Olfa Messaoud

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 43 publications

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

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

Novel and Extremely Sensitive NiAl2O4-NiO Nanostructures on an ITO Sensing Electrode for Enhanced Detection of Ascorbic Acid.

Novel and Extremely Sensitive NiAl2O4-NiO Nanostructures on an ITO Sensing Electrode for Enhanced Detection of Ascorbic Acid.

Journal: Molecules (Basel, Switzerland)

Published: May 22, 2024

Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

Journal: Frontiers in genetics

Published: February 08, 2024

The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes.

The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes.

Journal: Frontiers in endocrinology

Published: September 12, 2023

First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP-C founder mutation.

First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP-C founder mutation.

Journal: Molecular genetics & genomic medicine

Published: September 27, 2022

When to Recommend a Peripheral Blood Smear to Patients with Congenital Ichthyosiform Erythroderma.

When to Recommend a Peripheral Blood Smear to Patients with Congenital Ichthyosiform Erythroderma.

Journal: Skinmed

Published: August 17, 2022

Editorial: Monogenic vs. Oligogenic Reclassification.

Editorial: Monogenic vs. Oligogenic Reclassification.

Journal: Frontiers in genetics

Published: November 24, 2021

Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved.

Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved.

Journal: Genes

Published: September 27, 2021

Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers.

Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers.

Journal: Frontiers in oncology

Published: March 02, 2021

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism.

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism.

Journal: Frontiers in genetics

Published: February 07, 2021

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.

Journal: PloS one

Published: January 29, 2021

Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype.

Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype.

Journal: Frontiers in genetics

Published: January 07, 2021

Showing 1-12 of 43

Last Updated: 09/26/2026