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scopus: 7005566654

Heutink, P.

(Peter Heutink)

Supervisor (promotor) of 6 dissertations


patient disease mutation study family dementia population protein analysis chromosome region brain control alzheimer allele association marker frontotemporal dementia sample parkinson genet frontotemporal parkinsonism linkage onset disorder table genotype neurology netherland factor neurol result polymorphism group diabetes genetic research university haplotype effect type 2 diabetes expression frequency department supranuclear palsy individual locus subject sequence cohort rotterdam tau gene family history genomic inclusion frontotemporal lobar degeneration score level evidence diagnosis signi pathology antibody autosomal neuron number history center supranuclear isoform model microtubule tau mutations degeneration early-onset dutch tau protein change syndrome




10 Most Recent Publications

Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's disease (Article)
Lau, L. de Verbaan, D. Marinus, J. Heutink, P. Hilten, J.J. van
2012-01-01
Genome-wide association study confirms extant PD risk loci among the Dutch (Article)
Simón-Sánchez, J. Hilten, J.J. van Bloem, B. Dijk, K.D. van Rivadeneira Ramirez, F. Hofman, A. Uitterlinden, A.G. Rizzu, P. Bochdanovits, Z. Singleton, A.B. Heutink, P. Warrenburg, B. van de Post, B. Berendse, H.W. Arepalli, S. Hernandez, D.G. Bie, R.M.A. de Velseboer, D. Scheffer, H.
2011-06-01
Translational research in genomics of Alzheimer's disease: A review of current practice and future perspectives (Article)
Mihaescu, R. Detmar, S.B. Cornel, M.C. Flier, W.M. van der Heutink, P. Hol, E.M. Olde Rikkert, M.G.M. Duijn, C.M. van Janssens, A.C.J.W.
2010-07-19
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
Variation at GRN3′-UTR rs5848 is not associated with a risk of frontotemporal lobar degenerationin Dutch population (Article)
Simón-Sánchez, J. Seelaar, H. Bochdanovits, Z. Deeg, D.J.H. Swieten, J.C. van Heutink, P.
2009-10-22
Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways (Article)
Bronner, I.F. Bochdanovits, Z. Rizzu, P. Kamphorst, W. Ravid, R. Swieten, J.C. van Heutink, P.
2009-08-28
Familial aggregation of parkinsonism in progressive supranuclear palsy (Article)
Donker Kaat, L. Boon, A.J.W. Azmani, A. Kamphorst, W. Breteler, M.M.B. Anar, B. Heutink, P. Swieten, J.C. van
2009-07-01
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
Tauopathies with parkinsonism: Clinical spectrum, neuropathologic basis, biological markers, and treatment options (Article)
Ludolph, A.C. Kassubek, J. Hoglinger, G. Jamrozik, Z. Jellinger, K.A. Kazantsev, A. Kretzschmar, H. Lang, A.E. Litvan, I. Lucas, J.J. McGeer, P.L. Melquist, S. Landwehrmeyer, B.G. Oertel, W. Otto, M. Paviour, D. Reum, T. Saint-Raymond, A. Steele, J.C. Tolnay, M. Tumani, H. Swieten, J.C. van Vanier, M.T. Mandelkow, E. Vonsattel, J.P. Wagner, S. Wszolek, Z.K. Burn, D.J. Caparros-Lefebvre, D. Frey, K.A. Yebenes, J.G. de Gasser, T. Heutink, P.
2009-03-01
A functional polymorphism under positive evolutionary selection in ADRB2 is associated with human intelligence with opposite effects in the young and the elderly (Article)
Bochdanovits, Z. Gosso, F.M. Deary, I.J. Geus, E.J.C. de Boomsma, D.I. Heutink, P. Posthuma, D. Berg, L. van den Rizzu, P. Polderman, T.J.C. Pardo Cortes, L.M. Houlihan, L.M. Luciano, M. Starr, J.M. Harris, S.E.
2009-01-01