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Browsing by Author Burdon, Kathryn Penelope

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PreviewIssue DateTitleAuthor(s)
2010Aldose reductase gene polymorphisms and diabetic retinopathy susceptibilityThorpe, Stacey; Abhary, Sotoodeh; Burdon, Kathryn Penelope; Laurie, Kate; Landers, John A; Goold, L; Lake, Stewart; Petrovsky, Nikolai; Craig, Jamie
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
2008Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel lociGiunta, Cecilia; Hewitt, Alex W; Craig, Jamie E; Latimer, Paul; Burdon, Kathryn Penelope; Coster, Douglas John; Charlesworth, Jac C; Mills, Richard Arthur; Laurie, Kate
2006Association analysis of genes in the renin-angiotensin system with subclinical cardiovascular disease in families with type 2 diabetes mellitus: The Diabetes Heart StudyBurdon, Kathryn Penelope; Langefeld, Carl D; Wagenknecht, Lynne M; Carr, John Jeffery; Freedman, Barry I; Herrington, David M; Bowden, Donald W
2010Association between erythropoietin gene polymorphisms and diabetic retinopathyAbhary, Sotoodeh; Burdon, Kathryn Penelope; Casson, R J; Goggin, M; Petrovsky, Nikolai; Craig, Jamie
2007Association of alpha2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosisLehtinen, Allison B; Burdon, Kathryn Penelope; Lewis, Joshua P; Langefeld, Carl D; Ziegler, Julie T; Rich, Stephen S; Register, Thomas C; Carr, John Jeffery; Freedman, Barry I; Bowden, Donald W
2008Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetesHerrington, David M; Bowden, Donald W; Wagenknecht, Lynne M; Hedrick, Catherine C; Rich, Stephen S; Langefeld, Carl D; Goff, David C; Freedman, Barry I; Burdon, Kathryn Penelope; Howard, Timothy; Liu, Yongmei
Mar-2013Association of eNOS polymorphisms with primary angle-closure glaucomaAwadalla, Mona S; Thapa, Suman S; Hewitt, Alex W; Craig, Jamie E; Burdon, Kathryn Penelope
2005Association of genes of lipid metabolism with measures of subclinical cardiovascular disease in the diabetes heart studyBurdon, Kathryn Penelope; Langefeld, Carl D; Beck, Stephanie R; Wagenknecht, Lynne M; Carr, John Jeffery; Freedman, Barry I; Herrington, David M; Bowden, Donald W
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
2006Association of protein tyrosine phosphatase-N1 polymorphisms with coronary calcified plaque in the diabetes heart studyBurdon, Kathryn Penelope; Bento, Jennifer L; Langefeld, Carl D; Campbell, Joel K; Carr, John Jeffery; Wagenknecht, Lynne M; Herrington, David M; Freedman, Barry I; Rich, Stephen S; Bowden, Donald W
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
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
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