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authFullName_s : Hicham Charoute

X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations

Zahra Aadam , Nadia Kechout , Abdelhamid Barakat , Koon-Wing Chan , Meriem Ben-Ali , et al.
Journal of Clinical Immunology, 2016, 36 (3), pp.187-194. ⟨10.1007/s10875-016-0251-z⟩
Journal articles pasteur-01374987v1
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Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies

Aymane Bouzidi , Hicham Charoute , Majida Charif , Ghita Amalou , Mostafa Kandil , et al.
Orphanet Journal of Rare Diseases, 2022, 17 (1), pp.197. ⟨10.1186/s13023-022-02340-7⟩
Journal articles hal-03861095v1

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family

Soukaina Elrharchi , Zied Riahi , Sara Salime , Hicham Charoute , Lamiae Elkhattabi , et al.
Human Heredity, 2021, 85 (1), pp.35-39. ⟨10.1159/000512712⟩
Journal articles pasteur-03219602v1

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family

Sara Salime , Zied Riahi , Soukaina Elrharchi , Lamiae Elkhattabi , Hicham Charoute , et al.
Gene, 2018, 659, pp.89-92. ⟨10.1016/j.gene.2018.03.042⟩
Journal articles pasteur-03219641v1

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD

Yassine Naasse , Amina Bakhchane , Hicham Charoute , Farida Jennane , Joelle Bignon-Topalovic , et al.
Sexual Development, 2017, 11 (5-6), pp.269-274. ⟨10.1159/000485393⟩
Journal articles pasteur-03521891v1

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco

Imane Aitraise , Ghita Amalou , Amale Bousfiha , Hicham Charoute , Hassan Rouba , et al.
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Journal articles pasteur-03985530v1

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

Houda Benrahma , Hicham Charoute , Khaled Lasram , Redouane Boulouiz , Rym Kefi-Ben Atig , et al.
Biochemical Genetics, 2014, 52 (9-10), pp.430-42. ⟨10.1007/s10528-014-9658-5⟩
Journal articles pasteur-01375062v1

Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population.

Imane Morjane , Rym Kefi , Hicham Charoute , Fouzia Lakbakbi El Yaagoubi , Meryem Hechmi , et al.
Diabetes & Metabolic Syndrome: Clinical Research & Reviews, 2017, 11 (supplement 2), pp.S853-S857. ⟨10.1016/j.dsx.2017.07.005⟩
Journal articles hal-01571303v1
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A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

Amale Bousfiha , Amina Bakhchane , Hicham Charoute , Zied Riahi , Khalid Snoussi , et al.
Human Genome Variation, 2017, 4 (1), pp.17009. ⟨10.1038/hgv.2017.9⟩
Journal articles pasteur-03219646v1

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness

Amale Bousfiha , Zied Riahi , Lamiae Elkhattabi , Amina Bakhchane , Hicham Charoute , et al.
Human Heredity, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Journal articles pasteur-03219615v1

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population

Hicham Charoute , Rym Kefi , Safaa Bounaceur , Houda Benrahma , Ahmed Reguig , et al.
Mitochondrial DNA Part A, 2017, 29 (1), pp.9-13. ⟨10.1080/24701394.2016.1233530⟩
Journal articles pasteur-01966344v1

A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability

Al Mehdi Krami , Aymane Bouzidi , Majida Charif , Ghita Amalou , Hicham Charoute , et al.
European Journal of Medical Genetics, 2022, 65 (6), pp.104515. ⟨10.1016/j.ejmg.2022.104515⟩
Journal articles hal-03861096v1