Abnormal development and dysconnectivity of distinct thalamic nuclei in patients with 22q11.2 deletion syndrome experiencing auditory hallucinations
ContributorsMancini, Valentina
; Zoeller, Daniela; Schneider, Maude; Schaer, Marie
; Eliez, Stéphan
Published inBiological Psychiatry
Publication date2020
Abstract
Keywords
- Auditory cortex
- Medial geniculate nucleus
- Nucleus reuniens
- Psychosis
- Thalamocortical comaturation
- Wernicke's area
Funding
- Swiss National Science Foundation - Geneva VCFS longitudinal project: neurobehavioral outcomes in adolescents and adults [121996]
- 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 [144260]
- Swiss National Science Foundation - NCCR SYNAPSY: The synaptic bases of mental diseases (phase II) [158776]
- Swiss National Science Foundation - Towards an embodied and ecological understanding of social impairments in neurodevelopmental disorders [174206]
- Swiss National Science Foundation - Measuring trajectories of cerebral development associated with autism in the first years of life [163859]
Citation (ISO format)
MANCINI, Valentina et al. Abnormal development and dysconnectivity of distinct thalamic nuclei in patients with 22q11.2 deletion syndrome experiencing auditory hallucinations. In: Biological Psychiatry, 2020. doi: 10.1016/j.bpsc.2020.04.015
Main files (1)
Article (Published version)
Secondary files (1)
Supplemental data
Identifiers
- PID : unige:139054
- DOI : 10.1016/j.bpsc.2020.04.015
- PMID : 32620531
Additional URL for this publicationhttps://www.sciencedirect.com/science/article/pii/S2451902220301099
Journal ISSN0006-3223
