Craig JE - Search Results

1

The genetics of central corneal thickness.

Dimasi DP, Burdon KP, Craig JE. Dimasi DP, et al. Among authors: craig je. Br J Ophthalmol. 2010 Aug;94(8):971-6. doi: 10.1136/bjo.2009.162735. Epub 2009 Jun 24. Br J Ophthalmol. 2010. PMID: 19556215 Review.

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

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

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: craig je. 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

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: craig je. J Med Genet. 2004 Aug;41(8):e106. doi: 10.1136/jmg.2004.018333. J Med Genet. 2004. PMID: 15286166 Free PMC article. No abstract available.

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: 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.

7

Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma.

Dimasi DP, Hewitt AW, Green CM, Mackey DA, Craig JE. Dimasi DP, et al. Among authors: craig je. J Med Genet. 2005 Sep;42(9):e55. doi: 10.1136/jmg.2005.032458. J Med Genet. 2005. PMID: 16140998 Free PMC article.

8

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: craig je. 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.

9

The role of the Met98Lys optineurin variant in inherited optic nerve diseases.

Craig JE, Hewitt AW, Dimasi DP, Howell N, Toomes C, Cohn AC, Mackey DA. Craig JE, et al. Br J Ophthalmol. 2006 Nov;90(11):1420-4. doi: 10.1136/bjo.2006.099333. Epub 2006 Aug 2. Br J Ophthalmol. 2006. PMID: 16885188 Free PMC article.

10

Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma.

Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, Craig JE. Dimasi DP, et al. Among authors: craig je. Clin Genet. 2007 Sep;72(3):255-60. doi: 10.1111/j.1399-0004.2007.00864.x. Clin Genet. 2007. PMID: 17718864

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