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Journal of Clinical Medicine|February 22, 2020
Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic VariantsRob W Roudijk, Laurens P Bosman, Jeroen F van der Heijden, et al.
Plos One|December 19, 2017
High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutationBaerbel Klauke, Anna Gaertner-Rommel, Uwe Schulz, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac DiseasesEline A Nannenberg, Ingrid A W van Rijsingen, Paul A van der Zwaag, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 20, 2025
Different underlying aetiologies in patients presenting with ventricular tachycardia fulfilling task force criteria for arrhythmogenic right ventricular cardiomyopathy: initial suspicion based on the 12-lead electrocardiogramJarieke C Hoogendoorn, Laurens P Bosman, Jeroen F van der Heijden, et al.
International Journal of Cardiology|March 4, 2026
Population and family data support TNNT2 p.Arg288Cys as an intermediate effect variant in hypertrophic cardiomyopathyTalitha C F Spanjersberg, Fahima Hassanzada, Jan D H Jongbloed, et al.
Heart Rhythm|April 29, 2010
Desmin mutations as a cause of right ventricular heart failure affect the intercalated disksEllen Otten, Angeliki Asimaki, Alexander Maass, et al.
Animals : an Open Access Journal From MDPI|July 9, 2022
Genetic Basis of Dilated Cardiomyopathy in Dogs and Its Potential as a Bidirectional ModelKaren R Gaar-Humphreys, Talitha C F Spanjersberg, Giorgia Santarelli, et al.
Circulation|September 19, 2007
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic featuresZahurul A Bhuiyan, Maarten P van den Berg, J Peter van Tintelen, et al.
Heart Failure Reviews|March 24, 2017
Redefining the role of biomarkers in heart failure trials: expert consensus documentFrank Kramer, Hani N Sabbah, James J Januzzi, et al.
Human Mutation|April 10, 2013
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnosticsBirgit Sikkema-Raddatz, Lennart F Johansson, Eddy N de Boer, et al.
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