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Number of items: 9.

Franke, Maximilian; Conzelmann, Annette; Grünblatt, Edna; Werling, Anna M; Spieles, Helen; Wewetzer, Christoph; Warnke, Andreas; Romanos, Marcel; Walitza, Susanne; Renner, Tobias J (2019). No Association of Variants of the NPY-System With Obsessive-Compulsive Disorder in Children and Adolescents. Frontiers in Molecular Neuroscience, 12:112.

Gerlach, Manfred; Sharma, Manu; Romanos, Marcel; Lesch, Klaus-Peter; Walitza, Susanne; Conzelmann, H Annette; Krüger, Rejko; Renner, Tobias J (2019). Family-based association study on functional α-synuclein polymorphisms in attention-deficit/hyperactivity disorder. ADHD Attention Deficit and Hyperactivity Disorders, 11(1):107-111.

Freitag, Christine M; Lempp, Thomas; Nguyen, T Trang; Jacob, Christian P; Weissflog, Lena; Romanos, Marcel; Renner, Tobias J; Walitza, Susanne; Warnke, Andreas; Rujescu, Dan; Lesch, Klaus-Peter; Reif, Andreas (2016). The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits. Journal of Neural Transmission, 123(8):849-858.

Jarick, Ivonne; Volckmar, Anna-Lena; Pütter, Carolin; Pechlivanis, Sonali; Nguyen, Trang T; Dauvermann, Maria R; Beck, Sebastian; Albayrak, Özgür; Scherag, Susann; Gilsbach, Susanne; Cichon, Sven; Hoffmann, Per; Degenhardt, Franziska A; Nöthen, Markus M; Schreiber, Stefan; Wichmann, H-Erich; Jöckel, Karl-Heinz; Heinrich, Joachim; Tiesler, Carla M T; Faraone, Stephen V; Walitza, Susanne; Sinzig, Judith; Freitag, Christine; Meyer, Jobst; Herpertz-Dahlmann, Beate; Lehmkuhl, Gerd; Renner, Tobias J; Warnke, Andreas; Romanos, Marcel; Lesch, Klaus-Peter; Reif, Andreas; Schimmelmann, Benno G; Hebebrand, Johannes; Scherag, André; Hinney, Anke (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular Psychiatry, 19(1):115-121.

Lin, Michelle K; Freitag, Christine M; Schote, Andrea B; Pálmason, Haukur; Seitz, Christiane; Renner, Tobias J; Romanos, Marcel; Walitza, Susanne; Jacob, Christian P; Reif, Andreas; Warnke, Andreas; Cantor, Rita M; Lesch, Klaus-Peter; Meyer, Jobst (2013). Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 162(8):855-863.

Hamshere, Marian L; Langley, Kate; Martin, Joanna; Agha, Sharifah Shameem; Stergiakouli, Evangelia; Anney, Richard J L; Buitelaar, Jan; Faraone, Stephen V; Lesch, Klaus-Peter; Neale, Benjamin M; Franke, Barbara; Sonuga-Barke, Edmund; Asherson, Philip; Merwood, Andrew; Kuntsi, Jonna; Medland, Sarah E; Ripke, Stephan; Steinhausen, Hans-Christoph; Freitag, Christine; Reif, Andreas; Renner, Tobias J; Romanos, Marcel; Romanos, Jasmin; Warnke, Andreas; Meyer, Jobst; Palmason, Haukur; Vasquez, Alejandro Arias; Lambregts-Rommelse, Nanda; Roeyers, Herbert; Biederman, Joseph; Doyle, Alysa E; Hakonarson, Hakon; Rothenberger, Aribert; Banaschewski, Tobias; Oades, Robert D; McGough, James J; Kent, Lindsey; Williams, Nigel; Owen, Michael J; Holmans, Peter; O'Donovan, Michael C; Thapar, Anita (2013). High loading of polygenic risk for ADHD in children with comorbid aggression. American Journal of Psychiatry, 170(8):909-916.

Weißflog, Lena; Scholz, Claus-Jürgen; Jacob, Christian P; Nguyen, Thuy Trang; Zamzow, Karin; Groß-Lesch, Silke; Renner, Tobias J; Romanos, Marcel; Rujescu, Dan; Walitza, Susanne; Kneitz, Susanne; Lesch, Klaus-Peter; Reif, Andreas (2013). KCNIP4 as a candidate gene for personality disorders and adult ADHD. European Neuropsychopharmacology, 23(6):436-447.

