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Browsing by Author Burdon, Kathryn Penelope

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PreviewIssue DateTitleAuthor(s)
2009Rapid inexpensive genome-wide association using pooled whole bloodCraig, Jamie; Sharma, Shiwani; Hewitt, Alex W; McMellon, Amy E; Henders, Anjali K; Wallace, Leanne; Ma, Lingjun; Burdon, Kathryn Penelope; Visscher, Peter; Montgomery, Grant; Macgregor, Stuart
30-Jul-2013Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconusBae, HA; Mills, RA; Lindsay, RG; Phillips, T; Mitchell, P; Wang, JJ; Coster, Douglas John; Craig, Jamie E; Burdon, Kathryn Penelope
Mar-2014Screening of the COL8A2 gene in an Australian family with early-onset Fuchs’ endothelial corneal dystrophyKuot, Abraham; Mills, Richard Arthur; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope
2010Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetesKuot, Abraham; Javadiyan, Shahrbanou; Abhary, Sotoodeh; Burdon, Kathryn Penelope; Whiting, Malcolm John; Kasmeridis, Nicholas; Petrovsky, Nikolai; Craig, Jamie
2009A systematic meta-analysis of genetic association studies for diabetic retinopathyAbhary, Sotoodeh; Hewitt, Alex W; Craig, Jamie; Burdon, Kathryn Penelope
2005T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart studyBurdon, Kathryn Penelope; Rich, Stephen S; Bowden, Donald W; Langefeld, Carl D; Beck, Stephanie R; Liu, Yongmei; Wagenknecht, Lynne E; Freedman, Barry I
2010Tag SNPs detect association of teh CYP1B1 gene with primary open angle glaucomaBurdon, Kathryn Penelope; Hewitt, Alex W; Mackey, David A; Craig, Jamie; Mitchell, Paul
Jul-2005The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.McKay, James D; Patterson, B; Craig, Jamie E; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Hewitt, Alex W; Cohn, Amy C; Kerdraon, Y; Mackey, David A
2005The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesMcKay, James D; Patterson, B; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Cohn, Amy C; Kerdraon, Y; Mackey, David A; Craig, Jamie E; Hewitt, Alex W
2004Variability of serum soluble intercellular adhesion molecule-1 measurements attributable to a common polymorphismRegister, Thomas C; Lenchik, Leon; Burdon, Kathryn Penelope; Bowden, Donald W; Hawkins, Gregory A; Nicklas, Barbara J; Lolman, Kurt; Hsu, Fang-Chi; Langefeld, Carl D; Carr, John Jeffery
2006Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS)Burdon, Kathryn Penelope; Langefeld, Carl D; Beck, Stephanie R; Wagenknecht, Lynne M; Carr, John Jeffery; Rich, Stephen S; Freedman, Barry I; Herrington, David M; Bowden, Donald W
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