Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
https://www.nature.com/articles/s41582-023-00896-x.pdf
Reference196 articles.
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2. Cunningham, A. C. et al. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Mov. Disord. 35, 1272–1274 (2020).
3. Liu, Y. et al. A selective review of the excitatory-inhibitory imbalance in schizophrenia: underlying biology, genetics, microcircuits, and symptoms. Front. Cell Dev. Biol. 9, 664535 (2021).
4. Thygesen, J. H. et al. Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders. Br. J. Psychiatry 212, 287–294 (2018).
5. Mollon, J., Almasy, L., Jacquemont, S. & Glahn, D. C. The contribution of copy number variants to psychiatric symptoms and cognitive ability. Mol. Psychiatry https://doi.org/10.1038/s41380-023-01978-4 (2023).
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