Hao Meng

788 total citations
22 papers, 580 citations indexed

About

Hao Meng is a scholar working on Molecular Biology, Plant Science and Oncology. According to data from OpenAlex, Hao Meng has authored 22 papers receiving a total of 580 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 4 papers in Plant Science and 2 papers in Oncology. Recurrent topics in Hao Meng's work include Genomics, phytochemicals, and oxidative stress (4 papers), Identification and Quantification in Food (2 papers) and Inflammasome and immune disorders (2 papers). Hao Meng is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (4 papers), Identification and Quantification in Food (2 papers) and Inflammasome and immune disorders (2 papers). Hao Meng collaborates with scholars based in China, Germany and Australia. Hao Meng's co-authors include Lei Du, Xiaoxing Yin, Qian Lü, Xi Lin, Zhiming Li, Jiaxin Du, Yizhou Zhong, Zhenlie Huang, Xingfen Yang and Yuji Huang and has published in prestigious journals such as Nature Communications, Journal of Hazardous Materials and Biochemical and Biophysical Research Communications.

In The Last Decade

Hao Meng

20 papers receiving 572 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hao Meng China 12 300 128 78 65 63 22 580
Shali Yu China 19 246 0.8× 226 1.8× 69 0.9× 89 1.4× 87 1.4× 43 826
Liqin Wang China 12 153 0.5× 106 0.8× 39 0.5× 34 0.5× 17 0.3× 38 655
Muyao Li United States 16 393 1.3× 38 0.3× 89 1.1× 43 0.7× 73 1.2× 32 821
Gautam K. Ginjupalli United States 8 187 0.6× 67 0.5× 66 0.8× 130 2.0× 35 0.6× 18 702
Xue Qi China 17 222 0.7× 99 0.8× 33 0.4× 43 0.7× 54 0.9× 30 634
Linqing Yang China 16 472 1.6× 77 0.6× 79 1.0× 139 2.1× 184 2.9× 40 916
Kaiwen Guo China 14 272 0.9× 114 0.9× 50 0.6× 53 0.8× 41 0.7× 42 836
Pallab Shaw India 12 381 1.3× 48 0.4× 36 0.5× 69 1.1× 67 1.1× 26 896
Lingyue Zou China 17 249 0.8× 258 2.0× 96 1.2× 257 4.0× 86 1.4× 28 901

Countries citing papers authored by Hao Meng

Since Specialization
Citations

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

Fields of papers citing papers by Hao Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hao Meng

This figure shows the co-authorship network connecting the top 25 collaborators of Hao Meng. A scholar is included among the top collaborators of Hao Meng 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 Hao Meng. Hao Meng 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.
Yang, Shengyong, Shanshan Jiang, Qian Wu, et al.. (2025). Transcription factor KLF5 regulates MsrB1 to promote colorectal cancer progression by inhibiting ferroptosis through β-catenin. Free Radical Biology and Medicine. 234. 34–48.
2.
Meng, Hao, et al.. (2024). Establishing a straightforward I‐ SceI ‐mediated recombination one‐plasmid system for efficient genome editing in P. putida KT2440. Microbial Biotechnology. 17(7). e14531–e14531. 2 indexed citations
3.
Song, Fuqiang, Zhijie Qin, Lian Wang, et al.. (2024). Development of a vitamin B5 hyperproducer in Escherichia coli by multiple metabolic engineering. Metabolic Engineering. 84. 158–168. 21 indexed citations
4.
Zhang, Mengmeng, Guo‐Liang Wang, Xiaoyan Deng, et al.. (2024). Loss of ADAR1 induces ferroptosis of breast cancer cells. Cellular Signalling. 121. 111258–111258. 14 indexed citations
6.
Liu, Jianming, Han Zhang, Yingying Xu, Hao Meng, & An‐Ping Zeng. (2023). Turn air-captured CO2 with methanol into amino acid and pyruvate in an ATP/NAD(P)H-free chemoenzymatic system. Nature Communications. 14(1). 2772–2772. 40 indexed citations
7.
Zhang, Meng, et al.. (2023). Sequential expression of small heat shock proteins contributing to the cold response of Haemaphysalis longicornis (Acari: Ixodidae). Pest Management Science. 80(4). 2061–2071. 7 indexed citations
8.
Lin, Xi, Rongyi Ye, Zhiming Li, et al.. (2022). KIAA1429 promotes tumorigenesis and gefitinib resistance in lung adenocarcinoma by activating the JNK/ MAPK pathway in an m6A-dependent manner. Drug Resistance Updates. 66. 100908–100908. 59 indexed citations
9.
Liang, Boxuan, Yuji Huang, Yizhou Zhong, et al.. (2022). Brain single-nucleus transcriptomics highlights that polystyrene nanoplastics potentially induce Parkinson’s disease-like neurodegeneration by causing energy metabolism disorders in mice. Journal of Hazardous Materials. 430. 128459–128459. 151 indexed citations
10.
Jiang, Yan, Xiaodi Hu, Yuan Yuan, et al.. (2022). The Gastrodia menghaiensis (Orchidaceae) genome provides new insights of orchid mycorrhizal interactions. BMC Plant Biology. 22(1). 179–179. 22 indexed citations
11.
Zhong, Yizhou, Boxuan Liang, Hao Meng, et al.. (2022). 1,2-Dichloroethane induces cortex demyelination by depressing myelin basic protein via inhibiting aquaporin 4 in mice. Ecotoxicology and Environmental Safety. 231. 113180–113180. 12 indexed citations
12.
Hu, Manjiang, Yizhou Zhong, Jun Liu, et al.. (2022). An adverse outcome pathway-based approach to assess aurantio-obtusin-induced hepatotoxicity. Toxicology. 478. 153293–153293. 9 indexed citations
13.
Hu, Manjiang, Lin Li, Jun Liu, et al.. (2021). Aurantio-obtusin induces hepatotoxicity through activation of NLRP3 inflammasome signaling. Toxicology Letters. 354. 1–13. 7 indexed citations
14.
Adelusi, Temitope Isaac, Xizhi Li, Xu Liu, et al.. (2021). Novel Chalcone BDD-39 Mitigated Diabetic Nephropathy through the Activationof Nrf2/ARE Signaling. Current Molecular Pharmacology. 15(4). 658–675. 3 indexed citations
15.
Adelusi, Temitope Isaac, Lei Du, Hao Meng, et al.. (2020). Keap1/Nrf2/ARE signaling unfolds therapeutic targets for redox imbalanced-mediated diseases and diabetic nephropathy. Biomedicine & Pharmacotherapy. 123. 109732–109732. 106 indexed citations
16.
17.
Du, Lei, Jin Wang, Yibing Chen, et al.. (2019). Novel biphenyl diester derivative AB-38b inhibits NLRP3 inflammasome through Nrf2 activation in diabetic nephropathy. Cell Biology and Toxicology. 36(3). 243–260. 41 indexed citations
18.
Du, Lei, Lei Wang, Bo Wang, et al.. (2019). A novel compound AB38b attenuates oxidative stress and ECM protein accumulation in kidneys of diabetic mice through modulation of Keap1/Nrf2 signaling. Acta Pharmacologica Sinica. 41(3). 358–372. 38 indexed citations
20.
Du, Fengxia, Minjie Zhang, Xiaohua Li, et al.. (2014). Dimer monomer transition and dimer re-formation play important role for ATM cellular function during DNA repair. Biochemical and Biophysical Research Communications. 452(4). 1034–1039. 7 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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