Myriam Berthet

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Jamie D. Kapplinger, David J. Tester, Mariëlle Alders et al. · Heart Rhythm · 2009 · 753 citations · Full text

Channelopathies, Cardiomyopathy, Genetic Disorder +7

<i>KVLQT1</i> C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome

Claire Donger, Isabelle Denjoy, Myriam Berthet et al. · Circulation · 1997 · 346 citations

The genetics underlying acquired long QT syndrome: impact for genetic screening

Hideki Itoh, Lia Crotti, Takeshi Aiba et al. · European Heart Journal · 2015 · 209 citations · Full text

<i>MOG1</i>

Darouna Kattygnarath, Svetlana Maugenre, Nathalie Neyroud et al. · Circulation Cardiovascular Genetics · 2011 · 159 citations · Full text

Long QT syndrome in neonates

Jean‐Marc Lupoglazoff, Isabelle Denjoy, E Villain et al. · Journal of the American College of Cardiology · 2004 · 130 citations

Neonatology, Pediatrics, Newborn Medicine +3