cetylpyridinium chloride anhydrous and Genetic Predisposition

cetylpyridinium chloride anhydrous has been researched along with Genetic Predisposition in 89 studies

Research

Studies (89)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	11 (12.36)	18.2507
2000's	23 (25.84)	29.6817
2010's	51 (57.30)	24.3611
2020's	4 (4.49)	2.80

Authors

Authors	Studies
Azeloglu, EU; Beaumont, KG; Berger, SI; Birtwistle, MR; D'Souza, SL; Dariolli, R; Dhanan, P; Dubois, NC; Garg, J; Goldfarb, J; Gonzalez, DM; Hansen, J; Hu, B; Iyengar, R; Jayaraman, G; Kovacic, JC; Machado, M; Mahajan, M; Mathew, B; Michelis, KC; Miller, M; Najfeld, V; Raghunandan, T; Schadt, E; Schaniel, C; Schürer, SC; Sebra, R; Sobie, EA; Surlyn, CS; Tangirala, NC; Thomas, DC; Tripodi, J; Vidovic, D; Weerahandi, H; Xiong, Y; Yadaw, AS	1
Arnold, M; Baird, D; Benner, C; Black, MH; Burkitt-Gray, L; Burren, OS; Chen, CY; Chiou, J; Cule, M; Davitte, J; Deaton, AM; Fauman, EB; Ferber, KL; Gibson, BW; Gillies, CE; Hedman, ÅK; Hou, L; Howson, JMM; Hsu, YH; Hu, S; Kang, HM; Kastenmüller, G; Kvikstad, EM; Lehner, N; Lin, T; Mahajan, A; McCarthy, MI; Melamud, E; Mikkilineni, R; Miller, MR; Mitnaul, LJ; Nioi, P; Pendergrass, RK; Petrovski, S; Pickering, C; Prins, B; Raj, A; Richardson, TG; Robins, C; Scott, RA; Sethi, A; Smith, EN; Suhre, K; Sun, BB; Surendran, P; Szalma, S; Szustakowski, JD; Traylor, M; Vasquez-Grinnell, SG; Ward, LD; Waterworth, DM; Welsh, S; Whelan, CD; Willis, CM; Wörheide, MA	1
Abdellaoui, A; Amin, N; Baselmans, BML; Boomsma, DI; Cacioppo, JT; Cacioppo, S; Davis, LK; Dennis, J; Denys, D; Elson, S; Fontanillas, P; Hottenga, JJ; Ip, HF; Lu, Y; M van Duijn, C; Mosing, M; Neumann, A; Nivard, MG; Palmer, AA; Pedersen, NL; Sanchez-Roige, S; Sealock, J; Szilagyi, I; Tiemeier, H; Treur, JL; van der Zee, M; Verweij, KJH; Willemsen, G	1
Banks, MA	1
Fraternali, F; Laddach, A; Ng, JCF	1
Adeyemo, A; Bentley, AR; Chen, G; Doumatey, AP; Rotimi, CN; Shriner, D	1
Ouimette, JF; Rougeulle, C; Veitia, RA	1
Abelson, S; Awadalla, P; Balicer, RD; Barda, N; Barricarte, A; Beer, P; Behjati, S; Boeing, H; Bowles, KM; Bratman, SV; Brennan, P; Britten, A; Campbell, PJ; Cirlan, I; Collord, G; Costa, R; Dick, JE; Eagles, J; Foll, M; Gerstung, M; Hardy, C; Hayat, S; Heisler, L; Hoult, D; Huerta, JM; Johansson, M; Jones, D; Kaaks, R; Karakatsani, A; Khaw, KT; Krämer, A; Krzyzanowski, P; La Vecchia, C; Latimer, C; Luben, R; Martincorena, I; Masala, G; Mbabaali, F; McKay, J; McPherson, JD; Mendelson Cohen, N; Miller, JK; Minden, MD; Ng, K; Ng, SWK; Niemeyer, E; Panico, S; Papaemmanuil, E; Pasternack, D; Polidoro, S; Pugh, TJ; Quirós, JR; Raine, K; Riboli, E; Sala, N; Salamanca-Fernández, E; Segal, E; Shlush, LI; Sieri, S; Soave, D; Sundaravadanam, Y; Tanay, A; Timms, L; Travis, RC; Trichopoulou, A; Tumino, R; Vassiliou, GS; Vermeulen, R; Vineis, P; Wang, JCY; Wang, TT; Wareham, NJ; Weissbrod, O; Zhao, Z; Zuzarte, PC	1
Khorrami-Nezhad, L; Maghbooli, Z; Mirzaei, K; Mollahosseini, M; Nasir, Y; Pooyan, S; Rahimi, MH	1
Agrawal, PB; Beggs, AH; Ceyhan-Birsoy, O; Fayer, S; Genetti, CA; Green, RC; Holm, IA; Lebo, MS; Machini, K; McGuire, AL; Murry, JB; Parad, RB; Rehm, HL; Schwartz, TS; Yu, TW	1
Alham, NK; Andev, RS; Antanaviciute, A; Ashley, N; Aulicino, A; Bao, L; Björklund, E; Chen, HH; Davis, S; Fawkner-Corbett, D; Fischer, R; Goldin, R; Hublitz, P; Jagielowicz, M; Johnson, E; Kessler, BM; Kinchen, J; Koohy, H; Lagerholm, C; Lukomska, J; Parikh, K; Simmons, A	1
Fu, WZ; He, JW; Zhang, CQ; Zhang, Z; Zhang, ZL	1
Aleman, A; Bochdanovits, Z; Hoogendijk, WJ; Opmeer, EM; Penninx, BW; van Buchem, MA; van der Wee, NJ; van Tol, MJ; Veltman, DJ; Woudstra, S; Zitman, FG	1
Artiges, E; Banaschewski, T; Barker, GJ; Büchel, C; Conrod, PJ; Flor, H; Frank, J; Gallinat, J; Garavan, H; Heinz, A; Ittermann, B; Loth, E; Lourdusamy, A; Mann, K; Nees, F; Paus, T; Pausova, Z; Poustka, L; Rietschel, M; Schumann, G; Smolka, MN; Steiner, S; Struve, M; Vollstädt-Klein, S; Witt, SH	1
Huang, Y; Jin, Q; Li, J; Ma, H; Wang, Y; Zhang, B; Zhao, X; Zhu, G	1
Ahrens, W; Bailey, ME; Bammann, K; Cugino, D; Gianfagna, F; Herrmann, D; Iacoviello, L; Koni, AC; Kourides, Y; Marild, S; Molnár, D; Moreno, LA; Pitsiladis, YP; Russo, P; Siani, A; Sieri, S; Sioen, I; Veidebaum, T	1
Bookheimer, SY; Burggren, AC; Donix, M; Ercoli, LM; Holthoff, VA; Jones, M; Krupa, AK; Marschner, K; Martin-Harris, L; Miller, KJ; Sauer, C; Scharf, M; Siddarth, P; Small, GW; Suthana, NA; von Kummer, R; Werner, A	1
Accardi, G; Candore, G; Caruso, C; Di Bona, D; Virruso, C	1
Chen, Z; Gross, MD; Hsu, C; Koh, WP; Koratkar, R; Liu, J; Odegaard, AO; Pereira, MA; Seielstad, M; Stram, DO; Tai, ES; Teo, YY; Thyagarajan, B; Wang, R; Yuan, JM	1
