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Browsing by Author Mackey, David A

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PreviewIssue DateTitleAuthor(s)
2008Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleBaird, Paul N; Wang, Jie Jin; Mackey, David A; Mitchell, Paul; Sharma, Shiwani; Burdon, Kathryn Penelope; Hewitt, Alex W; Dimasi, David Paul; Craig, Jamie E
6-Jun-2012Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterisation of the protein in the eyeSharma, Shiwani; Burdon, Kathryn Penelope; Chidlow, Glyn; Klebe, Sonja; Crawford, April; Dimasi, David Paul; Dave, Alpana; Martin, Sarah; Javadiyan, Shahrbanou; Wood, John P M; Casson, Robert; Danoy, Patrick; Griggs, Kim Marie; Hewitt, Alex W; Landers, John; Mitchell, Paul; Mackey, David A; Craig, Jamie E
2004Attitudes to predictive DNA testing for myocilin glaucoma: experience with a large Australian familyWilkinson, C H; Craig, Jamie E; Mackey, David A; Healey, D L; Stone, Edwin M
13-Aug-2013Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentSouzeau, Emmanuelle; Goldberg, Ivan; Healey, Paul R; Mills, Richard Arthur; Landers, John; Graham, Stuart L; Grigg, John RB; Usher, Bronwyn; Straga, Tania; Crawford, April; Casson, Robert J; Morgan, William H; Ruddle, Jonathan B; Coote, Michael A; White, Andrew; Stewart, James; Hewitt, Alex W; Mackey, David A; Burdon, Kathryn Penelope; Craig, Jamie E
2006Complex genetics of complex traits: the case of primary open-angle glaucomaHewitt, Alex W; Craig, Jamie E; Mackey, David A
2006Disease severity of familial glaucoma compared with sporadic glaucomaWu, Johnny; Green, Catherine M; Hewitt, Alex W; McCartney, Paul J; Craig, Jamie E; Mackey, David A
2003Evaluation of optinueurin sequence variations in 1,048 patients with open-angle glaucomaYamamoto, 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
2006Familial transmission risk of infantile glaucoma in AustraliaHewitt, Alex W; MacKinnon, Jane R; Giubilato, Antonio; Elder, James E; Craig, Jamie E; Mackey, David A
2008Genetic 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
2008Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qBrown, Shayne A; MacKinnon, Jane R; Chen, Christine Y; Craig, Jamie E; Martin, Nicholas G; Mackey, David A; Zhu, G; Hewitt, Alex W; Ruddle, Jonathan B; Kearns, Lisa S; Hammond, Christopher J; Montgomery, G W
30-Jul-2012Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucomaDimasi, David Paul; Burdon, Kathryn Penelope; Hewitt, Alex W; Fitzgerald, J; Wang, Jie Jin; Healey, Paul R; Mitchell, Paul; Mackey, David A; Craig, Jamie E
2006A glaucoma case-control study of the WDR36 gene D658G sequence variantHewitt, Alex W; Mackey, David A; Craig, Jamie E; Dimasi, David Paul
2003Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutationWong, 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
1-Aug-2012Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal tension glaucoma, and advanced glaucomaBurdon, Kathryn Penelope; Crawford, April; Casson, Robert J; Hewitt, Alex W; Landers, John; Danoy, Patrick; Mackey, David A; Mitchell, Paul; Healey, Paul R; Craig, Jamie E
2003Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentationsToohey, 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
2007Heritable features of the optic disc: a novel twin method for determining genetic significanceAlward, 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
28-Feb-2013Higher prevalence of Myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registrySouzeau, Emmanuelle; Burdon, Kathryn Penelope; Dubowsky, A; Grist, S; Usher, Bronwyn; Fitzgerald, JT; Crawford, April; Hewitt, Alex W; Goldberg, Ivan; Mills, Richard Arthur; Ruddle, Jonathan B; Landers, John; Mackey, David A; Craig, Jamie E
2003Investigation of albinism genes in congenital esotropiaBurdon, Kathryn Penelope; Wilkinson, Robin M; Barbour, Julie M; Dickinson, Joanne L; Stankovich, Jim M; Mackey, David A; Sale, Michele M
Jan-2004Investigation 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
2008Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataractMackey, David A; Craig, Jamie E; Burdon, Kathryn Penelope; Lachke, Salil A; Hattersely, Kathryn; Laurie, Kate; Maas, Richard L
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