This title appears in the Scientific Report : 2014 

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders
Hammer, Christian (Corresponding Author)
Degenhardt, Franziska / Priebe, Lutz / Stütz, Adrian M / Heilmann, Stefanie / Waszak, Sebastian M / Schlattl, Andreas / Mangold, Elisabeth / Hoffmann, Per / Nöthen, Markus M / Rietschel, Marcella / Rappold, Gudrun / Korbel, Jan / Cichon, Sven / Niesler, Beate
Strukturelle und funktionelle Organisation des Gehirns; INM-1
Bipolar disorders, 16 (2014) 7, S. 764–768
Oxford Wiley-Blackwell 2014
10.1111/bdi.12207
24754353
Journal Article
Connectivity and Activity
Pathophysiological Mechanisms of Neurological and Psychiatric Diseases
Please use the identifier: http://dx.doi.org/10.1111/bdi.12207 in citations.
Copy number variants (CNVs) have been shown to affect susceptibility for neuropsychiatric disorders. To date, studies implicating the serotonergic system in complex conditions have just focused on single nucleotide polymorphisms (SNPs). We therefore sought to identify novel common genetic copy number polymorphisms affecting genes of the serotonergic system, and to assess their putative role in bipolar affective disorder (BPAD) and major depressive disorder (MDD).