Kim, Wonji
Assessing the Contribution of Rare Genetic Variants to Phenotypes of Chronic Obstructive Pulmonary Disease Using Whole-Genome Sequencing Data
Hum Mol Genet.
2022
35766891
Shabani, Mahsima
Rare Genetic Variants Associated with Myocardial Fibrosis; Multi-Ethnic Study of Atherosclerosis (MESA)
Frontiers in Cardiovascular Medicine
2022
35265679
Page, Grier
GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing
Commun Biol
2022
35953715
Li, Zilin
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Nat Methods
2022
36303018
Kelly, Tanika
Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease
Hum Mol Genet.
2022
36444934
Bhattacharya, Romit
Clonal Hematopoiesis Is Associated With Higher Risk of Stroke
Stroke
2022
34743536
Selvaraj, Margaret Sunitha
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Nat Commun
2022
36220816
Ma, Jiantao
Diet Quality Scores are Positively Associated with Whole Blood-derived Mitochondrial DNA Copy Number in the Framingham Heart Study
journal of nutrition
2022
34875096
Blue, Elizabeth
Accounting for population structure in genetic studies of cystic fibrosis
Human Genetics and Genomic Advances
2022
35647563
Blobner, Brandon
Rare Variants in Genes Encoding Subunits of the Epithelial Na+ Channel Are Associated With Blood Pressure and Kidney Function
Hypertension
2022
36193739