Works matching AU Mead, Simon


Results: 111
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    Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease.

    Published in:
    JAMA Neurology, 2016, v. 73, n. 4, p. 447, doi. 10.1001/jamaneurol.2015.4885
    By:
    • Mead, Simon;
    • Burnell, Matthew;
    • Lowe, Jessica;
    • Thompson, Andrew;
    • Lukic, Ana;
    • Porter, Marie-Claire;
    • Carswell, Christopher;
    • Kaski, Diego;
    • Kenny, Janna;
    • Mok, Tze How;
    • Bjurstrom, Nina;
    • Franko, Edit;
    • Gorham, Michele;
    • Druyeh, Ronald;
    • Wadsworth, Jonathan D. F.;
    • Jaunmuktane, Zane;
    • Brandner, Sebastian;
    • Hyare, Harpreet;
    • Rudge, Peter;
    • Sarah Walker, A.
    Publication type:
    Article
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    Population Screening for Variant Creutzfeldt-Jakob Disease Using a Novel Blood Test.

    Published in:
    JAMA Neurology, 2014, v. 71, n. 4, p. 421, doi. 10.1001/jamaneurol.2013.6001
    By:
    • Jackson, Graham S.;
    • Burk-Rafel, Jesse;
    • Edgeworth, Julie Ann;
    • Sicilia, Anita;
    • Abdilahi, Sabah;
    • Korteweg, Justine;
    • Mackey, Jonathan;
    • Thomas, Claire;
    • Wang, Guosu;
    • Schott, Jonathan M.;
    • Mummery, Catherine;
    • Chinnery, Patrick F.;
    • Mead, Simon;
    • Collinge, John
    Publication type:
    Article
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    Creutzfeldt-Jakob Disease.

    Published in:
    JAMA Neurology, 2013, v. 70, n. 12, p. 1588, doi. 10.1001/jamaneurol.2013.4412
    By:
    • Benninger, Felix F.;
    • Steiner, Israel;
    • Angus-Leppan, Heather;
    • Rudge, Peter;
    • Mead, Simon;
    • Collinge, John;
    • Vincent, Angela
    Publication type:
    Article
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    Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications.

    Published in:
    2015
    By:
    • Maheshwari, Atul;
    • Fischer, Michael;
    • Gambetti, Pierluigi;
    • Parker, Alicia;
    • Ram, Aarthi;
    • Soto, Claudio;
    • Concha-Marambio, Luis;
    • Cohen, Yvonne;
    • Belay, Ermias D;
    • Maddox, Ryan A;
    • Mead, Simon;
    • Goodman, Clay;
    • Kass, Joseph S;
    • Schonberger, Lawrence B;
    • Hussein, Haitham M
    Publication type:
    journal article
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    Recent US Case of Variant Creutzfeldt-Jakob Disease--Global Implications.

    Published in:
    2015
    By:
    • Maheshwari, Atul;
    • Fischer, Michael;
    • Gambetti, Pierluigi;
    • Parker, Alicia;
    • Ram, Aarthi;
    • Soto, Claudio;
    • Concha-Marambio, Luis;
    • Cohen, Yvonne;
    • Belay, Ermias D.;
    • Maddox, Ryan A.;
    • Mead, Simon;
    • Goodman, Clay;
    • Kass, Joseph S.;
    • Schonberger, Lawrence B.;
    • Hussein, Haitham M.
    Publication type:
    Case Study
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    Prion disease genetics.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 3, p. 273, doi. 10.1038/sj.ejhg.5201544
    By:
    • Mead, Simon
    Publication type:
    Article
    19

    A common single-nucleotide variant in T is strongly associated with chordoma.

