Haichuan Wang

3.2k total citations · 1 hit paper
92 papers, 2.0k citations indexed

About

Haichuan Wang is a scholar working on Molecular Biology, Surgery and Cell Biology. According to data from OpenAlex, Haichuan Wang has authored 92 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 17 papers in Surgery and 14 papers in Cell Biology. Recurrent topics in Haichuan Wang's work include Insect Resistance and Genetics (22 papers), Hippo pathway signaling and YAP/TAZ (8 papers) and Liver physiology and pathology (7 papers). Haichuan Wang is often cited by papers focused on Insect Resistance and Genetics (22 papers), Hippo pathway signaling and YAP/TAZ (8 papers) and Liver physiology and pathology (7 papers). Haichuan Wang collaborates with scholars based in United States, China and Germany. Haichuan Wang's co-authors include Blair D. Siegfried, Murugesan Rangasamy, Xin Chen, Sek Yee Tan, Diego F. Calvisi, Hong Chen, Ana M. Vélez, Chitvan Khajuria, Matthias Evert and Kenneth E. Narva and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Haichuan Wang

87 papers receiving 2.0k citations

Hit Papers

PPAR-γ signaling in nonalcoholic fatty liver disease: Pat... 2023 2026 2024 2025 2023 50 100 150

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Haichuan Wang United States 25 1.3k 475 323 270 195 92 2.0k
Mengmeng Yang China 21 1.0k 0.8× 177 0.4× 489 1.5× 281 1.0× 94 0.5× 84 1.8k
Qingxin Liu China 22 536 0.4× 145 0.3× 166 0.5× 177 0.7× 166 0.9× 92 1.4k
Qingwei Zhang China 19 732 0.6× 100 0.2× 340 1.1× 323 1.2× 105 0.5× 52 1.6k
Guanglu Shi China 19 1.1k 0.8× 235 0.5× 449 1.4× 288 1.1× 103 0.5× 45 2.0k
N. Ferry France 28 1.4k 1.1× 578 1.2× 599 1.9× 39 0.1× 124 0.6× 69 2.2k
Fenghua Yuan United States 25 1.5k 1.2× 54 0.1× 360 1.1× 410 1.5× 90 0.5× 59 2.2k
José A. Pintor‐Toro Spain 29 1.9k 1.5× 182 0.4× 1.5k 4.6× 285 1.1× 104 0.5× 55 3.1k
Jean‐William Dupuy France 23 749 0.6× 61 0.1× 323 1.0× 114 0.4× 215 1.1× 77 1.4k
Hye Jin You South Korea 22 903 0.7× 819 1.7× 108 0.3× 226 0.8× 71 0.4× 65 2.5k
Toshio Ito Japan 25 486 0.4× 514 1.1× 131 0.4× 101 0.4× 424 2.2× 200 2.2k

