PubMed

Rapid inexpensive genome-wide association using pooled whole blood.

Craig JE, Hewitt AW, McMellon AE, Henders AK, Ma L, Wallace L, Sharma S, Burdon KP, Visscher PM, Montgomery GW, MacGregor S.

Genome Res. 2009 Nov;19(11):2075-80. Epub 2009 Oct 3.PMID: 19801603 [PubMed - in process]Related articles

Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.

Dimasi DP, Chen JY, Hewitt AW, Klebe S, Davey R, Stirling J, Thompson E, Forbes R, Tan TY, Savarirayan R, Mackey DA, Healey PR, Mitchell P, Burdon KP, Craig JE.

Hum Genet. 2009 Aug 28. [Epub ahead of print]PMID: 19714363 [PubMed - as supplied by publisher]Related articles

Diabetic retinopathy is associated with elevated serum asymmetric and symmetric dimethylarginines.

Abhary S, Kasmeridis N, Burdon KP, Kuot A, Whiting MJ, Yew WP, Petrovsky N, Craig JE.

Diabetes Care. 2009 Nov;32(11):2084-6. Epub 2009 Aug 12.PMID: 19675197 [PubMed - in process]Related articles

A systematic meta-analysis of genetic association studies for diabetic retinopathy.

Abhary S, Hewitt AW, Burdon KP, Craig JE.

Diabetes. 2009 Sep;58(9):2137-47. Epub 2009 Jul 8.PMID: 19587357 [PubMed - indexed for MEDLINE]Related articles

The genetics of central corneal thickness.

Dimasi DP, Burdon KP, Craig JE.

Br J Ophthalmol. 2009 Jun 24. [Epub ahead of print]PMID: 19556215 [PubMed - as supplied by publisher]Related articles

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.

Invest Ophthalmol Vis Sci. 2009 Jun 24. [Epub ahead of print]PMID: 19553626 [PubMed - as supplied by publisher]Related articles

Diabetic retinopathy is not associated with carbonic anhydrase gene polymorphisms.

Abhary S, Burdon KP, Gupta A, Petrovsky N, Craig JE.

Mol Vis. 2009 Jun 13;15:1179-84.PMID: 19536309 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Exp Eye Res. 2009 Oct;89(4):479-85. Epub 2009 May 12.PMID: 19442659 [PubMed - in process]Related articles

Heritability of central corneal thickness in nuclear families.

Landers JA, Hewitt AW, Dimasi DP, Charlesworth JC, Straga T, Mills RA, Savarirayan R, Mackey DA, Burdon KP, Craig JE.

Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4087-90. Epub 2009 May 6.PMID: 19420341 [PubMed - indexed for MEDLINE]Related articles

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract.

Zhang T, Hua R, Xiao W, Burdon KP, Bhattacharya SS, Craig JE, Shang D, Zhao X, Mackey DA, Moore AT, Luo Y, Zhang J, Zhang X.

Hum Mutat. 2009 May;30(5):E603-11.PMID: 19306328 [PubMed - indexed for MEDLINE]Related articles

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.

Am J Med Genet A. 2009 Feb 15;149A(4):633-9.PMID: 19291767 [PubMed - indexed for MEDLINE]Related articles

Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform.

Sharma S, Burdon KP, Dave A, Jamieson RV, Yaron Y, Billson F, Van Maldergem L, Lorenz B, Gécz J, Craig JE.

Mol Vis. 2008;14:1856-64. Epub 2008 Oct 20.PMID: 18949062 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Mol Vis. 2008;14:1799-804. Epub 2008 Sep 30.PMID: 18843385 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Mol Vis. 2008 Sep 22;14:1727-36.PMID: 18806885 [PubMed - indexed for MEDLINE]Related articlesFree article

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, Hewitt AW, Latimer P, Craig JE.

Hum Genet. 2008 Nov;124(4):379-86. Epub 2008 Sep 5.PMID: 18795334 [PubMed - indexed for MEDLINE]Related articles

Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes.

Liu Y, Freedman BI, Burdon KP, Langefeld CD, Howard T, Herrington D, Goff DC Jr, Bowden DW, Wagenknecht LE, Hedrick CC, Rich SS.

Am J Kidney Dis. 2008 Aug;52(2):242-50. Epub 2008 Mar 25.PMID: 18640486 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study.

Burdon KP, Lehtinen AB, Langefeld CD, Carr JJ, Rich SS, Freedman BI, Herrington D, Bowden DW.

Diab Vasc Dis Res. 2008 Jun;5(2):128-34.PMID: 18537101 [PubMed - indexed for MEDLINE]Related articles

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

Craig JE, Friend KL, Gecz J, Rattray KM, Troski M, Mackey DA, Burdon KP.

Mol Vis. 2008 Apr 18;14:721-6.PMID: 18431456 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration.

Ormsby RJ, Ranganathan S, Tong JC, Griggs KM, Dimasi DP, Hewitt AW, Burdon KP, Craig JE, Hoh J, Gordon DL.

Invest Ophthalmol Vis Sci. 2008 May;49(5):1763-70. Epub 2008 Feb 8.PMID: 18263814 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Hum Mol Genet. 2008 Mar 1;17(5):710-6. Epub 2007 Nov 23.PMID: 18037624 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Hum Mutat. 2007 Jul;28(7):742.PMID: 17579362 [PubMed - indexed for MEDLINE]Related articles

Association of alpha2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis.

Lehtinen AB, Burdon KP, Lewis JP, Langefeld CD, Ziegler JT, Rich SS, Register TC, Carr JJ, Freedman BI, Bowden DW.

