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2021
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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
Not available
S-EPMC8394596
|
biostudies-literature
Cite
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Not available
S-EPMC6107638
|
biostudies-literature
Cite
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Not available
S-EPMC6031652
|
biostudies-literature
Cite
Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma.
Not available
S-EPMC6904857
|
biostudies-literature
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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Not available
S-EPMC10360040
|
biostudies-literature
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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
Not available
S-EPMC9119698
|
biostudies-literature
Cite
Effect 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
Cite
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Not available
S-EPMC7944936
|
biostudies-literature
Cite
Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease.
Not available
S-EPMC9158509
|
biostudies-literature
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Powerful, 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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