Jianwen Deng (Jiaxi Yu)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Venues

Cell discovery

Journal of medical genetics

Journal of neurology

Proceedings of the National Academy of Sciences of the United States of America

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

Publications

Yilei Zheng, Tongling Liufu, Bing Wen, Chao Zhou, Lingchun Liu, Yusen Qiu, Wenquan Zou, Wei Zhang, Yu Li, Jianfeng Pei, Yiheng Zeng, Wanjin Chen, Chunhua Zhang, Yun Yuan, Guochun Wang, Chuanzhu Yan, Xin Lu, Jianwen Deng, Zhaoxia Wang, Daojun Hong
COASY variant as a new genetic cause of riboflavin-responsive lipid storage myopathy. Cell discovery 10 (1) (2024)
Yilei Zheng, Tongling Liufu, Bing Wen, Chao Zhou, Lingchun Liu, Yusen Qiu, Wenquan Zou, Wei Zhang, Yu Li, Jianfeng Pei, Yiheng Zeng, Wanjin Chen, Chunhua Zhang, Yun Yuan, Guochun Wang, Chuanzhu Yan, Xin Lu, Jianwen Deng, Zhaoxia Wang, Daojun Hong
COASY variant as a new genetic cause of riboflavin-responsive lipid storage myopathy. Cell discovery 10 (1) (2024)
Yilei Zheng, Tongling Liufu, Bing Wen, Chao Zhou, Lingchun Liu, Yusen Qiu, Wenquan Zou, Wei Zhang, Yu Li, Jianfeng Pei, Yiheng Zeng, Wanjin Chen, Chunhua Zhang, Yun Yuan, Guochun Wang, Chuanzhu Yan, Xin Lu, Jianwen Deng, Zhaoxia Wang, Daojun Hong
COASY variant as a new genetic cause of riboflavin-responsive lipid storage myopathy. Cell discovery 10 (1) (2024)
Yilei Zheng, Tongling Liufu, Bing Wen, Chao Zhou, Lingchun Liu, Yusen Qiu, Wenquan Zou, Wei Zhang, Yu Li, Jianfeng Pei, Yiheng Zeng, Wanjin Chen, Chunhua Zhang, Yun Yuan, Guochun Wang, Chuanzhu Yan, Xin Lu, Jianwen Deng, Zhaoxia Wang, Daojun Hong
COASY variant as a new genetic cause of riboflavin-responsive lipid storage myopathy. Cell discovery 10 (1) (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)
Jiaxi Yu, Tongling Liufu, Yilei Zheng, Jin Xu, Lingchao Meng, Wei Zhang, Yun Yuan, Daojun Hong, Nicolas Charlet-Berguerand, Zhaoxia Wang, Jianwen Deng
CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model. Proceedings of the National Academy of Sciences of the United States of America 119 (41) (2022)
Jiayu Sun, Wenwen Su, Jianwen Deng, Yao Qin, Zhaoxia Wang, Yuhe Liu
DNA2 mutation causing multisystemic disorder with impaired mitochondrial DNA maintenance. Journal of human genetics 67 (12) (2022)
Xutong Zhao, Meng Yu, Yawen Zhao, Yiming Zheng, Lingchao Meng, Kang Du, Zhiying Xie, He Lv, Wei Zhang, Jing Liu, Qingqing Wang, Yun Yuan, Zhaoxia Wang, Jianwen Deng
Circulating cell-free mtDNA release is associated with the activation of cGAS-STING pathway and inflammation in mitochondrial diseases. Journal of neurology 269 (9) (2022)
Mingyue Luan, Yunchuang Sun, Jing Chen, Yanyan Jiang, Fan Li, Luhua Wei, Wei Sun, Jinfa Ma, Lu Song, Jianghong Liu, Bing Liu, Yaohua Pei, Zhaoxia Wang, Li Zhu, Jianwen Deng
Diagnostic Value of Salivary Real-Time Quaking-Induced Conversion in Parkinson's Disease and Multiple System Atrophy. Movement disorders : official journal of the Movement Disorder Society 37 (5) (2022)
Jianwen Deng, Binbin Zhou, Jiaxi Yu, Xiaochen Han, Jianhui Fu, Xiaobin Li, Xufang Xie, Min Zhu, Yilei Zheng, Xueyu Guo, Pidong Li, Qingqing Wang, Jing Liu, Wei Zhang, Yun Yuan, Sheng Yao, Zhaoxia Wang, Daojun Hong
Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease. Journal of medical genetics (2021)
Jianwen Deng, Jianwen Deng, Xueyu Guo, Jingli Shan, Xinghua Luan, Li Cao, Juan Zhao, Meng Yu, Wei Zhang, He Lv, Zhiying Xie, LingChao Meng, Yiming Zheng, Yawen Zhao, Qiang Gang, Qingqing Wang, Jing Liu, Min Zhu, Binbin Zhou, Pidong Li, Yinzhe Liu, Yang Wang, Chuanzhu Yan, Daojun Hong, Yun Yuan, Zhaoxia Wang
The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3. Brain : a journal of neurology 144 (6) (2021)
Jianwen Deng, Muliang Gu, Yu Miao, Sheng Yao, Min Zhu, Pu Fang, Xuefan Yu, Pidong Li, Yanan Su, Jian Huang, Jun Zhang, Jiaxi Yu, Fan Li, Jing Bai, Wei Sun, Yining Huang, Yun Yuan, Daojun Hong, Zhaoxia Wang
Long-read sequencing identified repeat expansions in the 5'UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease. Journal of medical genetics 56 (11) (2019)

Jianwen Deng.css-eqlu8i{font-size:small;padding-left:4px;} (Jiaxi Yu)

Publication Activity (10 Years)

Top Topics

Top Venues

Jianwen Deng (Jiaxi Yu)