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The International HapMap Project
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The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with ancestry from parts of Africa, Asia and Europe. The HapMap will allow the discovery of sequence variants that affect common disease, will facilitate development of diagnostic tools, and will enhance our ability to choose targets for therapeutic intervention.
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“Increasing availability of reference datasets cataloguing population genetic variation across diverse ethnic backgrounds has supported robust causal inference2,3,5,6.”
From A brief history of human disease genetics (2020) · cites this paper as [2]
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“Systematic efforts to characterize genome-wide patterns of genomic variation, initially through the HapMap Consortium2, proved catalytic, demonstrating that the allelic structure of the genome was segmented into haplotype blocks, each containing sets of correlated variants.”
From A brief history of human disease genetics (2020) · cites this paper as [2]
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“For the common variants that underlie the bulk of complex-disease risk, the resolution of association mapping is often limited by the haplotype structure of the human genome2–4.”
From A brief history of human disease genetics (2020) · cites this paper as [2]
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Cites
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
Self-citationThe sequence of the human genome
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909
Self-citationdbSNP: the NCBI database of genetic variation
Sherry, S. T. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.1.308 · Cited by 7,502
Self-citationThe Structure of Haplotype Blocks in the Human Genome
Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., et al. (2002) · Science · doi:10.1126/science.1069424 · Cited by 5,863
Self-citationAssociation of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591
The Future of Genetic Studies of Complex Human Diseases
Risch, N., & Merikangas, K. (1996) · Science · doi:10.1126/science.273.5281.1516 · Cited by 5,355
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030
Identification of the Cystic Fibrosis Gene: Genetic Analysis
Kerem, B.-S., Rommens, J. M., Buchanan, J. A., Markiewicz, D., Cox, T. K., Chakravarti, A., Buchwald, M., & Tsui, L.-C. (1989) · Science · doi:10.1126/science.2570460 · Cited by 4,142
Self-citationThe History and Geography of Human Genes
Cavalli-Sforza, L. L., Menozzi, P., & Piazza, A. (2018) · Princeton University Press eBooks · doi:10.2307/j.ctv301gjp · Cited by 3,175
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
The International SNP Map Working Group, Laboratories:, C. S. H., Sachidanandam, R., Weissman, D., Schmidt, S. C., Kakol, J. M., Stein, L. D., National Center for Biotechnology Information:, Marth, G., Sherry, S., et al. (2001) · Nature · doi:10.1038/35057149 · Cited by 2,977
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Signorello, L. B., Shi, J., Cai, Q., Zheng, W., Williams, S. M., Long, J., Cohen, S. S., Li, G., Hollis, B. W., Smith, J. R., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028623 · Cited by 118
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Hertz, D. L., Roy, S., Motsinger‐Reif, A. A., Drobish, A. A., Clark, L. S., McLeod, H. L., Carey, L., & Dees, E. C. (2013) · Annals of Oncology · doi:10.1093/annonc/mdt018 · Cited by 116
