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Cardiovascular Research|September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesisEdgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.Molecular Genetics & Genomic Medicine|November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variantEline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.Nederlands Tijdschrift Voor Geneeskunde|February 8, 2019
[Hypertrophic cardiomyopathy]Beau van Driel, Folkert W Asselbergs, Rudolf A de Boer, et al.European Journal of Human Genetics : EJHG|November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.Circulation Research|July 11, 2009
Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathySebastian Carballo, Paul Robinson, Robyn Otway, et al.European Journal of Human Genetics : EJHG|December 1, 2016
Follow-up care by a genetic counsellor for relatives at risk for cardiomyopathies is cost-saving and well-appreciated: a randomised comparisonKarin Nieuwhof, Erwin Birnie, Maarten P van den Berg, et al.Cardiovascular Research|June 1, 2005
Genetic aspects of atrial fibrillationAns C P Wiesfeld, Martin E W Hemels, J Peter Van Tintelen, et al.Stem Cell Research|September 25, 2023
Generation and characterization of novel human induced pluripotent stem cell (iPSC) lines originating from five asymptomatic individuals carrying the PLN-R14del pathogenic variant and a non-carrier relativeValentina Balducci, Francesco Scardigli, Magdalena Harakalova, et al.Genes|October 23, 2021
Uptake and Patient Perspectives on Additional Testing for Novel Disease-Associated Genes: Lessons from a PAH CohortSamara M A Jansen, Lieke M van de Heuvel, Arjan C Houweling, et al.Journal of the American College of Cardiology|February 11, 2022
Echocardiographic Deformation Imaging for Early Detection of Genetic Cardiomyopathies: JACC Review Topic of the WeekKarim Taha, Feddo P Kirkels, Arco J Teske, et al.Pageof 21