The Journal of Infectious Diseases · 2010 · 160 citations · 17 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsImmunogeneticsMolecular VirologyGenome-wide Association StudiesHiv EpidemiologyHla TypingPopulation ImmunogeneticsCommon Variant AnalysisCommon Variant ContributionCommon Variant EffectsHla Allele PolymorphismHla AllelesHla Genotype AssociationsHla Risk AllelesViral Load Assessment
We performed a whole-genome association study of human immunodeficiency virus type 1 (HIV-1) set point among a cohort of African Americans (n = 515), and an intronic single-nucleotide polymorphism (SNP) in the HLA-B gene showed one of the strongest associations. We use a subset of patients to demonstrate that this SNP reflects the effect of the HLA-B*5703 allele, which shows a genome-wide statistically significant association with viral load set point (P = 5.6 x 10(-10)). These analyses therefore confirm a member of the HLA-B*57 group of alleles as the most important common variant that influences viral load variation in African Americans, which is consistent with what has been observed for individuals of European ancestry, among whom the most important common variant is HLA-B*5701.
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Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price, Nick J. Patterson, Robert M. Plenge et al. · Nature Genetics · 2006 · 10.7K citations
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
Dongliang Ge, Jacques Fellay, Alexander Thompson et al. · Nature · 2009 · 3.5K citations · Full text
Life Sciences, Genetics, Immunology +13