The International HapMap Project
†The International HapMap Consortium, Genotyping centres: Baylor College of Medicine and ParAllele BioScience, Gibbs, Richard A., Belmont, John W., Hardenbol, Paul, Willis, Thomas D., Yu, Fuli, Chinese HapMap Consortium, Yang, Huanming, Ch'ang, Lan-Yang, Huang, Wei, Liu, Bin, Shen, Yan, Tam, Paul Kwong-Hang, Tsui, Lap-Chee, Waye, Mary Miu Yee, Wong, Jeffrey Tze-Fei, Zeng, Changqing, Zhang, Qingrun, Illumina, Chee, Mark S., Galver, Luana M., Kruglyak, Semyon, Murray, Sarah S., Oliphant, Arnold R., McGill University and Génome Québec Innovation Centre, Montpetit, Alexandre, Hudson, Thomas J., Chagnon, Fanny, Ferretti, Vincent, Leboeuf, Martin, Phillips, Michael S., Verner, Andrei, University of California at San Francisco and Washington University, Kwok, Pui-Yan, Duan, Shenghui, Lind, Denise L., Miller, Raymond D., Rice, John P., Saccone, Nancy L., Taillon-Miller, Patricia, Xiao, Ming, University of Tokyo and RIKEN, Nakamura, Yusuke, Sekine, Akihiro, Sorimachi, Koki, Tanaka, Toshihiro, Tanaka, Yoichi, Tsunoda, Tatsuhiko, Yoshino, Eiji, Wellcome Trust Sanger Institute, Bentley, David R., Deloukas, Panos, Hunt, Sarah, Powell, Don, Whitehead Institute/MIT Center for Genome Research, Altshuler, David, Gabriel, Stacey B., Community engagement/public consultation and sample-collection groups: Beijing Normal University and Beijing Genomics Institute, Zhang, Houcan, Zeng, Changqing, Health Sciences University of Hokkaido, Eubios Ethics Institute and Shinshu University, Matsuda, Ichiro, Fukushima, Yoshimitsu, Macer, Darryl R., Suda, Eiko, Howard University and University of Ibadan, Rotimi, Charles N., Adebamowo, Clement A., Aniagwu, Toyin, Marshall, Patricia A., Matthew, Olayemi, Nkwodimmah, Chibuzor, Royal, Charmaine D. M., University of Utah, Leppert, Mark F., Dixon, Missy, Analysis Groups: Cold Spring Harbor Laboratory, Stein, Lincoln D., Cunningham, Fiona, Kanani, Ardavan, Thorisson, Gudmundur A., Johns Hopkins University School of Medicine, Chakravarti, Aravinda, Chen, Peter E., Cutler, David J., Kashuk, Carl S., University of Oxford, Donnelly, Peter, Marchini, Jonathan, McVean, Gilean A. T., Myers, Simon R., University of Oxford, Wellcome Trust Centre for Human Genetics, Cardon, Lon R., Abecasis, Gonçalo R., Morris, Andrew, Weir, Bruce S., US National Institutes of Health, Mullikin, James C., Sherry, Stephen T., Feolo, Michael, Whitehead Institute/MIT Center for Genome Research, Altshuler, David, Daly, Mark J., Schaffner, Stephen F., Ethical, Legal and Social Issues: Chinese Academy of Social Sciences, Qiu, Renzong, Genetic Interest Group, Kent, Alastair, Howard University, Dunston, Georgia M., Kyoto University, Kato, Kazuto, Nagasaki University, Niikawa, Norio, University of Montréal, Knoppers, Bartha M., University of Oklahoma, Foster, Morris W., Vanderbilt University, Clayton, Ellen Wright, Wang, Vivian Ota, Wellcome Trust, Watkin, Jessica, SNP Discovery: Baylor College of Medicine, Gibbs, Richard A., Belmont, John W., Sodergren, Erica, Weinstock, George M., Washington University, Wilson, Richard K., Fulton, Lucinda L., Wellcome Trust Sanger Institute, Rogers, Jane, Whitehead Institute/MIT Center for Genome Research, Birren, Bruce W., Scientific Management: Chinese Academy of