Hao‐Bing Yu

1.2k total citations
55 papers, 959 citations indexed

About

Hao‐Bing Yu is a scholar working on Pharmacology, Biotechnology and Organic Chemistry. According to data from OpenAlex, Hao‐Bing Yu has authored 55 papers receiving a total of 959 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Pharmacology, 39 papers in Biotechnology and 19 papers in Organic Chemistry. Recurrent topics in Hao‐Bing Yu's work include Microbial Natural Products and Biosynthesis (40 papers), Marine Sponges and Natural Products (38 papers) and Synthetic Organic Chemistry Methods (12 papers). Hao‐Bing Yu is often cited by papers focused on Microbial Natural Products and Biosynthesis (40 papers), Marine Sponges and Natural Products (38 papers) and Synthetic Organic Chemistry Methods (12 papers). Hao‐Bing Yu collaborates with scholars based in China, United States and Japan. Hao‐Bing Yu's co-authors include Hou‐Wen Lin, Fan Yang, Wei‐Hua Jiao, Xiaoling Lu, Binghua Jiao, Bingnan Han, Jianhong Gan, Binbin Gu, Fan Sun and Tingting Xu and has published in prestigious journals such as Scientific Reports, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Hao‐Bing Yu

52 papers receiving 941 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‐Bing Yu China 21 532 521 330 308 153 55 959
Chong‐O. Lee South Korea 23 602 1.1× 499 1.0× 489 1.5× 311 1.0× 210 1.4× 38 1.1k
Taro Amagata United States 18 410 0.8× 469 0.9× 321 1.0× 265 0.9× 73 0.5× 22 843
Shamil Sh. Afiyatullov Russia 21 595 1.1× 759 1.5× 250 0.8× 327 1.1× 96 0.6× 54 1.1k
Xiaowei Luo China 21 583 1.1× 827 1.6× 193 0.6× 320 1.0× 110 0.7× 67 1.1k
Naoyuki Kotoku Japan 19 384 0.7× 312 0.6× 629 1.9× 455 1.5× 108 0.7× 56 1.2k
Rajendra P. Maskey Germany 20 402 0.8× 609 1.2× 395 1.2× 380 1.2× 84 0.5× 38 1.0k
Yongxiang Song China 23 539 1.0× 994 1.9× 364 1.1× 671 2.2× 83 0.5× 55 1.4k
Binbin Gu China 19 354 0.7× 435 0.8× 201 0.6× 300 1.0× 109 0.7× 50 744
Anja Krick Germany 19 368 0.7× 486 0.9× 265 0.8× 267 0.9× 45 0.3× 25 932
Siwen Niu China 23 604 1.1× 819 1.6× 207 0.6× 447 1.5× 65 0.4× 51 1.1k

Countries citing papers authored by Hao‐Bing Yu

Since Specialization
Citations

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

Fields of papers citing papers by Hao‐Bing Yu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hao‐Bing Yu

