Prof Stuart Pickering-BrownPhD

Professor of Neurogenetics

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  1. Article › Research › Peer-reviewed
  2. Published

    Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource

    Keogh, M. J., Wei, W., Wilson, I., Coxhead, J., Ryan, S., Rollinson, S., Griffin, H., Kurzawa-Akanbi, M., Santibanez-Koref, M., Talbot, K., Turner, M. R., McKenzie, C. A., Troakes, C., Attems, J., Smith, C., Al Sarraj, S., Morris, C. M., Ansorge, O., Pickering-Brown, S., Ironside, J. W. & 1 others, Chinnery, P. F., 1 Jan 2017, In : Genome research. 27, 1, p. 165-173 9 p.

    Research output: Contribution to journalArticle

  3. Published

    Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Alzheimer Disease Genetics Consortium (ADGC), European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE), & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), 2019, In : Nature Genetics. 51, 3, p. 414-430 17 p.

    Research output: Contribution to journalArticle

  4. Published

    Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

    Schott, J. M., Crutch, S. J., Carrasquillo, M. M., Uphill, J., Shakespeare, T. J., Ryan, N. S., Yong, K. X. X., Lehmann, M., Ertekin-Taner, N., Graff-Radford, N. R., Boeve, B. F., Murray, M. E., Khan, Q. U. A., Petersen, R. C., Dickson, D. W., Knopman, D. S., Rabinovici, G. D., Miller, B. L., Gonzalez, A. S., Gil-Néciga, E. & 24 others, Snowden, J. S., Harris, J., Pickering-Brown, S. M., Louwersheimer, E., van der Flier, W. M., Scheltens, P., Pijnenburg, Y. A., Galasko, D., Sarazin, M., Dubois, B., Magnin, E., Galimberti, D., Scarpini, E., Cappa, S. F., Hodges, J. R., Halliday, G. M., Bartley, L., Carrillo, M. C., Bras, J. T., Hardy, J., Rossor, M. N., Collinge, J., Fox, N. C. & Mead, S., 15 Mar 2016, In : Alzheimer's and Dementia.

    Research output: Contribution to journalArticle

  5. Published

    Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

    ITALSGEN Consortium, 2018, In : Neuron. 97, 6, p. 1268-1283.e6

    Research output: Contribution to journalArticle

  6. Published

    Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases.

    Guerreiro, R., Escott-Price, V., Darwent, L., Parkkinen, L., Ansorge, O., Hernandez, D. G., Nalls, M. A., Clark, L., Honig, L., Marder, K., van der Flier, W., Holstege, H., Louwersheimer, E., Lemstra, A., Scheltens, P., Rogaeva, E., St George-Hyslop, P., Londos, E., Zetterberg, H., Ortega-Cubero, S. & 27 others, Pastor, P., Ferman, T. J., Graff-Radford, N. R., Ross, O. A., Barber, I., Braae, A., Brown, K., Morgan, K., Maetzler, W., Berg, D., Troakes, C., Al-Sarraj, S., Lashley, T., Compta, Y., Revesz, T., Lees, A., Cairns, N. J., Halliday, G. M., Mann, D., Pickering-Brown, S., Powell, J., Lunnon, K., Lupton, M. K., Dickson, D., Hardy, J., Singleton, A. & Bras, J., 2 Nov 2015, In : Neurobiology of Aging.

    Research output: Contribution to journalArticle

  7. Published

    Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.

    Mok, K. Y., Schneider, S. A., Trabzuni, D., Stamelou, M., Edwards, M., Kasperaviciute, D., Pickering-Brown, S., Silverdale, M., Hardy, J. & Bhatia, K. P., Feb 2014, In : Movement disorders : official journal of the Movement Disorder Society. 29, 2

    Research output: Contribution to journalArticle

  8. Published

    Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: Classification and relation to clinical phenotype

    Mackenzie, I. R. A., Baborie, A., Pickering-Brown, S., Plessis, D. D., Jaros, E., Perry, R. H., Neary, D., Snowden, J. S. & Mann, D. M. A., Nov 2006, In : Acta neuropathologica. 112, 5, p. 539-549 10 p.

    Research output: Contribution to journalArticle

  9. Published

    Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene

    Davidson, Y. S., Flood, L., Robinson, A. C., Nihei, Y., Mori, K., Rollinson, S., Richardson, A., Benson, B. C., Jones, M., Snowden, J. S., Pickering-Brown, S., Haass, C., Lashley, T. & Mann, D. M. A., 21 Apr 2017, In : Acta Neuropathologica Communications. 5, 1, p. 31

    Research output: Contribution to journalArticle

  10. Published

    Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration

    Davidson, Y. S., Robinson, A. C., Flood, L., Rollinson, S., Benson, B. C., Asi, Y. T., Richardson, A., Jones, M., Snowden, J. S., Pickering-Brown, S., Lashley, T. & Mann, D. M. A., 30 Jun 2017, In : Acta Neuropathologica Communications. 5, 1, 12 p., 54.

    Research output: Contribution to journalArticle

  11. Published

    Histone deacetylases (HDACs) in Frontotemporal Lobar Degeneration.

    Whitehouse, A., Doherty, K., Yeh, H. H., Robinson, A. C., Rollinson, S., Pickering-Brown, S., Snowden, J., Thompson, J. C., Davidson, Y. S. & Mann, D. M. A., 2015, In : Neuropathology and Applied Neurobiology. 41, 2, p. 245-57 187 p.

    Research output: Contribution to journalArticle

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