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Number of items: 9.

Van Deerlin, V M; Sleiman, P M A; Martinez-Lage, M; Chen-Plotkin, A; Wang, L S; Graff-Radford, N R; Dickson, D W; Rademakers, R; Boeve, B F; Grossman, M; Arnold, S E; Mann, D M A; Pickering-Brown, S M; Seelaar, H; Heutink, P; van Swieten, J C; Murrell, J R; Ghetti, B; Spina, S; Grafman, J; 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; Rosenberg, R N; White, C L; Ferrer, I; Lladó, A; Neumann, M; Kretzschmar, H A; Hulette, C M; Welsh-Bohmer, K A; Miller, B L; Alzualde, A; Lopez de Munain, A; 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; Hamilton, R L; Dekosky, S T; van der Zee, J; Kumar-Singh, S; Van Broeckhoven, C; Mayeux, R; Vonsattel, J P G; Troncoso, J C; Kril, J J; Kwok, J B J; 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; 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; Vinters, H V; Miller, C A; Chui, H C; Alafuzoff, I; Hartikainen, P; Seilhean, D; Galasko, D; Masliah, E; Cotman, C W; Tuñón, M T; 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). Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nature Genetics, 42(3):234-239.

Webster, J A; Myers, A J; Pearson, J V; Craig, D W; Hu-Lince, D; Coon, K D; Zismann, V L; Beach, T; Leung, D; Bryden, L; Halperin, R F; Marlowe, L; Kaleem, M; Huentelman, M J; Joshipura, K; Walker, D; Heward, C B; Ravid, R; Rogers, J; Papassotiropoulos, A; Hardy, J; Reiman, E M; Stephan, D A (2008). Sorl1 as an Alzheimer's disease predisposition gene? Neurodegenerative Diseases, 5(2):60-64.

Huentelman, M J; Papassotiropoulos, A; Craig, D W; Hoerndli, F J; Pearson, J; Huynh, K; Corneveaux, J; Hänggi, Jürgen; Mondadori, C R A; Buchmann, A; Reiman, E M; Henke, K; de Quervain, D; Stephan, D A (2007). Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. Human Molecular Genetics, 16(12):1469-1477.

Coon, K D; Myers, A J; Craig, D W; Webster, J A; Pearson, J V; Lince, D H; Zismann, V L; Beach, T G; Leung, D; Bryden, L; Halperin, R F; Marlowe, L; Kaleem, M; Walker, D G; Ravid, R; Heward, C B; Rogers, J; Papassotiropoulos, A; Reiman, E M; Hardy, J; Stephan, D A (2007). A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. Journal of Clinical Psychiatry, 68(4):613-618.

Pearson, J V; Huentelman, M J; Halperin, R F; Tembe, W D; Melquist, S; Homer, N; Brun, M; Szelinger, S; Coon, K D; Zismann, V L; Webster, J A; Beach, T; Sando, S B; Aasly, J O; Heun, R; Jessen, F; Kölsch, H; Tsolaki, M; Daniilidou, M; Reiman, E M; Papassotiropoulos, A; Hutton, M L; Stephan, D A; Craig, D W (2007). Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. American Journal of Human Genetics, 80(1):126-139.

Papassotiropoulos, A; Stephan, D A; Huentelman, M J; Hoerndli, F J; Craig, D W; Pearson, J V; Huynh, K D; Brunner, F; Corneveaux, J; Osborne, D; Wollmer, M A; Aerni, A; Coluccia, D; Hänggi, Jürgen; Mondadori, C R A; Buchmann, A; Reiman, E M; Caselli, R J; Henke, K; de Quervain, D J F (2006). Common Kibra alleles are associated with human memory performance. Science, 314(5798):475-478.

Papassotiropoulos, A; Fountoulakis, M; Dunckley, T; Stephan, D A; Reiman, E M (2006). Genetics, transcriptomics, and proteomics of Alzheimer's disease. Journal of Clinical Psychiatry, 67(4):652-670.

Coon, K D; Siegel, A M; Yee, S J; Dunckley, T L; Mueller, C; Nagra, R M; Tourtellotte, W W; Reiman, E M; Papassotiropoulos, A; Petersen, F F; Stephan, D A; Kirsch, W M (2006). Preliminary demonstration of an allelic association of the IREB2 gene with Alzheimer's disease. Journal of Alzheimer's Disease, 9(3):225-233.

Coon, K D; Valla, J; Szelinger, S; Schneider, L E; Niedzielko, T L; Brown, K M; Pearson, J V; Halperin, R; Dunckley, T L; Papassotiropoulos, A; Caselli, R J; Reiman, E M; Stephan, D A (2006). Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencing. Mitochondrion, 6(4):194-210.

This list was generated on Wed Jul 26 02:17:35 2017 CEST.