Hewitt AW - Search Results

1

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

Hysi PG, Young TL, Mackey DA, Andrew T, Fernández-Medarde A, Solouki AM, Hewitt AW, Macgregor S, Vingerling JR, Li YJ, Ikram MK, Fai LY, Sham PC, Manyes L, Porteros A, Lopes MC, Carbonaro F, Fahy SJ, Martin NG, van Duijn CM, Spector TD, Rahi JS, Santos E, Klaver CC, Hammond CJ. Hysi PG, et al. Among authors: hewitt aw. Nat Genet. 2010 Oct;42(10):902-5. doi: 10.1038/ng.664. Epub 2010 Sep 12. Nat Genet. 2010. PMID: 20835236 Free PMC article.

2

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: hewitt aw. J Med Genet. 2005 Sep;42(9):e55. doi: 10.1136/jmg.2005.032458. J Med Genet. 2005. PMID: 16140998 Free PMC article.

3

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

Hewitt AW, Craig JE, Mackey DA. Hewitt AW, et al. 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.

4

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

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

5

Familial transmission risk of infantile glaucoma in Australia.

Hewitt AW, MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA. Hewitt AW, et al. Ophthalmic Genet. 2006 Sep;27(3):93-7. doi: 10.1080/13816810600870843. Ophthalmic Genet. 2006. PMID: 17050285

6

Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees.

Bennett SL, Hewitt AW, Poulsen JL, Kearns LS, Morgan JE, Craig JE, Mackey DA. Bennett SL, et al. Among authors: hewitt aw. Arch Ophthalmol. 2007 Jan;125(1):112-6. doi: 10.1001/archopht.125.1.112. Arch Ophthalmol. 2007. PMID: 17210861

7

PAX6 mutations may be associated with high myopia.

Hewitt AW, Kearns LS, Jamieson RV, Williamson KA, van Heyningen V, Mackey DA. Hewitt AW, et al. Ophthalmic Genet. 2007 Sep;28(3):179-82. doi: 10.1080/13816810701356676. Ophthalmic Genet. 2007. PMID: 17896318

8

Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q.

Zhu G, Hewitt AW, Ruddle JB, Kearns LS, Brown SA, Mackinnon JR, Chen CY, Hammond CJ, Craig JE, Montgomery GW, Martin NG, Mackey DA. Zhu G, et al. Among authors: hewitt aw. Ophthalmology. 2008 Jun;115(6):1053-1057.e2. doi: 10.1016/j.ophtha.2007.08.013. Epub 2007 Oct 26. Ophthalmology. 2008. PMID: 17964656

9

Myocilin allele-specific glaucoma phenotype database.

Hewitt AW, Mackey DA, Craig JE. Hewitt AW, et al. Hum Mutat. 2008 Feb;29(2):207-11. doi: 10.1002/humu.20634. Hum Mutat. 2008. PMID: 17966125

10

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.

Hewitt AW, Sharma S, Burdon KP, Wang JJ, Baird PN, Dimasi DP, Mackey DA, Mitchell P, Craig JE. Hewitt AW, et al. Hum Mol Genet. 2008 Mar 1;17(5):710-6. doi: 10.1093/hmg/ddm342. Epub 2007 Nov 23. Hum Mol Genet. 2008. PMID: 18037624

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