| Genistein induces alterations of epigenetic modulatory signatures in human cervical cancer cells MK Sundaram, MZ Ansari, A Al Mutery, M Ashraf, R Nasab, S Rai, N Rais, ... Anti-Cancer Agents in Medicinal Chemistry (Formerly Current Medicinal …, 2018 | 63 | 2018 |
| Novel tools for characterising inter and intra chromosomal rearrangements in avian microchromosomes PE Lithgow, R O’Connor, D Smith, G Fonseka, A Al Mutery, C Rathje, ... Chromosome research 22, 85-97, 2014 | 40 | 2014 |
| Chromosome level genome assembly and comparative genomics between three falcon species reveals an unusual pattern of genome organisation S Joseph, RE O’Connor, AF Al Mutery, M Watson, DM Larkin, DK Griffin Diversity 10 (4), 113, 2018 | 36 | 2018 |
| Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss A Tlili, A Al Mutery, W Kamal Eddine Ahmad Mohamed, M Mahfood, ... Genetic testing and molecular biomarkers 21 (11), 686-691, 2017 | 25 | 2017 |
| Global patterns of apparent copy number variation in birds revealed by cross-species comparative genomic hybridization BM Skinner, A Al Mutery, D Smith, M Völker, N Hojjat, S Raja, S Trim, ... Chromosome research 22, 59-70, 2014 | 19 | 2014 |
| Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism M Moalla, F Hadj Kacem, AF Al-Mutery, M Mahfood, N Mejdoub-Rekik, ... Journal of assisted reproduction and genetics 36, 1273-1280, 2019 | 13 | 2019 |
| Biodegradation and Decolorization of Textile Azo Dyes by Paramecium caudatum Isolated from Industrial Wastewater U Ramzan, FR Shakoori, MT Zahid, W Majeed, I Zahra, SZ Abbas, A Hedfi, ... Water 14 (21), 3553, 2022 | 9 | 2022 |
| Assessment of Uptake, Accumulation and Degradation of Paracetamol in Spinach (Spinacia oleracea L.) under Controlled Laboratory Conditions Z Badar, A Shanableh, A El-Keblawy, KA Mosa, L Semerjian, AA Mutery, ... Plants 11 (13), 1626, 2022 | 9 | 2022 |
| Genetic diversity, antifungal evaluation and molecular docking studies of Cu-chitosan nanoparticles as prospective stem rust inhibitor candidates among some Egyptian wheat … HS Omar, A Al Mutery, NH Osman, NEHA Reyad, MA Abou-Zeid PLoS One 16 (11), e0257959, 2021 | 9 | 2021 |
| Genetic etiology of hereditary hearing loss in the Gulf cooperation council countries A Al Mutery, M Mahfood, J Chouchen, A Tlili Human Genetics 141 (3), 595-605, 2022 | 7 | 2022 |
| Genetic Diversity in Casein Gene Cluster in a Dromedary Camel (C. dromedarius) Population from the United Arab Emirates AA Mutery, N Rais, WKE Mohamed, T Abdelaziz Genes 12 (9), 1417, 2021 | 7 | 2021 |
| Novel mutation in the DSG1 gene causes autosomal‐dominant striate palmoplantar keratoderma in a large Syrian family B Abi Zamer, M Mahfood, B Saleh, AF Al Mutery, A Tlili Annals of Human Genetics 83 (6), 472-476, 2019 | 7 | 2019 |
| Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation A Tlili, A Fahd Al Mutery, M Mahfood, W Kamal Eddine Ahmad Mohamed, ... Plos one 12 (9), e0185281, 2017 | 7 | 2017 |
| Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p. Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the … M Mahfood, J Chouchen, WKEA Mohamed, A Al Mutery, R Harati, A Tlili Saudi journal of biological sciences 28 (8), 4421-4429, 2021 | 6 | 2021 |
| Mitochondrial mutations in non-syndromic hearing loss at UAE WKE Mohamed, M Arnoux, THS Cardoso, A Almutery, A Tlili International Journal of Pediatric Otorhinolaryngology 138, 110286, 2020 | 6 | 2020 |
| Clinical Exome Sequencing Identifies a Frameshift Mutation Within the STRC Gene in a United Arab Emirates Family with Profound Nonsyndromic Hearing Loss M Mahfood, W Kamal Eddine Ahmad Mohamed, A Al Mutery, A Tlili Genetic Testing and Molecular Biomarkers 23 (3), 204-208, 2019 | 6 | 2019 |
| A Novel Nonsense Mutation (c.414G>A; p.Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report WKE Mohamed, M Mahfood, A Al Mutery, SH Abdallah, A Tlili Frontiers in genetics 10, 1087, 2019 | 4 | 2019 |
| Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families M Asaad, M Mahfood, A Al Mutery, A Tlili Human Genomics 17 (1), 42, 2023 | 2 | 2023 |
| Progress in research on the reproductive function in the sand rat (Psammomys obesus): A review WH Khati, AF Al Mutery, A Ricken, RE Akhigbe General and Comparative Endocrinology 331, 114161, 2023 | 2 | 2023 |
| Identification of nonsense mutation in TMC1 gene inducing hearing loss by clinical exome sequencing M Alobathani, A Al Mutery, WKEA Mohamed, A Tlili Journal of Biological Sciences and Medicine 4 (4), 1-6, 2018 | 2 | 2018 |
