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personal data approved: 2023. I. 01.
Personal data
Nikoletta Nagy
name Nikoletta Nagy
name of institution
doctoral school
SzTE Doctoral School of Interdisciplinary Medicine (Announcer of research topic)
SzTE Doctoral School of Clinical Medicine (Announcer of research topic)
accreditation statement submitted to: University of Szeged
Contact details
E-mail address nikoletta.nagygmail.com
phone number +36 62 545-134
mobile phone number +36 70 533-3834
own web page
Academic title
scientific degree, title Ph.D.
year degree was obtained 2007
discipline to which degree belongs clinical medicine
institution granting the degree University of Szeged
scientific degree, title Habilitation
year degree was obtained 2017
discipline to which degree belongs clinical medicine
institution granting the degree University of Szeged
scientific degree, title DSc
year degree was obtained 2022
discipline to which degree belongs clinical medicine
institution granting the degree HAS
Employment
2005 - University of Szeged
other (not specified) (egyetemi adjunktus)
Thesis topic supervisor
number of doctoral students supervised until now 0
number of students who fulfilled course requirements 0
students who obtained their degrees:
(50%) Éva Melinda Pap PhD 2020  DSCM-SzTE
Beáta Fábos PhD 2018  DSCM-SzTE
Adrienn Sulák PhD 2017  DSCM-SzTE
Kornélia Tripolszki PhD 2017  DSCM-SzTE
Katalin Farkas PhD 2016  DSCM-SzTE
(50%) Emese Beatrix Horváth PhD 2014  DSCM-SzTE
(50%) Péter Vályi PhD 2014  DSCM-SzTE

  Thesis topic proposals
Research
research area Investigations on the genetic background of rare monogenic diseases.
research field in which current research is conducted general health sciences
clinical medicine
Publications
2020

Pap É. M., Farkas K., Tóth L., Fábos B., Széll M., Németh G., Nagy N.: Identification of putative genetic modifying factors that influence the development of Papillon–Lefévre or Haim–Munk syndrome phenotypes, CLINICAL AND EXPERIMENTAL DERMATOLOGY 45: (5) pp. 555-559.
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL 
2019

Zombor Melinda, Kalmár Tibor, Nagy Nikoletta, Berényi Marianne, Telcs Borbála, Maróti Zoltán, Brandau Oliver, Sztriha László: A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature, JOURNAL OF APPLIED GENETICS 60: (2) pp. 151-162.
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL 
2019

Gál B, Göblös A, Danis J, Farkas K, Sulák A, Varga E, Nagy N, Széll M, Kemény L, Bata-Csörgő Z: The management and genetic background of pityriasis rubra pilaris, JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY 33: (5) pp. 944-949.
type of document: Journal paper/Article
language: English
URL 
2019

Széll Márta, Szabó Kornélia, Csoma Zsanett, Manczinger Máté, Nagy Nikoletta, Veréb Zoltán, Bata-Csörgő Zsuzsanna, Kemény Lajos: Bőrbetegségek immunpatogenezisének és genetikájának vizsgálata, BŐRGYÓGYÁSZATI ÉS VENEROLÓGIAI SZEMLE 95: (2) pp. 38-42.
type of document: Journal paper/Article
language: Hungarian
Full text 
2018

Marki S, Goblos A, Szlavicz E, Torok N, Balicza P, Bereznai B, Takats A, Engelhardt J, Klivenyi P, Vecsei L, Molnar MJ, Nagy N, Szell M: The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson’s Disease in the Hungarian Population, PARKINSONS DISEASE 2018: 9351598
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL 
2018

Danis J, Goblos A, Gal B, Sulak A, Farkas K, Torok D, Varga E, Korom I, Kemeny L, Szell M, Bata-Csorgo Z, Nagy N: Nuclear Factor kappaB Activation in a Type V Pityriasis Rubra Pilaris Patient Harboring Multiple CARD14 Variants., FRONTIERS IN IMMUNOLOGY 9: 1564
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL 
2017

Kornélia Tripolszki, Bernadett Csányi, Dóra Nagy, Antonia Ratti, Cinzia Tiloca, Vincenzo Silani, Éva Kereszty, Nóra Török, László Vécsei, József I Engelhardt, Péter Klivényi, Nikoletta Nagy, Márta Széll: Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis, NEUROBIOLOGY OF AGING: AGE-RELATED PHENOMENA NEURODEGENERATION AND NEUROPATHOLOGY 53: 195.e1
type of document: Journal paper/Article
number of independent citations: 9
language: English
URL 
2017

Lola Tóth, Beáta Fábos, Katalin Farkas, Adrienn Sulák, Kornélia Tripolszki, Márta Széll, Nikoletta Nagy: Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4, BMC MEDICAL GENETICS 18: (1) 27
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL 
2017

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) e00669
type of document: Journal paper/Article
number of independent citations: 9
language: English
URL 
2008

Szell M, Baltas E, Bodai L, Bata-Csorgo Z, Nagy N, Dallos A, Porfarzi R, Simics E, Kondorosi I, Szalai Z, Toth GK, Hunyadi J, Dobozy A, Kemeny L: The Arg160Trp allele of melanocortin-1 receptor gene might potect against vitiligo, PHOTOCHEMISTRY AND PHOTOBIOLOGY 84: (3) pp. 565-571.
type of document: Journal paper/Article
number of independent citations: 18
language: English
URL 
Number of independent citations to these publications:50 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
181
number of scientific publications:
175
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
0 
number of independent citations to scientific publications and creative works:
1187

 
All rights reserved © 2007, Hungarian Doctoral Council. Doctoral Council registration number at commissioner for data protection: 02003/0001. Program version: 2.2358 ( 2017. X. 31. )