Jean‐Jacques Schott

Congenital Heart Disease Caused by Mutations in the Transcription Factor <i>NKX2-5</i>

Jean‐Jacques Schott, D. Woodrow Benson, Craig T. Basson et al. · Science · 1998 · 1.3K citations

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Peter J. Mohler, Jean‐Jacques Schott, Anthony O. Gramolini et al. · Nature · 2003 · 959 citations

Cardiac Muscle, Cardiomyopathy, Cardiovascular Disease +10

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

Cardiac conduction defects associate with mutations in SCN5A

Jean‐Jacques Schott, Connie Alshinawi, Florence Kyndt et al. · Nature Genetics · 1999 · 629 citations

Cardiac Muscle, Cardiomyopathy, Genetics +6

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Connie R. Bezzina, Julien Barc, Yuka Mizusawa et al. · Nature Genetics · 2013 · 540 citations · Full text

Cardiomyopathy, Genetic Disorder, Genetics +9