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UnknownCommon and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.
Not available
S-EPMC5951629 | biostudies-literature
UnknownMulti-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Not available
S-EPMC7242331 | biostudies-literature
UnknownWhole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
Not available
S-EPMC8394596 | biostudies-literature
UnknownInherited causes of clonal haematopoiesis in 97,691 whole genomes.
Not available
S-EPMC7944936 | 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
UnknownClonal haematopoiesis and risk of chronic liver disease.
Not available
S-EPMC10405350 | biostudies-literature
UnknownDeep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Not available
S-EPMC6107638 | biostudies-literature
UnknownDeep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Not available
S-EPMC6031652 | biostudies-literature
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