Rate My Professor Belinda Gray

Her research centers on the genetics, risk stratification, and prevention of sudden cardiac death in young people and athletes, including inherited cardiomyopathies such as hypertrophic cardiomyopathy, arrhythmogenic cardiomyopathy, and dilated cardiomyopathy, as well as channelopathies like Brugada syndrome and long QT syndrome. She investigates ECG patterns in athletes, genetic testing utility, and exercise safety in genetic heart conditions. Key publications include "Sudden death and left ventricular involvement in arrhythmogenic cardiomyopathy" (2019), "Vigorous Exercise in Patients With Hypertrophic Cardiomyopathy" (2023), "The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy" (2018), "Accuracy of the 2017 international recommendations for clinicians who interpret adolescent athletes’ ECGs: a cohort study of 11 168 British white and black soccer players" (2020), and "Natural History of Genotype Positive Phenotype Negative Patients with Hypertrophic Cardiomyopathy" (2011). Gray chairs the Cardiac Society of Australia and New Zealand Genetic Council, co-founded its Sports Cardiology Working Group, and lectures in the Masters of Sports Cardiology at St George’s University of London. She has secured funding through NHMRC Early Career Fellowship and University of Sydney Cardiovascular Initiative Catalyst Grant, and presented the Ralph Reader Prize at CSANZ.