Publications by authors named "Samya Hagos"

11Publications

Comprehensive Genomic Analysis of Noonan Syndrome and Acute Myeloid Leukemia in Adults: A Review and Future Directions.

Acta Haematol 2020 15;143(6):583-593. Epub 2020 Jun 15.

Department of Adult Hematology and Stem Cell Transplant, Oncology Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia,

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January 2021

New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.

OMICS 2020 01 19;24(1):16-28. Epub 2019 Dec 19.

Departments Biostatistics, Epidemiology and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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January 2020

Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice.

Am J Hum Genet 2016 Apr 24;98(4):643-52. Epub 2016 Mar 24.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia. Electronic address:

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April 2016

A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.

Atherosclerosis 2016 Feb 22;245:62-70. Epub 2015 Nov 22.

Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia. Electronic address:

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February 2016

A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders.

Hum Genomics 2013 Dec 12;7:25. Epub 2013 Dec 12.

Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.

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December 2013

A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family.

Eur J Med Genet 2013 Jan 18;56(1):43-5. Epub 2012 Oct 18.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia.

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January 2013