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UnknownSequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Not available
S-EPMC7875770 | biostudies-literature
UnknownImplicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
Not available
S-EPMC9793579 | biostudies-literature
UnknownAssessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
Not available
S-EPMC9119698 | biostudies-literature
UnknownInherited causes of clonal haematopoiesis in 97,691 whole genomes.
Not available
S-EPMC7944936 | biostudies-literature
UnknownGenetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Not available
S-EPMC3340926 | biostudies-literature
UnknownA statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
Not available
S-EPMC11981678 | biostudies-literature
UnknownAberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Not available
S-EPMC10360040 | biostudies-literature
UnknownA multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Not available
S-EPMC9388392 | 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
UnknownWhole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease.
Not available
S-EPMC9158509 | biostudies-literature
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