Bodian, DL; Huddleston, KC; Iyer, RK; Kothiyal, P; McCutcheon, JN; Niederhuber, JE; Vockley, JG	1
Friend, SH; Schadt, EE	1
Arias-Vásquez, A; Fernández, G; Franke, B; Schene, AH; Tendolkar, I; van Oostrom, I; Vrijsen, JN	1
Barrett, JC; Barroso, I; Crooks, L; Danecek, P; Durbin, R; Floyd, J; Futema, M; Greenwood, CM; Hendricks, AE; Huang, J; Humphries, SE; Hurles, ME; Iotchkova, V; Lawson, D; Li, R; McCarthy, S; Memari, Y; Min, JL; Perry, JR; Plagnol, V; Richards, JB; Schiffels, S; Soranzo, N; Timpson, NJ; Wain, LV; Walter, K; Xu, C; Zeggini, E	1
Huang, L; Li, M; Luo, XJ; Su, B; Wang, J	1
Cullen, B; Davies, G; Deary, IJ; Fawns-Ritchie, C; Gale, CR; Gallacher, J; Hagenaars, SP; Harris, SE; Hill, WD; Liewald, DC; Malik, R; Marioni, RE; McIntosh, AM; Pell, J; Ritchie, SJ; Smith, DJ; Sudlow, CL; Wardlaw, JM; Worrall, BB	1
Bolnick, DA; Smart, A; Tutton, R	1
Makarchuk, MJ; Rose, K; Sherman, PM	1
Brigham, KL; Johns, MM	1
Berg, T; Hubácek, JA; Jirsa, M; Meitinger, T; Petrásek, J; Pfeufer, A; Ruf, E; Sperl, J; Spicák, J; Stickel, F; Trunecka, P; Wichmann, HE	1
Birmingham, DJ; Chung, EK; Hebert, LA; Kitzmiller, KJ; Nagaraja, HN; Rovin, BH; Savelli, SL; Tsao, BP; Wu, YL; Yang, Y; Yu, CY; Zhou, B	1
Bottini, E; Bottini, N; Chiarelli, F; D'Annibale, F; Gloria-Bottini, F; Manca Bitti, ML; Piccinini, S; Rapini, N; Saccucci, P; Verrotti, A	1
Convit, JR; Dumitrescu, RG; Freudenheim, JL; Kallakury, BV; Krishnan, SS; Marian, C; Perry, DJ; Seillier-Moiseiwitsch, F; Shields, PG; Spear, SL; Yang, Y	1
Beller, U; Eitan, R; Levavi, H; Michaelson-Cohen, R	1
Allanson, J; Carroll, J; Little, J; Qureshi, N; Raina, P; Santaguida, P; Wilson, B	1
Altmäe, S; Arenas, J; Arteta, D; Artieda, M; Buxens, A; Gómez-Gallego, F; González-Freire, M; Lao, JI; Lucia, A; Martínez, A; Ruiz, JR; Santiago, C; Tejedor, D; Verde, Z	1
Kream, RM; Mantione, K; Stefano, GB	1
Brasfield, J; Cubells, JF; Tang, YL; Trotman, HD; Walder, DJ; Walker, EF	1
Bakker, JA; Cavallaro, G; González-Luis, G; Moonen, RM; Reyes, I; Villamor, E	1
Collins, RE; Marteau, TM; Wright, AJ	1
Chasman, DI; Ridker, PM; Zee, RY	1
Chasman, DI; Perez-Fuentes, R; Pulido-Perez, P; Ridker, PM; Romero, JR; Zee, RY	1
Caulfield, T; Evans, JP; Marteau, TM; Meslin, EM	1
Bertolaso, L; Bolzonella, C; Gusella, M; Padrini, R; Pasini, F	1
Bellido, TM; Drezner, MK; Gordon, CM; Harris, TB; Khosla, S; Kiel, DP; Kream, BE; LeBoff, MS; Lian, JB; Peterson, CA; Rosen, CJ; Sherman, SS; Williams, JP; Winer, KK	1
Chibnik, LB; Costenbader, KH; Cui, J; Karlson, EW; Keenan, BT; Liao, KP; Plenge, RM	1
Almal, SH; Padh, H	1
Kaname, T	1
Akyüz, S; Bayer, H; Furuncuoğlu, H; Koç Öztürk, L; Ulucan, K; Yarat, A	1
Berg, JP; Endestad, T; Foss Haug, KB; Jonassen, R; Landrø, NI; Neumeister, A	1
Berenson, GS; Chen, W; Hernesniemi, JA; Hutri-Kähönen, N; Jula, A; Juonala, M; Kähönen, M; Kettunen, J; Laaksonen, R; Laitinen, T; Lehtimäki, T; Lyytikäinen, LP; Mononen, N; Murray, SS; Oksala, N; Raitakari, OT; Ripatti, S; Schork, NJ; Seppälä, I; Smith, EN; Srinivasan, SR; Taittonen, L; Viikari, J	1
Avramopoulos, D; Evdokimidis, I; Hatzimanolis, A; Smyrnis, N; Stefanis, CN; Stefanis, NC	1
Cruz, M; Fernández-Tilapa, G; Flores-Alfaro, E; Illades-Aguiar, B; Parra-Rojas, I; Salazar-Martínez, E	1
Agartz, I; Andreassen, OA; Brown, AA; Dale, AM; Djurovic, S; Hartberg, CB; Kähler, AK; Melle, I; Rimol, LM	1
Bai, LJ; Cheung, MN; Chow, LW; Dou, YD; Fan, CB; Li, JL; Liang, H; Loo, WT; Qing, L; Tian, Y; Wang, M; Yue, Y	1
Dyer, P; McGilvray, R; Robertson, V; Turner, D	1
Hesketh, J	1
Minihane, AM	1
de Roos, B	1
Eisenstein, M	1
Huang, Y; Jin, Q; Li, J; Ma, H; Wang, M; Wang, Y; Zhang, B; Zhao, X; Zhu, G	1
Baird, P	1
Jackson, FL	1
Scully, JL	1
Tauer, CA	1
Goldstein, DB; Stumpf, MP; Wood, NW	1
Bamshad, M	1
Kono, S; Mineshita, M; Ogawa, S; Tabata, S; Yamaguchi, K; Yin, G	1
Dato, S; De Benedictis, G; Domma, F; Feraco, E; Giordano, S; Mari, V; Montesanto, A; Passarino, G	1
Barancoková, M; Dusinská, M; Horská, A; Kazimírová, A; Tulinská, J; Wsólová, L	1
Adams, S; Adorno, D; Bouaouina, N; Chen, D; Chouchane, L; Ghandri, N; Li, X; Marincola, FM; Monaco, A; Piancatelli, D; Robbins, FM; Selleri, S; Stroncek, D; Wang, E	1
Breunis, WB; Bruin, M; de Boer, M; de Haas, M; Geissler, J; Koene, HR; Kuijpers, TW; Peters, M; Roos, D; van Mirre, E	1
Ahaghotu, C; Akereyeni, F; Bonilla, C; Hooker, S; Kittles, RA	1
Dolinoy, DC; Jirtle, RL	1
Bradley, LA; Gwinn, M; Janssens, AC; Khoury, MJ; Oostra, BA; van Duijn, CM	1
Begun, AZ; Harris, JR; Holm, NV; Iachina, MK; Iachine, IA; Kaprio, J; Laitinen, M; Yashin, AI	1
Nilsonne, A	1
Kahn, RL; Rowe, JW	1
Makalowska, I; Makalowski, W; Wolfsberg, TG	1
Kuhse, H; Singer, P	1
Kennedy, I	1
Hubbard, R	1
Fitzgerald, WA	1
Leenen, H	1
Strudler, A	1
Fenner, DE	1
Robertson, JA	1

