Mackey DA - Search Results

1

Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology.

Han X, Qassim A, An J, Marshall H, Zhou T, Ong JS, Hassall MM, Hysi PG, Foster PJ, Khaw PT, Mackey DA, Gharahkhani P, Khawaja AP, Hewitt AW, Craig JE, MacGregor S. Han X, et al. Among authors: mackey da. Hum Mol Genet. 2019 Nov 1;28(21):3680-3690. doi: 10.1093/hmg/ddz193. Hum Mol Genet. 2019. PMID: 31809533

2

Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.

Fingert JH, Héon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey DA, Alward WL, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: mackey da. Hum Mol Genet. 1999 May;8(5):899-905. doi: 10.1093/hmg/8.5.899. Hum Mol Genet. 1999. PMID: 10196380

3

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.

4

Normal range of hearing associated with myocilin Thr377Met.

Simm RM, Fingert JH, Craig JE, McNaught AI, Mackey DA. Simm RM, et al. Among authors: mackey da. Ophthalmic Genet. 1999 Sep;20(3):205-7. doi: 10.1076/opge.20.3.205.2279. Ophthalmic Genet. 1999. PMID: 10610189 No abstract available.

5

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

6

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.

7

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

8

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.

Toomes C, Marchbank NJ, Mackey DA, Craig JE, Newbury-Ecob RA, Bennett CP, Vize CJ, Desai SP, Black GC, Patel N, Teimory M, Markham AF, Inglehearn CF, Churchill AJ. Toomes C, et al. Among authors: mackey da. Hum Mol Genet. 2001 Jun 15;10(13):1369-78. doi: 10.1093/hmg/10.13.1369. Hum Mol Genet. 2001. PMID: 11440989

9

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

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. 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.

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