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Hamza Chouk
Affiliation : University of Monastir · Hôpital Farhat Hached · University of Sousse
- 19Publications (affiliation in Tunisia)
- 26Total publications
- 49Citations
- 4h-index
Research profile
Hamza Chouk has 19 indexed publications (2019–2026). Their work appears mainly in “Research Square”, “Annales de Dermatologie et de Vénéréologie” and “Journal of Community Genetics”. Their most cited article, “Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC” (2021), has been cited 19 times. 5 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in South Africa, France, Germany.
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Create my free profile Add my publicationsResearch areas
- Genetic and rare skin diseases.
- Genomics and Rare Diseases
- Histiocytic Disorders and Treatments
- Skin and Cellular Biology Research
- Immunodeficiency and Autoimmune Disorders
Publications (19)
- Retrospective analysis of spinal muscular atrophy in tunisian population: phenotypic-genotypic associations and considerations for therapeutic advancement
- 1st Congress of the Tunisian Society of Human Genomics October 17–18 & 19, 2024, Sousse, Tunisia Genomics for a sustainable healthcare system
- Socio-genomics of intellectual disability in African populations: top research-producing countries
- Is Tunisia ready for precision medicine? Challenges of medical genomics within a LMIC healthcare system
- Honey-based therapeutics: a comprehensive review of anticancer, antioxidant, and prognostic impacts in breast cancer treatment
- Molecular characterization of Porokeratosis in Tunisian patients with intraindividual and intrafamilial clinical heterogeneity
- X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
- Unusual facial lesions in H syndrome
- X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
- X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
- 213 Genetic study of the largest Tunisian cohort of 15 patients with Netherton syndrome: Two new SPINK5 mutations and founder effect
- Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene
- Les manifestations systémiques et auto-immunes au cours du syndrome H : une série de 13 cas
- Phenotypic intrafamilial variability including H syndrome and Rosai Dorfman Disease associated with the same c.1088G>A mutation in the SLC29A3 gene.
- Phenotypic Intrafamilial Variability Including H Syndrome and Rosai Dorfman Disease Associated With the Same c.1088G>A mutation in the SLC29A3 gene.
- Syndrome de Netherton : une série de 14 patients tunisiens porteurs de 4 nouvelles mutations du gène SPINK5
- Ichtyose récessive liée à l’X : nouvelle mutation fondatrice tunisienne
- Variabilité phénotypique intrafamiliale du gène SLC29A3 : cas d’une famille tunisienne
- Étude génétique de la porokératose chez 2 familles tunisiennes
Publication venues
- Research Square × 5
- Annales de Dermatologie et de Vénéréologie × 4
- Journal of Community Genetics × 3
- Neurogenetics × 1
- Journal of Cancer Prevention & Current Research × 1
- BMC Medical Genomics × 1
Publications per year
- 20263
- 20242
- 20231
- 20225
- 20214
- 20202
- 20192
Collaborations
Partner institutions : University of Sfax · Hopital Universitaire Hedi Chaker · Institut Pasteur de Tunis · Manouba University · Tunis University
Co-authors’ countries : South Africa · France · Germany
Co-authors
- Dorra Hmida
- Haïfa El Mabrouk
- Mohamed DENGUEZLI
- Ayda Bennour
- Lobna BOUSSOFARA
- Ali Saad
- Nadia Fetoui Ghariani
- A. Saad
- Rima Gammoudi
- Najet Ghariani
- Ali Saâd
- Walid Sabri Hamadou
Bibliographic data from OpenAlex (open database).
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