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personal data approved: 2020. IX. 15.
Personal data
name László Sztriha
name of institution
doctoral school
SzTE Doctoral School of Clinical Medicine (Announcer of research topic)
Contact details
E-mail address sztriha.laszlomed.u-szeged.hu
phone number +36 62 342-076
mobile phone number +36 20 535-1323
Academic title
scientific degree, title Ph.D.
year degree was obtained 1989
discipline to which degree belongs clinical medicine
institution granting the degree HAS
scientific degree, title DSc
year degree was obtained 2002
discipline to which degree belongs clinical medicine
institution granting the degree HAS
Employment
2005 - Szegedi Tudományegyetem Általános Orvostudományi Kar Gyermekgyógyászati Klinika (research institute, not university)
Thesis topic supervisor
number of doctoral students supervised until now 2
number of students who fulfilled course requirements 0
students who obtained their degrees:
Melinda Zombor PhD 2020  DSCM-SzTE
Gyurgyinka Gergev PhD 2015  DSCM-SzTE
(50%) Emese Beatrix Horváth PhD 2014  DSCM-SzTE
Nóra Zsuzsanna Szabó PhD 2012  DSCM-SzTE

  Thesis topic proposals
Research
research area Neurodevelopmental disabilities in infancy and childhood: aetiology, clinical features, management and epidemiology
research field in which current research is conducted clinical medicine
Publications
2019

Zombor Melinda, Kalmár Tibor, Nagy Nikoletta, Berényi Marianne, Telcs Borbála, Maróti Zoltán, Brandau Oliver, Sztriha László: A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature, JOURNAL OF APPLIED GENETICS 60: (2) pp. 151-162.
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL 
2017

Alcantara D, Timms AE, Gripp K, Baker L, Park K, Collins S, Cheng C, Stewart F, Mehta SG, Saggar A, Sztriha L, Zombor M, Caluseriu O, Mesterman R, Van Allen MI, Jacquinet A, Ygberg S, Bernstein JA, Wenger AM, Guturu H, Bejerano G, Gomez-Ospina N, Lehman A, Alfei E, Pantaleoni C, Conti V, Guerrini R, Moog U, Graham JM Jr, Hevner R, Dobyns WB, O'Driscoll M, Mirzaa GM: Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly, BRAIN 140: (10) pp. 2610-2622.
type of document:
number of independent citations: 21
language: English
URL 
2016

Carter J, Zombor M, Mate A, Sztriha L, Waters JJ: De Novo Interstitial Microdeletion at 1q32.1 in a 10-Year-Old Boy with Developmental Delay and Dysmorphism., CASE REPORTS IN GENETICS 2016: 2501741
type of document:
language: English
URL 
2015

Alby C, Piquand K, Huber C, Megarbane A, Ichkou A, Legendre M, Pelluard F, Encha-Ravazi F, Abi-Tayeh G, Bessieres B, El Chehadeh-Djebbar S, Laurent N, Faivre L, Sztriha L, Zombor M, Szabo H, Failler M, Garfa-Traore M, Bole C, Nitschke P, Nizon M, Elkhartoufi N, Clerget-Darpoux F, Munnich A, Lyonnet S, Vekemans M, Saunier S, Cormier-Daire V, Attie-Bitach T, Thomas S: Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome, AMERICAN JOURNAL OF HUMAN GENETICS 97: (2) pp. 311-318.
type of document: Journal paper/Article
number of independent citations: 38
language: English
URL 
2015

Kodani Andrew, Yu Timothy W, Johnson Jeffrey R, Jayaraman Divya, Johnson Tasha L, Al-Gazali Lihadh, Sztriha Lāszló, Partlow Jennifer N, Kim Hanjun, Krup Alexis L, Dammermann Alexander, Krogan Nevan J, Walsh Christopher A, Reiter Jeremy F: Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication, ELIFE 4: p. e07519.
type of document: Journal paper/Article
number of independent citations: 43
language: English
URL 
2015

Thiffault I, Wolf NI, Forget D, Guerrero K, Tran LT, Choquet K, Lavalleee-Adam M, Poitras C, Brais B, Yoon G, Sztriha L, Webster RI, Timmann D, de Warrenburg BPV, Seeger J, Zimmermann A, Mate A, Goizet C, Fung E, van der Knaap MS, Fribourg S, Vanderver A, Simons C, Taft RJ, Yates JR, Coulombe B, Bernard G: Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III, NATURE COMMUNICATIONS 6: 7623
type of document: Journal paper/Article
number of independent citations: 39
language: English
URL 
2015

Gergev G, Mate A, Zimmermann A, Rarosi F, Sztriha L: Spectrum of Neurodevelopmental Disabilities: A Cohort Study in Hungary, JOURNAL OF CHILD NEUROLOGY 30: (3) pp. 344-356.
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL 
2012

Mokánszki Attila, Körhegyi Ivett, Szabó Nóra, Bereg Edit, Gergev Gyurgyinka, Balogh Erzsébet, Bessenyei Beáta, Sümegi Andrea, Morris-Rosendahl DeborahJ, Sztriha László, Oláh Éva: Lissencephaly and Band Heterotopia : LIS1, TUBA1A, and DCX Mutations in Hungary, JOURNAL OF CHILD NEUROLOGY 27: (12) pp. 1534-1540.
type of document: Journal paper/Article
number of independent citations: 18
language: English
URL 
1999

Saar K, Al-Gazali L, Sztriha L, Rueschendorf F, Nur-E-Kamal M, Reis A, Bayoumi R: Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity, AMERICAN JOURNAL OF HUMAN GENETICS 65: (6) pp. 1666-1671.
type of document: Journal paper/Article
number of independent citations: 94
language: English
URL 
1998

Sztriha L, Al-Gazali L, Dawodu A, Bakir M, Chandran P: Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death., NEUROLOGY 50: (5) pp. 1466-1469.
type of document: Journal paper/Article
number of independent citations: 6
language: English
Number of independent citations to these publications:263 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
169
number of scientific publications:
167
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
1 
number of independent citations to scientific publications and creative works:
2096

 
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. )