Dr. Afif Ben Mahmoud | Genomics | Excellence in Research
Dr at Qatar Biomedical Research Institute, Qatar
Profile
Publications Top Notes
- Antagonist effects of Bacillus spp. strains against Fusarium graminearum for protection of durum wheat (Triticum turgidum L. subsp. durum)
- Authors: I Zalila-Kolsi, AB Mahmoud, H Ali, S Sellami, Z Nasfi, S Tounsi, …
- Journal: Microbiological Research, 2016
- Pages: 148-158
- Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men
- Authors: S Baklouti-Gargouri, M Ghorbel, A Ben Mahmoud, E Mkaouar-Rebai, …
- Journal: Molecular Biology Reports, 2013
- Volume/Pages: 40, 4705-4712
- A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD)
- Authors: M Tabebi, E Mkaouar-Rebai, M Mnif, F Kallabi, AB Mahmoud, WB Saad, …
- Journal: Biochemical and Biophysical Research Communications, 2015
- Volume/Pages: 459(3), 353-360
- Genetics of hypogonadotropic hypogonadism—Human and mouse genes, inheritance, oligogenicity, and genetic counseling
- Authors: ED Louden, A Poch, HG Kim, A Ben-Mahmoud, SH Kim, LC Layman
- Journal: Molecular and Cellular Endocrinology, 2021
- Volume: 534, 111334
- Identification of a novel m.9588G>A missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men
- Authors: S Baklouti-Gargouri, M Ghorbel, A Ben Mahmoud, E Mkaouar-Rebai, …
- Journal: Journal of Assisted Reproduction and Genetics, 2014
- Volume/Pages: 31, 595-600
- A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing loss
- Authors: N Gariballa, A Ben-Mahoud, M Komara, AM Al-Shamsi, …
- Journal: American Journal of Medical Genetics Part A, 2017
- Volume/Pages: 173(5), 1257-1263
- Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and its phenotypic implications
- Authors: M Tabebi, N Charfi, F Kallabi, O Alila-Fersi, AB Mahmoud, A Tlili, …
- Journal: Journal of Diabetes and its Complications, 2017
- Volume/Pages: 31(1), 253-259
- Two novel mutations in COII and tRNAHis mitochondrial genes in asthenozoospermic infertiles men
- Authors: BG Siwar, G Myriam, BM Afif, MR Emna, C Nozha, S Afifa, F Faiza, …
- Journal: Biochemical and Biophysical Research Communications, 2014
- Volume/Pages: 450(1), 610-615
- A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men
- Authors: S Baklouti-Gargouri, M Ghorbel, A Ben Mahmoud, E Mkaouar-Rebai, …
- Journal: Molecular Reproduction and Development, 2013
- Volume/Pages: 80(7), 581-587
- Bacillus amyloliquefaciens: Harnessing Its Potential for Industrial, Medical, and Agricultural Applications—A Comprehensive Review
- Authors: I Zalila-Kolsi, A Ben-Mahmoud, R Al-Barazie
- Journal: Microorganisms, 2023
- Volume/Pages: 11(9), 2215
- Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect
- Authors: BB Rhouma, F Kallabi, N Mahfoudh, AB Mahmoud, RT Engeli, H Kamoun, …
- Journal: The Journal of Steroid Biochemistry and Molecular Biology, 2017
- Volume/Pages: 165, 86-94
- Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish
- Authors: YR Lee, SH Kim, A Ben-Mahmoud, OH Kim, TI Choi, KH Lee, B Ku, J Eum, …
- Journal: Human Molecular Genetics, 2021
- Volume/Pages: 30(5), 331-342