<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Park BY</submitter><funding>Canada First Research Excellence Fund (Fonds d'excellence en recherche Apogée Canada)</funding><funding>Norges Forskningsråd (Research Council of Norway)</funding><pagination>1024</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9515219</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>It is increasingly recognized that multiple psychiatric conditions are underpinned by shared neural pathways, affecting similar brain systems. Here, we carried out a multiscale neural contextualization of shared alterations of cortical morphology across six major psychiatric conditions (autism spectrum disorder, attention deficit/hyperactivity disorder, major depression disorder, obsessive-compulsive disorder, bipolar disorder, and schizophrenia). Our framework cross-referenced shared morphological anomalies with respect to cortical myeloarchitecture and cytoarchitecture, as well as connectome and neurotransmitter organization. Pooling disease-related effects on MRI-based cortical thickness measures across six ENIGMA working groups, including a total of 28,546 participants (12,876 patients</pubmed_abstract><journal>Communications biology</journal><pubmed_title>Multiscale neural gradients reflect transdiagnostic effects of major psychiatric conditions on cortical morphology.</pubmed_title><pmcid>PMC9515219</pmcid><funding_grant_id>223273</funding_grant_id><funding_grant_id>CFREF Competition 2, 2015-2016</funding_grant_id><funding_grant_id>283798</funding_grant_id><pubmed_authors>Veltman DJ</pubmed_authors><pubmed_authors>Hettwer MD</pubmed_authors><pubmed_authors>van den Heuvel OA</pubmed_authors><pubmed_authors>Franke B</pubmed_authors><pubmed_authors>Hoogman M</pubmed_authors><pubmed_authors>Valk SL</pubmed_authors><pubmed_authors>Bernhardt BC</pubmed_authors><pubmed_authors>Buitelaar J</pubmed_authors><pubmed_authors>Turner JA</pubmed_authors><pubmed_authors>Lariviere S</pubmed_authors><pubmed_authors>Schmaal L</pubmed_authors><pubmed_authors>Andreassen OA</pubmed_authors><pubmed_authors>Evans AC</pubmed_authors><pubmed_authors>Dagher A</pubmed_authors><pubmed_authors>Stein DJ</pubmed_authors><pubmed_authors>Thomopoulos SI</pubmed_authors><pubmed_authors>Paquola C</pubmed_authors><pubmed_authors>Ching CRK</pubmed_authors><pubmed_authors>Kirschner M</pubmed_authors><pubmed_authors>van Rooij D</pubmed_authors><pubmed_authors>Thompson PM</pubmed_authors><pubmed_authors>Kebets V</pubmed_authors><pubmed_authors>van Erp TGM</pubmed_authors><pubmed_authors>Park BY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiscale neural gradients reflect transdiagnostic effects of major psychiatric conditions on cortical morphology.</name><description>It is increasingly recognized that multiple psychiatric conditions are underpinned by shared neural pathways, affecting similar brain systems. Here, we carried out a multiscale neural contextualization of shared alterations of cortical morphology across six major psychiatric conditions (autism spectrum disorder, attention deficit/hyperactivity disorder, major depression disorder, obsessive-compulsive disorder, bipolar disorder, and schizophrenia). Our framework cross-referenced shared morphological anomalies with respect to cortical myeloarchitecture and cytoarchitecture, as well as connectome and neurotransmitter organization. Pooling disease-related effects on MRI-based cortical thickness measures across six ENIGMA working groups, including a total of 28,546 participants (12,876 patients</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-19T05:19:28.763Z</modification><creation>2025-04-19T05:19:28.763Z</creation></dates><accession>S-EPMC9515219</accession><cross_references><pubmed>36168040</pubmed><doi>10.1038/s42003-022-03963-z</doi></cross_references></HashMap>