Reviews

16 review(s) available for cetylpyridinium chloride anhydrous and Genetic Predisposition

Article	Year
The genomic landscape of African populations in health and disease. Human molecular genetics, 2017, 10-01, Volume: 26, Issue:R2 Topics: Alleles; Biological Evolution; Black People; Disease; Genetic Predisposition to Disease; Genetic Variation; Genetics, Population; Genome, Human; Genomics; Haplotypes; Health; Humans; Pharmacogenetics; Polymorphism, Single Nucleotide	2017
Three-dimensional genome architecture in health and disease. Clinical genetics, 2019, Volume: 95, Issue:2 Topics: Chromosomes, Human; Gene Expression Regulation; Genetic Association Studies; Genetic Predisposition to Disease; Genome, Human; Genomics; Gonads; Health; Humans; Muscle Development	2019
Association of Klotho polymorphisms with healthy aging: a systematic review and meta-analysis. Rejuvenation research, 2014, Volume: 17, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Aging; Case-Control Studies; Genetic Predisposition to Disease; Genome-Wide Association Study; Glucuronidase; Health; Humans; Infant; Infant, Newborn; Klotho Proteins; Middle Aged; Polymorphism, Single Nucleotide; Young Adult	2014
Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus. Cytogenetic and genome research, 2008, Volume: 123, Issue:1-4 Topics: Animals; Complement C4; Genetic Predisposition to Disease; Genotype; Health; Humans; Lupus Erythematosus, Systemic; Phenotype	2008
The counseling and management of young healthy BRCA mutation carriers. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 2009, Volume: 19, Issue:7 Topics: Breast Neoplasms; Counseling; Disease Management; Female; Genes, BRCA1; Genes, BRCA2; Genetic Predisposition to Disease; Health; Heterozygote; Humans; Mutation; Ovarian Neoplasms	2009
Family history and improving health. Evidence report/technology assessment, 2009, Issue:186 Topics: Family; Genetic Predisposition to Disease; Health; Humans; Medical History Taking; Risk Factors	2009
Variations in critical morphine biosynthesis genes and their potential to influence human health. Neuro endocrinology letters, 2010, Volume: 31, Issue:1 Topics: Cannabinoid Receptor Modulators; Catechol O-Methyltransferase; Cytochrome P-450 CYP2D6; Enzymes; Genetic Predisposition to Disease; Health; Humans; Mental Disorders; Metabolic Networks and Pathways; Models, Biological; Morphine; Phenylethanolamine N-Methyltransferase; Polymorphism, Genetic	2010
Impact of communicating personalized genetic risk information on perceived control over the risk: a systematic review. Genetics in medicine : official journal of the American College of Medical Genetics, 2011, Volume: 13, Issue:4 Topics: Adult; Culture; Female; Genetic Predisposition to Disease; Health; Health Communication; Humans; Male; Middle Aged; Research Design; Risk Assessment; Risk Factors; Social Environment	2011
Implications of gene copy-number variation in health and diseases. Journal of human genetics, 2012, Volume: 57, Issue:1 Topics: Disease; DNA Copy Number Variations; Genetic Predisposition to Disease; Health; Humans; Pharmaceutical Preparations	2012
Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--a meta PloS one, 2012, Volume: 7, Issue:1 Topics: Adult; Carotid Intima-Media Thickness; Coronary Artery Disease; Data Collection; Female; Finland; Genetic Predisposition to Disease; Genome-Wide Association Study; Health; Humans; Louisiana; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors	2012
Status report from 'double agent HLA': health and disease. Molecular immunology, 2013, Volume: 55, Issue:1 Topics: Disease; Genetic Association Studies; Genetic Predisposition to Disease; Health; HLA Antigens; Humans; Immunity; Major Histocompatibility Complex; Models, Biological; Polymorphism, Genetic	2013
Personalised nutrition: how far has nutrigenomics progressed? European journal of clinical nutrition, 2013, Volume: 67, Issue:5 Topics: Diet; Genetic Predisposition to Disease; Genetic Variation; Health; Humans; Lipid Metabolism; Micronutrients; Nutrigenomics; Nutritional Physiological Phenomena; Nutritional Sciences; Nutritional Status; Precision Medicine	2013
Personalised nutrition: ready for practice? The Proceedings of the Nutrition Society, 2013, Volume: 72, Issue:1 Topics: Diet; Environment; Genetic Predisposition to Disease; Genetic Variation; Genotype; Health; Humans; Nutrigenomics; Nutritional Physiological Phenomena; Phenotype; Risk Factors	2013
Human genetic variation and health: new assessment approaches based on ethnogenetic layering. British medical bulletin, 2004, Volume: 69 Topics: Biodiversity; Culture; Environment; Genetic Predisposition to Disease; Genetic Variation; Health; Humans	2004
Environmental epigenomics in human health and disease. Environmental and molecular mutagenesis, 2008, Volume: 49, Issue:1 Topics: Animals; Computational Biology; Environment; Epigenesis, Genetic; Genetic Predisposition to Disease; Genomic Instability; Health; Humans; Phylogeny	2008
Successful aging and disease prevention. Advances in renal replacement therapy, 2000, Volume: 7, Issue:1 Topics: Aging; Cognition; Genetic Predisposition to Disease; Health; Humans; Interpersonal Relations; Life Style; Physical Fitness; Preventive Medicine; Research; Risk Factors	2000

