نتائج البحث - Kathryn P. Burdon

تنقيح النتائج
  1. 1
    A Systematic Meta-Analysis of Genetic Association Studies for Diabetic Retinopathy

    A Systematic Meta-Analysis of Genetic Association Studies for Diabetic Retinopathy حسب Sotoodeh Abhary, Alex W. Hewitt, Kathryn P. Burdon, Jamie E. Craig

    منشور في 2009
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    Revisão
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  2. 2
    Association of Genetic Variants with Primary Angle Closure Glaucoma in Two Different Populations

    Association of Genetic Variants with Primary Angle Closure Glaucoma in Two Different Populations حسب Mona S. Awadalla, Suman Thapa, Alex W. Hewitt, Kathryn P. Burdon, Jamie E. Craig

    منشور في 2013
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  3. 3
    Mutation in<i>TMEM98</i>in a Large White Kindred With Autosomal Dominant Nanophthalmos Linked to 17p12-q12

    Mutation in<i>TMEM98</i>in a Large White Kindred With Autosomal Dominant Nanophthalmos Linked to 17p12-q12 حسب Mona S. Awadalla, Kathryn P. Burdon, Emmanuelle Souzeau, John Landers, Alex W. Hewitt, Shiwani Sharma, Jamie E. Craig

    منشور في 2014
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  4. 4
    Sequence Variation in DDAH1 and DDAH2 Genes Is Strongly and Additively Associated with Serum ADMA Concentrations in Individuals with Type 2 Diabetes

    Sequence Variation in DDAH1 and DDAH2 Genes Is Strongly and Additively Associated with Serum ADMA Concentrations in Individuals with Type 2 Diabetes حسب Sotoodeh Abhary, Kathryn P. Burdon, Abraham Kuot, Shahrbanou Javadiyan, Malcolm J. Whiting, Nicholas Kasmeridis, Nikolai Petrovsky, Jamie E. Craig

    منشور في 2010
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  5. 5
    Diabetic Retinopathy Is Associated With Elevated Serum Asymmetric and Symmetric Dimethylarginines

    Diabetic Retinopathy Is Associated With Elevated Serum Asymmetric and Symmetric Dimethylarginines حسب Sotoodeh Abhary, Nicholas Kasmeridis, Kathryn P. Burdon, Abraham Kuot, Malcolm J. Whiting, Wai Ping Yew, Nikolai Petrovsky, Jamie E. Craig

    منشور في 2009
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  6. 6
    Association of TCF4 and CLU polymorphisms with Fuchs’ endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process

    Association of TCF4 and CLU polymorphisms with Fuchs’ endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process حسب Abraham Kuot, Alex W. Hewitt, Kim Griggs, Sonja Klebe, Richard Mills, Vishal Jhanji, Jamie E. Craig, Shiwani Sharma, Kathryn P. Burdon

    منشور في 2012
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  7. 7
    Serum selenium status in <scp>G</scp>raves’ disease with and without orbitopathy: a case–control study

    Serum selenium status in <scp>G</scp>raves’ disease with and without orbitopathy: a case–control study حسب Jwu Jin Khong, Rebecca F. Goldstein, Kerrie M. Sanders, Hans G. Schneider, Jeffrey Pope, Kathryn P. Burdon, Jamie E. Craig, Peter R. Ebeling

    منشور في 2013
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  8. 8
    Genetic analysis of the soluble epoxide hydrolase gene, <i>EPHX2</i>, in subclinical cardiovascular disease in the Diabetes Heart Study

    Genetic analysis of the soluble epoxide hydrolase gene, <i>EPHX2</i>, in subclinical cardiovascular disease in the Diabetes Heart Study حسب Kathryn P. Burdon, Allison B. Lehtinen, Carl D. Langefeld, J. Jeffrey Carr, Stephen S. Rich, Barry I. Freedman, David M. Herrington, Donald W. Bowden

    منشور في 2008
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  9. 9
    Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people

    Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people حسب Alex W. Hewitt, Shiwani Sharma, Kathryn P. Burdon, J. J. Wang, Paul N. Baird, David P. Dimasi, David A. Mackey, Paul Mitchell, Jamie E. Craig

    منشور في 2007
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  10. 10
    Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy

    Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy حسب Nicole J. Van Bergen, Jonathan G. Crowston, Jamie E. Craig, Kathryn P. Burdon, Lisa S. Kearns, Shiwani Sharma, Alex W. Hewitt, David A. Mackey, Ian A. Trounce

    منشور في 2015
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  11. 11
    Mutations of the<i>EPHA2</i>receptor tyrosine kinase gene cause autosomal dominant congenital cataract

    Mutations of the<i>EPHA2</i>receptor tyrosine kinase gene cause autosomal dominant congenital cataract حسب 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

    منشور في 2009
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  12. 12
    Mutations in the <i>NDP</i> gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity

