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2021
(6)
2023
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2020
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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
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response.
Not available
S-EPMC8959399
|
biostudies-literature
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
Not available
S-EPMC7483769
|
biostudies-literature
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Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals.
Not available
S-EPMC9395431
|
biostudies-literature
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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Not available
S-EPMC6107638
|
biostudies-literature
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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Not available
S-EPMC6031652
|
biostudies-literature
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De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
Not available
S-EPMC7007577
|
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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Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Not available
S-EPMC7944936
|
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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