Publications by authors named "Samya Hagos"

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Pharmacogenomic testing implementation: Tertiary care center experience and results of a pilot of 512 patients.
Dana Bakheet, Hana Al Alshaykh, Ghadi Askar, Sateesh Maddirevula, Samya Hagos

Genet Med Open· March 2025

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Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases.
Lama AlAbdi, Hanan E Shamseldin, Ebtissal Khouj, Rana Helaby, Bayan Aljamal, Samya T Hagos

Genome Med· December 2023

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Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis.
Mohammed S Aldughaim, Mashael R Al-Anazi, Marie Fe F Bohol, Dilek Colak, Hani Alothaid, Samya T Hagos

Dose Response· June 2021

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Comprehensive Genomic Analysis of Noonan Syndrome and Acute Myeloid Leukemia in Adults: A Review and Future Directions.
Muhned S Alhumaid, Majed J Dasouki, Syed O Ahmed, Halah AbalKhail, Samya Hagos

Acta Haematol· January 2021

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New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Majed J Dasouki, Salma M Wakil, Olfat Al-Harazi, Maarab Alkorashy, Nzioka P Muiya, Samya Hagos

OMICS· January 2020

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Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene.
Salma M Wakil, Dorota Monies, Samya Hagos, Fahad Al-Ajlan, Josef Finsterer

Case Rep Genet· December 2018

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Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs.
Salma M Wakil, Ramesh Ram, Nzioka P Muiya, Munish Mehta, Editha Andres, Samya Hagos

Data Brief· June 2016

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Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice.
Ranad Shaheen, Shams Anazi, Tawfeg Ben-Omran, Mohammed Zain Seidahmed, L Brianna Caddle, Samya Hagos

Am J Hum Genet· April 2016

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A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
Salma M Wakil, Ramesh Ram, Nzioka P Muiya, Munish Mehta, Editha Andres, Samya Hagos

Atherosclerosis· February 2016

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The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.
Sarah M Al-Qattan, Salma M Wakil, Shamsa Anazi, Anas M Alazami, Nisha Patel, Samya T Hagos

Genet Med· September 2015

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Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T.
Salma M Wakil, Khushnooda Ramzan, Rula Abuthuraya, Samya Hagos, Haya Al-Dossari

Gene· February 2014

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A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders.
Nzioka P Muiya, Salma M Wakil, Asma I Tahir, Samya Hagos, Mohammed Najai

Hum Genomics· December 2013

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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family.
Salma M Wakil, Saeed Bohlega, Samya Hagos, Batoul Baz, Haya Al Dossari

Eur J Med Genet· January 2013

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Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosity.
Hanif G Khalak, Salma M Wakil, Faiqa Imtiaz, Khushnooda Ramzan, Batoul Baz, Samya Hagos

Genet Med· May 2012

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