Area of research
Genetics · Cancer Research
Research interest
Research focused on Genetics and Mendelian randomization, with related work in Atrial fibrillation, Whole genome sequencing, Genome-wide association study. Notable publications include 'Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes', 'Improving reporting standards for polygenic scores in risk prediction studies', and 'Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use'.
Correlates and consequences of clonal hematopoiesis expansion rate: a 16-year longitudinal study of 6976 women
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals
Integrative proteomic analyses across common cardiac diseases yield mechanistic insights and enhanced prediction
Prevalence of frequent premature ventricular contractions and nonsustained ventricular tachycardia in older women screened for atrial fibrillation in the Women’s Health Initiative
Genome-Wide Epistatic Interaction between DEF1B and APOL1 High-Risk Genotypes for Chronic Kidney Disease
Improving reporting standards for polygenic scores in risk prediction studies
Serum magnesium and calcium levels in relation to ischemic stroke
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use