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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.

Larkin, Daniel FP, Chowdhury, Kashfia, Burr, Jennifer M, Raynor, Mathew, Edwards, Matthew, Tuft, Stephen J, Bunce, Catey ORCID: 0000-0002-0935-3713, Caverly, Emilia, Doré, Caroline and KERALINK Trial Study Group, (2021) Effect of Corneal Cross-linking versus Standard Care on Keratoconus Progression in Young Patients: The KERALINK Randomized Controlled Trial. Ophthalmology, 128 (11). pp. 1516-1526.

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Ansari, Morad, Rainger, Jacqueline, Hanson, Isabel M, Williamson, Kathleen A, Sharkey, Freddie, Harewood, Louise, Sandilands, Angela, Clayton-Smith, Jill, Dollfus, Helene, Bitoun, Pierre et al (show 43 more authors) , Meire, Francoise, Fantes, Judy, Franco, Brunella, Lorenz, Birgit, Taylor, David S, Stewart, Fiona, Willoughby, Colin E, McEntagart, Meriel, Khaw, Peng Tee, Clericuzio, Carol, Van Maldergem, Lionel, Williams, Denise, Newbury-Ecob, Ruth, Traboulsi, Elias I, Silva, Eduardo D, Madlom, Mukhlis M, Goudie, David R, Fleck, Brian W, Wieczorek, Dagmar, Kohlhase, Juergen, McTrusty, Alice D, Gardiner, Carol, Yale, Christopher, Moore, Anthony T, Russell-Eggitt, Isabelle, Islam, Lily, Lees, Melissa, Beales, Philip L, Tuft, Stephen J, Solano, Juan B, Splitt, Miranda, Hertz, Jens Michael, Prescott, Trine E, Shears, Deborah J, Nischal, Ken K, Doco-Fenzy, Martine, Prieur, Fabienne, Temple, I Karen, Lachlan, Katherine L, Damante, Giuseppe, Morrison, Danny A, van Heyningen, Veronica and FitzPatrick, David R (2016) Genetic Analysis of '<i>PAX6</i>-Negative' Individuals with Aniridia or Gillespie Syndrome. PLOS ONE, 11 (4). e0153757-.