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Number of items: 5.

Elia, J; Glessner, J T; Wang, K; Takahashi, N; Shtir, C J; Hadley, D; Sleiman, P M A; Zhang, H; Kim, C E; Robison, R; Lyon, G J; Flory, J H; Bradfield, J P; Imielinski, M; Hou, C; Frackelton, E C; Chiavacci, R M; Sakurai, T; Rabin, C; Middleton, F A; Thomas, K A; Garris, M; Mentch, F; Freitag, C M; Steinhausen, H C; Todorov, A A; Reif, A; Rothenberger, A; Franke, B; Mick, E O; Roeyers, H; Buitelaar, J; Lesch, K P; Banaschewski, T; Ebstein, R P; Mulas, F; Oades, R D; Sergeant, J; Sonuga-Barke, E; Renner, T J; Romanos, M; Romanos, J; Warnke, A; Walitza, S; Meyer, J; Pálmason, H; Seitz, C; Loo, S K; Smalley, S L; Biederman, J; Kent, L; Asherson, P; Anney, R J L; Gaynor, J W; Shaw, P; Devoto, M; White, P S; Grant, S F A; Buxbaum, J D; Rapoport, J L; Williams, N M; Nelson, S F; Faraone, S V; Hakonarson, H (2011). Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics, 44(1):78-84.

Lesch, K P; Selch, S; Renner, T J; Jacob, C; Nguyen, T T; Hahn, T; Romanos, M; Walitza, S; Shoichet, S; Dempfle, A; Heine, M; Boreatti-Hümmer, A; Romanos, J; Gross-Lesch, S; Zerlaut, H; Wultsch, T; Heinzel, S; Fassnacht, M; Fallgatter, A; Allolio, B; Schäfer, H; Warnke, A; Reif, A; Ropers, H H; Ullmann, R (2011). Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree. Molecular Psychiatry, 16(5):491-503.

Arcos-Burgos, M; Jain, M; Acosta, M T; Shively, S; Stanescu, H; Wallis, D; Domené, S; Vélez, J I; Karkera, J D; Balog, J; Berg, K; Kleta, R; Gahl, W A; Roessler, E; Long, R; Lie, J; Pineda, D; Londoño, A C; Palacio, J D; Arbelaez, A; Lopera, F; Elia, J; Hakonarson, H; Johansson, S; Knappskog, P M; Haavik, J; Ribases, M; Cormand, B; Bayes, M; Casas, M; Ramos-Quiroga, J A; Hervas, A; Maher, B S; Faraone, S V; Seitz, C; Freitag, C M; Palmason, H; Meyer, J; Romanos, M; Walitza, S; Hemminger, U; Warnke, A; Romanos, J; Renner, T; Jacob, C; Lesch, K P; Swanson, J; Vortmeyer, A; Bailey-Wilson, J E; Castellanos, F X; Muenke, M (2010). A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. Molecular Psychiatry, 15(11):1053-1066.

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.

This list was generated on Fri Jul 28 05:22:30 2017 CEST.