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Journal of the American College of Cardiology|August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathyAnnalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Cardiovascular Research|May 20, 2014
Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutationsE Rosalie Witjas-Paalberends, Ahmet Güçlü, Tjeerd Germans, et al.
European Journal of Heart Failure|January 26, 2013
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experienceKarin Y van Spaendonck-Zwarts, Ingrid A W van Rijsingen, Maarten P van den Berg, et al.
Human Molecular Genetics|October 21, 2022
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetranceJaël S Copier, Marianne Bootsma, Chai A Ng, et al.
International Journal of Cardiology|October 18, 2012
Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complicationsIngrid A W van Rijsingen, Annemieke Bakker, Donija Azim, et al.
JACC. Heart Failure|August 11, 2023
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort StudyMark Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Circulation. Cardiovascular Genetics|June 10, 2014
Outcome in phospholamban R14del carriers: results of a large multicentre cohort studyIngrid A W van Rijsingen, Paul A van der Zwaag, Judith A Groeneweg, et al.
International Journal of Molecular Sciences|February 25, 2023
Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder VariantsMark Jansen, Maike Schuldt, Beau O van Driel, et al.
European Journal of Heart Failure|November 28, 2012
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriersIngrid A W van Rijsingen, Eline A Nannenberg, Eloisa Arbustini, et al.
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