View Author
disease patient study mutation alzheimer dementia allele control association genotype family analysis polymorphism onset population table genet region protein frequency amyloid chromosome group department plaque university linkage apolipoprotein rotterdam carrier research haplotype brain effect neurology subject rotterdam study netherland model number atherosclerosi individual alzheimer disease sequence sample duijn reference score marker genetic apoe genotype pathology carotid result estrogen level evidence van duijn cm early-onset estrogen use frontotemporal artery neurol family history frontotemporal dementia app 692 mutation locus center broeckhoven factor presenilin prion population-based dutch diagnosis context link late-onset study population function carotid artery atherosclerosis
10 Most Recent Publications
|
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
|
|
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
|
|
A study of the SORL1 Gene in Alzheimer's disease and cognitive function
(Article)
Liu, F. Ikram, M.A. Bettens, K. Broeckhoven, C. van Swieten, J.C. van Hofman, A. Oostra, B.A. Aulchenko, Y.S. Breteler, M.M.B. Duijn, C.M. van Janssens, A.C.J.W. Schuur, M. Koning, I. de Isaacs, A. Struchalin, M.V. Uitterlinden, A.G. Dunnen, J.T. den Sleegers, K. |
2009-09-21
|
|
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
(Article)
Aulchenko, Y.S. Hoppenbrouwers, I.A. Goossens, D. Broeckhoven, C. van Del-Favero, J. Ebers, G.C. Oostra, B.A. Tikka-Kleemola, P. Hintzen, R.Q. Ramagopalan, S.V. Broer, L. Jafari, N. Hillert, J. Link, J. Lundström, W. Greiner, E. Dessa Sadovnick, A. |
2008-12-01
|
|
Cyclin-dependent kinase 5 is associated with risk for Alzheimer's disease in a Dutch population-based study
(Article)
Arias-Vásquez, A. Aulchenko, Y.S. Isaacs, A. Oosterhout, A.A.L.J. van Sleegers, K. Hofman, A. Broeckhoven, C. van Oostra, B.A. Breteler, M.M.B. Tikka-Kleemola, P. |
2008-05-01
|
|
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
(Article)
Haugarvoll, K. Rademakers, R. Guidi, M. Riboldazzi, G. Brown, L. Walter, U. Benecke, R. Berg, D. Gasser, T. Theuns, J. Pals, P. Cras, P. Kachergus, J. Deyn, P.P. de Engelborghs, S. Pickut, B. Uitti, R.J. Foroud, T. Nichols, W.C. Hagenah, J. Klein, C. Samii, A. Zabetian, C.P. Nuytemans, K. Bonifati, V. Broeckhoven, C. van Farrer, M.J. Wszolek, Z.K. Ross, O.A. Gibson, J.M. Tan, E.K. Gaig, C. Tolosa, E. Goldwurm, S. |
2008-04-01
|
|
A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population
(Article)
Liu, F. Arias-Vásquez, A. Heutink, P. Broeckhoven, C. van Oostra, B.A. Tikka-Kleemola, P. Sleegers, K. Aulchenko, Y.S. Kayser, M. Sanchez-Juan, P. Feng, B.-J. Bertoli Avella, A.M. Swieten, J.C. van Axenovich, T.I. |
2007-07-01
|
|
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample
(Article)
Rijk, P. de Cruts, M. Swieten, J.C. van Aulchenko, Y.S. Rademakers, R. Broeck, M. van den Broeckhoven, C. van Sleegers, K. Dermaut, B. Theuns, J. Weckx, S. Duijn, C.M. van Pooter, T. Corsmit, E. Del-Favero, J. |
2005-01-01
|
|
Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.
(Article)
Sleegers, K. Forey, F. Duijn, C.M. van Broeckhoven, C. van Theuns, J. Aulchenko, Y.S. Rademakers, S. Cruts, M. Gool, W.A. van Heutink, P. Oostra, B.A. Swieten, J.C. van |
2004-07-01
|
|
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease
(Article)
Croes, E.A. Alizadeh, B.Z. Duijn, C.M. van Bertoli Avella, A.M. Rademaker, T.A.M. Vergeer-Drop, J. Dermaut, B. Houwing-Duistermaat, J.J. Wientjens, D.P.W.M. Hofman, A. Broeckhoven, C. van |
2004-05-01
|
