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authFullName_s : Mariem Chargui

H syndrome: Clinical, histological and genetic investigation in Tunisian patients

Hager Jaouadi , Anissa Zaouak , Khadija Sellami , Olfa Messaoud , Mariem Chargui , et al.
Journal of Dermatology, 2018, 45 (8), pp.978 - 985. ⟨10.1111/1346-8138.14359⟩
Journal articles pasteur-03550642v1

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 , et al.
Metabolic Syndrome and Related Disorders, 2016, 14 (2), pp.121-128. ⟨10.1089/met.2015.0090⟩
Journal articles pasteur-01969533v1

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 , et al.
Endocrine Research, 2016, 41 (4), pp.300-309. ⟨10.3109/07435800.2016.1141945⟩
Journal articles hal-01356539v1
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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 , et al.
BioMed Research International , 2014, 2014, pp.256245. ⟨10.1155/2014/256245⟩
Journal articles pasteur-01060291v1

Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population.

Rym Kefi , Meriem Hechmi , Hamza Dallali , Sahar Elouej , Haifa Jmel , et al.
Annales d'Endocrinologie, 2017, 78 (3), pp.146--155. ⟨10.1016/j.ando.2017.01.005⟩
Journal articles hal-01571309v1
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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 , et al.
PLoS ONE, 2014, 9 (6), pp.e99797. ⟨10.1371/journal.pone.0099797⟩
Journal articles pasteur-01060192v1

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 , et al.
Journal of Dermatological Science, 2018, 89 (2), pp.172--180. ⟨10.1016/j.jdermsci.2017.10.015⟩
Journal articles hal-01876284v1

Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

Hamza Dallali , Serena Pezzilli , Meriem Hechmi , Om Kalthoum Sallem , Sahar Elouej , et al.
Acta Diabetologica, 2019, 56 (5), pp.515-523. ⟨10.1007/s00592-018-01283-5⟩
Journal articles pasteur-01999628v1

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 , et al.
Annals of Human Biology, 2018, 45 (1), pp.86--97. ⟨10.1080/03014460.2017.1414875⟩
Journal articles hal-01876264v1
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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 , et al.
Journal of Translational Medicine, 2018, 16 (1), pp.158. ⟨10.1186/s12967-018-1504-9⟩
Journal articles hal-01873768v1

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 , et al.
Journal of Diabetes and its Complications, 2016, 30 (2), pp.206-211. ⟨10.1016/j.jdiacomp.2015.11.013⟩
Journal articles pasteur-01374973v1