| Short-wavelength light sensitivity of circadian, pupillary, and visual awareness in humans lacking an outer retina FH Zaidi, JT Hull, SN Peirson, K Wulff, D Aeschbach, JJ Gooley, ... Current biology 17 (24), 2122-2128, 2007 | 500 | 2007 |
| Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q C Toomes, HM Bottomley, RM Jackson, KV Towns, S Scott, DA Mackey, ... The American Journal of Human Genetics 74 (4), 721-730, 2004 | 428 | 2004 |
| Ocular coloboma: a reassessment in the age of molecular neuroscience CY Gregory-Evans, MJ Williams, S Halford, K Gregory-Evans Journal of medical genetics 41 (12), 881-891, 2004 | 292 | 2004 |
| Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy RE Kelsell, K Gregory-Evans, AM Payne, I Perrault, J Kaplan, RB Yang, ... Human molecular genetics 7 (7), 1179-1184, 1998 | 267 | 1998 |
| Focused magnetic stem cell targeting to the retina using superparamagnetic iron oxide nanoparticles A Yanai, UO Häfeli, AL Metcalfe, P Soema, L Addo, CY Gregory-Evans, ... Cell transplantation 21 (6), 1137-1148, 2012 | 172 | 2012 |
| Postnatal manipulation of Pax6 dosage reverses congenital tissue malformation defects CY Gregory-Evans, X Wang, KM Wasan, J Zhao, AL Metcalfe, ... The Journal of clinical investigation 124 (1), 2013 | 138 | 2013 |
| Retinitis pigmentosa and allied disorders. RG Weleber (No Title), 395, 2006 | 130 | 2006 |
| Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion BS Evans K, Fryer A, Inglehearn C, Duvall-Young J, Whittaker JL, Gregory CY ... Nature Genetics 6 (2), 210-3, 1994 | 129 | 1994 |
| Autosomal dominant cone–rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase K Gregory-Evans, RE Kelsell, CY Gregory-Evans, SM Downes, FW Fitzke, ... Ophthalmology 107 (1), 55-61, 2000 | 114 | 2000 |
| Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development. LC Bibb, JKL Holt, EE Tarttelin, MD Hodges, K Gregory-Evans, ... Human Molecular Genetics 10 (15), 1571-1579, 2001 | 112 | 2001 |
| Management of ocular ischaemic syndrome R Malhotra, K Gregory-Evans British journal of ophthalmology 84 (12), 1428-1431, 2000 | 111 | 2000 |
| Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19 M Al-Maghtheh, CF Inglehearn, TK Jeffrey, K Evans, AT Moore, M Jay, ... Human molecular genetics 3 (2), 351-354, 1994 | 109 | 1994 |
| Expression of opsin genes early in ocular development of humans and mice EE Tarttelin, J Bellingham, LC Bibb, RG Foster, MW Hankins, ... Experimental eye research 76 (3), 393-396, 2003 | 103 | 2003 |
| Genetic blindness: current concepts in the pathogenesis of human outer retinal dystrophies K Gregory-Evans, SS Bhattacharya Trends in Genetics 14 (3), 103-108, 1998 | 97 | 1998 |
| NLRP3 inflammasome activation drives bystander cone photoreceptor cell death in a P23H rhodopsin model of retinal degeneration IA Viringipurampeer, AL Metcalfe, AE Bashar, O Sivak, A Yanai, ... Human molecular genetics 25 (8), 1501-1516, 2016 | 92 | 2016 |
| Mesenchymal stem cells and potential applications in treating ocular disease AW Joe, K Gregory-Evans Current eye research 35 (11), 941-952, 2010 | 91 | 2010 |
| Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype M Al-Maghtheh, E Vithana, E Tarttelin, M Jay, K Evans, T Moore, ... American Journal of Human Genetics 59 (4), 864-871, 1996 | 91 | 1996 |
| Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q RE Kelsell, K Gregory-Evans, CY Gregory-Evans, GE Holder, MR Jay, ... The American Journal of Human Genetics 63 (1), 274-279, 1998 | 83 | 1998 |
| Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration K Gregory-Evans, F Chang, MD Hodges, CY Gregory-Evans Molecular vision 15, 962, 2009 | 77 | 2009 |
| The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16. CY Gregory, K Evans, SD Wijesuriya, S Kermani, MR Jay, C Plant, N Cox, ... Human Molecular Genetics 5 (7), 1055-1059, 1996 | 75 | 1996 |