Jiaxi Yu

831 total citations
20 papers, 269 citations indexed

About

Jiaxi Yu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Jiaxi Yu has authored 20 papers receiving a total of 269 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Jiaxi Yu's work include Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Jiaxi Yu is often cited by papers focused on Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Jiaxi Yu collaborates with scholars based in China, Romania and France. Jiaxi Yu's co-authors include Jianwen Deng, Zhaoxia Wang, Yun Yuan, Daojun Hong, Yilei Zheng, Min Zhu, Wei Zhang, Sheng Yao, Pidong Li and Yanan Su and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurobiology of Aging and Neurobiology of Disease.

In The Last Decade

Jiaxi Yu

19 papers receiving 266 citations

Peers

Countries citing papers authored by Jiaxi Yu

Since Specialization

Citations

This map shows the geographic impact of Jiaxi Yu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jiaxi Yu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jiaxi Yu more than expected).

Fields of papers citing papers by Jiaxi Yu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jiaxi Yu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jiaxi Yu. The network helps show where Jiaxi Yu may publish in the future.

Co-authorship network of co-authors of Jiaxi Yu

This figure shows the co-authorship network connecting the top 25 collaborators of Jiaxi Yu. A scholar is included among the top collaborators of Jiaxi Yu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jiaxi Yu. Jiaxi Yu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Mutational and clinical spectrum of myofibrillar myopathy in one center from China 2024 ·Journal of Neuromuscular Diseases ·(unknown), Peng Sun, Meng Yu, Zhiying Xie, Jiaxi Yu, Xiujuan Liu, (unknown), He Lv, Jianwen Deng, Yun Yuan, Zhaoxia Wang, Wei Zhang	1
2	Novel TUBA4A variant causes congenital myopathy with focal myofibrillar disorganisation 2024 ·Journal of Medical Genetics ·(unknown), Chao Zhou, Xingzhi Chang, Liwen Wu, Yilei Zheng, Jiaxi Yu, Bai Li, (unknown), Meng Yu, (unknown), Wei Zhang, Yun Yuan, Jianwen Deng, Zhaoxia Wang	4
3	Disease Progression of GNE Myopathy and Its Relationship With Genotype 2024 ·Neurology Genetics ·Haozhe Sun, (unknown), Jiaxi Yu, Lingchao Meng, Qiang Gang, He Lv, Wei Zhang, Yun Yuan, Meng Yu, Zhao-xia Wang	0
4	Complex I deficiency in m.3243A>G fibroblasts is alleviated by reducing NADH accumulation 2023 ·Frontiers in Physiology ·(unknown), (unknown), Jiaxi Yu, Meng Yu, (unknown), (unknown), Jianwen Deng, Guo‐Gang Xing, Zhao-xia Wang	8
5	Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stress 2023 ·Neurobiology of Disease ·Hui Wang, Yilei Zheng, Jiaxi Yu, Lingchao Meng, Wei Zhang, Daojun Hong, Zhaoxia Wang, Yun Yuan, Jianwen Deng	2
6	Cryptic exon activation caused by a novel deep‐intronic splice‐altering variant in Becker muscular dystrophy 2023 ·Journal of Clinical Laboratory Analysis ·Zhiying Xie, (unknown), Chang Liu, Chengyue Sun, Jiaxi Yu, Ling Chen, Xinghua Luan, Wei Wang, Li Wang, (unknown), (unknown), Lingchao Meng, Zhaoxia Wang, Yun Yuan	1
7	Novel variants, muscle imaging, and myopathological changes in Chinese patients with VCP‐related multisystem proteinopathy 2023 ·Molecular Genetics & Genomic Medicine ·(unknown), Qi Wang, Yiming Zheng, Meng Yu, Zhiying Xie, Ling Chen, Lingchao Meng, Jiaxi Yu, Yilei Zheng, Yikang Wang, (unknown), Chang Liu, Yawen Zhao, Yun Yuan, Jianwen Deng, Qiang Gang, Zhaoxia Wang	3
