Area of research
Genetics · Surgery
Research interest
Research interests include Genetic Associations and Epidemiology, Lipoproteins and Cardiovascular Health, Genomics and Rare Diseases, and Diabetes, Cardiovascular Risks, and Lipoproteins.
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity
Inferring compound heterozygosity from large-scale exome sequencing data
Association of Habitual Alcohol Intake With Risk of Cardiovascular Disease
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
Clonal hematopoiesis associated with epigenetic aging and clinical outcomes
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Author Correction: A structural variation reference for medical and population genetics
A brief history of human disease genetics
Lp(a) (Lipoprotein[a]) Concentrations and Incident Atherosclerotic Cardiovascular Disease
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
Polygenic Risk Score Identifies Patients at Increased Risk for Abdominal Aortic Aneurysm and May Benefit from Ultrasound Screening
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood
Genetic Interleukin 6 Signaling Deficiency Attenuates Cardiovascular Risk in Clonal Hematopoiesis
Biological and clinical insights from genetics of insomnia symptoms
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction
Genome-wide association study of peripheral artery disease in the Million Veteran Program
Genetics of Common, Complex Coronary Artery Disease
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Association of <i>APOL1</i> Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
Multi-ethnic genome-wide association study for atrial fibrillation
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
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