Ketty Schwartz

Overview

Best Publications

• Genotype-Phenotype Correlation in the Long-QT Syndrome Gene-Specific Triggers for Life-Threatening Arrhythmias

  Peter J. Schwartz;Silvia G Priori;Carla Spazzolini;Arthur J Moss

  2168
  Citations

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

  Gisèle Bonne;M R Di Barletta;S Varnous;H M Bécane

  1627
  Citations

• Myoblast transplantation for heart failure.

  Philippe Menasché;Albert A Hagège;Marcio Scorsin;Bruno Pouzet

  1608
  Citations

• Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

  Philippe Menasché;Albert A Hagège;Jean-Thomas Vilquin;Michel Desnos

  1583
  Citations

• Genotype-Phenotype Correlation in the Long-QT Syndrome

  Peter J. Schwartz;Silvia G. Priori;Carla Spazzolini;Arthur J. Moss

  1555
  Citations

• Hypertrophic Cardiomyopathy Distribution of Disease Genes, Spectrum of Mutations, and Implications for a Molecular Diagnosis Strategy

  Pascale Richard;Philippe Charron;Lucie Carrier;Céline Ledeuil

  1395
  Citations

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

  Nathalie Neyroud;Frédérique Tesson;Isabelle Denjoy;Michel Leibovici

  1055
  Citations

• Three myosin heavy-chain isozymes appear sequentially in rat muscle development.

  R G Whalen;S M Sell;G S Butler-Browne;K Schwartz

  779
  Citations

• Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.

  A Helbling-Leclerc;X Zhang;H Topaloglu;C Cruaud

  744
  Citations

• Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

  Muchir A;Bonne G;van der Kooi Aj;van Meegen M

  733
  Citations

• Myosin isoenzyme redistribution in chronic heart overload

  Anne-Marie Lompre;Ketty Schwartz;Anne d'Albis;Gabrielle Lacombe

  709
  Citations

• Altered sarcoplasmic reticulum Ca2(+)-ATPase gene expression in the human ventricle during end-stage heart failure.

  Jean Jacques Mercadier;Anne Marie Lompré;Philippe Duc;Kenneth R. Boheler

  634
  Citations

• Familial Hypertrophic Cardiomyopathy: From Mutations to Functional Defects

  Gisèle Bonne;Lucie Carrier;Pascale Richard;Bernard Hainque

  616
  Citations

• Myosin isoenzyme changes in several models of rat cardiac hypertrophy.

  J J Mercadier;A M Lompré;C Wisnewsky;J L Samuel

  616
  Citations

• Guidelines for the study of familial dilated cardiomyopathies

  L. Mestroni;B. Maisch;W.J. McKenna;K. Schwartz

  594
  Citations

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

  Bonne G;Bercovici J;Cruaud C

  592
  Citations

• Clinical and molecular genetic spectrum of autosomal dominant Emery‐Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

  Bonne G;Mercuri E;Muchir A;Urtizberea A

  570
  Citations

• Apoptosis in pressure overload-induced heart hypertrophy in the rat.

  E Teiger;V D Than;L Richard;C Wisnewsky

  565
  Citations

• Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

  Marina Raffaele di Barletta;Enzo Ricci;Giuliana Galluzzi;Pietro Tonali

  505
  Citations

• KVLQT1 C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome

  Claire Donger;Isabelle Denjoy;Myriam Berthet;Nathalie Neyroud

  500
  Citations