valine and Genetic Predisposition

valine has been researched along with Genetic Predisposition in 333 studies

Research

Studies (333)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	10 (3.00)	18.2507
2000's	178 (53.45)	29.6817
2010's	138 (41.44)	24.3611
2020's	7 (2.10)	2.80

Authors

Authors	Studies
Chou, WP; Ko, CH; Lin, HC; Lin, PC; Lin, PY; Yen, JY	1
Andreou, AC; Eliopoulos, EE; Goulielmos, GN; Zervou, MI	1
Kumar, P; Rai, V	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
Bararpour, N; Darrous, L; Froguel, P; Gasser, M; Gilardi, F; Kutalik, Z; Marques-Vidal, P; Porcu, E; Thomas, A; Waeber, G; Yengo, L	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
Amemiya, F; Asahina, Y; Enomoto, N; Fukasawa, M; Inoue, T; Kuratomi, N; Maekawa, S; Matsuda, S; Miura, M; Murakawa, M; Muraoka, M; Nakagawa, M; Nakakuki, N; Nakayama, Y; Sakamoto, M; Sato, M; Sato, T; Suzuki, Y; Takano, S; Tatsumi, A; Yamaguchi, T	1
Hamaguchi, T; Hizume, M; Ito, Y; Kitamoto, T; Kobayashi, A; Mizusawa, H; Ohgami, T; Sanjo, N; Satoh, K; Yamada, M; Yokota, T	1
Alston, CL; Bonnen, PE; Crushell, E; Ferdinandusse, S; Fitzsimons, PE; Geraghty, MT; Hughes, J; Mayne, PD; O'Reilly, P; Pitt, JJ; Sheikh, Y; Taylor, RW; Tetreault, M; Twomey, E; Walsh, R; Wanders, RJA; Waterham, HR	1
Danzi, BA; La Greca, AM	1
Hällfors, J; Kaprio, J; Korhonen, T; Loukola, A; Salomaa, V	1
Khan, AJ; Mohindra, S; Negi, TS; Parmar, D; Ranjan, P; Saraswat, VA	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
Aurilia, C; Barbanti, P; De Marchis, ML; Della-Morte, D; Egeo, G; Fofi, L; Guadagni, F; Ialongo, C; Ludovici, G; Palmirotta, R	1
Sun, HM; Wang, ZZ; Zhang, Y	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
Abdelrahman, HM; Fattah, NR; Hashim, HM; Hassan, TH; Karam, RA; Mohammad, D; Rezk, NA	1
Darabi, M; Ghaleh, TD; Najafipour, R; Rashvand, Z; Sahmani, M	1
Boyd, A; Collins, SJ; Johanssen, V; Klug, G; Lewis, V; Li, QX; Masters, CL; McLean, C; Pamphlett, R; Simpson, M	1
Ermolenko, NA; Filipenko, ML; Gareeva, JV; Glushkov, AN; Gordeeva, LA; Simonova, TA; Sokolova, EA; Sutulina, IM; Voronina, EN	1
Gong, H; Guan, H; Guo, S; Lang, Z; Liu, B; Liu, L; Wang, H; Zhang, J	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
Eum, KD; Hersh, CP; Hu, H; Kelsey, K; Schwartz, J; Sparrow, D; Spiro, A; Wang, FT; Weisskopf, MG; Wright, RO	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
Cath, DC; Hemmings, SM; Lochner, C; Seedat, S; Stein, DJ; van der Merwe, L	1
Gharbi, O; Kassab, A; Lakhdar, R; Miled, A; Msolly, A	1
Alosco, ML; Cohen, RA; Gunstad, J; McGeary, JE; Miller, LA; Poppas, A; Szabo, AJ	1
Ambite-Quesada, S; Caminero, AB; Fernández-de-las-Peñas, C; Gil-Crujera, A; Ortega-Santiago, R; Ortíz-Gutiérrez, R	1
Furukawa, M; Hashida, S; Higasa, K; Ichimura, K; Kiura, K; Matsuda, F; Matsuo, K; Miyoshi, S; Sakaguchi, M; Shien, K; Soh, J; Takigawa, N; Toyooka, S; Tsukuda, K; Yamamoto, H	1
Chang, YH; Chen, PS; Chen, SH; Chen, SL; Chu, CH; Hong, JS; Lee, IH; Lee, SY; Lu, RB; Wang, TY; Yang, YK	1
Cheng, H; Lu, J; Qin, Q; Sun, X; Xu, L; Yang, X; Zhan, L; Zhang, C; Zhu, H	1
Alavantić, D; Dinčić, E; Djurić, T; Stanković, A; Stojković, L; Zivković, M	1
Cheng, FB; Feng, JC; Grundmann, K; Ma, LY; Miao, J; Ott, T; Wan, XH	1
Alonso-Canovas, A; Bernal-Bernal, I; Blanco-Ollero, A; Bonilla-Toribio, M; Burguera, JA; Cáceres-Redondo, MT; Carballo, M; Carrillo, F; Catalán-Alonso, MJ; Escamilla-Sevilla, F; Espinosa-Rosso, R; Fernández-Moreno, MC; García-Caldentey, J; García-Moreno, JM; García-Ruiz, PJ; Giacometti-Silveira, S; Gómez-Garre, P; Gutiérrez-García, J; Huertas-Fernández, I; Jesús, S; López-Valdés, E; Martínez-Castrillo, JC; Martínez-Torres, I; Medialdea-Natera, MP; Méndez-Lucena, C; Mínguez-Castellanos, A; Mir, P; Moya, M; Ochoa-Sepulveda, JJ; Ojea, T; Rodríguez, N; Sillero-Sánchez, M; Vargas-González, L	1
Betz, BL; Brown, NA; Elenitoba-Johnson, KS; Furtado, LV; Kiel, MJ; Lim, MS; Weigelin, HC	1
Chang, CC; Chang, HA; Chen, TY; Fang, WH; Huang, SY	1
Chen, SD; Dong, F; Liu, J; Quinn, TJ; Wang, Y; Wu, H; Xiao, Q; Yang, Q; Zhao, J	1
Dong, YL; He, HR; Hu, SS; Lu, J; Ma, Y; Sun, JY; You, HS	1
Chen, P; Guo, M; Li, L; Liu, J; Lu, L	1
Alberts, SR; Berenberg, JL; Diasio, RB; Goldberg, RM; Lee, AM; Pavey, E; Sargent, DJ; Shi, Q; Sinicrope, FA	1
Chao, HT; Chen, LF; Hsieh, JC; Lee, LC; Lin, MW; Shen, HD; Tu, CH	1
Bucossi, S; Mariani, S; R, RS; Simonelli, I; Siotto, M; Ventriglia, M	1
Fang, Y; Gao, K; Li, Z; Wang, Z	1
Amin, N; C 't Hoen, PA; de Vries, B; Deelder, AM; Demirkan, A; Dharuri, H; Göraler, S; Henneman, P; Karssen, LC; Meissner, A; van den Maagdenberg, AM; van Dijk, KW; van Duijn, CM; van Klinken, JB; Verhoeven, A	1
Ling, W; Mijiti, A; Moming, A	1
Hou, C; Huang, J; Li, N; Liu, Z; Pu, J; Shan, H	1
Alfimova, MV; Gabaeva, MV; Golimbet, VE; Korovaitseva, GI; Lezheiko, TV; Oleichik, IV; Stolyarov, SA	1
Wang, T	1
Bittencourt, G; Crispim, D; da Silva, RA; Fabião, JD; Ghisleni, G; Jansen, K; Kaster, MP; Lara, DR; Moreira, FP; Oses, JP; Pinheiro, RT; Portela, LV; Quevedo, Lde Á; Souza, LD; Wiener, CD	1
Antozzi, C; Brancati, F; D Apice, MR; Federici, L; Maggi, L; Marshall, CR; Massa, R; Minassian, BA; Mora, M; Morandi, L; Novelli, G; Pasanisi, MB; Ruggieri, A; Sangiuolo, F; Saredi, S; Scherer, SW; Terracciano, C; Zanotti, S	1
García-Cárdenas, JM; Leone, PE; López-Cortés, A; Paz-Y-Miño, CA; Salazar, C; Serrano, M	1
Andershed, AK; Andershed, H; Colins, OF; Comasco, E; Fanti, KA; Narusyte, J; Nilsson, KW; Tuvblad, C	1
Al-Maghrabi, JA; Bakarman, M; Gar, MA; Gazzaz, ZJ; Ibrahim, AM; Khabaz, MN; Nedjadi, T	1
Hemmings, S; Malan-Müller, S; Seedat, S; Suliman, S; van den Heuvel, L	1
Madra, M; Zeltser, LM	1
Jiang, JR; Jin, SQ; Liao, YJ	1
Askar, T; Mansour, AA; Mergani, A; Mohammed, MA; Mustafa, AM; Saleh, OM; Zahran, RN	1
Ye, B; Ye, X	1
Ambler, K; Casolari, DA; D'Andrea, RJ; Nguyen, T; Ross, DM; Tiong, IS; Van Velzen, MJ	1
Barrantes-Vidal, N; Cristóbal-Narváez, P; de Castro-Catala, M; Derom, C; Jacobs, N; Kwapil, TR; Peña, E; Rosa, A; Sheinbaum, T; Thiery, E; van Nierop, M; van Os, J; van Winkel, R	1
Devoto, M; Emanuel, BS; Franconi, CP; Gur, RE; McDonald-McGinn, D; McNamara, MA; Moss, E; Salmons, H; Zackai, EH	1
Barbosa, MR; Cagni, FC; Campêlo, CLDC; Coimbra, DG; Gomes de Andrade, T; Júnior, COG; Júnior, LGO; Neto, ABS; Ribeiro, AM; Silva, RH	1
Arango, C; Arias, B; Bernardo, M; Bioque, M; Bulbena, A; Cabrera, B; Castro-Fornieles, J; Corripio, I; Cuesta, MJ; Díaz-Caneja, CM; Fraguas, D; González-Pinto, A; Lobo, A; Parellada, M; Rodríguez-Toscano, E; Sanjuán, J; Sarró, S; Vieta, E	1
Ettinger, U; Haraldsson, HM; Ingason, A; Magnusdottir, BB; Petursson, H; Sigmundsson, T; Sigurdsson, E	2
Bellingham, J; Goto, Y; Grace, AA; Grizenko, N; Joober, R; Polotskaia, A; Schmitz, N; Schwartz, G; Sengupta, S; Stepanian, MT	1
Berrettini, WH; Bloch, PJ; Dackis, CA; Ferraro, TN; Kampman, KM; Lohoff, FW; Nall, AH; O'Brien, CP; Oslin, DW; Pettinati, HM; Weller, AE	1
An, H; Cho, SN; Choi, JE; Han, C; Joe, SH; Jung, IK; Kang, SG; Kim, L; Kim, SH; Kim, YK; Lee, HJ; Lee, MS; Park, YM	1
Adem, A; Al-Haj, M; Awad, S; Bernsen, R; Hassan, AH; Kamal, H; Mohamed, AO; Siddig, A; Zilahi, E	1
Fukushima, M; Higashiyama, T; Hirokawa, M; Inoue, H; Ito, Y; Kihara, M; Kobayashi, K; Maruo, R; Matsuzuka, F; Miya, A; Miyauchi, A; Morita, S; Takamura, Y; Takano, T; Tomoda, C; Uruno, T; Yabuta, T; Yoshida, H	1
Hong, JP; Joo, YH; Kim, B; Kim, CY; Kim, SY; Lee, C	1
Lachman, HM	1
Armamento-Villareal, R; Bucchieri, S; Camarda, L; Camarda, MR; Di Fede, G; Giri, T; Jain, S; Mumm, S; Napoli, N; Rini, GB; Serber, D; Yarramaneni, J	1
Jia, W; Jiang, J; Li, L; Li, M; Liu, L; Wang, F; Wang, N; Zhao, R; Zhao, W; Zheng, T; Zhu, Q	1
Ivanitsky, AM; Kulikova, MA; Maluchenko, NV; Schegolkova, JV; Shlepzova, VA; Sysoeva, OV; Timofeeva, MA; Tonevitsky, AG	1
Cetin, E; Kanigür-Sultuybek, G; Onaran, I; Ozdemir, AT; Ozgönenel, L; Tezcan, G	1
Girodon, F; Gisslinger, H; Hao-Shen, H; Hermouet, S; Jäger, R; Kralovics, R; Looser, R; Schaub, FX; Skoda, RC; Tichelli, A	1
Bag, A; Bag, N	1
Akev, N; Isbir, T; Yilmaz, H; Zejnilovic, J	1
Bové, A; Cervera, R; de la Red, G; Espinosa, G; Monteagudo, J; Plaza, J; Reverter, JC; Tàssies, D	1
Accili, E; Armstrong, L; Chapman, K; Demos, MK; Farrell, K; Macri, V; Nelson, TN	1
Chupin, M; Garnero, L; Leonard, G; Paus, T; Pausova, Z; Perron, M; Pike, B; Pitiot, A; Richer, L; Toro, R; Veillette, S	1
Abicht, A; Bender, A; Czermin, B; Holinski-Feder, E; Horváth, R; Klopstock, T; Lochmüller, H; Schneiderat, P; Trips, T	1
Bassols, J; Botas, P; Delgado, E; Fernández-Real, JM; Menéndez, JA; Moreno-Navarrete, JM; Ortega, FJ; Pardo, G; Ricart, W; Valdés, S; Vázquez-Martín, A	1
Ikeda, M; Inada, T; Iwata, N; Kawashima, K; Kinoshita, Y; Kishi, T; Kitajima, T; Okochi, T; Ozaki, N; Tomita, M; Yamanouchi, Y	1
Cheng, M; Lindpaintner, K; Liu, L; Liu, X; Ma, L; Ma, X; Peng, Z; Ruan, X; Wang, B; Wang, S; Wang, X; Zhang, J	1
Alvira-Botero, X; Aragüés, M; España-Serrano, L; Garrido, E; Hoenicka, J; Jiménez-Arriero, MA; Martínez, I; Palomo, T; Ponce, G; Rodríguez-Jiménez, R; Rubio, G; Santos, JL	1
Doi, A; Furukawa, Y; Furuta, H; Kusuyama, A; Matsuno, S; Nanjo, K; Nishi, M; Sanke, T; Sasaki, H; Shimada, T; Yasuda, K	1
Fukuda, M; Kasai, K; Kawakubo, Y; Marumo, K; Sasaki, T; Takizawa, R; Tochigi, M	1
Kim, JI; Kim, YH; Kong, BG; Lee, CH; Lee, JG; Lee, SJ; Park, SW	1
Agartz, I; Andreassen, OA; Andreou, D; Djurovic, S; Hall, H; Hansen, T; Jönsson, EG; Lundmark, P; Melle, I; Saetre, P; Terenius, L; Timm, S; Werge, T	1
Coste, J; Lehmann, S; Segarra, C	1
Akatsu, H; Arboleda, H; Asada, T; Combarros, O; Comings, DE; Fujii, T; Fukumoto, N; Goto, Y; Grupe, A; Hyman, BT; Ingelsson, M; Kamboh, MI; Kunugi, H; Matsushita, S; Mattila, KM; Nacmias, B; Nakamura, S; Nishimura, AL; Rinne, J; Tsai, SJ; Zatz, M	1
Casali, C; Di Lorenzo, C; Di Lorenzo, G; Ghiotto, N; Grieco, GS; Guaschino, E; Pierelli, F; Sances, G; Santorelli, FM; Siracusano, A; Troisi, A	1
Ammatuna, E; Antonioli, E; Barbui, T; Barosi, G; Bosi, A; Delaini, F; Guglielmelli, P; Liso, V; Lo Coco, F; Longo, G; Pancrazzi, A; Pieri, L; Ponziani, V; Rambaldi, A; Specchia, G; Vannucchi, AM	1
Ayoubi, TA; de Bruin, TW; Feskens, EJ; Glembotski, CC; Heldens, L; Hofker, MH; Kuusisto, J; Laakso, M; Meex, SJ; Pajukanta, P; Schalkwijk, CG; Sinsheimer, JS; Stehouwer, CD; Taskinen, MR; Thuerauf, DJ; van der Kallen, CJ; van Greevenbroek, MM; Vlietinck, R; Weissglas-Volkov, D; Wouters, BG	1
Block, W; Guttenthaler, V; Hofels, S; Jessen, F; Maier, W; Scheef, L; Schuhmacher, A; Suliman, H; Urbach, H; von Widdern, O; Zobel, A	1
Bakker, SC; Hoogendoorn, ML; Hulshoff Pol, HE; Kahn, RS; Koolschijn, PC; van Haren, NE	1
Catteruccia, M; Di Giacopo, R; Lo Monaco, M; Sanna, T; Santorelli, FM; Sauchelli, D; Servidei, S; Tessa, A; Verbo, A	1
Caron-Dorval, D; Couture, P; Lemieux, S; Paquet, P; Paradis, AM; Rudkowska, I; Vohl, MC	1
