Hewitt AW - Search Results

1

High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia.

Javadiyan S, Craig JE, Souzeau E, Sharma S, Lower KM, Mackey DA, Staffieri SE, Elder JE, Taranath D, Straga T, Black J, Pater J, Casey T, Hewitt AW, Burdon KP. Javadiyan S, et al. Among authors: hewitt aw. G3 (Bethesda). 2017 Oct 5;7(10):3257-3268. doi: 10.1534/g3.117.300109. G3 (Bethesda). 2017. PMID: 28839118 Free PMC article.

2

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.

Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA. Hewitt AW, et al. Clin Exp Ophthalmol. 2005 Jun;33(3):233-9. doi: 10.1111/j.1442-9071.2005.01018.x. Clin Exp Ophthalmol. 2005. PMID: 15932525

3

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: hewitt aw. Br J Ophthalmol. 2005 Jul;89(7):831-4. doi: 10.1136/bjo.2004.058495. Br J Ophthalmol. 2005. PMID: 15965161 Free PMC article.

4

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.

5

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: hewitt aw. 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.

6

The relative contribution of the X chromosome to ocular phenotypes.

Hewitt AW, Burdon KP. Hewitt AW, et al. Ophthalmic Genet. 2005 Dec;26(4):191-3. doi: 10.1080/13816810500374375. Ophthalmic Genet. 2005. PMID: 16352481

7

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. Am J Ophthalmol. 2006 Feb;141(2):402-3. doi: 10.1016/j.ajo.2005.08.073. Am J Ophthalmol. 2006. PMID: 16458712

8

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: hewitt aw. Arch Ophthalmol. 2006 Jul;124(7):950-4. doi: 10.1001/archopht.124.7.950. Arch Ophthalmol. 2006. PMID: 16832017

9

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.

10

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

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