Haisu Wan

872 total citations
30 papers, 596 citations indexed

About

Haisu Wan is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Haisu Wan has authored 30 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Cancer Research and 7 papers in Genetics. Recurrent topics in Haisu Wan's work include MicroRNA in disease regulation (5 papers), RNA modifications and cancer (5 papers) and Estrogen and related hormone effects (5 papers). Haisu Wan is often cited by papers focused on MicroRNA in disease regulation (5 papers), RNA modifications and cancer (5 papers) and Estrogen and related hormone effects (5 papers). Haisu Wan collaborates with scholars based in China, United States and Sweden. Haisu Wan's co-authors include Reuben Lotan, Waun Ki Hong, R Lotan, Ping Yue, W K Hong, Shi‐Yong Sun, Jingbo Wu, Heng Zhang, Ming Zhao and Linglin Yang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Haisu Wan

30 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Haisu Wan China 13 417 124 100 93 90 30 596
Mohammad Tariq Malik United States 14 444 1.1× 67 0.5× 76 0.8× 70 0.8× 96 1.1× 20 734
Weicai Chen China 15 495 1.2× 157 1.3× 91 0.9× 38 0.4× 117 1.3× 32 726
Donald L. Helseth United States 12 310 0.7× 67 0.5× 73 0.7× 95 1.0× 223 2.5× 19 744
Yong Pan China 12 298 0.7× 181 1.5× 74 0.7× 50 0.5× 57 0.6× 17 493
Elazer R. Edelman United States 4 390 0.9× 66 0.5× 49 0.5× 87 0.9× 78 0.9× 5 671
Shamik Das United States 15 475 1.1× 157 1.3× 259 2.6× 65 0.7× 29 0.3× 22 775
Yang Shi United States 16 402 1.0× 70 0.6× 131 1.3× 27 0.3× 37 0.4× 29 691
P. G. Montaldo Italy 14 391 0.9× 132 1.1× 96 1.0× 60 0.6× 58 0.6× 27 608
Hengliang Shi China 17 548 1.3× 154 1.2× 154 1.5× 33 0.4× 42 0.5× 52 774

Countries citing papers authored by Haisu Wan

Since Specialization
Citations

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

Fields of papers citing papers by Haisu Wan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haisu Wan

