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科研机构
北京大学 [32]
内容类型
期刊论文 [27]
其他 [5]
发表日期
2017 [10]
2016 [3]
2015 [12]
2014 [5]
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2012 [1]
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专题:北京大学
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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
Optogenetic activation of dorsal raphe neurons rescues the autistic-like social deficits in Shank3 knockout mice
期刊论文
CELL RESEARCH, 2017
Luo, Junyu
;
Feng, Qiru
;
Wei, Liping
;
Luo, Minmin
收藏
  |  
浏览/下载:119/0
  |  
提交时间:2017/12/03
SPECTRUM DISORDER
REWARD
DOPAMINE
BEHAVIOR
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
Recent Research Progress in Autism Spectrum Disorder
期刊论文
NEUROSCIENCE BULLETIN, 2017
Yu, Xiang
;
Qiu, Zilong
;
Zhang, Dai
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2017/12/03
autism
honor
occasion
Bulletin
Neuroscience
neurological
celebrate
focusing
heterogeneous
developmental
OXYTOCIN
BRAIN
VASOPRESSIN
GENETICS
ABNORMALITIES
NEUROSCIENCE
MEDICINE
BEHAVIOR
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
How Oxytocin Receptor (OXTR) Single Nucleotide Polymorphisms Act on Prosociality: The Mediation Role of Moral Evaluation
期刊论文
FRONTIERS IN PSYCHOLOGY, 2017
Shang, Siyuan
;
Wu, Nan
;
Su, Yanjie
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2017/12/03
moral evaluation
prosociality
oxytocin receptor gene
gender differences
mediation
AUTISM SPECTRUM DISORDER
GENE OXTR
BEHAVIOR
ASSOCIATION
ADOLESCENTS
ANXIETY
PSYCHOPATHOLOGY
PERSPECTIVE
POPULATION
COGNITION
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