Isabelle Baró

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

Novel<i>SCN5A</i>Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family

Florence Kyndt, Vincent Probst, F Potet et al. · Circulation · 2001 · 368 citations · Full text

Life Sciences, Cardiology, Genetics +15

Multifocal Ectopic Purkinje-Related Premature Contractions

Gabriel Laurent, Samuel Saal, Mohamed‐Yassine Amarouch et al. · Journal of the American College of Cardiology · 2012 · 184 citations · Full text

Life Sciences, Neuroscience, Electrophysiology +5

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Vincent Probst, Florence Kyndt, F Potet et al. · Journal of the American College of Cardiology · 2003 · 172 citations

Life Sciences, Genetics, Molecular Genetics +7

The KCNQ1 potassium channel is down-regulated by ubiquitylating enzymes of the Nedd4/Nedd4-like family

Thomas Jespersen, Mathieu Membrez, Céline S. Nicolas et al. · Cardiovascular Research · 2007 · 138 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17