Craig JE - Search Results

1

Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma.

Alward WL, Kwon YH, Kawase K, Craig JE, Hayreh SS, Johnson AT, Khanna CL, Yamamoto T, Mackey DA, Roos BR, Affatigato LM, Sheffield VC, Stone EM. Alward WL, et al. Among authors: craig je. Am J Ophthalmol. 2003 Nov;136(5):904-10. doi: 10.1016/s0002-9394(03)00577-4. Am J Ophthalmol. 2003. PMID: 14597044

2

Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene.

Sale MM, Craig JE, Charlesworth JC, FitzGerald LM, Hanson IM, Dickinson JL, Matthews SJ, Heyningen Vv Vv, Fingert JH, Mackey DA. Sale MM, et al. Among authors: craig je. Hum Mutat. 2002 Oct;20(4):322. doi: 10.1002/humu.9066. Hum Mutat. 2002. PMID: 12325030

3

The apolipoprotein epsilon4 gene is associated with elevated risk of normal tension glaucoma.

Vickers JC, Craig JE, Stankovich J, McCormack GH, West AK, Dickinson JL, McCartney PJ, Coote MA, Healey DL, Mackey DA. Vickers JC, et al. Among authors: craig je. Mol Vis. 2002 Oct 14;8:389-93. Mol Vis. 2002. PMID: 12379839 Free article.

4

Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilin.

Baird PN, Craig JE, Richardson AJ, Ring MA, Sim P, Stanwix S, Foote SJ, Mackey DA. Baird PN, et al. Among authors: craig je. Hum Genet. 2003 Feb;112(2):110-6. doi: 10.1007/s00439-002-0865-5. Epub 2002 Nov 21. Hum Genet. 2003. PMID: 12522550

5

Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriers.

Wilkinson CH, van der Straaten D, Craig JE, Coote MA, McCartney PJ, Stankovich J, Stone EM, Mackey DA. Wilkinson CH, et al. Among authors: craig je. J Glaucoma. 2003 Jun;12(3):237-42. doi: 10.1097/00061198-200306000-00010. J Glaucoma. 2003. PMID: 12782842

6

Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation.

Mackey DA, Healey DL, Fingert JH, Coote MA, Wong TL, Wilkinson CH, McCartney PJ, Rait JL, de Graaf AP, Stone EM, Craig JE. Mackey DA, et al. Among authors: craig je. Arch Ophthalmol. 2003 Aug;121(8):1172-80. doi: 10.1001/archopht.121.8.1172. Arch Ophthalmol. 2003. PMID: 12912696

7

Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations.

Craig JE, Clark JB, McLeod JL, Kirkland MA, Grant G, Elder JE, Toohey MG, Kowal L, Savoia HF, Chen C, Roberts S, Wirth MG, Mackey DA. Craig JE, et al. Arch Ophthalmol. 2003 Dec;121(12):1753-61. doi: 10.1001/archopht.121.12.1753. Arch Ophthalmol. 2003. PMID: 14662596

8

Predictive DNA testing for glaucoma: reality in 2003.

Mackey DA, Craig JE. Mackey DA, et al. Among authors: craig je. Ophthalmol Clin North Am. 2003 Dec;16(4):639-45. doi: 10.1016/s0896-1549(03)00066-x. Ophthalmol Clin North Am. 2003. PMID: 14741004 Review.

9

Primary infantile glaucoma in an Australian population.

MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA. MacKinnon JR, et al. Among authors: craig je. Clin Exp Ophthalmol. 2004 Feb;32(1):14-8. doi: 10.1046/j.1442-9071.2004.00750.x. Clin Exp Ophthalmol. 2004. PMID: 14746584

10

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

Toomes C, Bottomley HM, Jackson RM, Towns KV, Scott S, Mackey DA, Craig JE, Jiang L, Yang Z, Trembath R, Woodruff G, Gregory-Evans CY, Gregory-Evans K, Parker MJ, Black GC, Downey LM, Zhang K, Inglehearn CF. Toomes C, et al. Among authors: craig je. Am J Hum Genet. 2004 Apr;74(4):721-30. doi: 10.1086/383202. Epub 2004 Mar 11. Am J Hum Genet. 2004. PMID: 15024691 Free PMC article.

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