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科研机构
北京大学 [8]
内容类型
期刊论文 [5]
其他 [3]
发表日期
2017 [2]
2016 [1]
2015 [5]
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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
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
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
Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism
期刊论文
PLOS ONE, 2015
Li, Jun
;
Zhao, Linnan
;
You, Yang
;
Lu, Tianlan
;
Jia, Meixiang
;
Yu, Hao
;
Ruan, Yanyan
;
Yue, Weihua
;
Liu, Jing
;
Lu, Lin
;
Zhang, Dai
;
Wang, Lifang
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2017/12/03
GENOME-WIDE ASSOCIATION
SCAFFOLDING PROTEIN SHANK3
COMMON GENETIC-VARIANTS
DE-NOVO MUTATIONS
BIPOLAR DISORDER
SPECTRUM DISORDERS
ASPERGER-SYNDROME
SUBUNIT GENE
COPY NUMBER
CONNECTIVITY
Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population
期刊论文
PLOS ONE, 2015
Li, Jun
;
You, Yang
;
Yue, Weihua
;
Jia, Meixiang
;
Yu, Hao
;
Lu, Tianlan
;
Wu, Zhiliu
;
Ruan, Yanyan
;
Wang, Lifang
;
Zhang, Dai
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2017/12/03
HEMIPLEGIC MIGRAINE
GENOME-WIDE
DISORDERS
MUTATION
CEREBELLUM
HYPOPLASIA
VARIANTS
BEHAVIOR
REVEAL
LOCI
Positive association between CACNA1A polymorphisms and autism in Chinese Han population
其他
2015-01-01
Yang You
;
Jun Li
;
Weihua Yue
;
Meixiang Jia
;
Hao Yu
;
Jing Liu
;
Tianlan Lu
;
Zhiliu Wu
;
Yanyan Ruan
;
Dai Zhang
;
Lifang Wang
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2017/12/03
autism
CACNA1A
family-based association study
calcium channel
autism
CACNA1A
family-based association study
calcium channel
Evidence for chromatin remodeling gene EZH2 associated with autism in Chinese Han population
其他
2015-01-01
Jun Li
;
Yang You
;
Hao Yu
;
Weihua Yue
;
Tianlan Lu
;
Meixiang Jia
;
Yanyan Ruan
;
Jing Liu
;
Dai Zhang
;
Lifang Wang
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2017/12/03
autism
EZH2
family-based association test
chromatin remodeling gene
autism
EZH2
family-based association test
chromatin remodeling gene
Schizophrenia related variants in CACNA1C also confer risk of autism
其他
2015-01-01
Jun Li
;
Linnan Zhao
;
Yang You
;
Tianlan Lu
;
Meixiang Jia
;
Hao Yu
;
Yanyan Ruan
;
Weihua Yue
;
Jing Liu
;
Lin Lu
;
Dai Zhang
;
Lifang Wang
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2017/12/03
autism
CACNA1C
family-based association study
calcium channel
autism
CACNA1C
family-based association study
calcium channel
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