| A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ... Nature genetics 48 (2), 134-143, 2016 | 634 | 2016 |
| Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia VJM Verhoeven, PG Hysi, R Wojciechowski, Q Fan, JA Guggenheim, ... Nature genetics 45 (3), 314-318, 2013 | 368 | 2013 |
| Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1 KP Burdon, S Macgregor, AW Hewitt, S Sharma, G Chidlow, RA Mills, ... Nature genetics 43 (6), 574-578, 2011 | 359 | 2011 |
| 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 | 350 | 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, 2013 | 253 | 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 | 218 | 2009 |
| 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 | 167 | 2014 |
| 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 | 161 | 2008 |
| 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, 2015 | 157 | 2015 |
| 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 Genet 6 (5), e1000947, 2010 | 137 | 2010 |
| 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 | 134 | 2016 |
| 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 | 131 | 2014 |
| 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 | 113 | 2013 |
| 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 | 113 | 2003 |
| Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus KP Burdon, S Macgregor, Y Bykhovskaya, S Javadiyan, X Li, KJ Laurie, ... Investigative ophthalmology & visual science 52 (11), 8514-8519, 2011 | 112 | 2011 |
| The genetics of central corneal thickness DP Dimasi, KP Burdon, JE Craig British journal of ophthalmology 94 (8), 971-976, 2010 | 107 | 2010 |
| Meta‐analysis of genome‐wide association studies identifies novel loci associated with optic disc morphology H Springelkamp, A Mishra, PG Hysi, P Gharahkhani, R Höhn, CC Khor, ... Genetic epidemiology 39 (3), 207-216, 2015 | 106 | 2015 |
| Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract T Zhang, R Hua, W Xiao, KP Burdon, SS Bhattacharya, JE Craig, D Shang, ... Human mutation 30 (5), E603-E611, 2009 | 97 | 2009 |
| Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma CC Khor, T Do, H Jia, M Nakano, R George, K Abu-Amero, R Duvesh, ... Nature genetics 48 (5), 556-562, 2016 | 95 | 2016 |
| 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 | 92 | 2016 |
Alex HewittUniversity of TasmaniaVerified email at utas.edu.au
