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UnknownGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
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S-EPMC4835977 | biostudies-literature
UnknownA statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
Not available
S-EPMC11981678 | biostudies-literature
UnknownWhole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals.
Not available
S-EPMC12418676 | biostudies-literature
UnknownEpigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma.
Not available
S-EPMC10462855 | biostudies-literature
UnknownAssessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
Not available
S-EPMC9119698 | 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
UnknownInherited causes of clonal haematopoiesis in 97,691 whole genomes.
Not available
S-EPMC7944936 | biostudies-literature
UnknownAberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Not available
S-EPMC10360040 | biostudies-literature
UnknownWhole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease.
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S-EPMC9158509 | biostudies-literature
UnknownPowerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
Not available
S-EPMC10084891 | biostudies-literature
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