Yacen Hu

721 total citations
20 papers, 317 citations indexed

About

Yacen Hu is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Yacen Hu has authored 20 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Neurology, 9 papers in Cellular and Molecular Neuroscience and 9 papers in Neurology. Recurrent topics in Yacen Hu's work include Parkinson's Disease Mechanisms and Treatments (8 papers), Neurological diseases and metabolism (7 papers) and Nuclear Receptors and Signaling (4 papers). Yacen Hu is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (8 papers), Neurological diseases and metabolism (7 papers) and Nuclear Receptors and Signaling (4 papers). Yacen Hu collaborates with scholars based in China and United States. Yacen Hu's co-authors include Beisha Tang, Xinxiang Yan, Jifeng Guo, Lu Shen, Qian Xu, Qiying Sun, Hong Jiang, Lingyan Yao, Chengyuan Song and Chunrong Wang and has published in prestigious journals such as Neurology, Scientific Reports and Frontiers in Immunology.

In The Last Decade

Yacen Hu

19 papers receiving 309 citations

Peers

Yacen Hu
Yacen Hu
Citations per year, relative to Yacen Hu Yacen Hu (= 1×) peers Susen Schaake

Countries citing papers authored by Yacen Hu

Since Specialization
Citations

This map shows the geographic impact of Yacen Hu'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 Yacen Hu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yacen Hu more than expected).

Fields of papers citing papers by Yacen Hu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yacen Hu. 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 Yacen Hu. The network helps show where Yacen Hu may publish in the future.

Co-authorship network of co-authors of Yacen Hu

This figure shows the co-authorship network connecting the top 25 collaborators of Yacen Hu. A scholar is included among the top collaborators of Yacen Hu 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 Yacen Hu. Yacen Hu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hu, Yacen, Qiying Sun, Yi Fang, et al.. (2022). Age of onset correlates with clinical characteristics and prognostic outcomes in neuromyelitis optica spectrum disorder. Frontiers in Immunology. 13. 1056944–1056944. 15 indexed citations
2.
Hu, Yacen & Qiying Sun. (2022). Cerebellar Swelling Followed by Atrophy in Anti-Homer-3 Antibody–Associated Cerebellitis. Neurology. 99(14). 610–611. 2 indexed citations
3.
Hu, Yacen, Zhiqin Wang, Lin Zhou, & Qiying Sun. (2021). Prolonged Hemiplegic Migraine Led to Persistent Hyperperfusion and Cortical Necrosis: Case Report and Literature Review. Frontiers in Neurology. 12. 748034–748034. 3 indexed citations
4.
Hu, Yacen, Qiying Sun, Yafang Zhou, et al.. (2021). NOTCH3 Variants and Genotype-Phenotype Features in Chinese CADASIL Patients. Frontiers in Genetics. 12. 705284–705284. 17 indexed citations
5.
Zhou, Yangjie, Runcheng He, Yuwen Zhao, et al.. (2020). Olfactory Dysfunction and Its Relationship With Clinical Features of Parkinson's Disease. Frontiers in Neurology. 11. 526615–526615. 5 indexed citations
7.
Zhou, Yafang, Yacen Hu, Qiying Sun, & Nina Xie. (2019). Non-coding RNA in Fragile X Syndrome and Converging Mechanisms Shared by Related Disorders. Frontiers in Genetics. 10. 139–139. 7 indexed citations
8.
He, Runcheng, Yacen Hu, Lingyan Yao, et al.. (2019). Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia. Prion. 13(1). 116–123. 10 indexed citations
9.
Li, Wenwen, et al.. (2018). [Etiologies and risk factors for young people with intracerebral hemorrhage].. PubMed. 43(11). 1246–1250. 8 indexed citations
11.
Du, Juan, Yacen Hu, Beisha Tang, Hong Jiang, & Lu Shen. (2017). Identification of novel SPG11 mutations in a cohort of Chinese families with hereditary spastic paraplegia. International Journal of Neuroscience. 128(2). 146–150. 12 indexed citations
12.
Yang, Nannan, Yang Wei, Jifeng Guo, et al.. (2016). Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigra. Scientific Reports. 6(1). 28933–28933. 18 indexed citations
13.
Guo, Jifeng, Kai Li, Lei Wang, et al.. (2015). Polygenic determinants of Parkinson's disease in a Chinese population. Neurobiology of Aging. 36(4). 1765.e1–1765.e6. 56 indexed citations
14.
Guo, Jifeng, Shuang He, Qian Xu, et al.. (2015). Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagiline.. PubMed. 8(10). 18158–64. 8 indexed citations
15.
Xu, Qian, Yacen Hu, Chengyuan Song, et al.. (2013). Hypomethylation of SNCA in blood of patients with sporadic Parkinson's disease. Journal of the Neurological Sciences. 337(1-2). 123–128. 82 indexed citations
16.
Tian, Jinyong, Jifeng Guo, Lei Wang, et al.. (2012). Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease. Neuroscience Letters. 516(2). 207–211. 11 indexed citations
17.
Hu, Yacen, Beisha Tang, Jifeng Guo, et al.. (2011). Variant in the 3′ region of SNCA associated with Parkinson’s disease and serum α-synuclein levels. Journal of Neurology. 259(3). 497–504. 27 indexed citations
18.
Wang, Lei, Jifeng Guo, Wen‐Wen Zhang, et al.. (2011). Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease. Journal of Clinical Neuroscience. 18(12). 1699–1701. 7 indexed citations
19.
Du, Juan, Yacen Hu, Beisha Tang, et al.. (2011). Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1. Clinical Neurology and Neurosurgery. 113(6). 480–482. 16 indexed citations
20.
Wang, Lei, Jifeng Guo, Wenwen Zhang, et al.. (2010). Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population. Neuroscience Letters. 473(2). 131–135. 11 indexed citations

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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