| Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing H Dallali, S Pezzilli, M Hechmi, OK Sallem, S Elouej, H Jmel, ... Acta Diabetologica 56, 515-523, 2019 | 20 | 2019 |
| Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa M Hechmi, H Dallali, M Gharbi, H Jmel, M Fassatoui, Y Ben Halima, ... Bioscience Reports 40 (8), BSR20200706, 2020 | 16 | 2020 |
| On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations R Kefi, M Hechmi, C Naouali, H Jmel, S Hsouna, E Bouzaid, S Abdelhak, ... Mitochondrial DNA Part A 29 (1), 147-157, 2018 | 16 | 2018 |
| Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations H Jmel, L Romdhane, Y Ben Halima, M Hechmi, C Naouali, H Dallali, ... PLoS One 13 (4), e0194842, 2018 | 14 | 2018 |
| Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population R Kefi, M Hechmi, H Dallali, S Elouej, H Jmel, YB Halima, M Nagara, ... Annales D'endocrinologie 78 (3), 146-155, 2017 | 14 | 2017 |
| The Role of Dietary Intake in Type 2 Diabetes Mellitus: Importance of Macro and Micronutrients in Glucose Homeostasis N Kheriji, W Boukhalfa, F Mahjoub, M Hechmi, T Dakhlaoui, M Mrad, ... Nutrients 14 (10), 2132, 2022 | 10 | 2022 |
| Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis H Dallali, M Hechmi, I Morjane, S Elouej, H Jmel, Y Ben Halima, A Abid, ... Diabetology & metabolic syndrome 14 (1), 25, 2022 | 5 | 2022 |
| Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment M Hechmi, M Charif, I Kraoua, M Fassatoui, H Dallali, V Desquiret-Dumas, ... Bioscience reports 42 (9), BSR20220194, 2022 | 4 | 2022 |
| Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive … R Mkaouar, Z Riahi, C Charfeddine, I Chelly, H Boudabbous, H Dallali, ... Plos one 16 (10), e0258202, 2021 | 4 | 2021 |
| The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes H Dallali, W Boukhalfa, N Kheriji, M Fassatoui, H Jmel, M Hechmi, ... Frontiers in Endocrinology 14, 1293124, 2023 | 2 | 2023 |
| Thiamine responsive megaloblastic anemia mimicking mitochondrial disorders F Tinsa, M Hechmi, IB Hadj, F Khalsi, M Chargui, R Kefi, H Azouz, ... Revue neurologique 175 (5), 324-327, 2019 | 2 | 2019 |
| Decoding the genetic relationship between Alzheimer’s disease and type 2 diabetes: potential risk variants and future direction for North Africa W Boukhalfa, H Jmel, N Kheriji, I Gouiza, H Dallali, M Hechmi, R Kefi Frontiers in Aging Neuroscience 15, 1114810, 2023 | 1 | 2023 |
| Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing I Gouiza, M Hechmi, A Zioudi, H Dallali, N Kheriji, M Charif, M Le Mao, ... Frontiers in Genetics 14, 1259826, 2024 | | 2024 |
| Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare management N Kheriji, H Dallali, I Gouiza, M Hechmi, F Mahjoub, M Mrad, A Krir, ... Frontiers in Genetics 14, 1224284, 2023 | | 2023 |
| Gut microbiota profile and the influence of nutritional status on bacterial distribution in diabetic and healthy Tunisian subjects M Fassatoui, A Saffarian, C Mulet, H Jamoussi, A Gamoudi, Y Ben Halima, ... Bioscience Reports 43 (9), BSR20220803, 2023 | | 2023 |
| CASE/CONTROL STUDY OF HNF1A GENETIC VARIANTS WITH THE METABOLIC SYNDROME IN THE TUNISIAN POPULATION. H DALLALI, M HECHMI, S ELOUEJ, H JMEL, Y BEN HALIMA, ... Archives de l'Institut Pasteur de Tunis 97, 2020 | | 2020 |
