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

Primary open angle glaucoma in subjects harbouring the predicted GLC1L haplotype reveals a normotensive phenotype.

Sherwin JC, Hewitt AW, Bennett SL, Baird PN, Craig JE, Mackey DA.

Clin Experiment Ophthalmol. 2009 Mar;37(2):201-7. Epub 2009 Feb 3.PMID: 19723129 [PubMed - indexed for MEDLINE]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

Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye Study.

Sun C, Zhu G, Wong TY, Hewitt AW, Ruddle JB, Hodgson L, Montgomery GW, Young TL, Hammond CJ, Craig JE, Martin NG, He M, Mackey DA.

Hypertension. 2009 Oct;54(4):788-95. Epub 2009 Aug 17.PMID: 19687348 [PubMed - indexed for MEDLINE]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

NHS-A isoform of the NHS gene is a novel interactor of ZO-1.

Sharma S, Koh KS, Collin C, Dave A, McMellon A, Sugiyama Y, McAvoy JW, Voss AK, Gécz J, Craig JE.

Exp Cell Res. 2009 Aug 15;315(14):2358-72. Epub 2009 May 15.PMID: 19447104 [PubMed - indexed for MEDLINE]Related articles

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

Mortality in primary open-angle glaucoma: 'two cupped discs and a funeral'

Hewitt AW, Sanfilippo P, Ring MA, Craig JE, Mackey DA.

Eye (Lond). 2009 Feb 27. [Epub ahead of print]PMID: 19247389 [PubMed - as supplied by publisher]Related articles

Advances in telemetric continuous intraocular pressure assessment.

Kakaday T, Hewitt AW, Voelcker NH, Li JS, Craig JE.

Br J Ophthalmol. 2009 Aug;93(8):992-6. Epub 2009 Feb 24. Review.PMID: 19244268 [PubMed - indexed for MEDLINE]Related articles

Anterior segment optical coherence tomography in the investigation of an unusual case of entoptic phenomenon.

Durkin SR, Chappell A, Craig JE.

Clin Experiment Ophthalmol. 2008 Nov;36(8):796-7. No abstract available. PMID: 19128388 [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

The natural history of OPA1-related autosomal dominant optic atrophy.

Cohn AC, Toomes C, Hewitt AW, Kearns LS, Inglehearn CF, Craig JE, Mackey DA.

Br J Ophthalmol. 2008 Oct;92(10):1333-6. Epub 2008 Jul 24.PMID: 18653586 [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

'America's passing gear'.

Craig JE Jr.

Health Aff (Millwood). 2008 Jan-Feb;27(1):300-1. No abstract available. PMID: 18180510 [PubMed - indexed for MEDLINE]Related articles

Objective monitoring of papilloedema using confocal scanning laser ophthalmoscopy.

Chen JY, Taranath DA, Chappell AJ, Brophy BP, Craig JE.

Clin Experiment Ophthalmol. 2007 Dec;35(9):863-5.PMID: 18173418 [PubMed - indexed for MEDLINE]Related articles

How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania.

Green CM, Kearns LS, Wu J, Barbour JM, Wilkinson RM, Ring MA, Craig JE, Wong TL, Hewitt AW, Mackey DA.

Clin Experiment Ophthalmol. 2007 Dec;35(9):793-9.PMID: 18173405 [PubMed - indexed for MEDLINE]Related articles

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

Myocilin allele-specific glaucoma phenotype database.

Hewitt AW, Mackey DA, Craig JE.

Hum Mutat. 2008 Feb;29(2):207-11.PMID: 17966125 [PubMed - indexed for MEDLINE]Related articles

Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q.

Zhu G, Hewitt AW, Ruddle JB, Kearns LS, Brown SA, Mackinnon JR, Chen CY, Hammond CJ, Craig JE, Montgomery GW, Martin NG, Mackey DA.

Ophthalmology. 2008 Jun;115(6):1053-1057.e2. Epub 2007 Oct 26.PMID: 17964656 [PubMed - indexed for MEDLINE]Related articles

Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma.

Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, Craig JE.

Clin Genet. 2007 Sep;72(3):255-60.PMID: 17718864 [PubMed - indexed for MEDLINE]Related articles

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

Heritable features of the optic disc: a novel twin method for determining genetic significance.

Hewitt AW, Poulsen JP, Alward WL, Bennett SL, Budde WM, Cooper RL, Craig JE, Fingert JH, Foster PJ, Garway-Heath DF, Green CM, Hammond CJ, Hayreh SS, Jonas JB, Kaufman PL, Miller NR, Morgan WH, Newman NJ, Quigley HA, Samples JR, Spaeth GL, Pesudovs K, Mackey DA.

Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2469-75.PMID: 17525172 [PubMed - indexed for MEDLINE]Related articlesFree article

No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma.

Symons RC, Turakulov R, Foote SJ, Craig JE, McCartney PJ, Mackey DA.

