Samya T. Hagos

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 17 publications

Pharmacogenomic testing implementation: Tertiary care center experience and results of a pilot of 512 patients.

Pharmacogenomic testing implementation: Tertiary care center experience and results of a pilot of 512 patients.

Journal: Genetics in medicine open

Published: October 31, 2024

Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases.

Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases.

Journal: Genome medicine

Published: July 27, 2023

Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis.

Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis.

Journal: Dose-response : a publication of International Hormesis Society

Published: March 28, 2021

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

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

Journal: Omics : a journal of integrative biology

Published: December 20, 2019

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

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

Journal: Acta haematologica

Published: February 04, 2019

Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene.

Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene.

Journal: Case reports in genetics

Published: August 30, 2018

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.

Journal: Clinical genetics

Published: June 22, 2016

A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.

A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.

Journal: Clinical genetics

Published: January 21, 2016

Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs.

Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs.

Journal: Data in brief

Published: November 25, 2015

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

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

Journal: American journal of human genetics

Published: October 27, 2015

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

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

Journal: Atherosclerosis

Published: January 14, 2015

The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.

The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 03, 2014

Showing 1-12 of 17

Last Updated: 09/26/2026