Ataç, FB; Gökmen, Z; Gülcan, H; Ince, DA; Ozbek, N; Sezgin, E; Taneri, A; Tarcan, A; Verdi, H; Yazici, AC	1
Apud, J; Berman, KF; Eisenberg, DP; Kohn, PD; Kolachana, B; Meyer-Lindenberg, A; Sarpal, D; Weinberger, DR; Wint, D	1
Alatsatianos, A; Bimpaki, E; Boikos, S; Greene, E; Hes, FJ; Horvath, A; Nesterova, M; Pereira, AM; Romijn, JA; Smit, JW; Stratakis, CA; Woortman, S	1
De Quervain, DJ; Ertl, V; Kolassa, IT; Kolassa, S; Papassotiropoulos, A	1
Kim, YK; Lee, HY	1
Barzilai, N; Derby, CA; Katz, M; Lipton, RB; Ozelius, L; Sanders, AE; Wang, C	1
Chen, B; Li, Y; Qiu, LX; Wang, XL; Wu, JQ; Xu, W; Zhao, WH	1
Ferrell, R; Fiocco, AJ; Harris, TB; Li, R; Lindquist, K; Nalls, M; Simonsick, EM; Yaffe, K	1
Angelucci, F; Bernardini, S; Bonaviri, G; Bossù, P; Bria, P; Caltagirone, C; Corvin, AP; Donohoe, G; Gill, M; Martinotti, G; Morris, DW; Rubino, IA; Siracusano, A; Spalletta, G; Spoletini, I	1
Bobińska, K; Florkowski, A; Gałecki, P; Pietras, T; Smigielski, J; Szemraj, J	1
Agra, S; Arrojo, M; Brenlla, J; Costas, J; Ivorra, JL; Páramo, M; Paz, E; Ramos-Ríos, R; Sanjuán, J	1
Berry, MN; Howard, TD; Kaczorowski, J; Keshavan, MS; Kwapil, TR; Schoch, K; Shashi, V; Spence, EJ	1
Brodianskiĭ, VM; Chuprova, NA; Kibitov, AO; Smirnova, EV; Voskoboeva, EIu	1
Akkermann, K; Harro, J; Hiio, K; Villa, I	1
Duman, Z; Oztürk, M; Saruhan-Direskeneli, G; Uçok, A	1
Fan, M; Jiang, T; Liu, B; Song, M; Wang, Z; Xu, C; Zhen, X	1
Baggiani, A; Basolo, F; Berti, P; Elisei, R; Giannini, R; Lupi, C; Miccoli, M; Miccoli, P; Sensi, E; Torregrossa, L; Vitti, P	1
Hou, H; Hu, J; Hu, S; Jia, S; Qing, Z; Zhang, X	1
de Luca, V; Javaid, N; Kennedy, JL; Panariello, F; Souza, RP; Strauss, J; Tallerico, T; Wong, AH; Zai, CC	1
Clark, CR; Gatt, JM; Gordon, E; Nemeroff, CB; Paul, RH; Schofield, PR; Williams, LM	1
Botta, M; Catania, M; Di Fede, G; Giaccone, G; Mazzoleni, G; Moda, F; Morbin, M; Moro, ML; Redaelli, V; Rossi, RS; Salmona, M; Spagnoli, A; Tagliavini, F; Uggetti, A	1
Altink, ME; Buitelaar, JK; Buschgens, CJ; Fliers, EA; Franke, B; Hartman, CA; Hoekstra, PJ; Minderaa, RB; Nijmeijer, JS; Ormel, J; Rommelse, NN; Sergeant, JA; Verhulst, FC	1
Bernabeu, C; Campanera, S; Estrada, G; Fañanás, L; Fatjó-Vilas, M; Illa, JM; Martín, M; Miñano, MJ; Miralles, ML; Miret, S; Muñoz, MJ; Navarro, ME; Pulido, G; Toledo, E	1
Hsiao, HH; Hsu, JF; Lee, CP; Lin, SF; Liu, YC; Tsai, HJ	1
Agra, S; Arrojo, M; Brenlla, J; Costas, J; Páramo, M; Paz, E; Ramos-Ríos, R; Sanjuán, J; Tolosa, A	1
Anfossi, M; Bernardi, L; Bruni, AC; Bugiani, O; Clodomiro, A; Colao, R; Curcio, SA; Di Lorenzo, R; Frangipane, F; Gallo, M; Geracitano, S; Ghidoni, E; Giaccone, G; Maletta, R; Marcello, N; Mirabelli, M; Muraca, G; Puccio, G; Smirne, N; Tagliavini, F; Vasso, F	1
Banaschewski, T; Blomeyer, D; Buchmann, AF; Esser, G; Jennen-Steinmetz, C; Laucht, M; Rietschel, M; Schmidt, MH; Treutlein, J; Zimmermann, US	1
Feng, Y; Ji, X; Sun, X; Wang, H; Zhang, C	1
Hwang, TS; Jang, YM; Kim, DL; Kim, SK; Lee, EJ; Song, KH	1
Aguilera, M; Alemany, S; Arias, B; Fañanás, L; Gastó, C; Ibáñez, MI; Moya, J; Ortet, G; Villa, H; Vossen, H	1
Bellgrove, MA; Cho, SC; Chung, US; Cummins, TD; Han, DH; Hong, SB; Kim, BN; Kim, JH; Kim, JW; Shin, MS; Shin, YM; Son, JW; Song, SH	1
Capellari, S; Dopper, EG; Jansen, C; Kamphorst, W; Parchi, P; Rozemuller, AJ; Strammiello, R; van Swieten, JC	1
Becker, JA; Bianchin, MM; Blaya, C; Bortoluzzi, A; Isolan, L; Leistner-Segal, S; Manfro, GG; Rebelo E Silva, R; Rohde, LA; Salum, GA; Teche, S; Tocchetto, A	1
Biljan, I; Giachin, G; Ilc, G; Legname, G; Plavec, J; Raspadori, A; Zhukov, I	1
Barosi, G; Bergamaschi, G; Carolei, A; Catarsi, P; Poletto, V; Primignani, M; Rosti, V; Spolverini, A; Vannucchi, AM; Villani, L	1
Ferrando, T; Genovés, J; Martorell, L; Molero, M; Naudó, M; Poo, P; Tondo, M	1
Evans, J; Heron, J; Lewis, G; Owen, MJ; Zammit, S	1
Berghoff, AS; Birner, P; Capper, D; Habel, A; Hackl, M; Ilhan, A; Magerle, M; Meyer, J; Petzelbauer, P; Pichler, J; Preusser, M; Pusch, S; von Deimling, A; Wöhrer, A	1
Dong, JH; Li, HL; Ma, TY; Shi, W; Sun, L; Tian, XP; Wang, JJ; Wang, L; Xu, J; Yu, PB; Zhang, L; Zheng, Y	1
de Lau, LM; Heutink, P; Marinus, J; van Hilten, JJ; Verbaan, D	1
Hans, VM; Mehta, DS	1
Ehmann, TS; Honer, WG; Kennedy, JL; Kopala, LC; Lang, DJ; Macewan, GW; Shiau, G; Smith, GN; Tee, K; Thornton, AE; Voineskos, AN	1
Kim, JM; Kim, SW; Kim, SY; Kim, YH; Lee, JS; Park, MH; Park, SW; Shin, IS; Stewart, R; Yoon, JH; Yoon, JS	1
Alavantić, D; Dinčić, E; Djurić, T; Stančić, O; Stanković, A; Stojković, L; Veljković, N; Zivković, M	1
Aarseth, JH; Celius, EG; Harbo, HF; Landrø, NI; Lie, BA; Lorentzen, ÅR; Mero, IL; Myhr, KM; Sandvik, L; Smestad, C	1
Choi, SJ; Ji, JD; Lee, YH; Song, GG	1
Bai, H; Fan, P; He, G; Liang, S; Liu, R; Liu, X; Liu, Y; Zhang, J	1
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Habuchi, T; Ichimura, Y; Kato, T; Nishiyama, H; Ogawa, O; Oyama, C; Sato, K; Tsuchiya, N; Wang, L	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
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Frisén, L; Kalbasi, M; Kockum, I; Lagerstedt, K; Nordenskjöld, A; Thai, HT	1
Deichmann, KA; Haider, A; Heinzmann, A; Lau, S; Nickel, R; Niggemann, B; Sengler, C; Wahn, U	1
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Harrison, PJ; Tunbridge, EM; Weinberger, DR	1
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Jones, EM; Surewicz, K; Surewicz, WK	1
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O'Donovan, MC; Owen, MJ; Williams, HJ	1
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Chang, KH; Chao, CY; Chen, CM; Chen, IC; Chen, YC; Hu, FJ; Lee-Chen, GJ; Liu, YT; Lyu, RK; Wu, YR	1
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Kim, JM; Kim, SW; Kim, YH; Shin, IS; Stewart, R; Yang, SJ; Yoon, JS	1
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Arolt, V; Baune, BT; Berger, K; Deckert, J; Domschke, K; Hohoff, C; Mortensen, S; Neumann, A; Roehrs, T	1
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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
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Cao, LY; Kosten, TA; Kosten, TR; Li, J; Lu, L; Tan, YL; Wang, ZR; Wu, GY; Zhang, XY; Zhou, DF	1
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Chen, X; Chenevix-Trench, G; Johnatty, SE; Nagle, CM; Spurdle, AB; Webb, PM	1
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Silberschmidt, AL; Sponheim, SR	1
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Hong, CJ; Hsieh, CH; Liou, YJ; Liu, ME; Tsai, SJ; Tsai, YL	1
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Herzog, A; Herzog, AL; Marziniak, M; Mössner, R; Sommer, C	1
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Barclay, BW; Navarrete, AE; Sahota, P; Webb, RL; Wosu, NJ	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
Bagli, M; Feder, O; Heun, R; Jessen, F; Ludwig, M; Maier, W; Papassotiropoulos, A; Rao, ML; Schwab, SG	1
Akahoshi, M; Arinobu, Y; Inoue, H; Nagano, S; Nakashima, H; Niho, Y; Niiro, H; Ogami, E; Otsuka, T; Tanaka, Y; Yamaoka, K	1
Bennetts, BH; Buhler, MM; Heard, RN; Stewart, GJ; Teutsch, SM	1
Chang, KJ; Chern, HD; Hsu, SM; Huang, CS; Shen, CY	1
Andersen, PS; Bundgaard, H; Christiansen, M; Havndrup, O; Kjeldsen, K; Larsen, LA; Vuust, J	1
Aoki, Y; Brenner, M; Haginoya, K; Iinuma, K; Ito, T; Kure, S; Matsubara, Y; Munakata, M; Nishio, T; Suzuki, Y; Togashi, N; Yokoyama, H	1
Cadilla, CL; de la Vega, A; García-Fragoso, L; García-García, I; Renta, J	1
Gao, X; Gazit, E; Livneh, A; Stastny, P	1

Reviews

34 review(s) available for valine 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
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
A meta-analysis of the relationship of the Parkin p.Val380Leu polymorphism to Parkinson's disease. 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: Adult; Age of Onset; Aged; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Leucine; Male; Middle Aged; Odds Ratio; Parkinson Disease; Polymorphism, Genetic; Ubiquitin-Protein Ligases; Valine	2013
Polymorphisms of ERBB2 and breast cancer risk: a meta-analysis of 26 studies involving 35,088 subjects. Journal of surgical oncology, 2013, Volume: 108, Issue:6 Topics: Adult; Aged; Alanine; Alleles; Asian People; Black People; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Proline; Receptor, ErbB-2; Risk Factors; Valine; White People	2013
PARP-1 Val762Ala polymorphism and risk of cancer: a meta-analysis based on 39 case-control studies. PloS one, 2014, Volume: 9, Issue:5 Topics: Alanine; Case-Control Studies; Genetic Predisposition to Disease; Humans; Neoplasms; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Polymorphism, Genetic; Valine	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
Glutathione S-transferase gene polymorphisms and susceptibility to acute myeloid leukemia: meta-analyses. Japanese journal of clinical oncology, 2014, Volume: 44, Issue:11 Topics: Asian People; Genetic Predisposition to Disease; Genotype; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Isoleucine; Leukemia, Myeloid, Acute; Odds Ratio; Polymorphism, Genetic; Risk Factors; Valine; White People	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
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
Association between the Val34Leu polymorphism in blood coagulation factor XIII-A and intracerebral hemorrhage: a meta-analysis. Genetics and molecular research : GMR, 2016, Jul-25, Volume: 15, Issue:3 Topics: Amino Acid Substitution; Cerebral Hemorrhage; Factor XIIIa; Genetic Predisposition to Disease; Humans; Leucine; Polymorphism, Single Nucleotide; Valine	2016
Target sequence polymorphism of human manganese superoxide dismutase gene and its association with cancer risk: a review. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Volume: 17, Issue:12 Topics: Alanine; Alleles; Antioxidants; Breast Neoplasms; Genetic Predisposition to Disease; Humans; Neoplasms; Polymorphism, Genetic; Superoxide Dismutase; Valine	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 CYP1B1 Leu432Val polymorphism contributes to lung cancer risk: evidence from 6501 subjects. Lung cancer (Amsterdam, Netherlands), 2010, Volume: 70, Issue:3 Topics: Adenocarcinoma; Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 CYP1B1; Ethnicity; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Lung Neoplasms; Penetrance; Polymorphism, Genetic; Risk; Smoking; Valine	2010
CYP1A1 Ile462Val polymorphism and susceptibility to lung cancer: a meta-analysis based on 32 studies. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP), 2011, Volume: 20, Issue:6 Topics: Asian People; Case-Control Studies; Cytochrome P-450 CYP1A1; Genetic Markers; Genetic Predisposition to Disease; Humans; Isoleucine; Lung Neoplasms; Polymorphism, Genetic; Valine	2011
