The evolving SARS-CoV-2 epidemic in Africa: Insights from rapidly expanding genomic surveillance H Tegally, JE San, M Cotten, M Moir, B Tegomoh, G Mboowa, DP Martin, ... Science 378 (6615), eabq5358, 2022 | 97 | 2022 |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human A Imtiaz, IA Belyantseva, AJ Beirl, C Fenollar-Ferrer, R Bashir, I Bukhari, ... Human molecular genetics 27 (5), 780-798, 2018 | 59 | 2018 |
Down-expression of P2RX2, KCNQ5, ERBB3 and SOCS3 through DNA hypermethylation in elderly women with presbycusis A Bouzid, I Smeti, L Dhouib, M Roche, I Achour, A Khalfallah, AA Gibriel, ... Biomarkers 23 (4), 347-356, 2018 | 36 | 2018 |
CDH23 Methylation Status and Presbycusis Risk in Elderly Women A Bouzid, I Smeti, A Chakroun, S Loukil, AA Gibriel, M Grati, A Ghorbel, ... Frontiers in aging neuroscience 10, 241, 2018 | 35 | 2018 |
Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population A Souissi, MB Said, IB Ayed, I Elloumi, A Bouzid, MA Mosrati, M Hasnaoui, ... Journal of Advanced Research 31, 13-24, 2021 | 22 | 2021 |
SRD5A3‐CDG: 3D structure modeling, clinical spectrum, and computer‐based dysmorphic facial recognition I Ben Ayed, W Ouarda, F Frikha, F Kammoun, A Souissi, M Ben Said, ... American Journal of Medical Genetics Part A 185 (4), 1081-1090, 2021 | 16 | 2021 |
ACE2 polymorphisms impact COVID-19 severity in obese patients N Jalaleddine, A Bouzid, M Hachim, NS Sharif-Askari, B Mahboub, ... Scientific Reports 12 (1), 21491, 2022 | 11 | 2022 |
Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis A Bouzid, A Tekari, F Jbeli, A Chakroun, K Hansdah, A Souissi, N Singh, ... BMC Medical Genetics 21, 1-10, 2020 | 10 | 2020 |
Circulating microRNAs as potential biomarkers of early vascular damage in vitamin D deficiency, obese, and diabetic patients AB Elmoselhi, M Seif Allah, A Bouzid, Z Ibrahim, T Venkatachalam, ... Plos one 18 (3), e0283608, 2023 | 8 | 2023 |
KIBRA Gene Variant Is Associated with Ability in Chess and Science II Ahmetov, EV Valeeva, MB Yerdenova, GK Datkhabayeva, A Bouzid, ... Genes 14 (1), 204, 2023 | 7 | 2023 |
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing A Yahia, IB Ayed, AA Hamed, IN Mohammed, MA Elseed, AM Bakhiet, ... Annals of Human Genetics 86 (4), 181-194, 2022 | 7 | 2022 |
Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly IB Ayed, W Bouchaala, A Bouzid, W Feki, A Souissi, SB Nsir, MB Said, ... European Journal of Medical Genetics 64 (12), 104373, 2021 | 6 | 2021 |
Transcriptomic Changes Associated with ERBB2 Overexpression in Colorectal Cancer Implicate a Potential Role of the Wnt Signaling Pathway in Tumorigenesis EA Abdul Razzaq, K Bajbouj, A Bouzid, N Alkhayyal, R Hamoudi, ... Cancers 15 (1), 130, 2022 | 5 | 2022 |
Evaluation of the Genetic Association and mRNA Expression of the COL1A1, BMP2, and BMP4 Genes in the Development of Otosclerosis K Hansdah, N Singh, A Bouzid, S Priyadarshi, CS Ray, A Desai, ... Genetic Testing and Molecular Biomarkers 24 (6), 343-351, 2020 | 5 | 2020 |
Effect of aerobic/strength training on RANKL gene DNA methylation levels A Chelly, A Bouzid, F Neifar, I Kammoun, A Tekari, S Masmoudi, ... Journal of Physical Activity and Health 20 (10), 900-908, 2023 | 4 | 2023 |
Integrative bioinformatics and artificial intelligence analyses of transcriptomics data identified genes associated with major depressive disorders including NRG1 A Bouzid, A Almidani, M Zubrikhina, A Kamzanova, BY Ilce, ... Neurobiology of Stress 26, 100555, 2023 | 3 | 2023 |
Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritis HR Gouda, IM Talaat, A Bouzid, H El-Assi, A Nabil, T Venkatachalam, ... Frontiers in immunology 13, 960068, 2022 | 3 | 2022 |
The risks of RELN polymorphisms and its expression in the development of otosclerosis S Priyadarshi, K Hansdah, N Singh, A Bouzid, CS Ray, KC Panda, ... Plos one 17 (6), e0269558, 2022 | 3 | 2022 |
8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects I Ben Ayed, A Bouzid, F Kammoun, A Souissi, O Jallouli, S Mallouli, ... Molecular genetics & genomic medicine 9 (11), e1811, 2021 | 3 | 2021 |
Titanium Particles Modulate Lymphocyte and Macrophage Polarization in Peri-Implant Gingival Tissues W Kheder, A Bouzid, T Venkatachalam, IM Talaat, NM Elemam, TK Raju, ... International Journal of Molecular Sciences 24 (14), 11644, 2023 | 2 | 2023 |