Meriem Hechmi
Tunis, 1002, Tunisia
Last Updated: 09/26/2026
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Found 16 publications
Integrated exome and mitochondrial genome sequencing reveals the genetic landscape of primary mitochondrial diseases: findings from a large Tunisian cohort.
Journal: Mitochondrion
Published: March 02, 2026
A Tunisian POLG mutation expands the clinical spectrum of POLG-related disorders.
Journal: Mitochondrion
Published: April 27, 2025
The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes.
Journal: Frontiers in endocrinology
Published: September 12, 2023
Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare management.
Journal: Frontiers in genetics
Published: May 17, 2023
Gut microbiota profile and the influence of nutritional status on bacterial distribution in diabetic and healthy Tunisian subjects.
Journal: Bioscience reports
Published: April 11, 2022
Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment.
Journal: Bioscience reports
Published: January 29, 2022
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysis.
Journal: Diabetology & metabolic syndrome
Published: October 20, 2021
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.
Journal: PloS one
Published: January 29, 2021
Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa.
Journal: Bioscience reports
Published: March 19, 2020
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing.
Journal: Acta diabetologica
Published: October 13, 2018
Last Updated: 09/26/2026