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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  2. Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseases
    NERI, 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
  3. Effects of 16 Genetic Variants on Fasting Glucose and Type 2 Diabetes in South Asians: ADCY5 and GLIS3 Variants May Predispose to Type 2 Diabetes
    Rees, Simon D., Hydrie, M. Zafar I., O'Hare, J. Paul, Kumar, Sudhesh, Shera, A. Samad, Basit, Abdul, Barnett, Anthony H., Kelly, M. Ann · 2011 · PLoS ONE
  4. Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab Community
    Meng, Yan, Baldwin, Clinton T., Bowirrat, Abdalla, Waraska, Kristin, Inzelberg, Rivka, Friedland, Robert P., Farrer, Lindsay A. · 2006 · The American Journal of Human Genetics
  5. PBAT: A comprehensive software package for genome-wide association analysis of complex family-based studies.
    Van Steen, Kristel, Lange, Christoph · 2005 · Human Genomics
  6. Conserved rules govern genetic interaction degree across species
    Koch, 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
  7. Genome-wide association studies and the genetic dissection of complex traits
    Sebastiani, Paola, Timofeev, Nadia, Dworkis, Daniel A., Perls, Thomas T., Steinberg, Martin H. · 2009 · American Journal of Hematology
  8. Two Human MYD88 Variants, S34Y and R98C, Interfere with MyD88-IRAK4-Myddosome Assembly
    George, 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
  9. IL-1 receptor antagonist gene as a predictive biomarker of progression of knee osteoarthritis in a population cohort
    Wu, X., Kondragunta, V., Kornman, K.S., Wang, H.Y., Duff, G.W., Renner, J.B., Jordan, J.M. · 2013 · Osteoarthritis and Cartilage
  10. Optimal selection of SNP markers for disease association studies.
    Halldórsson, Bjarni V., Istrail, Sorin, De La Vega, Francisco M. · 2004 · Human Heredity
  11. Exercise genomics—a paradigm shift is needed: a commentary
    Bouchard, Claude · 2015 · British Journal of Sports Medicine
  12. Polymorphism in THBS1 gene is associated with post-refractive surgery chronic ocular surface inflammation
    Contreras-Ruiz, Laura, Ryan, Denise S., Sia, Rose K., Bower, Kraig S., Dartt, Darlene A., Masli, Sharmila · 2014 · Ophthalmology
  13. Autism: the quest for the genes
    Sykes, Nuala H., Lamb, Janine A. · 2007 · Expert Reviews in Molecular Medicine
  14. Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization
    Gage, Suzanne H., Jones, Hannah J., Taylor, Amy E., Burgess, Stephen, Zammit, Stanley, Munafò, Marcus R. · 2017 · Scientific Reports
  15. Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population
    Dong, 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
  16. Gene‐Trait Similarity Regression for Multimarker‐Based Association Analysis
    Tzeng, Jung‐Ying, Zhang, Daowen, Chang, Sheng‐Mao, Thomas, Duncan C., Davidian, Marie · 2009 · Biometrics
  17. Variants in striatin gene are associated with salt-sensitive blood pressure in mice and humans
    Garza, 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
  18. Vascular Endothelial Growth Factor Gene Variation and the Response to Photodynamic Therapy in Age-Related Macular Degeneration
    Immonen, Ilkka, Seitsonen, Sanna, Tommila, Petri, Kangas-Kontio, Tiia, Kakko, Sakari, Savolainen, Eeva-Riitta, Savolainen, Markku J., Liinamaa, M. Johanna · 2010 · Ophthalmology
  19. Additive effects of oxytocin receptor gene polymorphisms on reward circuitry in youth with autism
    Hernandez, 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
  20. Genetics of Polycystic Ovary Syndrome
    Welt, Corrine K. · 2021 · Endocrinology and Metabolism Clinics of North America
  21. Linking the genetic architecture of cytosine modifications with human complex traits
