Structural Connectivity and Emotion Recognition Impairment in Children and Adolescents with Chromosome 22q11.2 Deletion Syndrome
Author:
Funder
National Institute of Mental Health
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
Developmental and Educational Psychology
Link
https://link.springer.com/content/pdf/10.1007/s10803-022-05675-z.pdf
Reference87 articles.
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2. Andersson, F., Glaser, B., Spiridon, M., Debbané, M., Vuilleumier, P., & Eliez, S. (2008). Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome. Biological Psychiatry, 63(1), 49–57.
3. Angkustsiri, K., Goodlin-Jones, B., Deprey, L., Brahmbhatt, K., Harris, S., & Simon, T. J. (2014). Social impairments in chromosome 22q11.2 deletion syndrome (22q11. 2DS): Autism spectrum disorder or a different endophenotype? Journal of Autism and Developmental Disorders, 44, 739–746.
4. Baker, K. D., & Skuse, D. H. (2005). Adolescents and young adults with 22q11 deletion syndrome: Psychopathology in an at-risk group. The British Journal of Psychiatry, 186(2), 115–120.
5. Bassett, A. S., Chow, E. W., AbdelMalik, P., Gheorghiu, M., Husted, J., & Weksberg, R. (2014). The schizophrenia phenotype in 22q11 deletion syndrome. American Journal of Psychiatry, 160(9), 1580–1586.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion Syndrome;Genes;2024-03-30
2. The Relationship between Motor Symptoms, Signs, and Parkinsonism with Facial Emotion Recognition Deficits in Individuals with 22q11.2 Deletion Syndrome at High Genetic Risk for Psychosis;Acta Neurologica Scandinavica;2023-03-28
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