Hanan M. Fathy

Alexandria, ALX, Egypt

Last Updated: 09/26/2026

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Found 21 publications

Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.

Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 02, 2025

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

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

Published: July 08, 2024

Identifying distinct phenotypes of patients with juvenile systemic lupus erythematosus: results from a cluster analysis by the Egyptian college of rheumatology (ECR) study group.

Identifying distinct phenotypes of patients with juvenile systemic lupus erythematosus: results from a cluster analysis by the Egyptian college of rheumatology (ECR) study group.

Journal: BMC pediatrics

Published: January 20, 2024

Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome.

Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome.

Journal: Genes & diseases

Published: September 04, 2023

Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life.

Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: December 09, 2022

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.

Journal: European urology open science

Published: August 10, 2022

OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.

OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.

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

Published: August 08, 2022

Systemic lupus erythematosus children in Egypt: Homeland spectrum amid the global situation.

Systemic lupus erythematosus children in Egypt: Homeland spectrum amid the global situation.

Journal: Lupus

Published: September 16, 2021

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.

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

Published: June 08, 2021

Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression.

Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression.

Journal: Scientific reports

Published: March 22, 2021

Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome.

Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome.

Journal: Kidney international reports

Published: September 05, 2020

Lupus nephritis: correlation of immunohistochemical expression of C4d, CD163-positive M2c-like macrophages and Foxp3-expressing regulatory T cells with disease activity and chronicity.

Lupus nephritis: correlation of immunohistochemical expression of C4d, CD163-positive M2c-like macrophages and Foxp3-expressing regulatory T cells with disease activity and chronicity.

Journal: Lupus

Published: June 26, 2020

Showing 1-12 of 21

Last Updated: 09/26/2026