Agency Deficits in a Human Genetic Model of Schizophrenia: Insights From 22q11DS Patients
Published inSchizophrenia bulletin, vol. 48, no. 2, p. 495-504
Publication date2022-03-01
Abstract
Keywords
- Locomotion
- Psychosis
- Sense of agency
- Sensorimotor prediction
- Velocardiofacial syndrome
- Virtual reality
- 22q11 Deletion Syndrome / complications
- 22q11 Deletion Syndrome / genetics
- Adolescent
- Adult
- Child
- Female
- Humans
- Male
- Models, Genetic
- Schizophrenia / complications
- Schizophrenia / genetics
Funding
- Bertarelli Foundation -
- European Commission - The motor hypothesis for self-monitoring: A new framework to understand and treat metacognitive failures [803122]
- Swiss National Science Foundation - Swiss VCFS Cohort: a 10-year longitudinal investigation from genes to brain to cognition for understanding psychosis proneness in 22q11.2 deletion [324730_144260]
- Swiss National Science Foundation - The Swiss 22q11DS longitudinal cohort: understanding psychosis proneness through negative symptoms [320030_179404]
- Swiss National Science Foundation - Immersive Embodied Interactions in Virtual Environments [200020_159968]
- Swiss National Science Foundation - NCCR 'SYNAPSY - The synaptic bases of mental diseases' (phase III)
Citation (ISO format)
SALOMON, Roy et al. Agency Deficits in a Human Genetic Model of Schizophrenia: Insights From 22q11DS Patients. In: Schizophrenia bulletin, 2022, vol. 48, n° 2, p. 495–504. doi: 10.1093/schbul/sbab143
Main files (1)
Article (Published version)
Secondary files (1)
Identifiers
- PID : unige:161526
- DOI : 10.1093/schbul/sbab143
- PMID : 34935960
- PMCID : PMC8886583
ISSN of the journal0586-7614