Pascale Sébillon

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

Expanding the phenotype of <i>LMNA</i> mutations in dilated cardiomyopathy and functional consequences of these mutations

Pascale Sébillon · Journal of Medical Genetics · 2003 · 170 citations · Full text

Life Sciences, Cardiology, Genetics +12

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes

Jeanne Flavigny, Michel Souchet, Pascale Sébillon et al. · Journal of Molecular Biology · 1999 · 74 citations

Life Sciences, Genetics, Molecular Biology +9

Functional consequences of an<i>LMNA</i>mutation associated with a new cardiac and non-cardiac phenotype

Jean‐Christophe Charniot, Cécile Pascal, Christiane Bouchier et al. · Human Mutation · 2003 · 65 citations

Medicine, Genetics, Molecular Genetics +13

A T to G mutation in the polypyrimidine tract of the second intron of the human β-globin gene reduces<i>in vitro</i>splicing efficiency: evidence for an increased hnRNP C interaction

Pascale Sébillon, Chérif Beldjord, Jean-Claude Kaplan et al. · Nucleic Acids Research · 1995 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15