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authFullName_s : Ahmed Houmeida

Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness

Malak Salame , Crystel Bonnet , Ely Cheikh Mohamed Moctar , Selma Mohamed Brahim , Abdallahi Dedy , et al.
European Archives of Oto-Rhino-Laryngology, 2023, ⟨10.1007/s00405-023-07907-z⟩
Journal articles pasteur-04053511v1
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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 , Hala El Hachmi , Crystel Bonnet , et al.
American Journal of Human Genetics, 2016, 98 (6), pp.1266 - 1270. ⟨10.1016/j.ajhg.2016.04.015⟩
Journal articles hal-01329650v1
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A novel missense mutation of GJA8 causes congenital cataract in a large Mauritanian family

Mouna Hadrami , Crystel Bonnet , Fatimetou Veten , Christina Zeitz , Christel Condroyer , et al.
European Journal of Ophthalmology, 2019, 29 (6), pp.621-628. ⟨10.1177/1120672118804757⟩
Journal articles hal-01990091v1
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Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma.

Mouna Hadrami , Crystel Bonnet , Christina Zeitz , Fatimetou Veten , Med Biya , et al.
Molecular Vision, 2021, 25, pp.373-381
Journal articles pasteur-03219621v1
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Screening of BRCA1/2 variants in Mauritanian breast cancer patients

Selma Mohamed Brahim , Ekht Elbenina Zein , Crystel Bonnet , Cheikh Tijani Hamed , Malak Salame , et al.
BMC Cancer, 2022, 22 (1), pp.802. ⟨10.1186/s12885-022-09903-8⟩
Journal articles pasteur-04072696v1

Characteristics of Helicobacter pylori strains isolated from Mauritanian patients

Fatimetou Khiddi , Mohamed Val Mohamed Abdellahi , Mohamed Abdallah Horma , Annick Billoet , Ghislaine Collobert , et al.
Helicobacter, 2020, 25, ⟨10.1111/hel.12726⟩
Journal articles pasteur-03264978v1