19 Mar 2026
Using Exome Sequencing to Identify the Causes of Neurodevelopmental Disorders: Experience of a North African Genetic CenterPublisher siteClinical Genetics, Genomics and Rare Diseases
Active, last published 2026
Ilhem
Turki
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 Ilhem Turki will appear here once their profile is updated.
02 · Reach
Publication output and reach
Ilhem's work has been cited 16 times across 4 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 researchFaculté de médecine de Tunis, TunisiaDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
11 works26 Aug 2025Open access
Creation and Validation of the Major Pediatric Mitochondrial Cytopathies Minimum Data Set: Consensus from a Moroccan–Tunisian Delphi StudyPublisher siteChildren, Delphi Technique in Research
15 Jul 2025
A Tunisian POLG mutation expands the clinical spectrum of POLG-related disordersPublisher siteMitochondrion, Mitochondrial Function and Pathology
1 Feb 2025Open access1cites
Subacute Sclerosing Panencephalitis in a North African Cohort: Findings From the Post-Measles Epidemic EraPublisher siteSage Open Pediatrics, Virology and Viral Diseases
26 Nov 2024Open access2cites
Supplementation with nicotinamide limits accelerated aging in affected individuals with cockayne syndrome and restores antioxidant defensesPublisher siteAging, DNA Repair Mechanisms
3 Aug 2024Open access3cites
Clinical and genetic spectrum of Ataxia Telangiectasia Tunisian patients: Bioinformatic analysis unveil mechanisms of ATM variants pathogenicityPublisher siteInternational Journal of Biological Macromolecules, DNA Repair Mechanisms
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
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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