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The Canadian Journal of Cardiology|August 5, 2019
Blinded Randomized Trial of Anticoagulation to Prevent Ischemic Stroke and Neurocognitive Impairment in Atrial Fibrillation (BRAIN-AF): Methods and DesignLena Rivard, Paul Khairy, Mario Talajic, et al.
JAMA Cardiology|November 3, 2021
Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency SyndromeThomas M Roston, Jinhong Wei, Wenting Guo, et al.
European Heart Journal|May 28, 2026
Tetralogy of Fallot: electrophysiology-guided surgical ablation during pulmonary valve replacementNabil Dib, Nancy Poirier, Anna Kamp, et al.
Circulation|December 4, 2025
Safety, Utility, and Outcomes of Procainamide Challenge for the Diagnosis and Exclusion of Brugada SyndromeBenjamin M Moore, Douglas Chan, Brianna Davies, et al.
JACC. Clinical Electrophysiology|October 7, 2023
The Prevalence and Characteristics of Arrhythmic Mitral Valve Prolapse in Patients With Unexplained Cardiac ArrestWael Alqarawi, Rafik Tadros, Jason D Roberts, et al.
CJC Open|December 11, 2020
The Hearts in Rhythm Organization: A Canadian National Cardiogenetics NetworkBrianna Davies, Jason D Roberts, Rafik Tadros, et al.
Heart Rhythm|July 4, 2020
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in ThailandPattarapong Makarawate, Charlotte Glinge, Apichai Khongphatthanayothin, et al.
European Journal of Human Genetics : EJHG|September 22, 2022
Identification and in-silico characterization of splice-site variants from a large cardiogenetic national registryKaveh Rayani, Brianna Davies, Matthew Cheung, et al.
Journal of the American College of Cardiology|March 12, 2025
Clinical Effect of Genetic Testing in Inherited Cardiovascular Diseases: A 14-Year Retrospective StudySteffany Grondin, Benjamin Neveu, Iness Soltani, et al.
European Heart Journal|March 30, 2022
Importance of genetic testing in unexplained cardiac arrestSteffany Grondin, Brianna Davies, Julia Cadrin-Tourigny, et al.
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