Charles C. Hong

This study shows that a polygenic risk score for coronary artery disease is associated with more severe atherosclerosis features in autopsy samples of sudden death cases.

The paper investigates allele-specific enhancer-promoter interactions in an imprinted domain during mouse neural commitment, finding that biallelic interactions occur but only maternal ones are productive.

The paper analyzes exome array data from 9,721 ischemic stroke cases to identify coding variants associated with stroke, finding 15 significant variants, including 13 novel associations.

The paper shows that variant effect sizes on quantitative endophenotypes support pathogenicity in monogenic disease genes.

This paper identifies novel genetic loci for thoracic and abdominal aortic aneurysms using GWAS in the UK Biobank and finds distinct genetic architectures and shared pathophysiology with Marfan syndrome.

This study examines the association between pathogenic or likely pathogenic genetic variants in cardiomyopathy and arrhythmia genes and unexplained sudden cardiac death in adults with no gross pathological findings.