Dominique Weil

P-Body Purification Reveals the Condensation of Repressed mRNA Regulons

Arnaud Hubstenberger, Maïté Courel, Marianne Bénard et al. · Molecular Cell · 2017 · 773 citations · Full text

Transcriptional Regulation, Protein Expression, P-body Purification +5

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

Sonia Abdelhak, Vasiliki Kalatzis, Roland Heilig et al. · Nature Genetics · 1997 · 678 citations

Biology, Developmental Biology, Novel Gene Family +9

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

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 635 citations · Full text

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

Françoise Denoyelle, Sandrine Marlin, Dominique Weil et al. · The Lancet · 1999 · 437 citations

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +10

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 et al. · Nature Genetics · 1997 · 423 citations

Allelic Defects, Mendelian Disorder, Myosin-viia Gene +8