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Response to phenotypic hetergeneity of POMT2 variants.
Guerin A, Wilson G, Abdullah S, Mertens L, Yoon G, Carter M. Guerin A, et al. Among authors: abdullah s. Am J Med Genet A. 2018 Mar;176(3):746-747. doi: 10.1002/ajmg.a.38591. Epub 2018 Jan 25. Am J Med Genet A. 2018. PMID: 29368392 No abstract available.
16q22.1 microdeletion and anticipatory guidance.
Abdullah S, Helal M, Dupuis L, Stavropoulos DJ, Louro P, Ramos L, Mendoza-Londono R. Abdullah S, et al. Am J Med Genet A. 2019 Jul;179(7):1287-1292. doi: 10.1002/ajmg.a.61155. Epub 2019 May 29. Am J Med Genet A. 2019. PMID: 31141312
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.
Wojtal D, Kemaladewi DU, Malam Z, Abdullah S, Wong TW, Hyatt E, Baghestani Z, Pereira S, Stavropoulos J, Mouly V, Mamchaoui K, Muntoni F, Voit T, Gonorazky HD, Dowling JJ, Wilson MD, Mendoza-Londono R, Ivakine EA, Cohn RD. Wojtal D, et al. Among authors: abdullah s. Am J Hum Genet. 2016 Jan 7;98(1):90-101. doi: 10.1016/j.ajhg.2015.11.012. Epub 2015 Dec 10. Am J Hum Genet. 2016. PMID: 26686765 Free PMC article.
Bibliometric analysis: A few suggestions (Part Two).
Abdelwahab SI, Taha MME, Farasani A, Abdullah SM, Moshi JM, Alshahrani AF, Khamjan NA, Khired ZA, Assiri A, Alqassmi AM, Alhusayni AM, Ibrahim IAA, Alshahrani S, Hassan W. Abdelwahab SI, et al. Among authors: abdullah sm. Curr Probl Cardiol. 2025 Jan 7:102982. doi: 10.1016/j.cpcardiol.2025.102982. Online ahead of print. Curr Probl Cardiol. 2025. PMID: 39788466 Review.
1,252 results