Petra Liskova
Petra Liskova
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Keratoconus in 18 pairs of twins
SJ Tuft, H Hassan, S George, DG Frazer, CE Willoughby, P Liskova
Acta ophthalmologica 90 (6), e482-e486, 2012
Descemet membrane endothelial keratoplasty with a stromal rim (DMEK-S)
P Studeny, A Farkas, M Vokrojova, P Liskova, K Jirsova
British journal of ophthalmology 94 (7), 909-914, 2010
Changes in lysyl oxidase (LOX) distribution and its decreased activity in keratoconus corneas
L Dudakova, P Liskova, T Trojek, M Palos, S Kalasova, K Jirsova
Experimental eye research 104, 74-81, 2012
Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy
P Liskova, SJ Tuft, R Gwilliam, ND Ebenezer, K Jirsova, Q Prescott, ...
Human mutation 28 (6), 638-638, 2007
Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients
K Jirsova, S Merjava, R Martincova, R Gwilliam, ND Ebenezer, P Liskova, ...
Experimental eye research 84 (4), 680-686, 2007
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
M Khan, SS Cornelis, MD Pozo-Valero, L Whelan, EH Runhart, K Mishra, ...
Genetics in Medicine 22 (7), 1235-1246, 2020
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene
R Gwilliam, P Liskova, M Filipec, S Kmoch, K Jirsova, EJ Huckle, ...
Investigative ophthalmology & visual science 46 (12), 4480-4484, 2005
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2)
VL Ramprasad, ND Ebenezer, T Aung, R Rajagopal, VHK Yong, SJ Tuft, ...
Human mutation 28 (5), 522-523, 2007
Autosomal-dominant corneal endothelial dystrophies CHED1 and PPCD1 are allelic disorders caused by non-coding mutations in the promoter of OVOL2
AE Davidson, P Liskova, CJ Evans, L Dudakova, L Nosková, N Pontikos, ...
The American Journal of Human Genetics 98 (1), 75-89, 2016
Molecular analysis of the VSX1 gene in familial keratoconus
P Liskova, ND Ebenezer, PG Hysi, R Gwilliam, MF El-Ashry, LC Moodaley, ...
Molecular vision 13, 1887, 2007
Evidence for keratoconus susceptibility locus on chromosome 14: a genome-wide linkage screen using single-nucleotide polymorphism markers
P Liskova, PG Hysi, N Waseem, ND Ebenezer, SS Bhattacharya, SJ Tuft
Archives of ophthalmology 128 (9), 1191-1195, 2010
Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity
C Zarouchlioti, B Sanchez-Pintado, NJH Tear, P Klein, P Liskova, K Dulla, ...
American Journal of Human Genetics 102 (4), 528, 2018
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy–associated TCF4 triplet repeat
NJ Hafford-Tear, YC Tsai, AN Sadan, B Sanchez-Pintado, C Zarouchlioti, ...
Genetics in Medicine 21 (9), 2092-2102, 2019
Validation of rs2956540: G> C and rs3735520: G> A association with keratoconus in a population of European descent
L Dudakova, M Palos, K Jirsova, V Stranecky, A Krepelova, PG Hysi, ...
European Journal of Human Genetics 23 (11), 1581-1583, 2015
Matrix metalloproteinases in recurrent corneal melting associated with primary Sjörgen’s syndrome
K Brejchova, P Liskova, E Hrdlickova, M Filipec, K Jirsova
Molecular Vision 15, 2364, 2009
British family with early-onset Fuchs’ endothelial corneal dystrophy associated with p. L450W mutation in the COL8A2 gene
P Liskova, Q Prescott, SS Bhattacharya, SJ Tuft
British Journal of Ophthalmology 91 (12), 1717-1718, 2007
Ectopic GRHL2 expression due to non-coding mutations promotes cell state transition and causes posterior polymorphous corneal dystrophy 4
P Liskova, L Dudakova, CJ Evans, KER Lopez, N Pontikos, D Athanasiou, ...
The American Journal of Human Genetics 102 (3), 447-459, 2018
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus
AE Davidson, E Borasio, P Liskova, AO Khan, H Hassan, ME Cheetham, ...
Investigative ophthalmology & visual science 56 (1), 578-586, 2015
Role of matrix metalloproteinases in recurrent corneal melting
K Brejchova, P Liskova, J Cejkova, K Jirsova
Experimental eye research 90 (5), 583-590, 2010
Genetic variants associated with corneal biomechanical properties and potentially conferring susceptibility to keratoconus in a genome-wide association study
AP Khawaja, KER Lopez, AJ Hardcastle, CJ Hammond, P Liskova, ...
JAMA ophthalmology 137 (9), 1005-1012, 2019
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