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frontotemporal disease dementia mutation inclusion bvftd frontotemporal lobar degeneration pathology department frontotemporal dementia degeneration aftld-u protein university lobar neuropathol onset neurology ftld-fu subtype mackenzie ftld-up ftld-ups cases neurol family genotype alzheimer aftld-u cases hospital patient research apolipoprotein symptom centre chromosome mackenzie ir fus pathology brain filament -43 ftld cases family history allele filament inclusion disease group ubiquitin pickering-brown trojanowski study neumann dickson neuropathology variant ucl institute neumann m trojanowski jq ubiquitin-positive bigio institute cause rossor rademakers r motor tdp -43 isaac baker m inclusion body disease medicine chmp 2b mutation rademaker diagnosis queen square grossman m neary revesz t feature broeckhoven kumar-singh mayo clinic snowden js
6 Most Recent Publications
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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
(Article)
Hoglinger, G. Melhem, N.M. Swieten, J.C. van Pahwa, R. Pezzoli, G. Pickering-Brown, S. Poewe, W. Rabano, A. Rajput, A. Reich, S.G. Respondek, G. Roeber, S. Rohrer, J.D. Heutink, P. Ross, O.A. Rossor, M. Sacilotto, G. Seeley, W.W. Seppi, K. Silveira-Moriyama, L. Spina, S. Srulijes, K. St. George-Hyslop, P. Stamelou, M. Wszolek, Z.K. Standaert, D.G. Tesei, S. Tourtellotte, W.W. Trenkwalder, C. Troakes, C. Trojanowski, J.Q. Troncoso, J.C. Deerlin, V.M. Vonsattel, J.P.G. Wenning, G.K. Uitti, R.J. White, C.L. Winter, P. Zarow, C. Zecchinelli, A.L. Antonini, A. Vandrovcova, J. Hurtig, H.I. Gross, R.G. Maetzler, W. Goldwurm, S. Tolosa, E. Dickson, D. Borroni, B. Pastor, P. Cantwell, L.B. Han, M.R. Dillman, A. Brug, M.P. van der Gibbs, J. Cookson, M.R. Hernandez, D.G. Singleton, A. Sleiman, P.M.A. Farrer, M.J. Yu, C.-E. Golbe, L.I. Revesz, T. Hardy, J. Lees, A.J. Devlin, B. Hakonarson, H. Müller, U. Schellenberg, G.D. Wang, L.-S. Albin, R.L. Alonso, E. Apfelbacher, M. Arnold, S.E. Avila, J. Beach, T.G. Beecher, S. Berg, D. Bird, T.D. Bogdanovic, N. Klei, L. Boon, A.J.W. Bordelon, Y. Brice, A. Budka, H. Canesi, M. Chiu, W.Z. Cilia, R. Colosimo, C. Deyn, P.P. de Yebenes, J.G. de Rademakers, R. Donker Kaat, L. Duara, R. Durr, A. Engelborghs, S. Fabbrini, G. Finch, N.A. Flook, R. Frosch, M.P. Gaig, C. Galasko, D. Silva, R. de Gasser, T. Gearing, M. Geller, E.T. Ghetti, B. Graff-Radford, N.R. Grossman, M. Hall, D.A. Hazrati, L.-N. Höllerhage, M. Jankovic, J. Litvan, I. Juncos, J.L. Karydas, A. Kretzschmar, H.A. Leber, I. Lee, V.M.Y. Lieberman, A.P. Lyons, K.E. Mariani, C. Masliah, E. Massey, L.A. Riley, D.E. McLean, C.A. Meucci, N. Miller, B.L. Mollenhauer, B. Möller, J.C. Morris, H. O'Sullivan, S.S. Oertel, W. Ottaviani, D. Padovani, A. |
2011-07-01
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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
(Article)
