Works matching AU McLean, Rebecca J.

Results: 15
    1

    The retina as a window into detecting subclinical cardiovascular disease in type 2 diabetes.

    Published in:
    Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-13468-4
    By:
    • Alatrany, Abbas S.;
    • Lakhani, Kishan;
    • Cowley, Alice C.;
    • Yeo, Jian L.;
    • Dattani, Abhishek;
    • Ayton, Sarah L.;
    • Deshpande, Aparna;
    • Graham-Brown, Matthew P.M.;
    • Davies, Melanie J.;
    • Khunti, Kamlesh;
    • Yates, Thomas;
    • Sellers, Stephanie L.;
    • Zhou, Huiyu;
    • Brady, Emer M.;
    • Arnold, Jayanth R.;
    • Deane, James;
    • McLean, Rebecca J.;
    • Proudlock, Frank A.;
    • McCann, Gerry P.;
    • Gulsin, Gaurav S.
    Publication type:
    Article
    2

    The retina as a window into detecting subclinical cardiovascular disease in type 2 diabetes.

    Published in:
    Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-13468-4
    By:
    • Alatrany, Abbas S.;
    • Lakhani, Kishan;
    • Cowley, Alice C.;
    • Yeo, Jian L.;
    • Dattani, Abhishek;
    • Ayton, Sarah L.;
    • Deshpande, Aparna;
    • Graham-Brown, Matthew P.M.;
    • Davies, Melanie J.;
    • Khunti, Kamlesh;
    • Yates, Thomas;
    • Sellers, Stephanie L.;
    • Zhou, Huiyu;
    • Brady, Emer M.;
    • Arnold, Jayanth R.;
    • Deane, James;
    • McLean, Rebecca J.;
    • Proudlock, Frank A.;
    • McCann, Gerry P.;
    • Gulsin, Gaurav S.
    Publication type:
    Article
    3
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    Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

    Published in:
    2011
    By:
    • Tarpey, Patrick;
    • Thomas, Shery;
    • Sarvananthan, Nagini;
    • Mallya, Uma;
    • Lisgo, Steven;
    • Talbot, Chris J;
    • Roberts, Eryl O;
    • Awan, Musarat;
    • Surendran, Mylvaganam;
    • McLean, Rebecca J;
    • Reinecke, Robert D;
    • Langmann, Andrea;
    • Lindner, Susanne;
    • Koch, Martina;
    • Jain, Sunila;
    • Woodruff, Geoffrey;
    • Gale, Richard P;
    • Degg, Chris;
    • Droutsas, Konstantinos;
    • Asproudis, Ioannis
    Publication type:
    Correction Notice
    6

    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

    Published in:
    Nature Genetics, 2006, v. 38, n. 11, p. 1242, doi. 10.1038/ng1893
    By:
    • Tarpey, Patrick;
    • Thomas, Shery;
    • Sarvananthan, Nagini;
    • Mallya, Uma;
    • Lisgo, Steven;
    • Talbot, Chris J.;
    • Roberts, Eryl O.;
    • Awan, Musarat;
    • Surendran, Mylvaganam;
    • McLean, Rebecca J.;
    • Reinecke, Robert D.;
    • Langmann, Andrea;
    • Lindner, Susanne;
    • Koch, Martina;
    • Jain, Sunila;
    • Woodruff, Geoffrey;
    • Gale, Richard P.;
    • Degg, Chris;
    • Droutsas, Konstantinos;
    • Asproudis, Ioannis
    Publication type:
    Article
    7

    Discordant phenotypes in twins with infantile nystagmus.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-82368-0
    By:
    • Aamir, Abdullah;
    • Kuht, Helen J.;
    • McLean, Rebecca J.;
    • Maconachie, Gail D. E.;
    • Sheth, Viral;
    • Dawar, Basu;
    • Purohit, Ravi;
    • Sylvius, Nicolas;
    • Hisaund, Michael;
    • Zubcov-Iwantscheff, Alina;
    • Proudlock, Frank A.;
    • Gottlob, Irene;
    • Thomas, Mervyn G.
    Publication type:
    Article
    8

    Abnormal retinal development associated with FRMD7 mutations.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 15, p. 4086, doi. 10.1093/hmg/ddu122
    By:
    • Thomas, Mervyn G.;
    • Crosier, Moira;
    • Lindsay, Susan;
    • Kumar, Anil;
    • Araki, Masasuke;
    • Leroy, Bart P.;
    • McLean, Rebecca J.;
    • Sheth, Viral;
    • Maconachie, Gail;
    • Thomas, Shery;
    • Moore, Anthony T.;
    • Gottlob, Irene
    Publication type:
    Article
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    13

    Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia.

    Published in:
    Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.718958
    By:
    • Lowndes, Rebecca;
    • Molz, Barbara;
    • Warriner, Lucy;
    • Herbik, Anne;
    • de Best, Pieter B.;
    • Raz, Noa;
    • Gouws, Andre;
    • Ahmadi, Khazar;
    • McLean, Rebecca J.;
    • Gottlob, Irene;
    • Kohl, Susanne;
    • Choritz, Lars;
    • Maguire, John;
    • Kanowski, Martin;
    • Käsmann-Kellner, Barbara;
    • Wieland, Ilse;
    • Banin, Eyal;
    • Levin, Netta;
    • Hoffmann, Michael B.;
    • Morland, Antony B.
    Publication type:
    Article
    14

    Vertical optokinetic nystagmus in Parkinson's disease.

    Published in:
    Movement Disorders, 2009, v. 24, n. 10, p. 1533, doi. 10.1002/mds.22634
    By:
    • Knapp, Christopher M.;
    • Gottlob, Irene;
    • McLean, Rebecca J.;
    • Rajabally, Yusuf A.;
    • Abbott, Richard J.;
    • Rafelt, Suzanne;
    • Proudlock, Frank A.
    Publication type:
    Article
    15

    The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

    Published in:
    Brain: A Journal of Neurology, 2011, v. 134, n. 3, p. 892, doi. 10.1093/brain/awq373
    By:
    • Thomas, Mervyn G.;
    • Crosier, Moira;
    • Lindsay, Susan;
    • Kumar, Anil;
    • Thomas, Shery;
    • Araki, Masasuke;
    • Talbot, Chris J.;
    • McLean, Rebecca J.;
    • Surendran, Mylvaganam;
    • Taylor, Katie;
    • Leroy, Bart P.;
    • Moore, Anthony T.;
    • Hunter, David G.;
    • Hertle, Richard W.;
    • Tarpey, Patrick;
    • Langmann, Andrea;
    • Lindner, Susanne;
    • Brandner, Martina;
    • Gottlob, Irene
    Publication type:
    Article