    Mutations in the <i>NDP</i> gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity حسب Joanne L. Dickinson, Michèle M. Sale, Abraham Passmore, Liesel M. FitzGerald, Catherine Wheatley, Kathryn P. Burdon, Jamie E. Craig, Supaporn Tengtrisorn, Susan M. Carden, Hector Maclean, David A. Mackey

    منشور في 2006
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  13. 13
    Predictive factors for treatment outcomes with intravitreal anti-vascular endothelial growth factor injections in diabetic macular edema in clinical practice

    Predictive factors for treatment outcomes with intravitreal anti-vascular endothelial growth factor injections in diabetic macular edema in clinical practice حسب Rajya Laxmi Gurung, Liesel M. FitzGerald, Ebony Liu, Bennet J. McComish, Georgia Kaidonis, Bronwyn Ridge, Alex W. Hewitt, Brendan J. Vote, Nitin Verma, Jamie E. Craig, Kathryn P. Burdon

    منشور في 2023
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  14. 14
    Copy Number Variations of TBK1 in Australian Patients With Primary Open-Angle Glaucoma

    Copy Number Variations of TBK1 in Australian Patients With Primary Open-Angle Glaucoma حسب Mona S. Awadalla, John H. Fingert, Benjamin E. Roos, Simon Chen, Richard Holmes, Stuart L. Graham, Mark Chehade, Anna Galanopolous, Bronwyn Ridge, Emmanuelle Souzeau, Tiger Zhou, Owen M. Siggs, Alex W. Hewitt, David A. Mackey, Kathryn P. Burdon, Jamie E. Craig

    منشور في 2014
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  15. 15
    Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel

    Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel حسب Kathryn P. Burdon, Patricia Graham, Johanna Hadler, John D. Hulleman, Francesca Pasutto, Erin A. Boese, Jamie E. Craig, John H. Fingert, Alex W. Hewitt, Owen M. Siggs, Kristina N. Whisenhunt, Terri L. Young, David A. Mackey, Andrew Dubowsky, Emmanuelle Souzeau

    منشور في 2022
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  16. 16
    Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy

    Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy حسب Patricia Graham, Georgia Kaidonis, Sotoodeh Abhary, Mark Gillies, Mark Daniell, Rohan W. Essex, John H. Chang, Stewart Lake, Bishwanath Pal, Alicia J. Jenkins, Alex W. Hewitt, Ecosse L. Lamoureux, Philip Hykin, Nikolai Petrovsky, Matthew A. Brown, Jamie E. Craig, Kathryn P. Burdon

    منشور في 2018
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  17. 17
    Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma

    Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma حسب Owen M. Siggs, Emmanuelle Souzeau, Deepa Taranath, Andrew Dubowsky, Angela Chappell, Tiger Zhou, Shari Javadiyan, Jillian Nicholl, Lisa S. Kearns, Sandra E. Staffieri, Andrew Narita, James E. Smith, John Pater, Alex W. Hewitt, Jonathan B. Ruddle, James E. Elder, David A. Mackey, Kathryn P. Burdon, Jamie E. Craig

    منشور في 2020
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  18. 18
    Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma

    Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma حسب Tiger Zhou, Emmanuelle Souzeau, Shiwani Sharma, John Landers, Richard Mills, Ivan Goldberg, Paul R. Healey, Stuart L. Graham, Alex W. Hewitt, David A. Mackey, Anna Galanopoulos, Robert J. Casson, Jonathan B. Ruddle, Jonathan Ellis, Paul Leo, Matthew A. Brown, Stuart MacGregor, David J. Lynn, Kathryn P. Burdon, Jamie E. Craig

    منشور في 2017
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  19. 19
    Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based Studies

    Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based Studies حسب Xikun Han, Emmanuelle Souzeau, Jue‐Sheng Ong, Jiyuan An, Owen M. Siggs, Kathryn P. Burdon, Stephen Best, Ivan Goldberg, Paul R. Healey, Stuart L. Graham, Jonathan B. Ruddle, Richard Mills, John Landers, Anna Galanopoulos, Andrew White, Robert J. Casson, David A. Mackey, Alex W. Hewitt, Puya Gharahkhani, Jamie E. Craig, Stuart MacGregor

    منشور في 2018
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  20. 20
    Prevalence of<i>FOXC1</i>Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma

    Prevalence of<i>FOXC1</i>Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma حسب Owen M. Siggs, Emmanuelle Souzeau, Francesca Pasutto, Andrew Dubowsky, James E. Smith, Deepa Taranath, John Pater, Julian L Rait, Andrew Narita, Lucia Mauri, Alessandra Longo, André Reis, Angela Chappell, Lisa S. Kearns, Sandra E. Staffieri, James E. Elder, Jonathan B. Ruddle, Alex W. Hewitt, Kathryn P. Burdon, David A. Mackey, Jamie E. Craig

    منشور في 2019
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