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浏览/检索结果: 共5条，第1-5条 帮助 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 Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia 期刊论文 JOURNAL OF GENETICS AND GENOMICS, 2017, 卷号: 44, 期号: 6, 页码: 295-306 作者:  Tang, Jinsong;  Fan, Yu;  Li, Hong;  Xiang, Qun;  Zhang, Deng-Feng 收藏  |  浏览/下载：58/0  |  提交时间：2017/08/07 Whole-genome sequencing  Schizophrenia  Monozygotic twin  De novo mutation  Combined effect  Susceptibility   Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia 期刊论文 Journal of Genetics and Genomics, 2017, 卷号: 44, 期号: X, 页码: 295-306 作者:  Xiang Q;  Zhang DF;  yanqingtang@163.com;  rckchan@psych.ac.cn;  Cwang.cy@163.net 收藏  |  浏览/下载：58/0  |  提交时间：2017/06/26 Whole-genome Sequencing  Schizophrenia  Monozygotic Twi  De Novo Mutatio  Combined Effec  Susceptibility   Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia 期刊论文 JOURNAL OF GENETICS AND GENOMICS, 2017, 卷号: 44, 期号: 6, 页码: 295-306 作者:  Tang Jinsong;  Fan Yu;  Li Hong;  Xiang Qun;  Zhang DengFeng 收藏  |  浏览/下载：9/0  |  提交时间：2021/02/02 DE-NOVO MUTATIONS  STRUCTURAL VARIANT DISCOVERY  WIDE ASSOCIATION  PSYCHIATRIC-DISORDERS  SYNAPTIC PLASTICITY  BIPOLAR DISORDER  PROTEIN FUNCTION  COMPLEX TRAITS  MESSENGER-RNA  HUMAN-DISEASE  Whole-genome sequencing  Schizophrenia  Monozygotic twin  De novo mutation  Combined effect  Susceptibility   Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci 期刊论文 NEURON, 2015 Sanders, Stephan J.; Xin He; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H.; Bishop, Somer L.; Shan Dong; Goldberg, Arthur P.; Cai Jinlu; Keaney, John F., III; Klei, Lambertus; Mandell, Jeffrey D.; Moreno-De-Luca, Daniel; Poultney, Christopher S.; Robinson, Elise B.; Smith, Louw; Solli-Nowlan, Tor; Su, Mack Y.; Teran, Nicole A.; Walker, Michael F.; Werling, Donna M.; Beaudet, Arthur L.; Cantor, Rita M.; Fombonne, Eric; Geschwind, Daniel H.; Grice, Dorothy E. 收藏  |  浏览/下载：3/0  |  提交时间：2017/12/03 COPY-NUMBER VARIATION  DE-NOVO MUTATIONS  HIDDEN-MARKOV MODEL  SNP GENOTYPING DATA  TRUNCATING MUTATIONS  STRUCTURAL VARIATION  WILLIAMS-SYNDROME  SIMPLEX AUTISM  GENE  RARE   Hybridization and amplification rate correction for affymetrix SNP arrays 其他 2012-01-01 Wang, Quan; Peng, Peichao; Qian, Minping; Wan, Lin; Deng, Minghua 收藏  |  浏览/下载：5/0  |  提交时间：2015/11/11 SNP array  Copy number variation (CNV)  Cross-hybridization  Genomic waves  COPY-NUMBER VARIATION  SHORT OLIGONUCLEOTIDE MICROARRAYS  GENOME-WIDE ASSOCIATION  DE-NOVO CNVS  DNA MICROARRAYS  STRUCTURAL VARIATION  BIPOLAR-DISORDER  MODEL  INTENSITIES  EXPRESSION