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110 results for “Psychosis risk”
Learning and Executive Function Disorders in Children and Psychosis Risk at Adult-age
ClinicalTrials.gov study NCT04280367. IPD Sharing: NO. Countries: 1. Publications: 0.
Targeted Cognitive Training in Clinical High Risk (CHR) for Psychosis
ClinicalTrials.gov study NCT02404194. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Develop a Psychosis Risk Calculator for Chinese Mental Health Servises
ClinicalTrials.gov study NCT04509778. IPD Sharing: YES. Countries: 1. Publications: 0.
Cognitive Behavioral Social Skills Training for Youth at Risk of Psychosis
ClinicalTrials.gov study NCT02234258. IPD Sharing: Not stated. Countries: 1. Publications: 0.
A Study Exploring Changes in a Variety of Biomarkers Following Dosing With MT1988 in Participants at Clinical High Risk for Psychosis
ClinicalTrials.gov study NCT07226895. IPD Sharing: YES. Countries: 1. Publications: 0.
The psychosis risk gene RBM12 encodes a novel repressor of GPCR/cAMP signal transduction
GEO Series GSE219195. Homo sapiens. 25 samples. Type: Expression profiling by high throughput sequencing.
Effects of Cognitive Remediation on Cognition in Young People at Clinical High Risk of Psychosis
ClinicalTrials.gov study NCT01619319. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Perceived family functioning profile in adolescents at clinical high risk for psychosis: rigidity as a possible preventive target
<p><strong>Introduction</strong></p> <p>This database includes the raw data linked with the paper “Perceived family functioning profile in adolescents at Clinical High-Risk for Psychosis: rigidity as a possible preventive target”, currently under submission.</p> <p>In this paper, we reported sociodemographic characteristics, family history of any DSM-5 psychiatric disorder, personal history of any DSM-5 psychiatric disorder, psychopathological assessment, and level of functioning. We aimed at investigating the role of family functioning for APS adolescents compared to adolescents suffering from early onset psychosis and with other psychiatric disorders.</p> <p><strong>Methods</strong></p> <p>Participants were then divided into three groups: 1) adolescents with established Early Onset Psychosis (EOP), 2) adolescents meeting DSM-5 Attenuated psychotic Syndrome (APS) criteria and the attenuated psychotic symptoms subgroup of the Clinical High Risk for Psychosis (CHR-P), 3) adolescents with other DSM-5 psychiatric disorders who did not meet APS/EOP criteria.</p> <p><strong>Results</strong></p> <p>Our results suggest that family functioning has a central role and could represent a worthwhile target of intervention for adolescents at CHR-P, leading the way to new preventive approaches.</p>
Neurocognition and functioning in adolescents at clinical high risk for psychosis
<p><strong>Introduction. </strong>This database includes the raw data linked with the paper “Neurocognitive Functioning of Adolescents at Clinical High Risk for Psychosis”<strong>. </strong>In this paper, we reported sociodemographic characteristics, family history of any DSM-5 psychiatric disorder, personal history of any DSM-5 psychiatric disorder, psychopathological assessment, and level of functioning. We aimed to identify differences in overall and neurocognitive functioning in three groups of adolescent patients divided according to the semi-structured interview Comprehensive Assessment of At-Risk Mental States (CAARMS) criteria.</p> <p><strong>Methods </strong>Participants were divided into three groups: 1) adolescents with established Early Onset Psychosis (EOP), 2) adolescents meeting DSM-5 Attenuated psychotic Syndrome (APS) criteria and the attenuated psychotic symptoms subgroup of the Clinical High Risk for Psychosis (CHR-P), 3) adolescents with other DSM-5 psychiatric disorders who did not meet APS/EOP criteria.</p> <p><strong>Results . </strong>We found that non-CHR-P exhibited better functioning and performances than psychosis group in processing speed, forward and backward verbal digit span, visual attention, categorial fluency, executive functions, processing speed, and planning and attention. No differences emerged between non-CHR-P and CHR-P. CHR-P and psychosis groups differed in processing speed, in TMT-A, in BVN forward verbal digit span, visual attention, categorial fluency and in ROCF drawing from memory task.</p>
Data related to article "Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease"
<p>Raw data and additional material for genetic analysis of psychosis risk in Alzheimer's disease</p>
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Allen Brain Atlas
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.