Wenli Sheng

837 total citations
39 papers, 641 citations indexed

About

Wenli Sheng is a scholar working on Neurology, Molecular Biology and Rheumatology. According to data from OpenAlex, Wenli Sheng has authored 39 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 13 papers in Molecular Biology and 11 papers in Rheumatology. Recurrent topics in Wenli Sheng's work include Moyamoya disease diagnosis and treatment (9 papers), Cerebrovascular and genetic disorders (6 papers) and Intracranial Aneurysms: Treatment and Complications (4 papers). Wenli Sheng is often cited by papers focused on Moyamoya disease diagnosis and treatment (9 papers), Cerebrovascular and genetic disorders (6 papers) and Intracranial Aneurysms: Treatment and Complications (4 papers). Wenli Sheng collaborates with scholars based in China and United States. Wenli Sheng's co-authors include Jiejie Li, Zhiyi Zuo, Jiao Deng, Jiaoxing Li, Xiaowei Xu, Lin Liu, Man Luo, Rong Lai, Fei Ye and Xiaoxin Wu and has published in prestigious journals such as PLoS ONE, Brain and Brain Research.

In The Last Decade

Wenli Sheng

36 papers receiving 632 citations

Peers

Wenli Sheng

PHYSI

RHEUM

NEURO

EDM

Carolina Gravina Italy

Nadira Ali United Kingdom

Antonio Ruocco Italy

Jing-Cheng Li China

Brittany L. Adler United States

Yanlin Zhang China

Masaki Nakayama Japan

Toshio Asano Japan

Ali Sazcı Türkiye

Nobuyo Maeda United States

Carolina Gravina Italy

Wenli Sheng

348 ×1.7

240 ×1.6

PHYSI

124 ×0.8

RHEUM

48 ×0.3

NEURO

59 ×0.7

EDM

Citations per year, relative to Wenli Sheng Wenli Sheng (= 1×) peers Carolina Gravina

Countries citing papers authored by Wenli Sheng

Since Specialization

Citations

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

Fields of papers citing papers by Wenli Sheng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wenli Sheng

This figure shows the co-authorship network connecting the top 25 collaborators of Wenli Sheng. A scholar is included among the top collaborators of Wenli Sheng 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 Wenli Sheng. Wenli Sheng 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

Li, Shuai, et al.. (2025). Diagnostic Challenges of Cerebral Venous Thrombosis Mimicking Brain Tumor: A Case Report. American Journal of Case Reports. 26. e949234–e949234.

Luo, Man, Xiaoling Li, Jing Lin, et al.. (2025). The Guanylate Cyclase Soluble Subunit Alpha-1 Deficiency Impairs Angiogenesis in Zebrafishes and Mice: In Vivo and In Vitro Studies. Molecular Neurobiology. 62(7). 8248–8260. 2 indexed citations

Yuan, Kang, Wenbiao Xian, Lishan Lin, et al.. (2025). Effect of Preinfection Health Status on COVID‐19 Severity and Cognitive Function. Brain and Behavior. 15(10). e70793–e70793. 1 indexed citations

Li, Jiaoxing, et al.. (2024). Mapping cell diversity in human sporadic cerebral cavernous malformations. Gene. 924. 148605–148605.

Ye, Fei, Liang Feng, Yuanyuan Dai, et al.. (2023). RNF213 loss-of-function promotes pathological angiogenesis in moyamoya disease via the Hippo pathway. Brain. 146(11). 4674–4689. 34 indexed citations

Luo, Man, Jing Lin, Fei Ye, et al.. (2023). Loss of Gucy1a3 causes poor post-stroke recovery by reducing angiogenesis via the HIF-1α/VEGFA signaling pathway in mice. Journal of Stroke and Cerebrovascular Diseases. 33(2). 107484–107484. 1 indexed citations

Dai, Yuanyuan, et al.. (2023). Rnf-213 Knockout Induces Pericyte Reduction and Blood-Brain Barrier Impairment in Mouse. Molecular Neurobiology. 60(11). 6188–6200. 8 indexed citations

Ye, Fei, et al.. (2022). Bioinformatic Analysis of Coexpressed Differentially Expressed Genes and Potential Targets for Intracerebral and Subarachnoid Hemorrhage. World Neurosurgery. 159. e442–e452. 2 indexed citations

Ye, Fei, et al.. (2021). N6-Methyladenosine RNA modification in cerebrospinal fluid as a novel potential diagnostic biomarker for progressive multiple sclerosis. Journal of Translational Medicine. 19(1). 316–316. 23 indexed citations

10.

Ye, Fei, et al.. (2021). Identification of immune-associated gene signature and immune cell infiltration related to overall survival in progressive multiple sclerosis. Multiple Sclerosis and Related Disorders. 55. 103188–103188. 1 indexed citations

11.

Lin, Jing, Man Luo, Jiaoxing Li, et al.. (2020). Mutations of RNF213 are responsible for sporadic cerebral cavernous malformation and lead to a mulberry-like cluster in zebrafish. Journal of Cerebral Blood Flow & Metabolism. 41(6). 1251–1263. 14 indexed citations

12.

Lin, Jing, Wenbiao Xian, Rong Lai, et al.. (2019). Bilateral cerebral infarction associated with severe arteriosclerosis in the A1 segment: a case report. Journal of International Medical Research. 47(3). 1373–1377. 1 indexed citations

13.

Li, Jiaoxing, Yufang Wang, Jing Lin, et al.. (2019). AND score: a simple tool for predicting infection in acute ischemic stroke patients without a ventilator in the Chinese population. Journal of International Medical Research. 48(3). 1219687855–1219687855. 4 indexed citations

14.

Lin, Jing & Wenli Sheng. (2018). RNF213 Variant Diversity Predisposes Distinct Populations to Dissimilar Cerebrovascular Diseases. BioMed Research International. 2018. 1–7. 16 indexed citations

15.

Chen, Huimin, Huijiao Liu, Rong Lai, et al.. (2016). Mutation of rnf213a by TALEN causes abnormal angiogenesis and circulation defects in zebrafish. Brain Research. 1644. 70–78. 24 indexed citations

16.

Luo, Man, et al.. (2014). The Single Nucleotide Polymorphism rs2208454 Confers an Increased Risk for Ischemic Stroke: A Case–Control Study. CNS Neuroscience & Therapeutics. 20(10). 893–897. 6 indexed citations

17.

Xu, Xiaowei, Li Jiang, Man Luo, et al.. (2014). Perfusion-weighted magnetic resonance imaging detects recurrent isolated vertigo caused by cerebral hypoperfusion. International Journal of Neuroscience. 125(6). 449–455. 6 indexed citations

18.

Lai, Rong, et al.. (2013). The -7351C/T Polymorphism in the TPA Gene and Ischemic Stroke Risk: A Meta-Analysis. PLoS ONE. 8(1). e53558–e53558. 9 indexed citations

19.

Li, Jiaoxing, Man Luo, Xiaowei Xu, & Wenli Sheng. (2011). Association between 1425G/A SNP in PRKCH and ischemic stroke among Chinese and Japanese populations: A meta-analysis including 3686 cases and 4589 controls. Neuroscience Letters. 506(1). 55–58. 14 indexed citations

20.

Zeng, Jinsheng, Jian Yu, Zhan Zhao, et al.. (2005). Cultured human embryonic neocortical cells survive and grow in infarcted cavities of adult rat brains and interconnect with host brain.. PubMed. 118(4). 275–80. 2 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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