Gergely Losonczy

Summary

Publications

  1. pmc Effect of the Gas6 c.834+7G>A polymorphism and the interaction of known risk factors on AMD pathogenesis in Hungarian patients
    Gergely Losonczy
    Department of Ophthalmology, University of Debrecen, Debrecen, Hungary
    PLoS ONE 7:e50181. 2012
  2. pmc 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
    Gergely Losonczy
    Department of Ophthalmology, University of Debrecen, Medical and Health Science Center, 98 Nagyerdei bld, 4012, Debrecen, Hungary
    BMC Med Genet 14:3. 2013
  3. doi request reprint Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age-related macular degeneration in Hungarian patients
    Gergely Losonczy
    Department of Ophthalmology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary
    Acta Ophthalmol 89:255-62. 2011
  4. pmc Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene
    Orsolya Orosz
    Department of Ophthalmology, University of Debrecen, Clinical Center, Debrecen, Hungary
    Mol Vis 21:124-30. 2015
  5. doi request reprint Segregation analysis suggests that keratoconus is a complex non-mendelian disease
    Agnes Kriszt
    Department of Ophthalmology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary Department of Biophysics and Cell Biology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    Acta Ophthalmol 92:e562-8. 2014
  6. doi request reprint Differentially expressed genes associated with human limbal epithelial phenotypes: new molecules that potentially facilitate selection of stem cell-enriched populations
    Lili Takacs
    Department of Ophthalmology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Invest Ophthalmol Vis Sci 52:1252-60. 2011
  7. ncbi request reprint TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis
    Lili Takacs
    Department of Ophthalmology, University of Debrecen, Medical and Health Science Center, Debrecen, Hungary
    Mol Vis 13:1976-83. 2007

Collaborators

Detail Information

Publications7

  1. pmc Effect of the Gas6 c.834+7G>A polymorphism and the interaction of known risk factors on AMD pathogenesis in Hungarian patients
    Gergely Losonczy
    Department of Ophthalmology, University of Debrecen, Debrecen, Hungary
    PLoS ONE 7:e50181. 2012
    ..834+7G>A polymorphism in exudative AMD development. In addition, novel genetic interactions were revealed between CFH, HTRA1 and C3 polymorphisms that might contribute to the pathogenesis of dry AMD...
  2. pmc 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
    Gergely Losonczy
    Department of Ophthalmology, University of Debrecen, Medical and Health Science Center, 98 Nagyerdei bld, 4012, Debrecen, Hungary
    BMC Med Genet 14:3. 2013
    ....
  3. doi request reprint Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age-related macular degeneration in Hungarian patients
    Gergely Losonczy
    Department of Ophthalmology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary
    Acta Ophthalmol 89:255-62. 2011
    ....
  4. pmc Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene
    Orsolya Orosz
    Department of Ophthalmology, University of Debrecen, Clinical Center, Debrecen, Hungary
    Mol Vis 21:124-30. 2015
    ..Our aim was to characterize the ophthalmological phenotype associated with the previously reported homozygous c.427_428CT mutation in the NEUROD1 gene...
  5. doi request reprint Segregation analysis suggests that keratoconus is a complex non-mendelian disease
    Agnes Kriszt
    Department of Ophthalmology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary Department of Biophysics and Cell Biology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    Acta Ophthalmol 92:e562-8. 2014
    ..Complex segregation analysis of 60 unrelated sporadic keratoconus (KC) families was performed to reveal the presumed mode of inheritance in our dataset...
  6. doi request reprint Differentially expressed genes associated with human limbal epithelial phenotypes: new molecules that potentially facilitate selection of stem cell-enriched populations
    Lili Takacs
    Department of Ophthalmology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Invest Ophthalmol Vis Sci 52:1252-60. 2011
    ..The aim of this study was to identify differentially expressed genes in the human limbal epithelium by microarray analysis...
  7. ncbi request reprint TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis
    Lili Takacs
    Department of Ophthalmology, University of Debrecen, Medical and Health Science Center, Debrecen, Hungary
    Mol Vis 13:1976-83. 2007
    ..To identify mutations in the Transforming Growth Factor Beta Induced (TGFBI) gene in Hungarian patients with corneal dystrophy and to characterize histological features of their corneal buttons excised during penetrating keratoplasty...