Ridha Mrad
Tunis, 1002, Tunisia
Last Updated: 09/26/2026
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Found 50 publications
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 08, 2025
First Detection of 1p36 Deletion by Whole-Exome Sequencing in a Tunisian Patient.
Journal: Birth defects research
Published: September 19, 2025
Renal survival in hereditary urolithiasis: a monocentric cohort study from a Tunisian nephrology department.
Journal: The Pan African medical journal
Published: August 30, 2024
Interstitial 11q deletion in a patient with Sprengel's deformity: a case report and review of the literature.
Journal: Molecular cytogenetics
Published: August 08, 2024
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Journal: Frontiers in genetics
Published: May 23, 2024
Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy.
Journal: Molecular genetics & genomic medicine
Published: April 22, 2024
Genetic testing for hereditary cancer syndromes in Tunisian patients: Impact on health system.
Journal: Translational oncology
Published: December 12, 2023
Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome Sequencing.
Journal: Gene
Published: October 31, 2023
Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia.
Journal: La Tunisie medicale
Published: June 20, 2023
Last Updated: 09/26/2026