Area of research
Surgery · Genetics
Research interest
Research interests include Lipoproteins and Cardiovascular Health, Genetic Associations and Epidemiology, Diabetes, Cardiovascular Risks, and Lipoproteins, and Cancer, Lipids, and Metabolism.
Primary care providers’ perspectives on receiving opportunistic genomic results from a national study: The Million Veteran Program Return Of Actionable Results (MVP-ROAR) Study
Lac-Phe mediates the effects of metformin on food intake and body weight
X chromosome dosage drives statin-induced dysglycemia and mitochondrial dysfunction
A functional genomic framework to elucidate novel causal metabolic dysfunction–associated fatty liver disease genes
Trends of Lipid Concentrations, Awareness, Evaluation, and Treatment in Severe Dyslipidemia in US Adults
RNA Interference Therapy Targeting Apolipoprotein C-III in Hypertriglyceridemia
Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH Registry
Introducing return of results in the Million Veteran Program: Design and pilot results of the MVP-ROAR Familial Hypercholesterolemia Study
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting
Isthmin-1 is an adipokine that promotes glucose uptake and improves glucose tolerance and hepatic steatosis
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics
Properties of structural variants and short tandem repeats associated with gene expression and complex traits
FAM13A affects body fat distribution and adipocyte function
Abstract 15751: Pharmacodynamic Effect of ARO-ANG3, an Investigational RNA Interference Targeting Hepatic Angiopoietin-like Protein 3, in Patients With Hypercholesterolemia
Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats
Children with Heterozygous Familial Hypercholesterolemia in the United States: Data from the Cascade Screening for Awareness and Detection-FH Registry
Predictive network modeling in human induced pluripotent stem cells identifies key driver genes for insulin responsiveness
Clinical Genetic Testing for Familial Hypercholesterolemia
Distance to treatment as a factor for loss to follow up of hepatitis C patients in North East England
Health disparities among adult patients with a phenotypic diagnosis of familial hypercholesterolemia in the CASCADE-FH™ patient registry
Human induced pluripotent stem cell–derived cardiomyocytes recapitulate the predilection of breast cancer patients to doxorubicin-induced cardiotoxicity
Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity
Association Between Intensity of Statin Therapy and Mortality in Patients With Atherosclerotic Cardiovascular Disease
US physician practices for diagnosing familial hypercholesterolemia: data from the CASCADE-FH registry
Interdisciplinary psychosocial care for families with inherited cardiovascular diseases
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
Genetic Evidence for a Normal-Weight “Metabolically Obese” Phenotype Linking Insulin Resistance, Hypertension, Coronary Artery Disease, and Type 2 Diabetes
Reducing the burden of disease and death from familial hypercholesterolemia: A call to action
Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders