|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
|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
|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, 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
|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
|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
|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
|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, 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, 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 genetics 6 (5), 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, 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, 2014
|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
|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
|The genetics of central corneal thickness|
DP Dimasi, KP Burdon, JE Craig
British journal of ophthalmology 94 (8), 971-976, 2010
|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
|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
|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
|Insights into keratoconus from a genetic perspective|
KP Burdon, AL Vincent
Clinical and Experimental Optometry 96 (2), 146-154, 2013
|Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity|
JL Dickinson, MM Sale, A Passmore, LM FitzGerald, CM Wheatley, ...
Clinical & experimental ophthalmology 34 (7), 682-688, 2006