Burdon KP - Search Results

1

Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study.

Sobrin L, Chong YH, Fan Q, Gan A, Stanwyck LK, Kaidonis G, Craig JE, Kim J, Liao WL, Huang YC, Lee WJ, Hung YJ, Guo X, Hai Y, Ipp E, Pollack S, Hancock H, Price A, Penman A, Mitchell P, Liew G, Smith AV, Gudnason V, Tan G, Klein BEK, Kuo J, Li X, Christiansen MW, Psaty BM, Sandow K; Asian Genetic Epidemiology Network Consortium; Jensen RA, Klein R, Cotch MF, Wang JJ, Jia Y, Chen CJ, Chen YI, Rotter JI, Tsai FJ, Hanis CL, Burdon KP, Wong TY, Cheng CY. Sobrin L, et al. Among authors: burdon kp. Diabetes. 2017 Dec;66(12):3130-3141. doi: 10.2337/db17-0398. Epub 2017 Sep 26. Diabetes. 2017. PMID: 28951389 Free PMC article.

2

Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.

Dickinson JL, Sale MM, Passmore A, FitzGerald LM, Wheatley CM, Burdon KP, Craig JE, Tengtrisorn S, Carden SM, Maclean H, Mackey DA. Dickinson JL, et al. Among authors: burdon kp. Clin Exp Ophthalmol. 2006 Sep-Oct;34(7):682-8. doi: 10.1111/j.1442-9071.2006.01314.x. Clin Exp Ophthalmol. 2006. PMID: 16970763

3

A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.

Burdon KP, Sharma S, Chen CS, Dimasi DP, Mackey DA, Craig JE. Burdon KP, et al. Hum Mutat. 2007 Jul;28(7):742. doi: 10.1002/humu.9501. Hum Mutat. 2007. PMID: 17579362

4

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.

Hewitt AW, Sharma S, Burdon KP, Wang JJ, Baird PN, Dimasi DP, Mackey DA, Mitchell P, Craig JE. Hewitt AW, et al. Among authors: burdon kp. Hum Mol Genet. 2008 Mar 1;17(5):710-6. doi: 10.1093/hmg/ddm342. Epub 2007 Nov 23. Hum Mol Genet. 2008. PMID: 18037624

5

A novel locus for X-linked congenital cataract on Xq24.

Craig JE, Friend KL, Gecz J, Rattray KM, Troski M, Mackey DA, Burdon KP. Craig JE, et al. Among authors: burdon kp. Mol Vis. 2008 Apr 18;14:721-6. Mol Vis. 2008. PMID: 18431456 Free PMC article.

6

Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.

Burdon KP, Sharma S, Hewitt AW, McMellon AE, Wang JJ, Mackey DA, Mitchell P, Craig JE. Burdon KP, et al. Mol Vis. 2008 Sep 22;14:1727-36. Mol Vis. 2008. PMID: 18806885 Free PMC article.

7

Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.

Burdon KP, Hattersley K, Lachke SA, Laurie KJ, Maas RL, Mackey DA, Craig JE. Burdon KP, et al. Mol Vis. 2008;14:1799-804. Epub 2008 Sep 30. Mol Vis. 2008. PMID: 18843385 Free PMC article.

8

A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian family.

Burdon KP, Durkin SR, Burke M, Edwards M, Pater J, Straga T, Gecz J, Liebelt JE, Craig JE. Burdon KP, et al. Am J Med Genet A. 2009 Feb 15;149A(4):633-9. doi: 10.1002/ajmg.a.32726. Am J Med Genet A. 2009. PMID: 19291767

9

Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry.

Sharma S, Chataway T, Burdon KP, Jonavicius L, Klebe S, Hewitt AW, Mills RA, Craig JE. Sharma S, et al. Among authors: burdon kp. Exp Eye Res. 2009 Oct;89(4):479-85. doi: 10.1016/j.exer.2009.05.001. Epub 2009 May 12. Exp Eye Res. 2009. PMID: 19442659

10

Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathy.

Abhary S, Burdon KP, Gupta A, Lake S, Selva D, Petrovsky N, Craig JE. Abhary S, et al. Among authors: burdon kp. Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5552-8. doi: 10.1167/iovs.09-3694. Epub 2009 Jun 24. Invest Ophthalmol Vis Sci. 2009. PMID: 19553626

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