<HashMap><database>biostudies-literature</database><scores/><additional><submitter>ENIGMA Clinical High Risk for Psychosis Working Group</submitter><funding>NCATS NIH HHS</funding><funding>NIBIB NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Lundbeck Foundation</funding><pagination>77-88</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10568447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>81(1)</volume><pubmed_abstract>&lt;h4>Importance&lt;/h4>The lack of robust neuroanatomical markers of psychosis risk has been traditionally attributed to heterogeneity. A complementary hypothesis is that variation in neuroanatomical measures in individuals at psychosis risk may be nested within the range observed in healthy individuals.&lt;h4>Objective&lt;/h4>To quantify deviations from the normative range of neuroanatomical variation in individuals at clinical high risk for psychosis (CHR-P) and evaluate their overlap with healthy variation and their association with positive symptoms, cognition, and conversion to a psychotic disorder.&lt;h4>Design, setting, and participants&lt;/h4>This case-control study used clinical-, IQ-, and neuroimaging software (FreeSurfer)-derived regional measures of cortical thickness (CT), cortical surface ar</pubmed_abstract><journal>JAMA psychiatry</journal><pubmed_title>Normative Modeling of Brain Morphometry in Clinical High Risk for Psychosis.</pubmed_title><pmcid>PMC10568447</pmcid><funding_grant_id>R01 MH113564</funding_grant_id><funding_grant_id>R01 MH113533</funding_grant_id><funding_grant_id>UL1 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P</pubmed_authors><pubmed_authors>Hubl D</pubmed_authors><pubmed_authors>Jahanshad N</pubmed_authors><pubmed_authors>Haut KM</pubmed_authors><pubmed_authors>Omelchenko MA</pubmed_authors><pubmed_authors>Smigielski L</pubmed_authors><pubmed_authors>Rossler W</pubmed_authors><pubmed_authors>Kasai K</pubmed_authors><pubmed_authors>Nemoto T</pubmed_authors><pubmed_authors>Bartholomeusz CF</pubmed_authors><pubmed_authors>Lebedeva I</pubmed_authors><pubmed_authors>Thomopoulos SI</pubmed_authors><pubmed_authors>Horton LE</pubmed_authors><pubmed_authors>Glenthoj LB</pubmed_authors><pubmed_authors>Sugranyes G</pubmed_authors><pubmed_authors>Corcoran CM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Normative Modeling of Brain Morphometry in Clinical High Risk for Psychosis.</name><description>&lt;h4>Importance&lt;/h4>The lack of robust neuroanatomical markers of psychosis risk has been traditionally attributed to heterogeneity. A complementary hypothesis is that variation in neuroanatomical measures in individuals at psychosis risk may be nested within the range observed in healthy individuals.&lt;h4>Objective&lt;/h4>To quantify deviations from the normative range of neuroanatomical variation in individuals at clinical high risk for psychosis (CHR-P) and evaluate their overlap with healthy variation and their association with positive symptoms, cognition, and conversion to a psychotic disorder.&lt;h4>Design, setting, and participants&lt;/h4>This case-control study used clinical-, IQ-, and neuroimaging software (FreeSurfer)-derived regional measures of cortical thickness (CT), cortical surface ar</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2026-07-14T16:37:06.154Z</modification><creation>2025-04-06T16:00:06.25Z</creation></dates><accession>S-EPMC10568447</accession><cross_references><pubmed>37819650</pubmed><doi>10.1001/jamapsychiatry.2023.3850</doi></cross_references></HashMap>