Natasa Stajic

Belgrade, SE, Serbia

Last Updated: 09/26/2026

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Found 31 publications

IgA Nephropathy in Native Kidneys: Oxford and Banff Classifications Reveal Distinct Profiles and Predict Outcomes in Pediatric and Adult Patients.

IgA Nephropathy in Native Kidneys: Oxford and Banff Classifications Reveal Distinct Profiles and Predict Outcomes in Pediatric and Adult Patients.

Journal: Life (Basel, Switzerland)

Published: June 13, 2025

Genetic Susceptibility to Glomerulonephritis in Children: Analysis of Structural Kidney Genes and Immune System Genes.

Genetic Susceptibility to Glomerulonephritis in Children: Analysis of Structural Kidney Genes and Immune System Genes.

Journal: Journal of clinical medicine

Published: June 13, 2025

Whole-exome sequencing in pediatric patients with glomerulonephritis.

Whole-exome sequencing in pediatric patients with glomerulonephritis.

Journal: Frontiers in genetics

Published: April 14, 2025

N6-adenosine methylation enhances nuclear mRNA export through METTL3 and NUP93.

N6-adenosine methylation enhances nuclear mRNA export through METTL3 and NUP93.

Journal: Nature cell biology

Published: March 05, 2025

COL4A5-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype.

COL4A5-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype.

Journal: Kidney international reports

Published: October 01, 2024

Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21.

Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21.

Journal: Balkan journal of medical genetics : BJMG

Published: March 14, 2024

Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4?

Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4?

Journal: Clinical genetics

Published: October 29, 2023

Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.

Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.

Journal: European journal of human genetics : EJHG

Published: November 08, 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

The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.

The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.

Journal: Frontiers in medicine

Published: May 31, 2022

Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression.

Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 26, 2022

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: June 11, 2021

Showing 1-12 of 31

Last Updated: 09/26/2026