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Browsing by Author Craig, Jamie E

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PreviewIssue DateTitleAuthor(s)
2006Complex genetics of complex traits: the case of primary open-angle glaucomaHewitt, Alex W; Craig, Jamie E; Mackey, David A
28-Dec-2012Compound heterozygote myocilin mutations in a pedigree with high prevalence of primary open-angle glaucomaYoung, Thomas K; Souzeau, Emmanuelle; Liu, Lance; Kearns, Lisa S; Burdon, Kathryn Penelope; Craig, Jamie E; Ruddle, Jonathan B
2012A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucomaAwadalla, Mona S; Burdon, Kathryn Penelope; Thapa, Suman S; Hewitt, Alex W; Craig, Jamie E
2008Development of a wireless intra-ocular pressure monitoring system for incorporation into a therapeutic glaucoma drainage implantVoelcker, Nicolas Hans; Kakaday, Tarun; Plunkett, Malcolm; McInnes, Steven James; Craig, Jamie E; Li, Jimmy Siu
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
Apr-2012Epigenetic effects on eye diseasesHewitt, Alex W; Wang, Jie Jin; Liang, Helena; Craig, Jamie E
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
2008Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degenerationOrmsby, 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
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
30-Sep-2013Genetic study of Diabetic Retinopathy: recruitment methodology and analysis of baseline characteristicsKaidonis, Georgia; Abhary, Sotoodeh; Daniell, Mark; Gillies, Mark; Fogarty, Rhys Daniel; Petrovsky, Nikolai; Jenkins, Alicia; Essex, Rohan; Chang, John H; Pal, Bishwanath; Hewitt, Alex W; Burdon, Kathryn Penelope; Craig, Jamie E
10-Feb-2013Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaVerhoeven, VJM; Hysi, PG; Wojciechowski, R; Fan, Q; Guggenheim, JA; Höhn, R; Macgregor, S; Hewitt, AW; Nag, A; Cheng, CY; Yonova-Doing, E; Zhou, X; Ikram, MK; Buitendijk, GHS; McMahon, G; Kemp, JP; Pourcain, BS; Simpson, CL; Mäkelä, KM; Lehtimäki, T; Kähönen, M; Paterson, AD; Hosseini, SM; Wong, HS; Xu, L; Jonas, JB; Pärssinen, O; Wedenoja, J; Yip, SP; Ho, DWH; Pang, CP; Chen, LJ; Klein, BEK; Klein, R; Haller, T; Metspalu, A; Khor, CC; Tai, ES; Aung, T; Vithana, E; Tay, WT; Barathi, VA; Chen, P; Li, R; Liao, J; Zheng, Y; Ong, RT; Döring, A; Evans, DM; Timpson, NJ; Verkerk, AJMH; Meitinger, T; Raitakari, O; Hawthorne, F; Spector, TD; Karssen, LC; Pirastu, M; Murgia, F; Ang, W; Mishra, A; Montgomery, GW; Pennell, CE; Cumberland, PM; Cotlarciuc, I; Mitchell, P; Wang, JJ; Schache, M; Janmahasathian, S; Igo Jr, RP; Lass, JH; Chew, E; Iyengar, SK; Gorgels, TGMF; Rudan, I; Hayward, C; Wright, AF; Craig, Jamie E; Burdon, Kathryn Penelope
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
Showing results 7 to 26 of 60
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