Accueil › Annuaire des chercheurs › Khalid Snoussi

Khalid Snoussi

Affiliation : Université Mohammed VI des Sciences et de la Santé · Hôpital Universitaire International Cheikh Khalifa

• 19Publications (affiliation marocaine)
• 20Publications au total
• 96Citations
• 6Indice h

OpenAlex

Domaines de recherche

• 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
  2026 · Human Genetics
• Retropharyngeal abscess revealing Granulomatosis with polyangiitis GPA (Wegener’s): a case report
  2026 · Journal of Medical Case Reports
• Clinical evaluation of the SmartNav system contribution in cochlear implantation surgery
  2026 · Cochlear Implants International
• Ambulatory pediatric cochlear implantation: safety, efficacy, and feasibility – first multicentric Moroccan study on 681 children
  2025 · BMC Pediatrics · cité 1 fois
• Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
  2025 · Proceedings of the National Academy of Sciences · cité 1 fois
• Spontaneous Retropharyngeal and Cervical Hematoma: A Case Report
  2025 · Clinical Medicine Insights Case Reports · cité 1 fois
• Demographic and Clinical Profile of Cochlear Implant Patients in Morocco
  2025 · Indian Journal of Otolaryngology and Head & Neck Surgery
• CSF gushers in cochlear implantation: surgical planning and management
  2025 · BMC Surgery
• Sinonasal inverted papilloma: a rare case of isolated septal location
  2025 · International Journal of Surgery Open
• A case report of labyrinthine infarction: a ‘central’ cause of vertigo with ‘peripheral’ presentation
  2024 · Annals of Medicine and Surgery · cité 5 fois
• Intra-Parotid Recurrent Nasopharyngeal Carcinoma Following Intensity-Modulated Radiation Therapy: A Case Report
  2024 · Clinical Medicine Insights Case Reports · cité 1 fois
• Novel pathogenic WHRN variant causing hearing loss in a moroccan family
  2023 · Molecular Biology Reports · cité 4 fois
• The Role of Surgery in the Treatment of Cervical Lymph Node Tuberculosis
  2023 · Cureus · cité 3 fois
• Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco
  2022 · Molecular Biology Reports · cité 8 fois
• Melatonin is useful alternative for sedation in children undergoing auditory brainstem responses testing
  2020 · European Journal of Pediatrics · cité 9 fois
• Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
  2019 · Human Heredity · cité 7 fois
• Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
  2017 · International Journal of Pediatric Otorhinolaryngology · cité 20 fois
• A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
  2017 · Human Genome Variation · cité 10 fois
• Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss
  2016 · European Journal of Medical Genetics · cité 26 fois

Revues de publication

• 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 par année

• 20263
• 20256
• 20242
• 20232
• 20221
• 20201
• 20191
• 20172
• 20161

Collaborations

Établissements partenaires : Institut Pasteur du Maroc · University of Hassan II Casablanca · Université Hassan II Mohammedia · Chouaib Doukkali University · Institut Pasteur

Pays des co-auteurs : France

Co-auteurs

• 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

Données bibliographiques issues d’OpenAlex (base ouverte).