Gergely Losonczy

TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.

Lili Takács, Gergely Losonczy, Klára Matesz et al. · PubMed · 2007 · 58 citations

Segregation analysis suggests that keratoconus is a complex non‐mendelian disease

Ágnes Kriszt, Gergely Losonczy, András Berta et al. · Acta Ophthalmologica · 2014 · 38 citations · Full text

Myopia and Late-Onset Progressive Cone Dystrophy Associate to LVAVA/MVAVA Exon 3 Interchange Haplotypes of Opsin Genes on Chromosome X

Orsolya Orosz, I. Rajta, Attila Vajas et al. · Investigative Ophthalmology & Visual Science · 2017 · 31 citations · Full text

Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age‐related macular degeneration in Hungarian patients

Gergely Losonczy, Ágnes Fekete, Zoltán Vokó et al. · Acta Ophthalmologica · 2009 · 26 citations

Detection of factor <scp>XIII</scp>‐A is a valuable tool for distinguishing dendritic cells and tissue macrophages in granuloma annulare and necrobiosis lipoidica

Dániel Törőcsik, Helga Bárdos, Zs. Hatalyák et al. · Journal of the European Academy of Dermatology and Venereology · 2013 · 15 citations · Full text