Hollingworth, P. Harold, D. Dowzell, K. Tikka-Kleemola, P. Breteler, M.M.B. Ikram, M.A. DeStefano, A.L. Fitzpatrick, A.L. Lopez, O.L. Launer, L.J. Seshadri, S. Berr, C. Campion, D. Jones, N. Epelbaum, J. Dartigues, J.-F. Tzourio, C. Alperovitch, A. Lathrop, G.M. Feulner, T.M. Friedrich, P. Riehle, C. Krawczak, M. Schreiber, S. Stretton, A. Mayhaus, M. Nicolhaus, S. Wagenpfeil, S. Steinberg, S. Kallela, M. SnÆdal, J. Björnsson, S. Jonsson, P.V. Chouraki, V. Genier-Boley, B. Thomas, C. Hiltunen, M. Soininen, H. Combarros, O. Zelenika, D. Delepine, M. Bullido, M.J. Pasquier, F. Mateo, I. Frank-Garcia, A. Porcellini, E. Richards, A. Hanon, O. Coto, E. Alvarez, V. Bosco, P. Siciliano, G. Mancuso, M. Panza, F. Solfrizzi, V. Nacmias, B. Sorbi, S. Ivanov, D. Bossù, P. Piccardi, P. Arosio, B. Annoni, G. Seripa, D. Pilotto, A. Scarpini, E. Galimberti, D. Brice, A. Hannequin, D. Widdowson, C. Licastro, F. Holmans, P.A. Riemenschneider, M. Morgan, K. Younkin, S. Owen, M.J. O'Donovan, M. Amouyel, P. Williams, J. Chapman, J. Lovestone, S. Powell, J. Sims, R. Proitsi, P. Lupton, M.K. Brayne, C. Rubinsztein, D.C. Gill, M. Lawlor, B. Lynch, A. Brown, K. Passmore, P.A. Craig, D. Gerrish, A. McGuinness, B. Todd, S. Holmes, C. Mann, D. Smith, A.D. Beaumont, H. Warden, D.R. Wilcock, G.K. Love, S. Kehoe, P.G. Lambert, J.C. Hooper, N.M. Vardy, E.R.L.C. Hardy, J. Mead, S. Fox, N.C. Rossor, M. Collinge, J. Maier, W. Jessen, F. Rüther, E. Carrasquillo, M.M. Schürmann, B. Heun, R. Kölsch, H. Bussche, H. van den Heuser, I. Kornhuber, J. Wiltfang, J. Dichgans, M. Frölich, L. Hampel, H. Abraham, R. Gallacher, J. Hüll, M. Rujescu, D. Giegling, I. Goate, A.M. Kauwe, J.S.K. Cruchaga, C. Nowotny, P. Morris, J.C. Mayo, K. Hamshere, M.L. Sleegers, K. Bettens, K. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Livingston, G. Bass, N.J. Gurling, H. McQuillin, A. Gwilliam, R. Pahwa, J.S. Deloukas, P. Al-Chalabi, A. Shaw, C.E. Tsolaki, M. Singleton, A.B. Guerreiro, R. Mühleisen, T.W. Nöthen, M.M. Moebus, S. Jöckel, K.-H. Moskvina, V. Klopp, N. Wichmann, H.E. Pankratz, V.S. Sando, S.B. Aasly, J.O. Barcikowska, M. Wszolek, Z.K. Dickson, D. Graff-Radford, N.R. Petersen, R.C. |
2011-05-01
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Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
(Article)
Chen-Plotkin, A. Martinez-Lage, M. Weiner, M.F. White, C.L. Brooks, W.S. Halliday, G.M. Kril, J.J. Gearing, M. Beach, T.G. Graff-Radford, N.R. Dickson, D. Rademakers, R. Sleiman, P.M.A. Boeve, B.F. Pickering-Brown, S. Snowden, J. Swieten, J.C. van Heutink, P. Seelaar, H. Murrell, J.R. Ghetti, B. Spina, S. Grafman, J. Hu, W.T. Kaye, J.A. Woltjer, R.L. Mesulam, M. Bigio, E.H. Lladó, A. Miller, B.L. Alzualde, A. Moreno, F. Rohrer, J.D. Mackenzie, I.R.A. Greene, R. Feldman, H.H. Hamilton, R.L. Cruts, M. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Bird, T.D. Cairns, N.J. Goate, A.M. Frosch, M.P. Wood, E.M. Riederer, P.F. Bogdanovic, N. Lee, V.M.Y. Trojanowski, J.Q. Deerlin, V.M. Bing, S. Grossman, M. Schellenberg, G.D. Hatanpaa, K.J. |