Association between the valine/leucine247 polymorphism of β2-glycoprotein I and susceptibility to anti-phospholipid syndrome: a meta-analysis. Lupus, 2012, Volume: 21, Issue:8 Topics: Alleles; Antibodies; Antiphospholipid Syndrome; beta 2-Glycoprotein I; Genetic Predisposition to Disease; Humans; Leucine; Polymorphism, Genetic; Thrombosis; Valine	2012
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
CYP1A1 Ile462Val polymorphism contributes to lung cancer susceptibility among lung squamous carcinoma and smokers: a meta-analysis. PloS one, 2012, Volume: 7, Issue:8 Topics: Carcinoma, Squamous Cell; Case-Control Studies; Cytochrome P-450 CYP1A1; Exons; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Lung Neoplasms; Models, Genetic; Odds Ratio; Polymorphism, Genetic; Smoking; Valine	2012
BRAF V600E mutation and its association with clinicopathological features of papillary thyroid cancer: a meta-analysis. The Journal of clinical endocrinology and metabolism, 2012, Volume: 97, Issue:12 Topics: Age Factors; Amino Acid Substitution; Carcinoma; Carcinoma, Papillary; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lymphatic Metastasis; Male; Mutation, Missense; Proto-Oncogene Proteins B-raf; Sex Characteristics; Thyroid Cancer, Papillary; Thyroid Neoplasms; Tumor Burden; Valine	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
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
Factor XIII Val34Leu variant is protective against venous thromboembolism: a HuGE review and meta-analysis. American journal of epidemiology, 2006, Jul-15, Volume: 164, Issue:2 Topics: Amino Acid Substitution; Factor XIII; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Leucine; Point Mutation; Polymorphism, Genetic; Risk Factors; Thromboembolism; Valine; Venous Thrombosis	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
Factor XIII Val34Leu variant protects against coronary artery disease. A meta-analysis. Thrombosis and haemostasis, 2007, Volume: 97, Issue:3 Topics: Amino Acid Substitution; Bayes Theorem; Coronary Artery Disease; Factor VIII; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Leucine; Male; Odds Ratio; Polymorphism, Genetic; Risk Assessment; Risk Factors; Valine	2007
Factor XIII Val34Leu variant and the risk of myocardial infarction: a meta-analysis. Thrombosis and haemostasis, 2007, Volume: 97, Issue:4 Topics: Adult; Factor XIII; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Myocardial Infarction; Odds Ratio; Risk Assessment; Risk Factors; 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
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 polymorphisms of drug-metabolizing enzymes and lung cancer susceptibility. Pharmacogenetics, 1995, Volume: 5 Spec No Topics: Chromosome Aberrations; Cytochrome P-450 Enzyme System; Deoxyribonuclease HpaII; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Isoenzymes; Isoleucine; Lung Neoplasms; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Smoking; Valine	1995

Trials

10 trial(s) available for valine and Genetic Predisposition

Article	Year
DPYD variants as predictors of 5-fluorouracil toxicity in adjuvant colon cancer treatment (NCCTG N0147). Journal of the National Cancer Institute, 2014, Volume: 106, Issue:12 Topics: Adult; Aged; Aged, 80 and over; Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Aspartic Acid; Camptothecin; Chemotherapy, Adjuvant; Colonic Neoplasms; Diarrhea; Dihydrouracil Dehydrogenase (NADP); Drug-Related Side Effects and Adverse Reactions; Female; Fluorouracil; Genetic Predisposition to Disease; Humans; Leucovorin; Logistic Models; Male; Middle Aged; Nausea; Neoplasm Staging; Neutropenia; Organoplatinum Compounds; Polymorphism, Single Nucleotide; Prospective Studies; Severity of Illness Index; Thrombocytopenia; Valine; Vomiting	2014
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
The BRAF(V600E) mutation is associated with malignant ultrasonographic features in thyroid nodules. Clinical endocrinology, 2011, Volume: 75, Issue:6 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Biopsy, Fine-Needle; Carcinoma; Carcinoma, Papillary; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Mutation; Proto-Oncogene Proteins B-raf; Sensitivity and Specificity; Thyroid Cancer, Papillary; Thyroid Neoplasms; Thyroid Nodule; Ultrasonography; Valine; Young Adult	2011
Val/Val genotype of brain-derived neurotrophic factor (BDNF) Val⁶⁶Met polymorphism is associated with a better response to OROS-MPH in Korean ADHD children. The international journal of neuropsychopharmacology, 2011, Volume: 14, Issue:10 Topics: Administration, Oral; Age Factors; Analysis of Variance; Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Central Nervous System Stimulants; Chi-Square Distribution; Child; Child Behavior; Delayed-Action Preparations; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Male; Methylphenidate; Pharmacogenetics; Phenotype; Polymorphism, Single Nucleotide; Prospective Studies; Psychiatric Status Rating Scales; Regression Analysis; Republic of Korea; Time Factors; Treatment Outcome; Valine	2011
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
[The relationship between the gene polymorphism of TGF-beta1 and early renal injury in patients with essential hypertension, and the effect of the gene polymorphism of TGF- beta1 on the individual treatment with valsartan]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2007, Volume: 24, Issue:4 Topics: Aged; Albuminuria; Antihypertensive Agents; Blood Pressure; Female; Genetic Predisposition to Disease; Humans; Hypertension; Kidney Diseases; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Tetrazoles; Time Factors; Transforming Growth Factor beta1; Treatment Outcome; Valine; Valsartan	2007
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

289 other study(ies) available for valine and Genetic Predisposition

Article	Year
Association of Internet gaming disorder with catechol-O-methyltransferase: Role of impulsivity and fun-seeking. The Kaohsiung journal of medical sciences, 2022, Volume: 38, Issue:1 Topics: Adult; Behavior, Addictive; Case-Control Studies; Catechol O-Methyltransferase; Dopamine; Female; Genetic Predisposition to Disease; Genotype; Humans; Impulsive Behavior; Internet Addiction Disorder; Interviews as Topic; Male; Pleasure; Polymorphism, Genetic; Valine	2022
Functional significance of the rare rs35667974 Autoimmunity, 2022, Volume: 55, Issue:7 Topics: Arthritis, Psoriatic; Autoantigens; Autoimmune Diseases; Chemokines; DEAD-box RNA Helicases; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Interferon-Induced Helicase, IFIH1; Interferons; Isoleucine; Polymorphism, Genetic; RNA, Viral; Valine	2022
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
Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes. Scientific reports, 2021, 03-18, Volume: 11, Issue:1 Topics: Adult; Aged; Betaine; Biomarkers; Carnitine; Case-Control Studies; Diabetes Mellitus, Type 2; Early Diagnosis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Lysine; Male; Mannose; Mendelian Randomization Analysis; Metabolome; Middle Aged; Valine	2021
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
Association between alanine aminotransferase elevation and UGT1A16 polymorphisms in daclatasvir and asunaprevir combination therapy for chronic hepatitis C. Journal of gastroenterology, 2018, Volume: 53, Issue:6* Topics: Adult; Aged; Aged, 80 and over; Alanine Transaminase; Antiviral Agents; Biomarkers; Carbamates; Chemical and Drug Induced Liver Injury; Drug Therapy, Combination; Female; Genetic Predisposition to Disease; Glucuronosyltransferase; Hepatitis C, Chronic; Humans; Imidazoles; Isoquinolines; Male; Middle Aged; Polymorphism, Single Nucleotide; Pyrrolidines; Sulfonamides; Valine	2018
Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene. Biochemical and biophysical research communications, 2018, 02-19, Volume: 496, Issue:4 Topics: Aged, 80 and over; Amino Acid Substitution; Codon; Creutzfeldt-Jakob Syndrome; Female; Genetic Markers; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Neocortex; Prion Proteins; Valine	2018
Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiency. American journal of medical genetics. Part A, 2018, Volume: 176, Issue:5 Topics: Amino Acid Sequence; Biomarkers; Brain; Chromatography, Liquid; DNA Mutational Analysis; Enoyl-CoA Hydratase; Enzyme Activation; Female; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Metabolic Networks and Pathways; Metabolome; Metabolomics; Pedigree; Phenotype; Tandem Mass Spectrometry; Valine	2018
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
Polymorphism in interferon λ3/interleukin-28B gene and risk to noncirrhotic chronic hepatitis C genotype 3 virus infection and its effect on the response to combined daclatasvir and sofosbuvir therapy. Journal of medical virology, 2019, Volume: 91, Issue:4 Topics: Adult; Aged; Antiviral Agents; Carbamates; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; Hepacivirus; Hepatitis C, Chronic; Humans; Imidazoles; Interferons; Male; Middle Aged; Pyrrolidines; Recurrence; Sofosbuvir; Sustained Virologic Response; Treatment Outcome; Valine	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
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
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
I405V polymorphism of CETP gene and lipid profile in women with endometriosis. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 2013, Volume: 29, Issue:7 Topics: Adolescent; Adult; Amino Acid Substitution; Case-Control Studies; Cholesterol Ester Transfer Proteins; Cross-Sectional Studies; Endometriosis; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Lipid Metabolism; Lipids; Polymorphism, Single Nucleotide; Uterine Diseases; Valine; Young Adult	2013
Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G). JAMA neurology, 2013, Sep-01, Volume: 70, Issue:9 Topics: Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Gerstmann-Straussler-Scheinker Disease; Glycine; Humans; Middle Aged; Mutation; Neurofibrillary Tangles; Pedigree; Phenotype; Prion Proteins; Prions; Valine	2013
Association GSTT1, GSTM1 and GSTP1 (Ile105Val) genetic polymorphisms in mothers with risk of congenital malformations in their children in Western Siberia: a case-control study. Prenatal diagnosis, 2013, Volume: 33, Issue:11 Topics: Adolescent; Adult; Amino Acid Substitution; Case-Control Studies; Congenital Abnormalities; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Infant, Newborn; Isoleucine; Mothers; Polymorphism, Genetic; Pregnancy; Risk Factors; Siberia; Valine; Young Adult	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
Modifying roles of glutathione S-transferase polymorphisms on the association between cumulative lead exposure and cognitive function. Neurotoxicology, 2013, Volume: 39 Topics: Aged; Aged, 80 and over; Cognition Disorders; Cohort Studies; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Lead; Male; Mental Status Schedule; Middle Aged; Polymorphism, Genetic; Spectrometry, X-Ray Emission; Valine; Veterans	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
