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Khalid Snoussi
Affiliation : Université Mohammed VI des Sciences et de la Santé · Hôpital Universitaire International Cheikh Khalifa
- 19Publications (affiliation in Morocco)
- 20Total publications
- 96Citations
- 6h-index
Research profile
Khalid Snoussi has 19 indexed publications (2016–2026). Their work appears mainly in “Clinical Medicine Insights Case Reports”, “Molecular Biology Reports” and “Human Genetics”. Their most cited article, “Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss” (2016), has been cited 26 times. 11 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France.
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Create my free profile Add my publicationsResearch areas
- Hearing, Cochlea, Tinnitus, Genetics
- Hearing Loss and Rehabilitation
- Congenital Ear and Nasal Anomalies
- Ear Surgery and Otitis Media
- Hearing Impairment and Communication
Publications (19)
- Genetic diversity of Usher syndrome in Moroccan patients
- Retropharyngeal abscess revealing Granulomatosis with polyangiitis GPA (Wegener’s): a case report
- Clinical evaluation of the SmartNav system contribution in cochlear implantation surgery
- Ambulatory pediatric cochlear implantation: safety, efficacy, and feasibility – first multicentric Moroccan study on 681 children
- Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
- Spontaneous Retropharyngeal and Cervical Hematoma: A Case Report
- Demographic and Clinical Profile of Cochlear Implant Patients in Morocco
- CSF gushers in cochlear implantation: surgical planning and management
- Sinonasal inverted papilloma: a rare case of isolated septal location
- A case report of labyrinthine infarction: a ‘central’ cause of vertigo with ‘peripheral’ presentation
- Intra-Parotid Recurrent Nasopharyngeal Carcinoma Following Intensity-Modulated Radiation Therapy: A Case Report
- Novel pathogenic WHRN variant causing hearing loss in a moroccan family
- The Role of Surgery in the Treatment of Cervical Lymph Node Tuberculosis
- Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco
- Melatonin is useful alternative for sedation in children undergoing auditory brainstem responses testing
- Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
- Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
- A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
- Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss
Publication venues
- Clinical Medicine Insights Case Reports × 2
- Molecular Biology Reports × 2
- Human Genetics × 1
- Journal of Medical Case Reports × 1
- Cochlear Implants International × 1
- BMC Pediatrics × 1
Publications per year
- 20263
- 20256
- 20242
- 20232
- 20221
- 20201
- 20191
- 20172
- 20161
Collaborations
Partner institutions : Institut Pasteur du Maroc · University of Hassan II Casablanca · Université Hassan II Mohammedia · Chouaib Doukkali University · Institut Pasteur
Co-authors’ countries : France
Co-authors
- Amal Hajjij
- Abdelhamid Barakat
- Saïd Anajar
- Mustapha Essaadi
- Hicham Charoute
- Amale Bousfiha
- Amina Bakhchane
- Safa Darouich
- Hassan Rouba
- Ghita Amalou
- Khadija El Bouhmadi
- Loubna Taali
Bibliographic data from OpenAlex (open database).
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