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CORC

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Linear mixed models for association analysis of quantitative traits with next-generation sequencing data 期刊论文
GENETIC EPIDEMIOLOGY, 2019, 卷号: 43, 期号: 2
作者:  Chiu, Chi-yang;  Yuan, Fang;  Zhang, Bingsong;  Yuan, Ao;  Li, Xin
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/04
PTCH1 alterations are frequent but other genetic alterations are rare in sporadic odontogenic keratocysts. 期刊论文
Oral diseases, 2019
作者:  Qu Jiafei;  Zhang Jianyun;  Zhang Heyu;  Li Xuefen;  Hong Yingying
收藏  |  浏览/下载：22/0  |  提交时间：2019/12/04
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes 期刊论文
The American Journal of Human Genetics, 2019, 卷号: Vol.104 No.1, 页码: 21-34
作者:  Nasim Mavaddat;  Kyriaki Michailidou;  Joe Dennis;  Michael Lush;  Laura Fachal
收藏  |  浏览/下载：31/0  |  提交时间：2019/12/13
Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia 期刊论文
2019, 卷号: 104, 期号: 3, 页码: 439-453
作者:  Chang, Hae Ryung;  Cho, Sung Yoon;  Lee, Jae Hoon;  Lee, Eunkyung;  Seo, Jieun
收藏  |  浏览/下载：33/0  |  提交时间：2020/01/03
TNIP1 Polymorphisms with the Risk of Hepatocellular Carcinoma Based on Chronic Hepatitis B Infection in Chinese Han Population 期刊论文
BIOCHEMICAL GENETICS, 2019, 卷号: 57, 期号: 1, 页码: 117-128
作者:  Cheng, YJ;  Jiang, XC;  Jin, JQ;  Luo, XJ;  Chen, WL
收藏  |  浏览/下载：49/0  |  提交时间：2019/09/10
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patients. 期刊论文
Orphanet journal of rare diseases, 2019, 卷号: 14, 期号: 1, 页码: 221
作者:  Zhu, Guanghui;  Zheng, Yu;  Liu, Yaoxi;  Yan, An;  Hu, Zhengmao
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/27
Genetic Analysis of Reemerging GII.P16-GII.2 Noroviruses in 2016-2017 in China 期刊论文
JOURNAL OF INFECTIOUS DISEASES, 2018, 卷号: 218, 期号: 1, 页码: 133-143
作者:  Tan, Ming;  Ao, Yuanyun;  Duan, Zhaojun;  Cong, Xin;  Jin, Miao
收藏  |  浏览/下载：70/0  |  提交时间：2018/12/29
Comprehensive genetic characteristics of dystrophinopathies in China 期刊论文
ORPHANET JOURNAL OF RARE DISEASES, 2018, 卷号: 13
作者:  Ma, Peipei;  Zhang, Shu;  Zhang, Hao;  Fang, Siying;  Dong, Yuru
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa 期刊论文
HUMAN MOLECULAR GENETICS, 2018, 卷号: 27, 期号: 14, 页码: 2563-2572
作者:  Zhou, Yu;  Li, Shujin;  Huang, Lulin;  Yang, Yeming;  Zhang, Lin
收藏  |  浏览/下载：15/0  |  提交时间：2021/11/01
A Robust and Powerful Set-Valued Approach to Rare Variant Association Analyses of Secondary Traits in Case-Control Sequencing Studies 期刊论文
GENETICS, 2017, 卷号: 205, 期号: 3, 页码: 1049-1062
作者:  Kang, Guolian;  Bi, Wenjian;  Zhang, Hang;  Pounds, Stanley;  Cheng, Cheng
收藏  |  浏览/下载：24/0  |  提交时间：2018/07/30

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