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UnknownRare coding variants in RCN3 are associated with blood pressure.
Not available
S-EPMC8858539 | biostudies-literature
UnknownRare variant contribution to the heritability of coronary artery disease.
Not available
S-EPMC11464707 | biostudies-literature
UnknownGenetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study.
Not available
S-EPMC5697951 | biostudies-literature
UnknownImpact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
Not available
S-EPMC5595282 | biostudies-literature
UnknownWhole genome sequence analysis of blood lipid levels in >66,000 individuals.
Not available
S-EPMC9553944 | biostudies-literature
UnknownWhole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals.
Not available
S-EPMC12418676 | biostudies-literature
UnknownDynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
Not available
S-EPMC7483769 | biostudies-literature
UnknownSequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Not available
S-EPMC7875770 | biostudies-literature
UnknownEffect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans.
Not available
S-EPMC7863645 | biostudies-literature
UnknownThe trans-ancestral genomic architecture of glycemic traits.
Not available
S-EPMC7610958 | biostudies-literature
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