TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study von Tian, Wo‐Tu, Zhan, Fei‐Xia, Liu, Zhen‐Hua, Liu, Zhe, Liu, Qing, Guo, Xia‐Nan, Zhou, Zai‐Wei, Wang, Shi‐Ge, Liu, Xiao‐Rong, Jiang, Hong, Li, Xun‐Hua, Zhao, Guo‐Hua, Li, Hai‐Yan, Tang, Jian‐Guang, Bi, Guang‐Hui, Zhong, Ping, Yin, Xiao‐Meng, Liu, Tao‐Tao, Ni, Rui‐Long, Zheng, Hao‐Ran, Liu, Xiao‐Li, Qian, Xiao‐Hang, Wu, Jing‐Ying, Cao, Yu‐Wen, Zhang, Chao, Liu, Shi‐Hua, Wu, Ying‐Ying, Wang, Qun‐Feng, Xu, Ting, Hou, Wen‐Zhe, Li, Zi‐Yi, Ke, Hui‐Yi, Zhu, Ze‐Yu, Zheng, Lan, Wang, Tian, Rong, Tian‐Yi, Wu, Li, Zhang, Yu, Fang, Kan, Wang, Zhan‐Hang, Zhang, Ya‐Kun, Zhang, Mei, Zhao, Yu‐Wu, Tang, Bei‐Sha, Luan, Xing‐Hua, Huang, Xiao‐Jun, Cao, Li

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Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients von Tian, Wo‐Tu, Huang, Xiao‐Jun, Mao, Xiao, Liu, Qing, Liu, Xiao‐Li, Zeng, Sheng, Guo, Xia‐Nan, Shen, Jun‐Yi, Xu, Yang‐Qi, Tang, Hui‐Dong, Yin, Xiao‐Meng, Zhang, Mei, Tang, Wei‐Guo, Liu, Xiao‐Rong, Tang, Bei‐Sha, Chen, Sheng‐Di, Cao, Li

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The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China von Huang, Xiao‐Jun, Wang, Shi‐Ge, Guo, Xia‐Nan, Tian, Wo‐Tu, Zhan, Fei‐Xia, Zhu, Ze‐Yu, Yin, Xiao‐Meng, Liu, Qing, Yin, Kai‐Li, Liu, Xiao‐Rong, Zhang, Yu, Liu, Zhen‐Guo, Liu, Xiao‐Li, Zheng, Lan, Wang, Tian, Wu, Li, Rong, Tian‐Yi, Wang, Yan, Zhang, Mei, Bi, Guang‐Hui, Tang, Wei‐Guo, Zhang, Chao, Zhong, Ping, Wang, Chun‐Yu, Tang, Jian‐Guang, Lu, Wei, Zhang, Ru‐Xu, Zhao, Guo‐Hua, Li, Xun‐Hua, Li, Hua, Chen, Tao, Li, Hai‐Yan, Luo, Xiao‐Guang, Song, Yan‐Yan, Tang, Hui‐Dong, Luan, Xing‐Hua, Zhou, Hai‐Yan, Tang, Bei‐Sha, Chen, Sheng‐Di, Cao, Li

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The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype von Meng, Heng, Xu, Hai-Qing, Yu, Lu, Lin, Guo-Wang, He, Na, Su, Tao, Shi, Yi-Wu, Li, Bin, Wang, Jie, Liu, Xiao-Rong, Tang, Bin, Long, Yue-Sheng, Yi, Yong-Hong, Liao, Wei-Ping

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Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability von Tian, Mao‐Qiang, Liu, Xiao‐Rong, Lin, Si‐Mei, Wang, Jie, Luo, Sheng, Gao, Liang‐Di, Chen, Xiao‐Bin, Liang, Xiao‐Yu, Liu, Zhi‐Gang, He, Na, Yi, Yong‐Hong, Liao, Wei‐Ping

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CELSR1 variants are associated with partial epilepsy of childhood von Chen, Zheng, Luo, Sheng, Liu, Zhi‐Gang, Deng, Yan‐Chun, He, Su‐Li, Liu, Xiao‐Rong, Yi, Yong‐Hong, Wang, Jie, Gao, Liang‐Di, Li, Bing‐Mei, Wu, Zhi‐Jun, Ye, Zi‐Long, Liang, De‐Hai, Bian, Wen‐Jun, Liao, Wei‐Ping

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Regioselective synthesis of 3-nitroindoles under non-acidic and non-metallic conditions von Zhang, Hua, Su, Rong-Chuan, Qin, Yu-Li, Wang, Xiao-Juan, Chen, Dan, Liu, Xiao-Rong, Jiang, Yu-Xin, Zhao, Peng