Ribasés, Marta; Ramos-Quiroga, Josep Antoni; Hervás, Amaia; Sánchez-Mora, Cristina; Bosch, Rosa; Bielsa, Anna; Gastaminza, Xavier; Lesch, Klaus-Peter; Reif, Andreas; Renner, Tobias J; Romanos, Marcel; Warnke, Andreas; Walitza, Susanne; Freitag, Christine; Meyer, Jobst; Palmason, Haukur; Casas, Miquel; Bayes, Monica; Cormand, Bru (2012). Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies associsation with BRD1. World Journal of Biological Psychiatry, 13(4):281-292.

Davis, Lea K; Yu, Dongmei; Keenan, Clare L; Gamazon, Eric R; Konkashbaev, Anuar I; Derks, Eske M; Neale, Benjamin M; Yang, Jian; Lee, S Hong; Evans, Patrick; Barr, Cathy L; Bellodi, Laura; Benarroch, Fortu; Berrio, Gabriel Bedoya; Bienvenu, Oscar J; Bloch, Michael H; Blom, Rianne M; Bruun, Ruth D; Budman, Cathy L; Camarena, Beatriz; Campbell, Desmond; Cappi, Carolina; Cardona Silgado, Julio C; Cath, Danielle C; Cavallini, Maria C; Chavira, Denise A; Chouinard, Sylvain; Conti, David V; Cook, Edwin H; Coric, Vladimir; Cullen, Bernadette A; Deforce, Dieter; Delorme, Richard; Dion, Yves; Edlund, Christopher K; Egberts, Karin; Falkai, Peter; Fernandez, Thomas V; Gallagher, Patience J; Garrido, Helena; Geller, Daniel; Girard, Simon L; Grabe, Hans J; Grados, Marco A; Greenberg, Benjamin D; Gross-Tsur, Varda; Haddad, Stephen; Heiman, Gary A; Hemmings, Sian M J; Hounie, Ana G; Illmann, Cornelia; Jankovic, Joseph; Jenike, Michael A; Kennedy, James L; King, Robert A; Kremeyer, Barbara; Kurlan, Roger; Lanzagorta, Nuria; Leboyer, Marion; Leckman, James F; Lennertz, Leonhard; Liu, Chunyu; Lochner, Christine; Lowe, Thomas L; Macciardi, Fabio; McCracken, James T; McGrath, Lauren M; Mesa Restrepo, Sandra C; Moessner, Rainald; Morgan, Jubel; Muller, Heike; Murphy, Dennis L; Naarden, Allan L; Ochoa, William Cornejo; Ophoff, Roel A; Osiecki, Lisa; Pakstis, Andrew J; Pato, Michele T; Pato, Carlos N; Piacentini, John; Pittenger, Christopher; Pollak, Yehuda; Rauch, Scott L; Renner, Tobias J; Reus, Victor I; Richter, Margaret A; Riddle, Mark A; Robertson, Mary M; Romero, Roxana; Rosàrio, Maria C; Rosenberg, David; Rouleau, Guy A; Ruhrmann, Stephan; Ruiz-Linares, Andres; Sampaio, Aline S; Samuels, Jack; Sandor, Paul; Sheppard, Brooke; Singer, Harvey S; Smit, Jan H; Stein, Dan J; Strengman, E; Tischfield, Jay A; Valencia Duarte, Ana V; Vallada, Homero; Van Nieuwerburgh, Filip; Veenstra-Vanderweele, Jeremy; Walitza, Susanne; Wang, Ying; Wendland, Jens R; Westenberg, Herman G M; Shugart, Yin Yao; Miguel, Euripedes C; McMahon, William; Wagner, Michael; Nicolini, Humberto; Posthuma, Danielle; Hanna, Gregory L; Heutink, Peter; Denys, Damiaan; Arnold, Paul D; Oostra, Ben A; Nestadt, Gerald; Freimer, Nelson B; Pauls, David L; Wray, Naomi R; Stewart, S Evelyn; Mathews, Carol A; Knowles, James A; Cox, Nancy J; Scharf, Jeremiah M (2013). Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genetics, 9(10):e1003864.

This list was generated on Mon May 27 15:09:51 2019 CEST.