Mariem Ben Saïd

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Denise Yan, Demet Tekin, Güney Bademci et al. · Human Genetics · 2016 · 136 citations · Full text

Allelic Variant, Multiple Continents, Mendelian Disorder +12

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

M’hamed Grati, Imen Chakchouk, Qi Ma et al. · Human Molecular Genetics · 2015 · 97 citations · Full text

Genetics, Cytoskeleton, Disease Gene Identification +20

<i>TMC1</i> but Not <i>TMC2</i> Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families

Abdelaziz Tlili, Imen Ben Rebeh, Mounira Hmani‐Aifa et al. · Audiology and Neurotology · 2008 · 59 citations

High Frequency of the p.R34X Mutation in the <i>TMC1</i> Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects

Mariem Ben Saïd, Mounira Hmani‐Aifa, Imen Amar et al. · Genetic Testing and Molecular Biomarkers · 2010 · 44 citations

P.r34x Mutation, Mendelian Disorder, Tmc1 P.r34x Mutation +15

Screening of the <i>DFNB3</i> Locus: Identification of Three Novel Mutations of <i>MYO15A</i> Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus

Hanen Belguith, Mounira Hmani‐Aifa, Houria Dhouib et al. · Genetic Testing and Molecular Biomarkers · 2009 · 40 citations

Genetics, Pathology, Molecular Genetics +19