    Published in:
    Nature Genetics, 2012, v. 44, n. 11, p. 1185, doi. 10.1038/ng.2419
    By:
    • Pillay, Nischalan;
    • Plagnol, Vincent;
    • Tarpey, Patrick S;
    • Lobo, Samira B;
    • Presneau, Nadège;
    • Szuhai, Karoly;
    • Halai, Dina;
    • Berisha, Fitim;
    • Cannon, Stephen R;
    • Mead, Simon;
    • Kasperaviciute, Dalia;
    • Palmen, Jutta;
    • Talmud, Philippa J;
    • Kindblom, Lars-Gunnar;
    • Amary, M Fernanda;
    • Tirabosco, Roberto;
    • Flanagan, Adrienne M
    Publication type:
    Article
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    PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features.

    Published in:
    Journal of Neurology, 2025, v. 272, n. 4, p. 1, doi. 10.1007/s00415-025-13022-2
    By:
    • Coysh, Thomas;
    • Jaunmuktane, Zane;
    • Hosszu, Laszlo L. P.;
    • Majbour, Nour;
    • Zhang, Fuquan;
    • Campbell, Tracy;
    • Darwent, Lee;
    • Matus, Marcelo Barria;
    • Chan, Edgar;
    • Holm-Mercer, Leah;
    • Mok, Tze How;
    • Wadsworth, Jonathan D. F.;
    • Bieschke, Jan;
    • Nithi, Kannan;
    • Brandner, Sebastian;
    • Smith, Colin;
    • Esiri, Margaret;
    • Collinge, John;
    • Mead, Simon
    Publication type:
    Article
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    Assessing initial MRI reports for suspected CJD patients.

    Published in:
    Journal of Neurology, 2022, v. 269, n. 8, p. 4452, doi. 10.1007/s00415-022-11087-x
    By:
    • Jesuthasan, Aaron;
    • Sequeira, Danielle;
    • Hyare, Harpreet;
    • Odd, Hans;
    • Rudge, Peter;
    • Mok, Tze How;
    • Nihat, Akin;
    • Collinge, John;
    • Mead, Simon
    Publication type:
    Article
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    The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's disease.

    Published in:
    Journal of Neurogenetics, 2025, v. 39, n. 1, p. 16, doi. 10.1080/01677063.2024.2440395
    By:
    • Holm-Mercer, Leah;
    • Coysh, Thomas;
    • Mok, Tze How;
    • Rudge, Peter;
    • Reisz, Zita;
    • Troakes, Claire;
    • Al-Sarraj, Safa;
    • Campbell, Tracy;
    • Hosszu, Laszlo L.P.;
    • Bieschke, Jan;
    • Zhang, Fuquan;
    • Wadsworth, Jonathan D.F.;
    • Smith, Colin;
    • Jenkinson, Jenna;
    • Rittman, Timothy;
    • Brandner, Sebastian;
    • Jaunmuktane, Zane;
    • Collinge, John;
    • Mead, Simon
    Publication type:
    Article
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    Profiles of white matter tract pathology in frontotemporal dementia.

    Published in:
    Human Brain Mapping, 2014, v. 35, n. 8, p. 4163, doi. 10.1002/hbm.22468
    By:
    • Mahoney, Colin J.;
    • Ridgway, Gerard R.;
    • Malone, Ian B.;
    • Downey, Laura E.;
    • Beck, Jonathan;
    • Kinnunen, Kirsi M.;
    • Schmitz, Nicole;
    • Golden, Hannah L.;
    • Rohrer, Jonathan D.;
    • Schott, Jonathan M.;
    • Rossor, Martin N.;
    • Ourselin, Sebastien;
    • Mead, Simon;
    • Fox, Nick C.;
    • Warren, Jason D.
    Publication type:
    Article
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    Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease.

