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Vcjd: The Epidemic That Never Was

Autor: Will, R. G., Knight, R. S. G., Ward, H. J. T., Ironside, J. W., Reuber, Markus, Dealler, Steve, Stewart, Gordon T.

Publikováno v: BMJ: British Medical Journal, 2002 Jul . 325(7355), 102-103.

Externí odkaz: https://www.jstor.org/stable/25451821

New Variant Creutzfeldt-Jakob Disease Is More Common in Britain than Elsewhere

Autor: Ironside, J. W., Knight, R. S. G., Will, R. G., Smith, P. G., Cousens, S. N.

Publikováno v: BMJ: British Medical Journal, 1998 Aug 01. 317(7154), 352-352.

Externí odkaz: https://www.jstor.org/stable/25180011

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

Autor: van der Lee, S. J., Conway, O. J., Jansen, I., Carrasquillo, M. M., Kleineidam, L., van den Akker, E., Hernandez, I., van Eijk, K. R., Stringa, N., Chen, J. A., Zettergren, A., Andlauer, T. F. M., Diez-Fairen, M., Simon-Sanchez, J., Lleo, A., Zetterberg, H., Nygaard, M., Blauwendraat, C., Savage, J. E., Mengel-From, J., Moreno-Grau, S., Wagner, M., Fortea, J., Keogh, M. J., Blennow, K., Skoog, I., Friese, M. A., Pletnikova, O., Zulaica, M., Lage, C., de Rojas, I., Riedel-Heller, S., Illan-Gala, I., Wei, W., Jeune, B., Orellana, A., Then Bergh, F., Wang, X., Hulsman, M., Beker, N., Tesi, N., Morris, C. M., Indakoetxea, B., Collij, L. E., Scherer, M., Morenas-Rodriguez, E., Ironside, J. W., van Berckel, B. N. M., Alcolea, D., Wiendl, H., Strickland, S. L., Pastor, P., Rodriguez Rodriguez, E., Mead, S., Synofzik, M., van Swieten, J. C., Leber, I., Ferrari, R., Hernandez, D. G., Nalls, M. A., Rohrer, J. D., Ramasamy, A., Kwok, J. B. J., Dobson-Stone, C., Schofield, P. R., Halliday, G. M., Hodges, J. R., Piguet, O., Bartley, L., Thompson, E., Borroni, B., Padovani, A., Cruchaga, C., Cairns, N. J., Benussi, L., Binetti, G., Ghidoni, R., Forloni, G., Albani, D., Galimberti, D., Fenoglio, C., Serpente, M., Scarpini, E., Blesa, R., Landqvist Waldo, M., Nilsson, K., Nilsson, C., Mackenzie, I. R. A., Hsiung, G. -Y. R., Mann, D. M. A., Grafman, J., Attems, J., Griffiths, T. D., Mckeith, I. G., Thomas, A. J., Pietrini, P., Huey, E. D., Wassermann, E. M., Baborie, A., Jaros, E., Tierney, M. C., Razquin, C., Ortega-Cubero, S., Alonso, E., Perneczky, R., Diehl-Schmid, J., Alexopoulos, P., Kurz, A., Rainero, I., Rubino, E., Pinessi, L., Rogaeva, E., St George-Hyslop, P., Rossi, G., Tagliavini, F., Giaccone, G., Rowe, J. B., Schlachetzki, J. C. M., Uphill, J., Collinge, J., Danek, A., Van Deerlin, V. M., Grossman, M., Trojanowski, J. Q., van der Zee, J., Van Broeckhoven, C., Cappa, S. F., Hannequin, D., Golfier, V., Vercelletto, M., Brice, A., Nacmias, B., Sorbi, S., Bagnoli, S., Piaceri, I., Nielsen, J. E., Hjermind, L. E., Riemenschneider, M., Mayhaus, M., Ibach, B., Gasparoni, G., Pichler, S., Gu, W., Rossor, M. N., Fox, N. C., Warren, J. D., Spillantini, M. G., Morris, H. R., Rizzu, P., Snowden, J. S., Rollinson, S., Richardson, A., Gerhard, A., Bruni, A. C., Maletta, R., Frangipane, F., Cupidi, C., Bernardi, L., Anfossi, M., Gallo, M., Conidi, M. E., Smirne, N., Baker, M., Josephs, K. A., Parisi, J. E., Seeley, W. W., Miller, B. L., Karydas, A. M., Rosen, H., Dopper, E. G. P., Seelaar, H., Logroscino, G., Capozzo, R., Novelli, V., Puca, A. A., Franceschi, M., Postiglione, A., Milan, G., Sorrentino, P., Kristiansen, M., Chiang, H. -H., Graff, C., Pasquier, F., Rollin, A., Deramecourt, V., Lebouvier, T., Kapogiannis, D., Ferrucci, L., Pickering-Brown, S., Singleton, A. B., Hardy, J., Momeni, P., Boeve, B. F., Petersen, R. C., Ferman, T. J., van Gerpen, J. A., Reinders, M. J. T., Uitti, R. J., Tarraga, L., Maier, W., Dols-Icardo, O., Kawalia, A., Dalmasso, M. C., Boada, M., Zettl, U. K., van Schoor, N. M., Beekman, M., Allen, M., Masliah, E., de Munain, A. L., Pantelyat, A., Wszolek, Z. K., Ross, O. A., Dickson, D. W., Graff-Radford, N. R., Knopman, D., Rademakers, R., Lemstra, A. W., Pijnenburg, Y. A. L., Scheltens, P., Gasser, T., Chinnery, P. F., Hemmer, B., Huisman, M. A., Troncoso, J., Moreno, F., Nohr, E. A., Sorensen, T. I. A., Heutink, P., Sanchez-Juan, P., Posthuma, D., Coppola, G., Varpetian, A., Foroud, T. M., Levey, A. I., Kukull, W. A., Mendez, M. F., Ringman, J., Chui, H., Cotman, C., Decarli, C., Geschwind, D. H., Clarimon, J., Christensen, K., Ertekin-Taner, N., Scholz, S. W., Ramirez, A., Ruiz, A., Slagboom, E., van der Flier, W. M., Holstege, H.

