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The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar.
Sci Rep. 2024 Feb 20;14(1):4202. doi: 10.1038/s41598-024-52784-z.
Sci Rep. 2024.
PMID: 38378725
Free PMC article.
Genetic epidemiology of male infertility (MI) in Arabs: a systematic review.
Okashah S, Abunada T, Zayed H.
Okashah S, et al.
Reprod Fertil Dev. 2022 Sep;34(14):905-919. doi: 10.1071/RD21343.
Reprod Fertil Dev. 2022.
PMID: 36041737
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Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.
Okashah S, Vasudeva D, El Jerbi A, Khodjet-El-Khil H, Al-Shafai M, Syed N, Kambouris M, Udassi S, Saraiva LR, Al-Saloos H, Udassi J, Al-Shafai KN.
Okashah S, et al.
Genes (Basel). 2022 Jul 30;13(8):1369. doi: 10.3390/genes13081369.
Genes (Basel). 2022.
PMID: 36011280
Free PMC article.
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Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review.
Jemmeih S, Malik S, Okashah S, Zayed H.
Jemmeih S, et al. Among authors: okashah s.
Ophthalmic Epidemiol. 2022 Feb;29(1):1-12. doi: 10.1080/09286586.2021.1883676. Epub 2021 Feb 28.
Ophthalmic Epidemiol. 2022.
PMID: 33641569
Review.
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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 UK, Sankar S, Younes S, D TK, Ahmad MN, Okashah SS, Kamaraj B, Al-Subaie AM, C GPD, Zayed H.
S UK, et al. Among authors: okashah ss.
Molecules. 2020 Nov 26;25(23):5543. doi: 10.3390/molecules25235543.
Molecules. 2020.
PMID: 33255942
Free PMC article.
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Involvement of Essential Signaling Cascades and Analysis of Gene Networks in Diabesity.
S UK, Rajan B, D TK, V AP, Abunada T, Younes S, Okashah S, Ethiraj S, C GPD, Zayed H.
S UK, et al. Among authors: okashah s.
Genes (Basel). 2020 Oct 25;11(11):1256. doi: 10.3390/genes11111256.
Genes (Basel). 2020.
PMID: 33113859
Free PMC article.
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