A haplotype map of the human genome.

Keywords

International HapMap Project, Haplotype, Linkage disequilibrium, Haplotype estimation, Genetics

References

• Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot要之助 中西 — 2002
• High-resolution haplotype structure in the human genomeMark J. Daly, John D. Rioux, S. F. Schaffner — 2001
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• Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28Patricia Taillon‐Miller, Irma Bauer-Sardiña, Nancy L. Saccone — 2000
• Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn diseaseJohn D. Rioux, Mark J. Daly, Mark S. Silverberg — 2001
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• A frameshift mutation in NOD2 associated with susceptibility to Crohn's diseaseYasunori Ogura, Denise K. Bonen, Naohiro Inohara — 2001
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• Haplotype block structure and its applications to association studies: power and study designs.Kui Zhang, Peter Calabrese, Magnus Nordborg — 2002
• Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21.Michael Olivier, Valerie I. Bustos, Michelle R. Levy — 2001
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• Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase.Andrew G. Clark, Kenneth M. Weiss, Deborah A. Nickerson — 1998
• The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysisNikolas Maniatis, Andrew Collins, Chun‐Fang Xu — 2002
• Linkage disequilibrium in the human genomeDavid Reich, Michele Cargill, Stacey Bolk — 2001
• Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations.Katrina A.B. Goddard, Penelope J. Hopkins, Jeff Hall — 2000
• Conserved worldwide linkage disequilibrium in the human factor XI gene.Takashi Tarumi, Danko Martincic, James A. Whitlock — 2000
• A map of human genome sequence variation containing 1.42 million single nucleotide polymorphismsThe International SNP Map Working Group, Cold Spring Harbor Laboratories:, Ravi Sachidanandam — 2001
• A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease.Erik G. Puffenberger, Kiminori Hosoda, Sarah S. Washington — 1994

Cited by

• Functional analysis of human enhancers using the zebrafish embryoIrene Miguel Escalada — 2014
• Genetics of Multiple SclerosisVirpi Leppä — 2013
• Clinical Neurogenetics: StrokeNatalia S. Rost — 2013
• West African Bioethics Training Program: Raison D'être.Clement Adebamowo — 2007
• Influence of human genome polymorphism on gene expression.高雄 大内 — 2006
• HapMap, pharmacogenomics, and the goal of personalized prescribing.Mary S. Erbaugh — 2006
• The effective size of the Icelandic population and the prospects for LD mapping: inference from unphased microsatellite markersManuel Pulido Quecedo — 2006
• Integrating Molecular Genetics Analyses Into Clinical Research隆 無藤, 智子 安藤 — 2006
• Intra- and interindividual epigenetic variation in human germ cells.Pamela Ramming, Caroline S. Kyger, Stacy Thompson — 2006
• Human regulatory T cells and their role in autoimmune diseaseIldefonso Damas Hurtado — 2006
• Identifying genes for diabetic nephropathy--current difficulties and future directions.M. Molera Aparicio, J. Rodríguez Berrocal — 2006
• Identifying genes underlying skin pigmentation differences among human populationsJennifer Turns — 2006
• Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms.Juan Aranzadi — 2006
• Genome scanning by composite likelihood.Enric Bou — 2007
• Multipoint linkage-disequilibrium mapping with haplotype-block structure.Ю. И. Патютко, А. G. Kotelnikov, А. П. Борисов — 2007
• Population Structure and EigenanalysisV. K. Lukyanov — 2006
• Candidate gene study to investigate the genetic determinants of normal variation in central corneal thicknessDavid P. Dimasi, Kathryn P. Burdon, Alex W. Hewitt — 2010
• Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutationsSylvia M. Jacobs — 2007
• Tagging Single Nucleotide Polymorphisms in the BRIP1 Gene and Susceptibility to Breast and Ovarian CancerCsilla Albert, G. Pohn, Z. Mándoki — 2007
• High density SNP association study of a major autism linkage region on chromosome 17.Thorjørn Larssen — 2007

Related papers

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• Linkage disequilibrium patterns vary substantially among populationsSarah L. Sawyer, Namita Mukherjee, A.J. Pakstis — 2005
• Multi-marker-LD based genetic algorithm for tag SNP selectionAmer E. Mouawad, Nashat Mansour — 2014
• The effect of single-nucleotide polymorphism marker selection on patterns of haplotype blocks and haplotype frequency estimates.Michael Nothnagel, Klaus Rohde — 2005
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• Linkage disequilibrium and haplotypes in 5′-flanking region of the human protein phosphatase 2A-Bδ gene in the CantoneseLin Zhong-nin — 2011
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• Evaluating coverage of exons by HapMap SNPs.Xiao Dong, Tingyan Zhong, Tao Xu — 2013
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