Abeer Ramadan

Cairo, C, Egypt

Last Updated: 09/26/2026

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Found 13 publications

Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants.

Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants.

Journal: Molecular and cellular pediatrics

Published: May 17, 2025

Autophagy-related genes expression in children with cystic fibrosis.

Autophagy-related genes expression in children with cystic fibrosis.

Journal: Respiratory medicine

Published: March 07, 2025

Characterization of Egyptian cystic fibrosis children including genotypes and phenotypes: A single tertiary center experience.

Characterization of Egyptian cystic fibrosis children including genotypes and phenotypes: A single tertiary center experience.

Journal: Respiratory medicine

Published: February 25, 2025

Biallelic TYR and TKFC variants in Egyptian patients with OCA1 and new expanded TKFC features.

Biallelic TYR and TKFC variants in Egyptian patients with OCA1 and new expanded TKFC features.

Journal: BMC genomics

Published: March 30, 2024

Efficacy of Laser Acupuncture for Children With Autism Spectrum Disorder: Clinical, Molecular, and Biochemical Study.

Efficacy of Laser Acupuncture for Children With Autism Spectrum Disorder: Clinical, Molecular, and Biochemical Study.

Journal: Pediatric neurology

Published: March 30, 2023

Autophagy-related 5 gene mRNA expression and ATG5 rs510432 polymorphism in children with bronchial asthma.

Autophagy-related 5 gene mRNA expression and ATG5 rs510432 polymorphism in children with bronchial asthma.

Journal: Pediatric pulmonology

Published: April 09, 2022

Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.

Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.

Journal: Molecular genetics and genomics : MGG

Published: September 22, 2021

Dynamic disequilibrium-based pathogenicity model in mutated pyrin's B30.2 domain-Casp1/p20 complex.

Dynamic disequilibrium-based pathogenicity model in mutated pyrin's B30.2 domain-Casp1/p20 complex.

Journal: Journal, genetic engineering & biotechnology

Published: August 23, 2021

The potential impact of COMT gene variants on dopamine regulation and phenotypic traits of ASD patients.

The potential impact of COMT gene variants on dopamine regulation and phenotypic traits of ASD patients.

Journal: Behavioural brain research

Published: June 02, 2019

Micro-RNA 196a2 expression and miR-196a2 (rs11614913) polymorphism in T1DM: a pilot study.

Micro-RNA 196a2 expression and miR-196a2 (rs11614913) polymorphism in T1DM: a pilot study.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: May 20, 2019

Influence of Interleukin-6 (174G/C) Gene Polymorphism on Obesity in Egyptian Children.

Influence of Interleukin-6 (174G/C) Gene Polymorphism on Obesity in Egyptian Children.

Journal: Open access Macedonian journal of medical sciences

Published: June 24, 2017

A novel SNP in 3' UTR of INS gene: A case report of neonatal diabetes mellitus.

A novel SNP in 3' UTR of INS gene: A case report of neonatal diabetes mellitus.

Journal: Diabetes research and clinical practice

Published: May 22, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026