Showing 1 - 20 results of 36 for search 'Jamie E. Craig', query time: 0.06s Refine Results
  1. 1
    Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion

    Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion by Emmanuelle Souzeau, Andrew Dubowsky, Jonathan B. Ruddle, Jamie E. Craig

    Published 2019-08-01
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  2. 2
    Single Dose of Pseudoephedrine Induces Simultaneous Bilateral Acute Angle Closure Crisis

    Single Dose of Pseudoephedrine Induces Simultaneous Bilateral Acute Angle Closure Crisis by Benjamin G. Spencer, Jonathan Baskin, Blake F. Giarola, Jamie E. Craig

    Published 2019-10-01
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  3. 3
    An Assessment of GUCA1C Variants in Primary Congenital Glaucoma

    An Assessment of GUCA1C Variants in Primary Congenital Glaucoma by Emmanuelle Souzeau, Nicole Weisschuh, Jamie E. Craig, Francesca Pasutto, Karl-Wilhelm Koch

    Published 2021-03-01
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  4. 4
    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 S Thapa, Alex W Hewitt, Kathryn P Burdon, Jamie E Craig

    Published 2013-01-01
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  5. 5
    Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)

    Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome) by Shari Javadiyan, Jamie E. Craig, Shiwani Sharma, Karen M. Lower, Theresa Casey, Eric Haan, Emmanuelle Souzeau, Kathryn P. Burdon

    Published 2017-05-01
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  6. 6
    TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases.

    TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases. by Abraham Kuot, Alex W Hewitt, Grant R Snibson, Emmanuelle Souzeau, Richard Mills, Jamie E Craig, Kathryn P Burdon, Shiwani Sharma

    Published 2017-01-01
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  7. 7
    Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse

    Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse by Mark M. Hassall, Shari Javadiyan, Sonja Klebe, Mona S. Awadalla, Shiwani Sharma, Ayub Qassim, Melissa White, Paul Q. Thomas, Jamie E. Craig, Owen M. Siggs

    Published 2023-07-01
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  8. 8
    Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia.

    Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia. by Alpana Dave, Kate Laurie, Sandra E Staffieri, Deepa Taranath, David A Mackey, Paul Mitchell, Jie Jin Wang, Jamie E Craig, Kathryn P Burdon, Shiwani Sharma

    Published 2013-01-01
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  9. 9
    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. by 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

    Published 2015-01-01
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  10. 10
    Genetic Risk Assessment of Degenerative Eye Disease (GRADE): study protocol of a prospective assessment of polygenic risk scores to predict diagnosis of glaucoma and age-related macular degeneration

    Genetic Risk Assessment of Degenerative Eye Disease (GRADE): study protocol of a prospective assessment of polygenic risk scores to predict diagnosis of glaucoma and age-related ma... by Georgina L Hollitt, Ayub Qassim, Daniel Thomson, Joshua M Schmidt, Thi Thi Nguyen, John Landers, Stuart MacGregor, Owen M Siggs, Emmanuelle Souzeau, Jamie E Craig

    Published 2023-10-01
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  11. 11
    Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucoma

    Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucoma by Haojie Fu, Owen M. Siggs, Lachlan S.W. Knight, Sandra E. Staffieri, Jonathan B. Ruddle, Amy E. Birsner, Edward Ryan Collantes, Jamie E. Craig, Janey L. Wiggs, Robert J. D’Amato

    Published 2022-12-01
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  12. 12
    Identifying Genetic Biomarkers Predicting Response to Anti-Vascular Endothelial Growth Factor Injections in Diabetic Macular Edema

    Identifying Genetic Biomarkers Predicting Response to Anti-Vascular Endothelial Growth Factor Injections in Diabetic Macular Edema by Rajya L. 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

    Published 2022-04-01
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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 by Rajya L 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

    Published 2023-04-01
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  14. 14
    Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent.

    Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent. by Sionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, Richard A Mills, Jonathan Ellis, Paul Leo, Emmanuelle Souzeau, Bronwyn Ridge, Jac C Charlesworth, Richard Lindsay, Jamie E Craig, Kathryn P Burdon

    Published 2018-01-01
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  15. 15
    Screening of CRISPR/Cas base editors to target the AMD high-risk Y402H complement factor H variant

    Screening of CRISPR/Cas base editors to target the AMD high-risk Y402H complement factor H variant by Minh Thuan Nguyen Tran, Mohd Khairul Nizam Mohd Khalid, Alice Pébay, Anthony L. Cook, Helena H. Liang, Raymond C.B. Wong, Jamie E. Craig, Guei-Sheung Liu, Sandy S. Hung, Alex W. Hewitt

    Published 2019-03-01
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  16. 16
    Study profile: the Genetics of Glaucoma Study

    Study profile: the Genetics of Glaucoma Study by David A Mackey, Alex W Hewitt, Stuart MacGregor, Puya Gharahkhani, Jamie E Craig, Mathias Seviiri, Jue-Sheng Ong, Matthew H Law, Weixiong He, Santiago Diaz Torres, Yeda Wu, Nathan Ingold, Regina Yu

    Published 2023-08-01
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  17. 17
    High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia

    High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia by Shari Javadiyan, Jamie E. Craig, Emmanuelle Souzeau, Shiwani Sharma, Karen M. Lower, David A. Mackey, Sandra E. Staffieri, James E. Elder, Deepa Taranath, Tania Straga, Joanna Black, John Pater, Theresa Casey, Alex W. Hewitt, Kathryn P. Burdon

    Published 2017-10-01
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  18. 18
    Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance.

    Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance. by Mona S Awadalla, Jude Fitzgerald, Nicholas H Andrew, Tiger Zhou, Henry Marshall, Ayub Qassim, Mark Hassall, Robert J Casson, Stuart L Graham, Paul R Healey, Ashish Agar, Anna Galanopoulos, Simon Phipps, Angela Chappell, John Landers, Jamie E Craig

    Published 2018-01-01
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  19. 19
    Pathogenic genetic variants identified in Australian families with paediatric cataract

    Pathogenic genetic variants identified in Australian families with paediatric cataract by David A Mackey, Emmanuelle Souzeau, Jamie E Craig, Jonathan B Ruddle, Bennet J McComish, Kathryn P Burdon, Jac C Charlesworth, Sandra E Staffieri, Johanna L Jones, Lisa S Kearns, James E Elder, Deepa Taranath, John Pater, Theresa Casey

    Published 2022-10-01
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  20. 20
    Hypomethylation of the IL17RC Promoter in Peripheral Blood Leukocytes Is Not A Hallmark of Age-Related Macular Degeneration

    Hypomethylation of the IL17RC Promoter in Peripheral Blood Leukocytes Is Not A Hallmark of Age-Related Macular Degeneration by Verity F. Oliver, Maria Franchina, Andrew E. Jaffe, Kari E. Branham, Mohammad Othman, John R. Heckenlively, Anand Swaroop, Betsy Campochiaro, Brendan J. Vote, Jamie E. Craig, Richard Saffery, David A. Mackey, Jiang Qian, Donald J. Zack, Alex W. Hewitt, Shannath L. Merbs

    Published 2013-12-01
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