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Number of items: 6.

Becker, J; Czamara, D; Hoffmann, P; Landerl, K; Blomert, L; Brandeis, D; Vaessen, A; Maurer, U; Moll, K; Ludwig, K U; Müller-Myhsok, B; Nöthen, M M; Schulte-Körne, G; Schumacher, J (2012). Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. Translational Psychiatry, 2:e136.

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.

Reutter, H; Boyadjiev, S A; Gambhir, L; Ebert, A K; Rösch, W H; Stein, R; Schröder, A; Boemers, T M; Bartels, E; Vogt, H; Utsch, B; Müller, M; Detlefsen, B; Zwink, N; Rogenhofer, S; Gobet, R; Beckers, G M A; Bökenkamp, A; Kajbafzadeh, A M; Jaureguizar, E; Draaken, M; Lakshmanan, Y; Gearhart, J P; Ludwig, M; Nöthen, M M; Jenetzky, E (2011). Phenotype severity in the bladder exstrophy-epispadias complex: Analysis of genetic and nongenetic contributing factors in 441 families from North America and Europe. Journal of Pediatrics, 159(5):825-831.e1.

Suliman, H; Schumacher, J; Becker, T; Cichon, S; Schulze, T G; Propping, P; Rietschel, M; Nöthen, M M; Jamra, R A (2010). Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia. Psychiatric Genetics, 20(2):82-83.

Jamra, R A; Georgi, A; Suliman, H; Klein, K; Villela, A W; Schulze, T G; Propping, P; Cichon, S; Rietschel, M; Nöthen, M M; Schumacher, J (2009). No association between the D-aspartate oxidase locus and schizophrenia. Psychiatric Genetics, 19(1):56.

Abou Jamra, R; Schumacher, J; Becker, T; Dahdouh, F; Ohlraun, S; Suliman, H; Schulze, T G; Tullius, M; Kovalenko, S; Maier, W; Rietschel, M; Propping, P; Nöthen, M M; Cichon, S (2005). No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder. Psychiatric Genetics, 15(3):195-198.

This list was generated on Sun Dec 17 21:45:52 2017 CET.