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UnknownEfficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
Not available
S-EPMC6119127 | biostudies-literature
UnknownNo large-effect low-frequency coding variation found for myocardial infarction.
Not available
S-EPMC4119412 | biostudies-literature
UnknownMEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk.
Not available
S-EPMC7585430 | biostudies-literature
UnknownBiobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Not available
S-EPMC6530775 | biostudies-literature
UnknownRegulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
Not available
S-EPMC8456156 | biostudies-literature
UnknownGenome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Not available
S-EPMC5777936 | biostudies-literature
UnknownLoss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.
Not available
S-EPMC7749177 | biostudies-literature
UnknownGenome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target.
Not available
S-EPMC10632148 | biostudies-literature
UnknownWhole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Not available
S-EPMC3928660 | biostudies-literature
UnknownImplicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
Not available
S-EPMC9793579 | biostudies-literature
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