Page last updated: 2024-08-17

methionine and Genetic Predisposition

methionine has been researched along with Genetic Predisposition in 302 studies

Research

Studies (302)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	10 (3.31)	18.2507
2000's	159 (52.65)	29.6817
2010's	123 (40.73)	24.3611
2020's	10 (3.31)	2.80

Authors

Authors	Studies
Abbas, AM; Alenazy, FO; Alhassan, HH; Davuljigari, CB; Elderdery, AY; Elkhalifa, AME; Mills, J; Shalabi, MG; Tebein, EM	1
Kuttner, CS; Lammert, F; Mancina, R; Stokes, CS; Wagenpfeil, G	1
Kumar, P; Rai, V	1
Akolkar, B; Butterworth, MD; Fan, S; Fiehn, O; Hagopian, W; Krischer, JP; Lernmark, Å; Li, Q; Parikh, H; Rewers, M; She, JX; Toppari, J; Ziegler, AG	1
Bogunia-Kubik, K; Bugaj, B; Dratwa, M; Iwaszko, M; Jeka, S; Kolossa, K; Korman, L; Świerkot, J; Wiland, P; Wysoczańska, B	1
Abed, S; Azoulay, D; Bashkin, A; Kaykov, E; Nodelman, M; Sfadi, A; Shaoul, E; Shehadeh, M; Sheleg, O	1
González-Hormazábal, P; Leiva, N; Pantoja, R; Pardo, R; Recabarren, AS; Recabarren, PA; Salamanca, C; Suazo, J	1
Abbasi, S; Abd El-Wahab, A; Abdallah, M; Abebe, G; Aca-Aca, G; Adama, S; Adefegha, SA; Adidigue-Ndiome, R; Adiseshaiah, P; Adrario, E; Aghajanian, C; Agnese, W; Ahmad, A; Ahmad, I; Ahmed, MFE; Akcay, OF; Akinmoladun, AC; Akutagawa, T; Alakavuklar, MA; Álava-Rabasa, S; Albaladejo-Florín, MJ; Alexandra, AJE; Alfawares, R; Alferiev, IS; Alghamdi, HS; Ali, I; Allard, B; Allen, JD; Almada, E; Alobaid, A; Alonso, GL; Alqahtani, YS; Alqarawi, W; Alsaleh, H; Alyami, BA; Amaral, BPD; Amaro, JT; Amin, SAW; Amodio, E; Amoo, ZA; Andia Biraro, I; Angiolella, L; Anheyer, D; Anlay, DZ; Annex, BH; Antonio-Aguirre, B; Apple, S; Arbuznikov, AV; Arinsoy, T; Armstrong, DK; Ash, S; Aslam, M; Asrie, F; Astur, DC; Atzrodt, J; Au, DW; Aucoin, M; Auerbach, EJ; Azarian, S; Ba, D; Bai, Z; Baisch, PRM; Balkissou, AD; Baltzopoulos, V; Banaszewski, M; Banerjee, S; Bao, Y; Baradwan, A; Barandika, JF; Barger, PM; Barion, MRL; Barrett, CD; Basudan, AM; Baur, LE; Baz-Rodríguez, SA; Beamer, P; Beaulant, A; Becker, DF; Beckers, C; Bedel, J; Bedlack, R; Bermúdez de Castro, JM; Berry, JD; Berthier, C; Bhattacharya, D; Biadgo, B; Bianco, G; Bianco, M; Bibi, S; Bigliardi, AP; Billheimer, D; Birnie, DH; Biswas, K; Blair, HC; Bognetti, P; Bolan, PJ; Bolla, JR; Bolze, A; Bonnaillie, P; Borlimi, R; Bórquez, J; Bottari, NB; Boulleys-Nana, JR; Brighetti, G; Brodeur, GM; Budnyak, T; Budnyk, S; Bukirwa, VD; Bulman, DM; Burm, R; Busman-Sahay, K; Butcher, TW; Cai, C; Cai, H; Cai, L; Cairati, M; Calvano, CD; Camacho-Ordóñez, A; Camela, E; Cameron, T; Campbell, BS; Cansian, RL; Cao, Y; Caporale, AS; Carciofi, AC; Cardozo, V; Carè, J; Carlos, AF; Carozza, R; Carroll, CJW; Carsetti, A; Carubelli, V; Casarotta, E; Casas, M; Caselli, G; Castillo-Lora, J; Cataldi, TRI; Cavalcante, ELB; Cavaleiro, A; Cayci, Z; Cebrián-Tarancón, C; Cedrone, E; Cella, D; Cereda, C; Ceretti, A; Ceroni, M; Cha, YH; Chai, X; Chang, EF; Chang, TS; Chanteux, H; Chao, M; Chaplin, BP; Chaturvedi, S; Chaturvedi, V; Chaudhary, DK; Chen, A; Chen, C; Chen, HY; Chen, J; Chen, JJ; Chen, K; Chen, L; Chen, Q; Chen, R; Chen, SY; Chen, TY; Chen, WM; Chen, X; Chen, Y; Cheng, G; Cheng, GJ; Cheng, J; Cheng, YH; Cheon, HG; Chew, KW; Chhoker, S; Chiu, WN; Choi, ES; Choi, MJ; Choi, SD; Chokshi, S; Chorny, M; Chu, KI; Chu, WJ; Church, AL; Cirrincione, A; Clamp, AR; Cleff, MB; Cohen, M; Coleman, RL; Collins, SL; Colombo, N; Conduit, N; Cong, WL; Connelly, MA; Connor, J; Cooley, K; Correa Ramos Leal, I; Cose, S; Costantino, C; Cottrell, M; Cui, L; Cundall, J; Cutaia, C; Cutler, CW; Cuypers, ML; da Silva Júnior, FMR; Dahal, RH; Damiani, E; Damtie, D; Dan-Li, W; Dang, Z; Dasa, SSK; Davin, A; Davis, DR; de Andrade, CM; de Jong, PL; de Oliveira, D; de Paula Dorigam, JC; Dean, A; Deepa, M; Delatour, C; Dell'Aiera, S; Delley, MF; den Boer, RB; Deng, L; Deng, Q; Depner, RM; Derdau, V; Derici, U; DeSantis, AJ; Desmarini, D; Diffo-Sonkoue, L; Divizia, M; Djenabou, A; Djordjevic, JT; Dobrovolskaia, MA; Domizi, R; Donati, A; Dong, Y; Dos Santos, M; Dos Santos, MP; Douglas, RG; Duarte, PF; Dullaart, RPF; Duscha, BD; Edwards, LA; Edwards, TE; Eichenwald, EC; El-Baba, TJ; Elashiry, M; Elashiry, MM; Elashry, SH; Elliott, A; Elsayed, R; Emerson, MS; Emmanuel, YO; Emory, TH; Endale-Mangamba, LM; Enten, GA; Estefanía-Fernández, K; Estes, JD; Estrada-Mena, FJ; Evans, S; Ezra, L; Faria de, RO; Farraj, AK; Favre, C; Feng, B; Feng, J; Feng, L; Feng, W; Feng, X; Feng, Z; Fernandes, CLF; Fernández-Cuadros, ME; Fernie, AR; Ferrari, D; Florindo, PR; Fong, PC; Fontes, EPB; Fontinha, D; Fornari, VJ; Fox, NP; Fu, Q; Fujitaka, Y; Fukuhara, K; Fumeaux, T; Fuqua, C; Fustinoni, S; Gabbanelli, V; Gaikwad, S; Gall, ET; Galli, A; Gancedo, MA; Gandhi, MM; Gao, D; Gao, K; Gao, M; Gao, Q; Gao, X; Gao, Y; Gaponenko, V; Garber, A; Garcia, EM; García-Campos, C; García-Donas, J; García-Pérez, AL; Gasparri, F; Ge, C; Ge, D; Ge, JB; Ge, X; George, I; George, LA; Germani, G; Ghassemi Tabrizi, S; Gibon, Y; Gillent, E; Gillies, RS; Gilmour, MI; Goble, S; Goh, JC; Goiri, F; Goldfinger, LE; Golian, M; Gómez, MA; Gonçalves, J; Góngora-García, OR; Gonul, I; González, MA; Govers, TM; Grant, PC; Gray, EH; Gray, JE; Green, MS; Greenwald, I; Gregory, MJ; Gretzke, D; Griffin-Nolan, RJ; Griffith, DC; Gruppen, EG; Guaita, A; Guan, P; Guan, X; Guerci, P; Guerrero, DT; Guo, M; Guo, P; Guo, R; Guo, X; Gupta, J; Guz, G; Hajizadeh, N; Hamada, H; Haman-Wabi, AB; Han, TT; Hannan, N; Hao, S; Harjola, VP; Harmon, M; Hartmann, MSM; Hartwig, JF; Hasani, M; Hawthorne, WJ; Haykal-Coates, N; Hazari, MS; He, DL; He, P; He, SG; Héau, C; Hebbar Kannur, K; Helvaci, O; Heuberger, DM; Hidalgo, F; Hilty, MP; Hirata, K; Hirsch, A; Hoffman, AM; Hoffmann, JF; Holloway, RW; Holmes, RK; Hong, S; Hongisto, M; Hopf, NB; Hörlein, R; Hoshino, N; Hou, Y; Hoven, NF; Hsieh, YY; Hsu, CT; Hu, CW; Hu, JH; Hu, MY; Hu, Y; Hu, Z; Huang, C; Huang, D; Huang, DQ; Huang, L; Huang, Q; Huang, R; Huang, S; Huang, SC; Huang, W; Huang, Y; Huffman, KM; Hung, CH; Hung, CT; Huurman, R; Hwang, SM; Hyun, S; Ibrahim, AM; Iddi-Faical, A; Immordino, P; Isla, MI; Jacquemond, V; Jacques, T; Jankowska, E; Jansen, JA; Jäntti, T; Jaque-Fernandez, F; Jarvis, GA; Jatt, LP; Jeon, JW; Jeong, SH; Jhunjhunwala, R; Ji, F; Jia, X; Jia, Y; Jian-Bo, Z; Jiang, GD; Jiang, L; Jiang, W; Jiang, WD; Jiang, Z; Jiménez-Hoyos, CA; Jin, S; Jobling, MG; John, CM; John, T; Johnson, CB; Jones, KI; Jones, WS; Joseph, OO; Ju, C; Judeinstein, P; Junges, A; Junnarkar, M; Jurkko, R; Kaleka, CC; Kamath, AV; Kang, X; Kantsadi, AL; Kapoor, M; Karim, Z; Kashuba, ADM; Kassa, E; Kasztura, M; Kataja, A; Katoh, T; Kaufman, JS; Kaupp, M; Kehinde, O; Kehrenberg, C; Kemper, N; Kerr, CW; Khan, AU; Khan, MF; Khan, ZUH; Khojasteh, SC; Kilburn, S; Kim, CG; Kim, DU; Kim, DY; Kim, HJ; Kim, J; Kim, OH; Kim, YH; King, C; Klein, A; Klingler, L; Knapp, AK; Ko, TK; Kodavanti, UP; Kolla, V; Kong, L; Kong, RY; Kong, X; Kore, S; Kortz, U; Korucu, B; Kovacs, A; Krahnert, I; Kraus, WE; Kuang, SY; Kuehn-Hajder, JE; Kurz, M; Kuśtrowski, P; Kwak, YD; Kyttaris, VC; Laga, SM; Laguerre, A; Laloo, A; Langaro, MC; Langham, MC; Lao, X; Larocca, MC; Lassus, J; Lattimer, TA; Lazar, S; Le, MH; Leal, DB; Leal, M; Leary, A; Ledermann, JA; Lee, JF; Lee, MV; Lee, NH; Leeds, CM; Leeds, JS; Lefrandt, JD; Leicht, AS; Leonard, M; Lev, S; Levy, K; Li, B; Li, C; Li, CM; Li, DH; Li, H; Li, J; Li, L; Li, LJ; Li, N; Li, P; Li, T; Li, X; Li, XH; Li, XQ; Li, XX; Li, Y; Li, Z; Li, ZY; Liao, YF; Lin, CC; Lin, MH; Lin, Y; Ling, Y; Links, TP; Lira-Romero, E; Liu, C; Liu, D; Liu, H; Liu, J; Liu, L; Liu, LP; Liu, M; Liu, T; Liu, W; Liu, X; Liu, XH; Liu, Y; Liuwantara, D; Ljumanovic, N; Lobo, L; Lokhande, K; Lopes, A; Lopes, RMRM; López-Gutiérrez, JC; López-Muñoz, MJ; López-Santamaría, M; Lorenzo, C; Lorusso, D; Losito, I; Lu, C; Lu, H; Lu, HZ; Lu, SH; Lu, SN; Lu, Y; Lu, ZY; Luboga, F; Luo, JJ; Luo, KL; Luo, Y; Lutomski, CA; Lv, W; M Piedade, MF; Ma, J; Ma, JQ; Ma, JX; Ma, N; Ma, P; Ma, S; Maciel, M; Madureira, M; Maganaris, C; Maginn, EJ; Mahnashi, MH; Maierhofer, M; Majetschak, M; Malla, TR; Maloney, L; Mann, DL; Mansuri, A; Marelli, E; Margulis, CJ; Marrella, A; Martin, BL; Martín-Francés, L; Martínez de Pinillos, M; Martínez-Navarro, EM; Martinez-Quintanilla Jimenez, D; Martínez-Velasco, A; Martínez-Villaseñor, L; Martinón-Torres, M; Martins, BA; Massongo, M; Mathew, AP; Mathews, D; Matsui, J; Matsumoto, KI; Mau, T; Maves, RC; Mayclin, SJ; Mayer, JM; Maynard, ND; Mayr, T; Mboowa, MG; McEvoy, MP; McIntyre, RC; McKay, JA; McPhail, MJW; McVeigh, AL; Mebazaa, A; Medici, V; Medina, DN; Mehmood, T; Mei-Li, C; Melku, M; Meloncelli, S; Mendes, GC; Mendoza-Velásquez, C; Mercadante, R; Mercado, MI; Merenda, MEZ; Meunier, J; Mi, SL; Michels, M; Mijatovic, V; Mikhailov, V; Milheiro, SA; Miller, DC; Ming, F; Mitsuishi, M; Miyashita, T; Mo, J; Mo, S; Modesto-Mata, M; Moeller, S; Monte, A; Monteiro, L; Montomoli, J; Moore, EE; Moore, HB; Moore, PK; Mor, MK; Moratalla-López, N; Moratilla Lapeña, L; Moreira, R; Moreno, MA; Mörk, AC; Morton, M; Mosier, JM; Mou, LH; Mougharbel, AS; Muccillo-Baisch, AL; Muñoz-Serrano, AJ; Mustafa, B; Nair, GM; Nakanishi, I; Nakanjako, D; Naraparaju, K; Nawani, N; Neffati, R; Neil, EC; Neilipovitz, D; Neira-Borrajo, I; Nelson, MT; Nery, PB; Nese, M; Nguyen, F; Nguyen, MH; Niazy, AA; Nicolaï, J; Nogueira, F; Norbäck, D; Novaretti, JV; O'Donnell, T; O'Dowd, A; O'Malley, DM; Oaknin, A; Ogata, K; Ohkubo, K; Ojha, M; Olaleye, MT; Olawande, B; Olomo, EJ; Ong, EWY; Ono, A; Onwumere, J; Ortiz Bibriesca, DM; Ou, X; Oza, AM; Ozturk, K; Özütemiz, C; Palacio-Pastrana, C; Palaparthi, A; Palevsky, PM; Pan, K; Pantanetti, S; Papachristou, DJ; Pariani, A; Parikh, CR; Parissis, J; Paroul, N; Parry, S; Patel, N; Patel, SM; Patel, VC; Pawar, S; Pefura-Yone, EW; Peixoto Andrade, BCO; Pelepenko, LE; Peña-Lora, D; Peng, S; Pérez-Moro, OS; Perez-Ortiz, AC; Perry, LM; Peter, CM; Phillips, NJ; Phillips, P; Pia Tek, J; Piner, LW; Pinto, EA; Pinto, SN; Piyachaturawat, P; Poka-Mayap, V; Polledri, E; Poloni, TE; Ponessa, G; Poole, ST; Post, AK; Potter, TM; Pressly, BB; Prouty, MG; Prudêncio, M; Pulkki, K; Pupier, C; Qian, H; Qian, ZP; Qiu, Y; Qu, G; Rahimi, S; Rahman, AU; Ramadan, H; Ramanna, S; Ramirez, I; Randolph, GJ; Rasheed, A; Rault, J; Raviprakash, V; Reale, E; Redpath, C; Rema, V; Remucal, CK; Remy, D; Ren, T; Ribeiro, LB; Riboli, G; Richards, J; Rieger, V; Rieusset, J; Riva, A; Rivabella Maknis, T; Robbins, JL; Robinson, CV; Roche-Campo, F; Rodriguez, R; Rodríguez-de-Cía, J; Rollenhagen, JE; Rosen, EP; Rub, D; Rubin, N; Rubin, NT; Ruurda, JP; Saad, O; Sabell, T; Saber, SE; Sabet, M; Sadek, MM; Saejio, A; Salinas, RM; Saliu, IO; Sande, D; Sang, D; Sangenito, LS; Santos, ALSD; Sarmiento Caldas, MC; Sassaroli, S; Sassi, V; Sato, J; Sauaia, A; Saunders, K; Saunders, PR; Savarino, SJ; Scambia, G; Scanlon, N; Schetinger, MR; Schinkel, AFL; Schladweiler, MC; Schofield, CJ; Schuepbach, RA; Schulz, J; Schwartz, N; Scorcella, C; Seeley, J; Seemann, F; Seinige, D; Sengoku, T; Seravalli, J; Sgromo, B; Shaheen, MY; Shan, L; Shanmugam, S; Shao, H; Sharma, S; Shaw, KJ; Shen, BQ; Shen, CH; Shen, P; Shen, S; Shen, Y; Shen, Z; Shi, J; Shi-Li, L; Shimoda, K; Shoji, Y; Shun, C; Silva, MA; Silva-Cardoso, J; Simas, NK; Simirgiotis, MJ; Sincock, SA; Singh, MP; Sionis, A; Siu, J; Sivieri, EM; Sjerps, MJ; Skoczen, SL; Slabon, A; Slette, IJ; Smith, MD; Smith, S; Smith, TG; Snapp, KS; Snow, SJ; Soares, MCF; Soberman, D; Solares, MD; Soliman, I; Song, J; Sorooshian, A; Sorrell, TC; Spinar, J; Staudt, A; Steinhart, C; Stern, ST; Stevens, DM; Stiers, KM; Stimming, U; Su, YG; Subbian, V; Suga, H; Sukhija-Cohen, A; Suksamrarn, A; Suksen, K; Sun, J; Sun, M; Sun, P; Sun, W; Sun, XF; Sun, Y; Sundell, J; Susan, LF; Sutjarit, N; Swamy, KV; Swisher, EM; Sykes, C; Takahashi, JA; Talmor, DS; Tan, B; Tan, ZK; Tang, L; Tang, S; Tanner, JJ; Tanwar, M; Tarazi, Z; Tarvasmäki, T; Tay, FR; Teketel, A; Temitayo, GI; Thersleff, T; Thiessen Philbrook, H; Thompson, LC; Thongon, N; Tian, B; Tian, F; Tian, Q; Timothy, AT; Tingle, MD; Titze, IR; Tolppanen, H; Tong, W; Toyoda, H; Tronconi, L; Tseng, CH; Tu, H; Tu, YJ; Tung, SY; Turpault, S; Tuynman, JB; Uemoto, AT; Ugurlu, M; Ullah, S; Underwood, RS; Ungell, AL; Usandizaga-Elio, I; Vakonakis, I; van Boxel, GI; van den Beucken, JJJP; van der Boom, T; van Slegtenhorst, MA; Vanni, JR; Vaquera, A; Vasconcellos, RS; Velayos, M; Vena, R; Ventura, G; Verso, MG; Vincent, RP; Vitale, F; Vitali, S; Vlek, SL; Vleugels, MPH; Volkmann, N; Vukelic, M; Wagner Mackenzie, B; Wairagala, P; Waller, SB; Wan, J; Wan, MT; Wan, Y; Wang, CC; Wang, H; Wang, J; Wang, JF; Wang, K; Wang, L; Wang, M; Wang, S; Wang, WM; Wang, X; Wang, Y; Wang, YD; Wang, YF; Wang, Z; Wang, ZG; Warriner, K; Weberpals, JI; Weerachayaphorn, J; Wehrli, FW; Wei, J; Wei, KL; Weinheimer, CJ; Weisbord, SD; Wen, S; Wendel Garcia, PD; Williams, JW; Williams, R; Winkler, C; Wirman, AP; Wong, S; Woods, CM; Wu, B; Wu, C; Wu, F; Wu, P; Wu, S; Wu, Y; Wu, YN; Wu, ZH; Wurtzel, JGT; Xia, L; Xia, Z; Xia, ZZ; Xiao, H; Xie, C; Xin, ZM; Xing, Y; Xing, Z; Xu, S; Xu, SB; Xu, T; Xu, X; Xu, Y; Xue, L; Xun, J; Yaffe, MB; Yalew, A; Yamamoto, S; Yan, D; Yan, H; Yan, S; Yan, X; Yang, AD; Yang, E; Yang, H; Yang, J; Yang, JL; Yang, K; Yang, M; Yang, P; Yang, Q; Yang, S; Yang, W; Yang, X; Yang, Y; Yao, JC; Yao, WL; Yao, Y; Yaqub, TB; Ye, J; Ye, W; Yen, CW; Yeter, HH; Yin, C; Yip, V; Yong-Yi, J; Yu, HJ; Yu, MF; Yu, S; Yu, W; Yu, WW; Yu, X; Yuan, P; Yuan, Q; Yue, XY; Zaia, AA; Zakhary, SY; Zalwango, F; Zamalloa, A; Zamparo, P; Zampini, IC; Zani, JL; Zeitoun, R; Zeng, N; Zenteno, JC; Zepeda-Palacio, C; Zhai, C; Zhang, B; Zhang, G; Zhang, J; Zhang, K; Zhang, Q; Zhang, R; Zhang, T; Zhang, X; Zhang, Y; Zhang, YY; Zhao, B; Zhao, D; Zhao, G; Zhao, H; Zhao, Q; Zhao, R; Zhao, S; Zhao, T; Zhao, X; Zhao, XA; Zhao, Y; Zhao, Z; Zheng, Z; Zhi-Min, G; Zhou, CL; Zhou, HD; Zhou, J; Zhou, W; Zhou, XQ; Zhou, Z; Zhu, C; Zhu, H; Zhu, L; Zhu, Y; Zitzmann, N; Zou, L; Zou, Y	1