8	Non-coding CGG repeat expansion in LOC642361/NUTM2B-AS1 is associated with a phenotype of oculopharyngodistal myopathy 2023 ·Journal of Medical Genetics ·Xinyu Gu, Jiaxi Yu, (unknown), Jianwen Deng, (unknown), Kai Qiao, (unknown), Mingshi Gao, Chongbo Zhao, Jihong Dong, (unknown), Jingli Shan, Chuanzhu Yan, (unknown), Yuwei Da, Wenhua Zhu, Jianying Xi, Zhaoxia Wang	6
9	Unraveling rare form of adult-onset NIID by characteristic brain MRI features: A single-center retrospective review 2022 ·Frontiers in Neurology ·Fan Li, Qi Wang, Ying Zhu, Jiangxi Xiao, (unknown), Jiaxi Yu, Jianwen Deng, (unknown), Zhaoxia Wang	3
10	Intermediate-length CGG repeat expansion in NOTCH2NLC is associated with pathologically confirmed Alzheimer's disease 2022 ·Neurobiology of Aging ·Wei Wu, Jiaxi Yu, Xiaojing Qian, Xue Wang, Yuanyuan Xu, Zhaoxia Wang, Jianwen Deng	4
11	The polyG diseases: a new disease entity 2022 ·Acta Neuropathologica Communications ·(unknown), Yilei Zheng, Jiaxi Yu, Yun Yuan, Zhaoxia Wang, Jianwen Deng, Daojun Hong	20
12	FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALS 2022 ·Molecular Neurobiology ·(unknown), Yilei Zheng, Xiaobing Li, (unknown), Jiaxi Yu, Yang Zou, Min Zhu, Yanyan Yu, Xin Fang, (unknown), Wei Zhang, Yun Yuan, Zhaoxia Wang, Jianwen Deng, Daojun Hong	10
13	Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variants 2022 ·Journal of Neurology ·Zhiying Xie, Chengyue Sun, Chang Liu, (unknown), (unknown), Jiaxi Yu, Ling Chen, Xue‐Jun Guo, Yilin Liu, Meng Yu, (unknown), Lingchao Meng, (unknown), Jianwen Deng, Suzanne M. Leal, Isabelle Schrauwen, Zhaoxia Wang, Yun Yuan	7
14	Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy 2022 ·European Journal of Neurology ·Daojun Hong, Hui Wang, Min Zhu, Yun Peng, (unknown), Yilei Zheng, Meng Yu, Lingchao Meng, Fan Li, Jiaxi Yu, (unknown), Jianwen Deng, Zhaoxia Wang, Yun Yuan	7
15	Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation 2022 ·Frontiers in Molecular Neuroscience ·(unknown), Mengdie Wang, Ran Tang, Yanan Huang, Jiaxi Yu, (unknown), Yilei Zheng, (unknown), Jianwen Deng, Zhi Wang, Wei Ma, Wenjing Song, Wu Yuan, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Yu Liu, Lingchao Meng	3
16	Oculopharyngodistal myopathy 2022 ·Current Opinion in Neurology ·Jiaxi Yu, Jianwen Deng, Zhaoxia Wang	11
17	CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model 2022 ·Proceedings of the National Academy of Sciences ·Jiaxi Yu, (unknown), Yilei Zheng, Jin Xu, Lingchao Meng, Wei Zhang, Yun Yuan, Daojun Hong, Nicolas Charlet‐Berguerand, Zhaoxia Wang, Jianwen Deng	29
18	GGC Repeat Expansion in the NOTCH2NLC Gene Is Associated With a Phenotype of Predominant Motor–Sensory and Autonomic Neuropathy 2021 ·Frontiers in Genetics ·Hui Wang, Jiaxi Yu, Meng Yu, Jianwen Deng, Wei Zhang, He Lv, Jing Liu, (unknown), (unknown), (unknown), Daojun Hong, Lingchao Meng, Zhaoxia Wang, Yun Yuan	18
19	Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease 2021 ·Journal of Medical Genetics ·Jianwen Deng, (unknown), Jiaxi Yu, Xiaochen Han, (unknown), Xiaobin Li, (unknown), Min Zhu, Yilei Zheng, Xueyu Guo, Pidong Li, Qingqing Wang, Jing Liu, Wei Zhang, Yun Yuan, Sheng Yao, Zhaoxia Wang, Daojun Hong	35
20	Long-read sequencing identified repeat expansions in the 5′UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease 2019 ·Journal of Medical Genetics ·Jianwen Deng, (unknown), (unknown), Sheng Yao, Min Zhu, Fang Pu, (unknown), Pidong Li, Yanan Su, Jian Huang, Jun Zhang, Jiaxi Yu, Fan Li, Jing Bai, Wei Sun, Yining Huang, Yun Yuan, Daojun Hong, Zhaoxia Wang	97

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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