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. SequenÒage Ë haut debit de l’exome entier d’une famille Tunisienne atteinte d’Hypogonadisme Hypogonadotrope Congenital 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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