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Florez, J. C. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-1345 · Cited by 118
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Ma, B., Wilker, E. H., Willis‐Owen, S. A. G., Byun, H., Wong, K., Motta, V., Baccarelli, A., Schwartz, J. D., Cookson, W., Khabbaz, K. R., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1380 · Cited by 116
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Mitchell, K. J. (2012) · Genome biology · doi:10.1186/gb-2012-13-1-237 · Cited by 126
He, M., Xu, M., Zhang, B., Liang, J., Chen, P., Lee, J.-Y., Johnson, T. A., Li, H., Yang, X., Dai, J., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddu583 · Cited by 106
Self-citationVelmurugan, S., Kapil, V., Ghosh, S. M., Davies, S., McKnight, A., Aboud, Z., Khambata, R. S., Webb, A. J., Poole, A., & Ahluwalia, A. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.06.031 · Cited by 114
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Flister, M. J., Tsaih, S., O'Meara, C. C., Endres, B. T., Hoffman, M. J., Geurts, A. M., Dwinell, M. R., Lazar, J., Jacob, H. J., & Moreno, C. (2013) · Genome Research · doi:10.1101/gr.160283.113 · Cited by 116
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Bogaert, A. V. D., Sleegers, K., Zutter, S. D., Heyrman, L., Norrback, K., Adolfsson, R., Broeckhoven, C. V., & Del‐Favero, J. (2006) · Archives of General Psychiatry · doi:10.1001/archpsyc.63.10.1103 · Cited by 114
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Metadata
- Authors
- †The International HapMap Consortium, Genotyping centres: Baylor College of Medicine and ParAllele BioScience, Gibbs, R. A., Belmont, J. W., Hardenbol, P., Willis, T. D., Yu, F., Chinese HapMap Consortium, Yang, H., Ch'ang, L.-Y., Huang, W., Liu, B., Shen, Y., Tam, P. K.-H., Tsui, L.-C., Waye, M. M. Y., Wong, J. T.-F., Zeng, C., Zhang, Q., Illumina, Chee, M. S., Galver, L. M., Kruglyak, S., Murray, S. S., Oliphant, A. R., McGill University and Génome Québec Innovation Centre, Montpetit, A., Hudson, T. J., Chagnon, F., Ferretti, V., Leboeuf, M., Phillips, M. S., Verner, A., University of California at San Francisco and Washington University, Kwok, P.-Y., Duan, S., Lind, D. L., Miller, R. D., Rice, J. P., Saccone, N. L., Taillon-Miller, P., Xiao, M., University of Tokyo and RIKEN, Nakamura, Y., Sekine, A., Sorimachi, K., Tanaka, T., Tanaka, Y., Tsunoda, T., Yoshino, E., Wellcome Trust Sanger Institute, Bentley, D. R., Deloukas, P., Hunt, S., Powell, D., Whitehead Institute/MIT Center for Genome Research, Altshuler, D., Gabriel, S. B., Community engagement/public consultation and sample-collection groups: Beijing Normal University and Beijing Genomics Institute, Zhang, H., Zeng, C., Health Sciences University of Hokkaido, E. E. I. A. S. U., Matsuda, I., Fukushima, Y., Macer, D. R., Suda, E., Howard University and University of Ibadan, Rotimi, C. N., Adebamowo, C. A., Aniagwu, T., Marshall, P. A., Matthew, O., Nkwodimmah, C., Royal, C. D. M., University of Utah, Leppert, M. F., Dixon, M., Laboratory, A. G. C. S. H., Stein, L. D., Cunningham, F., Kanani, A., Thorisson, G. A., Johns Hopkins University School of Medicine, Chakravarti, A., Chen, P. E., Cutler, D. J., Kashuk, C. S., University of Oxford, Donnelly, P., Marchini, J., McVean, G. A. T., Myers, S. R., University of Oxford, W. T. C. F. H. G., Cardon, L. R., Abecasis, G. R., Morris, A., Weir, B. S., Health, U. N. I. O., Mullikin, J. C., Sherry, S. T., Feolo, M., Whitehead Institute/MIT Center for Genome Research, Altshuler, D., Daly, M. J., Schaffner, S. F., Ethical, L. A. S. I. C. A. O. S. S., Qiu, R., Genetic Interest Group, Kent, A., Howard University, Dunston, G. M., Kyoto