Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
Author:
Publisher
Springer Science and Business Media LLC
Subject
Behavioral Neuroscience,Experimental and Cognitive Psychology,Social Psychology
Link
https://www.nature.com/articles/s41562-023-01541-9.pdf
Reference81 articles.
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2. Conrad, D. F. et al. Origins and functional impact of copy number variation in the human genome. Nature 464, 704–712 (2010).
3. Auwerx, C. et al. The individual and global impact of copy-number variants on complex human traits. Am. J. Hum. Genet. https://doi.org/10.1016/j.ajhg.2022.02.010 (2022).
4. Jacquemont, S. et al. Genes to mental health (G2MH): a framework to map the combined effects of rare and common variants on dimensions of cognition and psychopathology. Am. J. Psychiatry 179, 189–203 (2021).
5. Rutkowski, T. P. et al. Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders. J. Neurosci. Res. 95, 1144–1160 (2017).
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2. Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders;Heliyon;2023-09
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