Dominique Weil

Dominique Weil publication distribution in Genetics in 2026

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

Dominique Weil D-index placement in Genetics in 2026

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

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