Mackey DA - Search Results

1

Association of Genetic Variation With Keratoconus.

McComish BJ, Sahebjada S, Bykhovskaya Y, Willoughby CE, Richardson AJ, Tenen A, Charlesworth JC, MacGregor S, Mitchell P, Lucas SEM, Mills RA, Mackey DA, Li X, Wang JJ, Jensen RA, Rotter JI, Taylor KD, Hewitt AW, Rabinowitz YS, Baird PN, Craig JE, Burdon KP. McComish BJ, et al. Among authors: mackey da. JAMA Ophthalmol. 2020 Feb 1;138(2):174-181. doi: 10.1001/jamaophthalmol.2019.5293. JAMA Ophthalmol. 2020. PMID: 31855235 Free PMC article.

2

Glaucoma genetics: where are we? Where will we go?

Craig JE, Mackey DA. Craig JE, et al. Among authors: mackey da. Curr Opin Ophthalmol. 1999 Apr;10(2):126-34. doi: 10.1097/00055735-199904000-00009. Curr Opin Ophthalmol. 1999. PMID: 10537763 Review.

3

Inhaled corticosteroids, family history, and risk of glaucoma.

Mitchell P, Cumming RG, Mackey DA. Mitchell P, et al. Among authors: mackey da. Ophthalmology. 1999 Dec;106(12):2301-6. doi: 10.1016/S0161-6420(99)90530-4. Ophthalmology. 1999. PMID: 10599661

4

Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in Tasmania.

McNaught AI, Allen JG, Healey DL, McCartney PJ, Coote MA, Wong TL, Craig JE, Green CM, Rait JL, Mackey DA. McNaught AI, et al. Among authors: mackey da. Arch Ophthalmol. 2000 Jul;118(7):900-4. Arch Ophthalmol. 2000. PMID: 10900101

5

Laboratory methods in ophthalmic genetics: obtaining DNA from patients.

Dickinson JL, Sale MM, Craig JE, Mackey DA. Dickinson JL, et al. Among authors: mackey da. Ophthalmic Genet. 2001 Mar;22(1):49-60. doi: 10.1076/opge.22.1.49.2240. Ophthalmic Genet. 2001. PMID: 11262650 Review.

6

The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucoma.

Baird PN, Dickinson J, Craig JE, Mackey DA. Baird PN, et al. Among authors: mackey da. Am J Ophthalmol. 2001 Apr;131(4):510-1. doi: 10.1016/s0002-9394(00)00812-6. Am J Ophthalmol. 2001. PMID: 11292420

7

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

8

Retinopathy of prematurity: recent advances in our understanding.

Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Wheatley CM, et al. Among authors: mackey da. Br J Ophthalmol. 2002 Jun;86(6):696-700. doi: 10.1136/bjo.86.6.696. Br J Ophthalmol. 2002. PMID: 12034695 Free PMC article. Review.

9

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.

10

Retinopathy of prematurity: recent advances in our understanding.

Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Wheatley CM, et al. Among authors: mackey da. Arch Dis Child Fetal Neonatal Ed. 2002 Sep;87(2):F78-82. doi: 10.1136/fn.87.2.f78. Arch Dis Child Fetal Neonatal Ed. 2002. PMID: 12193510 Free PMC article. Review.

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