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| 1 | The association of hepatocyte growth factor (HGF) gene with primary angle closure glaucoma in the Nepalese population 显示文摘 | Awadalla MS Thapa SS Burdon KP | 2011 | Mol Vis2011，17，： | 1 |
| 2 | Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people 显示文摘 | Hewitt A W Sharma S Burdon KP | 2008 | Hum Mol Genet2008，17，5： | 1 |
| 3 | Association of alpha 2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis显示文摘 | Lehtinen AB Burdon KP Lewis JP | | 0，，01： | 1 |
| 4 | Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syn- drome, including severe congenital cataract, dental anomalies, and mental retardation 显示文摘 | Burdon KP McKay JD Sale MM | 2003 | Am J Hum Genet2003，73，5： | 1 |
| 5 | Common variants near ABCA1,AFAP1 and GMDS confer risk of primary open-angle glaucoma显示文摘 | GHARAHKHANI P BURDON KP FOGARTY R | 2014 | Nat Genet2014，46，10： | 1 |
| 6 | A systematic meta- analysis of genetic association studies for diabetic retinopathy 显示文摘 | Abhary S Hewitt AW Burdon KP | 2009 | Diabetes2009，58，9： | 1 |
| 7 | Association analysis of genes in the renin-angiotensin system with subclinical cardiovascular disease in families with type 2 diabetes mellitus:the Diabetes Heart Study显示文摘 | Burdon KP Langefeld CD Carr JJ | 2006 | Diabet Med2006，23，3： | 1 |
| 8 | A systematic meta- analysis of genetic association studies for diabetic retinopathy 显示文摘 | Abhary S Hewitt AW Burdon KP | 2009 | Diabetes2009，58，9： | 1 |
| 9 | Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study显示文摘 | Burdon KP Lehtinen AB Langefeld CD | 2008 | Diab Vasc Dis Res2008，5，12： | 1 |
| 10 | Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1显示文摘 | BURDON KP MACGREGOR S HEWITT AW | 2011 | Nat Genet2011，43，6： | 1 |
| 11 | P-selectin gene haplotype associations with albuminuria in the Diabetic Heart Study显示文摘 | Liu Y Burdon KP Langefeld CD | 2005 | Kidney Int2005，68，2： | 1 |
| 12 | Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near theGRB2gene 显示文摘 | Burdon KP Fogarty RD Shen W | 2015 | Diabetologia2015，58，10： | 1 |
| 13 | Asso- ciation of eNOS polymorphisms with primary angle-closure glaucoma显示文摘 | Awadalla MS Thapa SS Hewitt AW Craig JE Burdon KP | 2013 | Invest Ophthalmol Vis Sci2013，54，3： | 1 |
| 14 | The PITX3 gene in posterior polar congenital cataract in Australia显示文摘 | Burdon KP Mckay JD Wirth MG Russell-Eggit 1M Bhatti S Ruddle JB | 2006 | Mol Vis2006，12，： | 1 |
| 15 | Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract显示文摘 | Zhang T Hua R Xiao W Burdon KP Bhattacharya SS Craig JE | 2009 | Hum Mutat2009，30，5： | 1 |
| 16 | Aldose reductase gene polymorphisms and diabetic retinopathy suscepibility显示文摘 | Abhery S Burdon KP Laurie KJ | 2010 | Diabetes Care2010，33，8： | 1 |
| 17 | Asso- ciation of genetic variants with primary angle closure glaucoma in two different populations显示文摘 | Awadalla MS Thapa SS Hewitt AW Burdon KP Craig JE | 2013 | PLoS One2013，8，67： | 1 |
| 18 | Variants of the CD40gene but not of the CD40L gene are associated with coronary arterycalcification in the Diabetes Heart Study(DHS)显示文摘 | Burdon KP Langefeld CD Beck SR | 2006 | Am Heart J2006，151，3： | 1 |
| 19 | Genetic analysis of the solu- ble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study 显示文摘 | Burdon KP Lehtinen AB Langefeld CD | 2008 | Diab Vasc Dis Res2008，5，2： | 1 |
| 20 | A sys- tematic meta- analysis of genetic association studies for dia- betic retinopathy显示文摘 | ABHARY S HEWITT AW BURDON KP CRAIG JE | 2009 | Diabetes2009，58，9： | 1 |
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