Søgeresultater - Andrew R. Webster

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  1. 1
    The zebrafish eye—a paradigm for investigating human ocular genetics

    The zebrafish eye—a paradigm for investigating human ocular genetics af Rose Richardson, Dhani Tracey‐White, Andrew R. Webster, Mariya Moosajee

    Udgivet 2016
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  2. 2
    QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY

    QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY af James Tee, Angelos Kalitzeos, Andrew R. Webster, Tünde Pető, Michel Michaelides

    Udgivet 2017
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  3. 3
    A rare canonical splice-site variant in VPS13B causes attenuated Cohen syndrome

    A rare canonical splice-site variant in VPS13B causes attenuated Cohen syndrome af Malena Daich Varela, Fabiana Louise Motta, Andrew R. Webster, Gavin Arno

    Udgivet 2021
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  4. 4
    Mechanism and evidence of nonsense suppression therapy for genetic eye disorders

    Mechanism and evidence of nonsense suppression therapy for genetic eye disorders af Rose Richardson, Matthew Smart, Dhani Tracey‐White, Andrew R. Webster, Mariya Moosajee

    Udgivet 2017
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  5. 5
    Natural History Study of Retinal Structure, Progression, and Symmetry Using Ellipzoid Zone Metrics in RPGR-Associated Retinopathy

    Natural History Study of Retinal Structure, Progression, and Symmetry Using Ellipzoid Zone Metrics in RPGR-Associated Retinopathy af James Tee, Yesa Yang, Angelos Kalitzeos, Andrew R. Webster, James Bainbridge, Michel Michaelides

    Udgivet 2018
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  6. 6
    FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHY

    FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHY af Kamron Khan, Omar A. Mahroo, Farrah Islam, Andrew R. Webster, Anthony T. Moore, Michel Michaelides

    Udgivet 2016
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  7. 7
    An Analysis of Phenotypic Variation in the Familial Cancer Syndrome von Hippel–Lindau Disease: Evidence for Modifier Effects

    An Analysis of Phenotypic Variation in the Familial Cancer Syndrome von Hippel–Lindau Disease: Evidence for Modifier Effects af Andrew R. Webster, Frances M. Richards, Fiona E. MacRonald, Anthony T. Moore, Eamonn R. Maher

    Udgivet 1998
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  8. 8
    Genetic influence on early age-related maculopathy

    Genetic influence on early age-related maculopathy af Christopher J. Hammond, Andrew R. Webster, Harold Snieder, Alan C. Bird, Clare Gilbert, Tim D. Spector

    Udgivet 2002
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  9. 9
    Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation

    Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation af Hannah Currant, Tomas Fitzgerald, Praveen J. Patel, Anthony P. Khawaja, Andrew R. Webster, Omar A. Mahroo, Ewan Birney

    Udgivet 2023
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  10. 10
    Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis

    Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis af Panagiotis I. Sergouniotis, Alice E. Davidson, Donna S. Mackay, Zheng Li, Yang Xu, Vincent Plagnol, Anthony T. Moore, Andrew R. Webster

    Udgivet 2011
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  11. 11
    Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

    Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. af Eamonn R. Maher, Andrew R. Webster, Frances M. Richards, J S Green, Paul A. Crossey, Stewart J. Payne, Anthony T. Moore

    Udgivet 1996
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  12. 12
    Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of <i>ABCA4</i>

    Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of <i>ABCA4</i> af Ana Fakin, Anthony G. Robson, Kaoru Fujinami, Anthony T. Moore, Michel Michaelides, John Chiang, Graham E. Holder, Andrew R. Webster

    Udgivet 2016
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  13. 13
    The Effect on Retinal Structure and Function of 15 Specific <i>ABCA4</i> Mutations: A Detailed Examination of 82 Hemizygous Patients

    The Effect on Retinal Structure and Function of 15 Specific <i>ABCA4</i> Mutations: A Detailed Examination of 82 Hemizygous Patients af Ana Fakin, Anthony G. Robson, John Chiang, Kaoru Fujinami, Anthony T. Moore, Michel Michaelides, Graham E. Holder, Andrew R. Webster

    Udgivet 2016
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  14. 14
    Coats-like Vasculopathy in Inherited Retinal Disease

    Coats-like Vasculopathy in Inherited Retinal Disease af Malena Daich Varela, Giovanni Conti, Samantha Malka, Veronika Vaclavik, Omar A. Mahroo, Andrew R. Webster, Hoai Viet Tran, Michel Michaelides

    Udgivet 2023
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  15. 15
    Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update

    Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update af Anthony G. Robson, Michel Michaelides, Zubin Saihan, Alan C. Bird, Andrew R. Webster, Anthony T. Moore, Fred W. Fitzke, Graham E. Holder

    Udgivet 2007
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  16. 16
    Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosa

    Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosa af Gerald Liew, Stacey A Strong, Patrick D. Bradley, Philip Severn, Anthony T. Moore, Andrew R. Webster, Paul Mitchell, Annette Kifley, Michel Michaelides

    Udgivet 2018
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  17. 17
    Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies

    Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies af Leo Sheck, Wayne I. L. Davies, Phillip Moradi, Anthony G. Robson, Neruban Kumaran, Alki Liasis, Andrew R. Webster, Anthony T. Moore, Michel Michaelides

    Udgivet 2018
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  18. 18
    Photoreceptor Structure in<i>GNAT2</i>-Associated Achromatopsia

    Photoreceptor Structure in<i>GNAT2</i>-Associated Achromatopsia af Michalis Georgiou, Navjit Singh, Thomas Kane, Anthony G. Robson, Angelos Kalitzeos, Nashila Hirji, Andrew R. Webster, Alfredo Dubra, Joseph Carroll, Michel Michaelides

    Udgivet 2020
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  19. 19
    Autosomal Recessive Bestrophinopathy

    Autosomal Recessive Bestrophinopathy af Giuseppe Casalino, Kamron Khan, Monica Armengol, Genevieve Wright, Nikolas Pontikos, Michalis Georgiou, Andrew R. Webster, Anthony G. Robson, Parampal S. Grewal, Michel Michaelides

    Udgivet 2020
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  20. 20
    <i>ABCA4</i>Gene Screening by Next-Generation Sequencing in a British Cohort

    <i>ABCA4</i>Gene Screening by Next-Generation Sequencing in a British Cohort af Kaoru Fujinami, Jana Zernant, Ravinder Chana, Genevieve Wright, Kazushige Tsunoda, Yoko Ozawa, Kazuo Tsubota, Andrew R. Webster, Anthony T. Moore, Rando Allikmets, Michel Michaelides

    Udgivet 2013
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