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personal data approved: 2019. VI. 25.
Personal data
György Fekete
name György Fekete
name of institution
doctoral school
SE Doctoral School of Molecular Medicine (Core member emeritus)
Council of the Doctoral School
the share of work in the different doctoral schools. SE Doctoral School of Molecular Medicine 99%
SE DSMM-SE Council of the Doctoral School 1%
accreditation statement submitted to: Semmelweis University, Budapest
Contact details
E-mail address fekete.gyorgygyer2.sote.hu
phone number +36 1 210-2245
Academic title
scientific degree, title Ph.D.
year degree was obtained 1981
discipline to which degree belongs clinical medicine
institution granting the degree Semmelweis Orvostudományi Egyetem (to be translated)
scientific degree, title DSc
year degree was obtained 1992
discipline to which degree belongs clinical medicine
institution granting the degree HAS
Employment
1968 - Semmelweis University, Budapest
professor emeritus
Thesis topic supervisor
number of doctoral students supervised until now 7
number of students who fulfilled course requirements 4
students who obtained their degrees:
Barbara Zentainé Patócs PhD 2015  DSMM-SE
Irén Haltrich PhD 2006  DSMM-SE
Miklós Garami PhD 2005  DSMM-SE
Zsolt Urbán PhD 1997  

  Thesis topic proposals
Research
research area Molecular genetic studies, clinical genetics
research field in which current research is conducted clinical medicine
Publications
2019

Hennermann Julia B, Arash-Kaps Laila, Fekete György, Schaaf Andreas, Busch Andreas, Frischmuth Thomas: Pharmacokinetics, pharmacodynamics, and safety of moss-aGalactosidase A in patients with Fabry disease., JOURNAL OF INHERITED METABOLIC DISEASE In Press: (In Press) pp. In Press-In Press.
type of document: Journal paper/Article
language: English
URL 
2019

Haltrich Irén, Fekete György: Új diagnosztikai módszerek a ritka betegségek felismerésében {Modern Diagnostic Techniques For Diagnosis Of Rare Diseases}, MAGYAR TUDOMÁNY 180: (5) pp. 669-678.
type of document: Journal paper/Article
language: Hungarian
URL 
2019

Madar László, Szakszon Katalin, Pfliegler György, Szabó Gabriella P, Brúgós Boglárka, Ronen Natali, Papp Judit, Zahuczky Katalin, Szakos Erzsébet, Fekete György, Oláh Éva, Koczok Katalin, Balogh István: FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies., JOURNAL OF BIOTECHNOLOGY In Press: (In Press) pp. In Press-In Press.
type of document: Journal paper/Article
language: English
URL 
2018

Acs OD, Peterfia B, Hollosi P, Haltrich I, Sallai A, Luczay A, Buiting K, Horsthemke B, Torok D, Szabo A, Fekete G: Elsődleges genetikai vizsgálat Prader–Willi-szindróma igazolására [Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome], ORVOSI HETILAP 159: (2) pp. 64-69.
type of document: Journal paper/Article
language: Hungarian
URL 
2018

Kiss N, Haluszka D, Lőrincz K, Kuroli E, Hársing J, Mayer B, Kárpáti S, Fekete G, Szipőcs R, Wikonkál N, Medvecz M: Ex vivo nonlinear microscopy imaging of Ehlers–Danlos syndrome-affected skin, ARCHIVES OF DERMATOLOGICAL RESEARCH 310: (5) pp. 463-473.
type of document: Journal paper/Article
language: English
URL 
2017

Meyer R, Soellner L, Begemann M, Dicks S, Fekete G, Rahner N, Zerres K, Elbracht M, Eggermann T: Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management, JOURNAL OF PEDIATRICS 187: pp. 206-212.
type of document: Journal paper/Article
language: English
URL 
2017

Odler B, Cseh A, Constantin T, Fekete G, Losonczy G, Tamasi L, Benke K, Szilveszter B, Muller V: Long time enzyme replacement therapy stabilizes obstructive lung disease and alters peripheral immune cell subsets in Fabry patients, CLINICAL RESPIRATORY JOURNAL 11: (6) pp. 942-950.
type of document: Journal paper/Article
number of independent citations: 4
language: English
URL 
2017

Sachwitz J, Meyer R, Fekete G, Spranger S, Matuleviciene A, Kucinskas V, Bach A, Luczay A, Bruchle NO, Eggermann K, Zerres K, Elbracht M, Eggermann T: NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS features, CLINICAL GENETICS 91: (1) pp. 73-78.
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL 
2015

Haltrich I, Piko H, Pamjav H, Somogyi A, Volgyi A, David D, Beke A, Garamvolgyi Z, Kiss E, Karcagi V, Fekete G: Complex X chromosome rearrangement associated with multiorgan autoimmunity., MOLECULAR CYTOGENETICS 8: 51
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL 
2015

David D, Almeida LS, Maggi M, Araujo C, Imreh S, Valentini G, Fekete G, Haltrich I: Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene., JOURNAL OF INHERITED METABOLIC DISEASE REPORTS 23: pp. 55-65.
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL 
Number of independent citations to these publications:10 
Scientometric data
Saját közlemény- és idézőlista list of publications and citations
number of scientific publications that meet accreditation criteria:
206
number of scientific publications:
349
monographs and professional books:
3
monographs/books in which chapters/sections were contributed:
32 
art/engineering creative works:
0
scientific publications published abroad that meet the accreditation criteria:
103
publications not in Hungarian, published in Hungary, meeting the accreditation criteria:
6
number of independent citations to scientific publications and creative works:
2025

 
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. )