Ophthalmic Genet. 2007 Mar;28(1):39-41. No abstract available. PMID: 17454746 [PubMed - indexed for MEDLINE]Related articles

Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations.

Cohn AC, Toomes C, Potter C, Towns KV, Hewitt AW, Inglehearn CF, Craig JE, Mackey DA.

Am J Ophthalmol. 2007 Apr;143(4):656-62. Epub 2007 Feb 15.PMID: 17306754 [PubMed - indexed for MEDLINE]Related articles

Classic features of multiple endocrine neoplasia type 2B.

Chen JY, Taranath DA, Chappell AJ, McMellon AE, Craig JE.

Arch Ophthalmol. 2007 Feb;125(2):280-1. No abstract available. PMID: 17296909 [PubMed - indexed for MEDLINE]Related articles

Central corneal thickness of indigenous Australians within Central Australia.

Landers JA, Billing KJ, Mills RA, Henderson TR, Craig JE.

Am J Ophthalmol. 2007 Feb;143(2):360-2. Epub 2006 Oct 19.PMID: 17258537 [PubMed - indexed for MEDLINE]Related articles

Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees.

Bennett SL, Hewitt AW, Poulsen JL, Kearns LS, Morgan JE, Craig JE, Mackey DA.

Arch Ophthalmol. 2007 Jan;125(1):112-6.PMID: 17210861 [PubMed - indexed for MEDLINE]Related articlesFree article

Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.

Hewitt AW, Bennett SL, Richards JE, Dimasi DP, Booth AP, Inglehearn C, Anwar R, Yamamoto T, Fingert JH, Héon E, Craig JE, Mackey DA.

Arch Ophthalmol. 2007 Jan;125(1):98-104.PMID: 17210859 [PubMed - indexed for MEDLINE]Related articlesFree article

The optic nerve head in myocilin glaucoma.

Hewitt AW, Bennett SL, Fingert JH, Cooper RL, Stone EM, Craig JE, Mackey DA.

Invest Ophthalmol Vis Sci. 2007 Jan;48(1):238-43.PMID: 17197538 [PubMed - indexed for MEDLINE]Related articlesFree article

Optic nerve head parameters of an indigenous population living within Central Australia.

Landers JA, Henderson TR, Craig JE.

Clin Experiment Ophthalmol. 2006 Dec;34(9):852-6.PMID: 17181616 [PubMed - indexed for MEDLINE]Related articles

Familial transmission risk of infantile glaucoma in Australia.

Hewitt AW, MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA.

Ophthalmic Genet. 2006 Sep;27(3):93-7.PMID: 17050285 [PubMed - indexed for MEDLINE]Related articles

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

Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer.

Chen CS, Phillips KD, Grist S, Bennet G, Craig JE, Muecke JS, Suthers GK.

Fam Cancer. 2006;5(4):397-404. Epub 2006 Aug 31.PMID: 16944273 [PubMed - indexed for MEDLINE]Related articles

The role of the Met98Lys optineurin variant in inherited optic nerve diseases.

Craig JE, Hewitt AW, Dimasi DP, Howell N, Toomes C, Cohn AC, Mackey DA.

Br J Ophthalmol. 2006 Nov;90(11):1420-4. Epub 2006 Aug 2.PMID: 16885188 [PubMed - indexed for MEDLINE]Related articlesFree article

A Glaucoma Case-control Study of the WDR36 Gene D658G sequence variant.

Hewitt AW, Dimasi DP, Mackey DA, Craig JE.

Am J Ophthalmol. 2006 Aug;142(2):324-5.PMID: 16876519 [PubMed - indexed for MEDLINE]Related articles

Complex genetics of complex traits: the case of primary open-angle glaucoma.

Hewitt AW, Craig JE, Mackey DA.

Clin Experiment Ophthalmol. 2006 Jul;34(5):472-84. Review.PMID: 16872346 [PubMed - indexed for MEDLINE]Related articles

Disease severity of familial glaucoma compared with sporadic glaucoma.

Wu J, Hewitt AW, Green CM, Ring MA, McCartney PJ, Craig JE, Mackey DA.

Arch Ophthalmol. 2006 Jul;124(7):950-4.PMID: 16832017 [PubMed - indexed for MEDLINE]Related articlesFree article

Nail-patella syndrome and its association with glaucoma: a review of eight families.

Mimiwati Z, Mackey DA, Craig JE, Mackinnon JR, Rait JL, Liebelt JE, Ayala-Lugo R, Vollrath D, Richards JE.

Br J Ophthalmol. 2006 Dec;90(12):1505-9. Epub 2006 Jul 6.PMID: 16825280 [PubMed - indexed for MEDLINE]Related articles

Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions.

Sharma S, Ang SL, Shaw M, Mackey DA, Gécz J, McAvoy JW, Craig JE.

Hum Mol Genet. 2006 Jun 15;15(12):1972-83. Epub 2006 May 4.PMID: 16675532 [PubMed - indexed for MEDLINE]Related articlesFree article