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Number of items: 10.

Romanos, M; Freitag, C; Jacob, C; Craig, D W; Dempfle, A; Nguyen, T T; Halperin, R; Walitza, S; Renner, T J; Seitz, C; Romanos, J; Palmason, H; Reif, A; Heine, M; Windemuth-Kieselbach, C; Vogler, C; Sigmund, J; Warnke, A; Schäfer, H; Meyer, J; Stephan, D A; Lesch, K P (2008). Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12. Molecular Psychiatry, 13(5):522-530.

Lesch, K P; Timmesfeld, N; Renner, T J; Halperin, R; Röser, C; Nguyen, T T; Craig, D W; Romanos, J; Heine, M; Meyer, J; Freitag, C; Warnke, A; Romanos, M; Schäfer, H; Walitza, S; Reif, A; Stephan, D A; Jacob, C (2008). Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. Journal of Neural Transmission, 115(11):1573-1585.

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 Sat Oct 21 12:49:15 2017 CEST.