University, Kato, K., Nagasaki University, Niikawa, N., University of Montréal, Knoppers, B. M., University of Oklahoma, Foster, M. W., Vanderbilt University, Clayton, E. W., Wang, V. O., Wellcome Trust, Watkin, J., SNP Discovery: Baylor College of Medicine, Gibbs, R. A., Belmont, J. W., Sodergren, E., Weinstock, G. M., Washington University, Wilson, R. K., Fulton, L. L., Wellcome Trust Sanger Institute, Rogers, J., Whitehead Institute/MIT Center for Genome Research, Birren, B. W., Scientific Management: Chinese Academy of Sciences, Han, H., Chinese Ministry of Science and Technology, Wang, H., Canada, G., Godbout, M., Wallenburg, J. C., Québec, G., L'Archevêque, P., Bellemare, G., Japanese Ministry of Education, C., Todani, K., Fujita, T., Tanaka, S., The SNP Consortium, Holden, A. L., Lai, E. H., Health, U. N. I. O., Collins, F. S., Brooks, L. D., McEwen, J. E., Guyer, M. S., Jordan, E., Peterson, J. L., Spiegel, J., Sung, L. M., Zacharia, L. F., Wellcome Trust, Kennedy, K., Dunn, M. G., Seabrook, R., Shillito, M., Skene, B., Stewart, J. G., Initial Planning Groups: Populations and Ethical, L. A. S. I. G., Valle, D. L., Clayton, E. W., Jorde, L. B., Belmont, J. W., Chakravarti, A., Cho, M. K., Duster, T., Foster, M. W., Jasperse, M., Knoppers, B. M., Kwok, P.-Y., Licinio, J., Long, J. C., Marshall, P. A., Ossorio, P. N., Wang, V. O., Rotimi, C. N., Royal, C. D. M., Spallone, P., Terry, S. F., Methods Group, Lander, E. S., Lai, E. H., Nickerson, D. A., Abecasis, G. R., Altshuler, D., Bentley, D. R., Boehnke, M., Cardon, L. R., Daly, M. J., Deloukas, P., Douglas, J. A., Gabriel, S. B., Hudson, R. R., Hudson, T. J., Kruglyak, L., Kwok, P.-Y., Nakamura, Y., Nussbaum, R. L., Royal, C. D. M., Schaffner, S. F., Sherry, S. T., Stein, L. D., & Tanaka, T.
- Affiliations
- Baylor College of Medicine (US)
- Chinese Academy of Sciences (CN)
- Institute of Biomedical Sciences, Academia Sinica (TW)
- Chinese National Human Genome Center (CN)
- University of Hong Kong (HK)
- Chinese University of Hong Kong (HK)
- Illumina (United States) (US)
- McGill University and Génome Québec Innovation Centre (CA)
- Washington University in St. Louis (US)
- University of California, San Francisco (US)
- RIKEN (JP)
- Health Sciences University of Hokkaido (JP)
- Shinshu University (JP)
- Howard University (US)
- University of Ibadan (NG)
- University of Tsukuba (JP)
- Johns Hopkins University (US)
- University of Utah (US)
- Cold Spring Harbor Laboratory (US)
- North Carolina State University (US)
- Chinese Academy of Social Sciences (CN)
- Kyoto University (JP)
- University of Oxford (GB)
- Centre for Human Genetics (GB)
- National Institutes of Health (US)
- Genetic Alliance UK (United Kingdom) (GB)
- Nagasaki University (JP)
- Wellcome Trust (GB)
- University of Maryland, Baltimore (US)
- Wellcome Sanger Institute (GB)
- Massachusetts Institute of Technology (US)
- Vanderbilt University (US)
- Stanford University (US)
- Génome Québec (CA)
- University of New Mexico (US)
- Ministry of Education, Culture, Sports, Science and Technology (JP)
- University of Michigan (US)
- Foundation for the National Institutes of Health (US)
- University of Chicago (US)
- McGill University (CA)
- Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA)
- The University of Tokyo (JP)
- New York University (US)
- University of New Mexico Health Sciences Center (US)
- University of Wisconsin–Madison (US)
- Genetic Alliance (US)
- Fred Hutch Cancer Center (US)
- ORCID
- Yang, Huanming
- Huang, Wei
- Liu, Bin
- Tam, Paul Kwong-Hang
- Waye, Mary Miu Yee
- Wong, Jeffrey Tze-Fei
- Zhang, Qingrun
- Kruglyak, Semyon
- Murray, Sarah S.
