This title appears in the Scientific Report :
2014
Please use the identifier:
http://dx.doi.org/10.1111/bdi.12207 in citations.
A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders
A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders
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 numbe...
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Personal Name(s): | Hammer, Christian (Corresponding Author) |
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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 | |
Contributing Institute: |
Strukturelle und funktionelle Organisation des Gehirns; INM-1 |
Published in: | Bipolar disorders, 16 (2014) 7, S. 764–768 |
Imprint: |
Oxford
Wiley-Blackwell
2014
|
DOI: |
10.1111/bdi.12207 |
PubMed ID: |
24754353 |
Document Type: |
Journal Article |
Research Program: |
Connectivity and Activity Pathophysiological Mechanisms of Neurological and Psychiatric Diseases |
Publikationsportal JuSER |
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). |