Amblyopia JM Holmes, MP Clarke The Lancet 367 (9519), 1343-1351, 2006 | 600 | 2006 |
The retina in Parkinson's disease NK Archibald, MP Clarke, UP Mosimann, DJ Burn Brain 132 (5), 1128-1145, 2009 | 512 | 2009 |
Multi-system neurological disease is common in patients with OPA1 mutations P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ... Brain 133 (3), 771-786, 2010 | 470 | 2010 |
Heterozygous mutations of OTX2 cause severe ocular malformations NK Ragge, AG Brown, CM Poloschek, B Lorenz, RA Henderson, ... The American Journal of Human Genetics 76 (6), 1008-1022, 2005 | 338 | 2005 |
The ocular manifestations of the Sturge-Weber syndrome TJ Sullivan, MP Clarke, JD Morin Journal of Pediatric Ophthalmology & Strabismus 29 (6), 349-356, 1992 | 289 | 1992 |
An efficient component model for the construction of adaptive middleware M Clarke, GS Blair, G Coulson, N Parlavantzas Middleware 2001: IFIP/ACM International Conference on Distributed Systems …, 2001 | 279 | 2001 |
Discovery of radio emission from the brown dwarf LP944-20 E Berger, S Ball, KM Becker, M Clarke, DA Frail, TA Fukuda, IM Hoffman, ... Nature 410 (6826), 338-340, 2001 | 250 | 2001 |
Visual symptoms in Parkinson's disease and Parkinson's disease dementia NK Archibald, MP Clarke, UP Mosimann, DJ Burn Movement disorders 26 (13), 2387-2395, 2011 | 247 | 2011 |
Randomised controlled trial of treatment of unilateral visual impairment detected at preschool vision screening MP Clarke, CM Wright, S Hrisos, JD Anderson, J Henderson, ... Bmj 327 (7426), 1251, 2003 | 237 | 2003 |
The prevalence and natural history of dominant optic atrophy due to OPA1 mutations P Yu-Wai-Man, PG Griffiths, A Burke, PW Sellar, MP Clarke, L Gnanaraj, ... Ophthalmology 117 (8), 1538-1546. e1, 2010 | 221 | 2010 |
International variations in amputation practice: a VASCUNET report CA Behrendt, B Sigvant, Z Szeberin, B Beiles, N Eldrup, IA Thomson, ... European Journal of Vascular and Endovascular Surgery 56 (3), 391-399, 2018 | 205 | 2018 |
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations I Hanson, A Churchill, J Love, R Axton, T Moore, M Clarke, F Meire, ... Human molecular genetics 8 (2), 165-172, 1999 | 200 | 1999 |
Retinal thickness in Parkinson's disease NK Archibald, MP Clarke, UP Mosimann, DJ Burn Parkinsonism & related disorders 17 (6), 431-436, 2011 | 171 | 2011 |
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation KP Burdon, JD McKay, MM Sale, IM Russell-Eggitt, DA Mackey, MG Wirth, ... The American Journal of Human Genetics 73 (5), 1120-1130, 2003 | 158 | 2003 |
The emotional impact of amblyopia treatment in preschool children: randomized controlled trial S Hrisos, MP Clarke, CM Wright Ophthalmology 111 (8), 1550-1556, 2004 | 155 | 2004 |
The Newcastle Control Score: a new method of grading the severity of intermittent distance exotropia H Haggerty, S Richardson, S Hrisos, NP Strong, MP Clarke British Journal of Ophthalmology 88 (2), 233-235, 2004 | 146 | 2004 |
A semi‐structured interview to assess visual hallucinations in older people UP Mosimann, D Collerton, R Dudley, TD Meyer, G Graham, JL Dean, ... International Journal of Geriatric Psychiatry: A journal of the psychiatry …, 2008 | 143 | 2008 |
Mitochondrial abnormalities in ageing macular photoreceptors MJ Barron, MA Johnson, RM Andrews, MP Clarke, PG Griffiths, E Bristow, ... Investigative ophthalmology & visual science 42 (12), 3016-3022, 2001 | 132 | 2001 |
Visual exploration in Parkinson’s disease and Parkinson’s disease dementia NK Archibald, SB Hutton, MP Clarke, UP Mosimann, DJ Burn Brain 136 (3), 739-750, 2013 | 113 | 2013 |
A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy KP Langton, N McKie, A Curtis, JA Goodship, PM Bond, MD Barker, ... Journal of Biological Chemistry 275 (35), 27027-27031, 2000 | 107 | 2000 |