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UnknownRare variant contribution to the heritability of coronary artery disease.
Not available
S-EPMC11464707 | biostudies-literature
UnknownRare genetic variants explain missing heritability in smoking.
Not available
S-EPMC9985486 | biostudies-literature
UnknownRecurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.
Not available
S-EPMC3738837 | biostudies-literature
UnknownWhole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
Not available
S-EPMC8394596 | biostudies-literature
UnknownLarge-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits.
Not available
S-EPMC11985957 | biostudies-literature
UnknownDeterminants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.
Not available
S-EPMC8190084 | biostudies-literature
UnknownExome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
Not available
S-EPMC6699738 | biostudies-literature
UnknownMendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.
Not available
S-EPMC8986098 | biostudies-literature
UnknownWhole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Not available
S-EPMC3928660 | biostudies-literature
UnknownRare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
Not available
S-EPMC8764201 | biostudies-literature
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