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
Polymorphisms of glutathione-S-transferases M1, T1, P1 and susceptibility to colorectal cancer in a sample of the Tunisian population. Medical oncology (Northwood, London, England), 2014, Volume: 31, Issue:1 Topics: Adult; Aged; Alleles; Case-Control Studies; Colorectal Neoplasms; Female; Genetic Predisposition to Disease; Genotype; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Isoleucine; Male; Middle Aged; Polymorphism, Genetic; Tunisia; Valine	2014
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
Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas. Journal of the National Cancer Institute, 2014, Volume: 106, Issue:1 Topics: Adenocarcinoma; Adenocarcinoma of Lung; Adult; Asian People; Aspartic Acid; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Glycine; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Pedigree; Receptor, ErbB-2; Valine	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
The gender-specific association of CXCL16 A181V gene polymorphism with susceptibility to multiple sclerosis, and its effects on PBMC mRNA and plasma soluble CXCL16 levels: preliminary findings. Journal of neurology, 2014, Volume: 261, Issue:8 Topics: Adult; Alanine; Analysis of Variance; Case-Control Studies; Chemokine CXCL16; Chemokines, CXC; Disability Evaluation; Enzyme-Linked Immunosorbent Assay; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leukocytes, Mononuclear; Male; Middle Aged; Multiple Sclerosis; Polymorphism, Single Nucleotide; Receptors, Scavenger; RNA, Messenger; Valine	2014
Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia. Movement disorders : official journal of the Movement Disorder Society, 2014, Volume: 29, Issue:8 Topics: Adult; Apoptosis Regulatory Proteins; Asian People; Aspartic Acid; Cell Line, Tumor; Cohort Studies; DNA Mutational Analysis; DNA-Binding Proteins; Dystonic Disorders; Female; Genetic Predisposition to Disease; Genotype; HEK293 Cells; Humans; Male; Molecular Chaperones; Mutation; Neuroblastoma; Nuclear Proteins; Transfection; Valine	2014
High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis. Blood, 2014, Sep-04, Volume: 124, Issue:10 Topics: Amino Acid Substitution; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Histiocytosis, Langerhans-Cell; Humans; Male; MAP Kinase Kinase 1; Mutation, Missense; Prevalence; Proto-Oncogene Proteins B-raf; Retrospective Studies; Valine	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
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
Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses. PLoS genetics, 2015, Volume: 11, Issue:1 Topics: Exome; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Glycine; Humans; Metabolism, Inborn Errors; Metabolome; Phenotype; Polymorphism, Single Nucleotide; Pyruvic Acid; Quantitative Trait Loci; Valine	2015
Association of single-nucleotide polymorphisms in the IRF6 gene with non-syndromic cleft lip with or without cleft palate in the Xinjiang Uyghur population. The British journal of oral & maxillofacial surgery, 2015, Volume: 53, Issue:3 Topics: 5' Flanking Region; 5' Untranslated Regions; Adenine; Case-Control Studies; Cleft Lip; Cleft Palate; Cytosine; Exons; Gene Frequency; Genes, Dominant; Genes, Recessive; Genetic Predisposition to Disease; Genotype; Guanine; Haplotypes; Humans; Infant; Interferon Regulatory Factors; Introns; Isoleucine; Linkage Disequilibrium; Mutation, Missense; Polymorphism, Single Nucleotide; Serine; Valine	2015
A novel lamin A/C gene missense mutation (445 V > E) in immunoglobulin-like fold associated with left ventricular non-compaction. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2016, Volume: 18, Issue:4 Topics: Adolescent; Death, Sudden, Cardiac; DNA Mutational Analysis; Echocardiography; Electrocardiography; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Heterozygote; Humans; Isolated Noncompaction of the Ventricular Myocardium; Lamin Type A; Male; Membrane Potentials; Microscopy, Fluorescence; Models, Molecular; Mutagenesis, Site-Directed; Mutation, Missense; Phenotype; Protein Aggregates; Protein Conformation, beta-Strand; Protein Folding; Structure-Activity Relationship; Tachycardia, Ventricular; Transfection; Valine; Ventricular Fibrillation; Young Adult	2016
[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
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy. Acta neuropathologica communications, 2015, Jul-25, Volume: 3 Topics: Adult; Aged; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; HSP40 Heat-Shock Proteins; HSP70 Heat-Shock Proteins; Humans; Italy; Male; Middle Aged; Models, Molecular; Molecular Chaperones; Muscular Diseases; Mutation, Missense; Nerve Tissue Proteins; Phenylalanine; Tomography Scanners, X-Ray Computed; Valine; Young Adult	2015
Positive Association of the Cathepsin D Ala224Val Gene Polymorphism With the Risk of Alzheimer's Disease. The American journal of the medical sciences, 2015, Volume: 350, Issue:4 Topics: Aged; Alanine; Alleles; Alzheimer Disease; Case-Control Studies; Cathepsin D; Cystatin C; Ecuador; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Male; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Prevalence; Risk Factors; Valine	2015
Physical and verbal aggressive behavior and COMT genotype: Sensitivity to the environment. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171, Issue:5 Topics: Adult; Aggression; Alleles; Catechol O-Methyltransferase; Environment; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Male; Parent-Child Relations; Polymorphism, Single Nucleotide; Risk Factors; Valine; Young Adult	2016
Does Val/Val genotype of GSTP1 enzyme affects susceptibility to colorectal cancer in Saudi Arabia?. Neuro endocrinology letters, 2016, Volume: 37, Issue:1 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Colorectal Neoplasms; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutathione S-Transferase pi; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Saudi Arabia; Valine	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
Glutathione S-Transferase Pi-Ile 105 Val Polymorphism and Susceptibility to T2DM in Population from Turabah Region of Saudi Arabia. Biochemical genetics, 2016, Volume: 54, Issue:4 Topics: Adult; Aged; Amplified Fragment Length Polymorphism Analysis; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Glutathione S-Transferase pi; Humans; Isoleucine; Middle Aged; Polymorphism, Single Nucleotide; Saudi Arabia; Valine	2016
Masked polycythaemia vera is genetically intermediate between JAK2V617F mutated essential thrombocythaemia and overt polycythaemia vera. Blood cancer journal, 2016, 08-19, Volume: 6, Issue:8 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Asymptomatic Diseases; Cohort Studies; Disease Progression; Female; Genetic Predisposition to Disease; Humans; Janus Kinase 2; Male; Middle Aged; Mutation, Missense; Phenylalanine; Polycythemia Vera; Polymorphism, Single Nucleotide; Prodromal Symptoms; Thrombocythemia, Essential; Valine	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
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
Manganese superoxide dismutase gene Ala-9Val polymorphism might be related to the severity of abnormal involuntary movements in Korean schizophrenic patients. Progress in neuro-psychopharmacology & biological psychiatry, 2008, Dec-12, Volume: 32, Issue:8 Topics: Adult; Alanine; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Korea; Logistic Models; Male; Middle Aged; Movement Disorders; Polymorphism, Genetic; Schizophrenia; Severity of Illness Index; Statistics, Nonparametric; Superoxide Dismutase; Valine	2008
HER-2/neu Ile655Val polymorphism and the risk of breast cancer. Annals of the New York Academy of Sciences, 2008, Volume: 1138 Topics: Breast Neoplasms; Case-Control Studies; Female; Genes, erbB-2; Genetic Predisposition to Disease; Humans; Isoleucine; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Proto-Oncogene Mas; Risk Factors; Valine	2008
BRAF mutation in papillary thyroid carcinoma in a Japanese population: its lack of correlation with high-risk clinicopathological features and disease-free survival of patients. Endocrine journal, 2009, Volume: 56, Issue:1 Topics: Adult; Amino Acid Substitution; Carcinoma, Papillary; Disease-Free Survival; Female; Genetic Linkage; Genetic Predisposition to Disease; Genetics, Population; Glutamic Acid; Humans; Japan; Male; Middle Aged; Neoplasm Staging; Point Mutation; Prognosis; Proto-Oncogene Proteins B-raf; Risk Factors; Thyroid Neoplasms; Valine	2009
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
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
The Val432Leu polymorphism of the CYP1B1 gene is associated with differences in estrogen metabolism and bone density. Bone, 2009, Volume: 44, Issue:3 Topics: Aryl Hydrocarbon Hydroxylases; Bone Density; Cytochrome P-450 CYP1B1; Estrogens; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Middle Aged; Polymorphism, Genetic; Risk Factors; Valine	2009
The manganese superoxide dismutase Val16Ala polymorphism is associated with decreased risk of diabetic nephropathy in Chinese patients with type 2 diabetes. Molecular and cellular biochemistry, 2009, Volume: 322, Issue:1-2 Topics: Aged; Alanine; Alleles; Asian People; Cohort Studies; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Genetic Predisposition to Disease; Humans; Middle Aged; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Risk; Superoxide Dismutase; Valine	2009
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
The Val762Ala polymorphism in the poly(ADP-ribose) polymerase-1 gene is not associated with susceptibility in Turkish rheumatoid arthritis patients. Rheumatology international, 2009, Volume: 29, Issue:7 Topics: Adult; Aged; Alanine; Amino Acid Substitution; Arthritis, Rheumatoid; DNA Mutational Analysis; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Middle Aged; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Polymorphism, Genetic; Turkey; Valine	2009
Clonal analysis of deletions on chromosome 20q and JAK2-V617F in MPD suggests that del20q acts independently and is not one of the predisposing mutations for JAK2-V617F. Blood, 2009, Feb-26, Volume: 113, Issue:9 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Chromosome Deletion; Chromosomes, Human, Pair 20; Clone Cells; Comparative Genomic Hybridization; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Janus Kinase 2; Male; Middle Aged; Mutation; Myeloproliferative Disorders; Phenylalanine; Valine	2009
