Olfa Messaoud

7PUBLICATIONS
131CO-AUTHORS
NeurogeneticsCell and nuclear divisionNeurology and neuromuscular diseasesMolecular and organic electronicsHaematological tumours
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Publications (7)

|May 18, 2026
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

|Apr 08, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rocio Rius, Alexander J M Blakes, Yuyang Chen

|Apr 08, 2026
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders.

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji

|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

|Jun 27, 2024
Novel and Extremely Sensitive NiAl2O4-NiO Nanostructures on an ITO Sensing Electrode for Enhanced Detection of Ascorbic Acid.

Asma Hammami, Afrah Bardaoui, Shimaa Eissa

|Feb 22, 2023
First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP-C founder mutation.

Najlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya

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Frequent Collaborators

4 joint publications

Caroline Nava

4 joint publications

Christel Depienne

4 joint publications

Salima El Chehadeh

4 joint publications

Pierre Marijon