8 Dec 2025Open access
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosityPublisher siteProceedings of the National Academy of Sciences, Hearing, Cochlea, Tinnitus, Genetics
Active, last published 2026
Sonia
Abdelhak
Scholar“Research profile drawn from open scholarly records.”
University of Tunis El Manar
Tunisia
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01 · About the work
What I study
research summary for Sonia Abdelhak will appear here once their profile is updated.
02 · Reach
Publication output and reach
Sonia's work has been cited 46 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
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
17 works19 Oct 2025Open access
Precision Medicine of Rare Genetic Diseases in AfricaPublisher site14 Oct 2025Open access
Exome sequencing reveals new insights into the germline landscape of inflammatory breast cancer among Tunisian patientsPublisher siteJournal of Translational Medicine, Breast Cancer Treatment Studies
1 Oct 2024Open access1cites
Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent <scp>POLR3A</scp> Mutation in Six Unrelated Tunisian FamiliesPublisher siteMolecular Genetics & Genomic Medicine, RNA regulation and disease
26 Aug 2024Open access10cites
Genome Tunisia Project: paving the way for precision medicine in North AfricaPublisher siteGenome Medicine, Genomics and Rare Diseases
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
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
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