Association between manganese superoxide dismutase polymorphism and risk of lung cancer. Cancer genetics and cytogenetics, 2009, Volume: 189, Issue:1 Topics: Case-Control Studies; Genetic Predisposition to Disease; Genotype; Humans; Lung Neoplasms; Oxidative Stress; Polymorphism, Genetic; Risk Factors; Superoxide Dismutase; Turkey; Valine	2009
Factor XIII-A subunit Val34Leu polymorphism is associated with the risk of thrombosis in patients with antiphospholipid antibodies and high fibrinogen levels. Thrombosis and haemostasis, 2009, Volume: 101, Issue:2 Topics: Adult; Antiphospholipid Syndrome; Case-Control Studies; Factor XIII; Female; Fibrinogen; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Odds Ratio; Polymorphism, Genetic; Protein Subunits; Risk Assessment; Risk Factors; Thrombosis; Up-Regulation; Valine	2009
A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. Movement disorders : official journal of the Movement Disorder Society, 2009, Apr-15, Volume: 24, Issue:5 Topics: Adult; Animals; Cerebellar Diseases; Child, Preschool; CHO Cells; Cricetinae; Cricetulus; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Kv1.1 Potassium Channel; Leucine; Magnetic Resonance Imaging; Male; Membrane Potentials; Mutation; Transfection; Valine	2009
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
Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexia. Journal of neurology, 2009, Volume: 256, Issue:5 Topics: Adolescent; Age of Onset; Anticodon; Base Sequence; Cachexia; DNA Mutational Analysis; Female; Gastrointestinal Diseases; Gastrointestinal Motility; Genes, Recessive; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Mitochondria; Mitochondrial Diseases; Mutation; RNA; RNA, Mitochondrial; RNA, Transfer, Val; Valine	2009
Val1483Ile in FASN gene is linked to central obesity and insulin sensitivity in adult white men. Obesity (Silver Spring, Md.), 2009, Volume: 17, Issue:9 Topics: Adipose Tissue; Adiposity; Adult; Age Factors; Blood Glucose; Blood Pressure; Body Mass Index; Case-Control Studies; Down-Regulation; Fatty Acid Synthase, Type I; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Insulin Resistance; Isoleucine; Male; Middle Aged; Obesity; Phenotype; Polymorphism, Single Nucleotide; Risk Factors; Sex Factors; Time Factors; Valine; Waist-Hip Ratio; Weight Gain	2009
TAQIB and I405V polymorphisms of CETP are moderately associated with obesity risk in the Chinese adult population. Acta diabetologica, 2010, Volume: 47, Issue:3 Topics: Adult; Amino Acid Substitution; Asian People; Case-Control Studies; Cholesterol Ester Transfer Proteins; Deoxyribonucleases, Type II Site-Specific; Female; Genetic Predisposition to Disease; Genetics, Population; Humans; Isoleucine; Male; Middle Aged; Obesity; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk; Valine	2010
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
Identification of patients with poorer survival in primary myelofibrosis based on the burden of JAK2V617F mutated allele. Blood, 2009, Aug-20, Volume: 114, Issue:8 Topics: Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Janus Kinase 2; Male; Middle Aged; Mutation, Missense; Phenylalanine; Primary Myelofibrosis; Prognosis; Survival Analysis; Valine; Young Adult	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
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
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene. Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:11 Topics: Adult; Alanine; Cardiomyopathies; Caveolin 3; Electrocardiography; Electromyography; Family Health; Female; Genetic Predisposition to Disease; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Muscle, Skeletal; Muscular Diseases; Mutation; Valine; Young Adult	2009
Effect of the PPAR-Alpha L162V polymorphism on the cardiovascular disease risk factor in response to n-3 polyunsaturated fatty acids. Journal of nutrigenetics and nutrigenomics, 2008, Volume: 1, Issue:4 Topics: Adult; Amino Acid Substitution; Cardiovascular Diseases; Fatty Acids, Omega-3; Fatty Acids, Unsaturated; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Middle Aged; Polymorphism, Single Nucleotide; PPAR alpha; Risk Factors; Valine; Young Adult	2008
Lack of association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor beta1 (915G/T) gene polymorphisms and bronchopulmonary dysplasia: a single-center study. DNA and cell biology, 2010, Volume: 29, Issue:1 Topics: Amino Acid Substitution; Bronchopulmonary Dysplasia; Factor VII; Factor VIII; Female; Genetic Predisposition to Disease; Humans; INDEL Mutation; Infant, Newborn; Leucine; Male; Polymorphism, Genetic; Transforming Growth Factor beta1; Turkey; Valine	2010
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
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
Association of a functional polymorphism in the cholesteryl ester transfer protein (CETP) gene with memory decline and incidence of dementia. JAMA, 2010, Jan-13, Volume: 303, Issue:2 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Cholesterol Ester Transfer Proteins; Dementia; Female; Genetic Predisposition to Disease; Genotype; Humans; Incidence; Male; Memory Disorders; New York; Polymorphism, Single Nucleotide; Prospective Studies; Valine	2010
COMT genotype and cognitive function: an 8-year longitudinal study in white and black elders. Neurology, 2010, Apr-20, Volume: 74, Issue:16 Topics: Age Factors; Aged; Aging; Amino Acid Sequence; Amino Acid Substitution; Black People; Brain Chemistry; Catechol O-Methyltransferase; Cognition Disorders; Cytoprotection; Dementia; DNA Mutational Analysis; Dopamine; Female; Gene Expression Regulation, Enzymologic; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Longitudinal Studies; Male; Neuropsychological Tests; Racial Groups; Time Factors; Valine; 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
Analysis of two polymorphisms of the manganese superoxide dismutase gene (Ile-58Thr and Ala-9Val) in patients with recurrent depressive disorder. Psychiatry research, 2010, Aug-30, Volume: 179, Issue:1 Topics: Alanine; Amino Acids; Case-Control Studies; Depression; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Male; Middle Aged; Polymorphism, Genetic; Sex Factors; Superoxide Dismutase; Threonine; Valine	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
Correlation between the BRAF V600E mutation and tumor invasiveness in papillary thyroid carcinomas smaller than 20 millimeters: analysis of 1060 cases. The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:9 Topics: Adult; Amino Acid Substitution; Carcinoma, Papillary; Cohort Studies; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Neoplasm Invasiveness; Point Mutation; Proto-Oncogene Proteins B-raf; Retrospective Studies; Thyroid Neoplasms; Tumor Burden; 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
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features. Acta neuropathologica, 2010, Volume: 120, Issue:6 Topics: Alanine; Alzheimer Disease; Amino Acid Substitution; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Genes, Recessive; Genetic Predisposition to Disease; Humans; Male; Middle Aged; 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
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
JAK2V617F mutation is associated with special alleles in essential thrombocythemia. Leukemia & lymphoma, 2011, Volume: 52, Issue:3 Topics: Alleles; Amino Acid Substitution; DNA Mutational Analysis; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genetic Testing; Humans; Janus Kinase 2; Leucine; Lysine; Mutation, Missense; Phenylalanine; Polymorphism, Single Nucleotide; Receptors, Thrombopoietin; Thrombocythemia, Essential; Tryptophan; Valine	2011
Interaction between COMT haplotypes and cannabis in schizophrenia: a case-only study in two samples from Spain. Schizophrenia research, 2011, Volume: 127, Issue:1-3 Topics: Catechol O-Methyltransferase; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Marijuana Smoking; Polymorphism, Single Nucleotide; Schizophrenia; Spain; Valine	2011
A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features. Journal of Alzheimer's disease : JAD, 2011, Volume: 25, Issue:3 Topics: Aged; Alzheimer Disease; Amyloid beta-Peptides; Brain; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Mental Status Schedule; Middle Aged; Mutation; Phenotype; Presenilin-1; Valine	2011
Catechol-O-methyltransferase Val158 Met genotype, parenting practices and adolescent alcohol use: testing the differential susceptibility hypothesis. Journal of child psychology and psychiatry, and allied disciplines, 2012, Volume: 53, Issue:4 Topics: Adolescent; Adolescent Behavior; Adult; Alcohol Drinking; Catechol O-Methyltransferase; Cohort Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Longitudinal Studies; Male; Parenting; Polymorphism, Genetic; Risk Factors; Valine; Young Adult	2012
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
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient. Journal of neuropathology and experimental neurology, 2011, Volume: 70, Issue:8 Topics: Adult; Brain; Genetic Predisposition to Disease; Genome-Wide Association Study; Gerstmann-Straussler-Scheinker Disease; Glycine; Humans; Male; Netherlands; Polymorphism, Genetic; Prions; Valine	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
Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation. Journal of molecular biology, 2011, Sep-30, Volume: 412, Issue:4 Topics: Amino Acid Sequence; Amino Acid Substitution; Genetic Predisposition to Disease; Humans; Hydrophobic and Hydrophilic Interactions; Isoleucine; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Nuclear Magnetic Resonance, Biomolecular; Prion Diseases; Prions; Protein Folding; Protein Structure, Secondary; Protein Structure, Tertiary; Signal Transduction; Valine	2011
JAK2 46/1 haplotype predisposes to splanchnic vein thrombosis-associated BCR-ABL negative classic myeloproliferative neoplasms. Leukemia research, 2012, Volume: 36, Issue:1 Topics: Bone Marrow Neoplasms; Case-Control Studies; Fusion Proteins, bcr-abl; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Humans; Janus Kinase 2; Mesenteric Vascular Occlusion; Mesenteric Veins; Mutation; Myeloproliferative Disorders; Phenylalanine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Splanchnic Circulation; Valine; Venous Thrombosis	2012
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
Immunohistochemical testing of BRAF V600E status in 1,120 tumor tissue samples of patients with brain metastases. Acta neuropathologica, 2012, Volume: 123, Issue:2 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Brain Neoplasms; Female; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Humans; Immunohistochemistry; Male; Middle Aged; Point Mutation; Proto-Oncogene Proteins B-raf; Valine; Young Adult	2012
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
