Correspondence (reply): In Reply

Por Walitza, Susanne
Publicado em 2011

Real-Time Impedance-based Cell Analyzer as a Tool to Delineate Molecular Pathways Involved in Neurotoxicity and Neuroprotection in a Neuronal Cell Line

Por Marinova, Zoya, Walitza, Susanne, Grünblatt, Edna
Publicado no J Vis Exp (2014)

The neurobiological link between OCD and ADHD

Por Brem, Silvia, Grünblatt, Edna, Drechsler, Renate, Riederer, Peter, Walitza, Susanne
Publicado em 2014

Association study in siblings and case-controls of serotonin- and oxytocin-related genes with high functioning autism

Por Nyffeler, Johanna, Walitza, Susanne, Bobrowski, Elise, Gundelfinger, Ronnie, Grünblatt, Edna
Publicado no J Mol Psychiatry (2014)

Cognitive flexibility in adolescence: Neural and behavioral mechanisms of reward prediction error processing in adaptive decision making during development

Por Hauser, Tobias U., Iannaccone, Reto, Walitza, Susanne, Brandeis, Daniel, Brem, Silvia
Publicado no Neuroimage (2015)

Does Methylphenidate Cause a Cytogenetic Effect in Children with Attention Deficit Hyperactivity Disorder?

Por Walitza, Susanne, Werner, Birgit, Romanos, Marcel, Warnke, Andreas, Gerlach, Manfred, Stopper, Helga
Publicado em 2007

Obsessive-Compulsive Disorder in Children and Adolescents

Por Walitza, Susanne, Melfsen, Siebke, Jans, Thomas, Zellmann, Henrike, Wewetzer, Christoph, Warnke, Andreas
Publicado em 2011

Increased frontal sleep slow wave activity in adolescents with major depression

Por Tesler, Noemi, Gerstenberg, Miriam, Franscini, Maurizia, Jenni, Oskar G., Walitza, Susanne, Huber, Reto
Publicado no Neuroimage Clin (2015)

Tetrahydroisoquinoline derivatives: a new perspective on monoaminergic dysfunction in children with ADHD?

Por Roessner, Veit, Walitza, Susanne, Riederer, Franz, Hünnerkopf, Regina, Rothenberger, Aribert, Gerlach, Manfred, Moser, Andreas
Publicado em 2007

Early somatosensory processing in individuals at risk for developing psychoses

Por Hagenmuller, Florence, Heekeren, Karsten, Theodoridou, Anastasia, Walitza, Susanne, Haker, Helene, Rössler, Wulf, Kawohl, Wolfram
Publicado em 2014

Temporally Dissociable Contributions of Human Medial Prefrontal Subregions to Reward-Guided Learning

Por Hauser, Tobias U., Hunt, Laurence T., Iannaccone, Reto, Walitza, Susanne, Brandeis, Daniel, Brem, Silvia, Dolan, Raymond J.
Publicado no J Neurosci (2015)

Trio study and meta-analysis support the association of genetic variation at the serotonin transporter with early-onset obsessive-compulsive disorder

Por Walitza, Susanne, Marinova, Zoya, Grünblatt, Edna, Lazic, Stanley E., Remschmidt, Helmut, Vloet, Timo D., Wendland, Jens R.
Publicado em 2014

Characterization of cognitive deficits in spontaneously hypertensive rats, accompanied by brain insulin receptor dysfunction

Por Grünblatt, Edna, Bartl, Jasmin, Iuhos, Diana-Iulia, Knezovic, Ana, Trkulja, Vladimir, Riederer, Peter, Walitza, Susanne, Salkovic-Petrisic, Melita
Publicado no J Mol Psychiatry (2015)

Aberrant Coupling Within and Across the Default Mode, Task-Positive, and Salience Network in Subjects at Risk for Psychosis

Por Wotruba, Diana, Michels, Lars, Buechler, Roman, Metzler, Sibylle, Theodoridou, Anastasia, Gerstenberg, Miriam, Walitza, Susanne, Kollias, Spyros, Rössler, Wulf, Heekeren, Karsten
Publicado em 2014

Early Recognition of High Risk of Bipolar Disorder and Psychosis: An Overview of the ZInEP “Early Recognition” Study