Sciences, Han, Hua, Chinese Ministry of Science and Technology, Wang, Hongguang, Genome Canada, Godbout, Martin, Wallenburg, John C., Génome Québec, L'Archevêque, Paul, Bellemare, Guy, Japanese Ministry of Education, Culture, Sports, Science and Technology, Todani, Kazuo, Fujita, Takashi, Tanaka, Satoshi, The SNP Consortium, Holden, Arthur L., Lai, Eric H., US National Institutes of Health, Collins, Francis S., Brooks, Lisa D., McEwen, Jean E., Guyer, Mark S., Jordan, Elke, Peterson, Jane L., Spiegel, Jack, Sung, Lawrence M., Zacharia, Lynn F., Wellcome Trust, Kennedy, Karen, Dunn, Michael G., Seabrook, Richard, Shillito, Mark, Skene, Barbara, Stewart, John G., Initial Planning Groups: Populations and Ethical, Legal and Social Issues Group, Valle, David L., Clayton, Ellen Wright, Jorde, Lynn B., Belmont, John W., Chakravarti, Aravinda, Cho, Mildred K., Duster, Troy, Foster, Morris W., Jasperse, Marla, Knoppers, Bartha M., Kwok, Pui-Yan, Licinio, Julio, Long, Jeffrey C., Marshall, Patricia A., Ossorio, Pilar N., Wang, Vivian Ota, Rotimi, Charles N., Royal, Charmaine D. M., Spallone, Patricia, Terry, Sharon F., Methods Group, Lander, Eric S., Lai, Eric H., Nickerson, Deborah A., Abecasis, Gonçalo R., Altshuler, David, Bentley, David R., Boehnke, Michael, Cardon, Lon R., Daly, Mark J., Deloukas, Panos, Douglas, Julie A., Gabriel, Stacey B., Hudson, Richard R., Hudson, Thomas J., Kruglyak, Leonid, Kwok, Pui-Yan, Nakamura, Yusuke, Nussbaum, Robert L., Royal, Charmaine D. M., Schaffner, Stephen F., Sherry, Stephen T., Stein, Lincoln D., Tanaka, Toshihiro·2003·Nature
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- Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseasesNERI, M, UGOLINI, D, DIANZANI, I, GEMIGNANI, F, LANDI, S, CESARIO, A, MAGNANI, C, MUTTI, L, PUNTONI, R, BONASSI, S · 2008 · Mutation Research/Reviews in Mutation Research
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- Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab CommunityMeng, Yan, Baldwin, Clinton T., Bowirrat, Abdalla, Waraska, Kristin, Inzelberg, Rivka, Friedland, Robert P., Farrer, Lindsay A. · 2006 · The American Journal of Human Genetics
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- Conserved rules govern genetic interaction degree across speciesKoch, Elizabeth N, Costanzo, Michael, Bellay, Jeremy, Deshpande, Raamesh, Chatfield-Reed, Kate, Chua, Gordon, D'Urso, Gennaro, Andrews, Brenda J, Boone, Charles, Myers, Chad L · 2012 · Genome Biology
- Genome-wide association studies and the genetic dissection of complex traitsSebastiani, Paola, Timofeev, Nadia, Dworkis, Daniel A., Perls, Thomas T., Steinberg, Martin H. · 2009 · American Journal of Hematology
- Two Human MYD88 Variants, S34Y and R98C, Interfere with MyD88-IRAK4-Myddosome AssemblyGeorge, Julie, Motshwene, Precious G., Wang, Hui, Kubarenko, Andriy V., Rautanen, Anna, Mills, Tara C., Hill, Adrian V.S., Gay, Nicholas J., Weber, Alexander N.R. · 2011 · Journal of Biological Chemistry
- IL-1 receptor antagonist gene as a predictive biomarker of progression of knee osteoarthritis in a population cohortWu, X., Kondragunta, V., Kornman, K.S., Wang, H.Y., Duff, G.W., Renner, J.B., Jordan, J.M. · 2013 · Osteoarthritis and Cartilage
