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Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?
Glob Cardiol Sci Pract. 2015 Jul 3;2015(2):29. doi: 10.5339/gcsp.2015.29. eCollection 2015.
Glob Cardiol Sci Pract. 2015.
PMID: 26535225
Free PMC article.
No abstract available.
Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs.
Al-Shafai KN, Al-Hashemi M, Manickam C, Musa R, Selvaraj S, Syed N, Vempalli F, Ali M, Yacoub M, Estivill X.
Al-Shafai KN, et al.
Mol Genet Genomic Med. 2021 Jul;9(7):e1709. doi: 10.1002/mgg3.1709. Epub 2021 Jun 17.
Mol Genet Genomic Med. 2021.
PMID: 34137518
Free PMC article.
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The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in Qatar.
AbouHashem N, Zaied RE, Al-Shafai K, Nofal M, Syed N, Al-Shafai M.
AbouHashem N, et al. Among authors: al shafai k.
Obes Facts. 2022;15(3):357-365. doi: 10.1159/000521851. Epub 2022 Jan 13.
Obes Facts. 2022.
PMID: 35026759
Free PMC article.
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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. Among authors: al shafai kn.
Genes (Basel). 2022 Jul 30;13(8):1369. doi: 10.3390/genes13081369.
Genes (Basel). 2022.
PMID: 36011280
Free PMC article.
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The genetic elucidation of monogenic obesity in the Arab world: a systematic review.
AbouHashem N, Al-Shafai K, Al-Shafai M.
AbouHashem N, et al. Among authors: al shafai k.
J Pediatr Endocrinol Metab. 2022 Apr 20;35(6):699-707. doi: 10.1515/jpem-2021-0710. Print 2022 Jun 27.
J Pediatr Endocrinol Metab. 2022.
PMID: 35437977
Free article.
Review.
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