Losonczy Gergely
Losonczy Gergely
Debreceni Egyetem
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Segregation analysis suggests that keratoconus is a complex non‐mendelian disease
Á Kriszt, G Losonczy, A Berta, G Vereb, L Takács
Acta ophthalmologica 92 (7), e562-e568, 2014
Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age‐related macular degeneration in Hungarian patients
G Losonczy, Á Fekete, Z Vokó, L Takács, I Káldi, É Ajzner, M Kasza, ...
Acta ophthalmologica 89 (3), 255-262, 2011
Differentially expressed genes associated with human limbal epithelial phenotypes: new molecules that potentially facilitate selection of stem cell-enriched populations
L Takács, E Tóth, G Losonczy, A Szanto, T Bähr-Ivacevic, V Benes, ...
Investigative ophthalmology & visual science 52 (3), 1252-1260, 2011
Effects of aging on corneal parameters measured with Pentacam in healthy subjects
G Vitályos, BL Kolozsvári, G Németh, G Losonczy, Z Hassan, D Pásztor, ...
Scientific reports 9 (1), 3419, 2019
Myopia and late-onset progressive cone dystrophy associate to LVAVA/MVAVA exon 3 interchange haplotypes of opsin genes on chromosome X
O Orosz, I Rajta, A Vajas, L Takács, A Csutak, M Fodor, B Kolozsvári, ...
Investigative Ophthalmology & Visual Science 58 (3), 1834-1842, 2017
High frequency of factor V Leiden mutation and prothrombin 20210A variant in Romanies of Eastern Hungary
I Balogh, R Poka, G Losonczy, L Muszbek
Thrombosis and haemostasis 82 (11), 1555-1556, 1999
Tear mediators NGF along with IL-13 predict keratoconus progression
M Fodor, G Vitályos, G Losonczy, Z Hassan, D Pásztor, P Gogolák, ...
Ocular Immunology and Inflammation 29 (6), 1090-1101, 2021
TGFBI (BIGH3) gene mutations in Hungary–report of the novel F547S mutation associated with polymorphic corneal amyloidosis
L Takács, G Losonczy, K Matesz, I Balogh, Z Sohajda, K Tóth, F Fazakas, ...
Mol Vis 13, 1976-1983, 2007
Detection of factor XIII‐A is a valuable tool for distinguishing dendritic cells and tissue macrophages in granuloma annulare and necrobiosis lipoidica
D Töröcsik, H Bárdos, Z Hatalyák, B Dezső, G Losonczy, L Paragh, ...
Journal of the European Academy of Dermatology and Venereology 28 (8), 1087-1096, 2014
Nivolumab-induced ulcerative keratitis—a case report
G Losonczy, M Gijs, RMMA Nuijts
Cornea 40 (5), 656-658, 2021
ADAMTS9 locus associates with increased risk of wet AMD.
S Helisalmi, I Immonen, G Losonczy, MD Resch, S Benedek, I Balogh, ...
Acta Ophthalmologica (1755375X) 92 (5), 2014
Three novel mutations in the glycoprotein IIb gene in a patient with type II Glanzmann thrombasthenia
G Losonczy, N Rosenberg, Z Boda, G Vereb, J Kappelmayer, ...
haematologica 92 (5), 698-701, 2007
Presence of Fleischer ring and prominent corneal nerves in keratoconus relatives and normal controls
Á Kriszt, G Losonczy, A Berta, L Takács
International Journal of Ophthalmology 8 (5), 922, 2015
Correction of irregular and induced regular corneal astigmatism with toric IOL after posterior segment surgery: a case series
BL Kolozsvári, G Losonczy, D Pásztor, M Fodor
BMC ophthalmology 17, 1-6, 2017
A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form …
G Losonczy, N Rosenberg, C Kiss, J Kappelmayer, G Vereb, A Kerényi, ...
Thrombosis and haemostasis 93 (05), 904-909, 2005
Effect of the Gas6 c. 834+ 7G> A polymorphism and the interaction of known risk factors on AMD pathogenesis in Hungarian patients
G Losonczy, A Vajas, L Takács, E Dzsudzsák, Á Fekete, É Márhoffer, ...
PLoS One 7 (11), e50181, 2012
Three novel germ-line VHL mutations in Hungarian von Hippel-Lindau patients, including a nonsense mutation in a fifteen-year-old boy with renal cell carcinoma
G Losonczy, F Fazakas, G Pfliegler, I Komáromi, E Balázs, K Pénzes, ...
BMC medical genetics 14, 1-8, 2013
Cultivation of human oral mucosal explants on contact lenses
B Zsebik, L Ujlaky-Nagy, G Losonczy, G Vereb, L Takács
Current Eye Research 42 (8), 1094-1099, 2017
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene
O Orosz, M Czeglédi, I Kántor, I Balogh, A Vajas, L Takács, A Berta, ...
Molecular vision 21, 124, 2015
Relative anterior microphthalmos in oculodentodigital dysplasia
O Orosz, M Fodor, I Balogh, G Losonczy
Indian Journal of Ophthalmology 66 (2), 334-336, 2018
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