Author

Wafa Cherif

Observed names: W Cherif, W. Cherif, WAFA CHERIF

Institutions: University of Carthage, Tunis El Manar University

Observed institutions: University of Carthage, Hôpital La Rabta, Institut Pasteur de Tunis, Tunis El Manar University

OpenAlex ID: A5088792756

Consanguinity, endogamy, and genetic disorders in Tunisia

2012 · Nizar Ben Halim, Nissaf Ben Alaya Bouafif, et al. · Journal of Community Genetics · 111

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Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia

2015 · Nizar Ben Halim, Sana Hsouna, et al. · American Journal of Human Biology · 33

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

2011 · Amira Mili, Ilhem Ben Charfeddine, et al. · Journal of Human Genetics · 28

Genetic homogeneity of mutational spectrum of group‐A xeroderma pigmentosum in Tunisian patients

2010 · Olfa Messaoud, Mariem Ben Rekaya, et al. · International Journal of Dermatology · 26

Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis

2007 · E. Barkaoui, W. Cherif, et al. · Journal of Inherited Metabolic Disease · 15

High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia

2012 · Wafa Cherif, Faten Ben Rhouma, et al. · Annales de biologie clinique · 8

Adult gaucher disease in southern Tunisia: report of three cases

2012 · Faten Ben Rhouma, Faten Kallel, et al. · Diagnostic Pathology · 8

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Gaucher disease in Tunisia: High frequency of the most common mutations

2009 · Wafa Cherif, Hadhami Ben Turkia, et al. · Blood Cells Molecules and Diseases · 8

[Phenotype and mutational spectrum in Tunisian pediatric gaucher disease].

2010 · Hadhami Ben Turkia, Imène Riahi, et al. · PubMed · 6

Glycogen storage disease type I in Tunisia: An epidemiological analysis

2008 · A. Ben Chehida, N. Tebib, et al. · Journal of Inherited Metabolic Disease · 6

[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous].

2007 · W Cherif, H Ben Turkia, et al. · PubMed · 6

Dépistage et confirmation des anticorps anti-VHC chez les donneurs de sang tunisiens

1997 · S. Abid, S. Fkih, et al. · Transfusion Clinique et Biologique · 6

History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation

2015 · Faten Ben Rhouma, Habib Messai, et al. · Mitochondrial DNA Part A · 5

Screening of three Mediterranean phenylketonuria mutations in Tunisian families

2012 · SAMEH KHEMIR, HAJER SIALA, et al. · Journal of Genetics · 5

Diagnostic moléculaire de la maladie de Gaucher en Tunisie

2012 · W. Cherif, H. Ben Turkia, et al. · Pathologie Biologie · 4

Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie

2009 · W. Cherif, F. Ben Rhouma, et al. · Pathologie Biologie · 2

Fatty acid profile, nutritional potential and biological activity of green macroalgae from the Northern Tunisian coast

2026 · Wafa Cherif, Leila Ktari, et al. · Frontiers in Marine Science · 1

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826 Molecular Tool in the Diagnosis and Antenatal Diagnosis in Glycogen Storage Disease Type Ia in Tunisian Patients

2010 · E Barkaoui, C Charfeddine, et al. · Pediatric Research

P0201 High Prevalence of R83c Mutation Among Glycogen Storage Disease Type Ia in Tunisian Patients

2004 · E. Berkaoui, N. Tebib, et al. · Journal of Pediatric Gastroenterology and Nutrition

[A human recombinant erythropoietin produced in human lymphoblastoid cells].

1997 · A Bounemra-Ben Ghanem, W Cherif, et al. · PubMed

Works count: 20

Citation count: 278

H-index: 8

I10-index: 5