Nikoletta Nagy

Szeged, CS, Hungary

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 64 publications

The importance of challenging dogma with patient data.

The importance of challenging dogma with patient data.

Journal: The Journal of investigative dermatology

Published: January 30, 2026

The importance of challenging dogma with patient data.

The importance of challenging dogma with patient data.

Journal: The Journal of investigative dermatology

Published: January 30, 2026

A Unique Patient Stratification Method Combined with a Machine Learning Approach Identifies Novel Genetic Susceptibility and Protective Factors for Severe COVID-19 in a Hungarian Population.

A Unique Patient Stratification Method Combined with a Machine Learning Approach Identifies Novel Genetic Susceptibility and Protective Factors for Severe COVID-19 in a Hungarian Population.

Journal: International journal of molecular sciences

Published: January 10, 2026

A Novel Germline Frameshift Variant in the Tumor Suppressor Gene OBSCN in a Melanoma Patient.

A Novel Germline Frameshift Variant in the Tumor Suppressor Gene OBSCN in a Melanoma Patient.

Journal: International journal of molecular sciences

Published: September 15, 2025

Population- and haplotype-dependent variation around TYR rs1126809: An in silico study for melanoma risk research.

Population- and haplotype-dependent variation around TYR rs1126809: An in silico study for melanoma risk research.

Journal: JID innovations : skin science from molecules to population health

Published: July 29, 2025

Targeting noncanonical nuclear factor kappa B signalling in CYLD cutaneous syndrome by selective inhibition of IκB kinase alpha.

Targeting noncanonical nuclear factor kappa B signalling in CYLD cutaneous syndrome by selective inhibition of IκB kinase alpha.

Journal: The British journal of dermatology

Published: February 06, 2025

Timely recognition of a probably life-threatening genodermatosis: familial case report of hereditary leiomyomatosis and renal cell cancer.

Timely recognition of a probably life-threatening genodermatosis: familial case report of hereditary leiomyomatosis and renal cell cancer.

Journal: Pathology oncology research : POR

Published: January 17, 2025

Novel Pathogenic Variant of the TRRAP Gene Detected in a Hungarian Family with Autosomal Dominant Non-Syndromic Hearing Loss.

Novel Pathogenic Variant of the TRRAP Gene Detected in a Hungarian Family with Autosomal Dominant Non-Syndromic Hearing Loss.

Journal: International journal of molecular sciences

Published: January 10, 2025

Novel FANCI and RAD54B Variants and the Observed Clinical Outcomes in a Hungarian Melanoma Cohort.

Novel FANCI and RAD54B Variants and the Observed Clinical Outcomes in a Hungarian Melanoma Cohort.

Journal: International journal of molecular sciences

Published: December 02, 2024

Oculocutaneous albinism type 1B associated with allelic combination of a risk haplotype.

Oculocutaneous albinism type 1B associated with allelic combination of a risk haplotype.

Journal: Journal of dermatological science

Published: November 13, 2024

Novel Variants in Medium and Low Penetrance Predisposing Genes in a Hungarian Malignant Melanoma Cohort With Increased Risk.

Novel Variants in Medium and Low Penetrance Predisposing Genes in a Hungarian Malignant Melanoma Cohort With Increased Risk.

Journal: Pigment cell & melanoma research

Published: July 03, 2024

Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.

Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.

Journal: International journal of molecular sciences

Published: November 10, 2023

Showing 1-12 of 64

Last Updated: 09/26/2026