Dagong Sun

476 total citations
33 papers, 379 citations indexed

About

Dagong Sun is a scholar working on Physiology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Dagong Sun has authored 33 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 12 papers in Molecular Biology and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Dagong Sun's work include Erythrocyte Function and Pathophysiology (16 papers), Blood properties and coagulation (10 papers) and Cell death mechanisms and regulation (7 papers). Dagong Sun is often cited by papers focused on Erythrocyte Function and Pathophysiology (16 papers), Blood properties and coagulation (10 papers) and Cell death mechanisms and regulation (7 papers). Dagong Sun collaborates with scholars based in China and United States. Dagong Sun's co-authors include Zongyao Wen, Weibo Ka, Weijuan Yao, Shu Chien, Li Gu, Shu Chien, Zhu Zeng, Zhiyu Tang, Dan Chen and Yuhui Jiang and has published in prestigious journals such as PLoS ONE, Journal of Biomechanics and Journal of Ethnopharmacology.

In The Last Decade

Dagong Sun

33 papers receiving 371 citations

Peers

Dagong Sun
Weibo Ka China
Sara C. Sebag United States
Alessandra Scarpellini United Kingdom
Ralph E. Bottenus United States
Xiao Wan China
L Gu United States
Weibo Ka China
Dagong Sun
Citations per year, relative to Dagong Sun Dagong Sun (= 1×) peers Weibo Ka

Countries citing papers authored by Dagong Sun

Since Specialization
Citations

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

Fields of papers citing papers by Dagong Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dagong Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Dagong Sun. A scholar is included among the top collaborators of Dagong Sun 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 Dagong Sun. Dagong Sun 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.
Wang, Wenjun, Lijun Zhong, Wenxi Zhang, et al.. (2019). Quantitative proteomics reveals TMOD1-related proteins associated with water balance regulation. PLoS ONE. 14(7). e0219932–e0219932. 7 indexed citations
2.
Sun, Dagong, et al.. (2012). Stress-deformation-temperature behavior of a rolling segmented constrained layer damped bogie wheel. Noise Control Engineering Journal. 60(6). 655–664. 5 indexed citations
3.
Chen, Xiaopeng, Xiaofeng Xu, Xianwei Wang, et al.. (2011). Knockdown of hTERT Alters Biophysical Properties of K562 Cells Resulting in Decreased Migration Rate In Vitro. Cell Biochemistry and Biophysics. 61(3). 595–603. 9 indexed citations
4.
Chen, Dan, Xiaolan Zhang, Weibo Ka, et al.. (2011). Effects of Gekko Sulfated Polysaccharide–Protein Complex on the Defective Biorheological Characters of Dendritic Cells Under Tumor Microenvironment. Cell Biochemistry and Biophysics. 62(1). 193–201. 15 indexed citations
5.
Xu, Xiaofeng, Zhu Zeng, Weijuan Yao, et al.. (2010). Biomechanical alterations of dendritic cells by co-culturing with K562 CML cells and their potential role in immune escape. Journal of Biomechanics. 43(12). 2339–2347. 9 indexed citations
6.
Wang, Xianwei, Dan Chen, Xiaolan Zhang, et al.. (2010). Biorheological changes of dendritic cells at the different differentiation stages. Clinical Hemorheology and Microcirculation. 46(4). 265–273. 3 indexed citations
7.
Chen, Dan, Weijuan Yao, Xiaolan Zhang, et al.. (2009). Effects of Gekko sulfated polysaccharide–protein complex on human hepatoma SMMC-7721 cells: Inhibition of proliferation and migration. Journal of Ethnopharmacology. 127(3). 702–708. 38 indexed citations
8.
Wang, Xianwei, Xi Chen, Zhiyu Tang, et al.. (2009). Ryanodine receptor 1 mediates Ca2+ transport and influences the biomechanical properties in RBCs. Journal of Biomechanics. 42(16). 2774–2779. 1 indexed citations
9.
Gu, Li, et al.. (2007). Effects of TFAR19 gene on the in vivo biorheological properties and pathogenicity of mouse erythroleukemia cell line MEL. Science in China Series C Life Sciences. 50(1). 111–119. 2 indexed citations
10.
Yao, Weijuan, Zhu Zeng, Xianwei Wang, et al.. (2007). Exogenous Wild‐Type p53 Gene Improved Survival of Nude Mice Injected with Murine Erythroleukemia Cell Line Through Amelioration of Hemorheological Changes. Microcirculation. 14(2). 155–166. 1 indexed citations
11.
Jiang, Yuhui, Kai Chen, Zhiyu Tang, et al.. (2006). TRAIL gene reorganizes the cytoskeleton and decreases the motility of human leukemic Jurkat cells. Cell Motility and the Cytoskeleton. 63(8). 471–482. 7 indexed citations
12.
Wang, Jinhua, Weibo Ka, Dagong Sun, et al.. (2006). Biochemical and Biophysical Studies on the Precursor Cells of Mouse Erythrocytes at Different Stages. Cell Biochemistry and Biophysics. 45(2). 147–156. 3 indexed citations
13.
Zeng, Zhu, Xiaofeng Xu, Yingyu Zhang, et al.. (2006). Tumor‐derived factors impaired motility and immune functions of dendritic cells through derangement of biophysical characteristics and reorganization of cytoskeleton. Cell Motility and the Cytoskeleton. 64(3). 186–198. 23 indexed citations
14.
Zeng, Zhu, Xiao Liu, Yuhui Jiang, et al.. (2006). Biophysical Studies on the Differentiation of Human CD14<sup>+</sup> Monocytes Into Dendritic Cells. Cell Biochemistry and Biophysics. 45(1). 19–30. 16 indexed citations
15.
Gu, Li, Yuhui Jiang, Ying Wang, et al.. (2005). TFAR19 Gene Changes the Biophysical Properties of Murine Erythroleukemia Cells. Cell Biochemistry and Biophysics. 43(3). 355–364. 11 indexed citations
16.
Jiang, Yuhui, Weijuan Yao, Li Gu, et al.. (2005). Studies on the biomechanical properties of maturing reticulocytes. Journal of Biomechanics. 39(3). 530–535. 14 indexed citations
17.
Yao, Weijuan, Li Gu, Dagong Sun, et al.. (2003). Wild type p53 gene causes reorganization of cytoskeleton and, therefore, the impaired deformability and difficult migration of murine erythroleukemia cells. Cell Motility and the Cytoskeleton. 56(1). 1–12. 29 indexed citations
18.
Yao, Weijuan, et al.. (2001). Low viscosity Ektacytometry and its validation tested by flow chamber. Journal of Biomechanics. 34(11). 1501–1509. 51 indexed citations
19.
Wen, Zongyao, et al.. (1998). Biophysical meanings of orientation and deformation of RBCs in shear flow field of low viscosity with new Ektacytometry. Science in China Series C Life Sciences. 41(2). 195–202. 13 indexed citations
20.
Wen, Zongyao, et al.. (1995). The study on RBC deformability of iron deficiency anemia. Clinical Hemorheology and Microcirculation. 15(1). 81–87. 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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