GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits

por Huang, Dandan, Yi, Xianfu, Zhang, Shijie, Zheng, Zhanye, Wang, Panwen, Xuan, Chenghao, Sham, Pak Chung, Wang, Junwen, Li, Mulin Jun
Publicado 2018

Cell-Type-Specific Gene Modules Related to the Regional Homogeneity of Spontaneous Brain Activity and Their Associations With Common Brain Disorders

por Shen, Junlin, Yang, Bingbing, Xie, Zhonghua, Wu, Heng, Zheng, Zhanye, Wang, Jianhua, Wang, Ping, Zhang, Peng, Li, Wei, Ye, Zhaoxiang, Yu, Chunshui
Publicado 2021

QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes

por Zheng, Zhanye, Huang, Dandan, Wang, Jianhua, Zhao, Ke, Zhou, Yao, Guo, Zhenyang, Zhai, Sinan, Xu, Hang, Cui, Hui, Yao, Hongcheng, Wang, Zhao, Yi, Xianfu, Zhang, Shijie, Sham, Pak Chung, Li, Mulin Jun
Publicado 2020

The support of genetic evidence for cardiovascular risk induced by antineoplastic drugs

por Cui, Hui, Zuo, Shengkai, Liu, Zipeng, Liu, Huanhuan, Wang, Jianhua, You, Tianyi, Zheng, Zhanye, Zhou, Yao, Qian, Xinyi, Yao, Hongcheng, Xie, Lu, Liu, Tong, Sham, Pak Chung, Yu, Ying, Li, Mulin Jun
Publicado 2020

Interrogating cell type-specific cooperation of transcriptional regulators in 3D chromatin

por Yi, Xianfu, Zheng, Zhanye, Xu, Hang, Zhou, Yao, Huang, Dandan, Wang, Jianhua, Feng, Xiangling, Zhao, Ke, Fan, Xutong, Zhang, Shijie, Dong, Xiaobao, Wang, Zhao, Shen, Yujun, Cheng, Hui, Shi, Lei, Li, Mulin Jun
Publicado 2021

Activation of P-TEFb by cAMP-PKA signaling in autosomal dominant polycystic kidney disease

por Sun, Yongzhan, Liu, Zhiheng, Cao, Xinyi, Lu, Yi, Mi, Zeyun, He, Chaoran, Liu, Jing, Zheng, Zhanye, Li, Mulin Jun, Li, Tiegang, Xu, Dechao, Wu, Ming, Cao, Ying, Li, Yuhao, Yang, Baoxue, Mei, Changlin, Zhang, Lirong, Chen, Yupeng
Publicado 2019

CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies

por Wang, Jianhua, Huang, Dandan, Zhou, Yao, Yao, Hongcheng, Liu, Huanhuan, Zhai, Sinan, Wu, Chengwei, Zheng, Zhanye, Zhao, Ke, Wang, Zhao, Yi, Xianfu, Zhang, Shijie, Liu, Xiaorong, Liu, Zipeng, Chen, Kexin, Yu, Ying, Sham, Pak Chung, Li, Mulin Jun
Publicado 2020

An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

por Wang, Zhao, Liang, Qian, Qian, Xinyi, Hu, Bolang, Zheng, Zhanye, Wang, Jianhua, Hu, Yuelin, Bao, Zhengkai, Zhao, Ke, Zhou, Yao, Feng, Xiangling, Yi, Xianfu, Li, Jin, Shi, Jiandang, Liu, Zhe, Hao, Jihui, Chen, Kexin, Yu, Ying, Sham, Pak Chung, Lu, Wange, Wang, Xiaoyan, Song, Weihong, Li, Mulin Jun
Publicado 2023

Genome-wide association and functional interrogation identified a variant at 3p26.1 modulating ovarian cancer survival among Chinese women

por Dai, Hongji, Chu, Xinlei, Liang, Qian, Wang, Mengyun, Li, Lian, Zhou, Yao, Zheng, Zhanye, Wang, Wei, Wang, Zhao, Li, Haixin, Wang, Jianhua, Zheng, Hong, Zhao, Yanrui, Liu, Luyang, Yao, Hongcheng, Luo, Menghan, Wang, Qiong, Kang, Shan, Li, Yan, Wang, Ke, Song, Fengju, Zhang, Ruoxin, Wu, Xiaohua, Cheng, Xi, Zhang, Wei, Wei, Qingyi, Li, Mulin Jun, Chen, Kexin
Publicado 2021