|
Patel, Roshni |
Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits
|
2021 |
bioRxiv |
|
Battle, Stephanie |
A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data
|
2021 |
medRxiv |
|
Sofer, Tamar |
A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood
|
2021 |
medRxiv |
|
Wheeler, Marsha |
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
|
2021 |
medRxiv |
|
Page, Grier |
GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing
|
2021 |
bioRxiv |
|
Li, Zilin |
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
|
2021 |
bioRxiv |
|
Selvaraj, Margaret Sunitha |
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
|
2021 |
bioRxiv |
|
Minster, Ryan L |
A population-specific missense variant rs1597000001 in CETP promotes a favorable lipid profile and reduces CETP activity
|
2021 |
medRxiv |
|
Elgart, Michael |
Correlations between complex human phenotypes vary by genetic background, gender, and environment
|
2021 |
medRxiv |
|
Lubitz, Steven |
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes
|
2021 |
medRxiv |
