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Heart Rhythm|June 3, 2014
Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-upChristian van der Werf, Lotte Stiekema, Hanno L Tan, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|August 21, 2008
Phenotypic variability in Caucasian and Japanese patients with matched LQT1 mutationsJudy F Liu, Ilan Goldenberg, Arthur J Moss, et al.
Heart Rhythm|July 22, 2010
Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The NetherlandsChristian van der Werf, Nynke Hofman, Hanno L Tan, et al.
Journal of the American College of Cardiology|November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysisArgelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
Circulation. Arrhythmia and Electrophysiology|March 31, 2017
Effect of Age and Sex on the QTc Interval in Children and Adolescents With Type 1 and 2 Long-QT SyndromeArja S Vink, Sally-Ann B Clur, Ronald B Geskus, et al.
European Heart Journal|November 9, 2006
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?Nynke Hofman, Arthur A M Wilde, Stefan Kääb, et al.
Circulation|August 22, 2013
Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experienceNynke Hofman, Hanno L Tan, Mariëlle Alders, et al.
International Journal of Cardiology|March 7, 2017
Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillationKrystien V Lieve, Arie O Verkerk, Svitlana Podliesna, et al.
European Journal of Human Genetics : EJHG|December 14, 2023
Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic reviewSaar van Pottelberghe, Nina Kupper, Esther Scheirlynck, et al.
Journal of Medical Genetics|June 21, 2013
Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnosticsOlaf R F Mook, Martin A Haagmans, Jean-François Soucy, et al.
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