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Bouchaïb Gazzaz

Observed names: B. Gazzaz, Bouchaib Gazzaz, Gazzaz Bouchaib, Gazzaz, Bouchaïb
ORCID: 0000-0001-6102-2148
Observed ORCID: 0000-0001-6102-2148
OpenAlex ID: A5075742270
Autosomal recessive and sporadic deafness in Morocco: High frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant
2005 · Bouchaïb Gazzaz, Dominique Weil, et al. · Hearing Research · 37
Assessment of phylogenetic structure of Berber-speaking population of Azrou using 15 STRs of Identifiler kit
2009 · Hicham El Ossmani, Brahim Bouchrif, et al. · Legal Medicine · 19
Novel FREM1 homozygous variant in an individual with an intermediate phenotype between Bifid Nose with or without Anorectal and Renal Anomalies and Manitoba-oculo-tricho-anal syndromes
2022 · Sarah Berrada, Amal Tazzite, et al. · Clinical Dysmorphology · 5
The impact of ABCB1 gene polymorphism (C3435T) and its expression on response to Donepezil in Moroccan patients with Alzheimer's disease
2021 · Sara Ben Halla, Amal Tazzite, et al. · Gene Reports · 5
Involvement of APOE polymorphism in Alzheimer's disease susceptibility and Donepezil response in Moroccan patients
2022 · Sara Ben Halla, Amal Tazzite, et al. · Gene Reports · 3
R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report
2022 · Wafaa Bouzroud, Amal Tazzite, et al. · Clinical Pathology · 3
Anthropogenetic study of the Arabic - speaking population of Chaouia Ouardigha (Morocco) based on autosomal STRs
2024 · Othmane Essoubaiy, Bouchaïb Gazzaz, et al. · Egyptian Journal of Forensic Sciences · 2
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Complement Factor I deficiency: A novel homozygous CFI gene mutation
2022 · Wafaa Bouzroud, Amal Tazzite, et al. · SAGE Open Medical Case Reports · 2
Genetic structure of Moroccan population using 15 STRs of NGM kit
2011 · H. El Amri, D. Squalli, et al. · Forensic science international. Genetics supplement series · 2
Phelan-Mcdermid syndrome: three case reports and a literature review
2024 · Berrada Sarah, Tazzite Amal, et al. · European Journal of Medical Case Reports · 1
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A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report
2023 · Wafaa Bouzroud, Amal Tazzite, et al. · Journal of International Medical Research · 1
Tuberous Sclerosis Complex: Clinical Case Presentation and Literature Review
2022 · Wafaa Bouzroud, Amal Tazzite, et al. · (IJRE) International Journal of Research and Ethics · 1
Globoid cell leukodystrophy: case report and literature review
2022 · Fatima Zahra Outtaleb, Amal Tazzite, et al. · Endocrine Abstracts · 1
Severe sepsis and genetic predisposition: systematic review
2026 · Hanane Ezzouine, Wafaa Bouzroud, et al. · Egyptian Journal of Medical Human Genetics
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Additional file 3 of Severe sepsis and genetic predisposition: systematic review
2026 · Ezzouine, Hanane, Bouzroud, Wafaa, et al. · Figshare
Severe sepsis and genetic predisposition: systematic review
2026 · Ezzouine, Hanane, Bouzroud, Wafaa, et al. · Figshare
Additional file 4 of Severe sepsis and genetic predisposition: systematic review
2026 · Ezzouine, Hanane, Bouzroud, Wafaa, et al. · Figshare
Additional file 1 of Severe sepsis and genetic predisposition: systematic review
2026 · Ezzouine, Hanane, Bouzroud, Wafaa, et al. · Figshare
Additional file 2 of Severe sepsis and genetic predisposition: systematic review
2026 · Ezzouine, Hanane, Bouzroud, Wafaa, et al. · Figshare
Two adult Moroccan women with phenotypes suggestive of TRRAPrelated neurodevelopmental disorder carrying TRRAP variants of uncertain significance: a case report of two patients
2026 · Fakir Zineb, Bouzroud Wafaa, et al. · European Journal of Medical Case Reports
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Next-generation technology in epilepsy diagnostic: First Moroccan pediatric case series and literature review.
2024 · Wafaa Bouzroud, Amal Tazzite, et al. · (IJRE) International Journal of Research and Ethics
Fanconi anemia diagnosed by genetic testing
2024 · Fatima Maarouf, Amal Tazzite, et al. · (IJRE) International Journal of Research and Ethics
Epilepsy in a Moroccan patient with Pitt-Hopkins syndrome
2024 · Fatima Maarouf, Amal Tazzite, et al. · (IJRE) International Journal of Research and Ethics
A novel variant of ATRX gene is potentially associated with alpha-thalassemia X-linked intellectual disability syndrome: Case report and literature review
2024 · Berrada Sarah, Tazzite Amal, et al. · SAGE Open Medical Case Reports
Terminal deletion of 18q: A case report
2023 · Yousra Ibenbrahim, Wafaa Bouzroud, et al. · (IJRE) International Journal of Research and Ethics
Works count: 35
Citation count: 82
H-index: 4
I10-index: 2
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