This figure shows the co-authorship network connecting the top 25 collaborators of Haisu Wan. A scholar is included among the top collaborators of Haisu Wan 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 Haisu Wan. Haisu Wan 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.
Jiang, Jie, Xueqin Song, Xiaoyan Wang, et al.. (2023). Engrailed 2 triggers the activation of multiple phosphorylation-induced signaling pathways in both transcription-dependent and -independent manners. Biochemical and Biophysical Research Communications. 680. 127–134. 1 indexed citations
2.
Wang, Jian, Zhiya Zhang, Jie Jiang, et al.. (2022). KDM2A plays a dual role in regulating the expression of malignancy-related genes in esophageal squamous cell carcinoma. Biochemical and Biophysical Research Communications. 624. 53–58. 7 indexed citations
3.
Cao, Yong, Xiaoyan Wang, Li Tang, et al.. (2020). Engrailed-2 promotes a malignant phenotype of esophageal squamous cell carcinoma through upregulating the expression of pro-oncogenic genes. PeerJ. 8. e8662–e8662. 7 indexed citations
5.
Yang, Yingcheng, Xiaoping Tang, Xueqin Song, et al.. (2019). Evidence for an oncogenic role of HOXC6 in human non-small cell lung cancer. PeerJ. 7. e6629–e6629. 18 indexed citations
6.
Tang, Xiaoping, Yingcheng Yang, Xueqin Song, et al.. (2019). SIX4 acts as a master regulator of oncogenes that promotes tumorigenesis in non-small-cell lung cancer cells. Biochemical and Biophysical Research Communications. 516(3). 851–857. 19 indexed citations
7.
Zhang, Heng, Ming Zhao, Biqiong Wang, et al.. (2016). Magnetic nanoparticle-loaded electrospun polymeric nanofibers for tissue engineering. Materials Science and Engineering C. 73. 537–543. 103 indexed citations
8.
Guan, Jikui, Elizabeth R. Tucker, Haisu Wan, et al.. (2016). The ALK inhibitor PF-06463922 is effective as a single agent in neuroblastoma driven by expression of ALK and MYCN. Disease Models & Mechanisms. 9(9). 941–952. 53 indexed citations
9.
Chen, Chen, Fanrong Meng, Haisu Wan, & Qinghua Zhou. (2015). [Interaction between microRNAs and OCT4].. SHILAP Revista de lepidopterología. 18(1). 55–8. 2 indexed citations
10.
Deng, Han‐Xiang, et al.. (2014). miR-1228 promotes the proliferation and metastasis of hepatoma cells through a p53 forward feedback loop. British Journal of Cancer. 112(2). 365–374. 41 indexed citations
11.
Meng, Fanrong, Chen Chen, Haisu Wan, & Qinghua Zhou. (2014). [Advances of lentiviral vectors].. SHILAP Revista de lepidopterología. 17(12). 870–6. 3 indexed citations
12.
Fan, Yu, Jun Wu, Haisu Wan, et al.. (2012). Potential application of non-small cell lung cancer-associated autoantibodies to early cancer diagnosis. Biochemical and Biophysical Research Communications. 423(3). 613–619. 40 indexed citations
13.
Fan, Yu, Lu Li, Zhihao Wu, et al.. (2012). nm23‐H1 gene driven by hTERT promoter induces inhibition of invasive phenotype and metastasis of lung cancer xenograft in mice. Thoracic Cancer. 4(1). 41–52. 12 indexed citations
14.
Wan, Haisu, Li Y, Yu Fan, et al.. (2011). A site-directed mutagenesis method particularly useful for creating otherwise difficult-to-make mutants and alanine scanning. Analytical Biochemistry. 420(2). 163–170. 10 indexed citations
15.
Feng, Hua, et al.. (2010). [Interference of homologous sequences on the SNP study of CYP2A13 gene].. Europe PMC (PubMed Central). 13(2). 94–7. 2 indexed citations
16.
Sun, Shi‐Yong, Haisu Wan, Ping Yue, Waun Ki Hong, & Reuben Lotan. (2000). Evidence That Retinoic Acid Receptor β Induction by Retinoids Is Important for Tumor Cell Growth Inhibition. Journal of Biological Chemistry. 275(22). 17149–17153. 96 indexed citations
17.
Wan, Haisu, Nobuhiko Oridate, Dafna Lotan, W K Hong, & R Lotan. (1999). Overexpression of retinoic acid receptor beta in head and neck squamous cell carcinoma cells increases their sensitivity to retinoid-induced suppression of squamous differentiation by retinoids.. PubMed. 59(14). 3518–26. 51 indexed citations
18.
Wan, Haisu, Marcia I. Dawson, Waun Ki Hong, & Reuben Lotan. (1998). Overexpressed Activated Retinoid X Receptors Can Mediate Growth Inhibitory Effects of Retinoids in Human Carcinoma Cells. Journal of Biological Chemistry. 273(41). 26915–26922. 18 indexed citations
19.
Wan, Haisu, Marcia I. Dawson, Waun Ki Hong, & Reuben Lotan. (1997). Enhancement of Calu-1 human lung carcinoma cell growth in serum-free medium by retinoids: dependence on AP-1 activation, but not on retinoid response element activation. Oncogene. 15(17). 2109–2118. 14 indexed citations
20.
Gogos, Joseph A., et al.. (1996). Recognition of diverse sequences by class I zinc fingers: asymmetries and indirect effects on specificity in the interaction between CF2II and A+T-rich elements.. Proceedings of the National Academy of Sciences. 93(5). 2159–2164. 23 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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