Marcel M. A. M. Mannens

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 · 641 citations · Full text

Medicine, Cardiology, Genetics +17

Cardiac conduction defects associate with mutations in SCN5A

Jean‐Jacques Schott, Connie Alshinawi, Florence Kyndt et al. · Nature Genetics · 1999 · 633 citations

Medicine, Cardiology, Genetics +12

Mutation in the <i>KCNQ1</i> Gene Leading to the Short QT-Interval Syndrome

Chloé Bellocq, Antoni C.G. van Ginneken, Connie R. Bezzina et al. · Circulation · 2004 · 627 citations

Medicine, Cardiology, Genetics +17

The Human Chitotriosidase Gene

Rolf G. Boot, G. Herma Renkema, Marri Verhoek et al. · Journal of Biological Chemistry · 1998 · 408 citations · Full text

Life Sciences, Biochemistry, Genetics +6

Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

Alex V. Postma, Isabelle Denjoy, Theo M. Hoorntje et al. · Circulation Research · 2002 · 400 citations · Full text

Medicine, Cardiology, Molecular Genetics +9