Found: 8
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Integrating common and rare genetic variation in diverse human populations.
- Published in:
- Nature, 2010, v. 467, n. 7311, p. 52, doi. 10.1038/nature09298
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- Publication type:
- Article
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1510, doi. 10.1093/hmg/ddp052
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- Publication type:
- Article
A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 3, p. 1, doi. 10.1371/journal.pgen.1000433
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- Publication type:
- Article
Population-Specific Risk of Type 2 Diabetes Conferred by HNF4A P2 Promoter Variants.
- Published in:
- Diabetes, 2008, v. 57, n. 11, p. 3161, doi. 10.2337/db08-0719
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- Publication type:
- Article
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Variation Within the Gene Encoding the Upstream Stimulatory Factor 1 Does Not Influence Susceptibility to Type 2 Diabetes in Samples From Populations With Replicated Evidence of Linkage to Chromosome 1q.
- Published in:
- Diabetes, 2006, v. 55, n. 9, p. 2541, doi. 10.2337/db06-0088
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- Publication type:
- Article
The impact of SNP density on fine-scale patterns of linkage disequilibrium.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 6, p. 577, doi. 10.1093/hmg/ddh060
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- Publication type:
- Article
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes.
- Published in:
- Oncogene, 2000, v. 19, n. 34, p. 3902
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- Publication type:
- Article