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Communications Biology|October 28, 2025
Modelling arrhythmogenic cardiomyopathy fattyfibro pathology with PKP2-deficient epicardial cells derived from human iPSCsSadia L Falana, Sobhi G Kazmouz, Jessika B Iwanski, et al.
Circulation. Genomic and Precision Medicine|February 19, 2025
Natural History, Phenotype Spectrum, and Clinical Outcomes of Desmin (DES)-Associated CardiomyopathyBabken Asatryan, Marina Rieder, Brittney Murray, et al.
Journal of the American College of Cardiology|July 2, 2013
Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriersAnneline S J M te Riele, Aditya Bhonsale, Cynthia A James, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
Natural History, Phenotype Spectrum and Clinical Outcomes of Desmin (DES)-Associated CardiomyopathyBabken Asatryan, Marina Rieder, Brittney Murray, et al.
The Canadian Journal of Cardiology|December 1, 2024
Impaired Atrial and Ventricular Strain Predicts Heart Failure in Arrhythmogenic Right Ventricular CardiomyopathyXander Jacquemyn, Jef Van den Eynde, Junzhen Zhan, et al.
Heart Rhythm|July 3, 2013
Malignant arrhythmogenic right ventricular dysplasia/cardiomyopathy with a normal 12-lead electrocardiogram: a rare but underrecognized clinical entityAnneline S J M te Riele, Cynthia A James, Aditya Bhonsale, et al.
Heart Rhythm|February 4, 2012
Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathyTing-Ting Hong, Rebecca Cogswell, Cynthia A James, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|September 3, 2017
Feature tracking CMR reveals abnormal strain in preclinical arrhythmogenic right ventricular dysplasia/ cardiomyopathy: a multisoftware feasibility and clinical implementation studyMimount Bourfiss, Davis M Vigneault, Mounes Aliyari Ghasebeh, et al.
Genetics in Medicine Open|May 8, 2026
Evidence of variations in genetic prevalence for loss-of-function PKP2 variants between individuals with European and African ancestryAlexandra Winters, Renae Judy, Choudhary Anwar A Chahal, et al.
European Heart Journal|August 29, 2015
Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathyAnneline S J M te Riele, Cynthia A James, Judith A Groeneweg, et al.
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