Wenjun Xu

795 total citations
54 papers, 615 citations indexed

About

Wenjun Xu is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Wenjun Xu has authored 54 papers receiving a total of 615 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 12 papers in Cardiology and Cardiovascular Medicine and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Wenjun Xu's work include Neurogenesis and neuroplasticity mechanisms (6 papers), Congenital heart defects research (5 papers) and Atrial Fibrillation Management and Outcomes (4 papers). Wenjun Xu is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (6 papers), Congenital heart defects research (5 papers) and Atrial Fibrillation Management and Outcomes (4 papers). Wenjun Xu collaborates with scholars based in China, Canada and Australia. Wenjun Xu's co-authors include Ji-Sook Han, Haoming Song, Cindi M. Morshead, Yi‐Qing Yang, Xing‐Biao Qiu, Nadia Sachewsky, Jinfa Jiang, Bing Dong, Zhisong Chen and Juan Wang and has published in prestigious journals such as PLoS ONE, Scientific Reports and The FASEB Journal.

In The Last Decade

Wenjun Xu

48 papers receiving 613 citations

Peers

Wenjun Xu
Yingxi Wu China
Inga Gurevich United States
Shixiang Wen United States
Scott Sayers United States
Yuxia Han United States
Bilal N. Sheikh Australia
Yingxi Wu China
Wenjun Xu
Citations per year, relative to Wenjun Xu Wenjun Xu (= 1×) peers Yingxi Wu

Countries citing papers authored by Wenjun Xu

Since Specialization
Citations

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

Fields of papers citing papers by Wenjun Xu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wenjun Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Wenjun Xu. A scholar is included among the top collaborators of Wenjun Xu 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 Wenjun Xu. Wenjun Xu 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.
Li, Congying, Ying Huang, Zihan Liu, et al.. (2025). The interplay between form deprivation and dopamine signaling in regulating the expression of circadian rhythm-related genes in the retina of mice. Graefe s Archive for Clinical and Experimental Ophthalmology. 263(12). 3413–3421.
2.
Wang, Jinjie, Hao Qiao, Ping Wang, et al.. (2024). Exploration of DNA nucleotide adsorption on GeTe monolayer through DFT analysis. Materials Science in Semiconductor Processing. 184. 108846–108846. 5 indexed citations
3.
Kang, Meng‐Tian, Yong Liu, Chi Zhang, et al.. (2024). SSVT: Self-Supervised Vision Transformer For Eye Disease Diagnosis Based On Fundus Images. 1–4.
5.
Liu, Yong, Meng‐Tian Kang, Shuo Gao, et al.. (2024). Diagnosis of Multiple Fundus Disorders Amidst a Scarcity of Medical Experts Via Self-Supervised Machine Learning. IEEE Internet of Things Journal. 1–1. 2 indexed citations
6.
Yang, Lin, et al.. (2023). Elevated plasma myoglobin level is closely associated with type 2 diabetic kidney disease. Journal of Diabetes. 16(3). e13508–e13508. 2 indexed citations
7.
Wang, Yingmei, Xing Ma, Xin Liu, et al.. (2022). Modification of alternative splicing in bovine somatic cell nuclear transfer embryos using engineered CRISPR-Cas13d. Science China Life Sciences. 65(11). 2257–2268. 5 indexed citations
8.
Li, Jiayong, Wenjun Xu, Zhe Zhou, et al.. (2021). Evaluation of atherogenic lipoprotein-cholesterol to HDL cholesterol ratio as a prognostic test for ST-segment elevation myocardial infarction. International Journal of Medical Sciences. 18(13). 2897–2904. 1 indexed citations
9.
Tan, Hong‐Wei, Zhisong Chen, Fei Chen, et al.. (2018). Tryptase Promotes the Profibrotic Phenotype Transfer of Atrial Fibroblasts by PAR2 and PPARγ Pathway. Archives of Medical Research. 49(8). 568–575. 19 indexed citations
10.
Xu, Wenjun, et al.. (2018). A Neurosphere Assay to Evaluate Endogenous Neural Stem Cell Activation in a Mouse Model of Minimal Spinal Cord Injury. Journal of Visualized Experiments. 6 indexed citations
11.
Yan, Wenwen, Haoming Song, Jinfa Jiang, et al.. (2016). Characteristics of B cell-associated gene expression in patients with coronary artery disease. Molecular Medicine Reports. 13(5). 4113–4121. 14 indexed citations
12.
Shen, Yuqin, Haoming Song, Wenlin Ma, et al.. (2016). The Prognostic Value of Peak Cardiac Power Output in Chinese Patients with Chronic Heart Failure. PLoS ONE. 11(1). e0147423–e0147423. 3 indexed citations
13.
14.
Yu, Hong, Jiahong Xu, Haoming Song, et al.. (2014). Mutational Spectrum of the NKX2-5 Gene in Patients with Lone Atrial Fibrillation. International Journal of Medical Sciences. 11(6). 554–563. 33 indexed citations
15.
Sachewsky, Nadia, et al.. (2014). Primitive Neural Stem Cells in the Adult Mammalian Brain Give Rise to GFAP-Expressing Neural Stem Cells. Stem Cell Reports. 2(6). 810–824. 36 indexed citations
16.
Wang, Juan, Yuanfeng Xin, Wenjun Xu, et al.. (2013). Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease. DNA and Cell Biology. 32(12). 708–716. 24 indexed citations
17.
Zhao, Lan, Jiahong Xu, Wenjun Xu, et al.. (2013). A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy. International Journal of Molecular Medicine. 33(3). 654–660. 32 indexed citations
18.
Xu, Wenjun, Jiahong Xu, Bing Sun, et al.. (2012). The effect of PPARG gene polymorphisms on the risk of coronary heart disease: a meta-analysis. Molecular Biology Reports. 40(2). 875–884. 15 indexed citations
19.
Zhang, Xinyuan, Wenjun Xu, Bing Dong, et al.. (2011). Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients. Eye. 25(12). 1581–1589. 12 indexed citations
20.
Xu, Wenjun, et al.. (2011). A novel missense mutation of the ECM1 gene in a Chinese patient with lipoid proteinosis. Clinical and Experimental Dermatology. 37(1). 28–30. 10 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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