Showing 1 - 8 results of 8 for search 'Bei-sha TANG', query time: 0.03s
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Parkinson’s Disease and Cognitive Impairment by Yang Yang, Bei-sha Tang, Ji-feng Guo
Published 2016-01-01
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The Progress of Induced Pluripotent Stem Cells as Models of Parkinson’s Disease by Ji-feng Kang, Bei-sha Tang, Ji-feng Guo
Published 2016-01-01
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High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease by Chaodong Wang, Hankui Liu, Xu-Ying Li, Jinghong Ma, Zhuqin Gu, Xiuli Feng, Shu Xie, Bei-Sha Tang, Shengdi Chen, Wei Wang, Jian Wang, Jianguo Zhang, Piu Chan
Published 2024-07-01
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Identification of clinically actionable secondary genetic variants from whole‐genome sequencing in a large‐scale Chinese population by Pei‐Kuan Cong, Saber Khederzadeh, Cheng‐Da Yuan, Rui‐Jie Ma, Yi‐Yao Zhang, Jun‐Quan Liu, Shi‐Hui Yu, Lin Xu, Jian‐Hua Gao, Hong‐Xu Pan, Jin‐Chen Li, Shu‐Yang Xie, Ke‐Qi Liu, Bei‐Sha Tang, Hou‐Feng Zheng
Published 2022-05-01
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Temporal trends and rural–urban disparities in cerebrovascular risk factors, in-hospital management and outcomes in ischaemic strokes in China from 2005 to 2015: a nationwide seria... by Yongjun Wang, Zixiao Li, Xin Yang, Ying Xian, Hao Li, Meng Wang, Gregg C Fonarow, Xia Meng, Yong Jiang, Guo-zhong Li, Li-Ping Liu, Yi-long Wang, Yi Yang, Lee H Schwamm, Hong-Qiu Gu, Janet Prvu Bettger, Xing-Quan Zhao, Chun-Juan Wang, Bei-Sha Tang, Yu-Ming Xu, Chelsea Liu, Winnie Yip, Zhi-Yi He, Xin-Miao Zhang, Ke-Hui Dong, Run-Qi Wangqin
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HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism by Na He, Bao‐Zhu Guan, Jie Wang, Han‐Kui Liu, Yong Mao, Zhi‐Gang Liu, Fei Yin, Jing Peng, Bo Xiao, Bei‐sha Tang, Dong Zhou, Guang Huang, Qi‐Lin Dai, Ying Zeng, Hong Han, Qiong‐Xiang Zhai, Bin Li, Bin Tang, Wen‐Bin Li, Wang Song, Liu Liu, Yi‐Wu Shi, Bing‐Mei Li, Tao Su, Peng Zhou, Xiao‐Rong Liu, Li‐Wu Guo, Yong‐Hong Yi, Wei‐Ping Liao
Published 2023-06-01
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SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populations by Meng-Yuan Yang, Jia-Dong Zhong, Xin Li, Geng Tian, Wei-Yang Bai, Yi-Hu Fang, Mo-Chang Qiu, Cheng-Da Yuan, Chun-Fu Yu, Nan Li, Ji-Jian Yang, Yu-Heng Liu, Shi-Hui Yu, Wei-Wei Zhao, Jun-Quan Liu, Yi Sun, Pei-Kuan Cong, Saber Khederzadeh, Pian-Pian Zhao, Yu Qian, Peng-Lin Guan, Jia-Xuan Gu, Si-Rui Gai, Xiang-Jiao Yi, Jian-Guo Tao, Xiang Chen, Mao-Mao Miao, Lan-Xin Lei, Lin Xu, Shu-Yang Xie, Jin-Chen Li, Ji-Feng Guo, David Karasik, Liu Yang, Bei-Sha Tang, Fei Huang, Hou-Feng Zheng
Published 2024-12-01
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