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Circulation. Cardiovascular Genetics|August 24, 2010
Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studiesRobert W Davies, Sonny Dandona, Alexandre F R Stewart, et al.Current Atherosclerosis Reports|August 11, 2011
Genetic testing for early detection of individuals at risk of coronary heart disease and monitoring response to therapy: challenges and promisesH Robert Superko, Robert Roberts, Arthur Agatston, et al.Nature Communications|January 30, 2016
Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery diseaseJaana A Hartiala, W H Wilson Tang, Zeneng Wang, et al.Pediatrics|October 26, 2011
Overlooked and underserved: "action signs" for identifying children with unmet mental health needsPeter S Jensen, Eliot Goldman, David Offord, et al.The Canadian Journal of Cardiology|June 9, 2026
Identification of a Novel Genetic Variant responsible for Familial Atrial FibrillationRebecca Martínez-Moreno, Alexandra Pérez-Serra, Gopi Shah, et al.Science (New York, N.Y.)|May 5, 2007
A common allele on chromosome 9 associated with coronary heart diseaseRuth McPherson, Alexander Pertsemlidis, Nihan Kavaslar, et al.Journal of the American College of Cardiology|July 31, 2010
Gene dosage of the common variant 9p21 predicts severity of coronary artery diseaseSonny Dandona, Alexandre F R Stewart, Li Chen, et al.Human Genetics|November 4, 2009
The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank StudiesSonny Dandona, Li Chen, Meng Fan, et al.Circulation. Cardiovascular Genetics|December 25, 2009
Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogenKaralyn D Folmes, Anita Y M Chan, Debby P Y Koonen, et al.Circulation|December 22, 2004
Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndromeJasvinder S Sidhu, Yadavendra S Rajawat, Tapan G Rami, et al.Pageof 11