Meta-analysis identifies six new susceptibility loci for atrial fibrillation PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ... Nature genetics 44 (6), 670-675, 2012 | 669 | 2012 |
Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial JD Roberts, GA Wells, MR Le May, M Labinaz, C Glover, M Froeschl, ... The Lancet 379 (9827), 1705-1711, 2012 | 460 | 2012 |
The short QT syndrome: proposed diagnostic criteria MH Gollob, CJ Redpath, JD Roberts Journal of the American College of Cardiology 57 (7), 802-812, 2011 | 366 | 2011 |
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect R Tadros, C Francis, X Xu, AMC Vermeer, AR Harper, R Huurman, ... Nature genetics 53 (2), 128-134, 2021 | 169 | 2021 |
Guidance on minimizing risk of drug-induced ventricular arrhythmia during treatment of COVID-19: a statement from the Canadian Heart Rhythm Society JL Sapp, W Alqarawi, CJ MacIntyre, R Tadros, C Steinberg, JD Roberts, ... Canadian Journal of Cardiology 36 (6), 948-951, 2020 | 133 | 2020 |
Impact of genetic discoveries on the classification of lone atrial fibrillation JD Roberts, MH Gollob Journal of the American College of Cardiology 55 (8), 705-712, 2010 | 123 | 2010 |
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest C Van Der Werf, KV Lieve, JM Bos, CM Lane, I Denjoy, F Roses-Noguer, ... European heart journal 40 (35), 2953-2961, 2019 | 101 | 2019 |
Genetic testing in the evaluation of unexplained cardiac arrest: from the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) G Mellor, ZWM Laksman, R Tadros, JD Roberts, B Gerull, CS Simpson, ... Circulation: Cardiovascular Genetics 10 (3), e001686, 2017 | 87 | 2017 |
Association between QT-interval components and sudden cardiac death: the ARIC study (Atherosclerosis Risk in Communities) WT O’Neal, MJ Singleton, JD Roberts, LG Tereshchenko, N Sotoodehnia, ... Circulation: Arrhythmia and Electrophysiology 10 (10), e005485, 2017 | 85 | 2017 |
Cardiac ryanodine receptor calcium release deficiency syndrome B Sun, J Yao, M Ni, J Wei, X Zhong, W Guo, L Zhang, R Wang, D Belke, ... Science translational medicine 13 (579), eaba7287, 2021 | 72 | 2021 |
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ... Nature genetics 54 (3), 232-239, 2022 | 61 | 2022 |
Short-coupled ventricular fibrillation represents a distinct phenotype among latent causes of unexplained cardiac arrest: a report from the CASPER registry C Steinberg, B Davies, G Mellor, R Tadros, ZW Laksman, JD Roberts, ... European Heart Journal 42 (29), 2827-2838, 2021 | 61 | 2021 |
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ... Genetics in medicine 23 (1), 47-58, 2021 | 61 | 2021 |
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic … K Ng, EW Titus, KV Lieve, TM Roston, A Mazzanti, FH Deiter, I Denjoy, ... Circulation 142 (10), 932-947, 2020 | 56 | 2020 |
Cardiac abnormalities in first-degree relatives of unexplained cardiac arrest victims: a report from the cardiac arrest survivors with preserved ejection fraction registry C Steinberg, GJ Padfield, J Champagne, S Sanatani, P Angaran, ... Circulation: Arrhythmia and Electrophysiology 9 (9), e004274, 2016 | 54 | 2016 |
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy JD Roberts, JC Herkert, J Rutberg, SM Nikkel, ACP Wiesfeld, D Dooijes, ... Clinical genetics 83 (5), 452-456, 2013 | 54 | 2013 |
Alcohol consumption and leukocyte telomere length S Dixit, MA Whooley, E Vittinghoff, JD Roberts, SR Heckbert, ... Scientific reports 9 (1), 1404, 2019 | 53 | 2019 |
Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a … LA Swayne, NP Murphy, S Asuri, L Chen, X Xu, S McIntosh, C Wang, ... Circulation: Cardiovascular Genetics 10 (1), e001537, 2017 | 51 | 2017 |
A prospective randomized evaluation of a pharmacogenomic approach to antiplatelet therapy among patients with ST-elevation myocardial infarction: the RAPID STEMI study DYF So, GA Wells, R McPherson, M Labinaz, MR Le May, C Glover, ... The Pharmacogenomics Journal 16 (1), 71-78, 2016 | 51 | 2016 |
Elevated lipoprotein (a) and risk of atrial fibrillation: an observational and Mendelian randomization study P Mohammadi-Shemirani, M Chong, S Narula, N Perrot, D Conen, ... Journal of the American College of Cardiology 79 (16), 1579-1590, 2022 | 50 | 2022 |