    Zhang, 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
  22. Polymorphisms in the GAD2 gene‐region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders
    Unschuld, 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
  23. Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate
    Herzberg, 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
  24. Identification of Quantitative Trait Loci Underlying Proteome Variation in Human Lymphoblastoid Cells
    Garge, Nikhil, Pan, Huaqin, Rowland, Megan D., Cargile, Benjamin J., Zhang, Xinxin, Cooley, Phillip C., Page, Grier P., Bunger, Maureen K. · 2010 · Molecular & Cellular Proteomics
  25. Genetic Variation in Sodium-Dependent Vitamin C Transporters SLC23A1 and SLC23A2 and Risk of Advanced Colorectal Adenoma
    Erichsen, Hans Christian, Peters, Ulrike, Eck, Peter, Welch, Robert, Schoen, Robert E., Yeager, Meredith, Levine, Mark, Hayes, Richard B., Chanock, Stephen · 2008 · Nutrition and Cancer
  26. Genetic variation in ATP5O is associated with skeletal muscle ATP50 mRNA expression and glucose uptake in young twins
    Rönn, Tina, Poulsen, Pernille, Tuomi, Tiinamaija, Isomaa, Bo, Groop, Leif, Vaag, Allan, Ling, Charlotte · 2009 · PLoS ONE
  27. Power comparisons between similarity‐based multilocus association methods, logistic regression, and score tests for haplotypes
    Lin, Wan‐Yu, Schaid, Daniel J. · 2009 · Genetic Epidemiology
  28. A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis
    Jongjaroenprasert, 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
  29. A functional brain-derived neurotrophic factor (BDNF) gene variant increases the risk of moderate-to-severe allergic rhinitis
    Jin, 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
  30. Susceptibility effects of GABA receptor subunit alpha-2 (GABRA2) variants and parental monitoring on externalizing behavior trajectories: Risk and protection conveyed by the minor allele
    Trucco, Elisa M., Villafuerte, Sandra, Heitzeg, Mary M., Burmeister, Margit, Zucker, Robert A. · 2016 · Development and Psychopathology
  31. Predicting Cognitive Executive Functioning with Polygenic Risk Scores for Psychiatric Disorders
    Benca, Chelsie E., Derringer, Jaime L., Corley, Robin P., Young, Susan E., Keller, Matthew C., Hewitt, John K., Friedman, Naomi P. · 2017 · Behavior Genetics
  32. Rare ABCA7 variants in 2 German families with Alzheimer disease
    May, Patrick, Pichler, Sabrina, Hartl, Daniela, Bobbili, Dheeraj R., Mayhaus, Manuel, Spaniol, Christian, Kurz, Alexander, Balling, Rudi, Schneider, Jochen G., Riemenschneider, Matthias · 2018 · Neurology Genetics
  33. Finding Associations in Dense Genetic Maps: A Genetic Algorithm Approach
    Clark, Taane G., De Iorio, Maria, Griffiths, Robert C., Farrall, Martin · 2005 · Human Heredity
  34. Functional evaluation of the role of C-type lectin domain family 16A at the chromosome 16p13 locus
    Zouk, H, D'Hennezel, E, Du, X, Ounissi-Benkalha, H, Piccirillo, C A, Polychronakos, C · 2014 · Clinical and Experimental Immunology
  35. Dietary macronutrients, genetic variation, and progression of coronary atherosclerosis among women
    Kalantarian, Shadi, Rimm, Eric B., Herrington, David M., Mozaffarian, Dariush · 2014 · American Heart Journal
  36. Association between oxytocin receptor gene polymorphisms and autistic traits as measured by the Autism‐Spectrum Quotient in a non‐clinical Japanese population
    Kawamura, Yoshiya, Liu, Xiaoxi, Shimada, Takafumi, Otowa, Takeshi, Kakiuchi, Chihiro, Akiyama, Tsuyoshi, Umekage, Tadashi, Sasaki, Tsukasa · 2011 · Asia-Pacific Psychiatry
  37. Interpreting noncoding genetic variation in complex traits and human disease
    Ward, Lucas D, Kellis, Manolis · 2012 · Nature Biotechnology