Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients

Published:2019-05-08 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Balicza Péter,Varga Noémi Ágnes,Bolgár Bence,Pentelényi Klára,Bencsik Renáta,Gál Anikó,Gézsi András,Prekop Csilla,Molnár Viktor,Molnár Mária Judit

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference53 articles.

1. A method and server for predicting damaging missense mutations.;Adzhubei;Nat. Methods,2010

2. Disruptive CHD8 mutations define a subtype of autism early in development.;Bernier;Cell,2014

3. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.;Betancur;Brain Res.,2011

4. From the genetic architecture to synaptic plasticity in autism spectrum disorder.;Bourgeron;Nat. Rev. Neurosci.,2015

5. Analysis of shared heritability in common disorders of the brain.;Brainstorm Consortium;Science,2018

Cited by 14 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. Genomic diversity in functionally relevant genes modifies neurodevelopmental versus neoplastic risks in individuals with germline PTEN variants;2023-12-14

2. Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis;Frontiers in Medicine;2023-05-05

3. Can the “female protective effect” liability threshold model explain sex differences in autism spectrum disorder?;Neuron;2022-10

4. Screening for Fragile X Syndrome Among Filipino Children with Autism Spectrum Disorder;Journal of Autism and Developmental Disorders;2022-08-16

5. Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders;Frontiers in Molecular Neuroscience;2022-06-23

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