Attar, R; Bar-Shira, A; Gana-Weisz, M; Giladi, N; Goldstein, O; Lederkremer, M; Mirelman, A; Orr-Urtreger, A; Shiner, T; Thaler, A	1
Barjola, P; Díaz-Gil, G; Écija, C; Fernandes-Magalhaes, R; Ferrera, D; Gómez-Esquer, F; Martínez-Iñigo, D; Mercado, F; Peláez, I	1
Bilgiç, B; Bonifati, V; Breedveld, GJ; Diler, Y; Doğan, T; Doğu, O; Elibol, B; Emre, M; Graafland, J; Gultekin, M; Hanagasi, HA; Kaleagasi, H; Kuipers, D; Olgiati, S; Quadri, M; Saka, E; Sünter, G; Sürmeli, R; Tufekcioglu, Z; Yalçın, AD	1
Badiali, S; Baselli, GA; Bassani, GA; Dongiovanni, P; Facciotti, F; Fargion, S; Gatti, S; Maggioni, M; Meroni, M; Pietrelli, A; Rametta, R; Trunzo, V; Valenti, L	1
Ariëns, RA; Auld, J; Bazzi, ZA; Boffa, MB; Gauld, JW; Gemin, M; Hegele, RA; Koschinsky, ML; Macrae, FL; McAiney, JT; Romagnuolo, R; Scipione, CA; Simard, DJ	1
Abaza, H; Ayari, F; Ben Chaaben, A; Benammar-Elgaaeid, A; Damak, T; Guemira, F; Harzallah, L; Kablouti, G; Lajnef, M; Ouni, N; Tamouza, R	1
Becquemont, L; Brailly-Tabard, S; Colle, R; Corruble, E; David, DJ; Falissard, B; Fève, B; Hardy, P; Trabado, S; Verstuyft, C	1
Danzi, BA; La Greca, AM	1
Hällfors, J; Kaprio, J; Korhonen, T; Loukola, A; Salomaa, V	1
Brown, BM; Castalanelli, N; Doecke, J; Laws, SM; Martins, RN; Peiffer, JJ; Rainey-Smith, SR; Sohrabi, HR; Weinborn, M	1
Jiang, SD; Pan, CD; Tan, LM; Tang, KY; Tang, MS; Wang, YC; Xiao, J; Yan, ZR; Zheng, ZJ; Zou, YB	1
Ahmadi, M; Behrouj, H; Dastghaib, S; Erfani, M; Hosseini, SV; Mokarram, P; Shamsdin, SA; Zamani, M	1
Atkinson, JH; Bush, WS; Ellis, RJ; Franklin, D; Keltner, J; Letendre, S; Umlauf, A; Xu, J	1
Dashti, S; Ghafouri-Fard, S; Keshtkar, A; Taherian-Esfahani, Z	1
Aurilia, C; Barbanti, P; De Marchis, ML; Della-Morte, D; Egeo, G; Fofi, L; Guadagni, F; Ialongo, C; Ludovici, G; Palmirotta, R	1
Akizu, N; Al-Tawari, A; Bastaki, L; Ben-Omran, T; Conlin, LK; da Gente, G; Deardorff, MA; Gabriel, S; Gleeson, JG; Horton, MA; Koul, R; Li, J; Nickerson, E; Rosti, RO; Scott, E; Shembesh, NM; Sherr, EH; Spencer, E; Zackai, EH; Zaki, MS	1
Bufferd, SJ; Dougherty, LR; Hayden, EP; Klein, DN; Kryski, KR; Sheikh, HI; Singh, SM; Smith, HJ	1
Kowalczyk, M; Kowalski, J; Kucia, K; Owczarek, A; Paul-Samojedny, M; Suchanek, R	1
Delaney, C; Hewagama, A; Hoeltzel, MF; Johnson, K; Mickelson, B; Richardson, BC; Sawalha, AH; Strickland, FM; Wu, A; Yung, R	1
Lv, J; You, T; Zhou, L	1
Abdelrahman, HM; Fattah, NR; Hashim, HM; Hassan, TH; Karam, RA; Mohammad, D; Rezk, NA	1
Gu, L; Liang, B; Qin, L; Su, L; Tan, J; Wei, H; Wu, G; Yan, Y	1
Anfossi, M; Bernardi, L; Bruni, AC; Clodomiro, A; Colao, R; Conidi, ME; Curcio, SA; Di Lorenzo, R; Frangipane, F; Gallo, M; Maletta, R; Mirabelli, M; Puccio, G; Smirne, N; Vasso, F	1
Boks, MP; Bruggeman, R; Cahn, W; de Haan, L; Joëls, M; Kahn, RS; Luykx, JJ; Meijer, CJ; Myin-Germeys, I; Ophoff, RA; Schubart, CD; Van Eijk, KR; Van Gastel, WA; van Os, J; Van Winkel, R; Vinkers, CH; Wiersma, D	1
Carmel, M; Chen, J; Frisch, A; Gothelf, D; Kolachana, B; Law, AJ; Lipska, BK; Michaelovsky, E; Ren-Patterson, R; Weinberger, DR; Weizman, A; Zarchi, O	1
Ambrosone, CB; Bandera, EV; Bovbjerg, DH; Chandran, U; Ciupak, G; Gong, Z; Hong, CC; Hwang, H; Jandorf, L; Khoury, T; Lu, Q; McCann, SE; Pawlish, K; Wiam, B; Zirpoli, G	1
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Hallmayer, J; Hill, SJ; Johnson, SL; Ketter, TA; Miller, S; Wang, PW	1
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Clarimon, J; Eerola, J; Hellström, O; Singleton, A; Tienari, PJ	1
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Cervenakova, L; Gajdusek, DC; Goldfarb, LG	1
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Fan, JB; Feng, GY; Gu, NF; He, L; Li, XW; St Clair, D; Sun, WW; Wang, HY; Zhang, CS	1
Jennings, CE; Owen, CJ; Pearce, SH; Wilson, V	1
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Barker, RA; Blackwell, AD; Foltynie, T; Goldberg, TE; Kolachana, BS; Lewis, SG; Robbins, TW; Weinberger, DR	1
Kawabe, M; Sakaue, M; Taniguchi, H	1
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Kaji, R; Kawakami, H; Kuno, S; Nishimura, M	1
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Fallin, MD; Gelernter, J; Schork, NJ; Stein, MB	1
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Glaser, B; Kirov, GK; MacGregor, S; Norton, N; O'Donovan, MC; Owen, MJ; Williams, HJ; Williams, NM; Zammit, S	1
Berrettini, WH; Dahl, JP; Ferraro, TN; Gallinat, J; Lohoff, FW; Sander, T	1
Alberch, J; Badenas, C; Canals, JM; Carrasco, JL; López, M; Milà, M; Muñoz, E	1
Mitchell, BD; O'Connell, JR; Pollin, TI; Shuldiner, AR; Steinle, NI	1
Borkowska, A; Hauser, J; Rybakowski, JK; Skibinska, M	1
Harrison, PJ; Tunbridge, EM; Weinberger, DR	1
Bell, DW; Brannigan, BW; Godin-Heymann, N; Gore, I; Haber, DA; Mohapatra, G; Mulloy, R; Okimoto, RA; Settleman, J; Sharma, SV; Sordella, R	1
Hong, CJ; Hwang, JP; Lirng, JF; Tsai, SJ; Yang, CH; Yang, YM	1
Han, DH; Kee, BS; Lee, YS; Lyoo, IK; Min, KJ; Na, C; Park, DB	1
Goldman, D; Lipsky, RH; Ryan, LM; Salazar, AM; Sparling, MB; Warden, DL; Xu, K	1
Baudry-Bluteau, D; Besson, C; Brousse, N; Junien, C; Landais, P; Macintyre, E; Niclot, S; Pruvot, Q; Salles, G; Savoy, D; Taupin, P; Varet, B	1
Jones, EM; Surewicz, K; Surewicz, WK	1
Fliessbach, K; Gärtner, J; Kemp, S; Kleijer, WJ; Klockgether, T; Köhler, W; Linnebank, M; Schlegel, U; Schmidt, S; Semmler, A; Sokolowski, P; van der Sterre, ML; Wanders, RJ; Wüllner, U	1
Antonarakis, SE; Dahoun, SP; Debbane, M; Eliez, S; Glaser, B; Hinard, C; Morris, MA	1
Buyan, N; Gönen, S; Hasanoğlu, E; Kalman, S; Misirlioğlu, M; Ozkaya, O; Söylemezoğlu, O; Tuncer, S	1
Bradwejn, J; Deckert, J; Deluca, V; Kennedy, JL; King, N; Koszycki, D; Macciardi, F; Rothe, C; Tharmalingam, S	1
Aono, M; Hongwei, S; Iga, J; Ishimoto, Y; Kameoka, N; Kaneda, Y; Kinouchi, S; Numata, S; Ohmori, T; Ohta, K; Shibuya-Tayoshi, S; Sumitani, S; Taniguchi, T; Tayoshi, S; Tomotake, M; Ueno, S; Yamauchi, K	1
Kim, CH; Kim, SJ; Kim, SY; Kim, YS; Lee, HS	1
Hagen, K; Pettersen, E; Skorpen, F; Stovner, LJ; Zwart, JA	1
Li, H; Lo, RY; Shyu, WC	1
Coppola, R; Egan, MF; Goldberg, TE; Kolachana, BS; Weinberger, DR; Winterer, G	1
Aziz, M; Habib, EE; Kotb, M	1
Bilbao, JR; Castaño, L; Echevarria, E; Galdos, P; Isusi, P; Krabbendam, L; Martin-Pagola, A; Papiol, S; Van Os, J	1
Archetti, S; Borroni, B; Caimi, L; Costanzi, C; Franzoni, S; Grassi, M; Padovani, A; Zanetti, M	1
Eichhammer, P; Hajak, G; Langguth, B; Sand, PG	1
Canestrelli, B; Castaldo, E; Gennarelli, M; Maj, M; Monteleone, P; Tortorella, A; Zanardini, R	1
Abbruzzese, G; Bellone, E; Cattaneo, E; Ciotti, P; Di Maria, E; Mandich, P; Marasco, A; Novelli, G; Tartari, M	1
Blom, HJ; den Heijer, M; Finnell, RH; Shaw, GM	1
Eberly, SW; Goldenberg, I; McNitt, S; Moss, AJ; Ryan, D; Zareba, W	1
Cortés, MJ; Gutiérrez-Zotes, A; Jariod, M; Labad, A; Martorell, L; Mulet, B; Pérez, M; Valero, J; Vilella, E	1
Gillis, T; Gusella, JF; Hakky, MM; Hayden, M; Kishikawa, S; Li, JL; MacDonald, ME; Myers, RH; Warby, S	1
Conceição, I; De Carvalho, M	1
Baig, BJ; Hall, J; Job, D; Johnstone, EC; Lawrie, SM; Lymer, GK; McIntosh, AM; Miller, P; Moorhead, TW; Owens, DG; Porteous, D; Whalley, HC	1
Borroni, B; Di Luca, M; Padovani, A	1
Grzywacz, A; Horodnicki, J; Jabłoński, M; Kucharska-Mazur, J; Pełka-Wysiecka, J; Rommelspacher, H; Sagan, L; Samochowiec, A; Samochowiec, J; Sznabowicz, M	1
Aguglia, U; Cittadella, R; Condino, F; Gambardella, A; La Russa, A; Labate, A; Le Piane, E; Manna, I; Quattrone, A	1
Park, Y; Rumba, I; Sanjeevi, CB; Sedimbi, SK; Shastry, A	1
Bratosiewicz-Wasik, J; Golanska, E; Jansen, GH; Liberski, PP; Wasik, TJ	1
Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J	1
Bajbouj, M; Gallinat, J; Hellweg, R; Lang, UE; Lohoff, FW; Sander, T; Winterer, G	1
Barnett, JH; Golding, J; Goldman, D; Heron, J; Jones, PB; Ring, SM; Xu, K	1
Chen, DF; Guo, S; Haile, CN; Kosten, TA; Kosten, TR; Sun, HQ; Wu, GY; Zhang, XY; Zhou, DF	1
Bassett, AS; Caluseriu, O; Chow, EW; Weksberg, R; Young, DA	1
de Cid, R; Estivill, X; González, JR; Gratacòs, M; Mercader, JM; Urretavizcaya, M	1
Caan, BJ; Curtin, K; Holubkov, R; Murtaugh, MA; Slattery, ML; Sweeney, C; Wolff, RK	1
Anselmetti, S; Bechi, M; Bosia, M; Cavallaro, R; Cocchi, F; Marino, E; Poletti, S; Smeraldi, E	1
Akisawa, N; Dong, H; Hirose, A; Iwasaki, S; Li, C; Nozaki, Y; Onishi, S; Ono, M; Saibara, T; Takahashi, M; Wang, J	1
Baghai, T; Bondy, B; Born, C; Bottlender, R; Frodl, T; Meisenzahl, EM; Möller, HJ; Reiser, M; Rupprecht, R; Schmitt, G; Schüle, C; Zill, P	1
O'Donovan, MC; Owen, MJ; Williams, HJ	1
Hosák, L	1
Chang, KH; Chao, CY; Chen, CM; Chen, IC; Chen, YC; Hu, FJ; Lee-Chen, GJ; Liu, YT; Lyu, RK; Wu, YR	1
Carracedo, A; Costas, J; Franco, N; Labad, A; Martorell, L; Roig, B; Valero, J; Vilella, E; Virgos, C	1
Kim, JM; Kim, SW; Kim, YH; Shin, IS; Stewart, R; Yang, SJ; Yoon, JS	1
de Groot, R; de Jongh, CE; Emonts, M; Hermans, PW; Houwing-Duistermaat, JJ; van Belkum, A; van Leeuwen, WB; Verbrugh, HA	1
Honmyo, R; Ishikawa, M; Kokaze, A; Masuda, Y; Matsunaga, N; Satoh, M; Takashima, Y; Teruya, K; Uchida, Y; Yoshida, M	1
Arolt, V; Baune, BT; Berger, K; Deckert, J; Domschke, K; Hohoff, C; Mortensen, S; Neumann, A; Roehrs, T	1
Dmitrzak-Weglarz, M; Hauser, J; Kramer, L; Rajewski, A; Rybakowski, F; Skibinska, M; Slopien, A; Szczepankiewicz, A	1
Busnello, JV; Cantor, RM; Deloukas, P; Licinio, J; Ribeiro, L; Whelan, F; Whittaker, P; Wong, ML	1
Cao, LY; Kosten, TA; Kosten, TR; Li, J; Lu, L; Tan, YL; Wang, ZR; Wu, GY; Zhang, XY; Zhou, DF	1
Apter, A; Burg, M; Carmel, M; Frisch, A; Gothelf, D; Inbar, D; Korostishevsky, M; Michaelovsky, E; Steinberg, T; Weizman, A	1
Hilt, LM; Nolen-Hoeksema, S; Sander, LC; Simen, AA	1
Horan, M; Jackson, A; Mayes, A; Miyajima, F; Ollier, W; Payton, A; Pendleton, N; Rabbitt, P; Thacker, N	1
Abrahamsen, B; Andersen, M; Balemans, W; Bathum, L; Beckers, S; Brasen, C; Brixen, K; Hagen, C; Nielsen, TL; Peeters, A; Piters, E; Van Hul, W; Wraae, K	1
Bermejo, JL; Gurzau, E; Hemminki, K; Koppova, K; Kumar, R; Rudnai, P; Scherer, D	1
Arranz, MJ; Carrasco-Marín, E; Crespo-Facorro, B; Leyva-Cobián, F; Mata, I; Pelayo-Terán, JM; Pérez-Iglesias, R; Vázquez-Barquero, JL	1
Silberschmidt, AL; Sponheim, SR	1
Bras, J; Calado, A; Dias, M; Guerreiro, R; Hardy, J; Januario, C; Morgadinho, A; Oliveira, C; Ribeiro, M; Semedo, C; Singleton, A	1
Bai, X; Liu, Z; Shu, C; Tang, J; Wang, G; Wang, H; Wang, X; Xiao, L	1
Caspi, A; Langley, K; Milne, B; Moffitt, TE; O'Donovan, M; Owen, MJ; Polo Tomas, M; Poulton, R; Rutter, M; Taylor, A; Thapar, A; Williams, B	1
Chen, CH; Chen, JY; Lai, IC; Liao, DL; Liou, YJ; Wang, LH; Wang, YC	1
Kawamura, Y; Kawasaki, Y; Kobayashi, S; Kurachi, M; Ozaki, N; Sasaoka, T; Seto, H; Suzuki, M; Takahashi, N; Takahashi, T; Tsuneki, H; Tsunoda, M; Zhou, SY	1
Bilbao, JR; Castaño, L; Echevarria, E; Galdos, P; Isusi, P; Krabbendam, L; Martin-Pagola, A; Mengelers, R; Myin-Germeys, I; Papiol, S; van Os, J; van Winkel, R	1
Ashton, K; Bartram, CR; Beesley, J; Brauch, H; Brüning, T; Bugert, P; Burwinkel, B; Chang-Claude, J; Chen, X; Chenevix-Trench, G; Dunning, AM; Easton, DF; Flesch-Janys, D; Fletcher, O; Frank, B; Hamann, U; Hemminki, K; Hopper, JL; Houlston, R; Johnson, N; Justenhoven, C; Kiechle, M; Ko, YD; Kropp, S; Meindl, A; Mutschelknauss, E; Peto, J; Pharoah, PP; Pooley, KA; Salazar, R; Schmutzler, RK; Silva, Idos S; Slanger, T; Spurdle, AB; Sutter, C; Wappenschmidt, B; Webb, E; Wiestler, M	1
Baccarelli, A; Cassano, PA; Litonjua, A; Park, SK; Schwartz, J; Sparrow, D; Suh, H; Vokonas, P	1
Hong, CJ; Hsieh, CH; Liou, YJ; Liu, ME; Tsai, SJ; Tsai, YL	1
Carrasco-Marin, E; Crespo-Facorro, B; Gonzalez-Blanch, C; Mata, I; Pelayo-Teran, JM; Perez-Iglesias, R; Rodríguez-Sanchez, JM; Vazquez-Barquero, JL	1
An, SS; Bukszar, J; Chen, X; Hettema, JM; Kendler, KS; Neale, MC; van den Oord, EJ	1
Linnebank, M; Moskau, S; Semmler, A; Simon, M	1
Hagino, H; Kawamura, Y; Kawasaki, Y; Kobayashi, S; Kurachi, M; Maeno, N; Niu, L; Ozaki, N; Sasaoka, T; Seto, H; Suzuki, M; Takahashi, N; Takahashi, T; Tsuneki, H; Tsunoda, M; Zhou, SY	1
Herzog, A; Herzog, AL; Marziniak, M; Mössner, R; Sommer, C	1
Buka, S; Cannon, TD; Torrey, EF; Yolken, R	1
Fan, J; Sklar, P	1
Bath, K; Chen, ZY; Hempstead, B; Lee, F; McEwen, B	1
Bóveda, MD; Castiñeiras, DE; Corrales, FJ; Couce, ML; Fraga, JM; Mora, MI; Mudd, SH	1
Kaminari, A; Leze, H; Mamuris, Z; Maridaki, H; Petsiava, E; Stathopoulos, C; Theotokis, P; Zifa, E	1
Kang, SS; Wong, PW	1
Arranz, M; Cai, G; Collier, DA; Curtis, D; Deng, H; Li, T; Liu, J; Liu, X; Murray, R; Vallada, H; Xu, K	1
Alatri, A; Franchi, F; Moia, M	1
Kitzler, H; Lampe, J; Lochmüller, H; Reichmann, H; Walter, MC	1
Cattaneo, M; Lecchi, A; Lombardi, R; Zighetti, ML	1
Albu, J; Allison, DB; Burn, P; Chin, W; Deng, N; Duprat, L; Fisher, SL; Franco, LS; Gu, W; Heymsfield, S; Kissebah, A; Kleyn, PW; Lee, J; Maruti, S; Nathan, J; Pi-Sunyer, FX; Tu, Z; Yagaloff, KA	1
Alders, D; de Jong, SC; Jakobs, C; Kostense, PJ; Pals, G; Rauwerda, JA; Stehouwer, CD; van den Berg, M	1
Akahoshi, M; Arinobu, Y; Inoue, H; Nagano, S; Nakashima, H; Niho, Y; Niiro, H; Ogami, E; Otsuka, T; Tanaka, Y; Yamaoka, K	1
Pyeritz, RE; Rogan, PK; von Kodolitsch, Y	1
Law, MR; Wald, NJ	1
Stehouwer, CD; van Guldener, C	1
Boers, GH; Naughten, ER; Wilcken, B; Wilcken, DE; Yap, S	1
Alpers, MP; Brown, P; Cervenáková, L; Gajdusek, DC; Garruto, RM; Goldfarb, LG; Lee, HS	1
Hashiramoto, M; Iwamoto, K; Kasuga, M; Maeda, E; Mori, H; Okazawa, H	1
Alvarez, L; An, W; Avila, MA; Chen, L; Corrales, FJ; Huang, ZZ; Kanel, G; Lu, SC; Mato, JM	1
Asakura, S; Hamajima, N; Kaba, S; Kagami, Y; Kondoh, E; Maeda, S; Matsuo, K; Morishima, Y; Nakamura, S; Ogura, M; Seto, M; Suzuki, R; Taji, H; Tajima, K	1
Andersen, PS; Bundgaard, H; Christiansen, M; Havndrup, O; Kjeldsen, K; Larsen, LA; Vuust, J	1
Allen, RH; Cottington, EM; LaMantia, C; Mudd, SH; Stabler, SP; Tangerman, A; Wagner, C; Zeisel, SH	1

