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scopus: 6602533808

Rademakers, R.

(Rosa Rademakers)


family disease patient mutation dementia frontotemporal bvftd inclusion frontotemporal lobar degeneration 7 q 36 linkage study alzheimer frontotemporal dementia allele onset pathology family 1270 protein analysis duijn degeneration aftld-u broeckhoven haplotype lobar neuropathol department van duijn research marker region individual early-onset ad university number ftld-fu candidate region cruts m sequence subtype mackenzie paxip chromosome control ftld-up table early-onset neurology ftld-ups cases van duijn cm rademaker frequency brain diagnosis mutation analysis alzheimer disease paxip 1 aftld-u cases center genet hofman symptom candidate centre mackenzie ir fus pathology dutch backhovens h sample presenilin proband -43 ftld cases neurol 80- bp allele population-based study flanders interuniversity institute family history coding




10 Most Recent Publications

Symmetrical corticobasal syndrome caused by a novel c.314dup progranulin mutation (Article)
Dopper, E.G.P. Seelaar, H. Chiu, W.Z. Koning, I. de Minkelen, R. van Baker, M.C. Rozemuller, A.J.M. Rademakers, R. Swieten, J.C. van
2011-11-01
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
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
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration (Article)
Rollinson, S. Rizzu, P. Mead, S. Collinge, J. Rossor, M. Akay, E. Guerreiro, R. Rademakers, R. Morrison, K.E. Pastor, P. Alonso, E. Martinez-Lage, P. Sikkink, S. Graff-Radford, N.R. Neary, D. Heutink, P. Mann, D.M.A. Swieten, J.C. van Pickering-Brown, S. Baker, M.C. Halliwell, N. Snowden, J. Traynor, B.J. Ruano, D. Cairns, N.J. Rohrer, J.D.
2009-04-01
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
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
Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family (Letter To Editor)
Rademakers, R. Broeck, M. van den Sleegers, K. Duijn, C.M. van Broeckhoven, C. van Cruts, M.
2004-02-01
Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease (Article)
Cruts, M. Dermaut, B. Rademakers, R. Roks, G. Munteanu, G. Duijn, C.M. van Broeck, M. van den Broeckhoven, C. van
2001-11-02
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