Area of research
Genetics · Pulmonary and Respiratory Medicine
Research interest
Research interests include Genetic Associations and Epidemiology, Aortic Disease and Treatment Approaches, Aortic aneurysm repair treatments, and Cardiomyopathy and Myosin Studies.
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Unsupervised deep learning of electrocardiograms enables scalable human disease profiling
A deep learning digital biomarker to detect hypertension and stratify cardiovascular risk from the electrocardiogram
Improved multiancestry fine-mapping identifies cis-regulatory variants underlying molecular traits and disease risk
Electrocardiogram-Based Artificial Intelligence to Identify Coronary Artery Disease
Pathogenic Cardiomyopathy-Associated Gene Variants and Prognosis in Atrial Fibrillation
Artificial Intelligence for Cardiovascular Care—Part 1: Advances
Associations of “Weekend Warrior” Physical Activity With Incident Disease and Cardiometabolic Health
Artificial Intelligence in Cardiovascular Care—Part 2: Applications
Rare coding variant analysis for human diseases across biobanks and ancestries
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
Clonal hematopoiesis, cardiovascular events and treatment benefit in 63,700 individuals from five TIMI randomized trials
Deep learning of left atrial structure and function provides link to atrial fibrillation risk
Noninvasive assessment of organ-specific and shared pathways in multi-organ fibrosis using T1 mapping
The AORTA Gene score for detection and risk stratification of ascending aortic dilation
Rare Genetic Variants in <i>LDLR</i> , <i>APOB</i> , and <i>PCSK9</i> Are Associated With Aortic Stenosis
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heart
Clonal haematopoiesis and risk of chronic liver disease
TP53-mediated clonal hematopoiesis confers increased risk for incident atherosclerotic disease
Genetics of myocardial interstitial fibrosis in the human heart and association with disease
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program
Adjusting for common variant polygenic scores improves yield in rare variant association analyses
Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass
The Genetic Determinants of Aortic Distention
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
Selenoprotein deficiency disorder predisposes to aortic aneurysm formation
Author Correction: Clonal haematopoiesis and risk of chronic liver disease
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention
Genetic analysis of right heart structure and function in 40,000 people