Works by Wood, Nicholas


Results: 293
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    Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.

    Published in:
    2022
    By:
    • Magrinelli, Francesca;
    • Mehta, Sahil;
    • Di Lazzaro, Giulia;
    • Latorre, Anna;
    • Edwards, Mark J.;
    • Balint, Bettina;
    • Basu, Purba;
    • Kobylecki, Christopher;
    • Groppa, Sergiu;
    • Hegde, Anaita;
    • Mulroy, Eoin;
    • Estevez‐Fraga, Carlos;
    • Arora, Anshita;
    • Kumar, Hrishikesh;
    • Schneider, Susanne A.;
    • Lewis, Patrick A.;
    • Jaunmuktane, Zane;
    • Revesz, Tamas;
    • Gandhi, Sonia;
    • Wood, Nicholas W.
    Publication type:
    journal article
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    Childhood‐Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.

    Published in:
    Movement Disorders, 2021, v. 36, n. 6, p. 1472, doi. 10.1002/mds.28634
    By:
    • Mencacci, Niccolò E.;
    • Steel, Dora;
    • Magrinelli, Francesca;
    • Hsu, Jerry;
    • Keller Sarmiento, Ignacio Juan;
    • Troncoso Schifferli, Mónica;
    • Muñoz, Daniela;
    • Stefanis, Leonidas;
    • Lubbe, Steven J.;
    • Wood, Nicholas W.;
    • Kurian, Manju A.;
    • Stamelou, Maria
    Publication type:
    Article
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    Childhood-Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.

    Published in:
    2021
    By:
    • Mencacci, Niccolò E.;
    • Steel, Dora;
    • Magrinelli, Francesca;
    • Hsu, Jerry;
    • Keller Sarmiento, Ignacio Juan;
    • Troncoso Schifferli, Mónica;
    • Muñoz, Daniela;
    • Stefanis, Leonidas;
    • Lubbe, Steven J.;
    • Wood, Nicholas W.;
    • Kurian, Manju A.;
    • Stamelou, Maria
    Publication type:
    Letter
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    Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.

    Published in:
    Movement Disorders, 2021, v. 36, n. 2, p. 424, doi. 10.1002/mds.28342
    By:
    • Tan, Manuela M.X.;
    • Lawton, Michael A.;
    • Jabbari, Edwin;
    • Reynolds, Regina H.;
    • Iwaki, Hirotaka;
    • Blauwendraat, Cornelis;
    • Kanavou, Sofia;
    • Pollard, Miriam I.;
    • Hubbard, Leon;
    • Malek, Naveed;
    • Grosset, Katherine A.;
    • Marrinan, Sarah L.;
    • Bajaj, Nin;
    • Barker, Roger A.;
    • Burn, David J.;
    • Bresner, Catherine;
    • Foltynie, Thomas;
    • Wood, Nicholas W.;
    • Williams‐Gray, Caroline H.;
    • Hardy, John
    Publication type:
    Article
    35

    Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement Disorders.

    Published in:
    Movement Disorders, 2021, v. 36, n. 1, p. 251, doi. 10.1002/mds.28302
    By:
    • Yau, Wai Yan;
    • Vandrovcova, Jana;
    • Sullivan, Roisin;
    • Chen, Zhongbo;
    • Zecchinelli, Anna;
    • Cilia, Roberto;
    • Stefano, Duga;
    • Murray, Malgorzata;
    • Carmona, Susana;
    • Chelban, Viorica;
    • Ishiura, Hiroyuki;
    • Tsuji, Shoji;
    • Jaunmuktane, Zane;
    • Turner, Chris;
    • Wood, Nicholas W.;
    • Houlden, Henry
    Publication type:
    Article
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    The Parkinson's Disease Mendelian Randomization Research Portal.

    Published in:
    2019
    By:
    • Noyce, Alastair J.;
    • Bandres‐Ciga, Sara;
    • Kim, Jonggeol;
    • Heilbron, Karl;
    • Kia, Demis;
    • Hemani, Gibran;
    • Xue, Angli;
    • Lawlor, Debbie A.;
    • Smith, George Davey;
    • Duran, Raquel;
    • Gan‐Or, Ziv;
    • Blauwendraat, Cornelis;
    • Gibbs, J. Raphael;
    • Hinds, David A.;
    • Yang, Jian;
    • Visscher, Peter;
    • Cuzick, Jack;
    • Morris, Huw;
    • Hardy, John;
    • Wood, Nicholas W.
    Publication type:
    journal article
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    Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.

    Published in:
    2018
    By:
    • Chelban, Viorica;
    • Wiethoff, Sarah;
    • Fabian‐Jessing, Bjørn K.;
    • Haridy, Nourelhoda A.;
    • Khan, Alaa;
    • Efthymiou, Stephanie;
    • Becker, Esther B. E.;
    • O'Connor, Emer;
    • Hersheson, Joshua;
    • Newland, Katrina;
    • Hojland, Allan Thomas;
    • Gregersen, Pernille A.;
    • Lindquist, Suzanne G.;
    • Petersen, Michael B.;
    • Nielsen, Jørgen E.;
    • Nielsen, Michael;
    • Wood, Nicholas W.;
    • Giunti, Paola;
    • Houlden, Henry;
    • Fabian-Jessing, Bjørn K
    Publication type:
    journal article
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    The phenotypic spectrum of DYT24 due to ANO3 mutations.

    Published in:
    Movement Disorders, 2014, v. 29, n. 7, p. 928, doi. 10.1002/mds.25802
    By:
    • Stamelou, Maria;
    • Charlesworth, Gavin;
    • Cordivari, Carla;
    • Schneider, Susanne A.;
    • Kägi, Georg;
    • Sheerin, Una‐Marie;
    • Rubio‐Agusti, Ignacio;
    • Batla, Amit;
    • Houlden, Henry;
    • Wood, Nicholas W.;
    • Bhatia, Kailash P.
    Publication type:
    Article
    47

    The Phenotypic Spectrum of DYT24 Due to ANO3 Mutations.

    Published in:
    Movement Disorders, 2014, v. 29, p. 928, doi. 10.1002/mds.25802
    By:
    • Stamelou, Maria;
    • Charlesworth, Gavin;
    • Cordivari, Carla;
    • Schneider, Susanne A.;
    • Kägi, Georg;
    • Sheerin, Una-Marie;
    • Rubio-Agusti, Ignacio;
    • Batla, Amit;
    • Houlden, Henry;
    • Wood, Nicholas W.;
    • Bhatia, Kailash P.
    Publication type:
    Article
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    The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 2, p. 232, doi. 10.1002/mds.25248
    By:
    • Duran, Raquel;
    • Mencacci, Niccolo E.;
    • Angeli, Aikaterini V.;
    • Shoai, Maryam;
    • Deas, Emma;
    • Houlden, Henry;
    • Mehta, Atul;
    • Hughes, Derralynn;
    • Cox, Timothy M.;
    • Deegan, Patrick;
    • Schapira, Anthony H.;
    • Lees, Andrew J.;
    • Limousin, Patricia;
    • Jarman, Paul R.;
    • Bhatia, Kailash P.;
    • Wood, Nicholas W.;
    • Hardy, John;
    • Foltynie, Tom
    Publication type:
    Article