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Flinders Academic Commons >
Browsing by Author Burdon, Kathryn Penelope
Showing results 8 to 27 of 32
| Issue Date | Title | Author(s) | | 2012 | A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucoma | Awadalla, Mona S; Burdon, Kathryn Penelope; Thapa, Suman S; Hewitt, Alex W; Craig, Jamie E |
| 2008 | Functional and structural implications of the
complement factor H Y402H polymorphism associated with age-related macular
degeneration | Ormsby, 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 |
| 2006 | A functional polymorphism in the lymphotoxin-alpha
gene is associated with carotid artery wall thickness: the Diabetes heart
Study | Liu, Yongmei; Herrington, David M; Burdon, Kathryn Penelope; Langefeld, Carl D; Rich, Stephen S; Bowden, Donald W; Freedman, Barry I; Wagenknecht, Lynne E |
| 2008 | Genetic 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 |
| 2008 | Genetic analysis of the soluble epoxide hydrolase
gene, EPHX2, in subclinical cardiovascular disease in the diabetes heart study | Herrington, David M; Burdon, Kathryn Penelope; Lehtinen, Allison B; Langefeld, Carl D; Carr, John Jeffery; Freedman, Barry I; Rich, Stephen S; Bowden, Donald W |
| 2006 | Heritability and expression of c-reactive protein
in type 2 diabetes in the diabetes heart study | Lange, 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 |
| 2005 | Identification of podocin (NPHS2) gene mutations
in African Americans with nondiabetic end-stage renal disease | Engeler Dusel, J A; Burdon, Kathryn Penelope; Hicks, P J; Bowden, Donald W; Freedman, Barry I |
| 2003 | Investigation of albinism genes in congenital
esotropia | Burdon, Kathryn Penelope; Wilkinson, Robin M; Barbour, Julie M; Dickinson, Joanne L; Stankovich, Jim M; Mackey, David A; Sale, Michele M |
| Jan-2004 | Investigation of crystallin genes in familial cataract, and report of two disease associated mutations. | Burdon, Kathryn Penelope; Wirth, M Gabriela; Mackey, David A; Russell-Eggit, Isabelle M; Craig, Jamie E; Elder, James E; Dickinson, Joanne L; Sale, Michele M |
| 2004 | Investigation of crystallin genes in familial
cataract, and report of two disease associated mutations | Mackay, D A; Craig, Jamie E; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Dickinson, Joanne L; Elder, James E; Burdon, Kathryn Penelope |
| 2008 | Investigation of eight candidate genes on
chromosome 1p36 for autosomal dominant total congenital cataract | Mackey, David A; Craig, Jamie E; Burdon, Kathryn Penelope; Lachke, Salil A; Hattersely, Kathryn; Laurie, Kate; Maas, Richard L |
| 2003 | Mutations in a novel gene, NHS, cause the
pleiotropic effects of Nance-Horan Syndrome including severe congenital cataract, dental
anomalies and mental retardation | Thomas, P; Thomas, T; Voss, A K; Sharma, Shiwani; Russell-Eggit, Isabelle M; Craig, Jamie E; Sale, Michele M; Mackey, David A; Wirth, M Gabriela; Gajovic, S; Clarke, M P; Gecz, Jozef; Elder, James E; Gruss, P; Fitzgerald, Liesel M; McKay, James D; Shaw, Marie A; Nicholl, A; Ross, S; Stankich, J M; Burdon, Kathryn Penelope |
| 2006 | Mutations in the NDP gene: contribution to Norrie
disease, familial exudative vitreoretinopathy and retinopathy of prematurity | Dickinson, Joanne L; Sale, Michele M; Passmore, Abraham; Fitzgerald, Liesel M; Wheatley, Catherine M; Burdon, Kathryn Penelope; Craig, Jamie E; Tengtrisorn, Supaporn; Carden, Susan M; Maclean, Hector; Mackey, David A |
| 2008 | Novel causative mutations in patients with
Nance-Horan Syndrome and altered localization of the mutant NHS-A protein
isoform | Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Dave, Alpana; Jamieson, Robyn; Yaron, Yuval; Billson, Frank; Maldergem, Lionel; Lorenz, Birgit; Gecz, Jozef |
| 2007 | A novel deletion in the FTL gene causes hereditary
hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start
site | Burdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia S |
| 2008 | A novel locus for X-lined congenital cataract on
Xq24 | Craig, Jamie E; Friend, K; Gecz, Jozef; Rattray, K M; Troski, Mark; Mackey, David A; Burdon, Kathryn Penelope |
| 2004 | A novel mutation in the Connexin 46 Gene causes
autosomal dominant congenital cataract with incomplete penetrance | Craig, Jamie E; Sale, Michele M; Mackey, David A; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Dickinson, Joanne L; Elder, James E; Burdon, Kathryn Penelope |
| 2006 | The PITX3 gene in posterior polar congenital
cataract in Australia | Burdon, Kathryn Penelope; McKay, James D; Wirth, M Gabriela; Ruddle, Jonathan; Russell-Eggit, Isabelle M; Bhatti, Samira; Dimasi, David Paul; Mackey, David A; Craig, Jamie E |
| 2007 | Prenatal detection of congenital bilateral
cataract leading to the diagnosis of Nance-Horan syndrome in the extended
family | Reches, Adi; Malcov, Mira; Tepper, Ron; Crystal-Shalit, Ornit; Kidron, Dvora; Yaron, Yuval; Burdon, Kathryn Penelope |
| 2005 | P-selectin gene haplotype associations with
albuminuria in the Diabetes Heart Study | Liu, Yongmei; Burdon, Kathryn Penelope; Langefeld, Carl D; Beck, Stephanie R; Wagenknecht, Lynne M; Rich, Stephen S; Bowden, Donald W; Freedman, Barry I |
Showing results 8 to 27 of 32
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