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Wafa Cherif
Affiliation : University of Carthage · Tunis El Manar University
- 18Publications (affiliation in Tunisia)
- 23Total publications
- 270Citations
- 8h-index
Research profile
Wafa Cherif has 18 indexed publications (2004–2026). Their work appears mainly in “Pathologie Biologie”, “Journal of Inherited Metabolic Disease” and “Journal of Pediatric Gastroenterology and Nutrition”. Their most cited article, “Consanguinity, endogamy, and genetic disorders in Tunisia” (2012), has been cited 107 times. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Metabolism and Genetic Disorders
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Publications (18)
- Fatty acid profile, nutritional potential and biological activity of green macroalgae from the Northern Tunisian coast
- Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia
- History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation
- Consanguinity, endogamy, and genetic disorders in Tunisia
- High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia
- Adult gaucher disease in southern Tunisia: report of three cases
- Screening of three Mediterranean phenylketonuria mutations in Tunisian families
- Diagnostic moléculaire de la maladie de Gaucher en Tunisie
- Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III
- Genetic homogeneity of mutational spectrum of group‐A xeroderma pigmentosum in Tunisian patients
- 826 Molecular Tool in the Diagnosis and Antenatal Diagnosis in Glycogen Storage Disease Type Ia in Tunisian Patients
- Gaucher disease in Tunisia: High frequency of the most common mutations
- Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
- Glycogen storage disease type I in Tunisia: An epidemiological analysis
- Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis
- [Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous].
- P0201 HIGH PREVALENCE OF R83C MUTATION AMONG GLYCOGEN STORAGE DISEASE TYPE IA IN TUNISIAN PATIENTS
- P0201 HIGH PREVALENCE OF R83C MUTATION AMONG GLYCOGEN STORAGE DISEASE TYPE IA IN TUNISIAN PATIENTS
Publication venues
- Pathologie Biologie × 2
- Journal of Inherited Metabolic Disease × 2
- Journal of Pediatric Gastroenterology and Nutrition × 2
- Frontiers in Marine Science × 1
- American Journal of Human Biology × 1
- Mitochondrial DNA Part A × 1
Publications per year
- 20261
- 20152
- 20125
- 20111
- 20102
- 20092
- 20081
- 20072
- 20042
Collaborations
Partner institutions : Institut Pasteur de Tunis · Hôpital La Rabta · Hôpital Farhat Hached · Tunis University · Faculté de médecine de Tunis
Co-authors
- Néji Tebib
- Sonia Abdelhak
- Faten Ben Rhouma
- Rym Kéfi
- M. F. Ben Dridi
- Marie‐Françoise Ben Dridi
- Naziha Kaabachi
- Hatem Azzouz
- Jalel Chemli
- Hadhami Ben Turkia
- Chérine Charfeddine
- Habib Messai
Bibliographic data from OpenAlex (open database).
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