Search Results - Jamie E. Craig

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  1. 1
    <i>Myocilin</i>allele-specific glaucoma phenotype database

    <i>Myocilin</i>allele-specific glaucoma phenotype database by Alex W. Hewitt, David A. Mackey, Jamie E. Craig

    Published 2007
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  2. 2
    Progress in Translating Glaucoma Genetics Into the Clinic: A Review

    Progress in Translating Glaucoma Genetics Into the Clinic: A Review by Antonia Kolovos, Giorgina Maxwell, Emmanuelle Souzeau, Jamie E. Craig

    Published 2025
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  3. 3
    A Systematic Meta-Analysis of Genetic Association Studies for Diabetic Retinopathy

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

    Published 2009
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  4. 4
    Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification

    Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification by Jamie E. Craig, RA Barnetson, John F. Prior, JL Raven, SL Thein

    Published 1994
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  5. 5
    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 by Mona S. Awadalla, Suman Thapa, Alex W. Hewitt, Kathryn P. Burdon, Jamie E. Craig

    Published 2013
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  6. 6
    Aetiology of congenital and paediatric cataract in an Australian population

    Aetiology of congenital and paediatric cataract in an Australian population by Manuel Wirth, I Russell‐Eggitt, Jamie E. Craig, James E. Elder, David A. Mackey

    Published 2002
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  7. 7
    Primary infantile glaucoma in an Australian population

    Primary infantile glaucoma in an Australian population by Jane R. MacKinnon, Antonio Giubilato, James E. Elder, Jamie E. Craig, David A. Mackey

    Published 2004
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  8. 8
    Pathogenesis of thyroid eye disease: review and update on molecular mechanisms

    Pathogenesis of thyroid eye disease: review and update on molecular mechanisms by Jwu Jin Khong, Alan A. McNab, Peter R. Ebeling, Jamie E. Craig, Dinesh Selva

    Published 2015
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  9. 9
    Assessing the Efficacy of Synthetic Optic Disc Images for Detecting Glaucomatous Optic Neuropathy Using Deep Learning

    Assessing the Efficacy of Synthetic Optic Disc Images for Detecting Glaucomatous Optic Neuropathy Using Deep Learning by Abadh K. Chaurasia, Stuart MacGregor, Jamie E. Craig, David A. Mackey, Alex W. Hewitt

    Published 2024
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  10. 10
    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 by Mona S. Awadalla, Kathryn P. Burdon, Emmanuelle Souzeau, John Landers, Alex W. Hewitt, Shiwani Sharma, Jamie E. Craig

    Published 2014
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  11. 11
    Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort

    Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort by Xikun Han, Jue‐Sheng Ong, Jiyuan An, Jamie E. Craig, Puya Gharahkhani, Alex W. Hewitt, Stuart MacGregor

    Published 2020
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  12. 12
    The natural history of OPA1-related autosomal dominant optic atrophy

    The natural history of OPA1-related autosomal dominant optic atrophy by Amy Cohn, Carmel Toomes, Alex W. Hewitt, Lisa S. Kearns, C.F. Inglehearn, Jamie E. Craig, David A. Mackey

    Published 2008
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  13. 13
    Risk Factors for Graves' Orbitopathy; the Australian Thyroid-Associated Orbitopathy Research (ATOR) Study

    Risk Factors for Graves' Orbitopathy; the Australian Thyroid-Associated Orbitopathy Research (ATOR) Study by Jwu Jin Khong, Sue Finch, Chamika De Silva, Stacey Rylander, Jamie E. Craig, Dinesh Selva, Peter R. Ebeling

    Published 2016
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  14. 14
    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 by Sotoodeh Abhary, Kathryn P. Burdon, Abraham Kuot, Shahrbanou Javadiyan, Malcolm J. Whiting, Nicholas Kasmeridis, Nikolai Petrovsky, Jamie E. Craig

    Published 2010
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  15. 15
    Diabetic Retinopathy Is Associated With Elevated Serum Asymmetric and Symmetric Dimethylarginines

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

    Published 2009
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  16. 16
    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 by Abraham Kuot, Alex W. Hewitt, Kim Griggs, Sonja Klebe, Richard Mills, Vishal Jhanji, Jamie E. Craig, Shiwani Sharma, Kathryn P. Burdon

    Published 2012
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  17. 17
    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 by Jwu Jin Khong, Rebecca F. Goldstein, Kerrie M. Sanders, Hans G. Schneider, Jeffrey Pope, Kathryn P. Burdon, Jamie E. Craig, Peter R. Ebeling

    Published 2013
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  18. 18
    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 by 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

    Published 2007
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  19. 19
    How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania

    How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania by Catherine Green, Lisa S. Kearns, Johnny Wu, Julie M. Barbour, Robyn M Wilkinson, Maree A. Ring, Jamie E. Craig, Tiffany Wong, Alex W. Hewitt, David A. Mackey

    Published 2007
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  20. 20
    The Path to Open-Angle Glaucoma Gene Discovery: Endophenotypic Status of Intraocular Pressure, Cup-to-Disc Ratio, and Central Corneal Thickness

    The Path to Open-Angle Glaucoma Gene Discovery: Endophenotypic Status of Intraocular Pressure, Cup-to-Disc Ratio, and Central Corneal Thickness by Jac Charlesworth, Patricia L. Kramer, Tom Dyer, Víctor Diego, John R. Samples, Jamie E. Craig, David A. Mackey, Alex W. Hewitt, John Blangero, Mary K. Wirtz

    Published 2010
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