| Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor CL Freund, CY Gregory-Evans, T Furukawa, M Papaioannou, J Looser, ... Cell 91 (4), 543-553, 1997 | 674 | 1997 |
| 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 | 425 | 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 | 291 | 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 | 266 | 1998 |
| Retinoblastoma has properties of a cone precursor tumor and depends upon cone-specific MDM2 signaling XL Xu, Y Fang, TC Lee, D Forrest, C Gregory-Evans, D Almeida, A Liu, ... Cell 137 (6), 1018-1031, 2009 | 252 | 2009 |
| 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 | 168 | 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 | 136 | 2013 |
| Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion. BSS Evans K, Fryer A, Inglehearn C, Duvall-Young J, Whittaker J, Gregory CY ... Nature Genetics 6, 210-213, 1994 | 129 | 1994 |
| RANTES stimulates Ca2+ mobilization and inositol trisphosphate (IP3) formation in cells transfected with G protein‐coupled receptor 75 A Ignatov, J Robert, C Gregory‐Evans, HC Schaller British journal of pharmacology 149 (5), 490-497, 2006 | 122 | 2006 |
| Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype I Filges, E Nosova, E Bruder, S Tercanli, K Townsend, WT Gibson, ... Clinical genetics 86 (3), 220-228, 2014 | 121 | 2014 |
| 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 | 111 | 2001 |
| Animal models of amyotrophic lateral sclerosis: A comparison of model validity JR Morrice, CY Gregory-Evans, CA Shaw Neural Regeneration Research 13 (12), 2050-2054, 2018 | 106 | 2018 |
| 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 | 102 | 2003 |
| Rhodopsin mutations in autosomal dominant retinitis pigmentosa. BSS Al-Maghtheh M, Gregory C, Inglehearn C, Hardcastle A Hum Mutat 2, 249-255, 1993 | 97 | 1993 |
| Rhodospin mutations in autosomal dominant retinitis pigmentosa. BSS Al-Maghtheh M, Gregory C, Inglehearn C, Hardcastle A Human Mutation 2, 249-255, 1993 | 97 | 1993 |
| 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 | 90 | 2016 |
| Neuropilin-1 is upregulated in the adaptive response of prostate tumors to androgen-targeted therapies and is prognostic of metastatic progression and patient mortality BWC Tse, M Volpert, E Ratther, N Stylianou, M Nouri, K McGowan, ... Oncogene 36 (24), 3417-3427, 2017 | 84 | 2017 |
| 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 |