The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar
Alkhidir, Shaza, El-Akouri, Karen, Al-Dewik, Nader, Khodjet-El-khil, Houssein, Okashah, Sarah, Islam, Nazmul, Ben-Omran, Tawfeg, Al-Shafai, Mashael
Published in Scientific reports (20.02.2024)
Published in Scientific reports (20.02.2024)
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Journal Article
Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach
S, Udhaya Kumar, Sankar, Srivarshini, Younes, Salma, D, Thirumal Kumar, Ahmad, Muneera Naseer, Okashah, Sarah Samer, Kamaraj, Balu, Al-Subaie, Abeer Mohammed, C, George Priya Doss, Zayed, Hatem
Published in Molecules (Basel, Switzerland) (26.11.2020)
Published in Molecules (Basel, Switzerland) (26.11.2020)
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Journal Article
Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review
Jemmeih, Sara, Malik, Shaza, Okashah, Sarah, Zayed, Hatem
Published in Ophthalmic epidemiology (01.02.2022)
Published in Ophthalmic epidemiology (01.02.2022)
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Journal Article
Involvement of Essential Signaling Cascades and Analysis of Gene Networks in Diabesity
S., Udhaya Kumar, Rajan, Bithia, D., Thirumal Kumar, V., Anu Preethi, Abunada, Taghreed, Younes, Salma, Okashah, Sarah, Ethiraj, Selvarajan, C., George Priya Doss, Zayed, Hatem
Published in Genes (25.10.2020)
Published in Genes (25.10.2020)
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Journal Article
Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry
Okashah, Sarah, Vasudeva, Dhanya, El Jerbi, Aya, Khodjet-El-khil, Houssein, Al-Shafai, Mashael, Syed, Najeeb, Kambouris, Marios, Udassi, Sharda, Saraiva, Luis R, Al-Saloos, Hesham, Udassi, Jai, Al-Shafai, Kholoud N
Published in Genes (30.07.2022)
Published in Genes (30.07.2022)
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Journal Article