From Whole Exome Sequencing to Patient‐Specific Therapy: Another Example of How Basic Research Pays Off in Patient Care by Arthur A. M. Wilde, Sami Viskin

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Catecholaminergic polymorphic ventricular tachycardia in 2012 by Christian van der Werf, Arthur A.M. Wilde, Ineke Nederend

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Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias by Maaike eHoekstra, Christine L. Mummery, Arthur A.M. Wilde, Connie R. Bezzina, Arie O. Verkerk

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Diagnostic Performance of Various QTc Interval Formulas in a Large Family with Long QT Syndrome Type 3: Bazett's Formula Not So Bad After All … by Jan Brouwer, Maarten P. Van Den Berg, Diederick E. Grobbee, Jaap Haaksma, Arthur A.M. Wilde

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Generation of iPSC lines from CPVT patient carrying heterozygous mutation p.A2254V in the ryanodine receptor 2 gene by Wener Li, Sarah Henze, Xiaojing Luo, Ying Ulbricht, Anja Richter, Nataliya Di Donato, Arthur A.M. Wilde, Kaomei Guan

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Genotype and clinical characteristics of congenital long QT syndrome in Thailand by Ankavipar Saprungruang, Apichai Khongphatthanayothin, John Mauleekoonphairoj, Pharawee Wandee, Supaluck Kanjanauthai, Zahurul A. Bhuiyan, Arthur A.M. Wilde, Yong Poovorawan

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Left Axis Deviation in Brugada Syndrome: Vectorcardiographic Evaluation during Ajmaline Provocation Testing Reveals Additional Depolarization Abnormalities by Martijn H. van der Ree, Jeroen Vendrik, Jan A. Kors, Ahmad S. Amin, Arthur A. M. Wilde, Hanno L. Tan, Pieter G. Postema

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A deep learning approach identifies new ECG features in congenital long QT syndrome by Simona Aufiero, Hidde Bleijendaal, Tomas Robyns, Bert Vandenberk, Christian Krijger, Connie Bezzina, Aeilko H. Zwinderman, Arthur A. M. Wilde, Yigal M. Pinto

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SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this... by Raha Pazoki, Jonas S S G de Jong, Roos F Marsman, Nienke Bruinsma, Lukas R C Dekker, Arthur A M Wilde, Connie R Bezzina, Michael W T Tanck

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The development and validation of an easy to use automatic QT-interval algorithm. by Ben J M Hermans, Arja S Vink, Frank C Bennis, Luc H Filippini, Veronique M F Meijborg, Arthur A M Wilde, Laurent Pison, Pieter G Postema, Tammo Delhaas

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Machine learning of electrophysiological signals for the prediction of ventricular arrhythmias: systematic review and examination of heterogeneity between studiesResearch in contex... by Maarten Z.H. Kolk, Brototo Deb, Samuel Ruipérez-Campillo, Neil K. Bhatia, Paul Clopton, Arthur A.M. Wilde, Sanjiv M. Narayan, Reinoud E. Knops, Fleur V.Y. Tjong

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Sex- and age specific association of new-onset atrial fibrillation with in-hospital mortality in hospitalised COVID-19 patients by Joost A. Offerhaus, Linda P.T. Joosten, Maarten van Smeden, Marijke Linschoten, Hidde Bleijendaal, Robert Tieleman, Arthur A.M. Wilde, Frans H. Rutten, Geert-Jan Geersing, Carol Ann Remme

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SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility. by Frans van Hoorn, Maria E Campian, Anje Spijkerboer, Marieke T Blom, R Nils Planken, Albert C van Rossum, Jacques M T de Bakker, Arthur A M Wilde, Maarten Groenink, Hanno L Tan

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Evaluation of the Impact of a Chronic Total Coronary Occlusion on Ventricular Arrhythmias and Long‐Term Mortality in Patients With Ischemic Cardiomyopathy and an Implantable Cardio... by Ivo M. van Dongen, Dilek Yilmaz, Joëlle Elias, Bimmer E. P. M. Claessen, Ronak Delewi, Reinoud E. Knops, Arthur A. M. Wilde, Lieselot van Erven, Martin J. Schalij, José P. S. Henriques

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Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease–Causing Mutation by Christiaan C. Veerman, Isabella Mengarelli, Elisabeth M. Lodder, Georgios Kosmidis, Milena Bellin, Miao Zhang, Sven Dittmann, Kaomei Guan, Arthur A. M. Wilde, Eric Schulze‐Bahr, Boris Greber, Connie R. Bezzina, Arie O. Verkerk

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Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long‐QT Syndrome by Arja S. Vink, Ben J. M. Hermans, Jean‐Luc Q. Hooglugt, Puck J. Peltenburg, Veronique M. F. Meijborg, Nynke Hofman, Sally‐Ann B. Clur, Nico A. Blom, Tammo Delhaas, Arthur A. M. Wilde, Pieter G. Postema

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Prevalence of Mitral Annulus Disjunction and Mitral Valve Prolapse in Patients With Idiopathic Ventricular Fibrillation by Sanne A. Groeneveld, Feddo P. Kirkels, Maarten J. Cramer, Reinder Evertz, Kristina H. Haugaa, Pieter G. Postema, Niek H. J. Prakken, Arco J. Teske, Arthur A. M. Wilde, Birgitta K. Velthuis, Robin Nijveldt, Rutger J. Hassink

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<i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy by Manal Alaamery, Nour Albesher, Fahad Alhabshan, Phil Barnett, Mohamed Salim Kabbani, Farah Chaikhouni, Aho Ilgun, Olaf R. F. Mook, Hessa Alsaif, Vincent M. Christoffels, Peter van Tintelen, Arthur A. M. Wilde, Arjan C. Houweling, Salam Massadeh, Alex V. Postma

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Dynamic prediction of malignant ventricular arrhythmias using neural networks in patients with an implantable cardioverter-defibrillatorResearch in context by Maarten Z.H. Kolk, Samuel Ruipérez-Campillo, Laura Alvarez-Florez, Brototo Deb, Erik J. Bekkers, Cornelis P. Allaart, Anne-Lotte C.J. Van Der Lingen, Paul Clopton, Ivana Išgum, Arthur A.M. Wilde, Reinoud E. Knops, Sanjiv M. Narayan, Fleur V.Y. Tjong

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Accuracy and clinical relevance of the single-lead Apple Watch electrocardiogram to identify atrial fibrillation by Shari Pepplinkhuizen, MD, FHRS, Wiert F. Hoeksema, MD, Willeke van der Stuijt, MD, Nicole J. van Steijn, MD, Michiel M. Winter, MD, PhD, Arthur A.M. Wilde, MD, PhD, FHRS, Lonneke Smeding, PhD, Reinoud E. Knops, MD, PhD

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