Kathryn Burdon - Dissemin

Papers authored by Kathryn Burdon

This paper was not found in any repository, but could be made available legally by the author.

2009 Shiwani Sharma, Tim Chataway, Kathryn P. Burdon

, Lisa Jonavicius, Sonja Klebe, Alex W. Hewitt, Richard A. Mills, Jamie E. Craig

Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry

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This paper is made freely available by the publisher.

John A. Landers, Alex W. Hewitt, David P. Dimasi, Jac C. Charlesworth, Tania Straga, Richard A. D. Mills, Ravi Savarirayan, David A. Mackey, Kathryn P. Burdon

, Jamie E. Craig

Heritability of Central Corneal Thickness in Nuclear Families

Download from iovs.arvojournals.org

David P. Dimasi, Jern Y. Chen, Alex W. Hewitt, Sonja Klebe, Richard Davey, John Stirling, Elizabeth Thompson, Robin Forbes, Tiong Y. Tan, Ravi Savarirayan, David A. Mackey, Paul R. Healey, Paul Mitchell, Kathryn P. Burdon

, Jamie E. Craig

Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes

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Sotoodeh Abhary, Nicholas Kasmeridis, Kathryn P. Burdon

, Abraham Kuot, Malcolm J. Whiting, Wai Ping Yew, Nikolai Petrovsky, Jamie E. Craig

Diabetic Retinopathy Is Associated With Elevated Serum Asymmetric and Symmetric Dimethylarginines

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Sotoodeh Abhary, Alex W. Hewitt, Kathryn P. Burdon

, Jamie E. Craig

A Systematic Meta-Analysis of Genetic Association Studies for Diabetic Retinopathy

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This paper is available in a repository.

D. P. Dimasi, K. P. Burdon

, J. E. Craig

The genetics of central corneal thickness

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S. Abhary, Kp P. Burdon

, A. Gupta, N. Petrovsky, Je E. Craig

Diabetic retinopathy is not associated with carbonic anhydrase gene polymorphisms

Download from www.ncbi.nlm.nih.gov

Tianxiao Zhang, Rui Hua, Wei Xiao, Kathryn P. Burdon

, Shomi S. Bhattacharya, Jamie E. Craig, Dandan Shang, Xiuli Zhao, David A. Mackey, Anthony T. Moore, Yang Luo, Jinsong Zhang, Xue Zhang

Mutations of theEPHA2receptor tyrosine kinase gene cause autosomal dominant congenital cataract

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Kp Burdon

, Shane R. Durkin, Mary Burke, Mj Edwards, John Pater, Tania Straga, Jozef Gecz

, Je Liebelt, Je Craig

A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian family

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2008 S. Shama, L. van Maldergem, Shiwani Sharma, Yuval Yaron, Lionel Van Maldergem, Robyn V. Jamieson, Birgit Lorenz, Kathryn P. Burdon

, Alpana Dave, Frank Billson, Jozef Gécz

, Jamie E. Craig

Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform

Download from orbi.ulg.ac.be

Kathryn P. Burdon

, Kathryn Hattersley, Kate J. Laurie, Richard L. Maas, Salil A. Lachke

, David A. Mackey, Jamie E. Craig

Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract

Download from www.ncbi.nlm.nih.gov

Kathryn P. Burdon

, Jie Jin Wang, Alex W. Hewitt, Shiwani Sharma, Amy E. McMellon, David A. Mackey, Paul Mitchell, Jamie E. Craig

Genetic analysis of the clusterin gene in pseudoexfoliation syndrome

Download from www.ncbi.nlm.nih.gov

Jamie E. Craig, M. Trotski, Kate M. Rattray, Mark Troski, David A. Mackey, Kathryn L. Friend, Jozef Gecz

, Kathryn P. Burdon

A novel locus for X-linked congenital cataract on Xq24

Download from www.ncbi.nlm.nih.gov

Yongmei Liu, Barry I. Freedman, Kathryn P. Burdon

, Carl D. Langefeld, Timothy Howard, David Herrington, Lynne E. Wagenknecht, David C. Goff, Donald W. Bowden, Stephen S. Rich, Catherine C. Hedrick

Association of Arachidonate 12 Lipoxygenase Genotype Variation and Glycemic Control With Albuminuria in Type 2 Diabetes

Download from www.ncbi.nlm.nih.gov

This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Kp Burdon

, Mg Wirth, Da Mackey

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance (vol 41, art no e106, 2004)

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Ra Mills, Kj Laurie, Kp Burdon

, Cecilia Giunta, Alex W. Hewitt, Paul Latimer, Je Craig, Dj Coster, Jc Charlesworth

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci

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Rebecca J. Ormsby

, Shoba Ranganathan, Kim M. Griggs, Joo Chuan Tong, David P. Dimasi, Alex W. Hewitt, Kathryn P. Burdon

, Jamie E. Craig, David L. Gordon, Josephine Hoh

Functional and structural implications of the complement factor H Y402H polymorphism associated with Age-Related macular degeneration

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2007 Aw W. Hewitt, Shiwani Sharma, Kp P. Burdon

, Jj J. Wang, Pn N. Baird, Dp P. Dimasi, Da A. Mackey, Paul Mitchell, Je E. Craig

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people

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Adi Reches, Yuval Yaron, Kathryn Burdon

, Ornit Crystal-Shalit, Dvora Kidron, Mira Malcov, Ron Tepper

Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended family

Download from www.researchgate.net

Lehtinen, Kp Burdon

, Jp Lewis

Association of alpha 2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis

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Papers authored by Kathryn Burdon