%0 Journal Article %A Guo, Hui %A Wang, Tianyun %A Wu, Huidan %A Long, Min %A Coe, Bradley %A Li, Honghui %A Xun, Guanglei %A Ou, Jianjun %A Chen, Biyuan %A Duan, Guiqin %A Bai, Ting %A Zhao, Ningxia %A Shen, Yidong %A Li, Yun %A Wang, Yazhe %A Zhang, Yu %A Baker, Carl %A Liu, Yanling %A Pang, Nan %A Huang, Lian %A Han, Lin %A Jia, Xiangbin %A Liu, Cenying %A Ni, Hailun %A Yang, Xinyi %A Xia, Lu %A Chen, Jingjing %A Shen, Lu %A Li, Ying %A Zhao, Rongjuan %A Zhao, Wenjing %A Peng, Jing %A Pan, Qian %A Long, Zhigao %A Su, Wei %A Tan, Jieqiong %A Du, Xiaogang %A Ke, Xiaoyan %A Yao, Meiling %A Hu, Zhengmao %A Zou, Xiaobing %A Zhao, Jingping %A Bernier, Raphael %A Eichler, Evan %A Xia, Kun %D 2018 %T Additional file 10: of Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model %U https://springernature.figshare.com/articles/journal_contribution/Additional_file_10_of_Inherited_and_multiple_de_novo_mutations_in_autism_developmental_delay_risk_genes_suggest_a_multifactorial_model/7465622 %R 10.6084/m9.figshare.7465622.v1 %2 https://springernature.figshare.com/ndownloader/files/13825247 %K Autism spectrum disorders %K Targeted sequencing %K De novo mutations %K Multiple hit %K Multifactorial model %K Genotype–phenotype relationship %X Figure S6. Distribution of mutations in some of the top mutated genes (DYRK1A, ASXL3, WDFY3 and MECP2) in the ACGC cohort (above) compared to previously published LGD and missense DNMs identified in the SSC and ASC cohorts. (PDF 896 kb) %I figshare