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personal data approved: 2016. IX. 15.
Personal data
name György Fekete
year of birth 1944
name of institution
doctoral school
SE Doctoral School of Molecular Medicine (Core member)
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
HAC accreditation
full compliance
(2015. I. 30.)
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
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: Paper 51. 11 p.
type of document: Journal paper/Article
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
language: English
URL 
2013

Komlosi K, Maasz A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Ablonczy M, Nemeth K, Fekete G, Melegh B: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNASer(UCN) and Review of Published Cases, JOURNAL OF INHERITED METABOLIC DISEASE REPORTS 9: pp. 105-111.
type of document: Journal paper/Article
language: English
URL 
2013

Patocs B, Nemeth K, Garami M, Arato G, Kovalszky I, Szendroi M, Fekete G: Multiple splice variants of EWSR1-ETS fusion transcripts co-existing in the Ewing sarcoma family of tumors., CELLULAR ONCOLOGY 36: (3) pp. 191-200.
type of document: Journal paper/Article
number of independent citations: 6
language: English
DOI 
2013

Haltrich I, Csoka M, Kovacs G, Torok D, Alpar D, Ottoffy G, Fekete G: Six Cases of Rare Gene Amplifications and Multiple Copy of Fusion Gene in Childhood Acute Lymphoblastic Leukemia., PATHOLOGY AND ONCOLOGY RESEARCH 19: (1) pp. 123-128.
type of document: Journal paper/Article
number of independent citations: 5
language: English
URL 
2010

Sallai A, Solyom J, Dobos M, Szabo J, Halasz Z, Sagodi L, Niederland T, Kozari A, Bertalan R, Ugocsai P, Fekete G: Y-chromosome markers in Turner syndrome: Screening of 130 patients., JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION 33: (4) pp. 222-227.
type of document: Journal paper/Article
number of independent citations: 25
language: English
DOI 
2010

Dajnoki A, Fekete G, Keutzer J, Orsini JJ, De Jesus VR, Chien YH, Hwu WL, Lukacs Z, Muhl A, Zhang XK, Bodamer O: Newborn screening for Fabry disease by measuring GLA activity using tandem mass spectrometry, CLINICA CHIMICA ACTA 411: (19-20) pp. 1428-1431.
type of document: Journal paper/Article
number of independent citations: 23
language: English
DOI 
2005

Horvath J, Fliegauf M, Olbrich H, Kispert A, King SM, Mitchison H, Zariwala MA, Knowles MR, Sudbrak R, Fekete G, Neesen J, Reinhardt R, Omran H: Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients., AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY 33: (1) pp. 41-47.
type of document: Journal paper/Article
number of independent citations: 21
language: English
DOI 
1999

Ferenczi A, Garami M, Kiss E, Pék M, Sasvári-Székely M, Barta Cs, Staub M, Sólyom J, Fekete Gy: Screening for Mutations of 21-Hydroxylase Gene in Hungarian Patients with Congenital Adrenal Hyperplasia., JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 84: (7) pp. 2369-2372.
type of document: Journal paper/Article
number of independent citations: 33
language: English
URL 
1989

Fekete G, Plattner R, Crabb DW, Zhang B, Harris RA, Heerema N, Palmer CG: Localization of the human gene for the El alpha subunit of branched chain keto acid dehydrogenase (BCKDHA) to chromosome 19q13.1----q13.2, CYTOGENETICS AND CELL GENETICS 50: pp. 236-237.
type of document: Journal paper/Article
number of independent citations: 9
language: English
DOI 
Number of independent citations to these publications:122 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
191
number of scientific publications:
299
monographs and professional books:
1
monographs/books in which chapters/sections were contributed:
32 
number of independent citations to scientific publications and creative works:
1461

 
All rights reserved © 2007, Hungarian Doctoral Council. Doctoral Council registration number at commissioner for data protection: 02003/0001. Program version: 1.2318 ( 2016. XI. 26. )