The International HapMap Project.
- Authors
- International HapMap Consortium
- Year
- 2003
- Journal
- Nature
- PMID
- 14685227
- DOI
- 10.1038/nature02168
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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| Genetic Predisposition to Glioma Mediated by a MAPKAP1 Enhancer Variant. | Huang L et al. | β | 2020 | β |
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| Inauguration of the Tanzania Society of Human Genetics: Biomedical Research in Tanzania with Emphasis on Human Genetics and Genomics. | Alimohamed MZ et al. | β | 2020 | β |
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| Molecular Discordance between Myeloid Sarcomas and Concurrent Bone Marrows Occurs in Actionable Genes and Is Associated with Worse Overall Survival. | Werstein B et al. | β | 2020 | β |
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| Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs. | Treff NR et al. | β | 2020 | β |
| Refining the "double two-thirds" rule: Genotype-based breed grouping and clinical presentation help predict the diagnosis of canine splenic mass lesions in 288 dogs. | Davies O et al. | β | 2020 | β |
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| The Impact of <i>HMGB1</i> Polymorphisms on Prostate Cancer Progression and Clinicopathological Characteristics. | Chou YE et al. | β | 2020 | β |
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| The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. | Li D et al. | β | 2020 | β |
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| Population Structure and Implications on the Genetic Architecture of HIV-1 Phenotypes Within Southern Africa. | Thami PK et al. | β | 2019 | β |
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| Radiation-Induced Chromosomal Breaks may be DNA Repair Fragile Sites with Larger-scale Correlations to Eight Double-Strand-Break Related Data Sets over the Human Genome. | Brahme A et al. | β | 2019 | β |
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| Single nucleotide polymorphisms of let-7-related genes increase susceptibility to breast cancer. | Du Y et al. | β | 2019 | β |
| SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. | FernΓ‘ndez-Santiago R et al. | β | 2019 | β |
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| The Continuing Evolution of Precision Health in Type 2 Diabetes: Achievements and Challenges. | Lin Y et al. | β | 2019 | β |
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| Whole-genome re-sequencing reveals the impact of the interaction of copy number variants of the rhg1 and Rhg4 genes on broad-based resistance to soybean cyst nematode. | Patil GB et al. | β | 2019 | β |
| A common regulatory variant in SLC35B4 influences the recurrence and survival of prostate cancer. | Huang EY et al. | β | 2018 | β |
| A decade of genome-wide association studies for coronary artery disease: the challenges ahead. | Erdmann J et al. | β | 2018 | β |
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