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VALIDITY EXPIRED
personal data approved: 2011. IV. 14.
Personal data
name Veronika Karcagi
name of institution
doctoral school
ELTE Doctoral School of Biology (Academic staff member)
SE Doctoral School of Molecular Medicine (Academic staff member)
SE Doctoral School of University Semmelweis (Academic staff member)
the share of work in the different doctoral schools. ELTE Doctoral School of Biology 50%
SE Doctoral School of University Semmelweis 50%
accreditation statement submitted to: Eötvös Loránd University, Budapest
Contact details
E-mail address karcagi.veronikaoki.antsz.hu
phone number +36 1 476-1362
own web page
Academic title
scientific degree, title Ph.D.
year degree was obtained 1996
discipline to which degree belongs biology
institution granting the degree ELTE (to be translated)
Employment
1975 - Országos Környezetegészségügyi Intézet (research institute, not university)
Thesis topic supervisor
number of doctoral students supervised until now 1.5
number of students who fulfilled course requirements 1.5
students who obtained their degrees:
(50%) Ilona Milánkovics PhD 2010  DSMM-SE
Henriett Pikó PhD 2009  DSMM-SE

  Thesis topic proposals
Research
research area Neuromusculáris betegségek molekuláris genetikai diagnosztikai vizsgálatai. Geno- és fenotípus összefüggések elemzése, új mutációk keresése, valamint terápia kidolgozása nemzetközi együttműködésben. (to be translated)
research field in which current research is conducted clinical medicine
multidisciplinary medicine
Publications
2007

Juliane S. Müller, Agnes Herczegfalvi, Juan J. Vilchez, Jaume Colomer, Linda L.: Phenotypical spectrum of DOK7 mutations in congenital myasthenic, Brain, 130:1497-506, 2007
type of document: Journal paper
impact factor: 8.200
2006

Juliane S Müller, Henriett Pikó, Benedikt GH Schoser, Beate Schlotter-Weigel, Peter Reilich, Stefanie Gürster, Christine Born, Veronika Karcagi, Dieter Pongratz, Hanns Lochmüller, Maggie C. Walter: Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy, Neuromuscular Disorders, 16:432-436, 2006
type of document: Journal paper
impact factor: 3.040
number of independent citations: 1
2005

Gavin Hudson, Sharon Keers, Patrick Yu Wai Man, Philip Griffiths, Kirsi Huoponen, Marja-Liisa Savontaus, Eeva Nikoskelainen, Massimo Zeviani, Franco Carrara, Rita Horváth, Veronika Karcagi, Liesbeth S: Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder, Am. J. Hum. Genet. 77(6):1086-91. 2005
type of document: Journal paper
impact factor: 12.340
number of independent citations: 13
2005

Luba Kalaydjieva, Hanns Lochmüller, Ivailo Tournev, Frank Baas, Judit Beres, Jaume Colomer, Velina Guergueltcheva Ralf Herrmann, Veronika Karcagi, Rosalind King, Toshiyuki Miyata, Andrea Müllner-Eiden: 125th ENMC International Workshop: Neuromuscular Disorders in the Roma (Gypsy) Population, 23-25 April 2004, Naarden, The Netherlands, Neuromuscular Disorders 15: 65-71, 2005
type of document: Journal paper
impact factor: 3.040
2004

Morar B, Gresham D, Angelicheva D, Tournev I, Gooding R, Guergueltcheva V, Schmidt C, Abicht A, Lochmuller H, Tordai A, Kalmar L, Nagy M, Karcagi V, Jeanpierre M, Herczegfalvi A, Beeson D, Venkatarama: Mutation History of the Roma/Gypsies, Am. J. Hum. Genet. 75(4):596-609, 2004
type of document: Journal paper
impact factor: 10.540
number of independent citations: 11
2002

Jordanova, V. Karcagi, I. Kremensky, I. Litvinenko, M. Uzunova, I. Turnev, B. Ishpekova, A. Herczegfalvi, I. Simeonova and L. Kalaydjieva: Spinal Muscular Atrophy Among the Roma (Gypsies) in Bulgaria and Hungary, Neuromuscular Disorders, 12, 378-385, 2002
type of document: Journal paper
impact factor: 2.590
number of independent citations: 1
2002

Barisic N, Schmidt C, Sidorova OP, Herczegfalvi A, Gekht BM, Song IH, Stucka: Congenital myasthenic syndrome (CMS) in three European kinships due to a novel, Neuropediatrics. 2002 Oct;33(5):249-54
type of document: Journal paper
impact factor: 1.480
number of independent citations: 1
2001

M. Jaksch, R. Horvath, N. Horn, D. P. Auer, C. Macmillan, J. Peters, K-D. Gerbitz, I. Kraegeloh-Mann, A. Muntau, V. Karcagi, R. Kalmanchey, H. Lochmueller, E.A. Shoubridge, and P. Freisinger: Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy, Neurology, 57:1440-1446, 2001
type of document: Journal paper
impact factor: 5.230
number of independent citations: 23
1999

A. Abicht, R. Stucka, V. Karcagi, A. Herczegfalvi, R. Horvath, W. Mortier et al.: A common mutation (1267delG) in congenital myasthenic patients of Gypsy ethnic origin, Neurology, 1999, 53:1564-1569
type of document: Journal paper
impact factor: 5.230
number of independent citations: 34
1992

Venema, J., A. van Hoffe, Karcagi V., Natarajan A. T., van Zeeland A. A., Mullenders L. H. F.: Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from transcribed strand of active genes, Mol. Cell. Biol. 11:8, 4128-4134, 1992
type of document: Journal paper
impact factor: 7.580
number of independent citations: 244
Number of independent citations to these publications:328 
Scientometric data
Publication list in MTMT is not accessible.
number of scientific publications that meet accreditation criteria:
 
number of scientific publications:
26 
monographs and professional books:
3 
monographs/books in which chapters/sections were contributed:
3 
number of independent citations to scientific publications and creative works:
440 


2024. IV. 17.
ODT ülés
Az ODT következő ülésére 2024. június 14-én, pénteken 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. )