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Personal data sheet
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personal data approved: 2023. XI. 16.
Personal data
name Anikó Ujfalusi
name of institution
doctoral school
DE Kálmán Laki Doctoral School (Academic staff member)
DE Doctoral School of Clinical Medicine (Academic staff member)
the share of work in the different doctoral schools. DE Kálmán Laki Doctoral School 50%
DE Doctoral School of Clinical Medicine 50%
Contact details
E-mail address ujfalusi.anikomed.unideb.hu
phone number +36 52 411-717/56559
Academic title
scientific degree, title Ph.D.
year degree was obtained 1999
discipline to which degree belongs theoretical medicine
institution granting the degree University of Debrecen
Employment
1992 - University of Debrecen
university professor or researcher
Thesis topic supervisor
number of doctoral students supervised until now 1
number of students who fulfilled course requirements 0
students who obtained their degrees:
Orsolya Nagy PhD 2021  DSCM-DE
  Thesis topic proposals
Research
research area Genetic investigation in congenital heart diseases: detection of copy number variations by array CGH technique.
research field in which current research is conducted general health sciences
clinical medicine
Publications
2022

 Andó Szilvia, Koczok Katalin, Bessenyei Beáta, Balogh István, Ujfalusi Anikó: Cytogenetic Investigation of Infertile Patients in Hungary: A 10-Year Retrospective Study, GENES 13: (11) 2086
type of document: Journal paper/Article
language: English
URL 
2021

 Nagy Orsolya, Kárteszi Judit, Elmont Beatrix, Ujfalusi Anikó: Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 Gene, FRONTIERS IN PEDIATRICS 9: 664548
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL 
2020

 Ujfalusi Anikó, Nagy Orsolya, Bessenyei Beáta, Lente Györgyi, Kántor Irén, Borbély Ádám J., Szakszon Katalin: 22q13 Microduplication Syndrome in Siblings with Mild Clinical Phenotype: Broadening the Clinical and Behavioral Spectrum, MOLECULAR SYNDROMOLOGY 11: (3) pp. 146-152.
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL 
2019

 Nagy Orsolya, Szakszon Katalin, Biró Brigitta Orsolya, Mogyorósy Gábor, Nagy Dóra, Nagy Bálint, Balogh István, Ujfalusi Anikó: Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases, JOURNAL OF BIOTECHNOLOGY 299: pp. 86-95.
type of document: Journal paper/Article
number of independent citations: 10
language: English
URL 
2019

 Nagy Orsolya, Kárteszi Judit, Hartwig Marianna, Bertalan Rita, Jávorszky Eszter, Erhardt Éva, Patócs Attila, Tornóczky Tamás, Balogh István, Ujfalusi Anikó: The importance of the multiplex ligation-dependent probe amplification in the identification of a novel two-exon deletion of the NR5A1 gene in a patient with 46,XY differences of sex development, MOLECULAR BIOLOGY REPORTS 46: (5) pp. 5595-5601.
type of document:
number of independent citations: 4
language: English
URL 
2014

 Szakszon Katalin, Balogh Erzsébet, Ujfalusi Anikó, Bessenyei Beáta, P Szabó Gabriella, Balogh István, Oláh Éva dr: Ritka genetikai betegségek klinikai és genetikai diagnosztikájában szerzett tapasztalataink a kelet-magyarországi régióban (2007-2013), ORVOSI HETILAP 155: (9) pp. 348-357.
type of document: Journal paper/Article
number of independent citations: 2
language: Hungarian
URL 
2014

 Szakszon Katalin, Ujfalusi Anikó, Balogh Erzsébet, Mogyorósy Gábor, Felszeghy Enikő, Szilvássy Judit, Horkay Edit, Berényi Ervin, Merő Gabriella, Knegt Alida C További szerzőségek>>: 15q26-microdeletio-szindróma, ORVOSI HETILAP 155: (9) pp. 362-364.
type of document: Journal paper/Article
number of independent citations: 1
language: Hungarian
URL 
2013

 Mokánszki Attila, Ujfalusi Anikó, Balogh Erzsébet, Molnár Zsuzsanna, Sápy Tamás, Jakab Attila, Varga Attila, Oláh Éva: Infertilitásban végzett citogenetikai és molekuláris genetikai vizsgálatok a kelet-magyarországi régióban, ORVOSI HETILAP 154: (2) pp. 52-61.
type of document: Journal paper/Article
number of independent citations: 1
language: Hungarian
URL 
2012

 Szabó Gabriella P, Knegt Alida C, Ujfalusi Anikó, Balogh Erzsébet, Szabó Tamás, Oláh Éva: Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients, AMERICAN JOURNAL OF MEDICAL GENETICS PART A 158A: (4) pp. 869-876.
type of document: Journal paper/Article
number of independent citations: 6
language: English
URL 
2002

 Csiszár K, Fong F T S, Ujfalusi A, Krawetz S A, Salvati E P, Mackenzie J W, Boyd D C: Somatic mutations of the lysyl oxidase gene on chromosome 5q23.1 in colorectal tumors, INTERNATIONAL JOURNAL OF CANCER 97: (5) pp. 636-642.
type of document: Journal paper/Article
number of independent citations: 51
language: English
URL 
Number of independent citations to these publications:79 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
84
number of scientific publications:
92
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
0 
number of independent citations to scientific publications and creative works:
403

 
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. )