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authFullName_s : Ghazi Besbes

Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity

Nizar Ben Halim , Majdi Nagara , Béatrice Regnault , Sana Hsouna , Khaled Lasram , et al.
Annals of Human Genetics, 2015, 79 (6), pp.402 - 417. ⟨10.1111/ahg.12131⟩
Journal articles pasteur-01375019v1
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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.

Zied Riahi , Crystel Bonnet , Rim Zainine , Saida Lahbib , Yosra Bouyacoub , et al.
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
Journal articles pasteur-01221041v1
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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

Zied Riahi , Crystel Bonnet , Rim Zainine , Malek Louha , Yosra Bouyacoub , et al.
PLoS ONE, 2014, 9 (6), pp.e99797. ⟨10.1371/journal.pone.0099797⟩
Journal articles pasteur-01060192v1

A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.

Zied Riahi , Houda Chahed , Habib Jaafoura , Rim Zainine , Olfa Messaoud , et al.
International Journal of Pediatric Otorhinolaryngology, 2013, 77 (9), pp.1485-8. ⟨10.1016/j.ijporl.2013.06.015⟩
Journal articles pasteur-00861211v1
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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

Rahma Mkaouar , Zied Riahi , Cherine Charfeddine , Imen Chelly , Hela Boudabbous , et al.
PLoS ONE, 2021, 16 (10), pp.e0258202. ⟨10.1371/journal.pone.0258202⟩
Journal articles pasteur-04072687v1

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

Marwa Sayeb , Zied Riahi , Nadia Laroussi , Crystel Bonnet , Lilia Romdhane , et al.
International Journal of Dermatology, 2019, 58 (12), pp.1439-1443. ⟨10.1111/ijd.14452⟩
Journal articles pasteur-03219630v1

Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.

Zied Riahi , Rim Zainine , Yosra Mellouli , Raja Hannachi , Yosra Bouyacoub , et al.
International Journal of Pediatric Otorhinolaryngology, 2013, 77 (9), pp.1481-4. ⟨10.1016/j.ijporl.2013.06.013⟩
Journal articles pasteur-00860772v1

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

Zied Riahi , Hassen Hammami , Houyem Ouragini , Habib Messai , Rim Zainine , et al.
Gene, 2013, 525 (1), pp.1-4. ⟨10.1016/j.gene.2013.04.078⟩
Journal articles pasteur-00861409v1