Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Genetic Mapping and Diversity in Plants and Animals, Genomics and Rare Diseases, and RNA modifications and cancer.
Epigenome-wide DNA methylation association study of CHIP provides insight into perturbed gene regulation
Human plasma proteomic profile of clonal hematopoiesis
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Polygenic Risk for Type 2 Diabetes in African Americans
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk
Mendelian randomization study of diabetes and dementia in the Million Veteran Program
Genetic insights into resting heart rate and its role in cardiovascular disease
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations
A Diabetes Genetic Risk Score Is Associated With All-Cause Dementia and Clinically Diagnosed Vascular Dementia in the Million Veteran Program
The trans-ancestral genomic architecture of glycemic traits
Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes