Craig JE - Search Results

1

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: craig je. Br J Ophthalmol. 2005 Jul;89(7):831-4. doi: 10.1136/bjo.2004.058495. Br J Ophthalmol. 2005. PMID: 15965161 Free PMC article.

2

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

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

3

Normal range of hearing associated with myocilin Thr377Met.

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

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: craig je. Arch Ophthalmol. 2000 Jul;118(7):900-4. Arch Ophthalmol. 2000. PMID: 10900101

5

Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension.

Fingert JH, Clark AF, Craig JE, Alward WL, Snibson GR, McLaughlin M, Tuttle L, Mackey DA, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: craig je. Invest Ophthalmol Vis Sci. 2001 Jan;42(1):145-52. Invest Ophthalmol Vis Sci. 2001. PMID: 11133859

6

Laboratory methods in ophthalmic genetics: obtaining DNA from patients.

Dickinson JL, Sale MM, Craig JE, Mackey DA. Dickinson JL, et al. Among authors: craig je. 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: craig je. 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: craig je. 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. 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: craig je. 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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