Gisèle Bonne

Overview

Best Publications

• 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

• 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

• "Laminopathies": a wide spectrum of human diseases.

  Howard J. Worman;Gisèle Bonne;Gisèle Bonne

  710
  Citations

• Nuclear lamins: laminopathies and their role in premature ageing

  J. L. V. Broers;F. C. S. Ramaekers;G. Bonne;R. Ben Yaou

  652
  Citations

• Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C

  Giuseppe Novelli;Antoine Muchir;Federica Sangiuolo;Anne Helbling-Leclerc

  628
  Citations

• Familial Hypertrophic Cardiomyopathy: From Mutations to Functional Defects

  Gisèle Bonne;Lucie Carrier;Pascale Richard;Bernard Hainque

  616
  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

• Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

  Jop H. van Berlo;Willem G. de Voogt;Anneke J. van der Kooi;J. Peter van Tintelen

  504
  Citations

• Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

  Takuro Arimura;Anne Helbling-Leclerc;Catherine Massart;Shaida Varnous

  433
  Citations

• 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

  G Bonne;E Bährend;B Yu

  404
  Citations

• Primary prevention of sudden death in patients with lamin A/C gene mutations

  Christophe Meune;Jop H. Van Berlo;Frédéric Anselme;Gisèle Bonne

  404
  Citations

• Clinical Features and Prognostic Implications of Familial Hypertrophic Cardiomyopathy Related to the Cardiac Myosin-Binding Protein C Gene

  P Charron;O Dubourg;M Desnos;M Bennaceur

  363
  Citations

• The Ig-like Structure of the C-Terminal Domain of Lamin A/C, Mutated in Muscular Dystrophies, Cardiomyopathy, and Partial Lipodystrophy

  Isabelle Krimm;Cecilia Östlund;Bernard Gilquin;Joël Couprie

  335
  Citations

• Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy

  Antoine Muchir;Paul Pavlidis;Valérie Decostre;Alan J. Herron

  321
  Citations

• De Novo LMNA Mutations Cause a New Form of Congenital Muscular Dystrophy

  Susana Quijano-Roy;Blaise Mbieleu;Carsten G. Bönnemann;Pierre Yves Jeannet

  294
  Citations

• Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy

  Cecilia Östlund;Gisèle Bonne;Ketty Schwartz;Howard J. Worman

  291
  Citations

• High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation.

  Henri‐Marc Bécane;Gisèle Bonne;Shaida Varnous;Antoine Muchir

  277
  Citations

• Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

  Lucie Gueneau;Lucie Gueneau;Anne T. Bertrand;Anne T. Bertrand;Jean-Philippe Jais;Mustafa A. Salih

  253
  Citations

• LMNA mutations in atypical Werner's syndrome [5] (multiple letters)

  C. Vigouroux;F. Caux;J. Capeau;S. Christin-Maitre

  27
  Citations