Craig JE - Search Results

1

Pooled genome wide association detects association upstream of FCRL3 with Graves' disease.

Khong JJ, Burdon KP, Lu Y, Laurie K, Leonardos L, Baird PN, Sahebjada S, Walsh JP, Gajdatsy A, Ebeling PR, Hamblin PS, Wong R, Forehan SP, Fourlanos S, Roberts AP, Doogue M, Selva D, Montgomery GW, Macgregor S, Craig JE. Khong JJ, et al. Among authors: craig je. BMC Genomics. 2016 Nov 18;17(1):939. doi: 10.1186/s12864-016-3276-z. BMC Genomics. 2016. PMID: 27863461 Free PMC article.

2

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

3

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

Burdon KP, McKay JD, Sale MM, Russell-Eggitt IM, Mackey DA, Wirth MG, Elder JE, Nicoll A, Clarke MP, FitzGerald LM, Stankovich JM, Shaw MA, Sharma S, Gajovic S, Gruss P, Ross S, Thomas P, Voss AK, Thomas T, Gécz J, Craig JE. Burdon KP, et al. Among authors: craig je. Am J Hum Genet. 2003 Nov;73(5):1120-30. doi: 10.1086/379381. Epub 2003 Oct 16. Am J Hum Genet. 2003. PMID: 14564667 Free PMC article.

4

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: craig je. Clin Exp Ophthalmol. 2004 Oct;32(5):518-22. doi: 10.1111/j.1442-9071.2004.00886.x. Clin Exp Ophthalmol. 2004. PMID: 15498064

5

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: craig je. Am J Ophthalmol. 2005 Jun;139(6):1125-6. doi: 10.1016/j.ajo.2004.11.061. Am J Ophthalmol. 2005. PMID: 15953455

6

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree.

Charlesworth JC, Dyer TD, Stankovich JM, Blangero J, Mackey DA, Craig JE, Green CM, Foote SJ, Baird PN, Sale MM. Charlesworth JC, et al. Among authors: craig je. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3723-9. doi: 10.1167/iovs.05-0312. Invest Ophthalmol Vis Sci. 2005. PMID: 16186355

7

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: craig je. Am J Ophthalmol. 2005 Oct;140(4):760-2. doi: 10.1016/j.ajo.2005.04.043. Am J Ophthalmol. 2005. PMID: 16226543

8

The PITX3 gene in posterior polar congenital cataract in Australia.

Burdon KP, McKay JD, Wirth MG, Russell-Eggit IM, Bhatti S, Ruddle JB, Dimasi D, Mackey DA, Craig JE. Burdon KP, et al. Among authors: craig je. Mol Vis. 2006 Apr 18;12:367-71. Mol Vis. 2006. PMID: 16636655 Free article.

9

Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.

Dickinson JL, Sale MM, Passmore A, FitzGerald LM, Wheatley CM, Burdon KP, Craig JE, Tengtrisorn S, Carden SM, Maclean H, Mackey DA. Dickinson JL, et al. Among authors: craig je. Clin Exp Ophthalmol. 2006 Sep-Oct;34(7):682-8. doi: 10.1111/j.1442-9071.2006.01314.x. Clin Exp Ophthalmol. 2006. PMID: 16970763

10

A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.

Burdon KP, Sharma S, Chen CS, Dimasi DP, Mackey DA, Craig JE. Burdon KP, et al. Among authors: craig je. Hum Mutat. 2007 Jul;28(7):742. doi: 10.1002/humu.9501. Hum Mutat. 2007. PMID: 17579362

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