Sarah S. Okashah

Doha, DA, Qatar

Last Updated: 09/26/2026

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Found 9 publications

First National Expanded Genomic Newborn Screening Program in Qatar; A Pilot Study, Doha-Heidelberg Collaboration.

First National Expanded Genomic Newborn Screening Program in Qatar; A Pilot Study, Doha-Heidelberg Collaboration.

Journal: American journal of medical genetics. Part A

Published: December 13, 2025

Exploring the Genetic Causes of Nonsyndromic Retinal Dystrophies in Qatar.

Exploring the Genetic Causes of Nonsyndromic Retinal Dystrophies in Qatar.

Journal: Genes

Published: October 27, 2025

Spectrum of genetic variants associated with maple syrup urine disease in the Middle East, North Africa, and Türkiye (MENAT): a systematic review.

Spectrum of genetic variants associated with maple syrup urine disease in the Middle East, North Africa, and Türkiye (MENAT): a systematic review.

Journal: BMC medical genomics

Published: July 08, 2024

The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar.

The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar.

Journal: Scientific reports

Published: May 29, 2023

Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.

Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.

Journal: Genes

Published: June 25, 2022

Genetic epidemiology of male infertility (MI) in Arabs: a systematic review.

Genetic epidemiology of male infertility (MI) in Arabs: a systematic review.

Journal: Reproduction, fertility, and development

Published: November 25, 2021

Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review.

Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review.

Journal: Ophthalmic epidemiology

Published: March 01, 2021

Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.

Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.

Journal: Molecules (Basel, Switzerland)

Published: October 19, 2020

Involvement of Essential Signaling Cascades and Analysis of Gene Networks in Diabesity.

Involvement of Essential Signaling Cascades and Analysis of Gene Networks in Diabesity.

Journal: Genes

Published: September 21, 2020

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Last Updated: 09/26/2026