PubMed

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

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

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

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

Abnormal iris processes may be a marker of glaucoma gene carrier status in some cases of primary infantile glaucoma.

Balaratnasingam C, Morgan WH, Nelson J, Mackey DA, Dimasi DP, Lam G.

Ophthalmic Genet. 2007 Sep;28(3):157-62.PMID: 17896314 [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

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 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

A myocilin Gln368STOP homozygote does not exhibit a more severe glaucoma phenotype than heterozygous cases.

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

Am J Ophthalmol. 2006 Feb;141(2):402-3.PMID: 16458712 [PubMed - indexed for MEDLINE]Related articles

Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma.

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

J Med Genet. 2005 Sep;42(9):e55.PMID: 16140998 [PubMed - indexed for MEDLINE]Related articlesFree article