Pascale Richard

Hypertrophic Cardiomyopathy

Pascale Richard, Philippe Charron, Lucie Carrier et al. · Circulation · 2003 · 1.3K citations · Full text

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Gisèle Bonne, Lucie Carrier, J. Bercovici et al. · Nature Genetics · 1995 · 443 citations

Cardiac Muscle, Cardiomyopathy, Heart Failure +10

Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies

Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau et al. · The American Journal of Human Genetics · 2002 · 361 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Classical Phenotype +9

Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy

Lucie Carrier, Gisèle Bonne, Ellen Bährend et al. · Circulation Research · 1997 · 302 citations

Cardiac Muscle, Cardiomyopathy, Molecular Physiology +15

Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers

Saurabh Kumar, Samuel H. Baldinger, Estelle Gandjbakhch et al. · Journal of the American College of Cardiology · 2016 · 286 citations · Full text

Long-term Arrhythmic, Pathology, Medicine +2