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科研机构
北京大学 [33]
内容类型
期刊论文 [29]
其他 [4]
发表日期
2017 [8]
2016 [5]
2015 [12]
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专题:北京大学
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Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population
期刊论文
SCIENTIFIC REPORTS, 2017
Wu, Zhiliu
;
Qin, Jian
;
You, Yang
;
Ma, Yuanlin
;
Jia, Meixiang
;
Wang, Linyan
;
Lu, Tianlan
;
Yue, Weihua
;
Ruan, Yanyan
;
Zhang, Dai
;
Li, Jun
;
Wang, Lifang
收藏
  |  
浏览/下载:123/0
  |  
提交时间:2017/12/03
SCAFFOLDING PROTEIN SHANK3
CELL CORPSE ENGULFMENT
COPY NUMBER VARIATION
DE-NOVO MUTATIONS
SPECTRUM DISORDERS
SCHIZOPHRENIA
EXPRESSION
BRAIN
NEUROLIGINS
ASTROCYTES
Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation
期刊论文
MOLECULAR AUTISM, 2017
Wen, Zhu
;
Cheng, Tian-Lin
;
Li, Gai-Zhi
;
Sun, Shi-Bang
;
Yu, Shun-Ying
;
Zhang, Yi
;
Du, Ya-Song
;
Qiu, Zilong
收藏
  |  
浏览/下载:117/0
  |  
提交时间:2017/12/03
Autism spectrum disorder
Methyl-CpG-binding protein-2 (MeCP2)
Whole-exome sequencing
Neural development
CPG-BINDING PROTEIN-2
RETT-SYNDROME
DENDRITIC GROWTH
GENE
MICE
TRANSCRIPTION
MATURATION
DISORDER
Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations
期刊论文
HUMAN MUTATION, 2017
Dou, Yanmei
;
Yang, Xiaoxu
;
Li, Ziyi
;
Wang, Sheng
;
Zhang, Zheng
;
Ye, Adam Yongxin
;
Yan, Linlin
;
Yang, Changhong
;
Wu, Qixi
;
Li, Jiarui
;
Zhao, Boxun
;
Huang, August Yue
;
Wei, Liping
收藏
  |  
浏览/下载:121/0
  |  
提交时间:2017/12/03
autism spectrum disorder
autistic traits
parental mosaicism
single-nucleotide mosaicism
DE-NOVO MUTATIONS
INTERACTION NETWORKS
SOMATIC MOSAICISM
DRAVET SYNDROME
HUMAN-DISEASE
GENETIC RISK
HUMAN BRAIN
EVOLUTION
PATTERNS
GENOME
Identification of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing
期刊论文
NEUROSCIENCE BULLETIN, 2017
Wen, Zhu
;
Cheng, Tian-Lin
;
Yin, Da-Zhi
;
Sun, Shi-Bang
;
Wang, Zheng
;
Yu, Shun-Ying
;
Zhang, Yi
;
Qiu, Zilong
;
Du, Ya-Song
收藏
  |  
浏览/下载:119/0
  |  
提交时间:2017/12/03
Genetic Cause
Childhood
syndrome
AUTISM SPECTRUM DISORDER
SANFILIPPO-SYNDROME
MUCOPOLYSACCHARIDOSIS
CHILDREN
Meta-analyses of RELN variants in neuropsychiatric disorders
期刊论文
BEHAVIOURAL BRAIN RESEARCH, 2017
Chen, Na
;
Bao, Yanping
;
Xue, Yanxue
;
Sun, Yan
;
Hu, Die
;
Meng, Shiqiu
;
Lu, Lin
;
Shi, Jie
收藏
  |  
浏览/下载:117/0
  |  
提交时间:2017/12/03
RELN gene
Psychiatric disorders
Single nucleotide polymorphism
Meta-analysis
CHINESE HAN POPULATION
REELIN GENE RELN
BIPOLAR DISORDER
ALZHEIMERS-DISEASE
SPECTRUM DISORDER
MAJOR DEPRESSION
SCHIZOPHRENIA
ASSOCIATION
EXPRESSION
AUTISM
Development and evaluation of a speech-generating AAC mobile app for minimally verbal children with autism spectrum disorder in Mainland China
期刊论文
MOLECULAR AUTISM, 2017
An, Sainan
;
Feng, Xiaoping
;
Dai, Yue
;
Bo, Hongli
;
Wang, Xiuqing
;
Li, Mu
;
Woo, John Zhuohao
;
Liang, Xingmei
;
Guo, Cheng
;
Liu, Charles Xingchao
;
Wei, Liping
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2017/12/03
Augmentative and alternative communication
App
Development
Training effectiveness
Mainland China
EXCHANGE COMMUNICATION-SYSTEM
REQUESTING SKILLS
DEVICE
PECS
INTERVENTIONS
METAANALYSIS
ACQUISITION
ASD
INDIVIDUALS
TRIAL
Association of oligodendrocytes differentiation regulator gene DUSP15 with autism
期刊论文
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2017
Tian, Ye
;
Wang, Lifang
;
Jia, Meixiang
;
Lu, Tianlan
;
Ruan, Yanyan
;
Wu, Zhiliu
;
Wang, Linyan
;
Liu, Jing
;
Zhang, Dai
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2017/12/03
Autistic disorder
genetics
oligodendrocytes
DUSP15
polymorphism
MYELIN GLYCOPROTEIN GENE
DE-NOVO MUTATIONS
SPECTRUM DISORDERS
CORPUS-CALLOSUM
YOUNG-CHILDREN
TWIN PAIRS
RISK
DISEQUILIBRIUM
SCHIZOPHRENIA
CONNECTIVITY
Trust and Deception in Children with Autism Spectrum Disorders: A Social Learning Perspective
期刊论文
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2017
Yang, Yiying
;
Tian, Yuan
;
Fang, Jing
;
Lu, Haoyang
;
Wei, Kunlin
;
Yi, Li
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2017/12/03
Autism Spectrum Disorder
Trust
Deception
Social learning
CULTURAL-DIFFERENCES
JOINT ATTENTION
BEHAVIOR
ABILITY
LIES
MIND
INDIVIDUALS
DISTRUST
LANGUAGE
CONTEXT
Chromatin remodeling gene EZH2 involved in the genetic etiology of autism in Chinese Han population
期刊论文
NEUROSCIENCE LETTERS, 2016
Li, Jun
;
You, Yang
;
Yue, Weihua
;
Yu, Hao
;
Lu, Tianlan
;
Wu, Zhiliu
;
Jia, Meixiang
;
Ruan, Yanyan
;
Liu, Jing
;
Zhang, Dai
;
Wang, Lifang
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2017/12/03
Autism
EZH2
Chromatin remodeling gene
Family-based association test
DE-NOVO MUTATIONS
SPECTRUM DISORDERS
NEURAL DEVELOPMENT
ASSOCIATION
EXPRESSION
METHYLTRANSFERASE
DIFFERENTIATION
REVEALS
CNTNAP2
Dendritic spine pathology in autism: lessons learned from mouse models
期刊论文
转化神经科学电子杂志(英文), 2016
Qiangge Zhang
;
Dingxi Zhou
;
Guoping Feng
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2017/12/03
synapse dendritic spine autism FMR1 MECP2 SHANK3 animal model
synapse
dendritic spine
autism
FMR1
MECP2
SHANK3
animal model
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