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UnknownEmergency Consent: Patients' and Surrogates' Perspectives on Consent for Clinical Trials in Acute Stroke and Myocardial Infarction.
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S-EPMC6497349 | biostudies-literature
UnknownRare variant contribution to the heritability of coronary artery disease.
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S-EPMC11464707 | biostudies-literature
UnknownWhole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program.
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S-EPMC9334637 | biostudies-literature
UnknownGenomics yields biological and phenotypic insights into bipolar disorder.
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S-EPMC12163093 | biostudies-literature
UnknownWhole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma.
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S-EPMC6904857 | biostudies-literature
UnknownDeep-coverage whole genome sequences and blood lipids among 16,324 individuals.
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S-EPMC6107638 | biostudies-literature
UnknownDe novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
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S-EPMC7007577 | biostudies-literature
UnknownThe Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits.
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S-EPMC10231654 | biostudies-literature
UnknownA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
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S-EPMC10008172 | biostudies-literature
UnknownPowerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
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S-EPMC10084891 | biostudies-literature
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