Unraveling genetic risk contributions to nonverbal status in autism spectrum disorder probands

Unraveling genetic risk contributions to nonverbal status in autism spectrum disorder probands

Abstract Autism spectrum disorder (ASD) presents a wide range of cognitive and language impairments. In this study, we investigated the genetic basis of non-verbal status in ASD using a comprehensive genomic approach. We identified a novel common variant, rs1944180 in CNTN5, significantly associated...

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Main Authors: Huan Liu, Shenghan Wang, Binbin Cao, Jijun Zhu, Zhifang Huang, Pan Li, Shunjie Zhang, Xian Liu, Jing Yu, Zhongting Huang, Linzhuo Lv, Fuqiang Cai, Weixin Liu, Zhijian Song, Yuxin Liu, Tao Pang, Suhua Chang, Ying Chen, Junfang Chen, Wen-Xiong Chen
Format: Article
Language:English
Published: BMC 2025-06-01
Series:Behavioral and Brain Functions
Subjects:
Autism spectrum disorder
Common variants
De Novo mutations
Whole-exome sequencing
Non-verbal status
Online Access:https://doi.org/10.1186/s12993-025-00278-x
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https://doi.org/10.1186/s12993-025-00278-x

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