This publications search provides an entry for Group and Investigator associated publications. Please use the associated fields to refine your search for publications. The Group section will auto-populate from selections within the Department.

Rare variant contribution to the heritability of coronary artery disease. (Pubmed Abstract)

Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification. (Pubmed Abstract)

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. (Pubmed Abstract)

Carriers of rare damaging genetic variants are at lower risk of atherosclerotic disease. (Pubmed Abstract)

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing. (Pubmed Abstract)

Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease. (Pubmed Abstract)

Genome-wide association analysis of COVID-19 mortality risk in SARS-CoV-2 genomes identifies mutation in the SARS-CoV-2 spike protein that colocalizes with P.1 of the Brazilian strain. (Pubmed Abstract)

A Risk Prediction Model for Mortality Among Smokers in the COPDGene® Study. (Pubmed Abstract)