<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guimond S</submitter><funding>NCATS NIH HHS</funding><funding>Emerging Research Innovators in Mental Health</funding><funding>NIMH NIH HHS</funding><funding>National Institute of Mental Health</funding><funding>Fonds de recherche du Québec – Santé</funding><pagination>1706-1717</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8530385</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>47(6)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Brain-based Biotypes for psychotic disorders have been developed as part of the B-SNIP consortium to create neurobiologically distinct subgroups within idiopathic psychosis, independent from traditional phenomenological diagnostic methods. In the current study, we aimed to validate the Biotype model by assessing differences in volume and shape of the amygdala and hippocampus contrasting traditional clinical diagnoses with Biotype classification.&lt;h4>Methods&lt;/h4>A total of 811 participants from 6 sites were included: probands with schizophrenia (n = 199), schizoaffective disorder (n = 122), psychotic bipolar disorder with psychosis (n = 160), and healthy controls (n = 330). Biotype classification, previously developed using cognitive and electrophysiological data and K-mean</pubmed_abstract><journal>Schizophrenia bulletin</journal><pubmed_title>A Diagnosis and Biotype Comparison Across the Psychosis Spectrum: Investigating Volume and Shape Amygdala-Hippocampal Differences from the B-SNIP Study.</pubmed_title><pmcid>PMC8530385</pmcid><funding_grant_id>MH077945</funding_grant_id><funding_grant_id>R01 MH077862</funding_grant_id><funding_grant_id>MH078113</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>MH077862</funding_grant_id><funding_grant_id>MH077851</funding_grant_id><pubmed_authors>Kelly S</pubmed_authors><pubmed_authors>Guimond S</pubmed_authors><pubmed_authors>Clementz BA</pubmed_authors><pubmed_authors>Gu F</pubmed_authors><pubmed_authors>Tamminga C</pubmed_authors><pubmed_authors>Chakravarty MM</pubmed_authors><pubmed_authors>Keshavan M</pubmed_authors><pubmed_authors>Mike L</pubmed_authors><pubmed_authors>Devenyi GA</pubmed_authors><pubmed_authors>Pearlson G</pubmed_authors><pubmed_authors>Shannon H</pubmed_authors><pubmed_authors>Sweeney JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Diagnosis and Biotype Comparison Across the Psychosis Spectrum: Investigating Volume and Shape Amygdala-Hippocampal Differences from the B-SNIP Study.</name><description>&lt;h4>Objective&lt;/h4>Brain-based Biotypes for psychotic disorders have been developed as part of the B-SNIP consortium to create neurobiologically distinct subgroups within idiopathic psychosis, independent from traditional phenomenological diagnostic methods. In the current study, we aimed to validate the Biotype model by assessing differences in volume and shape of the amygdala and hippocampus contrasting traditional clinical diagnoses with Biotype classification.&lt;h4>Methods&lt;/h4>A total of 811 participants from 6 sites were included: probands with schizophrenia (n = 199), schizoaffective disorder (n = 122), psychotic bipolar disorder with psychosis (n = 160), and healthy controls (n = 330). Biotype classification, previously developed using cognitive and electrophysiological data and K-mean</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-09T02:49:54.037Z</modification><creation>2026-05-04T03:11:11.031Z</creation></dates><accession>S-EPMC8530385</accession><cross_references><pubmed>34254147</pubmed><doi>10.1093/schbul/sbab071</doi></cross_references></HashMap>