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scopus: 35261965000

Heutink, P.

(Peter Heutink)


disease mutation university patient region association control department chromosome study expansion grn mutations alzheimer research analysis ftld-tdp sample neurology linkage protein family stage institute genet table center hexanucleotide expression brain frontotemporal health medicine dementia neuron individual population hospital grn − ftld-tdp result frontotemporal lobar degeneration cause onset genetic number allele finnish marker genome frontotemporal dementia genotype progranulin pedigree identi parkinson figure value ancestry c .26c haplotype c 9orf frequency genome-wide association study c .1477c european identi fied degeneration als cases c 9orf protein grn mutation american journal lobar american variant neurol locus european ancestry late-onset linkage analysis supranuclear palsy late-onset ad




4 Most Recent Publications

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (Article)
Renton, A. Majounie, E. Kalimo, H. Paetau, A. Abramzon, Y. Remes, A. Kaganovich, A. Scholz, S. Duckworth, J. Ding, J. Harmer, D. Hernandez, D.G. Waite, A. Johnson, J. Mok, K. Ryten, M. Trabzuni, D. Guerreiro, R. Orrell, R. Neal, J. Murray, A. Pearson, J. Jansen, I. Simón-Sánchez, J. Sondervan, D. Seelaar, H. Blake, D. Young, K. Halliwell, N. Callister, J. Toulson, G. Richardson, A. Gerhard, A. Snowden, J. Rollinson, S. Mann, D. Neary, D. Nalls, M.A. Peuralinna, T. Jansson, L. Isoviita, V.-M. Kaivorinne, A.-L. Hölttä-Vuori, M. Ikonen, E. Sulkava, R. Gibbs, J. Benatar, M. Wuu, J. Chiò, A. Restagno, G. Borghero, G. Sabatelli, M. Heckerman, D. Rogaeva, E. Zinman, L. Rothstein, J. Schymick, J. Sendtner, M. Drepper, C. Eichler, E. Alkan, C. Abdullaev, Z. Pack, S. Dutra, A. Pak, E. Hardy, J. Singleton, A. Laaksovirta, H. Williams, N. Heutink, P. Pickering-Brown, S. Morris, H. Tienari, P.J. Traynor, B. Swieten, J.C. van Myllykangas, L.
2011-10-20
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
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