Trials

1 trial(s) available for cetylpyridinium chloride anhydrous and Genetic Predisposition

Article	Year
Serotonin transporter polymorphism modulates N-back task performance and fMRI BOLD signal intensity in healthy women. PloS one, 2012, Volume: 7, Issue:1 Topics: Adult; Brain Mapping; Computer Simulation; Depressive Disorder, Major; Female; Genetic Predisposition to Disease; Genotype; Health; Humans; Image Interpretation, Computer-Assisted; Magnetic Resonance Imaging; Middle Aged; Polymorphism, Genetic; Serotonin Plasma Membrane Transport Proteins; Task Performance and Analysis; Young Adult	2012

Article

Year

Serotonin transporter polymorphism modulates N-back task performance and fMRI BOLD signal intensity in healthy women.

PloS one, 2012, Volume: 7, Issue:1

Topics: Adult; Brain Mapping; Computer Simulation; Depressive Disorder, Major; Female; Genetic Predisposition to Disease; Genotype; Health; Humans; Image Interpretation, Computer-Assisted; Magnetic Resonance Imaging; Middle Aged; Polymorphism, Genetic; Serotonin Plasma Membrane Transport Proteins; Task Performance and Analysis; Young Adult

2012

Other Studies

72 other study(ies) available for cetylpyridinium chloride anhydrous and Genetic Predisposition