    Published in:
    PLoS ONE, 2019, v. 14, n. 7, p. 1, doi. 10.1371/journal.pone.0218111
    By:
    • Baker, Emily;
    • Sims, Rebecca;
    • Leonenko, Ganna;
    • Frizzati, Aura;
    • Harwood, Janet C.;
    • Grozeva, Detelina;
    • null, null;
    • Morgan, Kevin;
    • Passmore, Peter;
    • Holmes, Clive;
    • Powell, John;
    • Brayne, Carol;
    • Gill, Michael;
    • Mead, Simon;
    • Bossù, Paola;
    • Spalletta, Gianfranco;
    • Goate, Alison M.;
    • Cruchaga, Carlos;
    • Maier, Wolfgang;
    • Heun, Reinhard
    Publication type:
    Article
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    Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patient.

    Published in:
    PLoS Pathogens, 2025, v. 21, n. 2, p. 1, doi. 10.1371/journal.ppat.1012904
    By:
    • Zhang, Fuquan;
    • Joiner, Susan;
    • Linehan, Jacqueline M.;
    • Pintilii, Florin;
    • Nazari, Tamsin;
    • Argentina, Fabio;
    • Preston, Connor;
    • Taema, Maged;
    • Cunningham, Thomas J.;
    • Asante, Emmanuel A.;
    • Mok, Tzehow;
    • Mead, Simon;
    • Brandner, Sebastian;
    • Collinge, John;
    • Wadsworth, Jonathan D.F.
    Publication type:
    Article
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    Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 6, p. 965, doi. 10.1007/s00401-020-02153-7
    By:
    • Gill, O. Noel;
    • Spencer, Yvonne;
    • Richard-Loendt, Angela;
    • Kelly, Carole;
    • Brown, David;
    • Sinka, Katy;
    • Andrews, Nick;
    • Dabaghian, Reza;
    • Simmons, Marion;
    • Edwards, Philip;
    • Bellerby, Peter;
    • Everest, David J.;
    • McCall, Mark;
    • McCardle, Linda M.;
    • Linehan, Jacqueline;
    • Mead, Simon;
    • Hilton, David A.;
    • Ironside, James W.;
    • Brandner, Sebastian
    Publication type:
    Article
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    Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

    Published in:
    Acta Neuropathologica, 2013, v. 126, n. 3, p. 401, doi. 10.1007/s00401-013-1147-0
    By:
    • Fratta, Pietro;
    • Poulter, Mark;
    • Lashley, Tammaryn;
    • Rohrer, Jonathan;
    • Polke, James;
    • Beck, Jon;
    • Ryan, Natalie;
    • Hensman, Davina;
    • Mizielinska, Sarah;
    • Waite, Adrian;
    • Lai, Mang-Ching;
    • Gendron, Tania;
    • Petrucelli, Leonard;
    • Fisher, Elizabeth;
    • Revesz, Tamas;
    • Warren, Jason;
    • Collinge, John;
    • Isaacs, Adrian;
    • Mead, Simon
    Publication type:
    Article
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    Tau, prions and Aβ: the triad of neurodegeneration.

    Published in:
    Acta Neuropathologica, 2011, v. 121, n. 1, p. 5, doi. 10.1007/s00401-010-0691-0
    By:
    • Reiniger, Lilla;
    • Lukic, Ana;
    • Linehan, Jacqueline;
    • Rudge, Peter;
    • Collinge, John;
    • Mead, Simon;
    • Brandner, Sebastian
    Publication type:
    Article
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    Plasma amyloid-β ratios in autosomal dominant Alzheimer's disease: the influence of genotype.

    Published in:
    2021
    By:
    • O'Connor, Antoinette;
    • Pannee, Josef;
    • Poole, Teresa;
    • Arber, Charles;
    • Portelius, Erik;
    • Swift, Imogen J;
    • Heslegrave, Amanda J;
    • Abel, Emily;
    • Willumsen, Nanet;
    • Rice, Helen;
    • Weston, Philip S J;
    • Ryan, Natalie S;
    • Polke, James M;
    • Nicholas, Jennifer M;
    • Mead, Simon;
    • Wray, Selina;
    • Chávez-Gutiérrez, Lucía;
    • Frost, Chris;
    • Blennow, Kaj;
    • Zetterberg, Henrik
    Publication type:
    journal article
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