Mackey DA - Search Results

1

A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions.

Oliver VF, van Bysterveldt KA, Cadzow M, Steger B, Romano V, Markie D, Hewitt AW, Mackey DA, Willoughby CE, Sherwin T, Crosier PS, McGhee CN, Vincent AL. Oliver VF, et al. Among authors: mackey da. Ophthalmology. 2016 Apr;123(4):709-22. doi: 10.1016/j.ophtha.2015.12.008. Epub 2016 Jan 16. Ophthalmology. 2016. PMID: 26786512 Free article.

2

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier.

Craig JE, Baird PN, Healey DL, McNaught AI, McCartney PJ, Rait JL, Dickinson JL, Roe L, Fingert JH, Stone EM, Mackey DA. Craig JE, et al. Among authors: mackey da. Ophthalmology. 2001 Sep;108(9):1607-20. doi: 10.1016/s0161-6420(01)00654-6. Ophthalmology. 2001. PMID: 11535458

3

Aetiology of congenital and paediatric cataract in an Australian population.

Wirth MG, Russell-Eggitt IM, Craig JE, Elder JE, Mackey DA. Wirth MG, et al. Among authors: mackey da. Br J Ophthalmol. 2002 Jul;86(7):782-6. doi: 10.1136/bjo.86.7.782. Br J Ophthalmol. 2002. PMID: 12084750 Free PMC article.

4

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. Burdon KP, et al. Among authors: mackey da. Br J Ophthalmol. 2004 Jan;88(1):79-83. doi: 10.1136/bjo.88.1.79. Br J Ophthalmol. 2004. PMID: 14693780 Free PMC article.

5

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.

Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA. Hewitt AW, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2005 Jun;33(3):233-9. doi: 10.1111/j.1442-9071.2005.01018.x. Clin Exp Ophthalmol. 2005. PMID: 15932525

6

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. McKay JD, et al. Among authors: mackey da. Br J Ophthalmol. 2005 Jul;89(7):831-4. doi: 10.1136/bjo.2004.058495. Br J Ophthalmol. 2005. PMID: 15965161 Free PMC article.

7

Central corneal thickness is highly heritable: the twin eye studies.

Toh T, Liew SH, MacKinnon JR, Hewitt AW, Poulsen JL, Spector TD, Gilbert CE, Craig JE, Hammond CJ, Mackey DA. Toh T, et al. Among authors: mackey da. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3718-22. doi: 10.1167/iovs.04-1497. Invest Ophthalmol Vis Sci. 2005. PMID: 16186354 Free article.

8

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: mackey da. Am J Ophthalmol. 2006 Feb;141(2):402-3. doi: 10.1016/j.ajo.2005.08.073. Am J Ophthalmol. 2006. PMID: 16458712

9

Tools for cup:disc ratio measurement.

Hewitt AW, Traill A, Cooper RL, Morgan JE, Mackey DA. Hewitt AW, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2006 Apr;34(3):288-9; author reply 289. doi: 10.1111/j.1442-9071.2006.01209.x. Clin Exp Ophthalmol. 2006. PMID: 16671916 No abstract available.

10

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. Mimiwati Z, et al. Among authors: mackey da. Br J Ophthalmol. 2006 Dec;90(12):1505-9. doi: 10.1136/bjo.2006.092619. Epub 2006 Jul 6. Br J Ophthalmol. 2006. PMID: 16825280 Free PMC article.

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