Mariem Ben Said

5PUBLICATIONS
9CO-AUTHORS
GenomicsForensic epidemiologyGene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (5)

|Oct 23, 2023
Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy.

Mariem Ben Said, Olfa Jallouli, Abir Ben Aissa

|Sep 13, 2023
First report of Tunisian patients with CDKL5-related encephalopathy.

Chahnez Charfi Triki, Salma Zouari Mallouli, Marwa Ben Jdila

|Jan 08, 2022
Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys.

Mariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi

|Sep 13, 2021
Deep analysis of the LRTOMTc.242G>A variant in non-syndromic hearing loss North African patients and the Berber population: Implications for genetic diagnosis and genealogical studies.

Mohamed Ali Mosrati, Karima Fadhlaoui-Zid, Amel Benammar-Elgaaied

|Aug 18, 2021
Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene.

Amal Souissi, Mariem Ben Said, Fakher Frikha

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Frequent Collaborators

2 joint publications

Chahnez Charfi Triki

1 joint publications

Mohamed Ali Mosrati

1 joint publications

Karima Fadhlaoui-Zid

1 joint publications

Amel Benammar-Elgaaied