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CORC

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BiTSC2: Bayesian inference of tumor clonal tree by joint analysis of single-cell SNV and CNA data 期刊论文
BRIEFINGS IN BIOINFORMATICS, 2022, 页码: 12
作者:  Chen, Ziwei;  Gong, Fuzhou;  Wan, Lin;  Ma, Liang
收藏  |  浏览/下载：24/0  |  提交时间：2022/06/21
Glucose disturbances, cognitive deficits and white matter abnormalities in first-episode drug-naive schizophrenia 期刊论文
Molecular Psychiatry, 2020, 卷号: 25, 期号: 12, 页码: 3220–3230
作者:  Xiangyang Zhang;  Mi Yang;  Xiangdong Du;  Wei Liao;  Dachun Chen
收藏  |  浏览/下载：22/0  |  提交时间：2021/01/28
An epistasis between dopaminergic and oxytocinergic systems confers risk of post-traumatic stress disorder in a traumatized Chinese cohort 期刊论文
SCIENTIFIC REPORTS, 2019, 卷号: 9, 页码: 8
作者:  Zhang, Kunlin;  Li, Gen;  Wang, Li;  Cao, Chengqi;  Fang, Ruojiao
收藏  |  浏览/下载：28/0  |  提交时间：2020/02/29
Genome-Wide Comparisons of Mutations Induced by Carbon-Ion Beam and Gamma-Rays Irradiation in Rice via Resequencing Multiple Mutants 期刊论文
FRONTIERS IN PLANT SCIENCE, 2019, 卷号: 10, 页码: 13
作者:  Yang, Guili;  Luo, Wenlong;  Zhang, Jian;  Yan, Xiancheng;  Du, Yan
收藏  |  浏览/下载：13/0  |  提交时间：2022/01/19
The TNF-Alpha Gene-1031T > C Polymorphism Is Associated With Onset Age but Not With Risk of Schizophrenia in a Chinese Population 期刊论文
NEUROPSYCHOLOGY, 2019, 卷号: 33, 期号: 4, 页码: 482-489
作者:  Xiu, Meihong;  Zhang, Guangya;  Chen, Nan;  Chen, Song;  Tan, Yunlong
收藏  |  浏览/下载：71/0  |  提交时间：2019/06/03
A regulatory variant in TBX2 promoter is related to the decreased susceptibility of congenital heart disease in the Han Chinese population 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 2
作者:  Zhang, Ran-ran;  Cai, Ke;  Liu, Lian;  Yang, Qian;  Zhang, Ping
收藏  |  浏览/下载：0/0  |  提交时间：2019/12/05
Schizophrenia Patient Shows a Rare Interleukin 15 Receptor alpha Variant Disrupting Signal Transduction 期刊论文
CURRENT MOLECULAR MEDICINE, 2019, 卷号: 19, 期号: 8
作者:  Pan, Yanli
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/05
Significant association of rare variant p.Gly8Ser in cardiac sodium channel beta 4-subunit SCN4B with atrial fibrillation 期刊论文
ANNALS OF HUMAN GENETICS, 2019, 卷号: 83, 期号: 4
作者:  Xiong, Hongbo;  Yang, Qin;  Zhang, Xiaoping;  Wang, Pengxia;  Chen, Feifei
收藏  |  浏览/下载：43/0  |  提交时间：2019/12/05
Genetic polymorphisms in complement receptor 1 gene and its association with HBV-related liver disease: A case-control study 期刊论文
Gene, 2019, 卷号: Vol.688, 页码: 107-118
作者:  Jingrong Luo;  Siyuan Chen;  Jin Wang;  Shan Ou;  Wei Zhang
收藏  |  浏览/下载：14/0  |  提交时间：2019/12/13
Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome 期刊论文
2019, 卷号: 98, 期号: 2
作者:  Wang, Enshi;  Nie, Yu;  Fan, Xuesong;  Zheng, Zhe;  Gu, Haiyong
收藏  |  浏览/下载：28/0  |  提交时间：2020/01/03

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