Reviews

40 review(s) available for methionine and Genetic Predisposition

Article	Year
Catechol-O-methyltransferase gene Val158Met polymorphism and obsessive compulsive disorder susceptibility: a meta-analysis. Metabolic brain disease, 2020, Volume: 35, Issue:2 Topics: Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Methionine; Observational Studies as Topic; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Valine	2020
Zeitschrift fur Gesundheitswissenschaften = Journal of public health, 2022, Volume: 30, Issue:2 Topics: 3T3-L1 Cells; A Kinase Anchor Proteins; Acetates; Achilles Tendon; Acute Kidney Injury; Acute Pain; Acyclic Monoterpenes; Adenine Nucleotides; Adhesins, Escherichia coli; Adipocytes; Adipocytes, Brown; Adipogenesis; Administration, Inhalation; Administration, Oral; Adrenal Cortex Hormones; Adsorption; Adult; Aeromonas hydrophila; Africa; Aged; Aged, 80 and over; Agrobacterium tumefaciens; Air; Air Pollutants; Air Pollution; Air Pollution, Indoor; Algorithms; Alkaloids; Alkynes; Allosteric Regulation; Amines; Amino Acid Sequence; Amino Acids; Amino Acids, Branched-Chain; Aminoisobutyric Acids; Aminopyridines; Amyotrophic Lateral Sclerosis; Anaerobic Threshold; Angiography; Angiotensin II Type 1 Receptor Blockers; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Animal Distribution; Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Ankle Joint; Anti-Bacterial Agents; Anti-HIV Agents; Anti-Inflammatory Agents; Antibodies, Bacterial; Antifungal Agents; Antimalarials; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Antioxidants; Antiretroviral Therapy, Highly Active; Antiviral Agents; Aotidae; Apelin; Apoptosis; Arabidopsis Proteins; Argentina; Arginine; Artemisinins; Arthritis, Experimental; Arthritis, Rheumatoid; Arthroscopy; Aspergillus; Aspergillus niger; Asteraceae; Asthma; ATP Binding Cassette Transporter, Subfamily B, Member 1; ATP Binding Cassette Transporter, Subfamily G, Member 2; Auditory Cortex; Autoantibodies; Autophagy; Bacteria; Bacterial Infections; Bacterial Proteins; Bacterial Typing Techniques; Base Composition; Base Sequence; Basketball; Beclin-1; Benzhydryl Compounds; Benzimidazoles; Benzo(a)pyrene; Benzofurans; Benzoxazines; Bereavement; beta Catenin; beta-Lactamase Inhibitors; beta-Lactamases; beta-Lactams; Betacoronavirus; Betaine; Binding Sites; Biofilms; Biological Assay; Biological Availability; Biological Evolution; Biomarkers; Biomechanical Phenomena; Biopolymers; Biopsy; Bismuth; Blood Glucose; Blood Platelets; Blood Pressure; Body Composition; Body Weight; Bone Marrow; Bone Marrow Cells; Bone Regeneration; Boron; Botrytis; Brain Ischemia; Brain Neoplasms; Brain-Derived Neurotrophic Factor; Brazil; Breast Neoplasms; Breath Tests; Bronchoalveolar Lavage Fluid; Burkholderia; C-Reactive Protein; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Calcification, Physiologic; Calcium; Calcium Signaling; Calorimetry, Differential Scanning; Cameroon; Camptothecin; Candida; Candida albicans; Capillaries; Carbapenem-Resistant Enterobacteriaceae; Carbapenems; Carbohydrate Conformation; Carbon; Carbon Dioxide; Carbon Isotopes; Carcinoma, Ovarian Epithelial; Cardiac Output; Cardiomyopathy, Hypertrophic; Cardiotonic Agents; Cardiovascular Diseases; Caregivers; Carps; Case-Control Studies; Catalase; Catalysis; Cats; CD4 Lymphocyte Count; Cell Culture Techniques; Cell Differentiation; Cell Line, Tumor; Cell Membrane; Cell Movement; Cell Proliferation; Cell Survival; Cells, Cultured; Cellulose; Centrosome; Ceratopogonidae; Chickens; Child; China; Cholera Toxin; Choline; Cholinesterases; Chromatography, High Pressure Liquid; Chromatography, Liquid; Chromatography, Micellar Electrokinetic Capillary; Chromatography, Reverse-Phase; Chronic Disease; Cinnamates; Cities; Citrates; Climate Change; Clinical Trials, Phase III as Topic; Coal; Coal Mining; Cohort Studies; Coinfection; Colchicine; Colony Count, Microbial; Colorectal Neoplasms; Coloring Agents; Common Cold; Complement Factor H; Computational Biology; Computer Simulation; Continuous Positive Airway Pressure; Contrast Media; Coordination Complexes; Coronary Artery Bypass; Coronavirus 3C Proteases; Coronavirus Infections; Coronavirus Protease Inhibitors; Corynebacterium glutamicum; Cosmetics; COVID-19; Creatinine; Cross-Sectional Studies; Crotonates; Crystallography, X-Ray; Cues; Culicidae; Culture Media; Curcuma; Cyclopentanes; Cyclopropanes; Cymbopogon; Cystine; Cytochrome P-450 CYP2B6; Cytochrome P-450 CYP2C19; Cytochrome P-450 CYP2C19 Inhibitors; Cytokines; Databases, Genetic; Death; Dendritic Cells; Density Functional Theory; Depsides; Diabetes Mellitus, Type 2; Diamond; Diarylheptanoids; Dibenzofurans; Dibenzofurans, Polychlorinated; Diclofenac; Diet; Dietary Carbohydrates; Dietary Supplements; Diffusion Magnetic Resonance Imaging; Dioxins; Diphenylamine; Disease Outbreaks; Disease Susceptibility; Disulfides; Dithiothreitol; Dizocilpine Maleate; DNA Methylation; DNA-Binding Proteins; DNA, Bacterial; Dogs; Dose-Response Relationship, Drug; Double-Blind Method; Doublecortin Protein; Drosophila melanogaster; Droughts; Drug Carriers; Drug Combinations; Drug Delivery Systems; Drug Liberation; Drug Resistance; Drug Resistance, Bacterial; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Dust; Dynactin Complex; Dysferlin; Echo-Planar Imaging; Echocardiography; Edaravone; Egypt; Elasticity; Electrodes; Electrolytes; Emodin; Emtricitabine; Endometriosis; Endothelium, Vascular; Endotoxins; Energy Metabolism; Energy Transfer; Enterobacteriaceae; Enterococcus faecalis; Enterotoxigenic Escherichia coli; Environmental Monitoring; Enzyme Inhibitors; Epidemiologic Factors; Epigenesis, Genetic; Erythrocytes; Escherichia coli; Escherichia coli Infections; Escherichia coli Vaccines; Esophageal Neoplasms; Esophagectomy; Esophagogastric Junction; Esterases; Esterification; Ethanol; Ethiopia; Ethnicity; Eucalyptus; Evidence-Based Practice; Exercise; Exercise Tolerance; Extracorporeal Membrane Oxygenation; Family; Fatty Acids; Feedback; Female; Ferric Compounds; Fibrin Fibrinogen Degradation Products; Filtration; Fish Diseases; Flavonoids; Flavonols; Fluorodeoxyglucose F18; Follow-Up Studies; Food Microbiology; Food Preservation; Forests; Fossils; Free Radical Scavengers; Freund's Adjuvant; Fruit; Fungi; Gallium; Gender Identity; Gene Expression Regulation; Gene Expression Regulation, Neoplastic; Gene Expression Regulation, Plant; Gene Knockdown Techniques; Genes, Bacterial; Genes, Plant; Genetic Predisposition to Disease; Genitalia; Genotype; Glomerulonephritis, IGA; Glottis; Glucocorticoids; Glucose; Glucuronides; Glutathione Transferase; Glycogen Synthase Kinase 3 beta; Gram-Negative Bacterial Infections; Gram-Positive Bacterial Infections; Grassland; Guinea Pigs; Half-Life; Head Kidney; Heart Atria; Heart Rate; Heart Septum; HEK293 Cells; Hematopoietic Stem Cells; Hemodynamics; Hep G2 Cells; Hepacivirus; Hepatitis C; Hepatitis C, Chronic; Hepatocytes; Hesperidin; High-Frequency Ventilation; High-Temperature Requirement A Serine Peptidase 1; Hippocampus; Hirudins; History, 20th Century; History, 21st Century; HIV Infections; Homeostasis; Hominidae; Housing, Animal; Humans; Hydrocarbons, Brominated; Hydrogen Bonding; Hydrogen Peroxide; Hydrogen-Ion Concentration; Hydroxybutyrates; Hydroxyl Radical; Hypertension; Hypothyroidism; Image Interpretation, Computer-Assisted; Immunoconjugates; Immunogenic Cell Death; Indoles; Infant, Newborn; Infant, Premature; Infarction, Middle Cerebral Artery; Inflammation; Inflammation Mediators; Infrared Rays; Inhibitory Concentration 50; Injections, Intravenous; Interferon-gamma; Interleukin-23; Interleukin-4; Interleukin-6; Intermediate Filaments; Intermittent Claudication; Intestine, Small; Iridoid Glucosides; Iridoids; Iron; Isomerism; Isotope Labeling; Isoxazoles; Itraconazole; Kelch-Like ECH-Associated Protein 1; Ketoprofen; Kidney Failure, Chronic; Kinetics; Klebsiella pneumoniae; Lactams, Macrocyclic; Lactobacillus; Lactulose; Lakes; Lamivudine; Laparoscopy; Laparotomy; Laryngoscopy; Leucine; Limit of Detection; Linear Models; Lipid A; Lipopolysaccharides; Listeria monocytogenes; Liver; Liver Cirrhosis; Logistic Models; Longitudinal Studies; Losartan; Low Back Pain; Lung; Lupinus; Lupus Erythematosus, Systemic; Machine Learning; Macular Degeneration; Madin Darby Canine Kidney Cells; Magnetic Phenomena; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Magnetics; Malaria, Falciparum; Male; Mannans; MAP Kinase Signaling System; Mass Spectrometry; Melatonin; Membrane Glycoproteins; Membrane Proteins; Meniscectomy; Menisci, Tibial; Mephenytoin; Mesenchymal Stem Cells; Metal Nanoparticles; Metal-Organic Frameworks; Methionine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Nude; Mice, Obese; Mice, Transgenic; Microbial Sensitivity Tests; Microcirculation; MicroRNAs; Microscopy, Video; Microtubules; Microvascular Density; Microwaves; Middle Aged; Minimally Invasive Surgical Procedures; Models, Animal; Models, Biological; Models, Molecular; Models, Theoretical; Molecular Docking Simulation; Molecular Structure; Molecular Weight; Morus; Mouth Floor; Multicenter Studies as Topic; Multiple Sclerosis; Multiple Sclerosis, Relapsing-Remitting; Muscle, Skeletal; Myocardial Ischemia; Myocardium; NAD; NADP; Nanocomposites; Nanoparticles; Naphthols; Nasal Lavage Fluid; Nasal Mucosa; Neisseria meningitidis; Neoadjuvant Therapy; Neoplasm Invasiveness; Neoplasm Recurrence, Local; Neoplasms, Experimental; Neural Stem Cells; Neuroblastoma; Neurofilament Proteins; Neurogenesis; Neurons; New York; NF-E2-Related Factor 2; NF-kappa B; Nicotine; Nitriles; Nitrogen; Nitrogen Fixation; North America; Observer Variation; Occupational Exposure; Ochrobactrum; Oils, Volatile; Olea; Oligosaccharides; Omeprazole; Open Field Test; Optimism; Oregon; Oryzias; Osmolar Concentration; Osteoarthritis; Osteoblasts; Osteogenesis; Ovarian Neoplasms; Ovariectomy; Oxadiazoles; Oxidation-Reduction; Oxidative Stress; Oxygen; Ozone; p38 Mitogen-Activated Protein Kinases; Pakistan; Pandemics; Particle Size; Particulate Matter; Patient-Centered Care; Pelargonium; Peptides; Perception; Peripheral Arterial Disease; Peroxides; Pets; Pharmaceutical Preparations; Pharmacogenetics; Phenobarbital; Phenols; Phenotype; Phosphates; Phosphatidylethanolamines; Phosphines; Phospholipids; Phosphorus; Phosphorylation; Photoacoustic Techniques; Photochemotherapy; Photosensitizing Agents; Phylogeny; Phytoestrogens; Pilot Projects; Plant Components, Aerial; Plant Extracts; Plant Immunity; Plant Leaves; Plant Oils; Plants, Medicinal; Plasmodium berghei; Plasmodium falciparum; Platelet Activation; Platelet Function Tests; Pneumonia, Viral; Poaceae; Pogostemon; Poloxamer; Poly I; Poly(ADP-ribose) Polymerase Inhibitors; Polychlorinated Biphenyls; Polychlorinated Dibenzodioxins; Polycyclic Compounds; Polyethylene Glycols; Polylysine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Population Dynamics; Portasystemic Shunt, Transjugular Intrahepatic; Positron Emission Tomography Computed Tomography; Postoperative Complications; Postprandial Period; Potassium Cyanide; Predictive Value of Tests; Prefrontal Cortex; Pregnancy; Prepulse Inhibition; Prevalence; Procalcitonin; Prodrugs; Prognosis; Progression-Free Survival; Proline; Proof of Concept Study; Prospective Studies; Protein Binding; Protein Conformation; Protein Domains; Protein Folding; Protein Multimerization; Protein Sorting Signals; Protein Structure, Secondary; Proton Pump Inhibitors; Protozoan Proteins; Psychometrics; Pulse Wave Analysis; Pyridines; Pyrrolidines; Quality of Life; Quantum Dots; Quinoxalines; Quorum Sensing; Radiopharmaceuticals; Rain; Random Allocation; Randomized Controlled Trials as Topic; Rats; Rats, Sprague-Dawley; Rats, Wistar; RAW 264.7 Cells; Reactive Oxygen Species; Receptor, Angiotensin, Type 1; Receptor, PAR-1; Receptors, CXCR4; Receptors, Estrogen; Receptors, Glucocorticoid; Receptors, Interleukin-1; Receptors, Interleukin-17; Receptors, Notch; Recombinant Fusion Proteins; Recombinant Proteins; Reducing Agents; Reflex, Startle; Regional Blood Flow; Regression Analysis; Reperfusion Injury; Reproducibility of Results; Republic of Korea; Respiratory Tract Diseases; Retrospective Studies; Reverse Transcriptase Inhibitors; Rhinitis, Allergic; Risk Assessment; Risk Factors; Rituximab; RNA, Messenger; RNA, Ribosomal, 16S; ROC Curve; Rosmarinic Acid; Running; Ruthenium; Rutin; Sarcolemma; Sarcoma; Sarcopenia; Sarcoplasmic Reticulum; SARS-CoV-2; Scavenger Receptors, Class A; Schools; Seasons; Seeds; Sequence Analysis, DNA; Severity of Illness Index; Sex Factors; Shock, Cardiogenic; Short Chain Dehydrogenase-Reductases; Signal Transduction; Silver; Singlet Oxygen; Sinusitis; Skin; Skin Absorption; Small Molecule Libraries; Smoke; Socioeconomic Factors; Soil; Soil Microbiology; Solid Phase Extraction; Solubility; Solvents; Spain; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared; Speech; Speech Perception; Spindle Poles; Spleen; Sporothrix; Staphylococcal Infections; Staphylococcus aureus; Stereoisomerism; Stomach Neoplasms; Stress, Physiological; Stroke Volume; Structure-Activity Relationship; Substrate Specificity; Sulfonamides; Surface Properties; Surface-Active Agents; Surveys and Questionnaires; Survival Rate; T-Lymphocytes, Cytotoxic; Tandem Mass Spectrometry; Temperature; Tenofovir; Terpenes; Tetracycline; Tetrapleura; Textiles; Thermodynamics; Thiobarbituric Acid Reactive Substances; Thrombin; Thyroid Hormones; Thyroid Neoplasms; Tibial Meniscus Injuries; Time Factors; Tissue Distribution; Titanium; Toluidines; Tomography, X-Ray Computed; Tooth; Tramadol; Transcription Factor AP-1; Transcription, Genetic; Transfection; Transgender Persons; Translations; Treatment Outcome; Triglycerides; Ubiquinone; Ubiquitin-Specific Proteases; United Kingdom; United States; Up-Regulation; Vascular Stiffness; Veins; Ventricular Remodeling; Viral Load; Virulence Factors; Virus Replication; Vitis; Voice; Voice Quality; Wastewater; Water; Water Pollutants, Chemical; Water-Electrolyte Balance; Weather; Wildfires; Wnt Signaling Pathway; Wound Healing; X-Ray Diffraction; Xenograft Model Antitumor Assays; Young Adult; Zoogloea	2022
COMT Val158Met polymorphism and Parkinson's disease risk: a pooled analysis in different populations. Neurological research, 2019, Volume: 41, Issue:4 Topics: Catechol O-Methyltransferase; Databases, Bibliographic; Female; Genetic Predisposition to Disease; Global Health; Humans; Male; Methionine; Parkinson Disease; Polymorphism, Single Nucleotide; Valine	2019
Associations between XRCC3 Thr241Met polymorphisms and breast cancer risk: systematic-review and meta-analysis of 55 case-control studies. BMC medical genetics, 2019, 05-10, Volume: 20, Issue:1 Topics: Breast Neoplasms; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Homologous Recombination; Humans; Methionine; Polymorphism, Single Nucleotide; Threonine	2019
PON1 Q192R and L55M polymorphisms and organophosphate toxicity risk: a meta-analysis. DNA and cell biology, 2013, Volume: 32, Issue:5 Topics: Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Case-Control Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Methionine; Organophosphate Poisoning; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; White People	2013
AGT M235T polymorphisms and ischemic stroke risk: a meta-analysis. Journal of the neurological sciences, 2013, Aug-15, Volume: 331, Issue:1-2 Topics: Angiotensinogen; Asian People; Databases, Factual; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Ischemia; Methionine; Stroke; Threonine; White People	2013
Association of angiotensinogen gene M235T polymorphism with the risk of IgA nephropathy: a meta-analysis. Renal failure, 2014, Volume: 36, Issue:3 Topics: Alleles; Angiotensinogen; Asian People; Genetic Association Studies; Genetic Predisposition to Disease; Glomerulonephritis, IGA; Humans; Methionine; Polymorphism, Genetic; Risk Factors; Threonine; White People	2014
BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis. Movement disorders : official journal of the Movement Disorder Society, 2014, Volume: 29, Issue:8 Topics: Adult; Aged; Brain-Derived Neurotrophic Factor; Case-Control Studies; Dystonic Disorders; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Valine	2014
Meta-analysis study on the role of bone-derived neurotrophic factor Val66Met polymorphism in Parkinson's disease. Rejuvenation research, 2015, Volume: 18, Issue:1 Topics: Alleles; Brain-Derived Neurotrophic Factor; Case-Control Studies; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Methionine; Parkinson Disease; Polymorphism, Single Nucleotide; Regression Analysis; Valine	2015
Association between brain-derived neurotrophic factor genetic polymorphism Val66Met and susceptibility to bipolar disorder: a meta-analysis. BMC psychiatry, 2014, Dec-24, Volume: 14 Topics: Alleles; Amino Acid Substitution; Asian People; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Polymorphism, Genetic; Valine; White People	2014
Does BDNF Val66Met Polymorphism Confer Risk for Posttraumatic Stress Disorder? Neuropsychobiology, 2015, Volume: 71, Issue:3 Topics: Brain-Derived Neurotrophic Factor; Databases, Bibliographic; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Polymorphism, Single Nucleotide; Stress Disorders, Post-Traumatic; Valine	2015
Association Between X-Ray Cross-complementing Group 3 (XRCC3) Thr241Met Polymorphism and Risk of Thyroid Cancer: A Meta-Analysis. Medical science monitor : international medical journal of experimental and clinical research, 2015, Dec-21, Volume: 21 Topics: Amplified Fragment Length Polymorphism Analysis; DNA-Binding Proteins; Genetic Predisposition to Disease; Humans; Methionine; Threonine; Thyroid Neoplasms	2015
The association between COMT Val158Met polymorphism and migraine risk: A meta-analysis. Cephalalgia : an international journal of headache, 2017, Volume: 37, Issue:6 Topics: Catechol O-Methyltransferase; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Methionine; Migraine Disorders; Polymorphism, Single Nucleotide; Risk Factors; Valine	2017
Role of positron emission tomography imaging in Multiple Endocrine Neoplasia syndromes. Clinical physiology and functional imaging, 2018, Volume: 38, Issue:1 Topics: 5-Hydroxytryptophan; Biomarkers, Tumor; Dihydroxyphenylalanine; Ephedrine; Fluorodeoxyglucose F18; Genetic Predisposition to Disease; Humans; Methionine; Multiple Endocrine Neoplasia; Mutation; Phenotype; Positron-Emission Tomography; Predictive Value of Tests; Radiopharmaceuticals; Receptors, Somatostatin	2018
Potential Links between Impaired One-Carbon Metabolism Due to Polymorphisms, Inadequate B-Vitamin Status, and the Development of Alzheimer's Disease. Nutrients, 2016, Dec-10, Volume: 8, Issue:12 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Alzheimer Disease; Animals; Cystathionine beta-Synthase; Evidence-Based Medicine; Ferredoxin-NADP Reductase; Genetic Predisposition to Disease; Glycine Hydroxymethyltransferase; Humans; Hyperhomocysteinemia; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Models, Biological; Mutagenesis, Insertional; Nutrigenomics; Nutritional Status; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Tandem Repeat Sequences; Vitamin B Complex; Vitamin B Deficiency	2016
Animal models of NASH: getting both pathology and metabolic context right. Journal of gastroenterology and hepatology, 2008, Volume: 23, Issue:11 Topics: Animals; Choline Deficiency; Diet, Atherogenic; Dietary Fats; Disease Models, Animal; Disease Progression; Fatty Liver; Genetic Predisposition to Disease; Hyperphagia; Intubation, Gastrointestinal; Liver; Methionine; Overnutrition; Phenotype; Reproducibility of Results	2008
Meta-analysis of association between genetic variants in COMT and schizophrenia: an update. Schizophrenia research, 2009, Volume: 110, Issue:1-3 Topics: Adult; Case-Control Studies; Catechol O-Methyltransferase; Confidence Intervals; Databases, Bibliographic; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Japan; Male; Methionine; Middle Aged; Odds Ratio; Schizophrenia; Valine	2009
Sexually dimorphic effect of the Val66Met polymorphism of BDNF on susceptibility to Alzheimer's disease: New data and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2010, Jan-05, Volume: 153B, Issue:1 Topics: Aged; Alzheimer Disease; Base Sequence; Brain-Derived Neurotrophic Factor; Case-Control Studies; DNA Primers; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Sex Characteristics; Valine	2010
The ATF6-Met[67]Val substitution is associated with increased plasma cholesterol levels. Arteriosclerosis, thrombosis, and vascular biology, 2009, Volume: 29, Issue:9 Topics: Activating Transcription Factor 6; Amino Acid Substitution; Apolipoproteins B; Cardiovascular Diseases; Cholesterol; Cohort Studies; Endoplasmic Reticulum Chaperone BiP; Finland; Genetic Predisposition to Disease; Heat-Shock Proteins; HeLa Cells; Humans; Hyperlipidemia, Familial Combined; Membrane Glycoproteins; Methionine; Netherlands; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Risk Assessment; Transfection; Up-Regulation; Valine	2009
The COMT Met158 allele and violence in schizophrenia: a meta-analysis. Schizophrenia research, 2012, Volume: 140, Issue:1-3 Topics: Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; MEDLINE; Methionine; Polymorphism, Single Nucleotide; Schizophrenia; Schizophrenic Psychology; Valine; Violence	2012
No association between COMT Val158Met polymorphism and prostate cancer risk: a meta-analysis. Genetic testing and molecular biomarkers, 2013, Volume: 17, Issue:1 Topics: Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Male; Methionine; Polymorphism, Genetic; Prostatic Neoplasms; Risk Factors; Valine	2013
The association between the methionine/valine (M/V) polymorphism (rs1799990) in the PRNP gene and the risk of Alzheimer disease: an update by meta-analysis. Journal of the neurological sciences, 2013, Mar-15, Volume: 326, Issue:1-2 Topics: Alzheimer Disease; Case-Control Studies; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Methionine; Polymorphism, Genetic; Prion Proteins; Prions; Valine	2013
Epidemiologic studies of folate and colorectal neoplasia: a review. The Journal of nutrition, 2002, Volume: 132, Issue:8 Suppl Topics: Colorectal Neoplasms; Diet; Female; Folic Acid; Folic Acid Deficiency; Genetic Predisposition to Disease; Humans; Male; Methionine; Risk Factors	2002
[Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data]. Pathologie-biologie, 2003, Volume: 51, Issue:2 Topics: Animals; Arteriosclerosis; Biomarkers; Cystathionine beta-Synthase; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Models, Biological; Nitric Oxide; Oxidative Stress; Oxidoreductases Acting on CH-NH Group Donors; Rats; Risk Factors; S-Adenosylmethionine; Signal Transduction; Thrombophilia; Vascular Diseases; Vasodilation; Vitamin B 6 Deficiency	2003
Genetic variation in the epithelial sodium channel: a risk factor for hypertension in people of African origin. Advances in renal replacement therapy, 2004, Volume: 11, Issue:1 Topics: Amiloride; Black People; Diuretics; Epithelial Sodium Channels; Genetic Predisposition to Disease; Humans; Hypertension; London; Methionine; Polymorphism, Genetic; Risk Factors; Sodium Channels; Threonine	2004
Genetic studies in relation to kuru: an overview. Current molecular medicine, 2004, Volume: 4, Issue:4 Topics: Animals; Cattle; Creutzfeldt-Jakob Syndrome; Genetic Predisposition to Disease; Genotype; Humans; Kuru; Methionine; Papua New Guinea; Phenotype; Prions; Risk Factors	2004
Polymorphisms of the insertion / deletion ACE and M235T AGT genes and hypertension: surprising new findings and meta-analysis of data. BMC nephrology, 2005, Jan-11, Volume: 6 Topics: Adult; Aged; Angiotensinogen; Cross-Sectional Studies; DNA Transposable Elements; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Hypertension; Male; Methionine; Middle Aged; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Severity of Illness Index; Threonine	2005
Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis. Biological psychiatry, 2005, Jan-15, Volume: 57, Issue:2 Topics: Amino Acid Substitution; Asian People; Case-Control Studies; Catechol O-Methyltransferase; China; Female; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Humans; Male; Methionine; Polymorphism, Single Nucleotide; Schizophrenia; Valine	2005
[Polymorphisms of uncoupling protein-1 gene in type 2 diabetes]. Nihon rinsho. Japanese journal of clinical medicine, 2005, Volume: 63 Suppl 2 Topics: 5' Untranslated Regions; Alleles; Amino Acid Substitution; Animals; Carrier Proteins; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Humans; Ion Channels; Leucine; Membrane Proteins; Methionine; Mitochondrial Proteins; Mutation, Missense; Polymorphism, Genetic; Promoter Regions, Genetic; Uncoupling Protein 1	2005
Neural tube defects and folate: case far from closed. Nature reviews. Neuroscience, 2006, Volume: 7, Issue:9 Topics: Animals; Central Nervous System; Folic Acid; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Humans; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Neural Tube Defects	2006
Brain-derived neurotrophic factor Val66Met and psychiatric disorders: meta-analysis of case-control studies confirm association to substance-related disorders, eating disorders, and schizophrenia. Biological psychiatry, 2007, Apr-01, Volume: 61, Issue:7 Topics: Adult; Aged; Aged, 80 and over; Brain-Derived Neurotrophic Factor; Case-Control Studies; Feeding and Eating Disorders; Female; Genetic Predisposition to Disease; Humans; Male; Mental Disorders; Methionine; Middle Aged; Polymorphism, Genetic; Schizophrenia; Substance-Related Disorders; Valine	2007
Is COMT a susceptibility gene for schizophrenia? Schizophrenia bulletin, 2007, Volume: 33, Issue:3 Topics: Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 22; Dopamine; Genetic Predisposition to Disease; Humans; Methionine; Polymorphism, Genetic; Prefrontal Cortex; Schizophrenia; Valine	2007
Role of the COMT gene Val158Met polymorphism in mental disorders: a review. European psychiatry : the journal of the Association of European Psychiatrists, 2007, Volume: 22, Issue:5 Topics: Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Mental Disorders; Methionine; Phenotype; Polymorphism, Single Nucleotide; Social Environment; Valine	2007
Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis. Journal of the National Cancer Institute, 2008, Mar-19, Volume: 100, Issue:6 Topics: A Kinase Anchor Proteins; Adult; Aged; Alleles; Australia; Breast Neoplasms; Case-Control Studies; Cytoskeletal Proteins; Europe; Female; Genetic Predisposition to Disease; Germany; Humans; Isoleucine; Linkage Disequilibrium; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Research Design; Risk Assessment; Risk Factors; White People	2008
Genetics of bipolar disorder: focus on BDNF Val66Met polymorphism. Novartis Foundation symposium, 2008, Volume: 289 Topics: Amino Acid Substitution; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Case-Control Studies; Confidence Intervals; Genetic Predisposition to Disease; Genetic Variation; Humans; Meta-Analysis as Topic; Methionine; Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Valine	2008
Impact of genetic variant BDNF (Val66Met) on brain structure and function. Novartis Foundation symposium, 2008, Volume: 289 Topics: Amino Acid Substitution; Animals; Anxiety Disorders; Brain; Brain-Derived Neurotrophic Factor; Depressive Disorder; Genetic Predisposition to Disease; Genetic Variation; Growth Substances; Humans; Mental Disorders; Methionine; Mice; Mice, Transgenic; Polymorphism, Single Nucleotide; Psychotic Disorders; Valine	2008
Genetic and nongenetic factors for moderate hyperhomocyst(e)inemia. Atherosclerosis, 1996, Jan-26, Volume: 119, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Cystathionine beta-Synthase; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Phenotype; Prevalence; Risk Factors; Vascular Diseases	1996
Homocysteine and ischaemic heart disease. Haematologica, 1999, Volume: 84 Suppl EHA-4 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Case-Control Studies; Cohort Studies; Comorbidity; Cystathionine beta-Synthase; Female; Folic Acid; Genetic Predisposition to Disease; Homocysteine; Humans; Hyperhomocysteinemia; Male; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Myocardial Ischemia; Odds Ratio; Oxidoreductases Acting on CH-NH Group Donors; Retrospective Studies	1999
Hyperhomocysteinemia, vascular pathology, and endothelial dysfunction. Seminars in thrombosis and hemostasis, 2000, Volume: 26, Issue:3 Topics: Adult; Animals; Arteriosclerosis; Biomarkers; Blood Vessels; Cardiovascular Diseases; Carotid Stenosis; Child; Comorbidity; Coronary Angiography; Endothelium, Vascular; Female; Genetic Predisposition to Disease; Genotype; Homocystinuria; Humans; Hyperhomocysteinemia; Hyperplasia; Hypertension; Kidney Failure, Chronic; Male; Methionine; Middle Aged; Muscle, Smooth, Vascular; Nitric Oxide; Oxidative Stress; Prevalence; Rabbits; Rats; Vasodilation	2000
Vascular complications of severe hyperhomocysteinemia in patients with homocystinuria due to cystathionine beta-synthase deficiency: effects of homocysteine-lowering therapy. Seminars in thrombosis and hemostasis, 2000, Volume: 26, Issue:3 Topics: Adolescent; Adult; Aged; Australia; Child; Child, Preschool; Cohort Studies; Cystine; Drug Resistance; Female; Folic Acid; Follow-Up Studies; Genetic Predisposition to Disease; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Infant; Ireland; Male; Methionine; Middle Aged; Netherlands; Pyridoxine; Risk; Risk Factors; Thrombophilia; Vascular Diseases; Vitamin B 12	2000

