• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Integrative Genomics for the Interpretation of Genetic Loci Implicated in Neurodevelopmental Disorders.

作者信息

Walker Rebecca L

机构信息

Department of Neurology, Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California; Broad Institute of MIT and Harvard, Cambridge, Massachusetts.

出版信息

Biol Psychiatry. 2020 Sep 15;88(6):438-439. doi: 10.1016/j.biopsych.2020.07.003.

DOI:10.1016/j.biopsych.2020.07.003
PMID:32854829
Abstract
摘要

相似文献

1
Integrative Genomics for the Interpretation of Genetic Loci Implicated in Neurodevelopmental Disorders.用于解释神经发育障碍相关基因座的整合基因组学
Biol Psychiatry. 2020 Sep 15;88(6):438-439. doi: 10.1016/j.biopsych.2020.07.003.
2
Introduction to the Special Issue on 'The Genetic Architecture of Neurodevelopmental Disorders'.“神经发育障碍的遗传结构”特刊引言
Behav Genet. 2020 Jul;50(4):185-190. doi: 10.1007/s10519-020-10007-x.
3
Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies.通过整合全基因组关联、基因表达和 DNA 甲基化研究的汇总数据，精确定位注意力缺陷/多动障碍和自闭症谱系障碍的遗传基因座。
Biol Psychiatry. 2020 Sep 15;88(6):470-479. doi: 10.1016/j.biopsych.2020.05.002. Epub 2020 May 16.
4
Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.特定语言损伤、注意缺陷多动障碍和自闭症谱系障碍中的语言缺陷：多基因风险分析。
Autism Res. 2020 Mar;13(3):369-381. doi: 10.1002/aur.2211. Epub 2019 Oct 2.
5
Genes as Unmeasured and Unknown Confounds in Studies of Neurodevelopmental Outcomes After Antidepressant Prescription During Pregnancy.孕期服用抗抑郁药与神经发育结局相关性研究中的未测量和未知混杂因素：基因
J Clin Psychiatry. 2020 May 26;81(3):20f13463. doi: 10.4088/JCP.20f13463.
6
Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders.神经纤维瘤病 1 型提示 Ras 通路参与神经发育障碍的遗传结构。
Behav Genet. 2020 Jul;50(4):191-202. doi: 10.1007/s10519-020-09991-x. Epub 2020 Feb 5.
7
ADGRL3 rs6551665 as a Common Vulnerability Factor Underlying Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder.ADGRL3 rs6551665 作为注意缺陷多动障碍和自闭症谱系障碍的共同脆弱性因素。
Neuromolecular Med. 2019 Mar;21(1):60-67. doi: 10.1007/s12017-019-08525-x. Epub 2019 Jan 16.
8
[Genetics applied to clinical practice in neurodevelopmental disorders].[遗传学在神经发育障碍临床实践中的应用]
Rev Neurol. 2014 Feb 24;58 Suppl 1:S65-70.
9
Risk of Psychiatric and Neurodevelopmental Disorders Among Siblings of Probands With Autism Spectrum Disorders.自闭症谱系障碍患者的兄弟姐妹患精神和神经发育障碍的风险。
JAMA Psychiatry. 2016 Jun 1;73(6):622-9. doi: 10.1001/jamapsychiatry.2016.0495.
10
Delivering paediatric precision medicine: Genomic and environmental considerations along the causal pathway of childhood neurodevelopmental disorders.实现儿科精准医学：儿童神经发育障碍因果途径中的基因组和环境考虑因素。
Dev Med Child Neurol. 2022 Sep;64(9):1077-1084. doi: 10.1111/dmcn.15289. Epub 2022 Jun 6.