25 Jun 2024Open access1cites
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthPublisher siteFrontiers in Genetics, Hearing, Cochlea, Tinnitus, Genetics
Active, last published 2026
In dna repair mechanisms
Mariem
Chargui
Scholar“Research focused on DNA Repair Mechanisms and adjacent fields.”
University of Tunis El Manar
Tunisia
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01 · About the work
What I study
ariem Chargui is a researcher working on DNA Repair Mechanisms. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Mariem's work has been cited 308 times across 2 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
DNA Repair Mechanisms×4Genetic Associations and Epidemiology×4Hearing, Cochlea, Tinnitus, Genetics×3Nutrition, Genetics, and Disease×3Adipokines, Inflammation, and Metabolic Diseases×2
04 · Where I am
Affiliations
Affiliation on published researchInstitut Pasteur de Tunis, TunisiaDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
3 works22 Apr 2024Open access1cites
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthPublisher siteFrontiers in Genetics, Hearing, Cochlea, Tinnitus, Genetics
22 Feb 2023Open access3cites
First genetic characterization of <i>Xeroderma pigmentosum</i> in Libya: High frequency of XP‐C founder mutationPublisher siteMolecular Genetics & Genomic Medicine, DNA Repair Mechanisms
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