Disrupted working memory circuitry and psychotic symptoms in 22q11.2 deletion syndrome
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psychosis. Behavioral research suggests that 22q11DS patients exhibit a characteristic neurocognitive phenotype that includes differential impairment in spatial working memory (WM). Notably, spatial WM h...
Main Authors: | C.A. Montojo, A. Ibrahim, K.H. Karlsgodt, C. Chow, A.E. Hilton, R.K. Jonas, T.K. Vesagas, C.E. Bearden |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2014-01-01
|
Series: | NeuroImage: Clinical |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2213158214000114 |
Similar Items
-
Acute dystonia in a patient with 22q11.2 deletion syndrome
by: Konstantinos Kontoangelos, et al.
Published: (2015-09-01) -
Genotype-phenotype correlation in 22q11.2 deletion syndrome
by: Michaelovsky Elena, et al.
Published: (2012-12-01) -
Neurocognitive and neurophysiological endophenotypes in schizophrenia: An overview
by: Francesco Luciano Donati, et al.
Published: (2020-12-01) -
Altered white matter microstructure is associated with social cognition and psychotic symptoms in 22q11.2 microdeletion syndrome
by: Maria eJalbrzikowski, et al.
Published: (2014-11-01) -
Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome
by: Tyler M. Moore, et al.
Published: (2021-06-01)