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Dr.Abdullah Al-Mutery Assistant Professor Academic RankAssistant Professor

Specialization:

  • Genetics

Research Interests:

  • 1.Genome evolution 2. Human mutation 3. Cytogenetics comparative studies of birds

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2012 Doctor of Philosophy in Genetics (PhD), University of Kent, School of Biosciences, Canterbury, UK. 2005 Master of Business Administration (MBA), University of Wales, Cardiff, UK. 2001 Bachelor of Zoology, Sciences College (B.Sc.), King Saud University, KSA.
Member of Advisory Board for Biotechnology Program, Applied Biology, Science faculty. University of Sharjah, UAE. · Member of International Academy of Handwriting Analysis, International Academy of Handwriting Analysis, Paris, France. · Member of International Chromosome and Genome Society (ICGS), Kent, UK.
Title: cytogenetics compartive study of different species in Houbara Molecular Amount: 80,000 AED Donor: University of Sharjah (2018) 2. Title: Evaluation genetics association of some common genetics variation with common Epilepsy in Emirati population. (Submitted to Hamdan Foundation)
Mariam Moalla, Faten Hadj kacem, Abdullah Fahad Al Mutery, Mona Mahfood, Nabila Mejdoub-Rekik, Mohamed Abid, Mouna Mnif-Feki and Hassen Hadj Kacem Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism. J Assist Reprod Genet. 2019 Jun;36(6):1273-1280. doi: 10.1007/s10815-019-01468-z. Epub 2019 May 9. Tlili, A., Al Mutery, A., Kamal Eddine Ahmad Mohamed, W., Mahfood, M. and Hadj Kacem, H., 2017. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss. Genetic testing and molecular biomarkers, 21(11), pp.686-691. doi: 10.1089/gtmb.2017.0130. Epub 2017 Oct 10. Tlili, A., Al Mutery, A.F., Mahfood, M., Mohamed, W.K.E.A. and Bajou, K., 2017. Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation. PloS one, 12(9), p.e0185281. Al Mutery, A., Kamal, W., Al Bloushi, H.A.H., Manjuran, M.S. and Rais, N., 2017. Genetic polymorphism of vesicular monoamine transporter 1 gene (SLC18A1) in Emirati population. International Journal of Genetics and Molecular Biology, 9(3), pp.1
The goal of education should be to encourage seeking answers. I always seek to facilitate this advancement of knowledge. I particularly emphasize learning to think about trends and directions, rather than rote memorization of facts. I believe that the students work hard, earn their grades, and are entitled to their opinions. My task is to facilitate their learning process.
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