Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions

Van Deerlin, V.M., Sleiman, P.M.A., Martinez-Lage, M. et al. (97 more authors) (2010) Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions. Nature Genetics, 42 (3). pp. 234-239. ISSN 1061-4036,

Metadata

Authors/Creators:
  • Van Deerlin, V.M.
  • Sleiman, P.M.A.
  • Martinez-Lage, M.
  • Chen-Plotkin, A.
  • Wang, L.S.
  • Graff-Radford, N.R.
  • Dickson, D.W.
  • Rademakers, R.
  • Boeve, B.F.
  • Grossman, M.
  • Arnold, S.E.
  • Mann, D.M.A.
  • Pickering-Brown, S.M.
  • Seelaar, H.
  • Heutink, P.
  • van Swieten, J.C.
  • Murrell, J.R.
  • Ghetti, B.
  • Spina, S.
  • Grafman, J.
  • 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.
  • Rosenberg, R.N.
  • White, C.L.
  • Ferrer, I.
  • Llado, A.
  • Neumann, M.
  • Kretzschmar, H.A.
  • Hulette, C.M.
  • Welsh-Bohmer, K.A.
  • Miller, B.L.
  • Alzualde, A.
  • de Munain, A.L.
  • 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.
  • Hamilton, R.L.
  • Dekosky, S.T.
  • van der Zee, J.
  • Kumar-Singh, S.
  • Van Broeckhoven, C.
  • Mayeux, R.
  • Vonsattel, J.P.G.
  • Troncoso, J.C.
  • Kril, J.J.
  • Kwok, J.B.J.
  • 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.
  • 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.
  • Vinters, H.V.
  • Miller, C.A.
  • Chui, H.C.
  • Alafuzoff, I.
  • Hartikainen, P.
  • Seilhean, D.
  • Galasko, D.
  • Masliah, E.
  • Cotman, C.W.
  • Tunon, M.T.
  • Martinez, 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.
Copyright, Publisher and Additional Information: © 2010 Nature America, Inc. This is an author produced version of a paper subsequently published in Mature Genetics. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: GENOME-WIDE ASSOCIATION; GLOBAL GENE-EXPRESSION; GENOTYPE DATA; DEMENTIA; PROGRANULIN; MUTATIONS; CONSENSUS; DISEASE; ONSET; FAMILIES
Dates:
  • Published: March 2010
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Neuroscience (Sheffield)
The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 21 Jan 2016 11:33
Last Modified: 21 Mar 2018 00:38
Published Version: http://dx.doi.org/10.1038/ng.536
Status: Published
Publisher: Nature Publishing Group
Identification Number: https://doi.org/10.1038/ng.536

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