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Browsing by Author Burdon, Kathryn Penelope

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PreviewIssue DateTitleAuthor(s)
2010Candidate gene study to investigate the genetic determinants of normal variation in central corneal thicknessDimasi, David Paul; Burdon, Kathryn Penelope; Hewitt, Alex W; Craig, Jamie; Savarirayan, Ravi; Healey, Paul R; Mitchell, Paul; Mackey, David A
2010Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness PublicationMartin, Nicholas G; Young, Terri L; Hammond, Christopher J; Li, Yi JU; Mitchell, P; Healey, Paul R; Montgomery, G W; Hansell, Narelle; Spector, Tim D; Macgregor, Stuart; Craig, Jamie; Mackey, David A; Lu, Y; Dimasi, David Paul; Hysi, Pirro G; Hewitt, Alex W; Burdon, Kathryn Penelope; Toh, Tze'Yo; Ruddle, Jonathan
2009Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathyLake, Stewart; Craig, Jamie; Abhary, Sotoodeh; Gupta, A; Selva, Dinesh; Petrovsky, Nikolai; Burdon, Kathryn Penelope
2010Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaJonasdottir, Adalbjorg; Gudjonsson, Sigurjon; Aldred, Michaela A; Mitchell, Paul; St Clair, David; Collier, David A; Sveinsson, Orn; Tang, Nelson; Macgregor, Stuart; Martin, Nicholas G; Cree, Angela J; Gibson, Jane; Macleod, Alex; Jacob, Aby; Ennis, Sarah; Young, Terri L; Chan, Juliana C N; Karwatowski, Wojciech S S; Hammond, Christopher J; Thordarson, Kristjan; Zhang, Mingzhi; Wadelius, Claes; Lotery, Andrew J; Trembath, Richard C; Pang, Chi Pui; Hoh, Josephine; Craig, Jamie; Kong, Augustine; Mackey, David A; Jonasson, Fridbert; Thorsteinsdottir, Unnur; Stefansson, Kari; Masson, Gisli; Helgason, A; DeWan, A; Sigurdsson, A; Magnusson, K P; Stefansson, H; Lam, D S; Tam, P O; Gudmundsdottir, G J; Thorleifsson, G; Walters, G B; Hewitt, Alex W; Southgate, L; Burdon, Kathryn Penelope; Gottfredsdottir, M S
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
2009Diabetic retinopathy is associated with elevated serum asymmetric and symmetric dimethylargininesCraig, Jamie; Yew, Wai Ping; Kasmeridis, Nicholas; Burdon, Kathryn Penelope; Petrovsky, Nikolai; Kuot, Abraham; Whiting, Malcolm John; Abhary, Sotoodeh
2009Diabetic retinopathy is not associated with carbonic anhydrase gene polymorphismsAbhary, Sotoodeh; Burdon, Kathryn Penelope; Gupta, A; Petrovsky, Nikolai; Craig, Jamie
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
2006A functional polymorphism in the lymphotoxin-alpha gene is associated with carotid artery wall thickness: the Diabetes heart StudyLiu, Yongmei; Herrington, David M; Burdon, Kathryn Penelope; Langefeld, Carl D; Rich, Stephen S; Bowden, Donald W; Freedman, Barry I; Wagenknecht, Lynne E
2008Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie; Hewitt, Alex W; JJ, Wang; DA, Mackey; P, Mitchell; McMellon, Amy E
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 analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the diabetes heart studyHerrington, David M; Burdon, Kathryn Penelope; Lehtinen, Allison B; Langefeld, Carl D; Carr, John Jeffery; Freedman, Barry I; Rich, Stephen S; Bowden, Donald 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
2010The genetics of central corneal thicknessDimasi, David Paul; Burdon, Kathryn Penelope; Craig, Jamie
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
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
2006Heritability and expression of c-reactive protein in type 2 diabetes in the diabetes heart studyLange, Leslie A; Burdon, Kathryn Penelope; Langefeld, Carl D; Liu, Yongmei; Beck, Stephanie R; Rich, Stephen S; Freedman, Barry I; Brosnihan, K Bridget; Herrington, David M; Wagenknecht, Lynne E; Bowden, Donald W
2009Heritability of central corneal thickness in nuclear familiesLanders, John A; Hewitt, Alex W; Dimasi, David Paul; Charlesworth, Jac C; Straga, Tania; Burdon, Kathryn Penelope; Craig, Jamie; Mills, Richard Arthur; Savarirayan, Ravi; Mackey, David A
Showing results 13 to 32 of 67
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