Craig JE - Search Results

1

Rapid inexpensive genome-wide association using pooled whole blood.

Craig JE, Hewitt AW, McMellon AE, Henders AK, Ma L, Wallace L, Sharma S, Burdon KP, Visscher PM, Montgomery GW, MacGregor S. Craig JE, et al. Genome Res. 2009 Nov;19(11):2075-80. doi: 10.1101/gr.094680.109. Epub 2009 Oct 3. Genome Res. 2009. PMID: 19801603 Free PMC article.

2

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.

3

Central corneal thickness is highly heritable: the twin eye studies.

Toh T, Liew SH, MacKinnon JR, Hewitt AW, Poulsen JL, Spector TD, Gilbert CE, Craig JE, Hammond CJ, Mackey DA. Toh T, et al. Among authors: craig je. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3718-22. doi: 10.1167/iovs.04-1497. Invest Ophthalmol Vis Sci. 2005. PMID: 16186354 Free article.

4

A myocilin Gln368STOP homozygote does not exhibit a more severe glaucoma phenotype than heterozygous cases.

Hewitt AW, Bennett SL, Dimasi DP, Craig JE, Mackey DA. Hewitt AW, et al. Among authors: craig je. Am J Ophthalmol. 2006 Feb;141(2):402-3. doi: 10.1016/j.ajo.2005.08.073. Am J Ophthalmol. 2006. PMID: 16458712

5

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.

6

Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions.

Sharma S, Ang SL, Shaw M, Mackey DA, Gécz J, McAvoy JW, Craig JE. Sharma S, et al. Among authors: craig je. Hum Mol Genet. 2006 Jun 15;15(12):1972-83. doi: 10.1093/hmg/ddl120. Epub 2006 May 4. Hum Mol Genet. 2006. PMID: 16675532

7

Disease severity of familial glaucoma compared with sporadic glaucoma.

Wu J, Hewitt AW, Green CM, Ring MA, McCartney PJ, Craig JE, Mackey DA. Wu J, et al. Among authors: craig je. Arch Ophthalmol. 2006 Jul;124(7):950-4. doi: 10.1001/archopht.124.7.950. Arch Ophthalmol. 2006. PMID: 16832017

8

Complex genetics of complex traits: the case of primary open-angle glaucoma.

Hewitt AW, Craig JE, Mackey DA. Hewitt AW, et al. Among authors: craig je. Clin Exp Ophthalmol. 2006 Jul;34(5):472-84. doi: 10.1111/j.1442-9071.2006.01268.x. Clin Exp Ophthalmol. 2006. PMID: 16872346 Review.

9

A Glaucoma Case-control Study of the WDR36 Gene D658G sequence variant.

Hewitt AW, Dimasi DP, Mackey DA, Craig JE. Hewitt AW, et al. Among authors: craig je. Am J Ophthalmol. 2006 Aug;142(2):324-5. doi: 10.1016/j.ajo.2006.02.041. Am J Ophthalmol. 2006. PMID: 16876519

10

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

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