This figure shows the co-authorship network connecting the top 25 collaborators of Hao‐Bing Yu. A scholar is included among the top collaborators of Hao‐Bing Yu 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‐Bing Yu. Hao‐Bing Yu 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.
Zhu, Yuping, Xiaoling Lü, Binghua Jiao, et al.. (2024). Brevetoxin Aptamer Selection and Biolayer Interferometry Biosensor Application. Toxins. 16(10). 411–411.
2.
Song, Li, Yuping Zhu, Bo Hu, et al.. (2024). Genome Mining Leads to Diverse Sesquiterpenes with Anti-inflammatory Activity from an Arctic-Derived Fungus. Journal of Natural Products. 87(5). 1426–1440. 10 indexed citations
3.
Yu, Hao‐Bing, et al.. (2024). Uncommon Epoxyquinols Pyrrolocytosporin A and Cytosporin E2 from the Fungus Eutypella sp. D‐1. Chemistry & Biodiversity. 21(8). e202401097–e202401097. 1 indexed citations
4.
Hu, Bo, Yuanyuan Sun, Jinfeng Ding, et al.. (2024). Eutypellaolides A–J, Sesquiterpene diversity expansion of the polar fungus Eutypella sp. D-1. Frontiers in Microbiology. 15. 1349151–1349151. 4 indexed citations
5.
Yu, Hao‐Bing, Bo Hu, Yuping Zhu, et al.. (2023). Cytosporin Derivatives from Arctic-Derived Fungus Eutypella sp. D-1 via the OSMAC Approach. Marine Drugs. 21(7). 382–382. 7 indexed citations
6.
Yu, Hao‐Bing, Ying He, Zifei Yin, et al.. (2023). Phyllofenones F–M, Scalarane Sesterterpenes from the Marine Sponge Phyllospongia foliascens. Marine Drugs. 21(10). 507–507. 2 indexed citations
7.
Hu, Bo, et al.. (2022). Optimization of Protoplast Preparation and Establishment of Genetic Transformation System of an Arctic-Derived Fungus Eutypella sp.. Frontiers in Microbiology. 13. 769008–769008. 15 indexed citations
8.
Jiang, Wen‐Li, et al.. (2021). Soft coral-derived Aspernolide A suppressed non-small cell lung cancer induced osteolytic bone invasion via the c-Fos/NFATC1 signaling pathway. Journal of Thoracic Disease. 13(10). 5996–6011. 2 indexed citations
9.
Gan, Jianhong, et al.. (2019). Leucandioxoles A and B, two 1,3-benzodioxole derivatives from the South China Sea sponge Leucandra sp.. Journal of Asian Natural Products Research. 23(1). 33–38.
10.
Hong, Li‐Li, Hao‐Bing Yu, Jie Wang, et al.. (2017). Unusual Anti-allergic Diterpenoids from the Marine Sponge Hippospongia lachne. Scientific Reports. 7(1). 43138–43138. 18 indexed citations
11.
Yu, Hao‐Bing, Binbin Gu, Shuping Wang, et al.. (2017). New diterpenoids from the marine sponge Dactylospongia elegans. Tetrahedron. 73(47). 6657–6661. 14 indexed citations
12.
Chianese, Giuseppina, Hao‐Bing Yu, Fan Yang, et al.. (2016). PPAR Modulating Polyketides from a Chinese Plakortis simplex and Clues on the Origin of Their Chemodiversity. The Journal of Organic Chemistry. 81(12). 5135–5143. 31 indexed citations
13.
Yang, Fan, et al.. (2016). New antimalarial norterpene cyclic peroxides from Xisha Islands sponge Diacarnus megaspinorhabdosa. Bioorganic & Medicinal Chemistry Letters. 26(8). 2084–2087. 17 indexed citations
14.
Zhu, Yan, Yan Wang, Binbin Gu, et al.. (2016). Antifungal bromopyrrole alkaloids from the South China Sea sponge Agelas sp.. Tetrahedron. 72(22). 2964–2971. 29 indexed citations
15.
Zhang, Ping, Peiqin Wang, Hao‐Bing Yu, et al.. (2015). The Cytotoxic and Mechanistic Effects of Aaptamine on Hepatocellular Carcinoma. Anti-Cancer Agents in Medicinal Chemistry. 15(3). 291–297. 17 indexed citations
16.
Gan, Jianhong, et al.. (2015). Three new aaptamine derivatives from the South China Sea sponge Aaptos aaptos. Journal of Asian Natural Products Research. 17(12). 1231–1238. 9 indexed citations
17.
Ding, Lijian, Binbin Gu, Wei‐Hua Jiao, et al.. (2015). New Furan and Cyclopentenone Derivatives from the Sponge-Associated Fungus Hypocrea Koningii PF04. Marine Drugs. 13(9). 5579–5592. 33 indexed citations
18.
Jiao, Wei‐Hua, Jing Li, Qian Liu, et al.. (2014). Dysidinoid A, an Unusual Meroterpenoid with Anti-MRSA Activity from the South China Sea Sponge Dysidea sp.. Molecules. 19(11). 18025–18032. 14 indexed citations
19.
20.
Zhao, Yue, Simon Parsons, David W. H. Rankin, et al.. (2002). Saluenolide A, a novel eremophilanolide from Senecio saluenensis. Chinese Chemical Letters. 13(4). 3 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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