View Author
mutation university disease grn mutations department ftld-tdp research neurology stage control study association patient brain center alzheimer table grn − ftld-tdp analysis sample frontotemporal institute frontotemporal lobar degeneration protein region medicine hospital progranulin health result parkinson expression ancestry c .26c dementia c .1477c genotype grn mutation frontotemporal dementia degeneration lobar neurol european ancestry supranuclear palsy subject frequency school erasmus mc onset feature grant pathology stage 1 h 1/h genet nature rotterdam user ©2011 american european genome-wide value family right inversion .1477c van deerlin association results genetic motor neuron disease p.r 493x genome-wide association study death clinic allele number spain individual p.a 9d laboratory medicine variant
2 Most Recent Publications
|
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
|
|
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
|