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- Exercise genomics—a paradigm shift is needed: a commentaryBouchard, Claude · 2015 · British Journal of Sports Medicine
- Polymorphism in THBS1 gene is associated with post-refractive surgery chronic ocular surface inflammationContreras-Ruiz, Laura, Ryan, Denise S., Sia, Rose K., Bower, Kraig S., Dartt, Darlene A., Masli, Sharmila · 2014 · Ophthalmology
- Autism: the quest for the genesSykes, Nuala H., Lamb, Janine A. · 2007 · Expert Reviews in Molecular Medicine
- Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomizationGage, Suzanne H., Jones, Hannah J., Taylor, Amy E., Burgess, Stephen, Zammit, Stanley, Munafò, Marcus R. · 2017 · Scientific Reports
- Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese populationDong, Ming, Li, Jinxin, Tang, Ruqi, Zhu, Ping, Qiu, Fang, Wang, Chan, Qiu, Jie, Wang, Lan, Dai, Yaping, Xu, Ping et al. · 2015 · Clinical Reviews in Allergy & Immunology
- Gene‐Trait Similarity Regression for Multimarker‐Based Association AnalysisTzeng, Jung‐Ying, Zhang, Daowen, Chang, Sheng‐Mao, Thomas, Duncan C., Davidian, Marie · 2009 · Biometrics
- Variants in striatin gene are associated with salt-sensitive blood pressure in mice and humansGarza, Amanda E., Rariy, Chevon M., Sun, Bei, Williams, Jonathan S., Lasky-Su, Jessica, Baudrand, Rene, Yao, Tham, Moize, Burhanuddin, Hafiz, Wan M., Romero, Jose R. et al. · 2015 · Hypertension
- Vascular Endothelial Growth Factor Gene Variation and the Response to Photodynamic Therapy in Age-Related Macular DegenerationImmonen, Ilkka, Seitsonen, Sanna, Tommila, Petri, Kangas-Kontio, Tiia, Kakko, Sakari, Savolainen, Eeva-Riitta, Savolainen, Markku J., Liinamaa, M. Johanna · 2010 · Ophthalmology
- Additive effects of oxytocin receptor gene polymorphisms on reward circuitry in youth with autismHernandez, L M, Krasileva, K, Green, S A, Sherman, L E, Ponting, C, McCarron, R, Lowe, J K, Geschwind, D H, Bookheimer, S Y, Dapretto, M · 2017 · Molecular Psychiatry
- Genetics of Polycystic Ovary SyndromeWelt, Corrine K. · 2021 · Endocrinology and Metabolism Clinics of North America
- Linking the genetic architecture of cytosine modifications with human complex traitsZhang, Xu, Moen, Erika L., Liu, Cong, Mu, Wenbo, Gamazon, Eric R., Delaney, Shannon M., Wing, Claudia, Godley, Lucy A., Dolan, M. Eileen, Zhang, Wei · 2014 · Human Molecular Genetics
- Polymorphisms in the GAD2 gene‐region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disordersUnschuld, Paul G., Ising, Marcus, Specht, Michael, Erhardt, Angelika, Ripke, Stephan, Heck, Angela, Kloiber, Stefan, Straub, Verica, Brueckl, Tanja, Müller‐Myhsok, Bertram et al. · 2009 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolateHerzberg, Ibi, Valencia-Duarte, Ana Victoria, Kay, Victoria A., White, Daniel J., Müller, Heike, Rivas, Isabel C., Mesa, Sandra Catalina, Cuartas, Mauricio, García, Jharley, Bedoya, Gabriel et al. · 2010 · Psychiatric Genetics
- Identification of Quantitative Trait Loci Underlying Proteome Variation in Human Lymphoblastoid CellsGarge, Nikhil, Pan, Huaqin, Rowland, Megan D., Cargile, Benjamin J., Zhang, Xinxin, Cooley, Phillip C., Page, Grier P., Bunger, Maureen K. · 2010 · Molecular & Cellular Proteomics
