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Browsing by Author Burdon, Kathryn Penelope

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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
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
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
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
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
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 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
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
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