Article	Year
A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals. Stem cell reports, 2021, 12-14, Volume: 16, Issue:12 Topics: Adult; Calcium Signaling; Cell Differentiation; Cell Line; Clone Cells; Ethnicity; Female; Gene Expression Profiling; Gene Expression Regulation; Genetic Predisposition to Disease; Genetic Variation; Health; Heart Atria; Heart Ventricles; Humans; Induced Pluripotent Stem Cells; Male; Middle Aged; Myocytes, Cardiac; Risk Factors; Young Adult	2021
Plasma proteomic associations with genetics and health in the UK Biobank. Nature, 2023, Volume: 622, Issue:7982 Topics: ABO Blood-Group System; Biological Specimen Banks; Blood Proteins; COVID-19; Databases, Factual; Drug Discovery; Epistasis, Genetic; Fucosyltransferases; Galactoside 2-alpha-L-fucosyltransferase; Genetic Predisposition to Disease; Genomics; Health; Humans; Plasma; Proprotein Convertase 9; Proteome; Proteomics; Public-Private Sector Partnerships; Quantitative Trait Loci; United Kingdom	2023
Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness. Human molecular genetics, 2019, 11-15, Volume: 28, Issue:22 Topics: Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Health; Humans; Loneliness; Male; Mendelian Randomization Analysis; Mental Disorders; Mental Health; Multifactorial Inheritance; Phenomics; Phenotype; Polymorphism, Single Nucleotide	2019
Sequencing effort in Africa fine-tunes data collection. Nature medicine, 2020, Volume: 26, Issue:1 Topics: Africa; Data Collection; Genetic Predisposition to Disease; Genome-Wide Association Study; Health; Heredity; Humans; Sequence Analysis, DNA	2020
Pathogenic missense protein variants affect different functional pathways and proteomic features than healthy population variants. PLoS biology, 2021, Volume: 19, Issue:4 Topics: Amino Acid Sequence; Computational Biology; Databases, Protein; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Germ-Line Mutation; Health; Humans; Mutant Proteins; Mutation, Missense; Protein Conformation; Protein Folding; Protein Interaction Domains and Motifs; Protein Processing, Post-Translational; Proteins; Proteome; Proteomics; Signal Transduction; Software	2021
Prediction of acute myeloid leukaemia risk in healthy individuals. Nature, 2018, Volume: 559, Issue:7714 Topics: Adult; Age Factors; Aged; Disease Progression; Electronic Health Records; Female; Genetic Predisposition to Disease; Health; Humans; Leukemia, Myeloid, Acute; Male; Middle Aged; Models, Genetic; Mutagenesis; Mutation; Prevalence; Risk Assessment	2018
A High-Protein/Low-Fat Diet May Interact with Vitamin D-Binding Protein Gene Variants to Moderate the Risk of Depression in Apparently Healthy Adults. Lifestyle genomics, 2018, Volume: 11, Issue:1 Topics: Adolescent; Adult; Asymptomatic Diseases; Depression; Diet, Fat-Restricted; Diet, High-Protein; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Health; Humans; Iran; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Vitamin D Deficiency; Vitamin D-Binding Protein; Young Adult	2018
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. American journal of human genetics, 2019, 01-03, Volume: 104, Issue:1 Topics: Age of Onset; Disease; Exome Sequencing; Female; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genome, Human; Genomics; Health; Heterozygote; Humans; Infant, Newborn; Male; Pharmacogenetics; Racial Groups; Sequence Analysis, DNA	2019
Colonic epithelial cell diversity in health and inflammatory bowel disease. Nature, 2019, Volume: 567, Issue:7746 Topics: Animals; Biomarkers; Colitis, Ulcerative; Colon; Epithelial Cells; Genetic Predisposition to Disease; Goblet Cells; Health; Humans; Hydrogen-Ion Concentration; Inflammatory Bowel Diseases; Intestinal Mucosa; Ion Channels; Male; Mice; Natriuretic Peptides; Proteins; Single-Cell Analysis; Stem Cells; Tight Junctions; Transcription, Genetic; WAP Four-Disulfide Core Domain Protein 2	2019
An analysis of the association between the vitamin D pathway and serum 25-hydroxyvitamin D levels in a healthy Chinese population. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2013, Volume: 28, Issue:8 Topics: Adult; Aged; Aged, 80 and over; Asian People; China; Female; Genetic Association Studies; Genetic Predisposition to Disease; Haplotypes; Health; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Signal Transduction; Vitamin D; Vitamin D Deficiency; Vitamin D-Binding Protein; Young Adult	2013
Modulatory effects of the piccolo genotype on emotional memory in health and depression. PloS one, 2013, Volume: 8, Issue:4 Topics: Adult; Cytoskeletal Proteins; Depressive Disorder, Major; Emotions; Female; Genetic Predisposition to Disease; Gyrus Cinguli; Health; Humans; Male; Memory; Neostriatum; Neuropeptides; Selective Serotonin Reuptake Inhibitors; Task Performance and Analysis	2013
Genetic risk for nicotine dependence in the cholinergic system and activation of the brain reward system in healthy adolescents. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2013, Volume: 38, Issue:11 Topics: Adolescent; Adolescent Behavior; Corpus Striatum; Female; Frontal Lobe; Functional Neuroimaging; Genetic Predisposition to Disease; Genotype; Gyrus Cinguli; Health; Humans; Male; Multigene Family; Nerve Tissue Proteins; Personality; Polymorphism, Single Nucleotide; Receptors, Nicotinic; Reward; Risk Factors; Tobacco Use Disorder; White People	2013
No association of neurotensin receptor 1 gene polymorphisms with coping styles in healthy Chinese-Han individuals. Psychiatric genetics, 2013, Volume: 23, Issue:4 Topics: Adaptation, Psychological; Adolescent; Adult; Asian People; Ethnicity; Female; Genetic Association Studies; Genetic Predisposition to Disease; Health; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Neurotensin; Young Adult	2013
Understanding the links among neuromedin U gene, beta2-adrenoceptor gene and bone health: an observational study in European children. PloS one, 2013, Volume: 8, Issue:8 Topics: Alleles; Biomechanical Phenomena; Bone and Bones; Bone Diseases; Child; Child, Preschool; Epistasis, Genetic; Europe; Female; Genetic Predisposition to Disease; Health; Humans; Male; Neuropeptides; Receptors, Adrenergic, beta-2; Sex Characteristics	2013
Sequenced from the start. Nature, 2013, Sep-12, Volume: 501, Issue:7466 Topics: Evaluation Studies as Topic; False Positive Reactions; Genetic Counseling; Genetic Predisposition to Disease; Genetic Privacy; Genetic Testing; Genome, Human; Genomics; Health; Humans; Infant, Newborn; Neonatal Screening; Preventive Medicine; United States	2013
APOE associated hemispheric asymmetry of entorhinal cortical thickness in aging and Alzheimer's disease. Psychiatry research, 2013, Dec-30, Volume: 214, Issue:3 Topics: Aged; Aging; Alleles; Alzheimer Disease; Apolipoprotein E4; Entorhinal Cortex; Female; Genetic Predisposition to Disease; Genotype; Health; Heterozygote; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Middle Aged	2013
Joint effects of known type 2 diabetes susceptibility loci in genome-wide association study of Singapore Chinese: the Singapore Chinese health study. PloS one, 2014, Volume: 9, Issue:2 Topics: Aged; Asian People; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study; Health; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Singapore	2014
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. PloS one, 2014, Volume: 9, Issue:4 Topics: Adolescent; Adult; Alleles; Cohort Studies; Female; Gene Frequency; Gene Pool; Genes, Neoplasm; Genetic Predisposition to Disease; Genome, Human; Germ-Line Mutation; Health; Humans; Male; Middle Aged; Models, Molecular; Neoplasms; Open Reading Frames; Phylogeny; Sequence Analysis, DNA; Young Adult	2014
