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Kathryn Burdon
Kathryn Burdon
Menzies Institute for Medical Research, University of Tasmania
Bestätigte E-Mail-Adresse bei utas.edu.au - Startseite
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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
11392016
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
4712013
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
4292011
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
4132010
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
3262013
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
2542009
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
2232014
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
2202015
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
2082016
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
1812014
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
1752008
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
1582013
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
1542015
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
1522016
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
1502016
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
1502010
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
1422017
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
1412003
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
1352020
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
1342011
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