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Ocular Immunology and Inflammation|March 5, 2020
Tear Mediators NGF along with IL-13 Predict Keratoconus ProgressionMariann Fodor, Géza Vitályos, Gergely Losonczy, et al.
Haematologica|May 10, 2007
Three novel mutations in the glycoprotein IIb gene in a patient with type II Glanzmann thrombastheniaGergely Losonczy, Nurit Rosenberg, Zoltán Boda, et al.
Molecular Vision|February 17, 2015
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 geneOrsolya Orosz, Miklós Czeglédi, Irén Kántor, et al.
Thrombosis and Haemostasis|May 12, 2005
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 complex with GPIIIaGergely Losonczy, Nurit Rosenberg, Csongor Kiss, et al.
Investigative Ophthalmology & Visual Science|November 13, 2010
Differentially expressed genes associated with human limbal epithelial phenotypes: new molecules that potentially facilitate selection of stem cell-enriched populationsLili Takács, Eniko Tóth, Gergely Losonczy, et al.
Molecular Vision|November 6, 2007
TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosisLili Takács, Gergely Losonczy, Klára Matesz, et al.
Acta Ophthalmologica|October 23, 2009
Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age-related macular degeneration in Hungarian patientsGergely Losonczy, Ágnes Fekete, Zoltán Vokó, et al.
Plos One|December 5, 2012
Effect of the Gas6 c.834+7G>A polymorphism and the interaction of known risk factors on AMD pathogenesis in Hungarian patientsGergely Losonczy, Attila Vajas, Lili Takács, et al.
Investigative Ophthalmology & Visual Science|March 31, 2017
Myopia and Late-Onset Progressive Cone Dystrophy Associate to LVAVA/MVAVA Exon 3 Interchange Haplotypes of Opsin Genes on Chromosome XOrsolya Orosz, István Rajta, Attila Vajas, et al.
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