Nikoletta Nagy (N Nagy)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 16

Top Topics

Congenital Heart Disease

High Throughput Sequencing

Top Venues

International journal of molecular sciences

Experimental dermatology

Clinical and experimental dermatology

This page only lists publications with an associated author ORCID identifier.

Publications

Nikoletta Nagy, Margit Pál, Dóra Nagy, Barbara Anna Bokor, Aliz Zimmermann, Balázs Gellén, András Salamon, László Sztriha, Péter Klivényi, Márta Széll
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder. BMC pediatrics 24 (1) (2024)
Nikoletta Nagy, Margit Pál, Jozsef Kun, Bence Gálik, Peter Urban, Marta Medvecz, Beata Fabos, Alexandra Neller, Aliasgari Abdolreza, Judit Danis, Viktoria Szabo, Zhuo Yang, Stefanie Fenske, Martin Biel, Attila Gyenesei, Eva Adam, Marta Szell
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease. International journal of molecular sciences 25 (2) (2024)
Nikoletta Nagy, Margit Pál, Jozsef Kun, Bence Gálik, Peter Urban, Marta Medvecz, Beata Fabos, Alexandra Neller, Aliasgari Abdolreza, Judit Danis, Viktoria Szabo, Zhuo Yang, Stefanie Fenske, Martin Biel, Attila Gyenesei, Eva Adam, Marta Szell
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease. International journal of molecular sciences 25 (2) (2024)
Nikoletta Nagy, Margit Pál, Dóra Nagy, Barbara Anna Bokor, Aliz Zimmermann, Balázs Gellén, András Salamon, László Sztriha, Péter Klivényi, Márta Széll
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder. BMC pediatrics 24 (1) (2024)
Nikoletta Nagy, Margit Pál, Dóra Nagy, Barbara Anna Bokor, Aliz Zimmermann, Balázs Gellén, András Salamon, László Sztriha, Péter Klivényi, Márta Széll
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder. BMC pediatrics 24 (1) (2024)
Nikoletta Nagy, Margit Pál, Dóra Nagy, Barbara Anna Bokor, Aliz Zimmermann, Balázs Gellén, András Salamon, László Sztriha, Péter Klivényi, Márta Széll
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder. BMC pediatrics 24 (1) (2024)
Margit Pál, Dóra Nagy, Alexandra Neller, Katalin Farkas, Dóra Leprán-Török, Nikoletta Nagy, Dalma Füstös, Roland Nagy, Adrienne Németh, Judit Szilvássy, László Rovó, Jozsef Geza Kiss, Márta Széll
Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients. International journal of molecular sciences 24 (8) (2023)
Margit Pál, Dóra Nagy, Alexandra Neller, Katalin Farkas, Dóra Leprán-Török, Nikoletta Nagy, Dalma Füstös, Roland Nagy, Adrienne Németh, Judit Szilvássy, László Rovó, Jozsef Geza Kiss, Márta Széll
Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients. International journal of molecular sciences 24 (8) (2023)
Margit Pál, Éva Vetró, Nikoletta Nagy, Dóra Nagy, Emese Horváth, Barbara Anna Bokor, Anita Varga, László Seres, Judit Oláh, József Piffkó, Márta Széll
Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS. Current issues in molecular biology 45 (7) (2023)
Margit Pál, Dóra Nagy, Alexandra Neller, Katalin Farkas, Dóra Leprán-Török, Nikoletta Nagy, Dalma Füstös, Roland Nagy, Adrienne Németh, Judit Szilvássy, László Rovó, Jozsef Geza Kiss, Márta Széll
Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients. International journal of molecular sciences 24 (8) (2023)
Judit Danis, Evelyn Kelemen, Neil Rajan, Nikoletta Nagy, Márta Széll, Éva Ádám
TRAF3 and NBR1 both influence the effect of the disease-causing CYLD(Arg936X) mutation on NF-κB activity. Experimental dermatology 30 (11) (2021)
Éva Melinda Pap, Katalin Farkas, Márta Széll, Gábor Németh, Neil Rajan, Nikoletta Nagy
Identification of putative phenotype-modifying genetic factors associated with phenotypic diversity in Brooke-Spiegler syndrome. Experimental dermatology 29 (10) (2020)
É M Pap, K Farkas, L Tóth, B Fábos, M Széll, G Németh, Nikoletta Nagy
Identification of putative genetic modifying factors that influence the development of Papillon-Lefévre or Haim-Munk syndrome phenotypes. Clinical and experimental dermatology 45 (5) (2020)
Sezgi Sarıkaya Solak, S Yalcıntepe, C Atahan, Nikoletta Nagy, N Can
A novel nonsense mutation of the CYLD gene in a Turkish family with multiple familial trichoepithelioma. Clinical and experimental dermatology 45 (4) (2019)
Sándor Márki, Anikó Göblös, Eszter Szlávicz, Nóra Török, Péter Balicza, Benjamin Bereznai, Annamária Takáts, József Engelhardt, Klivényi Péter, László Vécsei, Mária Judit Molnár, Nikoletta Nagy, Márta Széll
The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population. Parkinson's disease 2018 (2018)
Kornélia Tripolszki, Dóra Török, David Goudenège, Katalin Farkas, Adrienn Sulák, Nóra Török, József I Engelhardt, Péter Klivényi, Vincent Procaccio, Nikoletta Nagy, Márta Széll
High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis. Brain and behavior 7 (4) (2017)