Ketty Schwartz
Centre National de la Recherche Scientifique(FR)Inserm(FR)Sorbonne Université(FR)Astrophysique, Instrumentation et Modélisation(FR)Pitié-Salpêtrière Hospital(FR)Centre de Recherche en Myologie
Publications by Year
Research Areas
Cardiomyopathy and Myosin Studies, Cardiac electrophysiology and arrhythmias, Muscle Physiology and Disorders, Cardiovascular Effects of Exercise, Ion channel regulation and function
Most-Cited Works
- → Genotype-Phenotype Correlation in the Long-QT Syndrome(2001)1,739 cited
- → Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy(1999)1,339 cited
- → Hypertrophic Cardiomyopathy(2003)1,272 cited
- → Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction(2003)1,124 cited
- → Myoblast transplantation for heart failure(2001)1,123 cited
- → A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome(1997)881 cited