Françoise Gary

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Gisèle Bonne, Marina Raffaele di Barletta, Shaïda Varnous et al. · Nature Genetics · 1999 · 1.3K citations

Mendelian Disorder, Genetic Disorder, Genetics +3

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy et al. · Nature Genetics · 1997 · 881 citations

Novel Mutation, Channelopathies, Cardiomyopathy +10

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

Eric Villard, Claire Perret, Françoise Gary et al. · European Heart Journal · 2011 · 347 citations · Full text

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

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy

Benjamin Meder, Frank Rühle, Tanja Weis et al. · European Heart Journal · 2013 · 171 citations · Full text