Genetic polymorphism of Fcγ-receptors IIa, IIIa and IIIb in South Indian patients with generalized aggressive periodontitis. Journal of oral science, 2011, Volume: 53, Issue:4 Topics: Adult; Aggressive Periodontitis; Amino Acid Substitution; Analysis of Variance; Arginine; Case-Control Studies; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; GPI-Linked Proteins; Histidine; Humans; India; Isoantigens; Male; Mouth Mucosa; Odds Ratio; Periodontal Index; Phenylalanine; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Receptors, IgG; Risk Factors; Valine; White People; Young Adult	2011
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
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
Analysis of mitochondrial haplogroups associated with TTR Val30Ala familial amyloidotic polyneuropathy in Chinese patients. The International journal of neuroscience, 2012, Volume: 122, Issue:12 Topics: Adult; Age of Onset; Aged; Alanine; Amyloid Neuropathies, Familial; Asian People; DNA, Mitochondrial; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mitochondria; Prealbumin; Valine; Young Adult	2012
Association of manganese superoxide dismutase and glutathione S-transferases genotypes with myocardial infarction in patients with type 2 diabetes mellitus. Diabetes research and clinical practice, 2012, Volume: 98, Issue:1 Topics: Alanine; Biomarkers; Blood Glucose; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Diabetic Angiopathies; Female; Genetic Predisposition to Disease; Genotype; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Lipids; Logistic Models; Male; Middle Aged; Myocardial Infarction; Oxidative Stress; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Slovenia; Superoxide Dismutase; Valine; White People	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
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
The BRAF(V600E) mutation is an independent, poor prognostic factor for the outcome of patients with low-risk intrathyroid papillary thyroid carcinoma: single-institution results from a large cohort study. The Journal of clinical endocrinology and metabolism, 2012, Volume: 97, Issue:12 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Carcinoma; Carcinoma, Papillary; Cohort Studies; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Mutation, Missense; Prognosis; Proto-Oncogene Proteins B-raf; Risk Factors; Sample Size; Thyroid Cancer, Papillary; Thyroid Gland; Thyroid Neoplasms; Valine; Young Adult	2012
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
The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry. Journal of neurology, 2013, Volume: 260, Issue:5 Topics: Adult; Age of Onset; Alanine; ATPases Associated with Diverse Cellular Activities; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Magnetic Resonance Imaging; Male; Metalloendopeptidases; Middle Aged; Mutation; Pedigree; Spastic Paraplegia, Hereditary; United Kingdom; Valine; Vestibular Diseases; White People	2013
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
Genetic polymorphism of cytochrome P4501A1 and susceptibility to oral squamous cell carcinoma and oral precancer lesions associated with smoking/betel use. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2002, Volume: 31, Issue:9 Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Amino Acid Substitution; Areca; Carcinoma, Squamous Cell; Cytochrome P-450 CYP1A1; Exons; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mouth Neoplasms; Mutation, Missense; Polymorphism, Restriction Fragment Length; Precancerous Conditions; Smoking; Untranslated Regions; Valine	2002
Novel mutations and SNPs identified in CCR2 using a new comprehensive denaturing gradient gel electrophoresis assay. Human mutation, 2002, Volume: 20, Issue:4 Topics: Amino Acid Substitution; Cohort Studies; Electrophoresis, Polyacrylamide Gel; Female; Genetic Predisposition to Disease; Genetic Variation; HIV Infections; HIV Seronegativity; HIV Seropositivity; HIV-1; Humans; Isoleucine; Male; Mutation; Nucleic Acid Denaturation; Polymorphism, Single Nucleotide; Receptors, CCR2; Receptors, Chemokine; Valine	2002
Re: Population-based, case-control study of HER2 genetic polymorphism and breast cancer risk. Journal of the National Cancer Institute, 2002, Dec-04, Volume: 94, Issue:23 Topics: Alleles; Asian People; Breast Neoplasms; Case-Control Studies; Female; Genes, erbB-2; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Japan; Odds Ratio; Polymorphism, Genetic; Population Surveillance; Receptor, ErbB-2; Risk Assessment; Risk Factors; Valine	2002
Association between the Ala379Val variant of the lipoprotein associated phospholipase A2 and risk of myocardial infarction in the north and south of Europe. Atherosclerosis, 2003, Volume: 168, Issue:2 Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Alanine; Alleles; Case-Control Studies; Europe; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homozygote; Humans; Male; Middle Aged; Myocardial Infarction; Odds Ratio; Phospholipases A; Phospholipases A2; Valine	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
Glutathione S-transferase M1 and P1 metabolic polymorphism and lung cancer predisposition. Neoplasma, 2003, Volume: 50, Issue:5 Topics: Adenocarcinoma; Carcinoma, Non-Small-Cell Lung; Carcinoma, Small Cell; Carcinoma, Squamous Cell; Female; Gene Deletion; Genetic Predisposition to Disease; Genotype; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Isoenzymes; Isoleucine; Lung Neoplasms; Male; Mutation, Missense; Occupational Exposure; Poland; Polymorphism, Genetic; Risk Factors; Smoking; Valine	2003
CD24 is a genetic modifier for risk and progression of multiple sclerosis. Proceedings of the National Academy of Sciences of the United States of America, 2003, Dec-09, Volume: 100, Issue:25 Topics: Alanine; Alleles; Animals; Antigens, CD; CD24 Antigen; CD3 Complex; Cell Membrane; Cloning, Molecular; Disease Progression; DNA, Complementary; Dose-Response Relationship, Drug; Encephalomyelitis, Autoimmune, Experimental; Flow Cytometry; Genetic Predisposition to Disease; Genotype; Humans; Membrane Glycoproteins; Mice; Models, Genetic; Multiple Sclerosis; Open Reading Frames; Pedigree; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Risk Factors; Time Factors; Transfection; Valine	2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation. Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:10 Topics: Adult; Carbohydrate Epimerases; Diagnosis, Differential; DNA Mutational Analysis; Genetic Predisposition to Disease; Histocompatibility Antigens Class I; Homozygote; Humans; Inflammation; Iran; Male; Muscle Fibers, Skeletal; Muscle, Skeletal; Mutation, Missense; Myositis, Inclusion Body; Pedigree; Valine	2003
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. Archives of neurology, 2004, Volume: 61, Issue:3 Topics: Age of Onset; Aged; alpha-Macroglobulins; Alzheimer Disease; Apolipoproteins E; Case-Control Studies; Chi-Square Distribution; Confidence Intervals; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Italy; Male; Middle Aged; Odds Ratio; Peroxidase; Polymerase Chain Reaction; Polymorphism, Genetic; Risk; Valine	2004
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
Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case-control study of African Americans and whites. Breast cancer research : BCR, 2004, Volume: 6, Issue:4 Topics: Adult; Alanine; Alleles; Amino Acid Substitution; Black or African American; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Molecular Epidemiology; North Carolina; Polymorphism, Genetic; Population Surveillance; Superoxide Dismutase; Valine; White People	2004
Increased risk of bladder cancer associated with a glutathione peroxidase 1 codon 198 variant. The Journal of urology, 2004, Volume: 172, Issue:2 Topics: Aged; Alanine; Asian People; Carcinoma, Transitional Cell; Female; Genetic Predisposition to Disease; Genotype; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Humans; Leucine; Logistic Models; Male; Middle Aged; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Superoxide Dismutase; Urinary Bladder Neoplasms; Valine	2004
Glutathione S-transferase polymorphisms in patients with Behçet's disease. Archives of dermatological research, 2004, Volume: 296, Issue:4 Topics: Acyltransferases; Adult; Behcet Syndrome; Case-Control Studies; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Glutathione Transferase; Humans; Male; Middle Aged; Phenotype; Polymorphism, Genetic; Valine	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
The progesterone receptor Val660-->Leu polymorphism and breast cancer risk. Breast cancer research : BCR, 2004, Volume: 6, Issue:6 Topics: Breast Neoplasms; Case-Control Studies; Genetic Predisposition to Disease; Humans; Leucine; Middle Aged; Polymorphism, Single Nucleotide; Postmenopause; Premenopause; Receptors, Progesterone; Valine	2004
Genetic polymorphism in the manganese superoxide dismutase gene, antioxidant intake, and breast cancer risk: results from the Shanghai Breast Cancer Study. Breast cancer research : BCR, 2004, Volume: 6, Issue:6 Topics: Adult; Alanine; Alleles; Antioxidants; Breast Neoplasms; Case-Control Studies; Cocarcinogenesis; Diet; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Oxidative Stress; Polymorphism, Genetic; Postmenopause; Premenopause; Superoxide Dismutase; 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
The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk. Carcinogenesis, 2005, Volume: 26, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Breast Neoplasms; Case-Control Studies; Female; Genes, erbB-2; Genetic Carrier Screening; Genetic Predisposition to Disease; Humans; Isoleucine; Middle Aged; Polymerase Chain Reaction; Proto-Oncogene Mas; Risk Factors; Valine	2005
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
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
Her2 genotype and breast cancer progression in Korean women. Pathology international, 2005, Volume: 55, Issue:2 Topics: Adult; Aged; Breast Neoplasms; Carcinoma, Ductal, Breast; Carcinoma, Intraductal, Noninfiltrating; Disease Progression; Female; Genes, erbB-2; Genetic Predisposition to Disease; Genotype; Humans; Immunohistochemistry; Korea; Middle Aged; Odds Ratio; Oncogene Proteins v-erbB; Polymorphism, Genetic; Proto-Oncogene Mas; Risk Factors; Valine	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
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
