Noha M. Issa

Alexandria, ALX, Egypt

Last Updated: 09/26/2026

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Found 12 publications

Multi-Level Genomic and Computational Analyses Identify a Novel IFT122 Variant Associated With Cranioectodermal Dysplasia 1 in a Consanguineous Saudi Family.

Multi-Level Genomic and Computational Analyses Identify a Novel IFT122 Variant Associated With Cranioectodermal Dysplasia 1 in a Consanguineous Saudi Family.

Journal: Molecular genetics & genomic medicine

Published: January 19, 2026

Maternal experiences and family dynamics following Down syndrome diagnosis in Saudi Arabia.

Maternal experiences and family dynamics following Down syndrome diagnosis in Saudi Arabia.

Journal: Frontiers in psychology

Published: November 24, 2025

Clinical, genetic and bioinformatic analysis of Saudi families with Joubert syndrome and related disorders.

Clinical, genetic and bioinformatic analysis of Saudi families with Joubert syndrome and related disorders.

Journal: Human genomics

Published: November 15, 2025

Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing.

Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing.

Journal: Clinical genetics

Published: February 26, 2025

The Effect of Genetic Variants of SLC22A2 (rs662301 and rs315978) on the response to Metformin in type 2 Saudi diabetic patients.

The Effect of Genetic Variants of SLC22A2 (rs662301 and rs315978) on the response to Metformin in type 2 Saudi diabetic patients.

Journal: Gene

Published: January 13, 2024

Quality of life in children with Down syndrome and its association with parent and child demographic characteristics: Parent-reported measures.

Quality of life in children with Down syndrome and its association with parent and child demographic characteristics: Parent-reported measures.

Journal: Molecular genetics & genomic medicine

Published: December 09, 2022

Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.

Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.

Journal: Gene

Published: May 27, 2022

The Prevalence Of Specific Gene Polymorphisms Related To Thrombophilia In Egyptian Women With Recurrent Pregnancy Loss.

The Prevalence Of Specific Gene Polymorphisms Related To Thrombophilia In Egyptian Women With Recurrent Pregnancy Loss.

Journal: Journal of human reproductive sciences

Published: March 19, 2020

MicroRNA signature in patients with hepatocellular carcinoma associated with type 2 diabetes.

MicroRNA signature in patients with hepatocellular carcinoma associated with type 2 diabetes.

Journal: World journal of gastroenterology

Published: September 03, 2019

The clinical significance of serum miRNA-224 expression in hepatocellular carcinoma.

The clinical significance of serum miRNA-224 expression in hepatocellular carcinoma.

Journal: Clinical and experimental hepatology

Published: August 06, 2019

A Genetic Association Study of a Specific Gene and Severe Form of Resorption in the Edentulous Mandible in the Egyptian Population.

A Genetic Association Study of a Specific Gene and Severe Form of Resorption in the Edentulous Mandible in the Egyptian Population.

Journal: Journal of prosthodontics : official journal of the American College of Prosthodontists

Published: February 22, 2019

Effect of Balanites aegyptiaca on Ehrlich Ascitic carcinoma growth and metastasis in Swiss mice.

Effect of Balanites aegyptiaca on Ehrlich Ascitic carcinoma growth and metastasis in Swiss mice.

Journal: Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie

Published: November 23, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026