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Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ... Nature genetics 42 (10), 906-909, 2010 | 456 | 2010 |
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ... Nature genetics 45 (2), 155-163, 2013 | 356 | 2013 |
A systematic meta-analysis of genetic association studies for diabetic retinopathy S Abhary, AW Hewitt, KP Burdon, JE Craig Diabetes 58 (9), 2137-2147, 2009 | 285 | 2009 |
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma JNC Bailey, SJ Loomis, JH Kang, RR Allingham, P Gharahkhani, CC Khor, ... Nature genetics 48 (2), 189-194, 2016 | 262 | 2016 |
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ... Nature genetics 46 (10), 1126-1130, 2014 | 256 | 2014 |
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma MH Law, DT Bishop, JE Lee, M Brossard, NG Martin, EK Moses, F Song, ... Nature genetics 47 (9), 987-995, 2015 | 251 | 2015 |
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 | 231 | 2020 |
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma P Gharahkhani, KP Burdon, R Fogarty, S Sharma, AW Hewitt, S Martin, ... Nature genetics 46 (10), 1120-1125, 2014 | 221 | 2014 |
Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity T Souma, SW Tompson, BR Thomson, OM Siggs, K Kizhatil, S Yamaguchi, ... The Journal of clinical investigation 126 (7), 2575-2587, 2016 | 197 | 2016 |
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Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error CY Cheng, M Schache, MK Ikram, TL Young, JA Guggenheim, V Vitart, ... The American Journal of Human Genetics 93 (2), 264-277, 2013 | 186 | 2013 |
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people AW Hewitt, S Sharma, KP Burdon, JJ Wang, PN Baird, DP Dimasi, ... Human molecular genetics 17 (5), 710-716, 2008 | 186 | 2008 |
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics H Springelkamp, AI Iglesias, A Mishra, R Höhn, R Wojciechowski, ... Human molecular genetics 26 (2), 438-453, 2017 | 180 | 2017 |
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Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility MT Landi, DT Bishop, S MacGregor, MJ Machiela, AJ Stratigos, P Ghiorzo, ... Nature genetics 52 (5), 494-504, 2020 | 171 | 2020 |
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma S MacGregor, JS Ong, J An, X Han, T Zhou, OM Siggs, MH Law, ... Nature genetics 50 (8), 1067-1071, 2018 | 171 | 2018 |
Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness Y Lu, DP Dimasi, PG Hysi, AW Hewitt, KP Burdon, TY Toh, JB Ruddle, ... PLoS genetics 6 (5), e1000947, 2010 | 163 | 2010 |