| Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) AI den Hollander, JB ten Brink, YJM de Kok, S van Soest, LI van den Born, ... Nature genetics 23 (2), 217-221, 1999 | 565 | 1999 |
| What works for wellbeing? A systematic review of wellbeing outcomes for music and singing in adults N Daykin, L Mansfield, C Meads, G Julier, A Tomlinson, A Payne, ... Perspectives in public health 138 (1), 39-46, 2018 | 355 | 2018 |
| Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis MM Sohocki, SJ Bowne, LS Sullivan, S Blackshaw, CL Cepko, AM Payne, ... Nature genetics 24 (1), 79-83, 2000 | 326 | 2000 |
| Machine learning with applications in breast cancer diagnosis and prognosis W Yue, Z Wang, H Chen, A Payne, X Liu Designs 2 (2), 13, 2018 | 308 | 2018 |
| A mutation in NRL is associated with autosomal dominant retinitis pigmentosa DAR Bessant, AM Payne, KP Mitton, QL Wang, PK Swain, C Plant, ... Nature genetics 21 (4), 355-356, 1999 | 288 | 1999 |
| 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 |
| A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21. 1 AM Payne, SM Downes, DAR Bessant, R Taylor, GE Holder, MJ Warren, ... Human molecular genetics 7 (2), 273-277, 1998 | 262 | 1998 |
| Prevalence of AIPL1 mutations in inherited retinal degenerative disease MM Sohocki, I Perrault, BP Leroy, AM Payne, S Dharmaraj, ... Molecular genetics and metabolism 70 (2), 142-150, 2000 | 206 | 2000 |
| Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma OJ Lehmann, ND Ebenezer, T Jordan, M Fox, L Ocaka, A Payne, ... The American Journal of Human Genetics 67 (5), 1129-1135, 2000 | 168 | 2000 |
| GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy I Sokal, N Li, I Surgucheva, MJ Warren, AM Payne, SS Bhattacharya, ... Molecular cell 2 (1), 129-133, 1998 | 154 | 1998 |
| The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations S Dharmaraj, BP Leroy, MM Sohocki, RK Koenekoop, I Perrault, K Anwar, ... Archives of ophthalmology 122 (7), 1029-1037, 2004 | 134 | 2004 |
| Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1 SM Downes, GE Holder, FW Fitzke, AM Payne, MJ Warren, ... Archives of ophthalmology 119 (1), 96-105, 2001 | 126 | 2001 |
| Computer simulations improve university instructional laboratories NJ Gibbons, C Evans, A Payne, K Shah, DK Griffin Cell Biology Education 3 (4), 263-269, 2004 | 108 | 2004 |
| Sport and dance interventions for healthy young people (15–24 years) to promote subjective well-being: a systematic review L Mansfield, T Kay, C Meads, L Grigsby-Duffy, J Lane, A John, N Daykin, ... BMJ open 8 (7), e020959, 2018 | 101 | 2018 |
| A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13 A Hameed, S Khaliq, M Ismail, K Anwar, ND Ebenezer, T Jordan, ... Investigative ophthalmology & visual science 41 (3), 629-633, 2000 | 90 | 2000 |
| Orexin receptors exert a neuroprotective effect in Alzheimer’s disease (AD) via heterodimerization with GPR103 J Davies, J Chen, R Pink, D Carter, N Saunders, G Sotiriadis, B Bai, Y Pan, ... Scientific reports 5 (1), 12584, 2015 | 87 | 2015 |
| The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report P Bennett, R Segurado, I Jones, S Bort, F McCandless, D Lambert, ... Molecular psychiatry 7 (2), 189-200, 2002 | 86 | 2002 |
| Clinical Features of Codon 172 RDSMacular Dystrophy: Similar Phenotype in 12 Families SM Downes, FW Fitzke, GE Holder, AM Payne, DAR Bessant, ... Archives of Ophthalmology 117 (10), 1373-1383, 1999 | 86 | 1999 |
| Filial cannibalism improves survival and development of beaugregory damselfish embryos AG Payne, C Smith, AC Campbell Proceedings of the Royal Society of London. Series B: Biological Sciences …, 2002 | 81 | 2002 |
| Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1 SM Downes, AM Payne, RE Kelsell, FW Fitzke, GE Holder, DM Hunt, ... Archives of ophthalmology 119 (11), 1667-1673, 2001 | 81 | 2001 |