Translational genomics. Clues from the resilient. Science (New York, N.Y.), 2014, May-30, Volume: 344, Issue:6187 Topics: DNA Mutational Analysis; Genetic Association Studies; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Genomics; Health; Humans; Molecular Targeted Therapy; Mutation	2014
Interaction of the 5-HTTLPR and childhood trauma influences memory bias in healthy individuals. Journal of affective disorders, 2015, Nov-01, Volume: 186 Topics: Adult Survivors of Child Adverse Events; Alleles; Depression; Female; Genetic Predisposition to Disease; Genotype; Health; Humans; Memory; Polymorphism, Genetic; Prejudice; Serotonin Plasma Membrane Transport Proteins	2015
The UK10K project identifies rare variants in health and disease. Nature, 2015, Oct-01, Volume: 526, Issue:7571 Topics: Adiponectin; Alleles; Cohort Studies; Disease; Exome; Female; Genetic Predisposition to Disease; Genetic Variation; Genetics, Medical; Genetics, Population; Genome-Wide Association Study; Genome, Human; Genomics; Health; Humans; Lipid Metabolism; Male; Molecular Sequence Annotation; Receptors, LDL; Reference Standards; Sequence Analysis, DNA; Triglycerides; United Kingdom	2015
No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171B, Issue:2 Topics: Adult; Asian People; Brain; Female; Genetic Association Studies; Genetic Predisposition to Disease; Health; Humans; Male; Organ Size; Polymorphism, Single Nucleotide; Schizophrenia; Young Adult	2016
Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (N=112 151) and 24 GWAS consortia. Molecular psychiatry, 2016, Volume: 21, Issue:11 Topics: Adult; Aged; Biological Specimen Banks; Cognition; Databases, Factual; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genome-Wide Association Study; Health; Humans; Linkage Disequilibrium; Male; Mental Health; Middle Aged; Multifactorial Inheritance; Polymorphism, Single Nucleotide	2016
Health and genetic ancestry testing: time to bridge the gap. BMC medical genomics, 2017, 01-09, Volume: 10, Issue:1 Topics: Disease; Genetic Predisposition to Disease; Genetic Testing; Health; Humans; Pedigree	2017
Refreshed Strategic Plan for the Canadian Institutes of Health Research Institute of Nutrition, Metabolism and Diabetes. Canadian journal of diabetes, 2017, Volume: 41, Issue:3 Topics: Biomedical Research; Canada; Chronic Disease; Diabetes Mellitus; Environment; Financing, Government; Genetic Predisposition to Disease; Government Agencies; Health; Humans; Nutritional Physiological Phenomena; Nutritional Sciences; Organizational Objectives	2017
Transforming health care through prospective medicine: the first step. Academic medicine : journal of the Association of American Medical Colleges, 2008, Volume: 83, Issue:8 Topics: Delivery of Health Care; Genetic Predisposition to Disease; Health; Humans; Preventive Medicine; United States	2008
Do common genetic variants in endotoxin signaling pathway contribute to predisposition to alcoholic liver cirrhosis? Clinical chemistry and laboratory medicine, 2009, Volume: 47, Issue:4 Topics: Case-Control Studies; Endotoxins; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Health; Humans; Liver Cirrhosis, Alcoholic; Male; Signal Transduction	2009
Type 1 diabetes: evidence of interaction between ACP1 and ADA1 gene polymorphisms. Medical science monitor : international medical journal of experimental and clinical research, 2009, Volume: 15, Issue:10 Topics: Adenosine Deaminase; Alleles; Case-Control Studies; Diabetes Mellitus, Type 1; Genetic Predisposition to Disease; Health; Humans; Infant, Newborn; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatases; Proto-Oncogene Proteins	2009
Familial and racial determinants of tumour suppressor genes promoter hypermethylation in breast tissues from healthy women. Journal of cellular and molecular medicine, 2010, Volume: 14, Issue:6B Topics: Adolescent; Adult; Aged; Black or African American; Breast; Breast Neoplasms; DNA Methylation; Family; Female; Genetic Predisposition to Disease; Health; Humans; Mammaplasty; Middle Aged; Promoter Regions, Genetic; Racial Groups; Risk Factors; Tumor Suppressor Proteins; Young Adult	2010
Are elite endurance athletes genetically predisposed to lower disease risk? Physiological genomics, 2010, Mar-03, Volume: 41, Issue:1 Topics: Adult; Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Health; Humans; Male; Physical Endurance; Quantitative Trait, Heritable; Spain; White People; Young Adult	2010
Catechol-O-methyltransferase modulation of cortisol secretion in psychiatrically at-risk and healthy adolescents. Psychiatric genetics, 2010, Volume: 20, Issue:4 Topics: Adolescent; Catechol O-Methyltransferase; Child; Genetic Predisposition to Disease; Health; Humans; Hydrocortisone; Mental Disorders; Risk Factors; Saliva	2010
The T1405N carbamoyl phosphate synthetase polymorphism does not affect plasma arginine concentrations in preterm infants. PloS one, 2010, May-25, Volume: 5, Issue:5 Topics: Amino Acid Substitution; Arginine; Carbamoyl-Phosphate Synthase (Ammonia); Female; Genetic Predisposition to Disease; Health; Humans; Infant, Newborn; Infant, Premature; Male; Polymorphism, Single Nucleotide; Pregnancy; Premature Birth; Urea	2010
Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study. Clinica chimica acta; international journal of clinical chemistry, 2011, Jan-14, Volume: 412, Issue:1-2 Topics: Aged; Cardiovascular Diseases; Cerebrovascular Disorders; Cohort Studies; Female; Genetic Predisposition to Disease; Genome, Human; Health; Humans; Middle Aged; Polymorphism, Single Nucleotide; Regression Analysis; Telomere	2011
Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Clinica chimica acta; international journal of clinical chemistry, 2011, Apr-11, Volume: 412, Issue:9-10 Topics: Body Mass Index; C-Reactive Protein; Cohort Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genome; Glycated Hemoglobin; Health; Humans; Islet Amyloid Polypeptide; Middle Aged; Polymorphism, Single Nucleotide; Regression Analysis; White People	2011
Genomics. Deflating the genomic bubble. Science (New York, N.Y.), 2011, Feb-18, Volume: 331, Issue:6019 Topics: Genetic Predisposition to Disease; Genetic Research; Genetic Testing; Genetics, Medical; Genomics; Health; Humans; Life Style; Pharmacogenetics; Translational Research, Biomedical	2011
Frequency of uridine monophosphate synthase Gly(213)Ala polymorphism in Caucasian gastrointestinal cancer patients and healthy subjects, investigated by means of new, rapid genotyping assays. Genetic testing and molecular biomarkers, 2011, Volume: 15, Issue:10 Topics: Adult; Aged; Aged, 80 and over; Alanine; Amino Acid Substitution; Carcinoma; Chromatography, High Pressure Liquid; Cost-Benefit Analysis; DNA Mutational Analysis; Female; Gastrointestinal Neoplasms; Gene Frequency; Genetic Predisposition to Disease; Genotyping Techniques; Glycine; Health; Humans; Male; Middle Aged; Multienzyme Complexes; Orotate Phosphoribosyltransferase; Orotidine-5'-Phosphate Decarboxylase; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Reproducibility of Results; White People	2011
Forum on aging and skeletal health: summary of the proceedings of an ASBMR workshop. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2011, Volume: 26, Issue:11 Topics: Aging; Biomedical Research; Bone and Bones; Bone Resorption; Cellular Senescence; Fractures, Bone; Genetic Predisposition to Disease; Health; Humans; Minerals; Motor Activity; Societies, Scientific	2011
