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personal data approved: 2017. I. 24.
Personal data
name Nikoletta Nagy
year of birth 1981
name of institution
doctoral school
SzTE Doctoral School of Interdisciplinary Medicine (Supervisor)
SzTE Doctoral School of Clinical Medicine (Supervisor)
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:
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 (2017/12)  IDS-SzTE
Kornélia Tripolszki PhD (2017/08)  DSCM-SzTE
present PhD students:
Adrienn Sulák (PhD) (2017/08)  DSCM-SzTE
Beáta Tóth (PhD) (2017/08)  IDS-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
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: 1
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: 3
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
language: English
URL 
2012

Tanaka A, Weinel S, Nagy N, O'Driscoll M, Lai-Cheong JE, Kulp-Shorten CL, Knable A, Carpenter G, Fisher SA, Hiragun M, Yanase Y, Hide M, Callen J, McGrath JA: Germline mutation in ATR in autosomal- dominant oropharyngeal cancer syndrome., AMERICAN JOURNAL OF HUMAN GENETICS 90: (3) pp. 511-517.
type of document: Journal paper/Article
number of independent citations: 21
language: English
DOI 
2012

Kis E, Baltas E, Kinyo A, Varga E, Nagy N, Gyulai R, Kemeny L, Olah J: Successful Treatment of Multiple Basaliomas with Bleomycin-based Electrochemotherapy: A Case Series of Three Patients with Gorlin-Goltz Syndrome., ACTA DERMATO-VENEREOLOGICA 92: (6) pp. 648-651.
type of document: Journal paper/Article
number of independent citations: 6
language: English
DOI 
2010

Szegedi K, Sonkoly E, Nagy N, Nemeth IB, Bata-Csorgo Z, Kemeny L, Dobozy A, Szell M: The anti-apoptotic protein G1P3 is overexpressed in psoriasis and regulated by the non-coding RNA, PRINS, EXPERIMENTAL DERMATOLOGY 19: (3) pp. 269-278.
type of document: Journal paper/Article
number of independent citations: 29
language: English
DOI 
2010

Tanaka A, Morice-Picard F, Lacombe D, Nagy N, Hide M, Taieb A, McGrath J: Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia., AMERICAN JOURNAL OF MEDICAL GENETICS PART A 152A: (6) pp. 1347-1348.
type of document: Journal paper/Article
number of independent citations: 17
language: English
DOI 
2010

Tanaka A, Lai-Cheong JE, van den Akker PC, Nagy N, Millington G, Diercks GF, van Voorst Vader PC, Clements SE, Almaani N, Techanukul T, Hide M, South AP, McGrath JA: The molecular skin pathology of familial primary localized cutaneous amyloidosis., EXPERIMENTAL DERMATOLOGY 19: (5) pp. 416-423.
type of document: Journal paper/Article
number of independent citations: 16
language: English
DOI 
2010

Nagy N, Grattan CE, McGrath JA: New insights into hereditary angio-oedema: Molecular diagnosis and therapy., AUSTRALASIAN JOURNAL OF DERMATOLOGY 51: (3) pp. 157-162.
type of document: Journal paper/Article
number of independent citations: 7
language: English
DOI 
2009

Nagy N, Greaves MW, Tanaka A, McGrath JA, Grattan CE: Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema., JOURNAL OF DERMATOLOGICAL SCIENCE 56: (1) pp. 62-64.
type of document: Journal paper/Article
number of independent citations: 13
language: English
DOI 
Number of independent citations to these publications:113 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
46
number of scientific publications:
130
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
0 
number of independent citations to scientific publications and creative works:
477


2017. I. 31.
ODT ülés
Az ODT következő ülésére 2017. március 10-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: 1.2334 ( 2017. I. 15. )