Mackey DA - Search Results

1

A genome-wide association study of corneal astigmatism: The CREAM Consortium.

Shah RL, Li Q, Zhao W, Tedja MS, Tideman JWL, Khawaja AP, Fan Q, Yazar S, Williams KM, Verhoeven VJM, Xie J, Wang YX, Hess M, Nickels S, Lackner KJ, Pärssinen O, Wedenoja J, Biino G, Concas MP, Uitterlinden A, Rivadeneira F, Jaddoe VWV, Hysi PG, Sim X, Tan N, Tham YC, Sensaki S, Hofman A, Vingerling JR, Jonas JB, Mitchell P, Hammond CJ, Höhn R, Baird PN, Wong TY, Cheng CY, Teo YY, Mackey DA, Williams C, Saw SM, Klaver CCW, Guggenheim JA, Bailey-Wilson JE; CREAM Consortium. Shah RL, et al. Among authors: mackey da. Mol Vis. 2018 Feb 5;24:127-142. eCollection 2018. Mol Vis. 2018. PMID: 29422769 Free PMC article.

2

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

3

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

4

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

5

Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye Study.

Baird PN, Richardson AJ, Craig JE, Mackey DA, Rochtchina E, Mitchell P. Baird PN, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2004 Oct;32(5):518-22. doi: 10.1111/j.1442-9071.2004.00886.x. Clin Exp Ophthalmol. 2004. PMID: 15498064

6

Evidence for a novel glaucoma locus at chromosome 3p21-22.

Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Baird PN, et al. Among authors: mackey da. Hum Genet. 2005 Jul;117(2-3):249-57. doi: 10.1007/s00439-005-1296-x. Epub 2005 May 20. Hum Genet. 2005. PMID: 15906098

7

The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye Study.

Baird PN, Richardson AJ, Craig JE, Rochtchina E, Mackey DA, Mitchell P. Baird PN, et al. Among authors: mackey da. Am J Ophthalmol. 2005 Jun;139(6):1125-6. doi: 10.1016/j.ajo.2004.11.061. Am J Ophthalmol. 2005. PMID: 15953455

8

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.

9

A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families.

Baird PN, Richardson AJ, Mackey DA, Craig JE, Faucher M, Raymond V. Baird PN, et al. Among authors: mackey da. Am J Ophthalmol. 2005 Oct;140(4):760-2. doi: 10.1016/j.ajo.2005.04.043. Am J Ophthalmol. 2005. PMID: 16226543

10

Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds.

Hewitt AW, Samples JR, Allingham RR, Järvelä I, Kitsos G, Krishnadas SR, Richards JE, Lichter PR, Petersen MB, Sundaresan P, Wiggs JL, Mackey DA, Wirtz MK. Hewitt AW, et al. Among authors: mackey da. Mol Vis. 2007 Mar 28;13:487-92. Mol Vis. 2007. PMID: 17417609 Free PMC article.

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