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Flinders Academic Commons >
Browsing by Author Hewitt, Alex W
Showing results 3 to 22 of 22
| Preview | Issue Date | Title | Author(s) | | 2006 | Complex genetics of complex traits: the case of
primary open-angle glaucoma | Hewitt, Alex W; Craig, Jamie E; Mackey, David A |
| 2012 | A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucoma | Awadalla, Mona S; Burdon, Kathryn Penelope; Thapa, Suman S; Hewitt, Alex W; Craig, Jamie E |
| 2006 | Disease severity of familial glaucoma compared
with sporadic glaucoma | Wu, Johnny; Green, Catherine M; Hewitt, Alex W; McCartney, Paul J; Craig, Jamie E; Mackey, David A |
| 2006 | Familial transmission risk of infantile glaucoma
in Australia | Hewitt, Alex W; MacKinnon, Jane R; Giubilato, Antonio; Elder, James E; Craig, Jamie E; Mackey, David A |
| 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 |
| 2008 | Genetic analysis of the clusterin gene in
pseudoexfoliation syndrome. | Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Hewitt, Alex W; Wang, Jie Jin; Mackey, David A; Mitchell, Paul; McMellon, Amy E |
| 2008 | Genetic dissection of myopia: evidence for linkage
of ocular axial length to chromosome 5q | Brown, Shayne A; MacKinnon, Jane R; Chen, Christine Y; Craig, Jamie E; Martin, Nicholas G; Mackey, David A; Zhu, G; Hewitt, Alex W; Ruddle, Jonathan; Kearns, Lisa S; Hammond, Christopher J; Montgomery, G W |
| 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 | Heritable features of the optic disc: a novel twin
method for determining genetic significance | Alward, Wallace L M; Hewitt, Alex W; Poulsen, Johan P; Bennett, Sonya L; Budde, Wido M; Cooper, Richard L; Craig, Jamie E; Fingert, John H; Foster, Paul J; Garway-Heath, David F; Green, Catherine M; Hammond, Christopher J; Hayreh, Sohan S; Jonas, Jost B; Kaufman, Paul L; Miller, Neil R; Morgan, William H; Newman, Nancy J; Quigley, Harry A; Samples, John R; Spaeth, George L; Pesudovs, Konrad; Mackey, David A |
| 2006 | Influence of photodynamic therapy for age related
macular degeneration upon subjective vision related quality of life | Hewitt, Alex W; Jeganathan, Swetha; Kidd, Juanita E; Pesudovs, Konrad; Verma, Nitin |
| 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 |
| 2008 | Myocilin allele-specific glaucoma phenotype
database | Craig, Jamie E; Hewitt, Alex W; Mackey, David A |
| 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 | The optic nerve head in myocilin
glaucoma | Hewitt, Alex W; Bennett, Sonya L; Fingert, John H; Cooper, Richard L; Stone, Edwin M; Craig, Jamie E; Mackey, David A |
| 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 |
| 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 |
| Jul-2005 | The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes. | McKay, James D; Patterson, B; Craig, Jamie E; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Hewitt, Alex W; Cohn, Amy C; Kerdraon, Y; Mackey, David A |
| 2005 | The telomere of human chromosome 1p contains at
least two independent autosomal dominant congenital cataract genes | McKay, James D; Patterson, B; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Cohn, Amy C; Kerdraon, Y; Mackey, David A; Craig, Jamie E; Hewitt, Alex W |
Showing results 3 to 22 of 22
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