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. 2022 Aug 10;27(11):4464–4473. doi: 10.1038/s41380-022-01722-4

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Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/

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Fig. 1 — A Common single-nucleotide variants in RBFOX1 showed a gene-based association with most disorders and traits tested; B Copy number variants (CNVs) identified in ASD and SCZ patients. Top panel, copy number gains identified in ASD and SCZ patients. Bottom panel, CN losses identified in ASD and SCZ patients. Each bar represents a CNV. ADHD attention-deficit/hyperactivity disorder, AGG aggression, ANO anorexia, ANX anxiety, ASD autism spectrum disorder, BIP bipolar disorder, MDD major depressive disorder, OCD obsessive-compulsive disorder, RT risk tolerance behaviour, SCZ schizophrenia, TS Tourette’s syndrome, CD cross-disorder meta-analysis. p-val p-value.