<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gottschalk MG</submitter><funding>Engineering and Physical Sciences Research Council</funding><pagination>pyu019</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4368887</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(2)</volume><pubmed_abstract>Although genetic studies suggest an overlap in risk alleles across the major psychiatric disorders, disease signatures reflecting overlapping symptoms have not been found. Profiling studies have identified candidate protein markers associated with specific disorders of the psychoaffective spectrum, but this has always been done in a selective fashion without accounting for the entire proteome composition of the system under investigation. Employing an orthogonal system-based proteomic enrichment approach based on label-free liquid chromatography mass spectrometry, we analyzed anterior prefrontal human post-mortem brain tissue of patients affected by schizophrenia (n = 23), bipolar disorder (n = 23), major depressive disorder with (n = 12) and without psychotic features (n = 11), and health</pubmed_abstract><journal>The international journal of neuropsychopharmacology</journal><pubmed_title>Proteomic enrichment analysis of psychotic and affective disorders reveals common signatures in presynaptic glutamatergic signaling and energy metabolism.</pubmed_title><pmcid>PMC4368887</pmcid><funding_grant_id>1351685</funding_grant_id><pubmed_authors>Gottschalk MG</pubmed_authors><pubmed_authors>Guest PC</pubmed_authors><pubmed_authors>Wesseling H</pubmed_authors><pubmed_authors>Bahn S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteomic enrichment analysis of psychotic and affective disorders reveals common signatures in presynaptic glutamatergic signaling and energy metabolism.</name><description>Although genetic studies suggest an overlap in risk alleles across the major psychiatric disorders, disease signatures reflecting overlapping symptoms have not been found. Profiling studies have identified candidate protein markers associated with specific disorders of the psychoaffective spectrum, but this has always been done in a selective fashion without accounting for the entire proteome composition of the system under investigation. Employing an orthogonal system-based proteomic enrichment approach based on label-free liquid chromatography mass spectrometry, we analyzed anterior prefrontal human post-mortem brain tissue of patients affected by schizophrenia (n = 23), bipolar disorder (n = 23), major depressive disorder with (n = 12) and without psychotic features (n = 11), and health</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2025-04-18T18:54:39.358Z</modification><creation>2019-03-27T01:48:36Z</creation></dates><accession>S-EPMC4368887</accession><cross_references><pubmed>25609598</pubmed><doi>10.1093/ijnp/pyu019</doi></cross_references></HashMap>