- Ferretti, Vincent
- Duan, Shenghui
- Rice, John P.
- Saccone, Nancy L.
- Xiao, Ming
- Sekine, Akihiro
- Tsunoda, Tatsuhiko
- Hunt, Sarah
- Matsuda, Ichiro
- Fukushima, Yoshimitsu
- Macer, Darryl R.
- Adebamowo, Clement A.
- Aniagwu, Toyin
- Cunningham, Fiona
- Chen, Peter E.
- Cutler, David J.
- Donnelly, Peter
- Marchini, Jonathan
- Myers, Simon R.
- Morris, Andrew
- Weir, Bruce S.
- Mullikin, James C.
- Feolo, Michael
- Kent, Alastair
- Sodergren, Erica
- Weinstock, George M.
- Fulton, Lucinda L.
- Birren, Bruce W.
- Han, Hua
- Wang, Hongguang
- Tanaka, Satoshi
- Collins, Francis S.
- Dunn, Michael G.
- Valle, David L.
- Jorde, Lynn B.
- Cho, Mildred K.
- Duster, Troy
- Long, Jeffrey C.
- Ossorio, Pilar N.
- Terry, Sharon F.
- Lander, Eric S.
- Nickerson, Deborah A.
- Boehnke, Michael
- Douglas, Julie A.
- Kruglyak, Leonid
- Nussbaum, Robert L.
- Venue
- Nature
- Published
- 2003-12-18
- Volume
- 426
- Issue
- 6968
- Pages
- 789-796
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2058401000
- Cited by
- 6,057
- References
- 73
- Citations by year
- 2026: 43 · 2025: 117 · 2024: 143 · 2023: 141 · 2022: 163 · 2021: 166 · 2020: 161 · 2019: 199 · 2018: 179 · 2017: 247 · 2016: 293 · 2015: 320 · 2014: 347 · 2013: 336 · 2012: 378
- FWCI
- 134.60
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Nature (publishedVersion, public-domain)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Deep Blue (University of Michigan) (submittedVersion, public-domain)
- The HKU Scholars Hub (University of Hong Kong) (submittedVersion, public-domain)
- Rare & Special e-Zone (The Hong Kong University of Science and Technology) (submittedVersion)
- DigitalGeorgetown (Georgetown University Library) (submittedVersion)
- Funders
- W. M. Keck Foundation
- McGill University
- Genome Canada
- Wellcome Trust
- Ministry of Education, Culture, Sports, Science and Technology
- National Natural Science Foundation of China
- University Grants Committee
- Chinese Academy of Sciences
- Beijing Normal University
- Ministry of Science and Technology of the People's Republic of China
- Innovation and Technology Commission
- National Institutes of Health
- National Institute on Alcohol Abuse and Alcoholism
- National Institute on Aging
- National Institute of Mental Health
- National Institute on Drug Abuse
- National Human Genome Research Institute
- National Eye Institute
- National Cancer Institute
- National Institute on Deafness and Other Communication Disorders
- National Institute of General Medical Sciences
- National Institute of Allergy and Infectious Diseases
- National Institute of Diabetes and Digestive and Kidney Diseases
- National Institute of Neurological Disorders and Stroke
- National Institute of Environmental Health Sciences
- National Institute of Arthritis and Musculoskeletal and Skin Diseases
- National Institute of Biomedical Imaging and Bioengineering
- National Institute of Dental and Craniofacial Research
- National Center for Research Resources
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Forensic and Genetic Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Keywords
- HapMap, human genome, DNA sequence variation, single nucleotide polymorphisms, genotype frequency, population genetic variation, common diseases, genetic association, diagnostic tools, therapeutic target
- MeSH terms
- Base Sequence, DNA, Gene Frequency, Haplotypes, Humans, International Cooperation, Genetic Variation, Genome, Human, Public Sector, Polymorphism, Single Nucleotide, Genomics, Racial Groups
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