Trials

8 trial(s) available for methionine and Genetic Predisposition

Article	Year
Four-Week Omega-3 Supplementation in Carriers of the Prosteatotic PNPLA3 p.I148M Genetic Variant: An Open-Label Study. Lifestyle genomics, 2019, Volume: 12, Issue:1-6 Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Dietary Supplements; Elasticity Imaging Techniques; Fatty Acids, Omega-3; Fatty Liver; Female; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Isoleucine; Lipase; Loss of Function Mutation; Male; Membrane Proteins; Methionine; Middle Aged; Non-alcoholic Fatty Liver Disease; Polymorphism, Single Nucleotide; Proteostasis; Time Factors; Young Adult	2019
Zeitschrift fur Gesundheitswissenschaften = Journal of public health, 2022, Volume: 30, Issue:2 Topics: 3T3-L1 Cells; A Kinase Anchor Proteins; Acetates; Achilles Tendon; Acute Kidney Injury; Acute Pain; Acyclic Monoterpenes; Adenine Nucleotides; Adhesins, Escherichia coli; Adipocytes; Adipocytes, Brown; Adipogenesis; Administration, Inhalation; Administration, Oral; Adrenal Cortex Hormones; Adsorption; Adult; Aeromonas hydrophila; Africa; Aged; Aged, 80 and over; Agrobacterium tumefaciens; Air; Air Pollutants; Air Pollution; Air Pollution, Indoor; Algorithms; Alkaloids; Alkynes; Allosteric Regulation; Amines; Amino Acid Sequence; Amino Acids; Amino Acids, Branched-Chain; Aminoisobutyric Acids; Aminopyridines; Amyotrophic Lateral Sclerosis; Anaerobic Threshold; Angiography; Angiotensin II Type 1 Receptor Blockers; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Animal Distribution; Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Ankle Joint; Anti-Bacterial Agents; Anti-HIV Agents; Anti-Inflammatory Agents; Antibodies, Bacterial; Antifungal Agents; Antimalarials; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Antioxidants; Antiretroviral Therapy, Highly Active; Antiviral Agents; Aotidae; Apelin; Apoptosis; Arabidopsis Proteins; Argentina; Arginine; Artemisinins; Arthritis, Experimental; Arthritis, Rheumatoid; Arthroscopy; Aspergillus; Aspergillus niger; Asteraceae; Asthma; ATP Binding Cassette Transporter, Subfamily B, Member 1; ATP Binding Cassette Transporter, Subfamily G, Member 2; Auditory Cortex; Autoantibodies; Autophagy; Bacteria; Bacterial Infections; Bacterial Proteins; Bacterial Typing Techniques; Base Composition; Base Sequence; Basketball; Beclin-1; Benzhydryl Compounds; Benzimidazoles; Benzo(a)pyrene; Benzofurans; Benzoxazines; Bereavement; beta Catenin; beta-Lactamase Inhibitors; beta-Lactamases; beta-Lactams; Betacoronavirus; Betaine; Binding Sites; Biofilms; Biological Assay; Biological Availability; Biological Evolution; Biomarkers; Biomechanical Phenomena; Biopolymers; Biopsy; Bismuth; Blood Glucose; Blood Platelets; Blood Pressure; Body Composition; Body Weight; Bone Marrow; Bone Marrow Cells; Bone Regeneration; Boron; Botrytis; Brain Ischemia; Brain Neoplasms; Brain-Derived Neurotrophic Factor; Brazil; Breast Neoplasms; Breath Tests; Bronchoalveolar Lavage Fluid; Burkholderia; C-Reactive Protein; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Calcification, Physiologic; Calcium; Calcium Signaling; Calorimetry, Differential Scanning; Cameroon; Camptothecin; Candida; Candida albicans; Capillaries; Carbapenem-Resistant Enterobacteriaceae; Carbapenems; Carbohydrate Conformation; Carbon; Carbon Dioxide; Carbon Isotopes; Carcinoma, Ovarian Epithelial; Cardiac Output; Cardiomyopathy, Hypertrophic; Cardiotonic Agents; Cardiovascular Diseases; Caregivers; Carps; Case-Control Studies; Catalase; Catalysis; Cats; CD4 Lymphocyte Count; Cell Culture Techniques; Cell Differentiation; Cell Line, Tumor; Cell Membrane; Cell Movement; Cell Proliferation; Cell Survival; Cells, Cultured; Cellulose; Centrosome; Ceratopogonidae; Chickens; Child; China; Cholera Toxin; Choline; Cholinesterases; Chromatography, High Pressure Liquid; Chromatography, Liquid; Chromatography, Micellar Electrokinetic Capillary; Chromatography, Reverse-Phase; Chronic Disease; Cinnamates; Cities; Citrates; Climate Change; Clinical Trials, Phase III as Topic; Coal; Coal Mining; Cohort Studies; Coinfection; Colchicine; Colony Count, Microbial; Colorectal Neoplasms; Coloring Agents; Common Cold; Complement Factor H; Computational Biology; Computer Simulation; Continuous Positive Airway Pressure; Contrast Media; Coordination Complexes; Coronary Artery Bypass; Coronavirus 3C Proteases; Coronavirus Infections; Coronavirus Protease Inhibitors; Corynebacterium glutamicum; Cosmetics; COVID-19; Creatinine; Cross-Sectional Studies; Crotonates; Crystallography, X-Ray; Cues; Culicidae; Culture Media; Curcuma; Cyclopentanes; Cyclopropanes; Cymbopogon; Cystine; Cytochrome P-450 CYP2B6; Cytochrome P-450 CYP2C19; Cytochrome P-450 CYP2C19 Inhibitors; Cytokines; Databases, Genetic; Death; Dendritic Cells; Density Functional Theory; Depsides; Diabetes Mellitus, Type 2; Diamond; Diarylheptanoids; Dibenzofurans; Dibenzofurans, Polychlorinated; Diclofenac; Diet; Dietary Carbohydrates; Dietary Supplements; Diffusion Magnetic Resonance Imaging; Dioxins; Diphenylamine; Disease Outbreaks; Disease Susceptibility; Disulfides; Dithiothreitol; Dizocilpine Maleate; DNA Methylation; DNA-Binding Proteins; DNA, Bacterial; Dogs; Dose-Response Relationship, Drug; Double-Blind Method; Doublecortin Protein; Drosophila melanogaster; Droughts; Drug Carriers; Drug Combinations; Drug Delivery Systems; Drug Liberation; Drug Resistance; Drug Resistance, Bacterial; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Dust; Dynactin Complex; Dysferlin; Echo-Planar Imaging; Echocardiography; Edaravone; Egypt; Elasticity; Electrodes; Electrolytes; Emodin; Emtricitabine; Endometriosis; Endothelium, Vascular; Endotoxins; Energy Metabolism; Energy Transfer; Enterobacteriaceae; Enterococcus faecalis; Enterotoxigenic Escherichia coli; Environmental Monitoring; Enzyme Inhibitors; Epidemiologic Factors; Epigenesis, Genetic; Erythrocytes; Escherichia coli; Escherichia coli Infections; Escherichia coli Vaccines; Esophageal Neoplasms; Esophagectomy; Esophagogastric Junction; Esterases; Esterification; Ethanol; Ethiopia; Ethnicity; Eucalyptus; Evidence-Based Practice; Exercise; Exercise Tolerance; Extracorporeal Membrane Oxygenation; Family; Fatty Acids; Feedback; Female; Ferric Compounds; Fibrin Fibrinogen Degradation Products; Filtration; Fish Diseases; Flavonoids; Flavonols; Fluorodeoxyglucose F18; Follow-Up Studies; Food Microbiology; Food Preservation; Forests; Fossils; Free Radical Scavengers; Freund's Adjuvant; Fruit; Fungi; Gallium; Gender Identity; Gene Expression Regulation; Gene Expression Regulation, Neoplastic; Gene Expression Regulation, Plant; Gene Knockdown Techniques; Genes, Bacterial; Genes, Plant; Genetic Predisposition to Disease; Genitalia; Genotype; Glomerulonephritis, IGA; Glottis; Glucocorticoids; Glucose; Glucuronides; Glutathione Transferase; Glycogen Synthase Kinase 3 beta; Gram-Negative Bacterial Infections; Gram-Positive Bacterial Infections; Grassland; Guinea Pigs; Half-Life; Head Kidney; Heart Atria; Heart Rate; Heart Septum; HEK293 Cells; Hematopoietic Stem Cells; Hemodynamics; Hep G2 Cells; Hepacivirus; Hepatitis C; Hepatitis C, Chronic; Hepatocytes; Hesperidin; High-Frequency Ventilation; High-Temperature Requirement A Serine Peptidase 1; Hippocampus; Hirudins; History, 20th Century; History, 21st Century; HIV Infections; Homeostasis; Hominidae; Housing, Animal; Humans; Hydrocarbons, Brominated; Hydrogen Bonding; Hydrogen Peroxide; Hydrogen-Ion Concentration; Hydroxybutyrates; Hydroxyl Radical; Hypertension; Hypothyroidism; Image Interpretation, Computer-Assisted; Immunoconjugates; Immunogenic Cell Death; Indoles; Infant, Newborn; Infant, Premature; Infarction, Middle Cerebral Artery; Inflammation; Inflammation Mediators; Infrared Rays; Inhibitory Concentration 50; Injections, Intravenous; Interferon-gamma; Interleukin-23; Interleukin-4; Interleukin-6; Intermediate Filaments; Intermittent Claudication; Intestine, Small; Iridoid Glucosides; Iridoids; Iron; Isomerism; Isotope Labeling; Isoxazoles; Itraconazole; Kelch-Like ECH-Associated Protein 1; Ketoprofen; Kidney Failure, Chronic; Kinetics; Klebsiella pneumoniae; Lactams, Macrocyclic; Lactobacillus; Lactulose; Lakes; Lamivudine; Laparoscopy; Laparotomy; Laryngoscopy; Leucine; Limit of Detection; Linear Models; Lipid A; Lipopolysaccharides; Listeria monocytogenes; Liver; Liver Cirrhosis; Logistic Models; Longitudinal Studies; Losartan; Low Back Pain; Lung; Lupinus; Lupus Erythematosus, Systemic; Machine Learning; Macular Degeneration; Madin Darby Canine Kidney Cells; Magnetic Phenomena; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Magnetics; Malaria, Falciparum; Male; Mannans; MAP Kinase Signaling System; Mass Spectrometry; Melatonin; Membrane Glycoproteins; Membrane Proteins; Meniscectomy; Menisci, Tibial; Mephenytoin; Mesenchymal Stem Cells; Metal Nanoparticles; Metal-Organic Frameworks; Methionine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Nude; Mice, Obese; Mice, Transgenic; Microbial Sensitivity Tests; Microcirculation; MicroRNAs; Microscopy, Video; Microtubules; Microvascular Density; Microwaves; Middle Aged; Minimally Invasive Surgical Procedures; Models, Animal; Models, Biological; Models, Molecular; Models, Theoretical; Molecular Docking Simulation; Molecular Structure; Molecular Weight; Morus; Mouth Floor; Multicenter Studies as Topic; Multiple Sclerosis; Multiple Sclerosis, Relapsing-Remitting; Muscle, Skeletal; Myocardial Ischemia; Myocardium; NAD; NADP; Nanocomposites; Nanoparticles; Naphthols; Nasal Lavage Fluid; Nasal Mucosa; Neisseria meningitidis; Neoadjuvant Therapy; Neoplasm Invasiveness; Neoplasm Recurrence, Local; Neoplasms, Experimental; Neural Stem Cells; Neuroblastoma; Neurofilament Proteins; Neurogenesis; Neurons; New York; NF-E2-Related Factor 2; NF-kappa B; Nicotine; Nitriles; Nitrogen; Nitrogen Fixation; North America; Observer Variation; Occupational Exposure; Ochrobactrum; Oils, Volatile; Olea; Oligosaccharides; Omeprazole; Open Field Test; Optimism; Oregon; Oryzias; Osmolar Concentration; Osteoarthritis; Osteoblasts; Osteogenesis; Ovarian Neoplasms; Ovariectomy; Oxadiazoles; Oxidation-Reduction; Oxidative Stress; Oxygen; Ozone; p38 Mitogen-Activated Protein Kinases; Pakistan; Pandemics; Particle Size; Particulate Matter; Patient-Centered Care; Pelargonium; Peptides; Perception; Peripheral Arterial Disease; Peroxides; Pets; Pharmaceutical Preparations; Pharmacogenetics; Phenobarbital; Phenols; Phenotype; Phosphates; Phosphatidylethanolamines; Phosphines; Phospholipids; Phosphorus; Phosphorylation; Photoacoustic Techniques; Photochemotherapy; Photosensitizing Agents; Phylogeny; Phytoestrogens; Pilot Projects; Plant Components, Aerial; Plant Extracts; Plant Immunity; Plant Leaves; Plant Oils; Plants, Medicinal; Plasmodium berghei; Plasmodium falciparum; Platelet Activation; Platelet Function Tests; Pneumonia, Viral; Poaceae; Pogostemon; Poloxamer; Poly I; Poly(ADP-ribose) Polymerase Inhibitors; Polychlorinated Biphenyls; Polychlorinated Dibenzodioxins; Polycyclic Compounds; Polyethylene Glycols; Polylysine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Population Dynamics; Portasystemic Shunt, Transjugular Intrahepatic; Positron Emission Tomography Computed Tomography; Postoperative Complications; Postprandial Period; Potassium Cyanide; Predictive Value of Tests; Prefrontal Cortex; Pregnancy; Prepulse Inhibition; Prevalence; Procalcitonin; Prodrugs; Prognosis; Progression-Free Survival; Proline; Proof of Concept Study; Prospective Studies; Protein Binding; Protein Conformation; Protein Domains; Protein Folding; Protein Multimerization; Protein Sorting Signals; Protein Structure, Secondary; Proton Pump Inhibitors; Protozoan Proteins; Psychometrics; Pulse Wave Analysis; Pyridines; Pyrrolidines; Quality of Life; Quantum Dots; Quinoxalines; Quorum Sensing; Radiopharmaceuticals; Rain; Random Allocation; Randomized Controlled Trials as Topic; Rats; Rats, Sprague-Dawley; Rats, Wistar; RAW 264.7 Cells; Reactive Oxygen Species; Receptor, Angiotensin, Type 1; Receptor, PAR-1; Receptors, CXCR4; Receptors, Estrogen; Receptors, Glucocorticoid; Receptors, Interleukin-1; Receptors, Interleukin-17; Receptors, Notch; Recombinant Fusion Proteins; Recombinant Proteins; Reducing Agents; Reflex, Startle; Regional Blood Flow; Regression Analysis; Reperfusion Injury; Reproducibility of Results; Republic of Korea; Respiratory Tract Diseases; Retrospective Studies; Reverse Transcriptase Inhibitors; Rhinitis, Allergic; Risk Assessment; Risk Factors; Rituximab; RNA, Messenger; RNA, Ribosomal, 16S; ROC Curve; Rosmarinic Acid; Running; Ruthenium; Rutin; Sarcolemma; Sarcoma; Sarcopenia; Sarcoplasmic Reticulum; SARS-CoV-2; Scavenger Receptors, Class A; Schools; Seasons; Seeds; Sequence Analysis, DNA; Severity of Illness Index; Sex Factors; Shock, Cardiogenic; Short Chain Dehydrogenase-Reductases; Signal Transduction; Silver; Singlet Oxygen; Sinusitis; Skin; Skin Absorption; Small Molecule Libraries; Smoke; Socioeconomic Factors; Soil; Soil Microbiology; Solid Phase Extraction; Solubility; Solvents; Spain; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared; Speech; Speech Perception; Spindle Poles; Spleen; Sporothrix; Staphylococcal Infections; Staphylococcus aureus; Stereoisomerism; Stomach Neoplasms; Stress, Physiological; Stroke Volume; Structure-Activity Relationship; Substrate Specificity; Sulfonamides; Surface Properties; Surface-Active Agents; Surveys and Questionnaires; Survival Rate; T-Lymphocytes, Cytotoxic; Tandem Mass Spectrometry; Temperature; Tenofovir; Terpenes; Tetracycline; Tetrapleura; Textiles; Thermodynamics; Thiobarbituric Acid Reactive Substances; Thrombin; Thyroid Hormones; Thyroid Neoplasms; Tibial Meniscus Injuries; Time Factors; Tissue Distribution; Titanium; Toluidines; Tomography, X-Ray Computed; Tooth; Tramadol; Transcription Factor AP-1; Transcription, Genetic; Transfection; Transgender Persons; Translations; Treatment Outcome; Triglycerides; Ubiquinone; Ubiquitin-Specific Proteases; United Kingdom; United States; Up-Regulation; Vascular Stiffness; Veins; Ventricular Remodeling; Viral Load; Virulence Factors; Virus Replication; Vitis; Voice; Voice Quality; Wastewater; Water; Water Pollutants, Chemical; Water-Electrolyte Balance; Weather; Wildfires; Wnt Signaling Pathway; Wound Healing; X-Ray Diffraction; Xenograft Model Antitumor Assays; Young Adult; Zoogloea	2022
COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:13 Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Central Nervous System Stimulants; Child; Cognition Disorders; Cross-Over Studies; DNA Mutational Analysis; Double-Blind Method; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Mental Processes; Methionine; Methylphenidate; Placebo Effect; Polymorphism, Genetic; Thinking; Valine	2008
Catechol-O-methyltransferase Val158Met polymorphism affects therapeutic response to mood stabilizer in symptomatic manic patients. Psychiatry research, 2010, Jan-30, Volume: 175, Issue:1-2 Topics: Adult; Antimanic Agents; Bipolar Disorder; Catechol O-Methyltransferase; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single-Stranded Conformational; Psychiatric Status Rating Scales; Retrospective Studies; Statistics, Nonparametric; Valine; Young Adult	2010
BDNF gene is a risk factor for schizophrenia in a Scottish population. Molecular psychiatry, 2005, Volume: 10, Issue:2 Topics: Adult; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Haplotypes; Humans; Linkage Disequilibrium; Methionine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Reference Values; Risk Factors; Schizophrenia; Scotland; Valine; White People	2005
Illness-specific association of val66met BDNF polymorphism with performance on Wisconsin Card Sorting Test in bipolar mood disorder. Molecular psychiatry, 2006, Volume: 11, Issue:2 Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Case-Control Studies; Female; Genetic Predisposition to Disease; Humans; Male; Memory, Short-Term; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Single Nucleotide; Prefrontal Cortex; Problem Solving; Reference Values; Severity of Illness Index; Valine	2006
A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val158Met genotype. Molecular psychiatry, 2006, Volume: 11, Issue:2 Topics: Amino Acid Substitution; Bipolar Disorder; Catechol O-Methyltransferase; Gene Expression; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Humans; Methionine; Polymorphism, Genetic; Prefrontal Cortex; Protein Isoforms; Schizophrenia; Valine	2006
Lack of influence of COMT Val158Met genotype on cognition in first-episode non-affective psychosis. Schizophrenia research, 2008, Volume: 102, Issue:1-3 Topics: Adult; Antipsychotic Agents; Catechol O-Methyltransferase; Cognition Disorders; Diagnostic and Statistical Manual of Mental Disorders; Female; Genetic Predisposition to Disease; Genotype; Humans; Longitudinal Studies; Male; Methionine; Neuropsychological Tests; Phenotype; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Schizophrenic Psychology; Valine	2008

