Natalia Dubrowinskaja

Hannover, NI, Germany

Last Updated: 09/26/2026

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Found 33 publications

Rare variants in genes related to inborn errors of immunity in patients with rheumatoid arthritis and secondary immunodeficiency.

Rare variants in genes related to inborn errors of immunity in patients with rheumatoid arthritis and secondary immunodeficiency.

Journal: RMD open

Published: April 10, 2026

A germline IκBα mutation outside the signal reception domain blocks nuclear translocation of NFκB1 and associates with autoinflammation-like features.

A germline IκBα mutation outside the signal reception domain blocks nuclear translocation of NFκB1 and associates with autoinflammation-like features.

Journal: Annals of the rheumatic diseases

Published: April 24, 2025

GWAS meta-analysis identifies five susceptibility loci for endometrial cancer.

GWAS meta-analysis identifies five susceptibility loci for endometrial cancer.

Journal: EBioMedicine

Published: January 23, 2025

Reappraisal of IgG subclass deficiencies: a retrospective comparative cohort study.

Reappraisal of IgG subclass deficiencies: a retrospective comparative cohort study.

Journal: Frontiers in immunology

Published: December 28, 2024

Comparative sequencing study of mismatch repair and homology-directed repair genes in endometrial cancer and breast cancer patients from Kazakhstan.

Comparative sequencing study of mismatch repair and homology-directed repair genes in endometrial cancer and breast cancer patients from Kazakhstan.

Journal: International journal of cancer

Published: February 05, 2024

Alteration of Cadherin 3 Expression and DNA Methylation in Association with Aggressive Renal Cell Carcinoma.

Alteration of Cadherin 3 Expression and DNA Methylation in Association with Aggressive Renal Cell Carcinoma.

Journal: International journal of molecular sciences

Published: September 28, 2023

Rituximab to treat prolidase deficiency due to a novel pathogenic copy number variation in PEPD.

Rituximab to treat prolidase deficiency due to a novel pathogenic copy number variation in PEPD.

Journal: RMD open

Published: July 17, 2023

Corrigendum: Vulnerability to meningococcal disease in immunodeficiency due to a novel pathogenic missense variant in NFKB1.

Corrigendum: Vulnerability to meningococcal disease in immunodeficiency due to a novel pathogenic missense variant in NFKB1.

Journal: Frontiers in immunology

Published: April 25, 2023

Identification of variants in genes associated with autoinflammatory disorders in a cohort of patients with psoriatic arthritis.

Identification of variants in genes associated with autoinflammatory disorders in a cohort of patients with psoriatic arthritis.

Journal: RMD open

Published: July 06, 2022

DNA Methylation in INA, NHLH2, and THBS4 Is Associated with Metastatic Disease in Renal Cell Carcinoma.

DNA Methylation in INA, NHLH2, and THBS4 Is Associated with Metastatic Disease in Renal Cell Carcinoma.

Journal: Cancers

Published: November 13, 2021

Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1.

Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1.

Journal: Frontiers in immunology

Published: August 30, 2021

Diagnostic Yield and Therapeutic Consequences of Targeted Next-Generation Sequencing in Sporadic Primary Immunodeficiency.

Diagnostic Yield and Therapeutic Consequences of Targeted Next-Generation Sequencing in Sporadic Primary Immunodeficiency.

Journal: International archives of allergy and immunology

Published: June 01, 2021

Showing 1-12 of 33

Last Updated: 09/26/2026