Genetic risk score predicting risk of rheumatoid arthritis phenotypes and age of symptom onset. PloS one, 2011, Volume: 6, Issue:9 Topics: Adult; Age of Onset; Alleles; Arthritis, Rheumatoid; Case-Control Studies; Female; Genetic Predisposition to Disease; Health; Humans; Middle Aged; Nurses; Odds Ratio; Phenotype; Risk Factors; ROC Curve; United States	2011
A commentary on implication of gene copy number variation in health and diseases. Journal of human genetics, 2012, Volume: 57, Issue:2 Topics: Disease; DNA Copy Number Variations; Genetic Predisposition to Disease; Genome-Wide Association Study; Genome, Human; Health; Humans; Pharmacogenetics; Polymorphism, Single Nucleotide	2012
The investigation of genetic polymorphisms in the carbonic anhydrase VI gene exon 2 and salivary parameters in type 2 diabetic patients and healthy adults. Molecular biology reports, 2012, Volume: 39, Issue:5 Topics: Adult; Aged; Base Sequence; Blood Glucose; Carbonic Anhydrases; Case-Control Studies; Diabetes Mellitus, Type 2; Exons; Female; Genetic Predisposition to Disease; Genotyping Techniques; Glycated Hemoglobin; Health; Humans; Male; Middle Aged; Molecular Sequence Data; Polymorphism, Single Nucleotide; Saliva; Young Adult	2012
Bipolar disorder ANK3 risk variant effect on sustained attention is replicated in a large healthy population. Psychiatric genetics, 2012, Volume: 22, Issue:4 Topics: Adolescent; Ankyrins; Attention; Bipolar Disorder; Cognition; Genetic Association Studies; Genetic Predisposition to Disease; Genetics, Population; Greece; Health; Humans; Male; Polymorphism, Single Nucleotide; Reproducibility of Results; Young Adult	2012
Common variants in the CRP gene are associated with serum C-reactive protein levels and body mass index in healthy individuals in Mexico. Genetics and molecular research : GMR, 2012, Aug-13, Volume: 11, Issue:3 Topics: Adolescent; Adult; Alleles; Body Mass Index; C-Reactive Protein; Cardiovascular Diseases; Demography; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Haplotypes; Health; Humans; Male; Mexico; Polymorphism, Single Nucleotide; Risk Factors; Young Adult	2012
Effect of DISC1 SNPs on brain structure in healthy controls and patients with a history of psychosis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2012, Volume: 159B, Issue:6 Topics: Adult; Brain; Case-Control Studies; Cerebral Cortex; Female; Genetic Association Studies; Genetic Predisposition to Disease; Health; Humans; Male; Nerve Tissue Proteins; Polymorphism, Single Nucleotide; Psychotic Disorders; Time Factors	2012
Gene polymorphism and protein of human pro- and anti-inflammatory cytokines in Chinese healthy subjects and chronic periodontitis patients. Journal of translational medicine, 2012, Sep-19, Volume: 10 Suppl 1 Topics: Adult; Aged; Anti-Inflammatory Agents; Asian People; Case-Control Studies; China; Chronic Periodontitis; Cytokines; Enzyme-Linked Immunosorbent Assay; Female; Gene Frequency; Genetic Predisposition to Disease; Health; Humans; Inflammation Mediators; Male; Middle Aged; Polymorphism, Genetic	2012
The genetic contribution to disease risk and variability in response to diet: where is the hidden heritability? The Proceedings of the Nutrition Society, 2013, Volume: 72, Issue:1 Topics: Diet; Environment; Genetic Predisposition to Disease; Genetic Variation; Health; Humans; Nutrigenomics; Nutritional Physiological Phenomena; Phenotype; Public Health; Risk Factors	2013
Centenarians: Great expectations. Nature, 2012, Dec-06, Volume: 492, Issue:7427 Topics: Age of Onset; Aged, 80 and over; Aging; Animals; Apolipoprotein C-III; Apolipoprotein E4; Biomedical Research; Cholesterol Ester Transfer Proteins; Forkhead Box Protein O3; Forkhead Transcription Factors; Genetic Predisposition to Disease; Genome-Wide Association Study; Geriatric Assessment; Health; Humans; Lipid Metabolism; Longevity; Middle Aged; Polymorphism, Single Nucleotide; Research Support as Topic	2012
No association of neurotensin receptor 1 (NTR1) gene polymorphisms with either trait or state anxiety in healthy Chinese-Han participants. Psychiatric genetics, 2013, Volume: 23, Issue:2 Topics: Adult; Anxiety; Asian People; Female; Genetic Association Studies; Genetic Predisposition to Disease; Health; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Neurotensin; Young Adult	2013
The Human Genome Project, genetics and health. Community genetics, 2001, Volume: 4, Issue:2 Topics: Environment; Genetic Predisposition to Disease; Genetic Testing; Genetics, Medical; Genotype; Health; Human Genome Project; Humans; Patient Compliance; Phenotype	2001
What is a disease? EMBO reports, 2004, Volume: 5, Issue:7 Topics: Chronic Disease; Clinical Medicine; Deafness; Decision Making; Disabled Persons; Disease; Genetic Predisposition to Disease; Health; Humans; Social Responsibility; Terminology as Topic	2004
Regulating preimplantation genetic diagnosis: the pathologization problem. Harvard law review, 2005, Volume: 118, Issue:8 Topics: Congenital Abnormalities; Disabled Persons; Fertilization in Vitro; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Genetic Testing; Government Regulation; Health; Humans; Preimplantation Diagnosis; Sex Preselection; Sexual Behavior; Social Values; United States	2005
The human significance of the genome project. Midwest medical ethics : a publication of the Midwest Bioethics Center, 1992,Summer, Volume: 8, Issue:1 Topics: Employment; Family; Genetic Determinism; Genetic Engineering; Genetic Predisposition to Disease; Genetic Privacy; Genetic Testing; Health; Human Genome Project; Humans; Insurance, Health; Metaphor; Prejudice; Prenatal Diagnosis	1992
Introduction: genetic variation and human health. Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2005, Aug-29, Volume: 360, Issue:1460 Topics: Genetic Predisposition to Disease; Genetic Variation; Genetics, Medical; Health; Humans	2005
Genetic influences on health: does race matter? JAMA, 2005, Aug-24, Volume: 294, Issue:8 Topics: Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genetics, Population; Health; Humans; Polymorphism, Genetic; Racial Groups; Risk Factors	2005
Genetic polymorphism of cholesterol 7alpha-hydroxylase (CYP7A1) and colorectal adenomas: Self Defense Forces Health Study. Cancer science, 2006, Volume: 97, Issue:5 Topics: Adenoma; Alcohol Drinking; Bile Acids and Salts; Case-Control Studies; Cholesterol 7-alpha-Hydroxylase; Colonoscopy; Colorectal Neoplasms; Genetic Predisposition to Disease; Genotype; Health; Humans; Male; Middle Aged; Polymorphism, Genetic; Smoking	2006
Sex and age specificity of susceptibility genes modulating survival at old age. Human heredity, 2006, Volume: 62, Issue:4 Topics: Adolescent; Adult; Age Distribution; Aged; Aged, 80 and over; Aging; Female; Genetic Predisposition to Disease; Health; Humans; Logistic Models; Longevity; Male; Middle Aged; Sex Characteristics	2006
Genetic predisposition and health effect of occupational exposure to asbestos. Neuro endocrinology letters, 2006, Volume: 27 Suppl 2 Topics: Asbestos; Asbestosis; Epoxide Hydrolases; Gene Frequency; Genetic Predisposition to Disease; Glutathione S-Transferase pi; Glutathione Transferase; Health; Humans; Micronuclei, Chromosome-Defective; Occupational Diseases; Occupational Exposure; Polymorphism, Genetic	2006
Associations between HLA class I alleles and the prevalence of nasopharyngeal carcinoma (NPC) among Tunisians. Journal of translational medicine, 2007, May-04, Volume: 5 Topics: Adult; Age Distribution; Alleles; Black People; Case-Control Studies; Gene Frequency; Genetic Loci; Genetic Predisposition to Disease; Haplotypes; Health; Histocompatibility Antigens Class I; HLA-A Antigens; HLA-B Antigens; HLA-C Antigens; Humans; Nasopharyngeal Neoplasms; Prevalence; Tunisia	2007
