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Browsing by Author Burdon, Kathryn Penelope

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PreviewIssue DateTitleAuthor(s)
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
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
2010Human Lipoxygenase Pathway Gene Variation and Association with Markers of Subclinical Atherosclerosis in the Diabetes Heart StudyHedrick, Catherine C; Rich, Stephen S; Rudock, Megan E; Lehtinen, Allison B; Langefeld, Carl D; Bowden, Donald W; Register, Thomas C; Liu, Yongmei; Freedman, Barry I; Carr, J Jeffery; Burdon, Kathryn Penelope
2014Identification of a novel MYOC mutation, p.Trp373X, in a family with open angle glaucomaCrawford, April; Souzeau, Emmanuelle; Agar, A; Ridge, B; Dubowsky, A; Burdon, Kathryn Penelope; Craig, Jamie E
Mar-2013Identification of a novel oligomerization disrupting mutation in CRYAA associated with congenital cataract in a South Australian familyLaurie, Kate; Dave, Alpana; Straga, Tania; Souzeau, Emmanuelle; Chataway, Timothy Kennion; Sykes, Matthew James; Casey, Theresa; Teo, Theodosia; Pater, John Brian; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope
2009Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry.Chataway, Timothy Kennion; Sharma, Shiwani; Burdon, Kathryn Penelope; Jonavicius, Lisa; Klebe, Sonja; Hewitt, Alex W; Mills, Richard Arthur; Craig, Jamie
2005Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal diseaseEngeler Dusel, J A; Burdon, Kathryn Penelope; Hicks, P J; Bowden, Donald W; Freedman, Barry I
Showing results 19 to 38 of 67
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