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Zarouchlioti, Christina, Sanchez-Pintado, Beatriz, Tear, Nathaniel J Hafford, Klein, Pontus, Liskova, Petra, Dulla, Kalyan, Semo, Ma'ayan, Vugler, Anthony A, Muthusamy, Kirithika, Dudakova, Lubica et al (show 8 more authors) , Levis, Hannah J ORCID: 0000-0002-3923-1178, Skalicka, Pavlina, Hysi, Pirro, Cheetham, Michael E, Tuft, Stephen J, Adamson, Peter, Hardcastle, Alison J and Davidson, Alice E (2018) Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity. American Journal of Human Genetics, 102 (4). pp. 528-539.

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Davidson, Alice E, Liskova, Petra, Evans, Cerys J, Dudakova, Lubica, Noskova, Lenka, Pontikos, Nikolas, Hartmannova, Hana, Hodanova, Katerina, Stranecky, Viktor, Kozmik, Zbynek et al (show 16 more authors) , Levis, Hannah J ORCID: 0000-0002-3923-1178, Idigo, Nwamaka, Sasai, Noriaki, Maher, Geoffrey J, Bellingham, James, Veli, Neyme, Ebenezer, Neil D, Cheetham, Michael E, Daniels, Julie T, Thaung, Caroline MH, Jirsova, Katerina, Plagnol, Vincent, Filipec, Martin, Kmoch, Stanislav, Tuft, Stephen J and Hardcastle, Alison J (2016) Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2. AMERICAN JOURNAL OF HUMAN GENETICS, 98 (1). pp. 75-89.

Skalicka, Pavlina, Porter, Louise F ORCID: 0000-0002-7406-0319, Brejchova, Kristyna, Malinka, Frantisek, Dudakova, Lubica and Liskova, Petra (2020) Brittle cornea syndrome: Disease-causing mutations in <i>ZNF469</i> and two novel variants identified in a patient followed for 26 years. BIOMEDICAL PAPERS-OLOMOUC, 164 (2). pp. 183-188.