Mariem Ben Said

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 5

Top Topics

Diabetic Retinopathy

Circulating Tumor

Top Venues

Molecular genetics & genomic medicine

Genetic testing and molecular biomarkers

This page only lists publications with an associated author ORCID identifier.

Publications

Chahnez Charfi Triki, Salma Zouari Mallouli, Marwa Ben Jdila, Mariem Ben Said, Fatma Kamoun Feki, Sarah Weckhuysen, Sabeur Masmoudi, Faiza Fakhfakh
First report of Tunisian patients with CDKL5-related encephalopathy. Epilepsia open (2023)
Mariem Ben Said, Olfa Jallouli, Abir Ben Aissa, Amal Souissi, Fatma Kamoun, Faiza Fakhfakh, Saber Masmoudi, Ikhlas Ben Ayed, Chahnez Charfi Triki
Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with Developmental and Epileptic Encephalopathy. Epilepsia open (2023)
Mariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi, Mehdi Hasnaoui, Amal Souissi, Nabil Idriss, Hajer Aloulou, Imen Chabchoub, Bayen Maâlej, Dorra Driss, Saber Masmoudi
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. Molecular genetics & genomic medicine 10 (2) (2022)
Amal Souissi, Mariem Ben Said, Fakher Frikha, Ines Elloumi, Saber Masmoudi, Andre Megarbane
Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene. Genetic testing and molecular biomarkers 25 (8) (2022)
Mohamed Ali Mosrati, Karima Fadhlaoui-Zid, Amel Benammar-Elgaaied, Abdullah Ahmed Gibriel, Mariem Ben Said, Saber Masmoudi
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. Molecular genetics & genomic medicine 9 (10) (2021)