Kunzhe Dong

1.8k total citations
46 papers, 1.1k citations indexed

About

Kunzhe Dong is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Kunzhe Dong has authored 46 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 12 papers in Genetics and 12 papers in Immunology. Recurrent topics in Kunzhe Dong's work include Cancer-related molecular mechanisms research (6 papers), Genetic and phenotypic traits in livestock (6 papers) and Herpesvirus Infections and Treatments (5 papers). Kunzhe Dong is often cited by papers focused on Cancer-related molecular mechanisms research (6 papers), Genetic and phenotypic traits in livestock (6 papers) and Herpesvirus Infections and Treatments (5 papers). Kunzhe Dong collaborates with scholars based in China, United States and Canada. Kunzhe Dong's co-authors include Jiliang Zhou, Deqiang Ding, Jiali Liu, Yuehui Ma, Qianjun Zhao, C. Chen, Lin Jiang, Xiaohong He, Uros Midic and Weijun Guan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Circulation.

In The Last Decade

Kunzhe Dong

44 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Kunzhe Dong China 20 614 323 286 157 122 46 1.1k
Walter Santana-Garcia France 4 1.1k 1.8× 195 0.6× 260 0.9× 176 1.1× 161 1.3× 4 1.4k
Yuanyan Xiong China 19 916 1.5× 277 0.9× 279 1.0× 192 1.2× 128 1.0× 56 1.4k
Noboru J. Sakabe United States 18 1.0k 1.7× 204 0.6× 148 0.5× 75 0.5× 100 0.8× 27 1.3k
D. Depétris France 23 1.1k 1.8× 447 1.4× 95 0.3× 173 1.1× 134 1.1× 44 1.5k
James Wettenhall Australia 8 562 0.9× 134 0.4× 152 0.5× 131 0.8× 238 2.0× 9 1.1k
Swarnaseetha Adusumalli Singapore 7 624 1.0× 408 1.3× 115 0.4× 109 0.7× 49 0.4× 8 1.1k
Shuai Xiao China 16 533 0.9× 178 0.6× 260 0.9× 186 1.2× 85 0.7× 61 1.1k
Chie Murata Japan 11 326 0.5× 168 0.5× 75 0.3× 78 0.5× 122 1.0× 21 771

Countries citing papers authored by Kunzhe Dong

Since Specialization
Citations

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

Fields of papers citing papers by Kunzhe Dong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kunzhe Dong

This figure shows the co-authorship network connecting the top 25 collaborators of Kunzhe Dong. A scholar is included among the top collaborators of Kunzhe Dong 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 Kunzhe Dong. Kunzhe Dong 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
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Bordán, Zsuzsanna, Stephen Haigh, Xueyi Li, et al.. (2024). PDZ-Binding Kinase, a Novel Regulator of Vascular Remodeling in Pulmonary Arterial Hypertension. Circulation. 150(5). 393–410. 5 indexed citations
3.
Zhou, Yaqi, Qiuhua Yang, Jiean Xu, et al.. (2024). Blockade of endothelial adenosine receptor 2 A suppresses atherosclerosis in vivo through inhibiting CREB-ALK5-mediated endothelial to mesenchymal transition. Pharmacological Research. 203. 107156–107156. 10 indexed citations
4.
Wang, Liang, Xiangqin He, Guoqing Hu, et al.. (2024). A novel mouse model carrying a gene trap insertion into the Hmgxb4 gene locus to examine Hmgxb4 expression in vivo. Physiological Reports. 12(8). e16014–e16014. 1 indexed citations
5.
Zhang, Wei, Li‐Hua Pan, Xiaoliang Wu, et al.. (2024). Functional characterization of human IL-8 in vascular stenosis using a novel humanized transgenic mouse model. Vascular Pharmacology. 157. 107438–107438.
6.
Zou, Jianqiu, Wenjuan Wang, Yi Lü, et al.. (2023). Neddylation is required for perinatal cardiac development through stimulation of metabolic maturation. Cell Reports. 42(1). 112018–112018. 13 indexed citations
7.
Pu, Yong, et al.. (2022). Sex-specific extracellular matrix remodeling during early adipogenic differentiation by gestational bisphenol A exposure. Chemosphere. 302. 134806–134806. 3 indexed citations
8.
Singla, Bhupesh, Pushpankur Ghoshal, Mary Cherian‐Shaw, et al.. (2022). Receptor-independent fluid-phase macropinocytosis promotes arterial foam cell formation and atherosclerosis. Science Translational Medicine. 14(663). eadd2376–eadd2376. 28 indexed citations
9.
Xu, Cheng, Hongyi Zhou, Yulan Jin, et al.. (2022). Hepatic neddylation deficiency triggers fatal liver injury via inducing NF-κB-inducing kinase in mice. Nature Communications. 13(1). 7782–7782. 25 indexed citations
10.
Lyu, Qing, Nunu Huang, Kunzhe Dong, et al.. (2021). The miR-378/PGC1β/mTOR axis as an alternative mechanism to promote autophagy during adipogenesis. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1866(6). 158921–158921. 1 indexed citations
11.
Singla, Bhupesh, Hui‐Ping Lin, Jiean Xu, et al.. (2021). Loss of myeloid cell-specific SIRPα, but not CD47, attenuates inflammation and suppresses atherosclerosis. Cardiovascular Research. 118(15). 3097–3111. 41 indexed citations
12.
He, Xiangqin, Kunzhe Dong, Jian Shen, et al.. (2021). Deficiency of the novel high mobility group protein HMGXB4 protects against systemic inflammation-induced endotoxemia in mice. Proceedings of the National Academy of Sciences. 118(7). 8 indexed citations
13.
Zhang, Lei, Chen Zhu, Mohammad Heidari, et al.. (2020). Marek’s disease vaccines-induced differential expression of known and novel microRNAs in primary lymphoid organ bursae of White Leghorn. Veterinary Research. 51(1). 19–19. 6 indexed citations
14.
Dong, Kunzhe, Min Yang, Qing Ma, et al.. (2020). Genomic analysis of worldwide sheep breeds reveals PDGFD as a major target of fat-tail selection in sheep. BMC Genomics. 21(1). 800–800. 39 indexed citations
15.
Wen, Tong, Jinhua Liu, Xiangqin He, et al.. (2019). Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation. Cell Death and Differentiation. 26(12). 2790–2806. 38 indexed citations
16.
Ahmed, Abu, Kunzhe Dong, Jinhua Liu, et al.. (2018). Long noncoding RNA NEAT1 (nuclear paraspeckle assembly transcript 1) is critical for phenotypic switching of vascular smooth muscle cells. PMC. 12 indexed citations
17.
Ding, Deqiang, Jiali Liu, Uros Midic, et al.. (2018). TDRD5 binds piRNA precursors and selectively enhances pachytene piRNA processing in mice. Nature Communications. 9(1). 127–127. 45 indexed citations
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Gorkhali, Neena Amatya, Kunzhe Dong, Min Yang, et al.. (2016). Genomic analysis identified a potential novel molecular mechanism for high-altitude adaptation in sheep at the Himalayas. Scientific Reports. 6(1). 29963–29963. 37 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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