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura. Blood, 2008, Feb-01, Volume: 111, Issue:3 Topics: Animals; Antibodies; Antigens, CD; Cells, Cultured; Genetic Predisposition to Disease; Genotype; Haplotypes; Health; Humans; Killer Cells, Natural; Lymphocyte Activation; Mice; Multigene Family; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Purpura, Thrombocytopenic, Idiopathic; Receptors, IgG	2008
NAT2 and NER genetic variants and sporadic prostate cancer susceptibility in African Americans. Prostate cancer and prostatic diseases, 2008, Volume: 11, Issue:4 Topics: Adult; Aged; Aged, 80 and over; Alleles; Arylamine N-Acetyltransferase; Black or African American; Genetic Markers; Genetic Predisposition to Disease; Genotype; Health; Humans; Liver X Receptors; Male; Middle Aged; Orphan Nuclear Receptors; Polymorphism, Single Nucleotide; Prostatic Neoplasms; Receptors, Cytoplasmic and Nuclear	2008
A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions. American journal of human genetics, 2008, Volume: 82, Issue:3 Topics: Commerce; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Genome, Human; Genomics; Health; Humans; Polymorphism, Genetic; Risk Factors	2008
How heritable is individual susceptibility to death? The results of an analysis of survival data on Danish, Swedish and Finnish twins. Twin research : the official journal of the International Society for Twin Studies, 1998, Volume: 1, Issue:4 Topics: Adult; Age Factors; Aged; Aged, 80 and over; Death; Denmark; Disease Susceptibility; Environment; Female; Finland; Forecasting; Genetic Predisposition to Disease; Health; Humans; Life Tables; Likelihood Functions; Longevity; Male; Middle Aged; Models, Genetic; Molecular Epidemiology; Sex Factors; Survival Analysis; Sweden; Twins	1998
[Why does illness exist? An evolutionary perspective. I: Health and illness in a wider biological context]. Lakartidningen, 1999, Oct-27, Volume: 96, Issue:43 Topics: Biological Evolution; Disease; Environmental Exposure; Genetic Predisposition to Disease; Genome, Human; Health; Humans; Models, Biological; Models, Theoretical	1999
Web alert. Genetics of disease. Current opinion in genetics & development, 2001, Volume: 11, Issue:3 Topics: Databases, Factual; Disease; Genetic Predisposition to Disease; Health; Humans; Internet; Oligonucleotide Array Sequence Analysis	2001
From the editors. Bioethics, 1993, Volume: 7, Issue:5 Topics: Abortion, Eugenic; Disease; Genetic Diseases, Inborn; Genetic Engineering; Genetic Predisposition to Disease; Genetics; Genetics, Behavioral; Health; Homosexuality; Humans; Morals; Prejudice; Prenatal Diagnosis; Sexuality; Social Problems	1993
Illness and treatment: meaning for purposes of insurance contract: Katskee v. Blue Cross/Blue Shield. Medical law review, 1995,Summer, Volume: 3, Issue:2 Topics: Breast Neoplasms; Contracts; Disease; General Surgery; Genetic Counseling; Genetic Predisposition to Disease; Health; Humans; Insurance, Health, Reimbursement; Jurisprudence; Nebraska; Neoplasms; Preventive Medicine; Terminology as Topic; United Kingdom	1995
Predictive genetics and the construction of the healthy ill. Suffolk University law review, 1993,Winter, Volume: 27, Issue:4 Topics: Abortion, Eugenic; Decision Making; Delivery of Health Care; Diagnosis; Disabled Persons; Disease; Family; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Genetic Testing; Genetics; Health; Humans; Industry; Mass Screening; Parents; Prejudice; Prenatal Diagnosis; Socioeconomic Factors	1993
Engineering perfect offspring: devaluing children and childhood. Hastings constitutional law quarterly, 1997,Summer, Volume: 24, Issue:4 Topics: Adult; Child; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Decision Making; Dehumanization; Dependency, Psychological; Disabled Persons; Down Syndrome; Eugenics; Euthanasia, Passive; Freedom; General Surgery; Genetic Counseling; Genetic Determinism; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Genetic Research; Genetic Therapy; Genetics; Genetics, Behavioral; Health; Health Care Rationing; Humans; Hyperkinesis; Individuality; Infant, Newborn; Jurisprudence; Life Support Care; Mental Disorders; Parents; Personal Autonomy; Personhood; Physicians; Prejudice; Prognosis; Quality of Life; Resource Allocation; Social Desirability; Social Values; Terminally Ill; Twins; Twins, Conjoined; United States; Value of Life; Withholding Treatment	1997
Health law in the twenty-first century. European journal of health law, 1998, Volume: 5, Issue:4 Topics: Bioethical Issues; Bioethics; Biomedical Technology; Civil Rights; Coercion; Computer Communication Networks; Delivery of Health Care; Developing Countries; Economics; Euthanasia; Euthanasia, Active, Voluntary; Evidence-Based Medicine; Genetic Predisposition to Disease; Genetic Privacy; Genetic Therapy; Germ Cells; Health; Health Promotion; History, 21st Century; Human Rights; Humans; International Cooperation; Internationality; Jurisprudence; Medicine; Pedigree; Persons; Physician-Patient Relations; Prejudice; Preventive Medicine; Privacy; Public Health; Social Change; Social Justice; Social Values; Stress, Psychological; Suicide, Assisted; Vulnerable Populations	1998
The social construction of genetic abnormality: ethical implications for managerial decisions in the workplace. Journal of business ethics : JBE, 1994, Volume: 13, Issue:11 Topics: Administrative Personnel; Decision Making; Economics; Employment; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Genetic Testing; Hazardous Substances; Health; Humans; Industry; Insurance, Health; Liability, Legal; Occupational Exposure; Organizational Policy; Prejudice; Public Policy; Reference Standards; Social Justice; Social Values; Stereotyping; United States	1994
Negative eugenics and ethical decisions. The Journal of medical humanities, 1996,Spring, Volume: 17, Issue:1 Topics: Abortion, Eugenic; Biological Evolution; Child; Ethics; Eugenics; Freedom; Gene Pool; Genetic Counseling; Genetic Diseases, Inborn; Genetic Engineering; Genetic Enhancement; Genetic Predisposition to Disease; Genetic Therapy; Health; Health Care Rationing; Humans; Moral Obligations; Parents; Personal Autonomy; Prenatal Diagnosis; Public Policy; Quality of Life; Reference Standards; Reproduction; Resource Allocation; Social Responsibility	1996
Genetic selection of offspring characteristics. Boston University law review. Boston University. School of Law, 1996, Volume: 76, Issue:3 Topics: Abortion, Eugenic; Age of Onset; Child; Cloning, Organism; Disabled Persons; Embryo Disposition; Embryo, Mammalian; Ethics; Eugenics; Family Relations; Female; Fetal Diseases; Fetus; Freedom; Genetic Counseling; Genetic Diseases, Inborn; Genetic Engineering; Genetic Enhancement; Genetic Predisposition to Disease; Genetic Privacy; Genetic Testing; Genetic Therapy; Germ Cells; Government Regulation; Health; Heterozygote; Human Genome Project; Human Rights; Humans; Jurisprudence; Mass Screening; Pedigree; Personal Autonomy; Preimplantation Diagnosis; Prejudice; Prenatal Diagnosis; Public Policy; Reproduction; Reproductive Techniques, Assisted; Sex Determination Analysis; Sex Preselection; Social Change; Social Control, Formal; Women; Women's Rights; Wounds and Injuries; Wrongful Life	1996
Nutrition and fitness: Diet, genes, physical activity and health. Proceedings of the 4th International Conference on Nutrition and Fitness. Athens, Greece, May 25-29, 2000. World review of nutrition and dietetics, 2001, Volume: 89 Topics: Diet; Exercise; Genetic Predisposition to Disease; Health; Health Status; Humans; Nutritional Physiological Phenomena	2001