Publications by authors named "Mariem Chargui"

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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Mariem Chargui

Front Genet· June 2024

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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Mariem Chargui

Front Genet· April 2024

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First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP-C founder mutation.
Najlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya, Mariem Chargui, Mohamed Zghal

Mol Genet Genomic Med· June 2023

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Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.
Ichraf Kraoua, Yosra Bouyacoub, Cyrine Drissi, Mariem Chargui, Ibtihel Rebai

Neuropediatrics· August 2021

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Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in the gene.
Yosra Bouyacoub, Yousra Falfoul, Mariem Ouederni, Marwa Sayeb, Aschraf Chedli, Mariem Chargui

Ophthalmic Genet· August 2019

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Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing.
Hamza Dallali, Serena Pezzilli, Meriem Hechmi, Om Kalthoum Sallem, Sahar Elouej, Mariem Chargui

Acta Diabetol· May 2019

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H syndrome: Clinical, histological and genetic investigation in Tunisian patients.
Hager Jaouadi, Anissa Zaouak, Khadija Sellami, Olfa Messaoud, Mariem Chargui

J Dermatol· August 2018

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Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases.
Yosr Hamdi, Maroua Boujemaa, Mariem Ben Rekaya, Cherif Ben Hamda, Najah Mighri, Mariem Chargui

J Transl Med· June 2018

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Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis.
Mariem Ben Rekaya, Chokri Naouali, Olfa Messaoud, Meriem Jones, Yosra Bouyacoub, Mariem Chargui

J Dermatol Sci· February 2018

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Mitochondrial DNA structure of an isolated Tunisian Berber population and its relationship with Mediterranean populations.
Nizar Ben Halim, Sana Hsouna, Khaled Lasram, Mariem Chargui, Laaroussi Khemira

Ann Hum Biol· February 2018

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Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population.
Rym Kefi, Meriem Hechmi, Hamza Dallali, Sahar Elouej, Haifa Jmel, Mariem Chargui

Ann Endocrinol (Paris)· July 2017

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Identification of a Novel Mutation of Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing.
Nadia Laroussi, Olfa Messaoud, Mariem Chargui, Chaima Ben Fayala, Abdelaziz Elahlafi

Ann Dermatol· April 2017

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Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population.
Sahar Elouej, Insaf Rejeb, Redha Attaoua, Majdi Nagara, Om Kalthoum Sallem, Mariem Chargui

Endocr Res· November 2016

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Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population.
Sahar Elouej, Majdi Nagara, Redha Attaoua, Om Kalthoum Sallem, Insaf Rejeb, Mariem Chargui

J Diabetes Complications· March 2016

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Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome.
Sahar Elouej, Hanen Belfki-Benali, Majdi Nagara, Khaled Lasram, Redha Attaoua, Mariem Chargui

Metab Syndr Relat Disord· March 2016

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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
Zied Riahi, Crystel Bonnet, Rim Zainine, Malek Louha, Yosra Bouyacoub, Mariem Chargui

PLoS One· May 2015

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A founder large deletion mutation in Xeroderma pigmentosum-Variant form in Tunisia: implication for molecular diagnosis and therapy.
Mariem Ben Rekaya, Nadia Laroussi, Olfa Messaoud, Mariem Jones, Manel Jerbi, Mariem Chargui

Biomed Res Int· February 2015

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