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Number of items: 34.


Willoughby, Colin (2018) Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nature Communications, NA . 0-0. [Journal article]

Willoughby, Colin (2018) Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nature Communications, NA . 0-0. [Journal article]

Willoughby, Colin (2018) Determination of the relationship between mechanical properties, ultrastructural changes and intrafibrillar bond formation in corneal UVA/riboflavin cross-linking treatment for keratoconus. Journal of Refractive Surgery, online . [Journal article]

Willoughby, Colin (2018) Imaging of Corneal Neovascularization: Optical Coherence Tomography Angiography and Fluorescence Angiography. Invest Ophthalmol Vis Sci., 59 . pp. 1263-1269. [Journal article]


Chiam, Patrick J, Cheeseman, Robert, Ho, Vivian W, Romano, Vito, Choudhary, Anshoo, Batterbury, Mark, Kaye, Stephen B and Willoughby, Colin (2017) Outcome of Descemet stripping automated endothelial keratoplasty in eyes with an Ahmed glaucoma valve. Graefe's Archive for Clinical and Experimental Ophthalmology, 255 (5). pp. 987-993. [Journal article]

Lawman, Samuel, Madden, Peter W., Romano, Vito, Dong, Yue, Mason, Sharon, Williams, Bryan M., Kaye, Stephen B., Willoughby, Colin, Harding, Simon P., Shen, Yao-Chun and Zheng, Yalin (2017) Deformation velocity imaging using optical coherence tomography and its applications to the cornea. Biomedical Optics Express, 8 (12). pp. 5579-5593. [Journal article]

Liu, Siyin, Romano, Vito, Steger, Bernhard, Kaye, Stephen B., Hamill, Kevin J. and Willoughby, Colin (2017) Gene-based antiangiogenic applications for corneal neovascularization. Survey of Ophthalmology, 63 (2). pp. 193-213. [Journal article]

Parekh, Mohit, Ruzza, Alessandro, Steger, Bernhard, Willoughby, Colin, Ferrari, Stefano, Ponzin, Diego, Kaye, Stephen B. and Romano, Vito (2017) Avoiding Complications Associated With Preloaded Ultrathin Descemet Stripping Automated Endothelial Keratoplasty. Cornea, 36 (4). e12-e13. [Journal article]

Romano, Vito, Parekh, Mohit, Ruzza, Alessandro, Willoughby, Colin, Ferrari, Stefano, Ponzin, Diego, Kaye, Stephen B and Levis, Hannah J (2017) Comparison of preservation and transportation protocols for preloaded Descemet membrane endothelial keratoplasty. British Journal of Ophthalmology, online . bjophthalmol-2017. [Journal article]

Romano, Vito, Steger, Bernhard, Brunner, Matthias, Kaye, Abigail, Zheng, Yalin, Willoughby, Colin and Kaye, Stephen B. (2017) Detecting Change in Conjunctival Hyperemia Using a Pixel Densitometry Index. Ocular Immunology and Inflammation, online . pp. 1-6. [Journal article]

Vallabh, Neeru A., Romano, Vito and Willoughby, Colin (2017) Mitochondrial dysfunction and oxidative stress in corneal disease. Mitochondrion, 36 . pp. 103-113. [Journal article]

Vinciguerra, Riccardo, Romano, Vito, Arbabi, Esmaeil M., Brunner, Matthias, Willoughby, Colin, Batterbury, Mark and Kaye, Stephen B. (2017) In Vivo Early Corneal Biomechanical Changes After Corneal Cross-linking in Patients With Progressive Keratoconus. Journal of Refractive Surgery, 33 (12). pp. 840-846. [Journal article]


Anderson, Michael G, Ansari, Morad, Rainger, Jacqueline, Hanson, Isabel M., Williamson, Kathleen A., Sharkey, Freddie, Harewood, Louise, Sandilands, Angela, Clayton-Smith, Jill, Dollfus, Helene, Bitoun, Pierre, Meire, Francoise, Fantes, Judy, Franco, Brunella, Lorenz, Birgit, Taylor, David S., Stewart, Fiona, Willoughby, Colin, 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 ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome. PLOS ONE, 11 (4). e0153757. [Journal article]

Barbaro, Vanessa, Nasti, Annamaria A., Del Vecchio, Claudia, Ferrari, Stefano, Migliorati, Angelo, Raffa, Paolo, Lariccia, Vincenzo, Nespeca, Patrizia, Biasolo, Mariangela, Willoughby, Colin, Ponzin, Diego, Palù, Giorgio, Parolin, Cristina and Di Iorio, Enzo (2016) Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele-Specific Silencing Restores Defective Stem Cell Function. STEM CELLS, 34 (6). pp. 1588-1600. [Journal article]

