Irene M. van Langen

A Single Na ⁺ Channel Mutation Causing Both Long-QT and Brugada Syndromes

Connie R. Bezzina, Marieke W. Veldkamp, Maarten P. van den Berg et al. · Circulation Research · 1999 · 637 citations · Full text

Cardiac Muscle, Family Members, Genetics +16

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Philippe Charron, Michael Arad, Eloisa Arbustini et al. · European Heart Journal · 2010 · 483 citations · Full text

Cardiomyopathy, Genetic Testing, Heart Failure +14

Sudden Unexplained Death

Hanno L. Tan, Nynke Hofman, Irene M. van Langen et al. · Circulation · 2005 · 414 citations · Full text

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands

Karuna R. M. van der Meij, Erik A. Sistermans, Merryn Macville et al. · The American Journal of Human Genetics · 2019 · 364 citations · Full text

Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

J. Peter van Tintelen, Mark M. Entius, Zahurul A. Bhuiyan et al. · Circulation · 2006 · 353 citations