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personal data approved: 2018. X. 07.
Personal data
name Nikoletta Nagy
name of institution
doctoral school
SzTE Doctoral School of Interdisciplinary Medicine (Academic staff member)
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
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:
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

students with degree granting in process:
Beáta Tóth PhD (2018/12)  
  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
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: pp. 195.e1-195.e5.
type of document: Journal paper/Article
number of independent citations: 2
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) Paper 27. 4 p.
type of document: Journal paper/Article
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) Paper e00669. 7 p.
type of document: Journal paper/Article
language: English
URL 
2017

Tripolszki K, Farkas K, Sulak A, Szolnoky G, Duga B, Melegh B, Knox RG, Parker VER, Semple RK, Kemeny L, Szell M, Nagy N: Atypical neurofibromatosis type 1 with unilateral limb hypertrophy mimicking overgrowth syndrome., CLINICAL AND EXPERIMENTAL DERMATOLOGY 42: (7) pp. 763-766.
type of document: Journal paper/Article
language: English
DOI 
2017

Fabos B, Farkas K, Toth L, Sulak A, Tripolszki K, Tihanyi M, Nemeth R, Vas K, Csoma Z, Kemeny L, Szell M, Nagy N: Delineating the genetic heterogeneity of OCA in Hungarian patients., EUROPEAN JOURNAL OF MEDICAL RESEARCH 22: (1) Paper 20. 8 p.
type of document: Journal paper/Article
language: English
URL 
2016

Tripolszki K, Knox R, Parker V, Semple R, Farkas K, Sulák A, Horváth E, Széll M, Nagy N: Somatic mosaicism of the PIK3CA gene identified in a Hungarian girl with macrodactyly and syndactyly, EUROPEAN JOURNAL OF MEDICAL GENETICS 59: (4) pp. 223-226.
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL 
2016

Kemeny L, Nagy N, Csoma Z, Szabo K, Eros G: Pharmacological Targeting of the Epidermal Barrier., CURRENT PHARMACEUTICAL DESIGN 22: (35) pp. 5373-5381.
type of document: Journal paper/Review paper
number of independent citations: 1
language: English
URL 
2016

Sulak A, Toth L, Farkas K, Tripolszki K, Fabos B, Kemeny L, Valyi P, Nagy K, Nagy N, Szell M: One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes, CLINICAL AND EXPERIMENTAL DERMATOLOGY 41: (2) pp. 190-195.
type of document: Journal paper/Article
number of independent citations: 5
language: English
URL 
2015

Nagy N, Farkas K, Kemény L, Széll M: Phenotype-genotype correlations for clinical variants caused by CYLD mutations, EUROPEAN JOURNAL OF MEDICAL GENETICS 58: (5) pp. 271-278.
type of document: Journal paper/Review paper
number of independent citations: 9
language: English
DOI 
2015

Nemes E, Farkas K, Kocsis-Deak B, Drubi A, Sulak A, Tripolszki K, Dosa P, Ferenc L, Nagy N, Szell M: Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation., ARCHIVES OF DERMATOLOGICAL RESEARCH 307: (10) pp. 891-895.
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL 
Number of independent citations to these publications:22 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
62
number of scientific publications:
158
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
0 
number of independent citations to scientific publications and creative works:
700


2019. I. 10.
ODT ülés
Az ODT következő ülésére 2019. február 22-én 10.00 órakor kerül sor a Semmelweis Egyetem Szenátusi termében (Bp. Üllői út 26. I. emelet).

 
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. )