Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variantsZhiying Xie, Yun Yuan, Yunchuang Sun et al.|Journal of Neurology|2022Cited by 13
A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology dataZhihao Xie, Chang Liu, Chengyue Sun et al.|Journal of Cachexia Sarcopenia and Muscle|2023Cited by 8
Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophyZhiying Xie, Yun Yuan, Chang Liu et al.|Frontiers in Genetics|2022Cited by 7
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A novel deep intronic variant introduce dystrophin pseudoexon in Becker muscular dystrophy: A case reportChang Liu, Yanyu Lu, Haiyan Yu et al.|Heliyon|2024Cited by 3