The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males. Neuroscience letters, 2005, Apr-29, Volume: 379, Issue:1 Topics: Adolescent; Alanine; Brazil; Child; Child, Preschool; DNA Mutational Analysis; DNA-Binding Proteins; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Mutation; Valine	2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds. Archives of neurology, 2005, Volume: 62, Issue:4 Topics: Alanine; Amino Acid Substitution; Chorea; Chromosome Mapping; Chromosomes, Human, Pair 2; DNA Mutational Analysis; Exons; Female; Genes, Dominant; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Haplotypes; Humans; Male; Muscle Proteins; Mutation, Missense; Pedigree; Protein Structure, Secondary; 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 5alpha-reductase type II A49T and V89L high-activity allelic variants are more common in men with prostate cancer compared with the general population. European urology, 2005, Volume: 48, Issue:4 Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Aged; Alanine; Alleles; Arginine; Biomarkers, Tumor; Case-Control Studies; Dihydrotestosterone; Disease Progression; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Luteinizing Hormone; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Prostatic Hyperplasia; Prostatic Neoplasms; Receptors, Androgen; Risk Factors; Sex Hormone-Binding Globulin; Sweden; Terminal Repeat Sequences; Testosterone; Threonine; 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
Cholesteryl ester transfer protein (CETP) polymorphism modifies the Alzheimer's disease risk associated with APOE epsilon4 allele. Journal of neurology, 2006, Volume: 253, Issue:2 Topics: Aged; Aged, 80 and over; Alleles; Alzheimer Disease; Apolipoprotein E4; Apolipoproteins E; Carrier Proteins; Cholesterol Ester Transfer Proteins; Confidence Intervals; DNA Mutational Analysis; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycoproteins; Humans; Isoleucine; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Promoter Regions, Genetic; Retrospective Studies; Risk Factors; Spain; Valine	2006
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
A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy. Archives of neurology, 2005, Volume: 62, Issue:9 Topics: Amino Acid Substitution; Blotting, Northern; Blotting, Western; Brain; Dihydroxyphenylalanine; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Glycine; Humans; Immunohistochemistry; Middle Aged; Mutation; Neurologic Examination; Positron-Emission Tomography; Protein Isoforms; Raclopride; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Supranuclear Palsy, Progressive; tau Proteins; Valine	2005
Assessment of the genetic risk and impact of lateral transmission in a valine-associated scrapie outbreak in sheep. American journal of veterinary research, 2005, Volume: 66, Issue:8 Topics: Amino Acid Substitution; Animals; Disease Outbreaks; Disease Transmission, Infectious; Female; Genetic Predisposition to Disease; Genotype; Male; Prions; Scrapie; Sheep; Valine	2005
The valine allele of the V89L polymorphism in the 5-alpha-reductase gene confers a reduced risk for hypospadias. The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:12 Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Alleles; Base Sequence; Case-Control Studies; DNA; Gene Frequency; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Hypospadias; Infant, Newborn; Leucine; Male; Molecular Sequence Data; Polymorphism, Genetic; Valine	2005
Association study of Glutathione S-transferase P1 (GSTP1) with asthma and bronchial hyper-responsiveness in two German pediatric populations. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2005, Volume: 16, Issue:6 Topics: Adolescent; Alanine; Asthma; Bronchial Hyperreactivity; Child; Child, Preschool; Dermatitis, Atopic; Follow-Up Studies; Forced Expiratory Volume; Gene Frequency; Genetic Predisposition to Disease; Genotype; Germany; Glutathione S-Transferase pi; Humans; Isoleucine; Polymorphism, Genetic; Respiratory Function Tests; Rhinitis, Allergic, Perennial; Valine	2005
Association of DRD2 gene variant with schizophrenia. Neuroscience letters, 2006, Jan-09, Volume: 392, Issue:1-2 Topics: Adolescent; Adult; Age of Onset; Case-Control Studies; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Histidine; Humans; Male; Polymorphism, Genetic; Psychiatric Status Rating Scales; Receptors, Dopamine D2; Schizophrenia; Valine	2006
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
Polymorphisms of ADPRT Val762Ala and XRCC1 Arg399Glu and risk of breast cancer in Chinese women: a case control analysis. Oncology reports, 2006, Volume: 15, Issue:1 Topics: Adult; Alanine; Amino Acid Substitution; Arginine; Asian People; Breast Neoplasms; Case-Control Studies; China; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Middle Aged; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Polymorphism, Genetic; Risk; Valine; X-ray Repair Cross Complementing Protein 1	2006
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
Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK. The British journal of psychiatry : the journal of mental science, 2006, Volume: 188 Topics: Bipolar Disorder; Brain-Derived Neurotrophic Factor; Case-Control Studies; England; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Valine; Wales	2006
Functional polymorphism 57Val>Ile of aurora kinase A associated with increased risk of gastric cancer progression. Cancer letters, 2006, Oct-28, Volume: 242, Issue:2 Topics: Alleles; Aurora Kinase A; Aurora Kinases; Case-Control Studies; Disease Progression; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Isoleucine; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Risk; Stomach Neoplasms; Valine	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
The association between factor XIII Val34Leu polymorphism and early myocardial infarction. Circulation journal : official journal of the Japanese Circulation Society, 2006, Volume: 70, Issue:3 Topics: Adult; Age Factors; Alleles; Case-Control Studies; Coronary Thrombosis; DNA; Factor XIII; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Myocardial Infarction; Polymerase Chain Reaction; Polymorphism, Genetic; Regression Analysis; Valine	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
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
A91V perforin variation in healthy subjects and FHLH patients. International journal of immunogenetics, 2006, Volume: 33, Issue:2 Topics: Alanine; Amino Acid Substitution; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Humans; Lymphohistiocytosis, Hemophagocytic; Membrane Glycoproteins; Perforin; Pore Forming Cytotoxic Proteins; Valine	2006
Association of the progesterone receptor gene with breast cancer risk: a single-nucleotide polymorphism tagging approach. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2006, Volume: 15, Issue:4 Topics: Aged; Breast Neoplasms; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Humans; Linkage Disequilibrium; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Progesterone; Risk; Sequence Tagged Sites; United Kingdom; 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
Natriuretic peptide Val7Met substitution and risk of coronary artery disease in Greek patients with familial hypercholesterolemia. Journal of clinical laboratory analysis, 2006, Volume: 20, Issue:3 Topics: Adult; Atrial Natriuretic Factor; Comorbidity; Coronary Artery Disease; Female; Genetic Predisposition to Disease; Greece; Humans; Hyperlipoproteinemia Type II; Lipids; Male; Polymorphism, Single Nucleotide; Risk Factors; Valine	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
A novel missense mutation in the transmembrane domain of neuregulin 1 is associated with schizophrenia. Biological psychiatry, 2006, Sep-15, Volume: 60, Issue:6 Topics: Animals; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Mutation, Missense; Neuregulin-1; Pedigree; Protein Structure, Tertiary; Schizophrenia; Sequence Homology; Valine	2006
Interaction of CTSD and A2M polymorphisms in the risk for Alzheimer's disease. Journal of the neurological sciences, 2006, Sep-25, Volume: 247, Issue:2 Topics: Aged; Aged, 80 and over; Alanine; alpha-Macroglobulins; Alzheimer Disease; Cathepsin D; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Odds Ratio; Polymorphism, Genetic; Risk; Valine	2006
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
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
The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer. Carcinogenesis, 2007, Volume: 28, Issue:2 Topics: A Kinase Anchor Proteins; Adaptor Proteins, Signal Transducing; Base Sequence; Breast Neoplasms; Cohort Studies; DNA Primers; Genetic Predisposition to Disease; Genetic Variation; Humans; Isoleucine; Risk Factors; Valine	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
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin. Annals of neurology, 2006, Volume: 60, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Aspartic Acid; Chromosomes, Human, Pair 17; Dementia; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Inclusion Bodies; Intercellular Signaling Peptides and Proteins; Male; Middle Aged; Mutation, Missense; Neuropsychological Tests; tau Proteins; Ubiquitin; Valine	2006
The factor XIII Val34Leu polymorphism: is it protective against idiopathic venous thromboembolism? Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2006, Volume: 17, Issue:7 Topics: Amino Acid Substitution; Case-Control Studies; Factor XIII; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Risk Assessment; Thromboembolism; Valine; Venous Thrombosis; White People	2006
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
No association between Ala9Val functional polymorphism of MnSOD gene and schizophrenia in a representative Italian sample. Neuroscience letters, 2006, Dec-27, Volume: 410, Issue:3 Topics: Adult; Alanine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Italy; Male; Middle Aged; Polymorphism, Genetic; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Schizophrenia; Superoxide Dismutase; Valine	2006
The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis. Journal of thrombosis and haemostasis : JTH, 2007, Volume: 5, Issue:1 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Child; Cohort Studies; Female; Follow-Up Studies; Gene Frequency; Genetic Predisposition to Disease; Humans; Italy; Janus Kinase 2; Male; Mesenteric Vascular Occlusion; Mesenteric Veins; Middle Aged; Mutation; Myeloproliferative Disorders; Odds Ratio; Phenylalanine; Portal Vein; Risk Factors; Time Factors; Valine; Venous Thrombosis; Von Hippel-Lindau Tumor Suppressor Protein	2007
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
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
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
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD. Journal of neural transmission (Vienna, Austria : 1996), 2007, Volume: 114, Issue:4 Topics: Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Child; Female; Genetic Predisposition to Disease; Humans; Male; Pedigree; Polymorphism, Single Nucleotide; Valine	2007
