Dr. Abdullah Fahad Al Mutery

Assistant Professor
Department of Applied Biology, College of Science, University of Sharjah, Sharjah, United Arab Emirates

Highest Degree
Ph.D. in Genetics from University of Kent, Canterbury, United Kingdom

My URL
https://livedna.org/971.39043

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Area of Interest:

Biomedical Sciences
Next-generation sequencing analysis
DNA Sequencing
Molecular Genetics
Human Genetics

Selected Publications

  1. Khati, W.H., O. Souilem, Abdullah F. Al Mutery, A.D. Rouibate, N. Benhafri and S.M. Issad, 2022. Advances in research on the biology of the desert rodent Gerbillus tarabuli: A review. Lab. Anim., 56: 319-330.
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  2. Abdullah Al Mutery, M. Mahfood, J. Chouchen and Abdelaziz Tlili, 2022. Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries. Hum. Genet., 141: 595-605.
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  3. Omar, H.S., Abdullah Al Mutery, N.H. Osman, N. El-Houda A. Reyad and M.A. Abou-Zeid, 2021. Genetic diversity, antifungal evaluation and molecular docking studies of Cu-chitosan nanoparticles as prospective stem rust inhibitor candidates among some Egyptian wheat genotypes. PLoS ONE, 10.1371/journal.pone.0257959.
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  4. Mahfood, M., J. Chouchen, W.K.E.A. Mohamed, Abdullah Al Mutery, R. Harati and Abdelaziz Tlili, 2021. 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 hearing process. Saudi J. Biol. Sci., 28: 4421-4429.
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  5. Khati, W.H., A.F. Al Mutery, E.N. Moudilou, J.M. Exbrayat and S. Hammouche, 2021. Distribution of the Novel RFRP-3/receptors system in the epididymis of the seasonal desert rodent, Gerbillus tarabuli, during sexual activity. Morphologie, 10.1016/j.morpho.2021.10.002.
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  6. Abdullah Al Mutery, N. Rais, W.K.E. Mohamed and T. Abdelaziz, 2021. Genetic diversity in casein gene cluster in a dromedary camel (C. dromedarius) population from the United Arab Emirates. Genes, 10.3390/genes12091417.
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  7. Moalla, M., W. Safi, D. Ghorbel, A.F. Al-Mutery and M. Mahfood, et al., 2020. Séquençage à haut débit de l’exome entier d’une famille Tunisienne atteinte d’Hypogonadisme Hypogonadotrope Congénital Normosmique. Annales d'Endocrinologie, 81: 215-216.
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  8. Khan, A.A., T.J. Huat, Abdullah Al Mutery, A.T. El-Serafi and H.H. Kacem, et al., 2020. Significant transcriptomic changes are associated with differentiation of bone marrow-derived mesenchymal stem cells into neural progenitor-like cells in the presence of bFGF and EGF. Cell Biosci., 10.1186/s13578-020-00487-z.
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  9. Eldin Mohamed, W.K., M. Mahfood, Abdullah Al Mutery, S.H. Abdallah and Abdelaziz Tlili, 2019. A novel nonsense mutation (c.414G>A; p.Trp138*) in CLDN14 causes hearing loss in Yemeni families: A case report. Front. Genet., 10.3389/fgene.2019.01087.
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  10. Abi Zamer, B., M. Mahfood, B. Saleh, Abdullah F. Al Mutery and Abdelaziz Tlili, 2019. Novel mutation in theDSG1gene causes autosomal‐dominant striate palmoplantar keratoderma in a large Syrian family. Ann. Hum. Genet., 83: 472-476.
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Member since October, 2022