Brian F. Meyer

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 100 publications

Building genomic medicine in Saudi Arabia.

Building genomic medicine in Saudi Arabia.

Journal: Nature genetics

Published: February 10, 2026

Circulating Tumour DNA Detection By The Urine-Informed Analysis Of Archival Serum Samples From Muscle-Invasive Bladder Cancer Patients.

Circulating Tumour DNA Detection By The Urine-Informed Analysis Of Archival Serum Samples From Muscle-Invasive Bladder Cancer Patients.

Journal: European urology

Published: December 01, 2023

Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population.

Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population.

Journal: Human genomics

Published: October 12, 2023

Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells.

Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells.

Journal: Frontiers in cell and developmental biology

Published: August 25, 2023

β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in BrafV600E-driven thyroid cancer cells.

β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in BrafV600E-driven thyroid cancer cells.

Journal: Frontiers in immunology

Published: February 22, 2023

The clinical utility of rapid exome sequencing in a consanguineous population.

The clinical utility of rapid exome sequencing in a consanguineous population.

Journal: Genome medicine

Published: November 04, 2022

Novel Homozygous Variants of SLC13A5 Expand the Functional Heterogeneity of a Homogeneous Syndrome of Early Infantile Epileptic Encephalopathy.

Novel Homozygous Variants of SLC13A5 Expand the Functional Heterogeneity of a Homogeneous Syndrome of Early Infantile Epileptic Encephalopathy.

Journal: Pediatric neurology

Published: June 27, 2022

Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia.

Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia.

Journal: Frontiers in neuroscience

Published: November 15, 2021

Identification of pharmacogenetic variants from large scale next generation sequencing data in the Saudi population.

Identification of pharmacogenetic variants from large scale next generation sequencing data in the Saudi population.

Journal: PloS one

Published: July 09, 2021

Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism.

Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 30, 2021

Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining.

Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining.

Journal: Human genomics

Published: April 01, 2021

β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model.

β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model.

Journal: Molecular cancer therapeutics

Published: January 13, 2021

Showing 1-12 of 100

Last Updated: 09/26/2026