Dominique Weil

Overview

Best Publications

• Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

  Françoise Denoyelle;Dominique Weil;Marion A. Maw;Stephen A. Wilcox

  844
  Citations

• A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

  Abdelhak S;Kalatzis;Heilig R;Compain S

  707
  Citations

• P-Body Purification Reveals the Condensation of Repressed mRNA Regulons

  Arnaud Hubstenberger;Arnaud Hubstenberger;Maïté Courel;Marianne Bénard;Sylvie Souquere

  681
  Citations

• Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

  Francoise Denoyelle;Sandrine Marlin;Dominique Weil;Lucien Moatti

  581
  Citations

• The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.

  Dominique Weil;Polonca Küssel;Stéphane Blanchard;Gallia Lévy

  492
  Citations

• SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.

  Rainer G. Ruf;Pin-Xian Xu;Derek Silvius;Edgar A. Otto

  488
  Citations

• A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

  F. J. Del Castillo;M. Rodriguez-Ballesteros;A. Alvarez;T. Hutchin

  432
  Citations

• Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

  Sedigheh Delmaghani;Francisco J del Castillo;Vincent Michel;Michel Leibovici

  413
  Citations

• Connexin 26 gene linked to a dominant deafness

  Françoise Denoyelle;Genevieve Lina-Granade;Henri Plauchu;Roberto Bruzzone

  392
  Citations

• Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

  Dominique Weil;Aziz El-Amraoui;Saber Masmoudi;Mirna Mustapha

  391
  Citations

• Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

  Philomena Mburu;Mirna Mustapha;Anabel Varela;Dominique Weil

  375
  Citations

• A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth

  Gaelle Lefèvre;Vincent Michel;Dominique Weil;Léa Lepelletier

  287
  Citations

• Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

  Sonia Abdelhak;Vasiliki Kalatzis;Roland Heilig;Sylvie Compain

  281
  Citations

• Interactions in the network of Usher syndrome type 1 proteins

  Avital Adato;Vincent Michel;Yoshiaki Kikkawa;Jan Reiners

  274
  Citations

• Translationally Repressed mRNA Transiently Cycles through Stress Granules during Stress

  Stephanie Mollet;Nicolas Cougot;Ania Wilczynska;François Dautry

  269
  Citations

• An α-Tectorin Gene Defect Causes a Newly Identified Autosomal Recessive Form of Sensorineural Pre-Lingual Non-Syndromic Deafness, DFNB21

  Mirna Mustapha;Dominique Weil;Sébastien Chardenoux;Sanaa Elias

  254
  Citations

• Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome

  Bethan E. Hoskins;Carl H. Cramer;Derek Silvius;Dan Zou

  246
  Citations

• Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning

  Nicolas Michalski;Vincent Michel;Amel Bahloul;Gaëlle Lefèvre

  240
  Citations

• Unravelling the ultrastructure of stress granules and associated P-bodies in human cells

  Sylvie Souquere;Stéphanie Mollet;Michel Kress;François Dautry

  233
  Citations

• P-Bodies: Cytosolic Droplets for Coordinated mRNA Storage.

  Nancy Standart;Dominique Weil

  218
  Citations