Lawman, Samuel, Dong, Yue, Williams, Bryan M., Romano, Vito, Kaye, Stephen, Harding, Simon P., Willoughby, Colin, Shen, Yao-Chun and Zheng, Yalin (2016) High resolution corneal and single pulse imaging with line field spectral domain optical coherence tomography. Optics Express, 24 (11). p. 12395. [Journal article]

Romano, Vito, Steger, Bernhard, Brunner, Matthias, Ahmad, Sajjad, Willoughby, Colin and Kaye, Stephen B. (2016) Method for Angiographically Guided Fine-Needle Diathermy in the Treatment of Corneal Neovascularization. Cornea, 35 (7). pp. 1029-1032. [Journal article]

Romano, Vito, Steger, Bernhard, Myneni, Jayavani, Batterbury, Mark, Willoughby, Colin and Kaye, Stephen B. (2016) Preparation of ultrathin grafts for Descemet-stripping endothelial keratoplasty with a single microkeratome pass. Journal of Cataract & Refractive Surgery, 43 (1). pp. 12-15. [Journal article]

Willoughby, Colin (2016) Estudio clínico y molecular en una familia con displasia ectodérmica hipohidrótica autosómica dominante. Archivos Argentinos de Pediatria, 115 (1). [Journal article]


Chamney, S, Cartmill, B, Earley, O, McConnell, V and Willoughby, Colin (2015) The ocular phenotype of stiff-skin syndrome. Eye, 30 (1). pp. 156-159. [Journal article]

Oliver, Verity F., van Bysterveldt, Katherine A., Cadzow, Murray, Steger, Bernhard, Romano, Vito, Markie, David, Hewitt, Alex W., Mackey, David A., Willoughby, Colin, Sherwin, Trevor, Crosier, Philip S., McGhee, Charles N. and Vincent, Andrea L. (2015) A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions. Ophthalmology, 123 (4). pp. 709-722. [Journal article]

Romano, Vito, Steger, Bernhard, Chen, Jern Y., Hassaan, Sherif, Batterbury, Mark, Willoughby, Colin, Ahmad, Sajjad, Elsheikh, Ahmed and Kaye, Stephen B. (2015) Reliability of the Effect of Artificial Anterior Chamber Pressure and Corneal Drying on Corneal Graft Thickness. Cornea, 34 (8). pp. 866-869. [Journal article]

Romano, Vito, Steger, Bernhard, Kovacova, Adriana, Kaye, Stephen B. and Willoughby, Colin (2015) Further evidence for heredity of pterygium. Ophthalmic Genetics, 37 (4). pp. 434-436. [Journal article]

Romano, Vito, Steger, Bernhard, Zheng, Yalin, Ahmad, Sajjad, Willoughby, Colin and Kaye, Stephen B. (2015) Angiographic and In Vivo Confocal Microscopic Characterization of Human Corneal Blood and Presumed Lymphatic Neovascularization. Cornea, 34 (11). pp. 1459-1465. [Journal article]

Spiteri, Natasha, Romano, Vito, Zheng, Yalin, Yadav, Sohraab, Dwivedi, Rahul, Chen, Jern, Ahmad, Sajjad, Willoughby, Colin and Kaye, Stephen B. (2015) Corneal Angiography for Guiding and Evaluating Fine-Needle Diathermy Treatment of Corneal Neovascularization. Ophthalmology, 122 (6). pp. 1079-1084. [Journal article]

Steger, Bernhard, Romano, Vito, Biddolph, Simon, Willoughby, Colin, Batterbury, Mark and Kaye, Stephen B. (2015) Femtosecond Laser–Assisted Lamellar Keratectomy for Corneal Opacities Secondary to Anterior Corneal Dystrophies. Cornea, 35 (1). pp. 6-13. [Journal article]

