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Flinders Academic Commons >
Browsing by Author Mackey, David A
Showing results 1 to 20 of 33
| 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 |
| 2004 | Attitudes to predictive DNA testing for myocilin
glaucoma: experience with a large Australian family | Wilkinson, C H; Craig, Jamie E; Mackey, David A; Healey, D L; Stone, Edwin M |
| 2006 | Complex genetics of complex traits: the case of
primary open-angle glaucoma | Hewitt, Alex W; Craig, Jamie E; Mackey, David A |
| 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 |
| 2003 | Evaluation of optinueurin sequence variations in
1,048 patients with open-angle glaucoma | Yamamoto, T; Craig, Jamie E; Affatigato, L M; Alward, Wallace L M; Mackey, David A; Kwon, Y H; Johnson, A T; Hayreh, Sohan S; Kawase, K; Khanna, C L; Sheffield, V; Roos, B R; Stone, Edwin M |
| 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 | 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 |
| 2003 | Glaucoma phenotype in pedigrees with the myocilin
Thr377Met mutation | Wong, T L; Wilkinson, C H; Craig, Jamie E; Mackey, David A; Coote, M A; De Graaf, A P; Fingert, John H; McCartney, Paul J; Healey, D L; Rait, J; Stone, Edwin M |
| 2003 | Hereditary hyperferritinemia-cataract syndrome:
prevalence, lens morphology, spectrum of mutations, and clinical presentations | Toohey, M G; Chen, Celia S; Craig, Jamie E; Mackey, David A; Wirth, M Gabriela; Clark, J B; Elder, James E; Grant, G; McLeod, J L; Kirkland, M A; Kowal, L; Roberts, S; Savoia, H F |
| 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 |
| 2003 | Investigation of albinism genes in congenital
esotropia | Burdon, Kathryn Penelope; Wilkinson, Robin M; Barbour, Julie M; Dickinson, Joanne L; Stankovich, Jim M; Mackey, David A; Sale, Michele M |
| Jan-2004 | Investigation of crystallin genes in familial cataract, and report of two disease associated mutations. | Burdon, Kathryn Penelope; Wirth, M Gabriela; Mackey, David A; Russell-Eggit, Isabelle M; Craig, Jamie E; Elder, James E; Dickinson, Joanne L; Sale, Michele M |
| 2008 | Investigation of eight candidate genes on
chromosome 1p36 for autosomal dominant total congenital cataract | Mackey, David A; Craig, Jamie E; Burdon, Kathryn Penelope; Lachke, Salil A; Hattersely, Kathryn; Laurie, Kate; Maas, Richard L |
| 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 |
| 2005 | Linkage to 10q22 for maximum intraocular pressure
and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma
pedigree | Charlesworth, Jac C; Dyer, Thomas D; Stankovich, Jim M; Blangero, John; Mackey, David A; Craig, Jamie E; Green, Catherine M; Baird, Paul N; Sale, Michele M; Foote, Simon J |
| 2003 | Mutations in a novel gene, NHS, cause the
pleiotropic effects of Nance-Horan Syndrome including severe congenital cataract, dental
anomalies and mental retardation | Thomas, P; Thomas, T; Voss, A K; Sharma, Shiwani; Russell-Eggit, Isabelle M; Craig, Jamie E; Sale, Michele M; Mackey, David A; Wirth, M Gabriela; Gajovic, S; Clarke, M P; Gecz, Jozef; Elder, James E; Gruss, P; Fitzgerald, Liesel M; McKay, James D; Shaw, Marie A; Nicholl, A; Ross, S; Stankich, J M; Burdon, Kathryn Penelope |
| 2006 | Mutations in the NDP gene: contribution to Norrie
disease, familial exudative vitreoretinopathy and retinopathy of prematurity | Dickinson, Joanne L; Sale, Michele M; Passmore, Abraham; Fitzgerald, Liesel M; Wheatley, Catherine M; Burdon, Kathryn Penelope; Craig, Jamie E; Tengtrisorn, Supaporn; Carden, Susan M; Maclean, Hector; Mackey, David A |
| 2008 | Myocilin allele-specific glaucoma phenotype
database | Craig, Jamie E; Hewitt, Alex W; Mackey, David A |
Showing results 1 to 20 of 33
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