Ketty Schwartz

Genotype-Phenotype Correlation in the Long-QT Syndrome

Peter J. Schwartz, Silvia G. Priori, Carla Spazzolini et al. · Circulation · 2001 · 1.7K citations

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

Hypertrophic Cardiomyopathy

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

Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

Philippe Menasché, Albert Hagège, Jean‐Thomas Vilquin et al. · Journal of the American College of Cardiology · 2003 · 1.1K citations

Regenerative Medicine, Cardiomyopathy, Heart Failure +6

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