19 Oct 2025Open access
Precision Medicine of Rare Genetic Diseases in AfricaPublisher siteUniversitiesNessrine Mezzi
Active, last published 2026
In genomics and rare diseases
Nessrine
Mezzi
Scholar“Research focused on Genomics and Rare Diseases and adjacent fields.”
Tunis University
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01 · About the work
What I study
essrine Mezzi is a researcher working on Genomics and Rare Diseases. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Nessrine's work has been cited 106 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Genomics and Rare Diseases×6Genomic variations and chromosomal abnormalities×5Hearing, Cochlea, Tinnitus, Genetics×2Hemoglobinopathies and Related Disorders×2
04 · Where I am
Affiliations
Affiliation on published researchTunis UniversityDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
7 works25 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
12 May 2024Open access2cites
Consanguinité et son impact sur la santé et la dynamique du génome : Un exemple de la TunisiePublisher siteLa Tunisie Médicale, Hemoglobinopathies and Related Disorders
22 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
26 Feb 2024Open access3cites
Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticityPublisher siteScientific Reports, Genomic variations and chromosomal abnormalities
3 Jan 2024
Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome SequencingPublisher siteGene, Lipid metabolism and biosynthesis
11 Feb 2022Open access4cites
African Genomic Medicine Portal: A Web Portal for Biomedical ApplicationsPublisher siteJournal of Personalized Medicine, Genetics, Bioinformatics, and Biomedical Research
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