Works by Wade-Martins, Richard


Results: 100
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    Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency.

    Published in:
    Human Mutation, 2004, v. 23, n. 6, p. 576, doi. 10.1002/humu.20040
    By:
    • Cosma, Maria Pia;
    • Pepe, Stefano;
    • Parenti, Giancarlo;
    • Settembre, Carmine;
    • Annunziata, Ida;
    • Wade-Martins, Richard;
    • Domenico, Carmela Di;
    • Natale, Paola Di;
    • Mankad, Anuj;
    • Cox, Barbara;
    • Uziel, Graziella;
    • Mancini, Grazia M.S.;
    • Zammarchi, Enrico;
    • Donati, Maria Alice;
    • Kleijer, Wim J.;
    • Filocamo, Mirella;
    • Carrozzo, Romeo;
    • Carella, Massimo;
    • Ballabio, Andrea
    Publication type:
    Article
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    Alpha-synuclein RT-Qu IC in the CSF of patients with alpha-synucleinopathies.

    Published in:
    Annals of Clinical & Translational Neurology, 2016, v. 3, n. 10, p. 812, doi. 10.1002/acn3.338
    By:
    • Fairfoul, Graham;
    • McGuire, Lynne I.;
    • Pal, Suvankar;
    • Ironside, James W.;
    • Neumann, Juliane;
    • Christie, Sharon;
    • Joachim, Catherine;
    • Esiri, Margaret;
    • Evetts, Samuel G.;
    • Rolinski, Michal;
    • Baig, Fahd;
    • Ruffmann, Claudio;
    • Wade‐Martins, Richard;
    • Hu, Michele T. M.;
    • Parkkinen, Laura;
    • Green, Alison J. E.
    Publication type:
    Article
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    Identification of distinct circulating exosomes in Parkinson's disease.

    Published in:
    Annals of Clinical & Translational Neurology, 2015, v. 2, n. 4, p. 353, doi. 10.1002/acn3.175
    By:
    • Tomlinson, Paul R.;
    • Zheng, Ying;
    • Fischer, Roman;
    • Heidasch, Ronny;
    • Gardiner, Chris;
    • Evetts, Samuel;
    • Hu, Michele;
    • Wade‐Martins, Richard;
    • Turner, Martin R.;
    • Morris, John;
    • Talbot, Kevin;
    • Kessler, Benedikt M.;
    • Tofaris, George K.
    Publication type:
    Article
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    Identification of a possible proteomic biomarker in Parkinson's disease: discovery and replication in blood, brain and cerebrospinal fluid.

    Published in:
    Brain Communications, 2023, v. 5, n. 1, p. 1, doi. 10.1093/braincomms/fcac343
    By:
    • Winchester, Laura;
    • Barber, Imelda;
    • Lawton, Michael;
    • Ash, Jessica;
    • Liu, Benjamine;
    • Evetts, Samuel;
    • Hopkins-Jones, Lucinda;
    • Lewis, Suppalak;
    • Bresner, Catherine;
    • Malpartida, Ana Belen;
    • Williams, Nigel;
    • Gentlemen, Steve;
    • Wade-Martins, Richard;
    • Ryan, Brent;
    • Holgado-Nevado, Alejo;
    • Hu, Michele;
    • Ben-Shlomo, Yoav;
    • Grosset, Donald;
    • Lovestone, Simon
    Publication type:
    Article
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    Mitochondrial dysfunction and mitophagy defects in LRRK2-R1441C Parkinson's disease models.

    Published in:
    Human Molecular Genetics, 2023, v. 32, n. 18, p. 2808, doi. 10.1093/hmg/ddad102
    By:
    • Williamson, Matthew G;
    • Madureira, Marta;
    • McGuinness, William;
    • Heon-Roberts, Rachel;
    • Mock, Elliot D;
    • Naidoo, Kalina;
    • Cramb, Kaitlyn M L;
    • Caiazza, Maria-Claudia;
    • Malpartida, Ana B;
    • Lavelle, Martha;
    • Savory, Katrina;
    • Humble, Stewart W;
    • Patterson, Ryan;
    • Davis, John B;
    • Connor-Robson, Natalie;
    • Ryan, Brent J;
    • Wade-Martins, Richard
    Publication type:
    Article
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    Cellular α -synuclein pathology is associated with bioenergetic dysfunction in Parkinson's iPSC-derived dopamine neurons.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 12, p. 2001, doi. 10.1093/hmg/ddz038
    By:
    • Zambon, Federico;
    • Cherubini, Marta;
    • Fernandes, Hugo J R;
    • Lang, Charmaine;
    • Ryan, Brent J;
    • Volpato, Viola;
    • Bengoa-Vergniory, Nora;
    • Vingill, Siv;
    • Attar, Moustafa;
    • Booth, Heather D E;
    • Haenseler, Walther;
    • Vowles, Jane;
    • Bowden, Rory;
    • Webber, Caleb;
    • Cowley, Sally A;
    • Wade-Martins, Richard
    Publication type:
    Article
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    LRRK2 BAC transgenic rats develop progressive, L-DOPA-responsive motor impairment, and deficits in dopamine circuit function.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 5, p. 951, doi. 10.1093/hmg/ddv628
    By:
    • Sloan, Max;
    • Alegre-Abarrategui, Javier;
    • Potgieter, Dawid;
    • Kaufmann, Anna-Kristin;
    • Exley, Richard;
    • Deltheil, Thierry;
    • Threlfell, Sarah;
    • Connor-Robson, Natalie;
    • Brimblecombe, Katherine;
    • Wallings, Rebecca;
    • Cioroch, Milena;
    • Bannerman, David M.;
    • Bolam, J. Paul;
    • Magill, Peter J.;
    • Cragg, Stephanie J.;
    • Dodson, Paul D.;
    • Wade-Martins, Richard
    Publication type:
    Article
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    Impaired dopamine release in Parkinson's disease.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 8, p. 3117, doi. 10.1093/brain/awad064
    By:
    • Cramb, Kaitlyn M L;
    • Beccano-Kelly, Dayne;
    • Cragg, Stephanie J;
    • Wade-Martins, Richard
    Publication type:
    Article
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    Whole-exome sequencing of 228 patients with sporadic Parkinson's disease.

    Published in:
    Scientific Reports, 2017, p. 41188, doi. 10.1038/srep41188
    By:
    • Sandor, Cynthia;
    • Honti, Frantisek;
    • Haerty, Wilfried;
    • Szewczyk-Krolikowski, Konrad;
    • Tomlinson, Paul;
    • Evetts, Sam;
    • Millin, Stephanie;
    • Keane, Thomas;
    • McCarthy, Shane A.;
    • Durbin, Richard;
    • Talbot, Kevin;
    • Hu, Michele;
    • Webber, Caleb;
    • Ponting, Chris P.;
    • Wade-Martins, Richard
    Publication type:
    Article
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