Other Studies

255 other study(ies) available for methionine and Genetic Predisposition

Article	Year
Impact of Methionine Synthase Reductase Polymorphisms in Chronic Myeloid Leukemia Patients. Genes, 2022, Sep-26, Volume: 13, Issue:10 Topics: Ferredoxin-NADP Reductase; Folic Acid; Genetic Predisposition to Disease; Humans; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Methionine	2022
Longitudinal Metabolome-Wide Signals Prior to the Appearance of a First Islet Autoantibody in Children Participating in the TEDDY Study. Diabetes, 2020, Volume: 69, Issue:3 Topics: Alanine; Amino Acids, Branched-Chain; Autoantibodies; Child, Preschool; Dehydroascorbic Acid; Diabetes Mellitus, Type 1; Fatty Acids; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamate Decarboxylase; Humans; Infant; Infant, Newborn; Insulin Antibodies; Longitudinal Studies; Male; Metabolome; Methionine; Phosphatidylethanolamines; Prodromal Symptoms; Proline; Risk; Triglycerides	2020
Association of MICA-129Met/Val polymorphism with clinical outcome of anti-TNF therapy and MICA serum levels in patients with rheumatoid arthritis. The pharmacogenomics journal, 2020, Volume: 20, Issue:6 Topics: Aged; Antirheumatic Agents; Arthritis, Rheumatoid; Biomarkers; Cohort Studies; Female; Follow-Up Studies; Genetic Predisposition to Disease; Histocompatibility Antigens Class I; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Treatment Outcome; Tumor Necrosis Factor-alpha; Valine	2020
Low brain-derived neurotrophic factor protein levels and single-nucleotide polymorphism Val66Met are associated with peripheral neuropathy in type II diabetic patients. Acta diabetologica, 2020, Volume: 57, Issue:7 Topics: Adult; Aged; Amino Acid Substitution; Biomarkers; Brain-Derived Neurotrophic Factor; Case-Control Studies; Diabetes Mellitus, Type 2; Diabetic Neuropathies; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Peripheral Nervous System Diseases; Polymorphism, Single Nucleotide; Valine	2020
Genetic variants in S-adenosyl-methionine synthesis pathway and nonsyndromic cleft lip with or without cleft palate in Chile. Pediatric research, 2021, Volume: 89, Issue:4 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adenosylhomocysteinase; Alleles; Chile; Cleft Lip; Cleft Palate; Female; Ferredoxin-NADP Reductase; Gene Frequency; Genes, Dominant; Genes, Recessive; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Male; Methionine; Methionine Adenosyltransferase; Odds Ratio; Polymorphism, Single Nucleotide; S-Adenosylmethionine	2021
The GBA-370Rec Parkinson's disease risk haplotype harbors a potentially pathogenic variant in the mitochondrial gene SLC25A44. Molecular genetics and metabolism, 2021, Volume: 133, Issue:1 Topics: Alleles; Amino Acid Transport Systems; Female; Genetic Predisposition to Disease; Genome, Human; Genotype; Haplotypes; Heterozygote; Humans; Jews; Male; Methionine; Mitochondria; Mitochondrial Proteins; Mutation; Parkinson Disease; Risk Factors; Solute Carrier Proteins; Whole Genome Sequencing	2021
Fear of pain moderates the relationship between self-reported fatigue and methionine allele of catechol-O-methyltransferase gene in patients with fibromyalgia. PloS one, 2021, Volume: 16, Issue:4 Topics: Adult; Aged; Alleles; Catechol O-Methyltransferase; Fatigue; Fear; Female; Fibromyalgia; Genetic Predisposition to Disease; Humans; Methionine; Middle Aged; Pain; Self Report	2021
The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN. Parkinsonism & related disorders, 2017, Volume: 39 Topics: Adolescent; Adult; Child; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Methionine; Mitochondrial Proteins; Mutation; Neurodegenerative Diseases; Threonine; Turkey; Young Adult	2017
Insulin resistance promotes Lysyl Oxidase Like 2 induction and fibrosis accumulation in non-alcoholic fatty liver disease. Clinical science (London, England : 1979), 2017, 06-01, Volume: 131, Issue:12 Topics: Amino Acid Oxidoreductases; Animals; Cell Proliferation; Cell Transdifferentiation; Cells, Cultured; Choline Deficiency; Diabetes Mellitus, Type 2; Disease Models, Animal; Enzyme Induction; Extracellular Matrix; Forkhead Box Protein O1; Genetic Predisposition to Disease; Hepatic Stellate Cells; Hepatocytes; Humans; Insulin Resistance; Liver; Liver Cirrhosis; Methionine; Mice, Inbred C57BL; Mice, Knockout; Non-alcoholic Fatty Liver Disease; Phenotype; Receptor, Insulin; Signal Transduction	2017
Characterization of the I4399M variant of apolipoprotein(a): implications for altered prothrombotic properties of lipoprotein(a). Journal of thrombosis and haemostasis : JTH, 2017, Volume: 15, Issue:9 Topics: Adult; Apoprotein(a); Blood Coagulation; Female; Fibrin; Fibrinolysis; Genetic Predisposition to Disease; HEK293 Cells; Homozygote; Humans; Lipoprotein(a); Male; Methionine; Middle Aged; Molecular Dynamics Simulation; Oxidation-Reduction; Phenotype; Polymorphism, Single Nucleotide; Protein Conformation; Recombinant Proteins; Structure-Activity Relationship; Thrombosis; Transfection	2017
MICA-129Met/Val Polymorphism Is Associated with Early-Onset Breast Cancer Risk. Immunological investigations, 2017, Volume: 46, Issue:6 Topics: Adult; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Histocompatibility Antigens Class I; Humans; Methionine; Middle Aged; Polymorphism, Genetic; Risk; Tunisia; Valine	2017
Plasma BDNF Level in Major Depression: Biomarker of the Val66Met BDNF Polymorphism and of the Clinical Course in Met Carrier Patients. Neuropsychobiology, 2017, Volume: 75, Issue:1 Topics: Adult; Analysis of Variance; Brain-Derived Neurotrophic Factor; Depressive Disorder, Major; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Valine; White People	2017
Genetic pathways to posttraumatic stress disorder and depression in children: Investigation of catechol-O-methyltransferase (COMT) Val158Met using different PTSD diagnostic models. Journal of psychiatric research, 2018, Volume: 102 Topics: Alleles; Catechol O-Methyltransferase; Child; Depression; Disasters; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Polymorphism, Genetic; Psychiatric Status Rating Scales; Stress Disorders, Post-Traumatic; Valine	2018
Is Brain-Derived Neurotrophic Factor Associated With Smoking Initiation? Replication Using a Large Finnish Population Sample. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco, 2020, 02-06, Volume: 22, Issue:2 Topics: Adult; Aged; Behavior, Addictive; Brain-Derived Neurotrophic Factor; Depressive Disorder; Female; Finland; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Population Surveillance; Tobacco Smoking; Valine; Young Adult	2020
Influence of BDNF Val66Met on the relationship between cardiorespiratory fitness and memory in cognitively normal older adults. Behavioural brain research, 2019, 04-19, Volume: 362 Topics: Aged; Aged, 80 and over; Aging; Brain-Derived Neurotrophic Factor; Cardiorespiratory Fitness; Cognition; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Memory, Episodic; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Single Nucleotide	2019
BDNF Val66Met genetic variation and its plasma level in patients with morbid obesity: A case-control study. Gene, 2019, Jul-15, Volume: 705 Topics: Adult; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; Case-Control Studies; Down-Regulation; Female; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Iran; Male; Methionine; Middle Aged; Obesity, Morbid; Polymorphism, Restriction Fragment Length; Sequence Analysis, DNA; Valine	2019
Catechol-O-methyltransferase polymorphism Val158Met is associated with distal neuropathic pain in HIV-associated sensory neuropathy. AIDS (London, England), 2019, 08-01, Volume: 33, Issue:10 Topics: Adult; AIDS-Associated Nephropathy; Amino Acid Substitution; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genotype; Genotyping Techniques; HIV Infections; Humans; Male; Methionine; Middle Aged; Neuralgia; Polymorphism, Single Nucleotide; Prospective Studies; United States; Valine	2019
Prion protein gene M129V polymorphism and variability in age at migraine onset. Headache, 2013, Volume: 53, Issue:3 Topics: Adult; Age of Onset; Aged; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Migraine Disorders; Polymorphism, Genetic; Prions; Retrospective Studies; Statistics as Topic; Valine	2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia. American journal of human genetics, 2013, Mar-07, Volume: 92, Issue:3 Topics: Agenesis of Corpus Callosum; Amino Acid Sequence; Cerebral Cortex; Codon; Corpus Callosum; Exome; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Molecular Sequence Data; Mutation; Sequence Analysis, DNA	2013
Catechol-O-methyltransferase gene val158met polymorphism and depressive symptoms during early childhood. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2013, Volume: 162B, Issue:3 Topics: Alleles; Anxiety; Catechol O-Methyltransferase; Child, Preschool; Depression; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Male; Methionine; Polymorphism, Genetic; Valine	2013
BDNF val66met polymorphism is associated with age at onset and intensity of symptoms of paranoid schizophrenia in a Polish population. The Journal of neuropsychiatry and clinical neurosciences, 2013,Winter, Volume: 25, Issue:1 Topics: Adult; Age of Onset; Analysis of Variance; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Poland; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Schizophrenia, Paranoid; Sex Factors; Valine	2013
Diet influences expression of autoimmune-associated genes and disease severity by epigenetic mechanisms in a transgenic mouse model of lupus. Arthritis and rheumatism, 2013, Volume: 65, Issue:7 Topics: Animals; Antibodies, Antinuclear; Betaine; CD40 Ligand; Choline; Coenzymes; Diet; Disease Models, Animal; DNA (Cytosine-5-)-Methyltransferase 1; DNA (Cytosine-5-)-Methyltransferases; DNA Methylation; Epigenesis, Genetic; Folic Acid; Gene Silencing; Genetic Predisposition to Disease; Lupus Erythematosus, Systemic; Methionine; Mice; Mice, Inbred C57BL; Mice, Transgenic; Micronutrients; Riboflavin; Vitamin B 12; Vitamin B 6; Zinc	2013
Catechol-O-methyltransferase Val158Met polymorphism and hyperactivity symptoms in Egyptian children with autism spectrum disorder. Research in developmental disabilities, 2013, Volume: 34, Issue:7 Topics: Case-Control Studies; Catechol O-Methyltransferase; Child; Child Development Disorders, Pervasive; Egypt; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Valine	2013
Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation. Journal of Alzheimer's disease : JAD, 2013, Volume: 37, Issue:2 Topics: Adult; Age of Onset; Alzheimer Disease; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Membrane Transport Proteins; Memory Disorders; Methionine; Middle Aged; Mitochondrial Precursor Protein Import Complex Proteins; Mutation; Neuropsychological Tests; Polymorphism, Genetic; Presenilin-1	2013
The effect of childhood maltreatment and cannabis use on adult psychotic symptoms is modified by the COMT Val¹⁵⁸Met polymorphism. Schizophrenia research, 2013, Volume: 150, Issue:1 Topics: Adolescent; Adult; Catechol O-Methyltransferase; Child; Child Abuse; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Humans; Male; Marijuana Abuse; Methionine; Multivariate Analysis; Polymorphism, Single Nucleotide; Psychotic Disorders; Surveys and Questionnaires; Valine; Young Adult	2013
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome. Biological psychiatry, 2014, Mar-01, Volume: 75, Issue:5 Topics: Adolescent; Adult; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Chromosome Deletion; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Methionine; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult	2014
Associations of dietary folate, Vitamins B6 and B12 and methionine intake with risk of breast cancer among African American and European American women. International journal of cancer, 2014, Mar-15, Volume: 134, Issue:6 Topics: Adolescent; Adult; Black or African American; Breast Neoplasms; Case-Control Studies; Diet; Female; Folic Acid; Follow-Up Studies; Genetic Predisposition to Disease; Humans; Methionine; Middle Aged; Neoplasm Staging; Premenopause; Prognosis; Receptors, Estrogen; Receptors, Progesterone; Risk Factors; Vitamin B 12; Vitamin B 6; Vitamins; White People; Young Adult	2014
BDNF Val66Met modifies the risk of childhood trauma on obsessive-compulsive disorder. Journal of psychiatric research, 2013, Volume: 47, Issue:12 Topics: Adolescent; Adult; Aged; Brain-Derived Neurotrophic Factor; Child; Child Abuse; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Linear Models; Male; Methionine; Middle Aged; Obsessive-Compulsive Disorder; Surveys and Questionnaires; Valine; Young Adult	2013
Brain-derived neurotrophic factor Val66Met polymorphism and cognitive function in persons with cardiovascular disease. Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society, 2013, Volume: 13, Issue:4 Topics: Aged; Aged, 80 and over; Alleles; Attention; Brain; Brain-Derived Neurotrophic Factor; Cardiovascular Diseases; Cognition; Cognition Disorders; Female; Genetic Markers; Genetic Predisposition to Disease; Geriatric Assessment; Humans; Male; Memory; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Genetic; Valine	2013
Catechol-O-methyltransferase Val158Met polymorphism (rs4680) is associated with pain in multiple sclerosis. The journal of pain, 2013, Volume: 14, Issue:12 Topics: Adult; Alleles; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Multiple Sclerosis; Pain; Pain Measurement; Polymorphism, Single Nucleotide; Risk Factors; Single-Blind Method; Valine	2013
Genetic variants of homocysteine metabolism and multiple sclerosis: a case-control study. Neuroscience letters, 2014, Mar-06, Volume: 562 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Case-Control Studies; Cystathionine beta-Synthase; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Homocysteine; Humans; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Multiple Sclerosis; Polymorphism, Genetic; S-Adenosylmethionine	2014
The BDNF Val66Met polymorphism and plasma brain-derived neurotrophic factor levels in Han Chinese patients with bipolar disorder and schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry, 2014, Jun-03, Volume: 51 Topics: Adult; Analysis of Variance; Asian People; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Schizophrenia; Valine; Young Adult	2014
Presence of the minor EGFR T790M mutation is associated with drug-sensitive EGFR mutations in lung adenocarcinoma patients. Oncology reports, 2014, Volume: 32, Issue:1 Topics: Adenocarcinoma; Adenocarcinoma of Lung; Adult; Aged; Aged, 80 and over; Cell Line, Tumor; Drug Resistance, Neoplasm; ErbB Receptors; Exons; Female; Genetic Predisposition to Disease; Humans; Lung Neoplasms; Male; Methionine; Middle Aged; Mutation; Sequence Deletion; Threonine	2014
Dietary B vitamin and methionine intake and MTHFR C677T genotype on risk of colorectal tumors in Lynch syndrome: the GEOLynch cohort study. Cancer causes & control : CCC, 2014, Volume: 25, Issue:9 Topics: Adult; Case-Control Studies; Cohort Studies; Colorectal Neoplasms, Hereditary Nonpolyposis; Diet; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Netherlands; Proportional Hazards Models; Prospective Studies; Riboflavin; Risk Factors; Surveys and Questionnaires; Vitamin B Complex; White People	2014
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism affects sympathetic tone in a gender-specific way. Psychoneuroendocrinology, 2014, Volume: 47 Topics: Adult; Amino Acid Substitution; Anxiety; Brain-Derived Neurotrophic Factor; Female; Genetic Predisposition to Disease; Genotype; Heart Rate; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Sympathetic Nervous System; Valine; Young Adult	2014
Catechol-O-methyltransferase Val158Met polymorphism: modulation of wearing-off susceptibility in a Chinese cohort of Parkinson's disease. Parkinsonism & related disorders, 2014, Volume: 20, Issue:10 Topics: Aged; Asian People; Catechol O-Methyltransferase; Cohort Studies; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Single Nucleotide; Valine	2014
Methionine oxidation accelerates the aggregation and enhances the neurotoxicity of the D178N variant of the human prion protein. Biochimica et biophysica acta, 2014, Volume: 1842, Issue:12 Pt A Topics: Animals; Apoptosis; Cell Line, Tumor; Chromatography, High Pressure Liquid; Circular Dichroism; Endopeptidase K; Genetic Predisposition to Disease; Humans; Hydrogen Peroxide; Insomnia, Fatal Familial; Mass Spectrometry; Methionine; Microscopy, Confocal; Mutation, Missense; Neurotoxicity Syndromes; Oxidants; Oxidation-Reduction; Prions; Protein Conformation; Protein Structure, Secondary	2014
Association of COMT Val158Met polymorphism with wearing-off susceptibility in Parkinson's disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2015, Volume: 36, Issue:4 Topics: Catechol O-Methyltransferase; Databases, Bibliographic; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Japan; Male; Methionine; Parkinson Disease; Polymorphism, Single Nucleotide; Valine	2015
Association of brain-derived neurotrophic factor gene Val66Met polymorphism with primary dysmenorrhea. PloS one, 2014, Volume: 9, Issue:11 Topics: Adult; Asian People; Brain-Derived Neurotrophic Factor; Case-Control Studies; Dysmenorrhea; Female; Genetic Predisposition to Disease; Humans; Methionine; Polymorphism, Single Nucleotide; Taiwan; Valine; Young Adult	2014
BDNF polymorphism associates with decline in set shifting in Parkinson's disease. Neurobiology of aging, 2015, Volume: 36, Issue:3 Topics: Aged; Alleles; Brain-Derived Neurotrophic Factor; Cohort Studies; Dopaminergic Neurons; Executive Function; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Neuronal Plasticity; Parkinson Disease; Polymorphism, Genetic	2015
[No effect of the BDNF Val66Met polymorphism on cognitive deficit in patients with schizophrenia and on the risk of the disease in their relatives]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2015, Volume: 115, Issue:1 Topics: Adult; Brain-Derived Neurotrophic Factor; Cognition Disorders; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Pedigree; Polymorphism, Genetic; Schizophrenia; Valine; Young Adult	2015
The Met allele of BDNF Val66Met polymorphism is associated with increased BDNF levels in generalized anxiety disorder. Psychiatric genetics, 2015, Volume: 25, Issue:5 Topics: Adult; Alleles; Anxiety Disorders; Brain-Derived Neurotrophic Factor; Cross-Sectional Studies; Female; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Male; Methionine; Polymorphism, Single Nucleotide; Valine; Young Adult	2015
Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma. Ophthalmic genetics, 2016, Volume: 37, Issue:4 Topics: Case-Control Studies; Child; Child, Preschool; Female; Folic Acid; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotyping Techniques; Humans; Iran; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Retinal Neoplasms; Retinoblastoma; Risk Factors; Tandem Repeat Sequences; Thymidylate Synthase	2016
Brain-derived neurotrophic factor Val66met polymorphism and plasma levels in road traffic accident survivors. Anxiety, stress, and coping, 2016, Volume: 29, Issue:6 Topics: Accidents, Traffic; Adult; Brain-Derived Neurotrophic Factor; Enzyme-Linked Immunosorbent Assay; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Polymorphism, Genetic; Prospective Studies; Stress Disorders, Post-Traumatic; Survivors; Valine	2016
BDNF-Val66Met variant and adolescent stress interact to promote susceptibility to anorexic behavior in mice. Translational psychiatry, 2016, Apr-05, Volume: 6 Topics: Animals; Anorexia Nervosa; Behavior, Animal; Brain-Derived Neurotrophic Factor; Caloric Restriction; Disease Models, Animal; Feeding Behavior; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Methionine; Mice; Polymorphism, Single Nucleotide; Risk Factors; Severity of Illness Index; Stress, Psychological; Valine	2016
DNA methylation regulates gabrb2 mRNA expression: developmental variations and disruptions in l-methionine-induced zebrafish with schizophrenia-like symptoms. Genes, brain, and behavior, 2016, Volume: 15, Issue:8 Topics: Animals; Disease Models, Animal; DNA Methylation; gamma-Aminobutyric Acid; Gene Expression Regulation; Genetic Predisposition to Disease; Methionine; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Receptors, GABA; RNA, Messenger; Schizophrenia; Zebrafish	2016
Childhood trauma, BDNF Val66Met and subclinical psychotic experiences. Attempt at replication in two independent samples. Journal of psychiatric research, 2016, Volume: 83 Topics: Adolescent; Adult; Brain-Derived Neurotrophic Factor; Child; Child Abuse; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Surveys and Questionnaires; Valine; Young Adult	2016
IQ and hemizygosity for the Val American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171, Issue:8 Topics: 22q11 Deletion Syndrome; Adolescent; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; Cognition Disorders; Female; Genetic Association Studies; Genetic Predisposition to Disease; Hemizygote; Humans; Intelligence Tests; Male; Methionine; Polymorphism, Single Nucleotide; Valine; Young Adult	2016
Association of BDNF Val66MET Polymorphism With Parkinson's Disease and Depression and Anxiety Symptoms. The Journal of neuropsychiatry and clinical neurosciences, 2017,Spring, Volume: 29, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Anxiety; Brain-Derived Neurotrophic Factor; Depression; Disease Progression; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic; Valine	2017
Gene-environment interaction as a predictor of early adjustment in first episode psychosis. Schizophrenia research, 2017, Volume: 189 Topics: Adult; Catechol O-Methyltransferase; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Parents; Polymorphism, Single Nucleotide; Psychotic Disorders; Retrospective Studies; Statistics, Nonparametric; Valine; Young Adult	2017
Catechol-O-methyltransferase Val 158 Met polymorphism and antisaccade eye movements in schizophrenia. Schizophrenia bulletin, 2010, Volume: 36, Issue:1 Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Catechol O-Methyltransferase; Dopamine; Female; Frontal Lobe; Gene Dosage; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Isoenzymes; Male; Methionine; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Reference Values; Saccades; Schizophrenia; Valine; Young Adult	2010
Angiotensinogen M235T polymorphism and symptoms of depression in a population-based study and a family-based study. Psychiatric genetics, 2008, Volume: 18, Issue:4 Topics: Aged; Aging; Amino Acid Substitution; Angiotensinogen; Antihypertensive Agents; Depression; Family; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Threonine	2008
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm. Journal of medical genetics, 2008, Volume: 45, Issue:11 Topics: Adult; Aged; Aged, 80 and over; Aortic Aneurysm, Abdominal; DNA Methylation; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Haplotypes; Homocysteine; Humans; Linkage Disequilibrium; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Proteins	2008
Association between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:13 Topics: Adult; Amino Acid Substitution; Black or African American; Brain Chemistry; Case-Control Studies; Catechol O-Methyltransferase; Cocaine; Cocaine-Related Disorders; DNA Mutational Analysis; Dopamine Uptake Inhibitors; Female; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype; Haplotypes; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Valine	2008
Brain-derived neurotrophic factor Val/Met polymorphism and bipolar disorder. Association of the Met allele with suicidal behavior of bipolar patients. Neuropsychobiology, 2008, Volume: 58, Issue:2 Topics: Adult; Analysis of Variance; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Granuloma, Lethal Midline; Humans; Male; Methionine; Middle Aged; Suicide; Valine	2008
The Leu72Met polymorphism of the ghrelin gene is associated with a decreased risk for type 2 diabetes. Clinica chimica acta; international journal of clinical chemistry, 2009, Volume: 399, Issue:1-2 Topics: Aged; Atherosclerosis; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Ghrelin; Humans; Leucine; Male; Methionine; Middle Aged; Polymorphism, Genetic; Reference Values; White People	2009
Does COMT val158met affect behavioral phenotypes: yes, no, maybe? Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:13 Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Behavior; Brain Chemistry; Catechol O-Methyltransferase; Catecholamines; Cocaine-Related Disorders; Genetic Predisposition to Disease; Humans; Methionine; Neurocognitive Disorders; Phenotype; Polymorphism, Genetic; Reward; Valine	2008
Effect of functional catechol-O-methyltransferase Val158Met polymorphism on physical aggression. Bulletin of experimental biology and medicine, 2008, Volume: 145, Issue:1 Topics: Adolescent; Aggression; Catechol O-Methyltransferase; Child; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Personality; Polymorphism, Single Nucleotide; Valine; Young Adult	2008
Brain volumes and Val66Met polymorphism of the BDNF gene: local or global effects? Brain structure & function, 2009, Volume: 213, Issue:6 Topics: Adolescent; Brain; Brain-Derived Neurotrophic Factor; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Image Processing, Computer-Assisted; Interviews as Topic; Magnetic Resonance Imaging; Male; Methionine; Organ Size; Polymorphism, Single Nucleotide; Protein Precursors; Surveys and Questionnaires; Valine; Young Adult	2009
One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders. Journal of cellular and molecular medicine, 2009, Volume: 13, Issue:10 Topics: Aminobutyrates; Carbon; Case-Control Studies; Child; Child Development Disorders, Pervasive; Female; Genetic Predisposition to Disease; Genotype; Glutathione; Homocysteine; Humans; Male; Metabolic Networks and Pathways; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Single Nucleotide	2009
Genetic variants of methionine metabolism and X-ALD phenotype generation: results of a new study sample. Journal of neurology, 2009, Volume: 256, Issue:8 Topics: Adrenoleukodystrophy; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Cerebral Cortex; Demyelinating Diseases; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype; Humans; Metabolic Diseases; Methionine; Peroxisomes; Phenotype; Polymorphism, Genetic	2009
Gender-specific COMT Val158Met polymorphism association in Spanish schizophrenic patients. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2010, Jan-05, Volume: 153B, Issue:1 Topics: Base Sequence; Catechol O-Methyltransferase; DNA Primers; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Schizophrenia; Sex Factors; Spain; Valine	2010
SUMO4 Met55Val polymorphism is associated with coronary heart disease in Japanese type 2 diabetes individuals. Diabetes research and clinical practice, 2009, Volume: 85, Issue:1 Topics: Aged; Amino Acid Substitution; Autoantibodies; Coronary Disease; Diabetes Mellitus, Type 2; Diabetic Angiopathies; Female; Genetic Predisposition to Disease; Glutamate Decarboxylase; Glycated Hemoglobin; Humans; Hypoglycemic Agents; Insulin; Japan; Male; Methionine; Middle Aged; Reference Values; Small Ubiquitin-Related Modifier Proteins; Valine	2009
Association between catechol-O-methyltrasferase Val108/158Met genotype and prefrontal hemodynamic response in schizophrenia. PloS one, 2009, Volume: 4, Issue:5 Topics: Adult; Amino Acid Substitution; Case-Control Studies; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Hemodynamics; Humans; Male; Methionine; Oxyhemoglobins; Polymorphism, Single Nucleotide; Prefrontal Cortex; Schizophrenia; Valine	2009
Genetic association of BDNF val66met and GSK-3beta-50T/C polymorphisms with tardive dyskinesia. Psychiatry and clinical neurosciences, 2009, Volume: 63, Issue:4 Topics: Adult; Alleles; Antipsychotic Agents; Asian People; Brain-Derived Neurotrophic Factor; Dyskinesia, Drug-Induced; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Genotype; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; Humans; Korea; Male; Methionine; Polymerase Chain Reaction; Polymorphism, Genetic; Schizophrenia; Valine	2009
Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia. Psychiatric genetics, 2009, Volume: 19, Issue:5 Topics: Amino Acid Substitution; Gene Frequency; Genetic Predisposition to Disease; Humans; Methionine; Polymorphism, Single Nucleotide; Schizophrenia; Tyrosine 3-Monooxygenase; Valine	2009
Prion protein expression and processing in human mononuclear cells: the impact of the codon 129 prion gene polymorphism. PloS one, 2009, Jun-04, Volume: 4, Issue:6 Topics: Brain; Codon; Enzyme-Linked Immunosorbent Assay; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Immunoblotting; Leukocytes, Mononuclear; Methionine; Polymorphism, Genetic; Prion Diseases; Prions; Reverse Transcriptase Polymerase Chain Reaction; Valine	2009
Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism. The journal of headache and pain, 2009, Volume: 10, Issue:5 Topics: Analgesics; Behavior, Addictive; Brain-Derived Neurotrophic Factor; Female; Genetic Predisposition to Disease; Headache; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Valine	2009
COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia. Psychiatry research, 2009, Sep-30, Volume: 169, Issue:2 Topics: Adult; Analysis of Variance; Catechol O-Methyltransferase; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Ocular Motility Disorders; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Pursuit, Smooth; Reaction Time; Schizophrenia; Valine	2009
No association of the Val66Met polymorphism of the brain-derived neurotrophic factor with hippocampal volume in major depression. Psychiatric genetics, 2009, Volume: 19, Issue:2 Topics: Adult; Aged; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; Case-Control Studies; Depressive Disorder, Major; Female; Genetic Predisposition to Disease; Hippocampus; Humans; Male; Methionine; Middle Aged; Organ Size; Polymorphism, Single Nucleotide; Valine; Young Adult	2009
Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers. Journal of cancer research and clinical oncology, 2010, Volume: 136, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Biomarkers, Tumor; Case-Control Studies; Colorectal Neoplasms; Esophageal Neoplasms; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Head and Neck Neoplasms; Humans; Incidence; Isoleucine; Japan; Lung Neoplasms; Male; Methionine; Middle Aged; Neoplasms; Polymorphism, Single Nucleotide; Proline; Protein Tyrosine Phosphatase, Non-Receptor Type 13; Receptor-Like Protein Tyrosine Phosphatases, Class 3; Risk Factors	2010
Sacroiliitis and muscle cramps in a healthy young man: some spearhead on MTHFR mutations. Rheumatology international, 2010, Volume: 30, Issue:7 Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Arthritis; Biomarkers; DNA Mutational Analysis; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Homocysteine; Humans; Hyperhomocysteinemia; Keratolytic Agents; Low Back Pain; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Cramp; Muscle, Skeletal; Mutation; Radiography; Sacroiliac Joint; Sulfasalazine; Tretinoin	2010
Effects of brain-derived neurotrophic factor Val66Met polymorphism on hippocampal volume change in schizophrenia. Hippocampus, 2010, Volume: 20, Issue:9 Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Atrophy; Brain-Derived Neurotrophic Factor; Female; Genetic Predisposition to Disease; Hippocampus; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Schizophrenia; Valine; Young Adult	2010
Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals. Molecular genetics and metabolism, 2009, Volume: 98, Issue:4 Topics: Amino Acid Substitution; Diabetes Mellitus, Type 2; Fatty Acid-Binding Proteins; Female; Gastrointestinal Hormones; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Methionine; Middle Aged; Molecular Weight; Obesity; Polymorphism, Single Nucleotide; Protein Isoforms; Threonine	2009
Catechol-o-methyltransferase valine(158)methionine genotype and resting regional cerebral blood flow in medication-free patients with schizophrenia. Biological psychiatry, 2010, Feb-01, Volume: 67, Issue:3 Topics: Adolescent; Adult; Brain Mapping; Catechol O-Methyltransferase; Cerebrovascular Circulation; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Positron-Emission Tomography; Prefrontal Cortex; Rest; Schizophrenia; Statistics as Topic; Valine; Young Adult	2010
One-carbon metabolism and schizophrenia: current challenges and future directions. Trends in molecular medicine, 2009, Volume: 15, Issue:12 Topics: Carbon; DNA Methylation; Environment; Epigenesis, Genetic; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Humans; Metabolic Networks and Pathways; Methionine; Mitochondrial Diseases; Receptors, Glutamate; Schizophrenia; Time Factors	2009
Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families. The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:1 Topics: Adrenal Cortex Diseases; Adult; Amino Acid Substitution; Cyclic AMP-Dependent Protein Kinase RIalpha Subunit; Family; Female; Genetic Linkage; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Pedigree; Point Mutation; Valine; Young Adult	2010
The risk of posttraumatic stress disorder after trauma depends on traumatic load and the catechol-o-methyltransferase Val(158)Met polymorphism. Biological psychiatry, 2010, Feb-15, Volume: 67, Issue:4 Topics: Adolescent; Adult; Africa; Aged; Catechol O-Methyltransferase; Chi-Square Distribution; Female; Genetic Predisposition to Disease; Humans; Life Change Events; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Probability; Risk Factors; Stress Disorders, Post-Traumatic; Valine; Young Adult	2010
Rare E196K mutation in the PRNP gene of a patient exhibiting behavioral abnormalities. Clinical neurology and neurosurgery, 2010, Volume: 112, Issue:3 Topics: 14-3-3 Proteins; Aged, 80 and over; Brain; Codon; Creutzfeldt-Jakob Syndrome; Electroencephalography; Genetic Predisposition to Disease; Homozygote; Humans; Magnetic Resonance Imaging; Male; Methionine; Mutation; Myoclonus; Polymorphism, Single Nucleotide; Prion Proteins; Prions	2010
Liver-specific beta-catenin knockout mice exhibit defective bile acid and cholesterol homeostasis and increased susceptibility to diet-induced steatohepatitis. The American journal of pathology, 2010, Volume: 176, Issue:2 Topics: Animals; beta Catenin; Bile Acids and Salts; Cholesterol; Choline Deficiency; Diet; Fatty Liver; Genetic Predisposition to Disease; Homeostasis; Liver; Liver Cirrhosis; Methionine; Mice; Mice, Knockout; Organ Specificity; Stress, Physiological	2010
MTHFR C677T and postmenopausal breast cancer risk by intakes of one-carbon metabolism nutrients: a nested case-control study. Breast cancer research : BCR, 2009, Volume: 11, Issue:6 Topics: Aged; Breast Neoplasms; Case-Control Studies; Dietary Supplements; Female; Folic Acid; Genetic Predisposition to Disease; Humans; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Polymorphism, Single Nucleotide; Postmenopause; Risk Factors; Vitamin B Complex	2009
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation. Neurology, 2010, Mar-09, Volume: 74, Issue:10 Topics: Adult; Alzheimer Disease; Brain; Cognition Disorders; Family Health; Female; Fluorodeoxyglucose F18; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Global Health; History, 17th Century; History, 21st Century; Humans; International Cooperation; Italy; Leucine; Male; Memory Disorders; Methionine; Middle Aged; Mutation; Phenotype; Positron-Emission Tomography; Presenilin-1	2010
Genetic variants of folate and methionine metabolism and PCNSL incidence in a German patient population. Journal of neuro-oncology, 2010, Volume: 100, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Central Nervous System Neoplasms; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Germany; Humans; Incidence; Lymphoma; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; White People	2010
BDNF Val66Met polymorphism is associated with aggressive behavior in schizophrenia. European psychiatry : the journal of the Association of European Psychiatrists, 2010, Volume: 25, Issue:6 Topics: Adult; Aggression; Brain-Derived Neurotrophic Factor; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Schizophrenia; Schizophrenic Psychology; Valine	2010
Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism. Thrombosis and haemostasis, 2010, Volume: 104, Issue:2 Topics: Adolescent; Adult; Age of Onset; Aged; Brain Ischemia; Case-Control Studies; Chi-Square Distribution; Child; Female; Genetic Predisposition to Disease; Haplotypes; Homocysteine; Humans; Italy; Logistic Models; Male; Methionine; Middle Aged; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Risk Assessment; Risk Factors; Stroke; Young Adult	2010
Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: new data and meta-analysis. Journal of psychiatric research, 2011, Volume: 45, Issue:1 Topics: Catechol O-Methyltransferase; Confidence Intervals; Europe; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Heterozygote; Humans; Male; Meta-Analysis as Topic; Methionine; Polymorphism, Single Nucleotide; Schizophrenia; Valine	2011
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome. Psychiatry research, 2010, Jul-30, Volume: 178, Issue:2 Topics: Adolescent; Anxiety; Catechol O-Methyltransferase; Child; Cognition Disorders; DiGeorge Syndrome; Executive Function; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Valine	2010
[Association study of the Val158Met polymorphism of the catechol-O-methyltransferase gene and alcoholism and heroin dependence: the role of a family history]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2010, Volume: 110, Issue:4 Topics: Adult; Alcoholism; Catechol O-Methyltransferase; Genetic Association Studies; Genetic Markers; Genetic Predisposition to Disease; Heroin Dependence; Humans; Male; Methionine; Pedigree; Polymorphism, Genetic; Valine	2010
Food restriction leads to binge eating dependent upon the effect of the brain-derived neurotrophic factor Val66Met polymorphism. Psychiatry research, 2011, Jan-30, Volume: 185, Issue:1-2 Topics: Adolescent; Analysis of Variance; Body Weight; Brain-Derived Neurotrophic Factor; Bulimia; Feeding Behavior; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Polymorphism, Single Nucleotide; Sex Factors; Starvation; Valine	2011
COMT Val 158 Met polymorphism is related with interpersonal problem solving in schizophrenia. European psychiatry : the journal of the Association of European Psychiatrists, 2010, Volume: 25, Issue:6 Topics: Adolescent; Adult; Alleles; Attention; Catechol O-Methyltransferase; Cognition; Female; Genetic Predisposition to Disease; Humans; Interpersonal Relations; Male; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Single Nucleotide; Problem Solving; Psychiatric Status Rating Scales; Schizophrenia; Schizophrenic Psychology; Valine; Young Adult	2010
Effects of BDNF Val66Met polymorphism on brain metabolism in Alzheimer's disease. Neuroreport, 2010, Aug-23, Volume: 21, Issue:12 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Amino Acid Substitution; Basal Metabolism; Brain; Brain Mapping; Brain-Derived Neurotrophic Factor; Cognition Disorders; Female; Genetic Carrier Screening; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Positron-Emission Tomography; Valine	2010
Influence of brain-derived neurotrophic factor (val66met) genetic polymorphism on the ages of onset for heroin abuse in males. Brain research, 2010, Sep-24, Volume: 1353 Topics: Adult; Age of Onset; Analysis of Variance; Brain-Derived Neurotrophic Factor; Chi-Square Distribution; Genetic Predisposition to Disease; Genotype; Heroin Dependence; Humans; Male; Methionine; Odds Ratio; Polymorphism, Single Nucleotide; Valine	2010
Parent of origin effect and differential allelic expression of BDNF Val66Met in suicidal behaviour. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry, 2011, Volume: 12, Issue:1 Topics: Adult; Alleles; Amino Acid Substitution; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Female; Gene Expression; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Parents; Polymorphism, Single Nucleotide; RNA, Messenger; Schizophrenia; Suicide; Suicide, Attempted; Valine	2011
Early life stress combined with serotonin 3A receptor and brain-derived neurotrophic factor valine 66 to methionine genotypes impacts emotional brain and arousal correlates of risk for depression. Biological psychiatry, 2010, Nov-01, Volume: 68, Issue:9 Topics: Adult; Arousal; Brain Waves; Brain-Derived Neurotrophic Factor; Depression; Electroencephalography; Emotions; Female; Genetic Predisposition to Disease; Genotype; Heart Rate; Humans; Male; Methionine; Polymorphism, Genetic; Receptors, Serotonin, 5-HT3; Stress, Psychological; Valine	2010
Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD. Journal of child psychology and psychiatry, and allied disciplines, 2010, Volume: 51, Issue:11 Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Birth Weight; Catechol O-Methyltransferase; Child; Child Development Disorders, Pervasive; Female; Genetic Predisposition to Disease; Genotype; Humans; INDEL Mutation; Interpersonal Relations; Linear Models; Male; Maternal Behavior; Methionine; Netherlands; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors; Sampling Studies; Serotonin Plasma Membrane Transport Proteins; Smoking; Stereotyped Behavior; Surveys and Questionnaires; Valine	2010
Dietary methyl donors, methyl metabolizing enzymes, and epigenetic regulators: diet-gene interactions and promoter CpG island hypermethylation in colorectal cancer. Cancer causes & control : CCC, 2011, Volume: 22, Issue:1 Topics: Aged; Colorectal Neoplasms; CpG Islands; Diet; DNA Methylation; Epigenesis, Genetic; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Methyltransferases; Middle Aged; Polymerase Chain Reaction; Promoter Regions, Genetic; Vitamin B 6	2011
Precancerous and non-cancer disease endpoints of chronic arsenic exposure: the level of chromosomal damage and XRCC3 T241M polymorphism. Mutation research, 2011, Jan-10, Volume: 706, Issue:1-2 Topics: Adult; Alleles; Amino Acid Substitution; Arsenic; Carcinogens; Case-Control Studies; Chromosome Aberrations; Conjunctivitis; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Methionine; Mutagens; Odds Ratio; Peripheral Nervous System Diseases; Polymorphism, Genetic; Precancerous Conditions; Skin Diseases; Threonine; Water Pollutants, Chemical	2011
Cannabis use and age at onset of psychosis: further evidence of interaction with COMT Val158Met polymorphism. Acta psychiatrica Scandinavica, 2011, Volume: 123, Issue:6 Topics: Adolescent; Age of Onset; Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Male; Marijuana Abuse; Marijuana Smoking; Methionine; Polymorphism, Genetic; Psychotic Disorders; Schizophrenia; Valine	2011
Nutrients in folate-mediated, one-carbon metabolism and the risk of rectal tumors in men and women. Nutrition and cancer, 2011, Volume: 63, Issue:3 Topics: Adult; Aged; Case-Control Studies; CpG Islands; Diet; Dietary Supplements; DNA Methylation; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Mutation; Phenotype; Polymorphism, Genetic; Proto-Oncogene Proteins; Proto-Oncogene Proteins p21(ras); ras Proteins; Rectal Neoplasms; Riboflavin; Risk Factors; Sex Factors; Tumor Suppressor Protein p53; Vitamin B 12; Vitamin B 6	2011
Renin-angiotensin-aldosterone system genes and nonarteritic anterior ischemic optic neuropathy. Molecular vision, 2011, Volume: 17 Topics: Age Factors; Aged; Aged, 80 and over; Alanine; Alleles; Angiotensinogen; Confidence Intervals; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Odds Ratio; Optic Neuropathy, Ischemic; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Sex Factors; Threonine	2011
Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2011, Volume: 18, Issue:8 Topics: China; DNA Mutational Analysis; Electromyography; Family Health; Genetic Predisposition to Disease; Humans; Methionine; Muscle, Skeletal; Mutation; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Neural Conduction; Phenotype; Sodium Channels; Valine	2011
Childhood abuse, the BDNF-Val66Met polymorphism and adult psychotic-like experiences. The British journal of psychiatry : the journal of mental science, 2011, Volume: 199, Issue:1 Topics: Adult; Adult Survivors of Child Abuse; Alleles; Brain-Derived Neurotrophic Factor; Child; Child Abuse; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Linear Models; Male; Methionine; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult	2011
Evidence of association between Val66Met polymorphism at BDNF gene and anxiety disorders in a community sample of children and adolescents. Neuroscience letters, 2011, Sep-20, Volume: 502, Issue:3 Topics: Adolescent; Amino Acid Substitution; Anxiety Disorders; Brain Chemistry; Brain-Derived Neurotrophic Factor; Child; Cohort Studies; Female; Genetic Predisposition to Disease; Genetic Testing; Humans; Male; Methionine; Polymorphism, Genetic; Valine	2011
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role? Epilepsy & behavior : E&B, 2011, Volume: 22, Issue:3 Topics: Adolescent; Adult; Aged; Brain-Derived Neurotrophic Factor; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy; Female; Fragile X Syndrome; Genetic Predisposition to Disease; Humans; Infant; Male; Methionine; Middle Aged; Polymorphism, Genetic; Valine; Young Adult	2011
Cannabis, COMT and psychotic experiences. The British journal of psychiatry : the journal of mental science, 2011, Volume: 199, Issue:5 Topics: Adolescent; Catechol O-Methyltransferase; Child; Dose-Response Relationship, Drug; Genetic Predisposition to Disease; Genotype; Hallucinations; Haplotypes; Humans; Longitudinal Studies; Male; Marijuana Abuse; Methionine; Polymorphism, Single Nucleotide; Psychotic Disorders; Risk; Self Report; Valine	2011
Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society, 2012, Volume: 27, Issue:1 Topics: Aged; Antiparasitic Agents; Catechol O-Methyltransferase; Cohort Studies; Dyskinesia, Drug-Induced; Dyskinesias; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic; Proportional Hazards Models; Valine	2012
Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2012, Volume: 41, Issue:4 Topics: Adult; Areca; Arginine; Arylamine N-Acetyltransferase; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Heterozygote; Homozygote; Humans; India; Lysine; Male; Methionine; Multifactor Dimensionality Reduction; Oral Submucous Fibrosis; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tobacco, Smokeless; Tryptophan; X-ray Repair Cross Complementing Protein 1	2012
Hippocampal volume and the brain-derived neurotrophic factor Val66Met polymorphism in first episode psychosis. Schizophrenia research, 2012, Volume: 134, Issue:2-3 Topics: Adolescent; Adult; Age Factors; Analysis of Variance; Brain-Derived Neurotrophic Factor; Cognition Disorders; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Memory; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychotic Disorders; Valine; Young Adult	2012
Serotonergic and BDNF genes associated with depression 1 week and 1 year after mastectomy for breast cancer. Psychosomatic medicine, 2012, Volume: 74, Issue:1 Topics: Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; Breast Neoplasms; Depressive Disorder; Diagnostic and Statistical Manual of Mental Disorders; Epistasis, Genetic; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Incidence; Interview, Psychological; Introns; Logistic Models; Mastectomy; Methionine; Middle Aged; Multifactor Dimensionality Reduction; Polymorphism, Genetic; Prevalence; Promoter Regions, Genetic; Risk Factors; Serotonin Plasma Membrane Transport Proteins; Tandem Repeat Sequences; Time Factors; Valine	2012
The association of V249I and T280M fractalkine receptor haplotypes with disease course of multiple sclerosis. Journal of neuroimmunology, 2012, Volume: 245, Issue:1-2 Topics: Adult; CX3C Chemokine Receptor 1; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Isoleucine; Male; Methionine; Middle Aged; Multiple Sclerosis, Chronic Progressive; Multiple Sclerosis, Relapsing-Remitting; Polymorphism, Genetic; Receptors, Chemokine; Threonine; Valine	2012
A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism. Pediatric research, 2012, Volume: 71, Issue:1 Topics: Adolescent; Adult; Collectins; Female; Genetic Predisposition to Disease; Gestational Age; Haplotypes; Humans; Infant, Newborn; Infant, Premature; Infant, Premature, Diseases; Linkage Disequilibrium; Mannose-Binding Lectin; Methionine; Middle Aged; Polymorphism, Genetic; Pregnancy; Premature Birth; Pulmonary Surfactant-Associated Protein A; Pulmonary Surfactant-Associated Protein D; Threonine; Young Adult	2012
Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course. Journal of neuroimmunology, 2012, Volume: 244, Issue:1-2 Topics: Adult; Age of Onset; Brain-Derived Neurotrophic Factor; Disease Progression; Female; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Male; Methionine; Multiple Sclerosis; Norway; Polymorphism, Genetic; Valine	2012
Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population. Archives of medical research, 2012, Volume: 43, Issue:2 Topics: Base Sequence; Case-Control Studies; Catechol O-Methyltransferase; China; DNA Primers; Genetic Predisposition to Disease; Humans; Methionine; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Valine	2012
COMT Val158Met modulates the effect of childhood adverse experiences on the risk of alcohol dependence. Addiction biology, 2013, Volume: 18, Issue:2 Topics: Adolescent; Adult; Age of Onset; Alcoholism; Alleles; Amino Acid Substitution; Analysis of Variance; Case-Control Studies; Catechol O-Methyltransferase; Child; Child Abuse; Dopamine; Gene-Environment Interaction; Genetic Predisposition to Disease; Humans; Life Change Events; Logistic Models; Male; Methionine; Polymorphism, Single Nucleotide; Prefrontal Cortex; Protein Serine-Threonine Kinases; Receptors, Dopamine D2; Self Report; Severity of Illness Index; Stress, Psychological; Valine	2013
Brain-derived neurotrophic factor Val66Met polymorphism and obsessive-compulsive symptoms in Egyptian schizophrenia patients. Journal of psychiatric research, 2012, Volume: 46, Issue:6 Topics: Adult; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Egypt; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Schizophrenia; Statistics, Nonparametric; Valine; Young Adult	2012
Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese population. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases, 2012, Volume: 13, Issue:6 Topics: Amyotrophic Lateral Sclerosis; Asian People; Cell Cycle Proteins; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Male; Membrane Transport Proteins; Methionine; Middle Aged; Mutation; Transcription Factor TFIIIA; Valine	2012
Genetic association between obstructive bronchitis and enzymes of oxidative stress. Metabolism: clinical and experimental, 2012, Volume: 61, Issue:12 Topics: Adult; Arginine; Aryldialkylphosphatase; Bronchitis; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Cohort Studies; Epoxide Hydrolases; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Germany; Histidine; Humans; Leucine; Lung Diseases, Obstructive; Male; Methionine; NAD(P)H Dehydrogenase (Quinone); Oxidative Stress; Polymorphism, Single Nucleotide; Pregnancy; Pregnancy Complications; Prenatal Exposure Delayed Effects; Proline; Prospective Studies; Risk Factors; Serine; Smoking; Valine	2012
BDNF Val66Met and spontaneous dyskinesias in non-clinical psychosis. Schizophrenia research, 2012, Volume: 140, Issue:1-3 Topics: Adolescent; Adult; Analysis of Variance; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Dyskinesias; Female; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult	2012
Allelic variants of XRCC1 and XRCC3 repair genes and susceptibility of oral cancer in Brazilian patients. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2013, Volume: 42, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Alleles; Arginine; Carcinoma, Squamous Cell; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Humans; Lymphatic Metastasis; Male; Methionine; Middle Aged; Mouth Neoplasms; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tryptophan; X-ray Repair Cross Complementing Protein 1; Young Adult	2013
A candidate gene study of one-carbon metabolism pathway genes and colorectal cancer risk. The British journal of nutrition, 2013, Mar-28, Volume: 109, Issue:6 Topics: Aged; Carbon; Case-Control Studies; Colorectal Neoplasms; Diet; Female; Folic Acid; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Mutagenesis, Insertional; Nucleotides; One-Carbon Group Transferases; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Transcobalamins; Vitamin B 12	2013
Functional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell death. Proceedings of the National Academy of Sciences of the United States of America, 2012, Aug-28, Volume: 109, Issue:35 Topics: Adult; Aged; Aged, 80 and over; Animals; Apoptosis; Apoptosis Regulatory Proteins; Bone Marrow Cells; Caspase 1; Caspase 9; Deoxyadenosines; Genetic Predisposition to Disease; Genetic Variation; HapMap Project; HEK293 Cells; Humans; Methionine; Mice; Mice, Inbred C57BL; Middle Aged; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Salmonella Infections; Salmonella typhimurium; Thionucleosides; Young Adult	2012
Influence of COMT Val158Met polymorphism on Alzheimer's disease and mild cognitive impairment in Italian patients. Journal of Alzheimer's disease : JAD, 2012, Volume: 32, Issue:4 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Apolipoprotein E4; Catechol O-Methyltransferase; Cognitive Dysfunction; Female; Genetic Predisposition to Disease; Humans; Italy; Male; Methionine; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk Factors; Valine	2012
Brain-derived neurotrophic factor gene Val66Met polymorphism and cognitive function in obsessive-compulsive disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2012, Volume: 159B, Issue:7 Topics: Adolescent; Adult; Alleles; Brain-Derived Neurotrophic Factor; Cognition; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Valine	2012
Fractalkine gene receptor polymorphism in patients with multiple sclerosis. The International journal of neuroscience, 2013, Volume: 123, Issue:1 Topics: Adolescent; Adult; Age of Onset; Analysis of Variance; Chemokine CX3CL1; Disability Evaluation; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Male; Methionine; Middle Aged; Multiple Sclerosis; Polymorphism, Single Nucleotide; Statistics, Nonparametric; Threonine; Valine; Young Adult	2013
Interacting effect of BDNF Val66Met polymorphism and stressful life events on adolescent depression. Genes, brain, and behavior, 2012, Volume: 11, Issue:8 Topics: Adolescent; Alleles; Brain-Derived Neurotrophic Factor; Child; China; Depressive Disorder; Diseases in Twins; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Humans; Life Change Events; Male; Methionine; Neuronal Plasticity; Polymorphism, Genetic; Random Allocation; Valine	2012
Gene-diet-interactions in folate-mediated one-carbon metabolism modify colon cancer risk. Molecular nutrition & food research, 2013, Volume: 57, Issue:4 Topics: Adult; Aged; Case-Control Studies; Colonic Neoplasms; Diet; DNA (Cytosine-5-)-Methyltransferase 1; DNA (Cytosine-5-)-Methyltransferases; Female; Folic Acid; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine Hydroxymethyltransferase; Humans; Male; Methionine; Methylenetetrahydrofolate Dehydrogenase (NADP); Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Minor Histocompatibility Antigens; Polymorphism, Genetic; Riboflavin; Risk Factors; Vitamin B 12; Vitamin B 6	2013
COMT and BDNF interacted in bipolar II disorder not comorbid with anxiety disorder. Behavioural brain research, 2013, Jan-15, Volume: 237 Topics: Adult; Anxiety Disorders; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Catechol O-Methyltransferase; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Polymorphism, Single Nucleotide; Valine; Young Adult	2013
