Hammadi Ayadi

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 · 636 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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 · 427 citations

Life Sciences, Genetics, Molecular Genetics +13

Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases

Ghazi Chabchoub, Elif Uz, Abdellatif Maalej et al. · Arthritis Research & Therapy · 2009 · 125 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

Avital Adato, Dominique Weil, Hagar Kalinski et al. · The American Journal of Human Genetics · 1997 · 116 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice

K. Saidas Nair, Mounira Hmani‐Aifa, Zain Ali et al. · Nature Genetics · 2011 · 111 citations

Medicine, Molecular Biology, Ophthalmology +9