Association between the MnSOD Ala-9Val polymorphism and development of schizophrenia and abnormal involuntary movements in the Xhosa population. Progress in neuro-psychopharmacology & biological psychiatry, 2007, Apr-13, Volume: 31, Issue:3 Topics: Adult; Africa, Southern; Alanine; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Movement Disorders; Polymorphism, Genetic; Schizophrenia; Superoxide Dismutase; Valine	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
655Val and 1170Pro ERBB2 SNPs in familial breast cancer risk and BRCA1 alterations. Cellular oncology : the official journal of the International Society for Cellular Oncology, 2007, Volume: 29, Issue:3 Topics: Adult; Age Distribution; Aged; BRCA1 Protein; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Polymorphism, Single Nucleotide; Proline; Receptor, ErbB-2; 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
Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation. Epilepsy research, 2007, Volume: 75, Issue:1 Topics: Adult; Child; DNA Mutational Analysis; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Mutation; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Pedigree; Phenotype; Sodium Channels; Valine	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
P27 V109G Polymorphism is associated with lymph node metastases but not with increased risk of breast cancer. Journal of experimental & clinical cancer research : CR, 2007, Volume: 26, Issue:1 Topics: Breast Neoplasms; Carcinoma, Ductal, Breast; Case-Control Studies; Cyclin-Dependent Kinase Inhibitor p27; Female; Gene Expression Regulation, Neoplastic; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Heterozygote; Homozygote; Humans; Intracellular Signaling Peptides and Proteins; Lymph Nodes; Lymphatic Metastasis; Malaysia; Middle Aged; Neoplasm Staging; Odds Ratio; Phenotype; Polymorphism, Restriction Fragment Length; Prognosis; Receptors, Estrogen; Risk Assessment; Risk Factors; Valine	2007
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
Potentially functional single nucleotide polymorphisms in the core nucleotide excision repair genes and risk of squamous cell carcinoma of the head and neck. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2007, Volume: 16, Issue:8 Topics: Age Factors; Aged; Carcinoma, Squamous Cell; Case-Control Studies; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genes, Recessive; Genetic Predisposition to Disease; Genetic Variation; Genotype; Head and Neck Neoplasms; Humans; Laryngeal Neoplasms; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Sex Factors; Transglutaminases; Valine	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
Impact of FXIII-A Val34Leu polymorphism on coronary artery disease in Croatian patients. Molecular biology reports, 2009, Volume: 36, Issue:1 Topics: Aged; Chi-Square Distribution; Coronary Artery Disease; Coronary Thrombosis; Croatia; Factor XIII; Female; Genetic Predisposition to Disease; Humans; Leucine; Logistic Models; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Risk Factors; Statistics, Nonparametric; Valine	2009
The MnSOD Val9Ala polymorphism, dietary antioxidant intake, risk and survival in ovarian cancer (Australia). Gynecologic oncology, 2007, Volume: 107, Issue:3 Topics: Adult; Alanine; Antioxidants; Australia; Case-Control Studies; Diet; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Ovarian Neoplasms; Polymorphism, Genetic; Superoxide Dismutase; 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
The orexin 1 receptor (HCRTR1) gene as a susceptibility gene contributing to polydipsia-hyponatremia in schizophrenia. Neuromolecular medicine, 2007, Volume: 9, Issue:4 Topics: Adult; Age of Onset; Aged; Amino Acid Substitution; Female; Genetic Predisposition to Disease; Genotype; Humans; Hyponatremia; Isoleucine; Male; Middle Aged; Orexin Receptors; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Receptors, G-Protein-Coupled; Receptors, Neuropeptide; Schizophrenia; Thirst; Valine	2007
Parkin polymorphisms in progressive supranuclear palsy. Journal of the neurological sciences, 2008, May-15, Volume: 268, Issue:1-2 Topics: Aged; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Polymorphism, Genetic; Supranuclear Palsy, Progressive; tau Proteins; Ubiquitin-Protein Ligases; Valine	2008
Genetic polymorphism in the manganese superoxide dismutase gene is associated with an increased risk for hepatocellular carcinoma in HCV-infected Moroccan patients. Mutation research, 2008, Jan-08, Volume: 649, Issue:1-2 Topics: Aged; Alanine; Carcinoma, Hepatocellular; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hepatitis C; Humans; Male; Middle Aged; Morocco; Odds Ratio; Polymorphism, Genetic; Risk Factors; Superoxide Dismutase; Valine	2008
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants? Breast cancer research : BCR, 2007, Volume: 9, Issue:6 Topics: Alanine; Arginine; Biomarkers, Tumor; Breast Neoplasms; Centrosome; DNA, Complementary; Factor Analysis, Statistical; Female; Genes, BRCA1; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Humans; Immunohistochemistry; Keratins; Mutation, Missense; Nucleic Acid Amplification Techniques; Plasmids; Polymorphism, Single Nucleotide; Predictive Value of Tests; Receptors, Estrogen; Risk Assessment; Risk Factors; Sequence Analysis, DNA; Valine	2007
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
A case-control study of the HER2 Ile655Val polymorphism and risk of breast cancer in Taiwan. Clinical biochemistry, 2008, Volume: 41, Issue:3 Topics: Adult; Age Factors; Breast Neoplasms; Case-Control Studies; Female; Genes, erbB-2; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Middle Aged; Neoplasm Staging; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Reference Values; Risk Factors; Taiwan; Valine	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
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 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
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
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
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Molecular vision, 2008, May-08, Volume: 14 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Aryl Hydrocarbon Hydroxylases; Asian People; Case-Control Studies; Cell Line; Child; Cytochrome P-450 CYP1B1; Cytochrome P-450 Enzyme System; Ethnicity; Gene Frequency; Genetic Predisposition to Disease; Geography; Glaucoma, Open-Angle; Haplotypes; Humans; India; Leucine; Linkage Disequilibrium; Middle Aged; Pigment Epithelium of Eye; Polymorphism, Single Nucleotide; Reactive Oxygen Species; Software; 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
HLA-DQ beta 1 typing and non-Asp57 alleles in the aborigine population of Senegal. Diabetes care, 1995, Volume: 18, Issue:5 Topics: Adolescent; Adult; Alleles; Aspartic Acid; Black People; Child; Diabetes Mellitus, Type 1; Female; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Histocompatibility Testing; HLA-DQ Antigens; HLA-DQ beta-Chains; Homozygote; Humans; Male; Native Hawaiian or Other Pacific Islander; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Racial Groups; Reference Values; Risk Factors; Senegal; Valine	1995
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
Protective effects of valsartan and benazeprilat in salt-loaded stroke-prone spontaneously hypertensive rats. Clinical and experimental hypertension (New York, N.Y. : 1993), 1998, Volume: 20, Issue:7 Topics: Angiotensin-Converting Enzyme Inhibitors; Animals; Antihypertensive Agents; Benzazepines; Blood Pressure; Cerebrovascular Disorders; Genetic Predisposition to Disease; Heart Rate; Hypertension; Infusion Pumps; Kidney; Myocardium; Proteinuria; Rats; Rats, Inbred SHR; Renin; Renin-Angiotensin System; Sodium Chloride; Tetrazoles; Valine; Valsartan	1998
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
Genetic polymorphism of cathepsin D is strongly associated with the risk for developing sporadic Alzheimer's disease. Neuroscience letters, 1999, Mar-12, Volume: 262, Issue:3 Topics: Aged; Aged, 80 and over; Alanine; Alzheimer Disease; Amino Acid Substitution; Apolipoprotein E4; Apolipoproteins E; Cathepsin D; Depression; Exons; Female; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Reference Values; Risk Factors; Valine	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
The DRB1 Val86/Val86 genotype associates with multiple sclerosis in Australian patients. Human immunology, 1999, Volume: 60, Issue:8 Topics: Alleles; Antigen Presentation; Australia; Genetic Predisposition to Disease; Genotype; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Multiple Sclerosis; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Valine	1999
Cytochrome P4501A1 polymorphism as a susceptibility factor for breast cancer in postmenopausal Chinese women in Taiwan. British journal of cancer, 1999, Volume: 80, Issue:11 Topics: Amino Acid Substitution; Asian People; Body Mass Index; Breast Neoplasms; China; Contraceptives, Oral; Cytochrome P-450 CYP1A1; Estrogen Replacement Therapy; Exons; Female; Genetic Carrier Screening; Genetic Predisposition to Disease; Genetic Variation; Humans; Incidence; Isoleucine; Menarche; Middle Aged; Parity; Polymorphism, Genetic; Pregnancy; Risk Factors; Smoking; Taiwan; Valine	1999
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
A novel mutation in glial fibrillary acidic protein gene in a patient with Alexander disease. Neuroscience letters, 2001, Oct-19, Volume: 312, Issue:2 Topics: Alanine; Brain; Child; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Glial Fibrillary Acidic Protein; Hereditary Central Nervous System Demyelinating Diseases; Heterozygote; Humans; Japan; Magnetic Resonance Imaging; Male; Mutation, Missense; Protein Structure, Tertiary; Tomography, Emission-Computed; Valine	2001
Presence of the 5,10-methylenetetrahydrofolate reductase C677T mutation in Puerto Rican patients with neural tube defects. Journal of child neurology, 2002, Volume: 17, Issue:1 Topics: Adult; Alanine; Alleles; Amino Acid Substitution; Female; Genetic Predisposition to Disease; Hispanic or Latino; Homozygote; Humans; Infant, Newborn; Male; Methylenetetrahydrofolate Dehydrogenase (NADP); Mutation; Neural Tube Defects; Pregnancy; Prenatal Diagnosis; Risk; Valine	2002
Rheumatoid arthritis in Israeli Jews: shared sequences in the third hypervariable region of DRB1 alleles are associated with susceptibility. The Journal of rheumatology, 1991, Volume: 18, Issue:6 Topics: Alanine; Alleles; Amino Acid Sequence; Arthritis, Rheumatoid; Genetic Predisposition to Disease; Glycine; Histocompatibility Antigens Class II; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Immunoglobulin Variable Region; Israel; Jews; Molecular Sequence Data; Oligonucleotides; Polymerase Chain Reaction; Risk Factors; Valine	1991