Ketty Schwartz

Ketty Schwartz publication distribution in Medicine in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Medicine in 2026. The highlighted bar marks where Ketty Schwartz sits on this spectrum.

Ketty Schwartz D-index placement in Medicine in 2026

The chart shows the D-index (discipline H-index) distribution of Medicine scientists ranked by Research.com in 2026. The highlighted bar marks where Ketty Schwartz sits on this spectrum.

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