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Genetic analysis for cognitive flexibility in the trail-making test in attention deficit hyperactivity disorder patients from single nucleotide polymorphism, gene to pathway level 期刊论文
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2019, 卷号: 20, 期号: 6, 页码: 476-485
作者:  Zhang, Kunlin;  Fan, Zili;  Wang, Yufeng;  Faraone, Stephen, V;  Yan, Li
收藏  |  浏览/下载:54/0  |  提交时间:2019/10/31
Genetic variant for behavioral regulation factor of executive function and its possible brain mechanism in attention deficit hyperactivity disorder 期刊论文
SCIENTIFIC REPORTS, 2018, 卷号: 8, 页码: 1-9
作者:  Sun, Xiao;  Wu, Zhaomin;  Cao, Qingjiu;  Qian, Ying;  Liu, Yong
收藏  |  浏览/下载:38/0  |  提交时间:2018/07/02
DLGAP1 and NMDA receptor-associated postsynaptic density protein genes influence executive function in attention deficit hyperactivity disorder 期刊论文
BRAIN AND BEHAVIOR, 2018, 卷号: 8, 期号: 2, 页码: 1-8
作者:  Fan, Zili;  Qian, Ying;  Lu, Qing;  Wang, Yufeng;  Chang, Suhua
收藏  |  浏览/下载:44/0  |  提交时间:2018/05/28
An overview of posttraumatic stress disorder genetic studies by analyzing and integrating genetic data into genetic database PTSDgene 期刊论文
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2017, 卷号: 83, 页码: 647-656
作者:  Zhang, Kunlin;  Qu, Susu;  Chang, Suhua;  Li, Gen;  Cao, Chengqi
收藏  |  浏览/下载:56/0  |  提交时间:2018/02/26
Common variants near IKZF1 are associated with primary Sjogren's syndrome in Han Chinese 期刊论文
PLOS ONE, 2017, 卷号: 12, 期号: 5
作者:  Qu, Susu;  Du, Yang;  Chang, Suhua;  Guo, Liyuan;  Fang, Kechi
收藏  |  浏览/下载:51/0  |  提交时间:2017/07/17
A combined analysis of genome-wide expression profiling of bipolar disorder in human prefrontal cortex 期刊论文
JOURNAL OF PSYCHIATRIC RESEARCH, 2016, 卷号: 82, 期号: 0, 页码: 23-29
作者:  Wang, Jinglu;  Qu, Susu;  Wang, Weixiao;  Guo, Liyuan;  Zhang, Kunlin
收藏  |  浏览/下载:30/0  |  提交时间:2016/12/19
Precision Medicine: What Challenges Are We Facing? 期刊论文
Genomics, proteomics & bioinformatics, 2016, 卷号: 14, 期号: 5, 页码: 253-261
作者:  Xue, Yu;  Lameijer, Eric-Wubbo;  Ye, Kai;  Zhang, Kunlin;  Chang, Suhua
收藏  |  浏览/下载:20/0  |  提交时间:2017/01/23
Pathway-based analysis for genome-wide association study data of bipolar disorder provides new insights for genetic study 期刊论文
PROTEIN & CELL, 2015, 卷号: 6, 期号: 12, 页码: 912-915
作者:  Chang, Suhua;  Wang, Jinglu;  Zhang, Kunlin;  Wang, Jing
收藏  |  浏览/下载:12/0  |  提交时间:2016/01/11
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder 期刊论文
JOURNAL OF MEDICAL GENETICS, 2015, 卷号: 52, 期号: 8, 页码: 523-531
作者:  Zong, Liang;  Guan, Jing;  Ealy, Megan;  Zhang, Qiujing;  Wang, Dayong
收藏  |  浏览/下载:52/0  |  提交时间:2015/12/07
Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals 期刊论文
PLOS ONE, 2015, 卷号: 10, 期号: 7, 页码: 1-16
作者:  Chang, Suhua;  Fang, Kechi;  Zhang, Kunlin;  Wang, Jing
收藏  |  浏览/下载:46/0  |  提交时间:2015/12/07


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