Journal
Nature Genetics
Publication Date
8-18-2022
Volume
54
Issue
9
First Page
1305
Last Page
1319
Document Type
Open Access Publication
DOI
10.1038/s41588-022-01148-2
Rights and Permissions
Zhou, X., Feliciano, P., Shu, C. et al. Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes. Nat Genet 54, 1305–1319 (2022). https://doi.org/10.1038/s41588-022-01148-2 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
Recommended Citation
Zhou, Xueya; Turner, Tychele N.; and et al, "Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes." Nature Genetics. 54, 9. 1305 - 1319. (2022).
https://digitalcommons.wustl.edu/oa_4/340
Supplementary Note, Supplementary Table Legends, Supplementary Figs. S1–S24, References
41588_2022_1148_MOESM2_ESM.pdf (2035 kB)
Reporting Summary
41588_2022_1148_MOESM3_ESM.pdf (1581 kB)
Peer Review File
41588_2022_1148_MOESM4_ESM.xlsx (6151 kB)
Supplementary Tables S1–S19
41588_2022_1148_MOESM5_ESM.xlsx (9427 kB)
Annotated de novo coding variants in ASD discovery cohorts
41588_2022_1148_MOESM6_ESM.xlsx (205 kB)
Annotated de novo coding variants identified in the SPARK replication cohort
41588_2022_1148_MOESM7_ESM.xlsx (14828 kB)
Annotated de novo coding variants collected from other NDD studies