Ashraf Dallol

P.O. Box 80218, Abdullah Sulayman St
Jeddah, 21589, Saudi Arabia

Last Updated: 09/26/2026

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Found 42 publications

Monitoring Cross-Border Dissemination of Antimicrobial Resistance (AMR) via Air Travel to Saudi Arabia: Formulation of Monitoring Strategies to Mitigate AMR Concerns.

Monitoring Cross-Border Dissemination of Antimicrobial Resistance (AMR) via Air Travel to Saudi Arabia: Formulation of Monitoring Strategies to Mitigate AMR Concerns.

Journal: Environmental science & technology

Published: December 24, 2025

Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature.

Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature.

Journal: Ophthalmic genetics

Published: June 29, 2025

Clinical relevance of the somatic mutational landscaping in predicting outcome of bladder cancer patients.

Clinical relevance of the somatic mutational landscaping in predicting outcome of bladder cancer patients.

Journal: Scientific reports

Published: February 09, 2025

Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap with Angelman syndrome.

Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap with Angelman syndrome.

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

Published: April 26, 2022

A paediatric dysembryoplastic neuroepithelial tumour (DNET) with deregulated stem cell markers: a case report.

A paediatric dysembryoplastic neuroepithelial tumour (DNET) with deregulated stem cell markers: a case report.

Journal: Translational pediatrics

Published: January 10, 2022

The Diagnostic Value of Pan-Trk Expression to Detect Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion in CNS Tumours: A Study Using Next-Generation Sequencing Platform.

The Diagnostic Value of Pan-Trk Expression to Detect Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion in CNS Tumours: A Study Using Next-Generation Sequencing Platform.

Journal: Pathology oncology research : POR

Published: December 03, 2021

Leptin Protein Expression and Promoter Methylation in Ovarian Cancer: A Strong Prognostic Value with Theranostic Promises.

Leptin Protein Expression and Promoter Methylation in Ovarian Cancer: A Strong Prognostic Value with Theranostic Promises.

Journal: International journal of molecular sciences

Published: November 04, 2021

Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia.

Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia.

Journal: Bioinformation

Published: October 12, 2021

Klotho promoter methylation status and its prognostic value in ovarian cancer.

Klotho promoter methylation status and its prognostic value in ovarian cancer.

Journal: Molecular and clinical oncology

Published: February 14, 2021

Prognostic value of TP53 expression and MGMT methylation in glioblastoma patients treated with temozolomide combined with other chemotherapies.

Prognostic value of TP53 expression and MGMT methylation in glioblastoma patients treated with temozolomide combined with other chemotherapies.

Journal: Journal of neuro-oncology

Published: February 02, 2021

Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes.

Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes.

Journal: Heliyon

Published: August 17, 2020

A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members.

A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members.

Journal: Heliyon

Published: August 10, 2020

Showing 1-12 of 42

Last Updated: 09/26/2026