Por Theodoridou, Anastasia, Heekeren, Karsten, Dvorsky, Diane, Metzler, Sibylle, Franscini, Maurizia, Haker, Helene, Kawohl, Wolfram, Rüsch, Nicolas, Walitza, Susanne, Rössler, Wulf
Publicado em 2014

Autism spectrum disorder associated with low serotonin in CSF and mutations in the SLC29A4 plasma membrane monoamine transporter (PMAT) gene

Por Adamsen, Dea, Ramaekers, Vincent, Ho, Horace TB, Britschgi, Corinne, Rüfenacht, Véronique, Meili, David, Bobrowski, Elise, Philippe, Paule, Nava, Caroline, Van Maldergem, Lionel, Bruggmann, Rémy, Walitza, Susanne, Wang, Joanne, Grünblatt, Edna, Thöny, Beat
Publicado no Mol Autism (2014)

Case-Control Genome-Wide Association of Attention-Deficit / Hyperactivity Disorder

Por Neale, Benjamin M., Medland, Sarah, Ripke, Stephan, Anney, Richard J.L., Asherson, Philip, Buitelaar, Jan, Franke, Barbara, Gill, Michael, Kent, Lindsey, Holmans, Peter, Middleton, Frank, Thapar, Anita, Lesch, Klaus-Peter, Faraone, Stephen V., Daly, Mark, Nguyen, Thuy Trang, Schäfer, Helmut, Steinhausen, Hans-Christoph, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Freitag, Christine, Meyer, Jobst, Palmason, Haukur, Rothenberger, Aribert, Hawi, Ziarih, Sergeant, Joseph, Roeyers, Herbert, Biederman, Joseph
Publicado em 2010

DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders

Por Reif, Andreas, Nguyen, T Trang, Weißflog, Lena, Jacob, Christian P, Romanos, Marcel, Renner, Tobias J, Buttenschon, Henriette N, Kittel-Schneider, Sarah, Gessner, Alexandra, Weber, Heike, Neuner, Maria, Gross-Lesch, Silke, Zamzow, Karin, Kreiker, Susanne, Walitza, Susanne, Meyer, Jobst, Freitag, Christine M, Bosch, Rosa, Casas, Miquel, Gómez, Nuria, Ribasès, Marta, Bayès, Mónica, Buitelaar, Jan K, Kiemeney, Lambertus ALM, Kooij, JJ Sandra, Kan, Cees C, Hoogman, Martine, Johansson, Stefan, Jacobsen, Kaya K, Knappskog, Per M, Fasmer, Ole B, Asherson, Phil, Warnke, Andreas, Grabe, Hans-Jörgen, Mahler, Jessie, Teumer, Alexander, Völzke, Henry, Mors, Ole N, Schäfer, Helmut
Publicado em 2012

DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders

Por Reif, Andreas, Nguyen, T Trang, Weißflog, Lena, Jacob, Christian P, Romanos, Marcel, Renner, Tobias J, Buttenschon, Henriette N, Kittel-Schneider, Sarah, Gessner, Alexandra, Weber, Heike, Neuner, Maria, Gross-Lesch, Silke, Zamzow, Karin, Kreiker, Susanne, Walitza, Susanne, Meyer, Jobst, Freitag, Christine M, Bosch, Rosa, Casas, Miquel, Gómez, Nuria, Ribasès, Marta, Bayès, Mónica, Buitelaar, Jan K, Kiemeney, Lambertus A L M, Kooij, J J Sandra, Kan, Cees C, Hoogman, Martine, Johansson, Stefan, Jacobsen, Kaya K, Knappskog, Per M, Fasmer, Ole B, Asherson, Phil, Warnke, Andreas, Grabe, Hans-Jörgen, Mahler, Jessie, Teumer, Alexander, Völzke, Henry, Mors, Ole N, Schäfer, Helmut, Ramos-Quiroga, Josep Antoni, Cormand, Bru, Haavik, Jan, Franke, Barbara, Lesch, Klaus-Peter
Publicado em 2011

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

Por Williams, Nigel M., Franke, Barbara, Mick, Eric, Anney, Richard J.L., Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael C., Owen, Michael J., Holmans, Peter, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter, Faraone, Stephen V.
Publicado em 2012