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Seizure|October 19, 2024
CCDC22 variants caused X-linked focal epilepsy and focal cortical dysplasiaYu-Lei He, Yi-Chen Ye, Peng-Yu Wang, et al.Frontiers in Molecular Neuroscience|January 22, 2024
DLG3 variants caused X-linked epilepsy with/without neurodevelopmental disorders and the genotype-phenotype correlationYun-Yan He, Sheng Luo, Liang Jin, et al.Epilepsia|October 27, 2025
De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrumXiao-Yu Liang, Xiang-Hong Meng, Wu-Chen Wu, et al.Epilepsia|March 20, 2025
De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsySheng Luo, Wen-Jun Zhang, Mi Jiang, et al.Nature Communications|December 30, 2025
Rapid endothelialization of printed vascular grafts by perivascular niche-circulating endothelial progenitors crosstalkZhe-Qian Zhang, Ping-Ping Yuan, Cong Yao, et al.Journal of Medical Genetics|March 20, 2024
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomesMing-Feng He, Li-Hong Liu, Sheng Luo, et al.Epilepsia|July 9, 2025
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsiesXiang Li, Lin Wang, Xiao-Yu Liang, et al.American Journal of Human Genetics|December 21, 2024
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disordersSheng Luo, Peng-Yu Wang, Peng Zhou, et al.Pageof 4