Zhiying Xie (Z Xie)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 20

Top Topics

Pulmonary Fibrosis

Magnetic Resonance

Muscular Dystrophy

Top Venues

Annals of clinical and translational neurology

Journal of cachexia, sarcopenia and muscle

Journal of neurology, neurosurgery, and psychiatry

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Zhihao Xie, Chang Liu, Chengyue Sun, Yilin Liu, Jieru Peng, Lingchao Meng, Jianwen Deng, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
Single-Nucleus RNA Sequencing Unravels Early Mechanisms of Human Becker Muscular Dystrophy. Annals of neurology (2024)
Tongling Liufu, Xutong Zhao, Meng Yu, Zhiying Xie, Lingchao Meng, He Lv, Wei Zhang, Yun Yuan, Guogang Xing, Jianwen Deng, Zhaoxia Wang
Multiomics analysis reveals serine catabolism as a potential therapeutic target for MELAS. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (12) (2024)
Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data. Journal of cachexia, sarcopenia and muscle 15 (1) (2023)
Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data. Journal of cachexia, sarcopenia and muscle (2023)
Zhiying Xie, Yunlong Lu, Chang Liu, Chengyue Sun, Jiaxi Yu, Chen Ling, Xinghua Luan, Wei Wang, Li Wang, Yanhong Liang, Qianbo Luo, Lingchao Meng, Zhaoxia Wang, Yun Yuan
Cryptic exon activation caused by a novel deep-intronic splice-altering variant in Becker muscular dystrophy. Journal of clinical laboratory analysis (2023)
Yang Zhao, Yue Hou, Xutong Zhao, Tongling Liufu, Meng Yu, Wei Zhang, Zhiying Xie, Victor Wei Zhang, Yun Yuan, Zhaoxia Wang
The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions. Molecular genetics & genomic medicine (2023)
Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data. Journal of cachexia, sarcopenia and muscle 15 (1) (2023)
Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data. Journal of cachexia, sarcopenia and muscle 15 (1) (2023)
Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data. Journal of cachexia, sarcopenia and muscle 15 (1) (2023)
Chengyue Sun, Zhiying Xie, Lu Cong, Yan Xu, Zunjing Liu
An in-frame pseudoexon activation caused by a novel deep-intronic variant in the dysferlin gene. Annals of clinical and translational neurology 10 (2) (2022)
Chengyue Sun, Zhiying Xie, Lu Cong, Yan Xu, Zunjing Liu
An in-frame pseudoexon activation caused by a novel deep-intronic variant in the dysferlin gene. Annals of clinical and translational neurology (2022)
Qi Wang, Meng Yu, Wei Zhang, Qiang Gang, Zhiying Xie, Jin Xu, Chao Zhou, Depeng Wang, Lingchao Meng, He Lv, Zhirong Jia, Jianwen Deng, Yun Yuan, Zhaoxia Wang
Subsarcolemmal and cytoplasmic p62 positivity and rimmed vacuoles are distinctive for PLIN4-myopathy. Annals of clinical and translational neurology 9 (11) (2022)
Zhiying Xie, Chengyue Sun, Chang Liu, Zhihao Xie, Luhua Wei, Jiaxi Yu, Chen Ling, Xuejun Guo, Yilin Liu, Meng Yu, Yinglin Leng, Lingchao Meng, Yunchuang Sun, Jianwen Deng, Suzanne M Leal, Isabelle Schrauwen, Zhaoxia Wang, Yun Yuan
Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variants. Journal of neurology (2022)
Chengyue Sun, Zhiying Xie, Lu Cong, Yan Xu, Zunjing Liu
An in-frame pseudoexon activation caused by a novel deep-intronic variant in the dysferlin gene. Annals of clinical and translational neurology 10 (2) (2022)
Chengyue Sun, Zhiying Xie, Lu Cong, Yan Xu, Zunjing Liu
An in-frame pseudoexon activation caused by a novel deep-intronic variant in the dysferlin gene. Annals of clinical and translational neurology 10 (2) (2022)
Chengyue Sun, Zhiying Xie, Lu Cong, Yan Xu, Zunjing Liu
An in-frame pseudoexon activation caused by a novel deep-intronic variant in the dysferlin gene. Annals of clinical and translational neurology 10 (2) (2022)
Chengyue Sun, Yue Wu, Chen Ling, Zhiying Xie, Yunchuang Sun, Zhihao Xie, Zhixin Li, Xiaojing Fang, Qingle Kong, Jing An, Bo Wang, Yan Zhuo, Wei Zhang, Zhaoxia Wang, Yun Yuan, Zihao Zhang
Reduced blood flow velocity in lenticulostriate arteries of patients with CADASIL assessed by PC-MRA at 7T. Journal of neurology, neurosurgery, and psychiatry (2021)
Zhiying Xie, Chengyue Sun, Yilin Liu, Meng Yu, Yiming Zheng, Lingchao Meng, Gao Wang, Diana M Cornejo-Sanchez, Thashi Bharadwaj, Jin Yan, Lingxiang Zhang, Nicolas Pineda-Trujillo, Wei Zhang, Suzanne M Leal, Isabelle Schrauwen, Zhaoxia Wang, Yun Yuan
Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise strategy in the genomic era. Journal of medical genetics 58 (11) (2020)
Zhiying Xie, Chengyue Sun, Siwen Zhang, Yilin Liu, Meng Yu, Yiming Zheng, Lingchao Meng, Anushree Acharya, Diana M Cornejo-Sanchez, Gao Wang, Wei Zhang, Isabelle Schrauwen, Suzanne M Leal, Zhaoxia Wang, Yun Yuan
Long-read whole-genome sequencing for the genetic diagnosis of dystrophinopathies. Annals of clinical and translational neurology 7 (10) (2020)
Yilin Liu, Y Zheng, Q Gang, Zhiying Xie, Y Jin, X Zhang, X Deng, H Hao, F Gao, Z Zhang, H Xiong, W Zhang, Z Wang, Y Yuan
Perimysial microarteriopathy in dermatomyositis with anti-nuclear matrix protein-2 antibodies. European journal of neurology 27 (3) (2019)