Hewitt AW - Search Results

1

Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene.

Burdon KP, Fogarty RD, Shen W, Abhary S, Kaidonis G, Appukuttan B, Hewitt AW, Sharma S, Daniell M, Essex RW, Chang JH, Klebe S, Lake SR, Pal B, Jenkins A, Govindarjan G, Sundaresan P, Lamoureux EL, Ramasamy K, Pefkianaki M, Hykin PG, Petrovsky N, Brown MA, Gillies MC, Craig JE. Burdon KP, et al. Among authors: hewitt aw. Diabetologia. 2015 Oct;58(10):2288-97. doi: 10.1007/s00125-015-3697-2. Epub 2015 Jul 19. Diabetologia. 2015. PMID: 26188370

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

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

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

5

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

6

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.

7

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

8

The role of the Met98Lys optineurin variant in inherited optic nerve diseases.

Craig JE, Hewitt AW, Dimasi DP, Howell N, Toomes C, Cohn AC, Mackey DA. Craig JE, et al. Among authors: hewitt aw. Br J Ophthalmol. 2006 Nov;90(11):1420-4. doi: 10.1136/bjo.2006.099333. Epub 2006 Aug 2. Br J Ophthalmol. 2006. PMID: 16885188 Free PMC article.

9

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

10

The optic nerve head in myocilin glaucoma.

Hewitt AW, Bennett SL, Fingert JH, Cooper RL, Stone EM, Craig JE, Mackey DA. Hewitt AW, et al. Invest Ophthalmol Vis Sci. 2007 Jan;48(1):238-43. doi: 10.1167/iovs.06-0611. Invest Ophthalmol Vis Sci. 2007. PMID: 17197538

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