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Mir20a/106a-WTX axis regulates RhoGDIa/CDC42 signaling and colon cancer progression von Zhu, Gui-Fang, Xu, Yang-Wei, Li, Jian, Niu, Hui-Lin, Ma, Wen-Xia, Xu, Jia, Zhou, Pei-Rong, Liu, Xia, Ye, Dan-Li, Liu, Xiao-Rong, Yan, Tao, Zhai, Wei-Ke, Xu, Zhi-Jun, Liu, Chun, Wang, Lei, Wang, Hao, Luo, Jia-Mao, Liu, Li, Li, Xuan-Qi, Guo, Suiqun, Jiang, Hui-Ping, Shen, Peng, Lin, Hui-Kuan, Yu, Di-Hua, Ding, Yan-Qing, Zhang, Qing-Ling

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Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies von He, Na, Lin, Zhi-Jian, Wang, Jie, Wei, Feng, Meng, Heng, Liu, Xiao-Rong, Chen, Qian, Su, Tao, Shi, Yi-Wu, Yi, Yong-Hong, Liao, Wei-Ping

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CCDC88C variants are associated with focal epilepsy and genotype–phenotype correlation von Chen, Yu‐Jie, Wang, Wen‐Jie, Zou, Dong‐Fang, Luo, Jun‐Xia, Jin, Pei‐Yan, Jin, Liang, Liu, Xiao‐Rong, Liao, Wei‐Ping, Li, Bin, Chen, Yong‐Jun

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Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratification von Tang, Bin, Li, Bin, Gao, Liang-Di, He, Na, Liu, Xiao-Rong, Long, Yue-Sheng, Zeng, Yang, Yi, Yong-Hong, Su, Tao, Liao, Wei-Ping

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CS2164, a novel multi‐target inhibitor against tumor angiogenesis, mitosis and chronic inflammation with anti‐tumor potency von Zhou, You, Shan, Song, Li, Zhi‐Bin, Xin, Li‐Jun, Pan, De‐Si, Yang, Qian‐Jiao, Liu, Ying‐Ping, Yue, Xu‐Peng, Liu, Xiao‐Rong, Gao, Ji‐Zhou, Zhang, Jin‐Wen, Ning, Zhi‐Qiang, Lu, Xian‐Ping

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ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation von Wang, Jing-Yang, Zhou, Peng, Wang, Jie, Tang, Bin, Su, Tao, Liu, Xiao-Rong, Li, Bing-Mei, Meng, Heng, Shi, Yi-Wu, Yi, Yong-Hong, He, Na, Liao, Wei-Ping

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CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures von Li, Jia, Lin, Si‐Mei, Qiao, Jing‐Da, Liu, Xiao‐Rong, Wang, Jie, Jiang, Mi, Zhang, Jing, Zhong, Min, Chen, Xu‐Qin, Zhu, Jing, He, Na, Su, Tao, Shi, Yi‐Wu, Yi, Yong‐Hong, Liao, Wei‐Ping

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RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia von Ma, Mei-Gang, Liu, Xiao-Rong, Wu, Yuan, Wang, Jie, Li, Bing-Mei, Shi, Yi-Wu, Su, Tao, Li, Bin, Liu, De-Tian, Yi, Yong-Hong, Liao, Wei-Ping

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Editorial: Sub-molecular mechanism of genetic epilepsy von Liao, Wei-Ping, Chen, Qian, Jiang, Yu-Wu, Luo, Sheng, Liu, Xiao-Rong

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DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect von Liu, Liu, Chen, Zi-Rong, Xu, Hai-Qing, Liu, De-Tian, Mao, Yong, Liu, Han-Kui, Liu, Xiao-Rong, Zhou, Peng, Lin, Si-Mei, Li, Bin, He, Na, Su, Tao, Zhai, Qiong-Xiang, Meng, Heng, Liao, Wei-Ping, Yi, Yong-Hong

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CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia von Liu, Xiao‐Rong, Ye, Ting‐Ting, Zhang, Wen‐Jun, Guo, Xuan, Wang, Jie, Huang, Shao‐Ping, Xie, Long‐Shan, Song, Xing‐Wang, Deng, Wei‐Wen, Li, Bing‐Mei, He, Na, Wu, Qian‐Yi, Zhuang, Min‐Zhi, Xu, Meng, Shi, Yi‐Wu, Su, Tao, Yi, Yong‐Hong, Liao, Wei‐Ping

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Immunological features and functional analysis of anti-CFH autoantibodies in patients with atypical hemolytic uremic syndrome von Guo, Wei-yi, Song, Di, Liu, Xiao-rong, Chen, Zhi, Xiao, Hui-jie, Ding, Jie, Sun, Shu-zhen, Liu, Hong-yan, Wang, Su-xia, Yu, Feng, Zhao, Ming-hui

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Tailoring microstructures of CoCrFeNiNb0.25 hypoeutectic high-entropy alloy by hot deformation von Liu, Xiao-Rong, He, Feng, Li, Jun-Jie, Dang, Ying-Ying, Wang, Zhi-Jun, Wang, Jin-Cheng

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