Brain-derived neurotrophic factor val66met genotype and early life stress effects upon bipolar course. Journal of psychiatric research, 2013, Volume: 47, Issue:2 Topics: Adult; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Stress, Psychological; Valine	2013
Association between the COMT gene and rumination in a Hungarian sample. Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology, 2012, Volume: 14, Issue:4 Topics: Adult; Catechol O-Methyltransferase; Depression; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Hungary; Male; Methionine; Middle Aged; Obsessive Behavior; Phenotype; Polymorphism, Single Nucleotide; Valine	2012
BDNF Val66Met variant and smoking in a Chinese population. PloS one, 2012, Volume: 7, Issue:12 Topics: Adult; Age of Onset; Aged; Amino Acid Substitution; Asian People; Brain-Derived Neurotrophic Factor; China; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Population; Smoking; Tobacco Use Disorder; Valine; Young Adult	2012
Modulation of brain structure by catechol-O-methyltransferase Val(158) Met polymorphism in chronic cannabis users. Addiction biology, 2014, Volume: 19, Issue:4 Topics: Adolescent; Adult; Amino Acid Substitution; Brain; Brain Mapping; Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Magnetic Resonance Imaging; Male; Marijuana Abuse; Methionine; Organ Size; Polymorphism, Single Nucleotide; Valine; Young Adult	2014
Gray matter volume in adolescent anxiety: an impact of the brain-derived neurotrophic factor Val(66)Met polymorphism? Journal of the American Academy of Child and Adolescent Psychiatry, 2013, Volume: 52, Issue:2 Topics: Adolescent; Adolescent Behavior; Amino Acid Substitution; Anxiety Disorders; Brain; Brain-Derived Neurotrophic Factor; Female; Functional Neuroimaging; Genetic Predisposition to Disease; Humans; Magnetic Resonance Imaging; Male; Methionine; Organ Size; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Valine	2013
A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia. Acta neurologica Belgica, 2013, Volume: 113, Issue:3 Topics: Adult; Age of Onset; Analysis of Variance; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Dystonic Disorders; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Odds Ratio; Parkinson Disease; Polymorphism, Single Nucleotide; Valine	2013
Mitochondrial 5178A/C genotype is associated with acute myocardial infarction. Circulation journal : official journal of the Japanese Circulation Society, 2003, Volume: 67, Issue:1 Topics: Aged; Aging; Alleles; Amino Acid Substitution; Diabetes Complications; DNA, Mitochondrial; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Hypercholesterolemia; Hypertension; Leucine; Male; Methionine; Middle Aged; Myocardial Infarction; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors	2003
Genetic determinants of fasting and post-methionine hyperhomocysteinemia in patients with retinal vein occlusion. Thrombosis research, 2003, Apr-15, Volume: 110, Issue:1 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Cystathionine beta-Synthase; Fasting; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Hyperhomocysteinemia; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Mutagenesis, Insertional; Mutation, Missense; Point Mutation; Polymorphism, Genetic; Retinal Vein Occlusion; Risk Factors; Thrombophilia	2003
Met66 in the brain-derived neurotrophic factor (BDNF) precursor is associated with anorexia nervosa restrictive type. Molecular psychiatry, 2003, Volume: 8, Issue:8 Topics: Adult; Anorexia Nervosa; Body Mass Index; Brain-Derived Neurotrophic Factor; Bulimia; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Phenotype; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Polymorphism, Single-Stranded Conformational	2003
An association study of a brain-derived neurotrophic factor Val66Met polymorphism and clozapine response of schizophrenic patients. Neuroscience letters, 2003, Oct-09, Volume: 349, Issue:3 Topics: Adult; Antipsychotic Agents; Brain; Brain-Derived Neurotrophic Factor; Clozapine; Drug Resistance; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Mutation; Polymorphism, Genetic; Schizophrenia; Valine	2003
The M98K variant of the OPTINEURIN (OPTN) gene modifies initial intraocular pressure in patients with primary open angle glaucoma. Journal of medical genetics, 2003, Volume: 40, Issue:11 Topics: Amino Acid Substitution; Cell Cycle Proteins; Eye Proteins; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glaucoma, Open-Angle; Humans; Intraocular Pressure; Lysine; Membrane Transport Proteins; Methionine; Nerve Tissue Proteins; Transcription Factor TFIIIA	2003
Association study of a functional catechol-O-methyltransferase genetic polymorphism with age of onset, cognitive function, symptomatology and prognosis in chronic schizophrenia. Neuropsychobiology, 2004, Volume: 49, Issue:4 Topics: Adolescent; Adult; Age of Onset; Aged; Catechol O-Methyltransferase; Chronic Disease; Cognition Disorders; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Prognosis; Psychiatric Status Rating Scales; Regression Analysis; Schizophrenia; Severity of Illness Index; Valine	2004
A M55V polymorphism in a novel SUMO gene (SUMO-4) differentially activates heat shock transcription factors and is associated with susceptibility to type I diabetes mellitus. The Journal of biological chemistry, 2004, Jun-25, Volume: 279, Issue:26 Topics: Amino Acid Sequence; Amino Acid Substitution; Cell Line; Diabetes Mellitus, Type 1; Genes, Reporter; Genetic Predisposition to Disease; Heat-Shock Proteins; Humans; Lysine; Methionine; Molecular Sequence Data; NF-kappa B; Oxidative Stress; Polymorphism, Genetic; Recombinant Proteins; Sequence Alignment; Small Ubiquitin-Related Modifier Proteins; Tissue Distribution; Transcription Factors; Valine	2004
The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPC. The Journal of biological chemistry, 2004, Jul-02, Volume: 279, Issue:27 Topics: Amides; Circular Dichroism; Creutzfeldt-Jakob Syndrome; Escherichia coli; Genetic Predisposition to Disease; Humans; Kinetics; Magnetic Resonance Spectroscopy; Methionine; Models, Molecular; Mutation; Plasmids; Polymorphism, Genetic; Protein Conformation; Protein Folding; Protein Structure, Secondary; Protein Structure, Tertiary; PrPC Proteins; Time Factors; Valine	2004
Association of paraoxonase-1 M55L genotype and alcohol consumption with coronary atherosclerosis: the Helsinki Sudden Death Study. Pharmacogenetics, 2004, Volume: 14, Issue:8 Topics: Adult; Aged; Alcohol Drinking; Amino Acid Substitution; Aryldialkylphosphatase; Autopsy; Coronary Artery Disease; Coronary Vessels; Finland; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Methionine; Middle Aged; Prospective Studies; Risk Factors	2004
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population. Neuroscience letters, 2004, Sep-02, Volume: 367, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Aryldialkylphosphatase; Case-Control Studies; DNA Mutational Analysis; Female; Finland; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic	2004
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. The American journal of psychiatry, 2004, Volume: 161, Issue:9 Topics: Alleles; Catechol O-Methyltransferase; Child; Chromosomes, Human, Pair 22; Cognition; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Prefrontal Cortex; Valine	2004
Taking stock: from chasing occlusal contacts to vulnerability alleles. Orthodontics & craniofacial research, 2004, Volume: 7, Issue:3 Topics: Alleles; Amino Acid Substitution; Catechol O-Methyltransferase; Dental Occlusion; Diagnosis, Differential; Disease Susceptibility; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Needs Assessment; Risk Factors; Temporomandibular Joint Disorders; Treatment Outcome; Valine	2004
Catechol-O-methyltransferase Val 108/158 Met polymorphism in premenopausal breast cancer patients. Toxicology, 2004, Nov-15, Volume: 204, Issue:2-3 Topics: Adult; Alleles; Breast Neoplasms; Case-Control Studies; Catechol O-Methyltransferase; Chi-Square Distribution; Confidence Intervals; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Methionine; Odds Ratio; Polymorphism, Genetic; Premenopause; Valine	2004
Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women. Brain research. Molecular brain research, 2004, Dec-06, Volume: 132, Issue:1 Topics: Adult; Amino Acid Substitution; Catechol O-Methyltransferase; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Mutation; Polymorphism, Genetic; Risk Factors; Schizophrenia; Sex Factors; Turkey; Valine	2004
Biomedicine. Prion dormancy and disease. Science (New York, N.Y.), 2004, Dec-03, Volume: 306, Issue:5702 Topics: Animals; Appendix; Brain; Carrier State; Cattle; Creutzfeldt-Jakob Syndrome; Disease Outbreaks; Encephalopathy, Bovine Spongiform; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Mice; Mice, Transgenic; Polymorphism, Genetic; Protein Conformation; PrPC Proteins; United Kingdom; Valine	2004
Negative association between catechol-O-methyltransferase (COMT) gene Val158Met polymorphism and persistent tardive dyskinesia in schizophrenia. Journal of neural transmission (Vienna, Austria : 1996), 2005, Volume: 112, Issue:8 Topics: Adult; Amino Acid Substitution; Antipsychotic Agents; Brain Chemistry; Catechol O-Methyltransferase; Cohort Studies; Disease Progression; DNA Mutational Analysis; Drug Administration Schedule; Dyskinesia, Drug-Induced; Female; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Schizophrenia; Valine	2005
Pick bodies in a family with presenilin-1 Alzheimer's disease. Annals of neurology, 2005, Volume: 57, Issue:1 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Blotting, Western; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Leucine; Male; Membrane Proteins; Methionine; Middle Aged; Mutation; Neurofibrillary Tangles; Pick Disease of the Brain; Plaque, Amyloid; Postmortem Changes; Presenilin-1; tau Proteins	2005
BDNF and COMT polymorphisms: relation to memory phenotypes in young adults with childhood-onset mood disorder. Neuromolecular medicine, 2004, Volume: 5, Issue:3 Topics: Adolescent; Adult; Age Factors; Age of Onset; Brain; Brain Chemistry; Brain-Derived Neurotrophic Factor; Catechol O-Methyltransferase; Child; Dopamine; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Intelligence; Male; Memory; Methionine; Mood Disorders; Phenotype; Polymorphism, Genetic; Sex Factors; Valine	2004
Genetic susceptibility to prion disease: new phenotypes? The Lancet. Neurology, 2005, Volume: 4, Issue:1 Topics: Animals; Cattle; Creutzfeldt-Jakob Syndrome; Encephalopathy, Bovine Spongiform; Genetic Predisposition to Disease; Homozygote; Humans; Methionine; Phenotype; Prion Diseases	2005
No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease. Clinical endocrinology, 2005, Volume: 62, Issue:3 Topics: Addison Disease; Case-Control Studies; Codon; Gene Frequency; Genetic Predisposition to Disease; Genotype; Graves Disease; Humans; Methionine; Polymorphism, Single Nucleotide; Small Ubiquitin-Related Modifier Proteins; Valine	2005
Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene. Neurology, 2005, Mar-08, Volume: 64, Issue:5 Topics: 14-3-3 Proteins; Amino Acid Substitution; Brain; Creutzfeldt-Jakob Syndrome; Disease Progression; DNA Mutational Analysis; Fatal Outcome; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Immunoblotting; Immunohistochemistry; Mass Spectrometry; Methionine; Middle Aged; Mutation; Neurons; Phenotype; PrPSc Proteins	2005
MTX-induced white matter changes are associated with polymorphisms of methionine metabolism. Neurology, 2005, Mar-08, Volume: 64, Issue:5 Topics: Aged; Brain; Central Nervous System Neoplasms; Demyelinating Diseases; DNA Mutational Analysis; Drug Resistance; Female; Folic Acid; Folic Acid Antagonists; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Haplotypes; Humans; Lymphoma; Male; Methionine; Methotrexate; Middle Aged; Myelin Sheath; Nerve Fibers, Myelinated; Neurotoxins; Polymorphism, Genetic; Risk Factors; S-Adenosylmethionine	2005
The BDNF Val66Met polymorphism has a gender specific influence on planning ability in Parkinson's disease. Journal of neurology, 2005, Volume: 252, Issue:7 Topics: Aged; Analysis of Variance; Brain-Derived Neurotrophic Factor; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Mental Processes; Methionine; Middle Aged; Neuropsychological Tests; Parkinson Disease; Polymorphism, Genetic; Sex Characteristics; Valine	2005
Phenotypic expression of familial amyloid polyneuropathy in Brazil. European journal of neurology, 2005, Volume: 12, Issue:4 Topics: Adult; Age Factors; Age of Onset; Amyloid Neuropathies, Familial; Body Mass Index; Brazil; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Mutation; Neurologic Examination; Phenotype; Prealbumin; Valine	2005
Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy. Movement disorders : official journal of the Movement Disorder Society, 2005, Volume: 20, Issue:8 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Brain-Derived Neurotrophic Factor; Cysteine; Female; Genetic Predisposition to Disease; Humans; Japan; Male; Methionine; Middle Aged; Multiple System Atrophy; Parkinson Disease; Polymorphism, Genetic; Threonine; Valine	2005
Investigation of the effect of brain-derived neurotrophic factor (BDNF) polymorphisms on the risk of late-onset Alzheimer's disease (AD) and quantitative measures of AD progression. Neuroscience letters, 2005, May-13, Volume: 379, Issue:3 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Black People; Brain-Derived Neurotrophic Factor; Case-Control Studies; Disease Progression; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Polymorphism, Genetic; Risk; Valine; White People	2005
COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome. Biological psychiatry, 2005, Jul-01, Volume: 58, Issue:1 Topics: Acoustic Stimulation; Adolescent; Adult; Catechol O-Methyltransferase; Child; Chromosomes, Human, Pair 22; Cognition Disorders; Electroencephalography; Evoked Potentials, Auditory; Female; Frontal Lobe; Gene Deletion; Genetic Predisposition to Disease; Humans; Male; Methionine; Neuropsychological Tests; Phenotype; Risk Factors; Schizophrenia; Temporal Lobe; Valine	2005
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular psychiatry, 2005, Volume: 10, Issue:10 Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Base Sequence; Brain-Derived Neurotrophic Factor; DNA Primers; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Molecular Sequence Data; Nuclear Family; Polymorphism, Single Nucleotide; Valine	2005
COMT polymorphisms and anxiety-related personality traits. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2005, Volume: 30, Issue:11 Topics: Adolescent; Adult; Anxiety; Catechol O-Methyltransferase; Chi-Square Distribution; Confidence Intervals; Demography; Extraversion, Psychological; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Male; Methionine; Neurotic Disorders; Odds Ratio; Personality; Personality Inventory; Polymorphism, Genetic; Sex Factors; Valine	2005
The BDNF-Val66Met polymorphism: implications for susceptibility to multiple sclerosis and severity of disease. Journal of neuroimmunology, 2005, Volume: 167, Issue:1-2 Topics: Brain-Derived Neurotrophic Factor; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Multiple Sclerosis; Polymorphism, Genetic; Valine	2005
The codon for the methionine at position 129 (M129) in the human prion protein provides an alternative initiation site for translation and renders individuals homozygous for M129 more susceptible to prion disease. Medical hypotheses, 2005, Volume: 65, Issue:5 Topics: Amino Acid Substitution; Animals; Clinical Trials as Topic; Codon, Initiator; DNA Mutational Analysis; Evidence-Based Medicine; Genetic Predisposition to Disease; Genetic Testing; Homozygote; Humans; Incidence; Methionine; Models, Genetic; Polymorphism, Genetic; Prion Diseases; Prions; Protein Biosynthesis; Risk Assessment; Risk Factors	2005
The Val158Met polymorphism of the catechol-O-methyltransferase gene is associated with the PSA-progression-free survival in prostate cancer patients treated with estramustine phosphate. European urology, 2005, Volume: 48, Issue:5 Topics: Aged; Aged, 80 and over; Antineoplastic Agents, Hormonal; Catechol O-Methyltransferase; Disease Progression; Disease-Free Survival; Estramustine; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Prodrugs; Prostate-Specific Antigen; Prostatic Neoplasms; Valine	2005
No association between schizophrenia and polymorphisms in COMT in two large samples. The American journal of psychiatry, 2005, Volume: 162, Issue:9 Topics: Case-Control Studies; Catechol O-Methyltransferase; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Ireland; Jews; Linkage Disequilibrium; Male; Methionine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Schizophrenia; Valine; White People	2005
Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2005, Nov-05, Volume: 139B, Issue:1 Topics: Adult; Alleles; Amino Acid Substitution; Bipolar Disorder; Brain-Derived Neurotrophic Factor; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Polymorphism, Genetic; Valine; White People	2005
Association between BDNF Val66Met polymorphism and age at onset in Huntington disease. Neurology, 2005, Sep-27, Volume: 65, Issue:6 Topics: Adult; Age of Onset; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Huntingtin Protein; Huntington Disease; Male; Methionine; Middle Aged; Mutation; Nerve Tissue Proteins; Nuclear Proteins; Polymorphism, Genetic; Trinucleotide Repeat Expansion; Valine	2005
Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish. The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:12 Topics: Adult; Arginine; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genetics, Population; Genotype; Ghrelin; Glutamine; Heterozygote; Humans; Hunger; Leucine; Male; Metabolic Syndrome; Methionine; Middle Aged; Peptide Hormones; United States	2005
Inherited susceptibility to lung cancer may be associated with the T790M drug resistance mutation in EGFR. Nature genetics, 2005, Volume: 37, Issue:12 Topics: Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Drug Resistance, Neoplasm; ErbB Receptors; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Lung Neoplasms; Male; Methionine; Middle Aged; Pedigree; Protein Kinase Inhibitors; Protein-Tyrosine Kinases; Threonine	2005
The Val66Met polymorphism of the brain-derived neurotrophic-factor gene is associated with geriatric depression. Neurobiology of aging, 2006, Volume: 27, Issue:12 Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; Depressive Disorder; Female; Genetic Markers; Genetic Predisposition to Disease; Humans; Male; Methionine; Mutation, Missense; Polymorphism, Genetic; Severity of Illness Index; Valine	2006
Effects of catechol-O-methyltransferase Val158Met polymorphism on the cognitive stability and aggression in the first-onset schizophrenic patients. Neuroreport, 2006, Jan-23, Volume: 17, Issue:1 Topics: Adult; Aggression; Catechol O-Methyltransferase; Cognition; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Polymorphism, Genetic; Schizophrenia; Schizophrenic Psychology; Valine	2006
Association of COMT Val158Met genotype with executive functioning following traumatic brain injury. The Journal of neuropsychiatry and clinical neurosciences, 2005,Fall, Volume: 17, Issue:4 Topics: Adult; Analysis of Variance; Brain Injuries; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Problem Solving; Valine	2005
Implication of the folate-methionine metabolism pathways in susceptibility to follicular lymphomas. Blood, 2006, Jul-01, Volume: 108, Issue:1 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Alleles; DNA; Enzymes; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Glycine Hydroxymethyltransferase; Humans; Lymphoma, Follicular; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Mutation; Polymorphism, Genetic; Risk Factors; Thymidylate Synthase	2006
Role of N-terminal familial mutations in prion protein fibrillization and prion amyloid propagation in vitro. The Journal of biological chemistry, 2006, Mar-24, Volume: 281, Issue:12 Topics: Amyloid; Benzothiazoles; Escherichia coli; Genetic Predisposition to Disease; Humans; In Vitro Techniques; Kinetics; Methionine; Microscopy, Atomic Force; Molecular Conformation; Mutation; Plasmids; Polymorphism, Genetic; Prion Diseases; Prions; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Spectroscopy, Fourier Transform Infrared; Thiazoles; Time Factors; Valine	2006
Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy. Neurology, 2006, Feb-14, Volume: 66, Issue:3 Topics: Adolescent; Adrenoleukodystrophy; Child; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Male; Methionine; Phenotype; Polymorphism, Genetic	2006
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome. The American journal of psychiatry, 2006, Volume: 163, Issue:3 Topics: Adolescent; Adult; Catechol O-Methyltransferase; Child; Cognition Disorders; DiGeorge Syndrome; Female; Frontal Lobe; Gene Expression; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Valine	2006
Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement. Clinical rheumatology, 2006, Volume: 25, Issue:6 Topics: Adolescent; Alanine; Angiotensinogen; Child; Child, Preschool; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; IgA Vasculitis; Kidney Diseases; Male; Methionine; Nephrotic Syndrome; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Proteinuria; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Severity of Illness Index; Threonine	2006
Association of the Val158Met catechol O-methyltransferase genetic polymorphism with panic disorder. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2006, Volume: 31, Issue:10 Topics: Animals; Case-Control Studies; Catechol O-Methyltransferase; DNA Mutational Analysis; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Male; Methionine; Panic Disorder; Polymorphism, Genetic; Sex Factors; Valine	2006
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism in schizophrenia is associated with age at onset and symptoms. Neuroscience letters, 2006, Jun-19, Volume: 401, Issue:1-2 Topics: Adult; Age of Onset; Aged; Amino Acid Substitution; Antipsychotic Agents; Brain; Brain Chemistry; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Drug Resistance; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Schizophrenia; Valine	2006
An association study of catechol-O-methyltransferase and monoamine oxidase A polymorphisms and personality traits in Koreans. Neuroscience letters, 2006, Jun-19, Volume: 401, Issue:1-2 Topics: Adult; Amino Acid Substitution; Asian People; Avoidance Learning; Brain; Brain Chemistry; Catechol O-Methyltransferase; Catecholamines; DNA Mutational Analysis; Fear; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype; Humans; Male; Methionine; Monoamine Oxidase; Neuropsychological Tests; Personality; Polymorphism, Genetic; Sex Characteristics; Valine	2006
The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study. The journal of headache and pain, 2006, Volume: 7, Issue:2 Topics: Adult; Catechol O-Methyltransferase; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Headache; Humans; Male; Methionine; Middle Aged; Norway; Polymorphism, Genetic; Sex Factors; Valine	2006
Long-duration sCJD with PRNP codon 129 methionine homozygosity and cerebral cortical plaques. Neurology, 2006, Jun-27, Volume: 66, Issue:12 Topics: Adult; Amyloid; Brain Diseases; Codon; Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Homozygote; Humans; Kuru; Methionine; Mutation; Plaque, Amyloid; Prion Proteins; Prions; Protein Precursors; Time Factors	2006
Prefrontal electrophysiologic "noise" and catechol-O-methyltransferase genotype in schizophrenia. Biological psychiatry, 2006, Sep-15, Volume: 60, Issue:6 Topics: Acoustic Stimulation; Adolescent; Adult; Analysis of Variance; Catechol O-Methyltransferase; Confidence Intervals; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Noise; Odds Ratio; Polymorphism, Single Nucleotide; Prefrontal Cortex; Retrospective Studies; Schizophrenia; Sex Factors; Valine	2006
Genetic polymorphism of folate and methionine metabolizing enzymes and their susceptibility to malignant lymphoma. Journal of the Egyptian National Cancer Institute, 2005, Volume: 17, Issue:3 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Child; Child, Preschool; DNA Methylation; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Humans; Lymphoma; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Genetic	2005
Associations between COMTVal158Met polymorphism and cognition: direct or indirect effects? European psychiatry : the journal of the Association of European Psychiatrists, 2006, Volume: 21, Issue:5 Topics: Adult; Alleles; Attention; Catechol O-Methyltransferase; Cognition Disorders; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Genetic; Reaction Time; Risk; Schizophrenia; Schizotypal Personality Disorder; Valine	2006
Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease. Neurobiology of aging, 2007, Volume: 28, Issue:8 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Catechol O-Methyltransferase; Chi-Square Distribution; Cognition; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Humans; Linkage Disequilibrium; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Psychotic Disorders; Risk; Valine	2007
COMT Association Data in Schizophrenia: New Caveats. Biological psychiatry, 2006, Sep-15, Volume: 60, Issue:6 Topics: Asia; Catechol O-Methyltransferase; Community Health Planning; Europe; Genetic Predisposition to Disease; Humans; Meta-Analysis as Topic; Methionine; Odds Ratio; Schizophrenia; Valine	2006
The 196G/A (val66met) polymorphism of the BDNF gene is significantly associated with binge eating behavior in women with bulimia nervosa or binge eating disorder. Neuroscience letters, 2006, Oct-02, Volume: 406, Issue:1-2 Topics: Amino Acid Substitution; Brain; Brain Chemistry; Brain-Derived Neurotrophic Factor; Bulimia Nervosa; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Methionine; Mutation; Polymorphism, Genetic; Valine; White People	2006
No evidence of association between BDNF gene variants and age-at-onset of Huntington's disease. Neurobiology of disease, 2006, Volume: 24, Issue:2 Topics: Adolescent; Adult; Age of Onset; Amino Acid Substitution; Brain; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype; Humans; Huntington Disease; Male; Methionine; Middle Aged; Polymorphism, Genetic; Promoter Regions, Genetic; Silencer Elements, Transcriptional; Trinucleotide Repeat Expansion; Valine	2006
Polymorphism in the angiotensinogen gene, hypertension, and ethnic differences in the risk of recurrent coronary events. Hypertension (Dallas, Tex. : 1979), 2006, Volume: 48, Issue:4 Topics: Aged; Angiotensin-Converting Enzyme Inhibitors; Angiotensinogen; Black People; Cardiovascular Diseases; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Hypertension; Male; Methionine; Middle Aged; Myocardial Infarction; Polymorphism, Genetic; Prospective Studies; Recurrence; Threonine; White People	2006
M129V variation in the prion protein gene and psychotic disorders: relationship to neuropsychological and psychopathological measures. Journal of psychiatric research, 2007, Volume: 41, Issue:10 Topics: Adult; Aged; Alleles; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homozygote; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Phenotype; Polymorphism, Genetic; Prion Proteins; Prions; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Schizophrenic Psychology; Valine; Wechsler Scales	2007
Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington's disease. Neurobiology of disease, 2006, Volume: 24, Issue:2 Topics: Age of Onset; Alzheimer Disease; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Haplotypes; Huntington Disease; Introns; Methionine; Polymorphism, Single Nucleotide; Trinucleotide Repeat Expansion; Valine	2006
Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal. Muscle & nerve, 2007, Volume: 35, Issue:1 Topics: Adult; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Amyloid Neuropathies, Familial; Autonomic Nervous System Diseases; Female; Genetic Predisposition to Disease; Geography; Humans; Inheritance Patterns; Longitudinal Studies; Male; Methionine; Middle Aged; Mutation; Neuralgia; Peripheral Nervous System Diseases; Portugal; Prospective Studies; Sex Distribution; Valine	2007
Relationship of catechol-O-methyltransferase variants to brain structure and function in a population at high risk of psychosis. Biological psychiatry, 2007, May-15, Volume: 61, Issue:10 Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Brain; Catechol O-Methyltransferase; Cohort Studies; Dominance, Cerebral; Dopamine; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Gyrus Cinguli; Humans; Image Processing, Computer-Assisted; Imaging, Three-Dimensional; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Prefrontal Cortex; Risk Factors; Schizophrenia; Schizophrenic Language; Schizophrenic Psychology; Scotland; Valine	2007
Catechol-o-methyltransferase gene polymorphism in dementia with Lewy bodies-related psychosis: evidence for a genetic predisposition. International psychogeriatrics, 2006, Volume: 18, Issue:4 Topics: Aged; Alleles; Catechol O-Methyltransferase; Corpus Striatum; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Humans; Lewy Body Disease; Methionine; Polymorphism, Genetic; Psychotic Disorders; Risk Factors; Valine	2006
Family-based and case-control study of DRD2, DAT, 5HTT, COMT genes polymorphisms in alcohol dependence. Neuroscience letters, 2006, Dec-13, Volume: 410, Issue:1 Topics: Adult; Alcoholism; Alleles; Case-Control Studies; Catechol O-Methyltransferase; Dopamine Plasma Membrane Transport Proteins; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Linkage Disequilibrium; Male; Methionine; Middle Aged; Minisatellite Repeats; Polymorphism, Genetic; Receptors, Dopamine D2; Serotonin Plasma Membrane Transport Proteins; Valine	2006
Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women. Neuroscience letters, 2007, Jun-21, Volume: 421, Issue:1 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Child; Epilepsy, Temporal Lobe; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Prion Proteins; Prions; Sex Characteristics; Valine	2007
Association of SUMO4 M55V polymorphism with autoimmune diabetes in Latvian patients. Annals of the New York Academy of Sciences, 2006, Volume: 1079 Topics: Adolescent; Alleles; Autoimmune Diseases; Case-Control Studies; Child; Child, Preschool; Diabetes Mellitus, Type 1; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Infant; Latvia; Male; Methionine; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Small Ubiquitin-Related Modifier Proteins	2006
Regulatory sequences of the PRNP gene influence susceptibility to sporadic Creutzfeldt-Jakob disease. Neuroscience letters, 2007, Jan-16, Volume: 411, Issue:3 Topics: Creutzfeldt-Jakob Syndrome; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Polymorphism, Single Nucleotide; Prion Proteins; Prions; Regulatory Elements, Transcriptional; Valine	2007
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human molecular genetics, 2007, Jan-01, Volume: 16, Issue:1 Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors	2007
Association of the met66 allele of brain-derived neurotrophic factor (BDNF) with smoking. Psychopharmacology, 2007, Volume: 190, Issue:4 Topics: Adult; Aged; Analysis of Variance; Brain-Derived Neurotrophic Factor; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Germany; Humans; Male; Methionine; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Reference Values; Risk Assessment; Smoking; Surveys and Questionnaires; Tobacco Use Disorder; Valine	2007
Gender-specific effects of the catechol-O-methyltransferase Val108/158Met polymorphism on cognitive function in children. The American journal of psychiatry, 2007, Volume: 164, Issue:1 Topics: Adolescent; Adult; Brain; Catechol O-Methyltransferase; Child; Child Development; Cognition; England; Female; Frontal Lobe; Genetic Predisposition to Disease; Genetic Testing; Humans; Intelligence; Longitudinal Studies; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Prefrontal Cortex; Puberty; Schizophrenia; Sex Factors; Valine	2007
Association of functional catechol O-methyl transferase (COMT) Val108Met polymorphism with smoking severity and age of smoking initiation in Chinese male smokers. Psychopharmacology, 2007, Volume: 190, Issue:4 Topics: Adult; Age Factors; Aged; Asian People; Catechol O-Methyltransferase; China; Cohort Studies; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Middle Aged; Odds Ratio; Polymorphism, Genetic; Smoking; Smoking Cessation; Tobacco Use Disorder; Valine	2007
Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome. Biological psychiatry, 2007, May-15, Volume: 61, Issue:10 Topics: Adult; Alleles; Amino Acid Substitution; Arousal; Chromosome Deletion; Chromosomes, Human, Pair 22; Female; Frontal Lobe; Gene Expression; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Schizophrenia; Syndrome; Valine	2007
Dietary intake of folate and co-factors in folate metabolism, MTHFR polymorphisms, and reduced rectal cancer. Cancer causes & control : CCC, 2007, Volume: 18, Issue:2 Topics: Adult; Aged; Alcohol Drinking; California; Case-Control Studies; Diet; Diet Surveys; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Rectal Neoplasms; Riboflavin; Risk; Utah; Vitamin B 12; Vitamin B 6	2007
Influence of catechol-O-methyltransferase Val158Met polymorphism on neuropsychological and functional outcomes of classical rehabilitation and cognitive remediation in schizophrenia. Neuroscience letters, 2007, May-07, Volume: 417, Issue:3 Topics: Amino Acid Substitution; Brain; Brain Chemistry; Catechol O-Methyltransferase; Cognition Disorders; Cognitive Behavioral Therapy; DNA Mutational Analysis; Female; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Quality of Life; Recovery of Function; Schizophrenia; Treatment Outcome; Valine	2007
The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers the susceptibility to NASH in Japanese population. Journal of hepatology, 2007, Volume: 46, Issue:5 Topics: Adult; Alleles; Asian People; DNA Primers; Fatty Liver; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Japan; Male; Methionine; Middle Aged; Phosphatidylethanolamine N-Methyltransferase; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Valine	2007
Association of the brain-derived neurotrophic factor Val66Met polymorphism with reduced hippocampal volumes in major depression. Archives of general psychiatry, 2007, Volume: 64, Issue:4 Topics: Adult; Amygdala; Atrophy; Brain-Derived Neurotrophic Factor; Cross-Sectional Studies; Depressive Disorder, Major; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Methionine; Neuronal Plasticity; Polymorphism, Genetic; Valine	2007
Nuclear receptor NR4A2 IVS6 +18insG and brain derived neurotrophic factor (BDNF) V66M polymorphisms and risk of Taiwanese Parkinson's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2007, Jun-05, Volume: 144B, Issue:4 Topics: Adult; Aged; Aged, 80 and over; Asian People; Brain-Derived Neurotrophic Factor; Case-Control Studies; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Nuclear Receptor Subfamily 4, Group A, Member 2; Parkinson Disease; Polymorphism, Genetic; Risk Factors; Sex Characteristics; Taiwan; Transcription Factors; Valine	2007
The discoidin domain receptor 1 as a novel susceptibility gene for schizophrenia. Molecular psychiatry, 2007, Volume: 12, Issue:9 Topics: Adult; Aged; Aged, 80 and over; Asparagine; Chi-Square Distribution; Discoidin Domain Receptor 1; DNA Mutational Analysis; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Receptor Protein-Tyrosine Kinases; Regression Analysis; Reverse Transcriptase Polymerase Chain Reaction; Schizophrenia; Serine; Valine	2007
Interactions between life stressors and susceptibility genes (5-HTTLPR and BDNF) on depression in Korean elders. Biological psychiatry, 2007, Sep-01, Volume: 62, Issue:5 Topics: Aged; Aged, 80 and over; Brain-Derived Neurotrophic Factor; Chi-Square Distribution; Cross-Sectional Studies; Depression; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Geriatrics; Humans; Korea; Male; Methionine; Polymorphism, Genetic; Predictive Value of Tests; Prospective Studies; Psychiatric Status Rating Scales; Serotonin Plasma Membrane Transport Proteins; Stress, Psychological; Valine	2007
Association between nasal carriage of Staphylococcus aureus and the human complement cascade activator serine protease C1 inhibitor (C1INH) valine vs. methionine polymorphism at amino acid position 480. FEMS immunology and medical microbiology, 2007, Volume: 50, Issue:3 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Sequence; Amino Acid Substitution; Carrier State; Complement C1 Inactivator Proteins; Complement C1 Inhibitor Protein; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Molecular Sequence Data; Nose; Polymorphism, Genetic; Serpins; Staphylococcal Infections; Staphylococcus aureus; Valine	2007
NADH dehydrogenase subunit-2 237 Leu/Met polymorphism modifies the effects of alcohol consumption on risk for hypertension in middle-aged Japanese men. Hypertension research : official journal of the Japanese Society of Hypertension, 2007, Volume: 30, Issue:3 Topics: Alcohol Drinking; Asian People; Blood Pressure; Cross-Sectional Studies; Genetic Predisposition to Disease; Genotype; Humans; Hypertension; Japan; Leucine; Male; Methionine; Middle Aged; NADH Dehydrogenase; Polymorphism, Restriction Fragment Length; Protein Subunits; Risk Factors	2007
Association of the COMT val158met variant with antidepressant treatment response in major depression. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:4 Topics: Adult; Antidepressive Agents; Bipolar Disorder; Catechol O-Methyltransferase; Depressive Disorder, Major; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Pharmacogenetics; Polymorphism, Genetic; Valine	2008
BDNF Met66 allele is associated with anorexia nervosa in the Polish population. Psychiatric genetics, 2007, Volume: 17, Issue:4 Topics: Amino Acid Substitution; Anorexia Nervosa; Brain-Derived Neurotrophic Factor; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Poland; Polymorphism, Single Nucleotide; Valine; White People	2007
The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans. Neuroreport, 2007, Aug-06, Volume: 18, Issue:12 Topics: Adult; Amino Acid Substitution; Brain; Brain Chemistry; Brain-Derived Neurotrophic Factor; Depressive Disorder; DNA Mutational Analysis; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Homozygote; Humans; Male; Methionine; Mexican Americans; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Valine	2007
Association analysis of gamma2 subunit of gamma-aminobutyric acid (GABA) type A receptor and voltage-gated sodium channel type II alpha-polypeptide gene mutation in southern Chinese children with febrile seizures. Journal of child neurology, 2007, Volume: 22, Issue:6 Topics: Arginine; Chi-Square Distribution; Child; Child, Preschool; China; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Infant; Lysine; Male; Methionine; Mutation; NAV1.2 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Polymorphism, Single Nucleotide; Receptors, GABA-A; Seizures, Febrile; Sodium Channels; Tryptophan	2007
Brain-derived neurotrophic factor polymorphisms and smoking in schizophrenia. Schizophrenia research, 2007, Volume: 97, Issue:1-3 Topics: Adult; Alleles; Asian People; Brain-Derived Neurotrophic Factor; Chromosomes, Human, Pair 11; Chronic Disease; Comorbidity; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; RNA, Messenger; Schizophrenia; Smoking; Tobacco Use Disorder; Valine	2007
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS. The international journal of neuropsychopharmacology, 2008, Volume: 11, Issue:3 Topics: Adolescent; Adult; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, Pair 22; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Single-Stranded Conformational; Valine	2008
The BDNF Val66Met polymorphism predicts rumination and depression differently in young adolescent girls and their mothers. Neuroscience letters, 2007, Dec-11, Volume: 429, Issue:1 Topics: Adolescent; Adult; Brain-Derived Neurotrophic Factor; Depression; DNA Mutational Analysis; Family Health; Feeding and Eating Disorders of Childhood; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Methionine; Middle Aged; Mother-Child Relations; Polymorphism, Genetic; Valine	2007
Brain-derived neurotrophic factor polymorphism Val66Met influences cognitive abilities in the elderly. Genes, brain, and behavior, 2008, Volume: 7, Issue:4 Topics: Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Atrophy; Brain-Derived Neurotrophic Factor; Cognition Disorders; Cohort Studies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Memory; Memory Disorders; Methionine; Middle Aged; Mutation; Neuropsychological Tests; Polymorphism, Genetic; Valine	2008
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen study. Calcified tissue international, 2007, Volume: 81, Issue:6 Topics: Absorptiometry, Photon; Alanine; Androgens; Bone Density; Gene Frequency; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; LDL-Receptor Related Proteins; Life Style; Low Density Lipoprotein Receptor-Related Protein-5; Male; Methionine; Polymorphism, Single Nucleotide; Valine; White People	2007
MC1R variants associated susceptibility to basal cell carcinoma of skin: interaction with host factors and XRCC3 polymorphism. International journal of cancer, 2008, Apr-15, Volume: 122, Issue:8 Topics: Adult; Aged; Arginine; Carcinoma, Basal Cell; Case-Control Studies; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Hungary; Male; Methionine; Middle Aged; Polymorphism, Genetic; Receptor, Melanocortin, Type 1; Risk Factors; Romania; Sequence Analysis, DNA; Skin Neoplasms; Slovakia; Threonine	2008
Catechol-O-methyltransferase Val158Met polymorphism and clinical characteristics in first episode non-affective psychosis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008, Jul-05, Volume: 147B, Issue:5 Topics: Adolescent; Adult; Affective Disorders, Psychotic; Age of Onset; Amino Acid Substitution; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Psychotic Disorders; Schizophrenia; Valine	2008
Personality in relation to genetic liability for schizophrenia and bipolar disorder: differential associations with the COMT Val 108/158 Met polymorphism. Schizophrenia research, 2008, Volume: 100, Issue:1-3 Topics: Adult; Bipolar Disorder; Catechol O-Methyltransferase; Depressive Disorder, Major; Family; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Male; Methionine; Middle Aged; Pedigree; Personality; Personality Assessment; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Schizophrenia; Schizophrenic Psychology; Schizotypal Personality Disorder; Self Concept; Surveys and Questionnaires; Valine	2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2. BMC neurology, 2008, Jan-22, Volume: 8 Topics: Aged; alpha-Synuclein; DNA Mutational Analysis; Exons; Family Health; Female; Genetic Predisposition to Disease; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Methionine; Middle Aged; Mutation; Parkinson Disease; Portugal; Protein Kinases; Protein Serine-Threonine Kinases; Threonine; Ubiquitin-Protein Ligases	2008
Association of the brain-derived neurotrophic factor gene and bipolar disorder with early age of onset in mainland China. Neuroscience letters, 2008, Mar-12, Volume: 433, Issue:2 Topics: Adult; Age of Onset; Bipolar Disorder; Brain-Derived Neurotrophic Factor; China; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Valine	2008
A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder. Archives of general psychiatry, 2008, Volume: 65, Issue:2 Topics: Adolescent; Adult; Aggression; Antisocial Personality Disorder; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Child, Preschool; Codon; Cohort Studies; Conduct Disorder; Crime; Diseases in Twins; England; Female; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Longitudinal Studies; Male; Methionine; New Zealand; Phenotype; Polymorphism, Genetic; Reproducibility of Results; Valine; Wales	2008
Association of missense variants of the PRKC, apoptosis, WT1, regulator (PAWR) gene with schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry, 2008, Apr-01, Volume: 32, Issue:3 Topics: 5' Untranslated Regions; Adult; Apoptosis Regulatory Proteins; Arginine; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Methionine; Middle Aged; Mutation, Missense; Polymorphism, Genetic; Proline; Schizophrenia; Sex Factors; Taiwan	2008
Association between the brain-derived neurotrophic factor Val66Met polymorphism and brain morphology in a Japanese sample of schizophrenia and healthy comparisons. Neuroscience letters, 2008, Apr-11, Volume: 435, Issue:1 Topics: Adult; Amino Acid Substitution; Atrophy; Brain; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Female; Functional Laterality; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Japan; Magnetic Resonance Imaging; Male; Methionine; Parahippocampal Gyrus; Polymorphism, Genetic; Schizophrenia; Valine	2008
Evidence that the COMTVal158Met polymorphism moderates subclinical psychotic and affective symptoms in unaffected first-degree relatives of patients with schizophrenia. European psychiatry : the journal of the Association of European Psychiatrists, 2008, Volume: 23, Issue:3 Topics: Adult; Brief Psychiatric Rating Scale; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Psychiatric Status Rating Scales; Psychotic Disorders; Risk Factors; Schizophrenia; Valine	2008
Cardiac autonomic dysfunction: effects from particulate air pollution and protection by dietary methyl nutrients and metabolic polymorphisms. Circulation, 2008, Apr-08, Volume: 117, Issue:14 Topics: Aged; Aged, 80 and over; Boston; Cardiotonic Agents; Case-Control Studies; Diet; Folic Acid; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glycine Hydroxymethyltransferase; Heart Conduction System; Heart Rate; Humans; Male; Meteorological Concepts; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Particulate Matter; Polymorphism, Single Nucleotide; Risk Factors; Vitamin B Complex	2008
Association study of a functional catechol-O-methyltransferase polymorphism and executive function in elderly males without dementia. Neuroscience letters, 2008, May-09, Volume: 436, Issue:2 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Attention; Catechol O-Methyltransferase; Cognition Disorders; Genetic Predisposition to Disease; Genotype; Geriatric Assessment; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Problem Solving; Psychomotor Performance; Valine	2008
Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes. Biological psychiatry, 2008, Aug-15, Volume: 64, Issue:4 Topics: Adult; Anxiety Disorders; Catechol O-Methyltransferase; Chi-Square Distribution; Community Health Planning; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Linkage Disequilibrium; Longitudinal Studies; Male; Methionine; Middle Aged; Odds Ratio; Phenotype; Polymorphism, Genetic; Valine	2008
Polymorphisms of methionine metabolism and susceptibility to meningioma formation: laboratory investigation. Journal of neurosurgery, 2008, Volume: 108, Issue:5 Topics: Brain Neoplasms; Female; Genetic Predisposition to Disease; Genetic Variation; Humans; Male; Meningioma; Methionine; Middle Aged; Polymorphism, Genetic	2008
The association of genotypic combination of the DRD3 and BDNF polymorphisms on the adhesio interthalamica and medial temporal lobe structures. Progress in neuro-psychopharmacology & biological psychiatry, 2008, Jul-01, Volume: 32, Issue:5 Topics: Adolescent; Adult; Brain-Derived Neurotrophic Factor; Dominance, Cerebral; Female; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Magnetic Resonance Imaging; Male; Methionine; Polymorphism, Genetic; Receptors, Dopamine D3; Schizophrenia; Serine; Temporal Lobe; Thalamus; Valine	2008
Investigation of the functional brain-derived neurotrophic factor gene variant Val66MET in migraine. Journal of neural transmission (Vienna, Austria : 1996), 2008, Volume: 115, Issue:9 Topics: Adult; Aged; Amino Acid Sequence; Amino Acid Substitution; Brain; Brain-Derived Neurotrophic Factor; Case-Control Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Migraine Disorders; Polymorphism, Genetic; Risk Factors; Valine	2008
Decreased neurotrophic response to birth hypoxia in the etiology of schizophrenia. Biological psychiatry, 2008, Nov-01, Volume: 64, Issue:9 Topics: Brain-Derived Neurotrophic Factor; Case-Control Studies; Cohort Studies; Female; Fetal Hypoxia; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Risk Factors; Schizophrenia; Valine	2008
Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programme. Journal of inherited metabolic disease, 2008, Volume: 31 Suppl 2 Topics: Amino Acid Metabolism, Inborn Errors; Biomarkers; Child Development; Child, Preschool; Early Diagnosis; Female; Genetic Predisposition to Disease; Homocysteine; Humans; Infant; Infant, Newborn; Male; Methionine; Methionine Adenosyltransferase; Mutation; Neonatal Screening; Pedigree; Phenotype; Predictive Value of Tests; Prognosis; Spain; Tandem Mass Spectrometry; Up-Regulation	2008
A novel G3337A mitochondrial ND1 mutation related to cardiomyopathy co-segregates with tRNALeu(CUN) A12308G and tRNAThr C15946T mutations. Mitochondrion, 2008, Volume: 8, Issue:3 Topics: Aged; Amino Acid Sequence; Amino Acid Substitution; Cardiomyopathies; Case-Control Studies; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Family; Female; Genetic Predisposition to Disease; Humans; Infant, Newborn; Methionine; Mitochondria; Molecular Sequence Data; Molecular Structure; Mutation; NADH Dehydrogenase; Pedigree; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Protein Structure, Secondary; RNA, Transfer, Leu; RNA, Transfer, Thr	2008
Catechol-O-methyltransferase Val158Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder. Pharmacogenetics, 1997, Volume: 7, Issue:5 Topics: Bipolar Disorder; Catechol O-Methyltransferase; China; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Point Mutation; Polymorphism, Genetic; Valine	1997
Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report. Thrombosis and haemostasis, 1998, Volume: 80, Issue:6 Topics: 3' Untranslated Regions; Adult; Aged; Brain Ischemia; Female; Genetic Predisposition to Disease; Homocysteine; Homozygote; Humans; Male; Methionine; Middle Aged; Prothrombin; Risk Factors; Thrombophilia; Thrombophlebitis	1998
Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis. Lancet (London, England), 1999, Feb-06, Volume: 353, Issue:9151 Topics: Codon; Genetic Predisposition to Disease; Homozygote; Humans; Methionine; Middle Aged; Myositis, Inclusion Body; Prions	1999
Is the oral methionine loading test insensitive to the remethylation pathway of homocysteine? Blood, 1999, Feb-01, Volume: 93, Issue:3 Topics: Artifacts; Folic Acid Deficiency; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Reproducibility of Results; Risk Factors; Thrombophilia	1999
Identification and functional analysis of novel human melanocortin-4 receptor variants. Diabetes, 1999, Volume: 48, Issue:3 Topics: Adolescent; Adult; Amino Acid Substitution; Animals; Body Mass Index; Cloning, Molecular; Diabetes Mellitus; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Isoleucine; Male; Methionine; Mice; Middle Aged; Obesity; Pedigree; Polymorphism, Single-Stranded Conformational; Receptor, Melanocortin, Type 4; Receptors, Peptide; Recombinant Proteins; Threonine; Valine	1999
Determinants of fasting and post-methionine homocysteine levels in families predisposed to hyperhomocysteinemia and premature vascular disease. Arteriosclerosis, thrombosis, and vascular biology, 1999, Volume: 19, Issue:5 Topics: Adult; Age Factors; Amino Acid Substitution; Arteriosclerosis; Body Mass Index; Comorbidity; Fasting; Female; Folic Acid; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Hyperhomocysteinemia; Hypertension; Lipids; Male; Menopause; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Oxidoreductases Acting on CH-NH Group Donors; Polymorphism, Genetic; Pyridoxine; Smoking; Vitamin B 12	1999
The combination of polymorphisms within interferon-gamma receptor 1 and receptor 2 associated with the risk of systemic lupus erythematosus. FEBS letters, 1999, Jun-18, Volume: 453, Issue:1-2 Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Interferon gamma Receptor; Lupus Erythematosus, Systemic; Male; Methionine; Middle Aged; Molecular Sequence Data; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Receptors, Interferon; Reverse Transcriptase Polymerase Chain Reaction; Valine	1999
Splice-site mutations in atherosclerosis candidate genes: relating individual information to phenotype. Circulation, 1999, Aug-17, Volume: 100, Issue:7 Topics: Amino Acid Substitution; Arteriosclerosis; DNA Mutational Analysis; Gene Expression Regulation; Genes; Genetic Predisposition to Disease; Humans; Hyperlipidemias; Information Theory; Lipid Metabolism; Methionine; Models, Genetic; Phenotype; Point Mutation; Protein Biosynthesis; Risk Factors; RNA Splicing; RNA, Messenger; Severity of Illness Index	1999
Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype. The Journal of infectious diseases, 2001, Jan-15, Volume: 183, Issue:2 Topics: Amyloid; Child; Child, Preschool; Codon; Disease Outbreaks; Female; Genetic Predisposition to Disease; Genotype; Humans; Infant; Kuru; Male; Methionine; Mutation; New Guinea; Polymorphism, Genetic; Prion Proteins; Prions; Protein Precursors; Sequence Analysis, DNA	2001
A polymorphism in the 5' untranslated region and a Met229-->Leu variant in exon 5 of the human UCP1 gene are associated with susceptibility to type II diabetes mellitus. Diabetologia, 2001, Volume: 44, Issue:3 Topics: 5' Untranslated Regions; Aged; Alleles; Amino Acid Substitution; Asian People; Carrier Proteins; Diabetes Mellitus, Type 2; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Ion Channels; Japan; Leucine; Male; Membrane Proteins; Methionine; Middle Aged; Mitochondria; Mitochondrial Proteins; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Reference Values; Uncoupling Protein 1	2001
Methionine adenosyltransferase 1A knockout mice are predisposed to liver injury and exhibit increased expression of genes involved in proliferation. Proceedings of the National Academy of Sciences of the United States of America, 2001, May-08, Volume: 98, Issue:10 Topics: Animals; Cell Division; Disease Models, Animal; DNA Methylation; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Liver; Liver Cirrhosis, Experimental; Methionine; Methionine Adenosyltransferase; Mice; Mice, Knockout; Phenotype	2001
Association between polymorphisms of folate- and methionine-metabolizing enzymes and susceptibility to malignant lymphoma. Blood, 2001, May-15, Volume: 97, Issue:10 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Aged; Aged, 80 and over; Case-Control Studies; DNA; DNA Methylation; Folic Acid; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Lymphoma; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Oxidoreductases Acting on CH-NH Group Donors; Polymorphism, Genetic	2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age. The American journal of cardiology, 2001, Jun-01, Volume: 87, Issue:11 Topics: Adolescent; Adult; Age Factors; Cardiomyopathy, Hypertrophic; Child; Cohort Studies; Death, Sudden, Cardiac; DNA Glycosylases; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Myosin Heavy Chains; N-Glycosyl Hydrolases; Nonmuscle Myosin Type IIB; Pedigree; Risk; Survival Analysis; Valine	2001
Adverse event associated with methionine loading test: a case report. Arteriosclerosis, thrombosis, and vascular biology, 2002, Jun-01, Volume: 22, Issue:6 Topics: Administration, Oral; Aged; Black or African American; Brain Death; Disease Susceptibility; Drug Contamination; Drug Overdose; Fatal Outcome; Female; Genetic Predisposition to Disease; Humans; Hyperhomocysteinemia; Inactivation, Metabolic; Metabolism, Inborn Errors; Methionine	2002