Both rare and common genetic variants contribute to autism in the Faroe Islands-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Both rare and common genetic variants contribute to autism in the Faroe Islands

Published:2019-01-21 Issue:1 Volume:4 Page:
ISSN:2056-7944
Container-title:npj Genomic Medicine
language:en
Short-container-title:npj Genomic Med

Author:

Leblond Claire S^ORCID,Cliquet Freddy^ORCID,Carton Coralie,Huguet Guillaume,Mathieu Alexandre,Kergrohen Thomas,Buratti Julien,Lemière Nathalie,Cuisset Laurence,Bienvenu Thierry,Boland Anne,Deleuze Jean-François,Stora Tormodur,Biskupstoe Rannva,Halling Jónrit,Andorsdóttir Guðrið,Billstedt Eva,Gillberg Christopher,Bourgeron Thomas

Funder

Institut Pasteur

Université Paris Diderot

Simons Foundation

Fondation Bettencourt Schueller

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

http://www.nature.com/articles/s41525-018-0075-2.pdf

Reference48 articles.

1. Gillberg, C. The ESSENCE in child psychiatry: Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations. Res. Dev. Disabil. 31, 1543–1551 (2010).

2. Sandin, S. et al. The heritability of autism spectrum disorder. JAMA 318, 1182–1184 (2017).

3. Yuen, R. K. C. et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nat. Neurosci. 20, 602 (2017).

4. Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Mol. Autism 8, 21 (2017).

5. Weiner, D. J. et al. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nat. Genet. 49, 978–985 (2017).

Cited by 58 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. Copy number deletion of PLA2G4A affects the susceptibility and clinical phenotypes of schizophrenia;Schizophrenia;2024-05-30

2. Identification of circRNA–miRNA–mRNA regulatory network associated to the autism spectrum disorder in children through integrated bioinformatics analysis;Egyptian Journal of Medical Human Genetics;2024-05-11

3. Landscape of NRXN1 Gene Variants in Phenotypic Manifestations of Autism Spectrum Disorder: A Systematic Review;Journal of Clinical Medicine;2024-04-02

4. A de novo variant in RERE causes autistic behavior by disrupting related genes and signaling pathway;Clinical Genetics;2023-11-28

5. SNP heterozygosity, relatedness and inbreeding of whole genomes from the isolated population of the Faroe Islands;BMC Genomics;2023-11-23

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3