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The International HapMap Project
scientific article (publication date: 18 December 2003)
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instance of
scholarly article
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title
The International HapMap Project
(English)
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language of work or name
English
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publication date
18 December 2003
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published in
Nature
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volume
426
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page(s)
789-96
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issue
6968
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cites work
Searching for genetic determinants in the new millennium
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7 January 2021
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Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
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7 January 2021
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The future of genetic studies of complex human diseases
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7 January 2021
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Worldwide differences in the incidence of type I diabetes are associated with amino acid variation at position 57 of the HLA-DQ beta chain
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A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus
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The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry
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Apolipoprotein E and Alzheimer's disease
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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
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Crossref
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7 January 2021
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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
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7 January 2021
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An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing
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7 January 2021
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A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
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https://api.crossref.org/works/10.1038%2FNATURE02168
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The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
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7 January 2021
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Neuregulin 1 and susceptibility to schizophrenia
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7 January 2021
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Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness
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7 January 2021
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The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.
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7 January 2021
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Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction
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7 January 2021
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Variations on a theme: cataloging human DNA sequence variation
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7 January 2021
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Variation is the spice of life
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7 January 2021
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Identification of the cystic fibrosis gene: genetic analysis
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7 January 2021
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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland
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7 January 2021
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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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Characterization of single-nucleotide polymorphisms in coding regions of human genes
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7 January 2021
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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
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7 January 2021
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Quality and completeness of SNP databases
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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The mosaic that is our genome
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7 January 2021
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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
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7 January 2021
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The structure of haplotype blocks in the human genome
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7 January 2021
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Linkage disequilibrium in the human genome
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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Extent and distribution of linkage disequilibrium in three genomic regions
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7 January 2021
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A first-generation linkage disequilibrium map of human chromosome 22
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7 January 2021
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High-resolution haplotype structure in the human genome
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
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7 January 2021
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Haplotype tagging for the identification of common disease genes
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7 January 2021
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Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans
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7 January 2021
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Genome scans and candidate gene approaches in the study of common diseases and variable drug responses
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7 January 2021
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Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28
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7 January 2021
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Population genetics--making sense out of sequence
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7 January 2021
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Global patterns of linkage disequilibrium at the CD4 locus and modern human origins
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7 January 2021
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Race, ethnicity, and genomics: social classifications as proxies of biological heterogeneity
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7 January 2021
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An apportionment of human DNA diversity
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7 January 2021
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Genetic structure of human populations
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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Microsatellite diversity and the demographic history of modern humans
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Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome
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7 January 2021
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dbSNP: the NCBI database of genetic variation
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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SSAHA: a fast search method for large DNA databases
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7 January 2021
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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
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7 January 2021
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The Sequence of the Human Genome
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7 January 2021
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Linkage disequilibrium in finite populations
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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The decay of linkage disequilibrium under random union of gametes: how to calculate Bennett's principal components.
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7 January 2021
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The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis
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Estimating the recombination parameter of a finite population model without selection
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https://api.crossref.org/works/10.1038%2FNATURE02168
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Initial sequencing and analysis of the human genome
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The complex relationship of genetics, groups, and health: what it means for public health
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7 January 2021
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Genetic research and culturally specific risks: one size does not fit all.
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https://api.crossref.org/works/10.1038%2FNATURE02168
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7 January 2021
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Involving study populations in the review of genetic research
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Ethical challenges in community-based research
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Commentary: what "community review" can and cannot do.
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Identifiers
DOI
10.1038/NATURE02168
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
138782
Dimensions Publication ID
1033654326
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OpenCitations bibliographic resource ID
138782
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
138782
PubMed ID
14685227
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
138782
ResearchGate publication ID
30863479
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Springer Nature article ID
10.1038/nature02168
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