Area of research
Genetics · Rheumatology
Research interest
Research interests include Genetic Associations and Epidemiology, Folate and B Vitamins Research, Cardiovascular Health and Risk Factors, and Congenital Heart Disease Studies.
Human plasma proteomic profile of clonal hematopoiesis
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes
Trajectory of C-Reactive Protein and Incident Heart Failure in Black Adults: The Jackson Heart Study
A genomic mutational constraint map using variation in 76,156 human genomes
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk
Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing
Centenarian clocks: epigenetic clocks for validating claims of exceptional longevity
Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups
Inferring compound heterozygosity from large-scale exome sequencing data
Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma
Protein Markers of Diabetes Discovered in an African American Cohort
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Investigating Gene–Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes
Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts
Impact of Diabetes and Hypertension on Left Ventricular Structure and Function: The Jackson Heart Study
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
DNA methylation GrimAge version 2
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood
Including measures of chronic kidney disease to improve cardiovascular risk prediction by SCORE2 and SCORE2-OP
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
Correlations between complex human phenotypes vary by genetic background, gender, and environment