De novo genic mutations among a Chinese autism spectrum disorder cohort

Recurrent sporadic mutations are important risk factors for autism spectrum disorders (ASDs) but have been primarily investigated in European cohorts. Here, Eichler, Xia and colleagues analyse risk genes in a large Chinese ASD cohort and find novel recurrences of potential pathogenic significance.

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Autores principales: Tianyun Wang, Hui Guo, Bo Xiong, Holly A.F. Stessman, Huidan Wu, Bradley P. Coe, Tychele N. Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Min Long, Janice Lin, Zev N. Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E. Eichler
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Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/e8317021f8e34afa82626d911d2284db
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spelling oai:doaj.org-article:e8317021f8e34afa82626d911d2284db2021-12-02T15:35:41ZDe novo genic mutations among a Chinese autism spectrum disorder cohort10.1038/ncomms133162041-1723https://doaj.org/article/e8317021f8e34afa82626d911d2284db2016-11-01T00:00:00Zhttps://doi.org/10.1038/ncomms13316https://doaj.org/toc/2041-1723Recurrent sporadic mutations are important risk factors for autism spectrum disorders (ASDs) but have been primarily investigated in European cohorts. Here, Eichler, Xia and colleagues analyse risk genes in a large Chinese ASD cohort and find novel recurrences of potential pathogenic significance.Tianyun WangHui GuoBo XiongHolly A.F. StessmanHuidan WuBradley P. CoeTychele N. TurnerYanling LiuWenjing ZhaoKendra HoekzemaLaura VivesLu XiaMeina TangJianjun OuBiyuan ChenYidong ShenGuanglei XunMin LongJanice LinZev N. KronenbergYu PengTing BaiHonghui LiXiaoyan KeZhengmao HuJingping ZhaoXiaobing ZouKun XiaEvan E. EichlerNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-10 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Tianyun Wang
Hui Guo
Bo Xiong
Holly A.F. Stessman
Huidan Wu
Bradley P. Coe
Tychele N. Turner
Yanling Liu
Wenjing Zhao
Kendra Hoekzema
Laura Vives
Lu Xia
Meina Tang
Jianjun Ou
Biyuan Chen
Yidong Shen
Guanglei Xun
Min Long
Janice Lin
Zev N. Kronenberg
Yu Peng
Ting Bai
Honghui Li
Xiaoyan Ke
Zhengmao Hu
Jingping Zhao
Xiaobing Zou
Kun Xia
Evan E. Eichler
De novo genic mutations among a Chinese autism spectrum disorder cohort
description Recurrent sporadic mutations are important risk factors for autism spectrum disorders (ASDs) but have been primarily investigated in European cohorts. Here, Eichler, Xia and colleagues analyse risk genes in a large Chinese ASD cohort and find novel recurrences of potential pathogenic significance.
format article
author Tianyun Wang
Hui Guo
Bo Xiong
Holly A.F. Stessman
Huidan Wu
Bradley P. Coe
Tychele N. Turner
Yanling Liu
Wenjing Zhao
Kendra Hoekzema
Laura Vives
Lu Xia
Meina Tang
Jianjun Ou
Biyuan Chen
Yidong Shen
Guanglei Xun
Min Long
Janice Lin
Zev N. Kronenberg
Yu Peng
Ting Bai
Honghui Li
Xiaoyan Ke
Zhengmao Hu
Jingping Zhao
Xiaobing Zou
Kun Xia
Evan E. Eichler
author_facet Tianyun Wang
Hui Guo
Bo Xiong
Holly A.F. Stessman
Huidan Wu
Bradley P. Coe
Tychele N. Turner
Yanling Liu
Wenjing Zhao
Kendra Hoekzema
Laura Vives
Lu Xia
Meina Tang
Jianjun Ou
Biyuan Chen
Yidong Shen
Guanglei Xun
Min Long
Janice Lin
Zev N. Kronenberg
Yu Peng
Ting Bai
Honghui Li
Xiaoyan Ke
Zhengmao Hu
Jingping Zhao
Xiaobing Zou
Kun Xia
Evan E. Eichler
author_sort Tianyun Wang
title De novo genic mutations among a Chinese autism spectrum disorder cohort
title_short De novo genic mutations among a Chinese autism spectrum disorder cohort
title_full De novo genic mutations among a Chinese autism spectrum disorder cohort
title_fullStr De novo genic mutations among a Chinese autism spectrum disorder cohort
title_full_unstemmed De novo genic mutations among a Chinese autism spectrum disorder cohort
title_sort de novo genic mutations among a chinese autism spectrum disorder cohort
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/e8317021f8e34afa82626d911d2284db
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