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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.Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.International Journal of Cardiology|April 13, 2025
Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variantE van Drie, J D H Jongbloed, E Hoorntje, 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.Circulation Research|June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates NaV1.5 at Intercalated DiscsGerard A Marchal, Mariam Jouni, David Y Chiang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologiesFrancesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.Circulation. Genomic and Precision Medicine|May 18, 2023
Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular ArrhythmiasCaroline Pham, Karolina Andrzejczyk, Sean J Jurgens, et al.Nature Communications|March 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactylyNajim Lahrouchi, Aman George, Ilham Ratbi, et al.European Journal of Human Genetics : EJHG|September 20, 2019
The yield of postmortem genetic testing in sudden death cases with structural findings at autopsyNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.Journal of the American College of Cardiology|April 29, 2017
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death SyndromeNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.Pageof 18