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. 2016 Oct 21;7:44. doi: 10.1186/s13229-016-0103-y

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Global overview of the data in this study. a A pie chart showing the number of publications reporting only common (red), rare (blue), or both common and rare (green) genetic variants associated with autism spectrum disorder (ASD) in our database. b A pie chart showing the number of genes including only common (red), rare (blue), or both common and rare (green) genetic variants associated with ASD in our database. c A distribution of the common (red) and rare (blue) genetic variation in our database within four mutation categories: nonsynonymous, synonymous, non-coding, and copy number variations (CNVs)