Wheway, Gabrielle, Schmidts, Miriam, Mans, Dorus A., Szymanska, Katarzyna, Nguyen, Thanh-Minh T., Racher, Hilary, Phelps, Ian G., Toedt, Grischa, Kennedy, Julie, Wunderlich, Kirsten A., Sorusch, Nasrin, Abdelhamed, Zakia A., Natarajan, Subaashini, Herridge, Warren, van Reeuwijk, Jeroen, Horn, Nicola, Boldt, Karsten, Parry, David A., Letteboer, Stef J. F., Roosing, Susanne, Adams, Matthew, Bell, Sandra M., Bond, Jacquelyn, Higgins, Julie, Morrison, Ewan E., Tomlinson, Darren C., Slaats, Gisela G., van Dam, Teunis J. P., Huang, Lijia, Kessler, Kristin, Giessl, Andreas, Logan, Clare V., Boyle, Evan A., Shendure, Jay, Anazi, Shamsa, Aldahmesh, Mohammed, Al Hazzaa, Selwa, Hegele, Robert A., Ober, Carole, Frosk, Patrick, Mhanni, Aizeddin A., Chodirker, Bernard N., Chudley, Albert E., Lamont, Ryan, Bernier, Francois P., Beaulieu, Chandree L., Gordon, Paul, Pon, Richard T., Donahue, Clem, Barkovich, A. James, Wolf, Louis, Toomes, Carmel, Thiel, Christian T., Boycott, Kym M., McKibbin, Martin, Inglehearn, Chris F., Stewart, Fiona, Omran, Heymut, Huynen, Martijn A., Sergouniotis, Panagiotis I., Alkuraya, Fowzan S., Parboosingh, Jillian S., Innes, A. Micheil, Willoughby, Colin, Giles, Rachel H., Webster, Andrew R., Ueffing, Marius, Blacque, Oliver, Gleeson, Joseph G., Wolfrum, Uwe, Beales, Philip L., Gibson, Toby, Doherty, Dan, Mitchison, Hannah M., Roepman, Ronald and Johnson, Colin A. (2015) An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. Nature Cell Biology, 17 (8). pp. 1074-1087. [Journal article]


Callea, M., Nieminen, P., Willoughby, Colin, Clarich, G., Yavuz, I., Vinciguerra, A., Di Stazio, M., Giglio, S., Sani, I., Maglione, M., Pensiero, S., Tadini, G. and Bellacchio, E. (2014) A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family. Journal of the European Academy of Dermatology and Venereology, 30 (2). pp. 341-343. [Journal article]

Callea, M., Willoughby, Colin, Nieminen, P., Di Stazio, M., Bellacchio, E., Giglio, S., Sani, I., Vinciguerra, A., Maglione, M., Tadini, G. and Clarich, G. (2014) Identification of a novel frameshift mutation in theEDARgene causing autosomal dominant hypohidrotic ectodermal dysplasia. Journal of the European Academy of Dermatology and Venereology, 29 (5). pp. 1032-1034. [Journal article]

Guazzarotti, L., Tadini, G., Mancini, G.E., Giglio, S., Willoughby, Colin, Callea, M., Sani, I., Nannini, P., Mameli, C., Tenconi, A.A., Mauri, S., Bottero, A., Caimi, A., Morelli, M. and Zuccotti, G.V. (2014) Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia. Clinical Genetics, 87 (4). pp. 338-342. [Journal article]

Lechner, Judith, Porter, Louise F., Rice, Aine, Vitart, Veronique, Armstrong, David J., Schorderet, Daniel F., Munier, Francis L., Wright, Alan F., Inglehearn, Chris F., Black, Graeme C., Simpson, David A., Manson, Forbes and Willoughby, Colin (2014) Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus. Human Molecular Genetics, 23 (20). pp. 5527-5535. [Journal article]

Napier, Maria L., Durga, Dash, Wolsley, Clive J., Chamney, Sarah, Alexander, Sharon, Brennan, Rosie, Simpson, David A., Silvestri, Giuliana and Willoughby, Colin (2014) Mutational Analysis of theRhodopsinGene in Sector Retinitis Pigmentosa. Ophthalmic Genetics, 36 (3). pp. 239-243. [Journal article]

Romano, Vito, Tey, Adrian, Hill, Natalie M E, Ahmad, Sajjad, Britten, Claire, Batterbury, Mark, Willoughby, Colin and Kaye, Stephen B (2014) Influence of graft size on graft survival following Descemet stripping automated endothelial keratoplasty. British Journal of Ophthalmology, 99 (6). pp. 784-788. [Journal article]

Sundaresan, Periasamy, Simpson, David A., Sambare, Chitra, Duffy, Seamus, Lechner, Judith, Dastane, Aditi, Dervan, Edward W., Vallabh, Neeru, Chelerkar, Vidya, Deshpande, Madan, O'Brien, Colm, McKnight, Amy Jayne and Willoughby, Colin (2014) Whole-mitochondrial genome sequencing in primary open-angle glaucoma using massively parallel sequencing identifies novel and known pathogenic variants. Genetics in Medicine, 17 (4). pp. 279-284. [Journal article]

Zhao, Li, Wang, Feng, Wang, Hui, Li, Yumei, Alexander, Sharon, Wang, Keqing, Willoughby, Colin, Zaneveld, Jacques E., Jiang, Lichun, Soens, Zachry T., Earle, Philip, Simpson, David, Silvestri, Giuliana and Chen, Rui (2014) Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland. Human Genetics, 134 (2). pp. 217-230. [Journal article]

This list was generated on Fri Aug 23 01:44:15 2019 BST.