Konstantinos Nikopoulos

Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy

Konstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen et al. · The American Journal of Human Genetics · 2010 · 231 citations · Full text

Mendelian Disorder, Familial Exudative Vitreoretinopathy, Genetic Disorder +8

L1 retrotransposition can occur early in human embryonic development

José A. J. M. van den Hurk, Iwan C. Meij, Maria del Carmen Seleme et al. · Human Molecular Genetics · 2007 · 187 citations · Full text

<i>ZNF408</i> is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

Rob W.J. Collin, Konstantinos Nikopoulos, Margo Dona et al. · Proceedings of the National Academy of Sciences · 2013 · 179 citations · Full text

Ocular Disease, Peripheral Retina, Exome Sequencing +17

Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP

Konstantinos Nikopoulos, Hanka Venselaar, Rob W.J. Collin et al. · Human Mutation · 2010 · 148 citations · Full text

Erosive Vitreoretinopathy and Wagner Disease Are Caused by Intronic Mutations in<i>CSPG2</i>/<i>Versican</i>That Result in an Imbalance of Splice Variants

Arijit Mukhopadhyay, Konstantinos Nikopoulos, Alessandra Maugeri et al. · Investigative Ophthalmology & Visual Science · 2006 · 89 citations · Full text