| Association of the methylene-tetrahydrofolate reductase gene rs1801133 C677T variant with serum homocysteine levels, and the severity of coronary artery disease N Bouzidi, M Hassine, H Fodha, M Ben Messaoud, F Maatouk, H Gamra, ... Scientific Reports 10 (1), 10064, 2020 | 19 | 2020 |
| Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction H Foddha, N Bouzidi, A Foddha, S Chouchene, R Touhami, N Leban, ... Advances in Clinical and Experimental Medicine 29 (4), 423-429, 2020 | 4 | 2020 |
| The association between Dental Fluorosis and COL1A2 gene polymorphism among a Tunisian Population R Kallala, A Slimani, Y Gassara, B Garrach, S Chouchen, H Foddha, ... BMC Oral Health 24 (1), 376, 2024 | 1 | 2024 |
| Case report: 7p22. 3 deletion and 8q24. 3 duplication in a patient with epilepsy and psychomotor delay—Does both possibly act to modulate a candidate gene region for the … R Touhami, H Foddha, E Alix, A Jalloul, S Mougou-Zerelli, A Saad, ... Frontiers in Genetics 13, 1061539, 2023 | 1 | 2023 |
| Antioxidant and inflammatory status of Tunisian patients with chronic spontaneous urticaria and effect of De-sloratadine: a case-control study A MAAOUIA, M YOUSSEF, N LEBAN, H FODDHA, JBEN CHIBANI, J ZILI, ... | 1 | |
| Comparing the SCN5A Gene Sequence and Expression in Three Different Brugada Syndrome Profiles of Patients: New Insights for Genotype-Phenotype Correlation H Foddha, H Daimi, A Foddha, N Leban, R Touhami, H Gamra, A Saad, ... Int J Hum Genet 20 (3), 138-146, 2020 | | 2020 |
| Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder H Foddha, GH Seo, H Lee, F Zemzem, AH Khelil Ann Mol Genet Med 6 (1), 001-004, 2020 | | 2020 |
| Expending the Mutational Spectrum of Xia-Gibbs and Bosch-Boonstra-Schaaf Optic Atrophy Syndromes R Touhami, H Foddha, S Dimassi, A Labalme, PA Rollat-Farnier, A Saad Ann Clin Case Rep. 2022; 7 2155, 0 | | |