Countries citing papers authored by Haichuan Wang

Since Specialization
Citations

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

Fields of papers citing papers by Haichuan Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haichuan Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Haichuan Wang. A scholar is included among the top collaborators of Haichuan Wang 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 Haichuan Wang. Haichuan Wang 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, Chuang, et al.. (2024). Anatomic versus nonanatomic resection for intrahepatic cholangiocarcinoma: a systematic review and meta-analysis. International Journal of Surgery. 111(1). 1440–1453.
2.
Zhou, Yi, Shu Zhang, Xue Wang, et al.. (2024). TSC/mTORC1 mediates mTORC2/AKT1 signaling in c-MYC–induced murine hepatocarcinogenesis via centromere protein M. Journal of Clinical Investigation. 134(22). 3 indexed citations
4.
Chen, Hao, Huabing Tan, Yong Zeng, et al.. (2023). PPAR-γ signaling in nonalcoholic fatty liver disease: Pathogenesis and therapeutic targets. Pharmacology & Therapeutics. 245. 108391–108391. 156 indexed citations breakdown →
5.
Wu, Yangping, Wenting Li, Xi Chen, et al.. (2023). DOG1 as a novel antibody-drug conjugate target for the treatment of multiple gastrointestinal tumors and liver metastasis. Frontiers in Immunology. 14. 1051506–1051506. 4 indexed citations
6.
Du, Jinpeng, Haichuan Wang, Xu Lin, et al.. (2023). MDIG-mediated H3K9me3 demethylation upregulates Myc by activating OTX2 and facilitates liver regeneration. Signal Transduction and Targeted Therapy. 8(1). 351–351. 6 indexed citations
7.
Xiao, Jie, et al.. (2023). Role of integrating cannabinoids and the endocannabinoid system in neonatal hypoxic-ischaemic encephalopathy. Frontiers in Molecular Neuroscience. 16. 1152167–1152167. 3 indexed citations
9.
Li, Hong‐Chun, et al.. (2022). Endocannabinoids regulate cocaine-associated memory through brain AEA–CB1R signalling activation. Molecular Metabolism. 65. 101597–101597. 4 indexed citations
10.
Liang, Bin-yong, Yi Zhou, Manning Qian, et al.. (2021). TBX3 functions as a tumor suppressor downstream of activated CTNNB1 mutants during hepatocarcinogenesis. Journal of Hepatology. 75(1). 120–131. 39 indexed citations
11.
Wang, Haichuan, Raj Bandaru, Matthew A. Lawlor, et al.. (2021). Selective targeting of MYC mRNA by stabilized antisense oligonucleotides. Oncogene. 40(47). 6527–6539. 10 indexed citations
12.
Xu, Meng, Haichuan Wang, Jingxiao Wang, et al.. (2020). mTORC2 Signaling Is Necessary for Timely Liver Regeneration after Partial Hepatectomy. American Journal Of Pathology. 190(4). 817–829. 14 indexed citations
13.
Wang, Jingxiao, Haichuan Wang, Ning Ding, et al.. (2019). Loss of Fbxw7 synergizes with activated Akt signaling to promote c-Myc dependent cholangiocarcinogenesis. Journal of Hepatology. 71(4). 742–752. 47 indexed citations
14.
Zhang, Shanshan, Jingxiao Wang, Haichuan Wang, et al.. (2018). Hippo Cascade Controls Lineage Commitment of Liver Tumors in Mice and Humans. American Journal Of Pathology. 188(4). 995–1006. 28 indexed citations
15.
Vélez, Ana M., Elane Fishilevich, Haichuan Wang, et al.. (2018). Clathrin-dependent endocytosis is associated with RNAi response in the western corn rootworm, Diabrotica virgifera virgifera LeConte. PLoS ONE. 13(8). e0201849–e0201849. 50 indexed citations
16.
Zhang, Qian, Haichuan Wang, Yingying Li, et al.. (2018). Roles of phospholipid methyltransferases in pycnidia development, stress tolerance and secondary metabolism in the taxol-producing fungus Pestalotiopsis microspore. Microbiological Research. 210. 33–42. 15 indexed citations
17.
Vellichirammal, Neetha Nanoth, Haichuan Wang, Seong‐il Eyun, et al.. (2015). Transcriptional analysis of susceptible and resistant European corn borer strains and their response to Cry1F protoxin. BMC Genomics. 16(1). 558–558. 34 indexed citations
18.
Xiong, Tian‐Yuan, Jiqiao Yang, Haichuan Wang, et al.. (2014). The association between the Lys751Gln polymorphism in the XPD gene and the risk of bladder cancer. Molecular Biology Reports. 41(4). 2629–2634. 8 indexed citations
19.
Huang, Jin, Jiqiao Yang, Haichuan Wang, et al.. (2013). The association between the poly(A) polymorphism in the VDR gene and cancer risk: a meta-analysis. Tumor Biology. 34(3). 1833–1838. 8 indexed citations
20.
Coates, Brad S., Douglas V. Sumerford, Miriam D. Lopez, et al.. (2011). A single major QTL controls expression of larval Cry1F resistance trait in Ostrinia nubilalis (Lepidoptera: Crambidae) and is independent of midgut receptor genes. Genetica. 139(8). 961–972. 18 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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