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Zied Riahi

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
2016 · Crystel Bonnet, Zied Riahi, et al. · European Journal of Human Genetics · 112
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Mutations in CDC14A , Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness
2016 · Sedigheh Delmaghani, Asadollah Aghaie, et al. · The American Journal of Human Genetics · 44
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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss
2013 · Zied Riahi, Hassen Hammami, et al. · Gene · 35
Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness
2014 · Zied Riahi, Crystel Bonnet, et al. · PLoS ONE · 33
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Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients
2015 · Zied Riahi, Crystel Bonnet, et al. · PLoS ONE · 26
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Specific Aspects of Consanguinity: Some Examples from the Tunisian Population
2014 · Lilia Romdhane, Nizar Ben Halim, et al. · Human Heredity · 25
Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province
2018 · Sonia Talbi, Crystel Bonnet, et al. · International Journal of Pediatric Otorhinolaryngology · 23
Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss
2016 · Ely Cheikh Mohamed Moctar, Zied Riahi, et al. · European Archives of Oto-Rhino-Laryngology · 22
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome
2013 · Zied Riahi, Rim Zainine, et al. · International Journal of Pediatric Otorhinolaryngology · 13
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
2017 · Amale Bousfiha, Amina Bakhchane, et al. · Human Genome Variation · 10
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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
2020 · Ghita Amalou, Crystel Bonnet, et al. · International Journal of Pediatric Otorhinolaryngology · 9
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
2020 · Soukaina Elrharchi, Zied Riahi, et al. · Human Heredity · 8
A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene
2019 · Marwa Sayeb, Zied Riahi, et al. · International Journal of Dermatology · 8
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
2019 · Amale Bousfiha, Zied Riahi, et al. · Human Heredity · 7
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family
2018 · Sara Salime, Zied Riahi, et al. · Gene · 7
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
2021 · Rahma Mkaouar, Zied Riahi, et al. · PLoS ONE · 6
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Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome
2018 · Soukaina Elrharchi, Zied Riahi, et al. · International Journal of Pediatric Otorhinolaryngology · 6
A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family
2014 · MAJDI NAGARA, KONSTANTINOS VOSKARIDES, et al. · Journal of Genetics · 4
A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families
2013 · Zied Riahi, Houda Chahed, et al. · International Journal of Pediatric Otorhinolaryngology · 3
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
2025 · Zied Riahi, Sophie Boucher, et al. · Proceedings of the National Academy of Sciences · 1
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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
2024 · Rahma Mkaouar, Zied Riahi, et al. · Frontiers in Genetics · 1
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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
2024 · Rahma Mkaouar, Zied Riahi, et al. · Frontiers in Genetics · 1
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Contents Vol. 77, 2014
2014 · Joël Zlotogora, Stavit A. Shalev, et al. · Human Heredity · 1
Nouvelle mutation du gène GJB2 (c.405delC) responsable de surdité autosomique récessive découverte chez deux familles tunisiennes
2014 · R. Zainine, Z. Riahi, et al. · Annales françaises d Oto-rhino-laryngologie et de Pathologie Cervico-faciale
Syndrome de Waardenburg : une cause non rare de surdité chez l’enfant
2014 · J. Marrakchi, R. Zainine, et al. · Annales françaises d Oto-rhino-laryngologie et de Pathologie Cervico-faciale
Works count: 29
Citation count: 405
H-index: 10
I10-index: 10
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