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Meriem Hechmi

Pasteur Institute

7

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30

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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.

2021 PLOS ONE
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Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

2019 Acta Diabetologica
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Pharmacogenetic landscape of metabolic syndrome components drug response in Tunisia and comparison with worldwide populations

2018 PLOS ONE
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On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations

2018 Mitochondrial DNA
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Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population

2017 Annales D Endocrinologie
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P34- Preliminary results of the association of apolipoprotein A5 gene with metabolic syndrome in Tunisian population

2016
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