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Flinders Academic Commons >
Browsing by Author Dimasi, David Paul
Showing results 1 to 13 of 13
| Issue Date | Title | Author(s) | | 2008 | Ancestral LOXL1 variants are associated with
pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in
Nordic people | Baird, Paul N; Wang, Jie Jin; Mackey, David A; Mitchell, Paul; Sharma, Shiwani; Burdon, Kathryn Penelope; Hewitt, Alex W; Dimasi, David Paul; Craig, Jamie E |
| 2008 | Functional and structural implications of the
complement factor H Y402H polymorphism associated with age-related macular
degeneration | Ormsby, Rebecca Jane; Ranganathan, S; Tong, Joo Chuan; Griggs, Kim Marie; Dimasi, David Paul; Hewitt, Alex W; Burdon, Kathryn Penelope; Craig, Jamie E; Hoh, Josephine; Gordon, David Llewellyn |
| 2006 | A glaucoma case-control study of the WDR36 gene
D658G sequence variant | Hewitt, Alex W; Mackey, David A; Craig, Jamie E; Dimasi, David Paul |
| 2007 | Heme carrier protein 1 (HCP1) expression and
functional analysis in the retina and retinal pigment epithelium | Broer, Stefan; Sharma, Shiwani; Dimasi, David Paul; Kumar, Raman; Della, N G |
| 2005 | Lack of association of p53 polymorphisms and
haplotypes in high and normal tension open angle glaucoma | Dimasi, David Paul; Hewitt, Alex W; Green, Catherine M; Mackey, David A; Craig, Jamie E |
| 2006 | A myocilin Gln368STOP homozygote does not exhibit
a more severe glaucoma phenotype than heterozygous cases | Hewitt, Alex W; Bennett, Sonya L; Dimasi, David Paul; Craig, Jamie E; Mackey, David A |
| 2007 | Myocilin Gly252Arg mutation and glaucoma of
intermediate severity in caucasian individuals | Hewitt, Alex W; Bennett, Sonya L; Richards, J E; Dimasi, David Paul; Booth, Adam P; Inglehearn, Chris; Anwar, Rashida; Yamamoto, Tetsuya; Fingert, John H; Heon, Elise; Craig, Jamie E; Mackey, David A |
| 2007 | A novel deletion in the FTL gene causes hereditary
hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start
site | Burdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia S |
| 26-Sep-2012 | The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucoma | Wiggs, Janey L; Hewitt, Alex W; Fan, Bao Jian; Wang, Dan Yi; O'Brien, Colm; Realini, Anthony; Craig, Jamie E; Dimasi, David Paul; Mackey, David A; Haines, Jonathan L; Pasquale, Louis R; Figueiredo Sena, Dayse R |
| 2006 | The PITX3 gene in posterior polar congenital
cataract in Australia | Burdon, Kathryn Penelope; McKay, James D; Wirth, M Gabriela; Ruddle, Jonathan; Russell-Eggit, Isabelle M; Bhatti, Samira; Dimasi, David Paul; Mackey, David A; Craig, Jamie E |
| 2007 | Prevalence of CYP1B1 mutations in Australian
patients with primary congenital glaucoma | Elder, James E; Casey, T; Mackey, David A; Craig, Jamie E; MacKinnon, Jane R; Hewitt, Alex W; Dimasi, David Paul; Pater, John Brian; Straga, Tania |
| 2006 | The role of the Met98Lys optineurin variant in
inherited optic nerve diseases | Craig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A |
| 2004 | RZF, a zinc-finger protein in the photoreceptors
of human retina | Higginson, K A; Sharma, Shiwani; Della, N G; Dimasi, David Paul |
Showing results 1 to 13 of 13
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