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Study Design of a Nationwide Network Indian Cohort of Pregnancy-Associated Acute Kidney Injury (iPRAKI NET)
Not available
S-EPMC11843178
|
biostudies-literature
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Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals.
Not available
S-EPMC12418676
|
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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Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Not available
S-EPMC7944936
|
biostudies-literature
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Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma.
Not available
S-EPMC6904857
|
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 analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
Not available
S-EPMC8394596
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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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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
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