- Genetic Variation in Sodium-Dependent Vitamin C Transporters SLC23A1 and SLC23A2 and Risk of Advanced Colorectal AdenomaErichsen, Hans Christian, Peters, Ulrike, Eck, Peter, Welch, Robert, Schoen, Robert E., Yeager, Meredith, Levine, Mark, Hayes, Richard B., Chanock, Stephen · 2008 · Nutrition and Cancer
- Genetic variation in ATP5O is associated with skeletal muscle ATP50 mRNA expression and glucose uptake in young twinsRönn, Tina, Poulsen, Pernille, Tuomi, Tiinamaija, Isomaa, Bo, Groop, Leif, Vaag, Allan, Ling, Charlotte · 2009 · PLoS ONE
- Power comparisons between similarity‐based multilocus association methods, logistic regression, and score tests for haplotypesLin, Wan‐Yu, Schaid, Daniel J. · 2009 · Genetic Epidemiology
- A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysisJongjaroenprasert, Wallaya, Phusantisampan, Theerawut, Mahasirimongkol, Surakameth, Mushiroda, Taisei, Hirankarn, Nattiya, Snabboon, Thiti, Chanprasertyotin, Suwannee, Tantiwong, Puntip, Soonthornpun, Supamai, Rattanapichart, Paninee et al. · 2012 · Journal of Human Genetics
- A functional brain-derived neurotrophic factor (BDNF) gene variant increases the risk of moderate-to-severe allergic rhinitisJin, Peng, Andiappan, Anand Kumar, Quek, Jia Min, Lee, Bernett, Au, Bijin, Sio, Yang Yie, Irwanto, Astrid, Schurmann, Claudia, Grabe, Hans Jörgen, Suri, Bani Kaur et al. · 2015 · Journal of Allergy and Clinical Immunology
- Susceptibility effects of GABA receptor subunit alpha-2 (GABRA2) variants and parental monitoring on externalizing behavior trajectories: Risk and protection conveyed by the minor alleleTrucco, Elisa M., Villafuerte, Sandra, Heitzeg, Mary M., Burmeister, Margit, Zucker, Robert A. · 2016 · Development and Psychopathology
- Predicting Cognitive Executive Functioning with Polygenic Risk Scores for Psychiatric DisordersBenca, Chelsie E., Derringer, Jaime L., Corley, Robin P., Young, Susan E., Keller, Matthew C., Hewitt, John K., Friedman, Naomi P. · 2017 · Behavior Genetics
- Rare ABCA7 variants in 2 German families with Alzheimer diseaseMay, Patrick, Pichler, Sabrina, Hartl, Daniela, Bobbili, Dheeraj R., Mayhaus, Manuel, Spaniol, Christian, Kurz, Alexander, Balling, Rudi, Schneider, Jochen G., Riemenschneider, Matthias · 2018 · Neurology Genetics
- Finding Associations in Dense Genetic Maps: A Genetic Algorithm ApproachClark, Taane G., De Iorio, Maria, Griffiths, Robert C., Farrall, Martin · 2005 · Human Heredity
- Functional evaluation of the role of C-type lectin domain family 16A at the chromosome 16p13 locusZouk, H, D'Hennezel, E, Du, X, Ounissi-Benkalha, H, Piccirillo, C A, Polychronakos, C · 2014 · Clinical and Experimental Immunology
- Dietary macronutrients, genetic variation, and progression of coronary atherosclerosis among womenKalantarian, Shadi, Rimm, Eric B., Herrington, David M., Mozaffarian, Dariush · 2014 · American Heart Journal
- Association between oxytocin receptor gene polymorphisms and autistic traits as measured by the Autism‐Spectrum Quotient in a non‐clinical Japanese populationKawamura, Yoshiya, Liu, Xiaoxi, Shimada, Takafumi, Otowa, Takeshi, Kakiuchi, Chihiro, Akiyama, Tsuyoshi, Umekage, Tadashi, Sasaki, Tsukasa · 2011 · Asia-Pacific Psychiatry
- Interpreting noncoding genetic variation in complex traits and human diseaseWard, Lucas D, Kellis, Manolis · 2012 · Nature Biotechnology