19 Apr 2026
Clinical and molecular spectrum of primary hyperoxaluria type 1 in Tunisia: pediatric presentation and minimum observed prevalencePublisher sitePediatric Nephrology, Kidney Stones and Urolithiasis Treatments
Active, last published 2026
Ridha
Mrad
Scholar“Research profile drawn from open scholarly records.”
University of Tunis El Manar
Tunisia
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UPGRADE
01 · About the work
What I study
research summary for Ridha Mrad will appear here once their profile is updated.
02 · Reach
Publication output and reach
Ridha's work has been cited 27 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 researchTunis El Manar University, TunisiaDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
19 works8 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
24 Jul 2025
Broad Clinical Spectrum of Mosaic Trisomy 2: Report of Two New Cases in TunisiaPublisher siteFetal and Pediatric Pathology, Prenatal Screening and Diagnostics
1 Jan 2025
Pharmacoepigenetics of autism spectrum disorderPublisher siteElsevier eBooks, Autism Spectrum Disorder Research
3 Dec 2024Open access
Interstitial 11q deletion in a patient with Sprengel’s deformity: a case report and review of the literaturePublisher siteMolecular Cytogenetics, Genomic variations and chromosomal abnormalities
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
1 Jun 2024Open access3cites
Homozygous <i>TNNI3</i> frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathyPublisher siteMolecular Genetics & Genomic Medicine, Cardiomyopathy and Myosin Studies
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