J Clin Endocrinol Metab. 2007 Jan;92(1):345-52. Epub 2006 Oct 24.PMID: 17062776 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Clin Experiment Ophthalmol. 2006 Sep-Oct;34(7):682-8.PMID: 16970763 [PubMed - indexed for MEDLINE]Related articles

A functional polymorphism in the lymphotoxin-alpha gene is associated with carotid artery wall thickness: the Diabetes Heart Study.

Liu Y, Herrington D, Burdon KP, Langefeld CD, Rich SS, Bowden DW, Freedman BI, Wagenknecht LE.

Eur J Cardiovasc Prev Rehabil. 2006 Aug;13(4):655-7.PMID: 16874159 [PubMed - indexed for MEDLINE]Related articles

The PITX3 gene in posterior polar congenital cataract in Australia.

Burdon KP, McKay JD, Wirth MG, Russell-Eggit IM, Bhatti S, Ruddle JB, Dimasi D, Mackey DA, Craig JE.

Mol Vis. 2006 Apr 18;12:367-71.PMID: 16636655 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of protein tyrosine phosphatase-N1 polymorphisms with coronary calcified plaque in the Diabetes Heart Study.

Burdon KP, Bento JL, Langefeld CD, Campbell JK, Carr JJ, Wagenknecht LM, Herrington DM, Freedman BI, Rich SS, Bowden DW.

Diabetes. 2006 Mar;55(3):651-8.PMID: 16505227 [PubMed - indexed for MEDLINE]Related articlesFree article

Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS).

Burdon KP, Langefeld CD, Beck SR, Wagenknecht LE, Carr JJ, Rich SS, Freedman BI, Herrington D, Bowden DW.

Am Heart J. 2006 Mar;151(3):706-11.PMID: 16504636 [PubMed - indexed for MEDLINE]Related articles

Association analysis of genes in the renin-angiotensin system with subclinical cardiovascular disease in families with Type 2 diabetes mellitus: the Diabetes Heart Study.

Burdon KP, Langefeld CD, Wagenknecht LE, Carr JJ, Freedman BI, Herrington D, Bowden DW.

Diabet Med. 2006 Mar;23(3):228-34.PMID: 16492203 [PubMed - indexed for MEDLINE]Related articles

The relative contribution of the X chromosome to ocular phenotypes.

Hewitt AW, Burdon KP.

Ophthalmic Genet. 2005 Dec;26(4):191-3.PMID: 16352481 [PubMed - indexed for MEDLINE]Related articles

Association of genes of lipid metabolism with measures of subclinical cardiovascular disease in the Diabetes Heart Study.

Burdon KP, Langefeld CD, Beck SR, Wagenknecht LE, Carr JJ, Freedman BI, Herrington D, Bowden DW.

J Med Genet. 2005 Sep;42(9):720-4.PMID: 16141008 [PubMed - indexed for MEDLINE]Related articlesFree article

P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study.

Liu Y, Burdon KP, Langefeld CD, Beck SR, Wagenknecht LE, Rich SS, Bowden DW, Freedman BI.

Kidney Int. 2005 Aug;68(2):741-6.PMID: 16014051 [PubMed - indexed for MEDLINE]Related articles

The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.

McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA.

Br J Ophthalmol. 2005 Jul;89(7):831-4.PMID: 15965161 [PubMed - indexed for MEDLINE]Related articlesFree article

Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease.

Dusel JA, Burdon KP, Hicks PJ, Hawkins GA, Bowden DW, Freedman BI.

Kidney Int. 2005 Jul;68(1):256-62.PMID: 15954915 [PubMed - indexed for MEDLINE]Related articles

T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study.

Liu Y, Burdon KP, Langefeld CD, Beck SR, Wagenknecht LE, Rich SS, Bowden DW, Freedman BI.

J Am Soc Nephrol. 2005 Apr;16(4):1085-90. Epub 2005 Mar 2.PMID: 15743995 [PubMed - indexed for MEDLINE]Related articlesFree article

Variability of serum soluble intercellular adhesion molecule-1 measurements attributable to a common polymorphism.

Register TC, Burdon KP, Lenchik L, Bowden DW, Hawkins GA, Nicklas BJ, Lohman K, Hsu FC, Langefeld CD, Carr JJ.

Clin Chem. 2004 Nov;50(11):2185-7. No abstract available. PMID: 15502096 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM.

J Med Genet. 2004 Aug;41(8):e106. No abstract available. Erratum in: J Med Genet. 2005 Mar;42(3):288. J Med Genet. 2008 Apr;45(4):256. PMID: 15286166 [PubMed - indexed for MEDLINE]Related articlesFree article

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM.

Br J Ophthalmol. 2004 Jan;88(1):79-83.PMID: 14693780 [PubMed - indexed for MEDLINE]Related articlesFree article

Investigation of albinism genes in congenital esotropia.

Burdon KP, Wilkinson RM, Barbour JM, Dickinson JL, Stankovich JM, Mackey DA, Sale MM.

Mol Vis. 2003 Dec 16;9:710-4.PMID: 14685142 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

Burdon KP, McKay JD, Sale MM, Russell-Eggitt IM, Mackey DA, Wirth MG, Elder JE, Nicoll A, Clarke MP, FitzGerald LM, Stankovich JM, Shaw MA, Sharma S, Gajovic S, Gruss P, Ross S, Thomas P, Voss AK, Thomas T, Gécz J, Craig JE.

Am J Hum Genet. 2003 Nov;73(5):1120-30. Epub 2003 Oct 16.PMID: 14564667 [PubMed - indexed for MEDLINE]Related articlesFree article