| Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene AL Vincent, G Billingsley, Y Buys, AV Levin, M Priston, G Trope, ... The American Journal of Human Genetics 70 (2), 448-460, 2002 | 387 | 2002 |
| VSX1: A gene for posterior polymorphous dystrophy and keratoconus E Heon, A Greenberg, KK Kopp, D Rootman, AL Vincent, G Billingsley, ... Human molecular genetics 11 (9), 1029-1036, 2002 | 355 | 2002 |
| Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression JE Craig, X Han, A Qassim, M Hassall, JN Cooke Bailey, TG Kinzy, ... Nature genetics 52 (2), 160-166, 2020 | 221 | 2020 |
| Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly A Vincent, G Billingsley, M Priston, D Williams-Lyn, J Sutherland, T Glaser, ... Journal of medical genetics 38 (5), 324-326, 2001 | 138 | 2001 |
| Insights into keratoconus from a genetic perspective KP Burdon, AL Vincent Clinical and Experimental Optometry 96 (2), 146-154, 2013 | 131 | 2013 |
| Impaired complex-I-linked respiration and ATP synthesis in primary open-angle glaucoma patient lymphoblasts S Lee, L Sheck, JG Crowston, NJ Van Bergen, EC O'Neill, F O'Hare, ... Investigative ophthalmology & visual science 53 (4), 2431-2437, 2012 | 131 | 2012 |
| Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics M Khan, SS Cornelis, MD Pozo-Valero, L Whelan, EH Runhart, K Mishra, ... Genetics in Medicine 22 (7), 1235-1246, 2020 | 107 | 2020 |
| Efficacy of wide‐field digital retinal imaging for retinopathy of prematurity screening S Dai, K Chow, A Vincent Clinical & experimental ophthalmology 39 (1), 23-29, 2011 | 99 | 2011 |
| Incidence and outcomes of infectious and noninfectious endophthalmitis after intravitreal injections for age-related macular degeneration V Daien, V Nguyen, RW Essex, N Morlet, D Barthelmes, MC Gillies, ... Ophthalmology 125 (1), 66-74, 2018 | 96 | 2018 |
| Abusive head trauma and accidental head injury: a 20-year comparative study of referrals to a hospital child protection team P Kelly, S John, AL Vincent, P Reed Archives of disease in childhood 100 (12), 1123-1130, 2015 | 93 | 2015 |
| Real-world clinical experience with idebenone in the treatment of Leber hereditary optic neuropathy CB Catarino, B von Livonius, C Priglinger, R Banik, S Matloob, ... Journal of Neuro-Ophthalmology 40 (4), 558-565, 2020 | 89 | 2020 |
| Further support of the role of CYP1B1 in patients with Peters anomaly A Vincent, G Billingsley, M Priston, T Glaser, E Oliver, M Walter, R Ritch, ... Mol Vis 12 (1), 506-510, 2006 | 80 | 2006 |
| Mutations in the zinc finger protein gene, ZNF469, contribute to the pathogenesis of keratoconus AL Vincent, CA Jordan, MJ Cadzow, TR Merriman, CN McGhee Investigative ophthalmology & visual science 55 (9), 5629-5635, 2014 | 72 | 2014 |
| Progression of diabetic retinopathy after bariatric surgery R Murphy, Y Jiang, M Booth, R Babor, A MacCormick, H Hammodat, ... Diabetic Medicine 32 (9), 1212-1220, 2015 | 51 | 2015 |
| Computerized corneal topography in a paediatric population with Down syndrome AL Vincent, BA Weiser, M Cupryn, RM Stein, M Abdolell, AV Levin Clinical & experimental ophthalmology 33 (1), 47-52, 2005 | 51 | 2005 |
| Corneal dystrophies and genetics in the I nternational C ommittee for C lassification of C orneal D ystrophies era: a review AL Vincent Clinical & experimental ophthalmology 42 (1), 4-12, 2014 | 47 | 2014 |
| Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma P Gharahkhani, KP Burdon, JN Cooke Bailey, AW Hewitt, MH Law, ... Scientific reports 8 (1), 3124, 2018 | 45 | 2018 |
| A COL17A1 splice-altering mutation is prevalent in inherited recurrent corneal erosions VF Oliver, KA van Bysterveldt, M Cadzow, B Steger, V Romano, D Markie, ... Ophthalmology 123 (4), 709-722, 2016 | 42 | 2016 |
| Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: genetic heterogeneity and exclusion of three candidate genes SM Hosseini, S Herd, AL Vincent, E Héon Molecular vision 14, 71, 2008 | 42 | 2008 |
| Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3 P Liskova, CJ Evans, AE Davidson, M Zaliova, L Dudakova, M Trkova, ... European Journal of Human Genetics 24 (7), 985-991, 2016 | 41 | 2016 |
