Family-based genetic association study of CNTNAP2 polymorphisms and sociality endophenotypes in Korean patients with autism spectrum disorders-Reference-Cited by-同舟云学术

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Family-based genetic association study of CNTNAP2 polymorphisms and sociality endophenotypes in Korean patients with autism spectrum disorders

Published:2017-02 Issue:1 Volume:27 Page:38-39
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:

Author:

Yoo Hee Jeong,Kim Boong-Nyun,Kim Jae-Won,Shin Min-Sup,Park Tae-Won,Son Jung-Woo,Chung Un-Sun,Park Mira,Kim Soon Ae

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics (clinical),Genetics

Reference5 articles.

1. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene;Alarcón;Am J Hum Genet,2008

2. Behavioral and neuroanatomical phenotypes in mouse models of autism;Ellegood;Neurotherapeutics,2015

3. Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population;Li;Psychiatr Genet,2010

4. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits;Peñagarikano;Cell,2011

5. Defining the contribution of CNTNAP2 to autism susceptibility;Sampath;PLoS One,2013

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL;European Journal of Endocrinology;2021-06-01

2. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder;Genes;2020-12-22

3. Association between CNTNAP2 polymorphisms and autism: A family‐based study in the chinese han population and a meta‐analysis combined with GWAS data of psychiatric genomics consortium;Autism Research;2019-01-25

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