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Number of items: 13.

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.

Renner, T J; Nguyen, T T; Romanos, M; Walitza, S; Röser, C; Reif, A; Schäfer, H; Warnke, A; Gerlach, M; Lesch, K P (2011). No evidence for association between a functional promoter variant of the Norepinephrine Transporter gene SLC6A2 and ADHD in a family-based sample. ADHD Attention Deficit and Hyperactivity Disorders, 3(3):285-289.

Reif, A; Nguyen, T T; Weissflog, L; Jacob, C P; Romanos, M; Renner, T J; Buttenschon, H N; Kittel-Schneider, S; Gessner, A; Weber, H; Neuner, M; Gross-Lesch, S; Zamzow, K; Kreiker, S; Walitza, S; Meyer, J; Freitag, C M; Bosch, R; Casas, M; Gómez, N; Ribasès, M; Bayès, M; Buitelaar, J K; Kiemeney, L A L M; Kooij, J J S; Kan, C C; Hoogman, M; Johansson, S; Jacobsen, K K; Knappskog, P M; Fasmer, O B; Asherson, P; Warnke, A; Grabe, H J; Mahler, J; Teumer, A; Völzke, H; Mors, O N; Schäfer, H; Ramos-Quiroga, J A; Cormand, B; Haavik, J; Franke, B; Lesch, K P (2011). DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders. Neuropsychopharmacology, 36(11):2318-2327.

Hinney, A; Scherag, A; Jarick, I; Albayrak, Ö; Pütter, C; Pechlivanis, S; Dauvermann, M R; Beck, S; Weber, H; Scherag, S; Nguyen, T T; Volckmar, A L; Knoll, N; Faraone, S V; Neale, B M; Franke, B; Cichon, S; Hoffmann, P; Nöthen, M M; Schreiber, S; Jöckel, K H; Wichmann, H E; Freitag, C; Lempp, T; Meyer, J; Gilsbach, S; Herpertz-Dahlmann, B; Sinzig, J; Lehmkuhl, G; Renner, T J; Warnke, A; Romanos, M; Lesch, K P; Reif, A; Schimmelmann, B G; Hebebrand, J; Psychiatric GWAS Consortium, ADHD subgroup (2011). Genome-wide association study in German patients with attention deficit/hyperactivity disorder. American Journal of Medical Genetics. Part B, 156B(8):888-897.

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.

Jans, T; Ball, J; Preiss, M; Haberhausen, M; Warnke, A; Renner, T J (2011). Pervasive refusal syndrome. Three German cases provide further illustration. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 39(5):351-359.

Romanos, M; Ehlis, A C; Baehne, C G; Jacob, C; Renner, T J; Storch, A; Briegel, W; Walitza, S; Lesch, K P; Fallgatter, A J (2010). Reduced NoGo-anteriorisation during continuous performance test in deletion syndrome 22q11.2. Journal of Psychiatric Research, 44(12):768-74.

Schimmelmann, B G; Friedel, S; Nguyen, T T; Sauer, S; Ganz Vogel, C I; Konrad, K; Wilhelm, C; Sinzig, J; Renner, T J; Romanos, M; Palmason, H; Dempfle, A; Walitza, S; Freitag, C; Meyer, J; Linder, M; Schäfer, H; Warnke, A; Lesch, K P; Herpertz-Dahlmann, B; Hinney, A; Hebebrand, J (2009). Exploring the genetic link between RLS and ADHD. Journal of Psychiatric Research, 43(10):941-945.

Walitza, S; Scherag, A; Renner, T J; Hinney, A; Remschmidt, H; Herpertz-Dahlmann, B; Schulze, E D; Schafer, H; Lange, K W; Wewetzer, C; Gerlach, M (2008). Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic system. Journal of Neural Transmission, 115(7):1071-1078.

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.

Renner, T J; Walitza, S; Dempfle, A; Eckert, L; Romanos, M; Gerlach, M; Schäfer, H; Warnke, A; Lesch, K P; Jacob, C (2008). Allelic variants of SNAP25 in a family-based sample of ADHD. Journal of Neural Transmission, 115(2):317-321.

Walitza, S; Renner, T J; Wewetzer, C; Warnke, A (2008). Genetische Befunde bei Zwangsstörungen im Kindes- und Jugendalter und bei Erwachsenen. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 36(1):45-52.

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 Sat Jul 22 01:54:37 2017 CEST.