2011-04-01
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FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration
(Article)
Urwin, H. Josephs, K.A. Nielsen, J.E. Holm, I.E. Dickson, D. Rademakers, R. Graff-Radford, N.R. Parisi, J.E. Petersen, R.C. Hatanpaa, K.J. White Iii, C.L. Weiner, M.F. Rohrer, J.D. Geser, F. Deerlin, V.M. Trojanowski, J.Q. Miller, B.L. Seeley, W.W. Zee, J. van der Kumar-Singh, S. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Mackenzie, I.R.A. Bigio, E.H. Deng, H-X. Halliday, G.M. Kril, J.J. Munoz, D.G. Mann, D. Pickering-Brown, S. Doodeman, V. Adamson, G. Ghazi-Noori, S Neumann, H.A.M. Fisher, E.M.C Holton, J.L. Revesz, T. Rossor, M.N. Collinge, J. Mead, S. Isaacs, A.M. Authier, A. Seelaar, H. Swieten, J.C. van Brown, J.M. Johannsen, P. |
2010-07-01
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
(Article)
Deerlin, V.M. Sleiman, P.M.A. Arnold, S.E. Mann, D. Pickering-Brown, S. Seelaar, H. Heutink, P. Swieten, J.C. van Murrell, J.R. Ghetti, B. Spina, S. Grafman, J. Martinez-Lage, M. Hodges, J. Spillantini, M.G. Gilman, S. Lieberman, A.P. Kaye, J.A. Woltjer, R.L. Bigio, E.H. Mesulam, M. Al-Sarraj, S. Troakes, C. Chen-Plotkin, A. Rosenberg, R.N. White, C.L. Ferrer, I. Lladó, A. Neumann, H.A.M. Kretzschmar, H.A. Hulette, C. Welsh-Bohmer, K.A. Miller, B.L. Alzualde, A. Wang, L. Munain, A.L. de McKee, A.C. Gearing, M. Levey, A.I. Lah, J.J. Hardy, J. Rohrer, J.D. Lashley, T. Mackenzie, I.R.A. Feldman, H.H. Graff-Radford, N.R. Hamilton, R.L. Dekosky, S.T. Zee, J. van der Kumar-Singh, S. Broeckhoven, C. van Mayeux, R. Vonsattel, J.P. Troncoso, J.C. Kril, J.J. Kwok, J.B.J. Dickson, D. Halliday, G.M. Bird, T.D. Ince, P.G. Shaw, P.J. Cairns, N.J. Morris, J.C. McLean, C.A. DeCarli, C. Ellis, W.G. Freeman, S.H. Rademakers, R. Frosch, M.P. Growdon, J.H. Perl, D.P. Sano, M. Bennett, D.A. Schneider, J.A. Beach, T.G. Reiman, E.M. Woodruff, B.K. Cummings, J.F. Boeve, B. Vinters, H.V. Miller, C.A. Chui, H. Alafuzoff, I. Hartikainen, P. Seilhean, D. Galasko, D. Masliah, E. Cotman, C.W. Tũón, M.T. Grossman, M. Martínez, M.C.C. Munoz, D.G. Carroll, S.L. Marson, D. Riederer, P.F. Bogdanovic, N. Schellenberg, G.D. Hakonarson, H. Trojanowski, J.Q. Lee, V.M.Y. |
2010-03-01
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Apolipoprotein E genotype does not affect the age of onset of dementia in families with define tau mutations
(Article)
Houlden, H. Stevens, M. Jannsen, J.C. Petersen, R.C. Dodd, P. Dark, F. Boeve, B. Dickson, D. Davies, P. Pickering-Brown, S. Mann, D. Adamson, J. Knijff, P. de Lynch, T. Payami, H. Poorkaj, P. Bird, T.D. Schellenberg, G.D. Chadraverty, S. Norton, J. Morris, F.C. Goate, A.M. Hutton, M. Duijn, C.M. van Hardy, J. Rizzu, P. Swieten, J.C. van Heutink, P. Perez-Tur, J. Thomas, V. Baker, M.C. Morris, H. Rossor, M. |
1999-02-05
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