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Number of items: 5.

Giegling, I; Drago, A; Dolžan, V; Plesničar, B K; Schäfer, M; Hartmann, A M; Sander, T; Toliat, M R; Möller, H J; Stassen, H H; Rujescu, D; Serretti, A (2011). Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol. Pharmacogenetics and Genomics, 21(4):206-216.

Giegling, I; Drago, A; Schäfer, M; Hartmann, A M; Sander, T; Toliat, M R; Möller, H J; De Ronchi, D; Stassen, H H; Rujescu, D; Serretti, A (2011). Lack of association between 71 variations located in candidate genes and response to acute haloperidol treatment. Psychopharmacology, 214(3):719-728.

Rutsch, F; Gailus, S; Miousse, I R; Suormala, T; Sagné, C; Toliat, M R; Nürnberg, G; Wittkampf, T; Buers, I; Sharifi, A; Stucki, M; Becker, C; Baumgartner, M; Robenek, H; Marquardt, T; Höhne, W; Gasnier, B; Rosenblatt, D S; Fowler, B; Nürnberg, P (2009). Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nature Genetics, 41(2):234-239.

Rakovic, A; Stiller, B; Djarmati, A; Flaquer, A; Freudenberg, J; Toliat, M R; Linnebank, M; Kostic, V; Lohmann, K; Paus, S; Nürnberg, P; Kubisch, C; Klein, C; Wüllner, U; Ramirez, A (2009). Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. Movement Disorders, 24(3):429-433.

Budde, B S; Namavar, Y; Barth, P G; Poll-The, B T; Nürnberg, G; Becker, C; van Ruissen, F; Weterman, M A J; Fluiter, K; te Beek, E T; Aronica, E; van der Knaap, M S; Höhne, W; Toliat, M R; Crow, Y J; Steinling, M; Voit, T; Roelens, F; Brussel, W; Brockmann, K; Kyllerman, M; Boltshauser, E; Hammersen, G; Willemsen, M A; Basel-Vanagaite, L; Krägeloh-Mann, I; de Vries, L S; Sztriha, L; Muntoni, F; Ferrie, C D; Battini, R; Hennekam, R C M; Grillo, E; Beemer, F A; Stoets, L M E; Wollnik, B; Nürnberg, P; Baas, F (2008). tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nature Genetics, 40(9):1113-1118.

This list was generated on Mon Jul 24 18:54:32 2017 CEST.