Zied Riahi

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet, Zied Riahi, Sandra Chantot‐Bastaraud et al. · European Journal of Human Genetics · 2016 · 106 citations · Full text

Mutations in CDC14A , Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness

Sedigheh Delmaghani, Asadollah Aghaie, Yosra Bouyacoub et al. · The American Journal of Human Genetics · 2016 · 46 citations · Full text

Signal Transduction, Developmental Biology, Mendelian Disorder +9

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss

Zied Riahi, H. Hammami, Houyem Ouragini et al. · Gene · 2013 · 35 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

Zied Riahi, Crystel Bonnet, Rim Zaïnine et al. · PLoS ONE · 2014 · 34 citations · Full text

Engineering, Genetics, Genetic Epidemiology +17

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

Zied Riahi, Crystel Bonnet, Rim Zaïnine et al. · PLoS ONE · 2015 · 24 citations · Full text

Genetics, Genetic Epidemiology, Molecular Genetics +21