Martin Filipec

Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2

Alice E. Davidson, Petra Lišková, Cerys J. Evans et al. · The American Journal of Human Genetics · 2015 · 78 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Novel mutations in theZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy

Petra Lišková, Stephen J. Tuft, Rhian Gwilliam et al. · Human Mutation · 2007 · 75 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Posterior Polymorphous Corneal Dystrophy in Czech Families Maps to Chromosome 20 and Excludes the<i>VSX1</i>Gene

Rhian Gwilliam, Petra Lišková, Martin Filipec et al. · Investigative Ophthalmology & Visual Science · 2005 · 64 citations

Life Sciences, Genetics, Ophthalmology +17

Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation

Petra Lišková, Brotati Kaur Veraitch, Kateřina Jirsová et al. · British Journal of Ophthalmology · 2007 · 60 citations

Medicine, Genetics, Molecular Genetics +15

Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients

Kateřina Jirsová, Stanislava Merjava, Radka Martincova et al. · Experimental Eye Research · 2006 · 56 citations

Medicine, Ophthalmology, Pathology +16