| Issue Date | Title | Author(s) |
| 2019 | A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavin | Shi, Kaili; Shi, Zhen; Yanu, Huifang; Wang, Xiaodong; Yang, Yanling; Xiong, Hui; Gu, Qiang; Wu, Ye; Jiang, Yuwu; Wang, Jingmin |
| 27-Oct-2023 | Detection of magnetospheric ion drift patterns at Mars | Zhang, Chi; Nilsson, Hans; Ebihara, Yusuke; Yamauchi, Masatoshi; Persson, Moa; Rong, Zhaojin; Zhong, Jun; Dong, Chuanfei; Chen, Yuxi; Zhou, Xuzhi; Sun, Yixin; Harada, Yuki; Halekas, Jasper; Xu, Shaosui; Futaana, Yoshifumi; Shi, Zhen; Yuan, Chongjing; Yun, Xiaotong; Fu, Song; Gao, Jiawei; Holmstrom, Mats; Wei, Yong; Barabash, Stas |
| 27-Oct-2023 | Detection of magnetospheric ion drift patterns at Mars | Zhang, Chi; Nilsson, Hans; Ebihara, Yusuke; Yamauchi, Masatoshi; Persson, Moa; Rong, Zhaojin; Zhong, Jun; Dong, Chuanfei; Chen, Yuxi; Zhou, Xuzhi; Sun, Yixin; Harada, Yuki; Halekas, Jasper; Xu, Shaosui; Futaana, Yoshifumi; Shi, Zhen; Yuan, Chongjing; Yun, Xiaotong; Fu, Song; Gao, Jiawei; Holmstrom, Mats; Wei, Yong; Barabash, Stas |
| May-2020 | Epilepsy in children with leukodystrophies | Zhang, Jie; Ban, Tingting; Zhou, Ling; Ji, Haoran; Yan, Huifang; Shi, Zhen; Cao, Binbin; Jiang, Yuwu; Wang, Jingmin; Wu, Ye |
| Feb-2021 | Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing | Yan, Huifang; Ji, Haoran; Kubisiak, Thomas; Wu, Ye; Xiao, Jiangxi; Gu, Qiang; Yang, Yanling; Xie, Han; Ji, Taoyun; Gao, Kai; Li, Dongxiao; Xiong, Hui; Shi, Zhen; Li, Ming; Zhang, Yuehua; Duan, Ruoyu; Bao, Xinhua; Jiang, Yuwu; Burmeister, Margit; Wang, Jingmin |
| 2019 | Identification in Chinese patients with GLIALCAM mutations of megalencephalic leukoencephalopathy with subcortical cysts and brain pathological study on Glialcam knock-in mouse models | Shi, Zhen; Yan, Hui-Fang; Cao, Bin-Bin; Guo, Mang-Mang; Xie, Han; Gao, Kai; Xiao, Jiang-Xi; Yang, Yan-Ling; Xiong, Hui; Gu, Qiang; Li, Ming; Wu, Ye; Jiang, Yu-Wu; Wang, Jing-Min |
| 2018 | Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy | Chen, Li; Yan, Huifang; Cao, Binbin; Wu, Ye; Gu, Qiang; Xiao, Jiangxi; Yang, Yanling; Yang, Huixia; Shi, Zhen; Yang, Zhixian; Pan, Hong; Chang, Xingzhi; Chen, Junya; Sun, Yu; Zhang, Yuehua; Wu, Xiru; Jiang, Yuwu; Wang, Jingmin |
| 2018 | De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism | Fan, Yanjie; Yin, Wu; Hu, Bing; Kline, Antonie D.; Zhang, Victor Wei; Liang, Desheng; Sun, Yu; Wang, Lili; Tang, Sha; Powis, Zoe; Li, Lei; Yan, Huifang; Shi, Zhen; Yang, Xiaoping; Chen, Yinyin; Wang, Jingmin; Jiang, Yuwu; Tan, Hu; Gu, Xuefan; Wu, Lingqian; Yu, Yongguo |
| Apr-2023 | Properties of Flapping Current Sheet of the Martian Magnetotail | Zhang, Chi; Rong, Zhaojin; Zhang, Lulu; Gao, Jiawei; Shi, Zhen; Klinger, Lucy; Shen, Chao; Wei, Yong |
| 2019 | Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene | Yan, Huifang; Shi, Zhen; Wu, Ye; Xiao, Jiangxi; Gu, Qiang; Yang, Yanling; Li, Ming; Gao, Kai; Chen, Yinyin; Yang, Xiaoping; Ji, Haoran; Cao, Binbin; Duan, Ruoyu; Jiang, Yuwu; Wang, Jingmin |
| Aug-2022 | Three-Dimensional Configuration of Induced Magnetic Fields Around Mars | Zhang, Chi; Rong, Zhaojin; Klinger, Lucy; Nilsson, Hans; Shi, Zhen; He, Fei; Gao, Jiawei; Li, Xinzhou; Futaana, Yoshifumi; Ramstad, Robin; Wang, Xiaodong; Holmstrom, Mats; Barabash, Stas; Fan, Kai; Wei, Yong |
