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浏览/检索结果: 共5条，第1-5条 帮助 限定条件 内容类型：期刊论文    专题：北京大学    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 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