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A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders

artículo científico publicado en 2014

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

artículo científico publicado en 2012

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

artículo científico publicado en 2012

Common and rare variant analysis in early-onset bipolar disorder vulnerability

artículo científico publicado en 2014

Copy number variants in German patients with schizophrenia

artículo científico publicado en 2013

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study reveals two new risk loci for bipolar disorder

artículo científico publicado en 2014

Implication of a rare deletion at distal 16p11.2 in schizophrenia

artículo científico publicado en 2013

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

artículo científico publicado en 2014

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

artículo científico publicado en 2013

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

artículo científico publicado en 2011