Publikováno v: Acta Neuropathologica, 139(5), 959-962. Springer Verlag

The IPDGC (The International Parkinson Disease Genomics Consortium) and EADB (Alzheimer Disease European DNA biobank) are listed correctly as an author to the article, however, they were incorrectly listed more than once.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::94e443ccb6785ad4f6a618b06412c43d
https://research.vumc.nl/en/publications/d26eb6fa-f1be-4970-b034-171276054602

Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains

Autor: Keogh, M, Wei, W, Aryaman, J, Wilson, I, Talbot, K, Turner, M, McKenzie, C, Troakes, C, Attems, J, Smith, C, Al Sarraj, S, Morris, C, Ansorge, O, Pickering-Brown, S, Jones, N, Ironside, J, Chinnery, P

Publikováno v: Keogh, M J, Wei, W, Aryaman, J, Wilson, I, 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, Jones, N, Ironside, J W & Chinnery, P F 2018, ' Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains ', Journal of Neurology, Neurosurgery & Psychiatry . https://doi.org/10.1136/jnnp-2017-317234
Journal of Neurology, Neurosurgery, and Psychiatry
Keogh, M J, Wei, W, Aryaman, J, Wilson, I, Talbot, K, Turner, M R, Mckenzie, C, Troakes, C, Attems, J, Smith, C, Al Sarraj, S, Morris, C M, Ansorge, O, Pickering-brown, S, Jones, N, Ironside, J W & Chinnery, P F 2018, ' Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains ', Journal of Neurology, Neurosurgery & Psychiatry, vol. 89, no. 8, pp. 813-816 . https://doi.org/10.1136/jnnp-2017-317234

Background Several studies suggest that multiple rare genetic variants in genes causing monogenic forms of neurodegenerative disorders interact synergistically to increase disease risk or reduce the age of onset, but these studies have not been valid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d38c99b145c49fc032a9e297e88f82eb
https://www.repository.cam.ac.uk/handle/1810/273241