A novel pathogenic splicing mutation of RPGR in a Chinese family with X-linked retinitis pigmentosa verified by minigene splicing assay by Hui-Qin Wang, Pei-Kuan Cong, Tian He, Xiao-Feng Yu, Ya-Nan Huo

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Observational and genetic evidence highlight the association of human sleep behaviors with the incidence of fracture by Yu Qian, Jiangwei Xia, Ke-Qi Liu, Lin Xu, Shu-Yang Xie, Guo-Bo Chen, Pei-Kuan Cong, Saber Khederzadeh, Hou-Feng Zheng

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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

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Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project by Pei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, Meng-Yuan Yang, Saber Khederzadeh, Si-Rui Gai, Nan Li, Yu-Heng Liu, Shi-Hui Yu, Wei-Wei Zhao, Jun-Quan Liu, Yi Sun, Xiao-Wei Zhu, Pian-Pian Zhao, Jiang-Wei Xia, Peng-Lin Guan, Yu Qian, Jian-Guo Tao, Lin Xu, Geng Tian, Ping-Yu Wang, Shu-Yang Xie, Mo-Chang Qiu, Ke-Qi Liu, Bei-Sha Tang, Hou-Feng Zheng

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