Dimasi DP - Search Results

1

Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucoma.

Dimasi DP, Burdon KP, Hewitt AW, Fitzgerald J, Wang JJ, Healey PR, Mitchell P, Mackey DA, Craig JE. Dimasi DP, et al. Am J Ophthalmol. 2012 Nov;154(5):833-842.e2. doi: 10.1016/j.ajo.2012.04.023. Epub 2012 Jul 27. Am J Ophthalmol. 2012. PMID: 22840486

2

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. Dimasi DP, et al. J Med Genet. 2005 Sep;42(9):e55. doi: 10.1136/jmg.2005.032458. J Med Genet. 2005. PMID: 16140998 Free PMC article.

3

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. Hewitt AW, et al. Among authors: dimasi dp. Am J Ophthalmol. 2006 Feb;141(2):402-3. doi: 10.1016/j.ajo.2005.08.073. Am J Ophthalmol. 2006. PMID: 16458712

4

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. Burdon KP, et al. Mol Vis. 2006 Apr 18;12:367-71. Mol Vis. 2006. PMID: 16636655 Free article.

5

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

Hewitt AW, Dimasi DP, Mackey DA, Craig JE. Hewitt AW, et al. Among authors: dimasi dp. Am J Ophthalmol. 2006 Aug;142(2):324-5. doi: 10.1016/j.ajo.2006.02.041. Am J Ophthalmol. 2006. PMID: 16876519

6

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. Craig JE, et al. Among authors: dimasi dp. Br J Ophthalmol. 2006 Nov;90(11):1420-4. doi: 10.1136/bjo.2006.099333. Epub 2006 Aug 2. Br J Ophthalmol. 2006. PMID: 16885188 Free PMC article.

7

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. Hewitt AW, et al. Among authors: dimasi dp. Arch Ophthalmol. 2007 Jan;125(1):98-104. doi: 10.1001/archopht.125.1.98. Arch Ophthalmol. 2007. PMID: 17210859

8

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. Among authors: dimasi dp. Hum Mutat. 2007 Jul;28(7):742. doi: 10.1002/humu.9501. Hum Mutat. 2007. PMID: 17579362

9

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. Dimasi DP, et al. Clin Genet. 2007 Sep;72(3):255-60. doi: 10.1111/j.1399-0004.2007.00864.x. Clin Genet. 2007. PMID: 17718864

10

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. Balaratnasingam C, et al. Among authors: dimasi dp. Ophthalmic Genet. 2007 Sep;28(3):157-62. doi: 10.1080/13816810701503715. Ophthalmic Genet. 2007. PMID: 17896314

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