Yongping Huang

8.0k total citations · 1 hit paper
169 papers, 5.5k citations indexed

About

Yongping Huang is a scholar working on Insect Science, Molecular Biology and Genetics. According to data from OpenAlex, Yongping Huang has authored 169 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 105 papers in Insect Science, 94 papers in Molecular Biology and 54 papers in Genetics. Recurrent topics in Yongping Huang's work include Insect Resistance and Genetics (47 papers), Silkworms and Sericulture Research (32 papers) and Neurobiology and Insect Physiology Research (31 papers). Yongping Huang is often cited by papers focused on Insect Resistance and Genetics (47 papers), Silkworms and Sericulture Research (32 papers) and Neurobiology and Insect Physiology Research (31 papers). Yongping Huang collaborates with scholars based in China, United States and Japan. Yongping Huang's co-authors include Jun Xu, Anjiang Tan, Xiao‐Ya Chen, Ying‐Bo Mao, Xiaoyuan Tao, Gaojie Hong, Wenjuan Cai, Ling-Jian Wang, Jiawei Wang and Muwang Li and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Yongping Huang

164 papers receiving 5.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Silencing a cotton bollworm P450 monooxygenase gene by plant-mediated RNAi impairs larval tolerance of gossypol

2007 990 citations Yongping Huang et al. profile →

Peers

Yongping Huang

IS

MB

PS

GENET

CMN

Zhonghuai Xiang China

Chuan‐Xi Zhang China

Qili Feng China

Wenqing Zhang China

Luc Swevers Greece

Kun Yan Zhu United States

Qisheng Song United States

Shogo Matsumoto Japan

Cheng Lu China

Tetsuro Shinoda Japan

Zhonghuai Xiang China

Yongping Huang

2.5k ×0.8

IS

3.3k ×1.1

MB

1.5k ×1.3

PS

1.4k ×1.2

GENET

1.4k ×1.5

CMN

Citations per year, relative to Yongping Huang Yongping Huang (= 1×) peers Zhonghuai Xiang

Countries citing papers authored by Yongping Huang

Since Specialization

Citations

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

Fields of papers citing papers by Yongping Huang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yongping Huang

This figure shows the co-authorship network connecting the top 25 collaborators of Yongping Huang. A scholar is included among the top collaborators of Yongping Huang 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 Yongping Huang. Yongping Huang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Xu, Xia, et al.. (2025). Black soldier fly: a new model for bioremediation of antibiotic pollutants. National Science Review. 12(3). nwaf043–nwaf043.

2.

Wu, Yining, Xiang Yan, Yongping Huang, et al.. (2024). Ultra-deep reservoirs gel fracturing fluid with stepwise reinforcement network from supramolecular force to chemical crosslinking. Energy. 293. 130632–130632. 12 indexed citations

3.

Wang, Jishi, et al.. (2024). Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry-Based Metabolic Characterization of Mango Ripened by Different Methods. Foods. 13(22). 3548–3548. 1 indexed citations

4.

Dong, Yongcheng, et al.. (2024). Genome‐wide identification of yellow gene family in Hermetia illucens and functional analysis of yellow‐y by CRISPR/Cas9. Insect Science. 32(1). 115–126. 3 indexed citations

5.

Xu, Yang, Shanshan Wang, Yongjian Liu, et al.. (2023). The Prmt5-Vasa module is essential for spermatogenesis in Bombyx mori. PLoS Genetics. 19(1). e1010600–e1010600. 13 indexed citations

6.

Luo, Xingyu, Peili Li, Kaiji Sun, et al.. (2023). Intersex is required for female sexual development in Hermetia illucens. Insect Science. 30(4). 901–911.

7.

Yang, Dehong, Jun Xu, Kai Chen, et al.. (2022). BmPMFBP1 regulates the development of eupyrene sperm in the silkworm, Bombyx mori. PLoS Genetics. 18(3). e1010131–e1010131. 19 indexed citations

8.

Wei, Yongjun, Yining Liu, Zhihua Zhou, et al.. (2021). De novo biosynthesis of sex pheromone components of Helicoverpa armigera through an artificial pathway in yeast. Green Chemistry. 24(2). 767–778. 10 indexed citations

9.

Wang, Yaohui, Yang Xu, Kai Chen, et al.. (2021). 5′-Nucleotidase Plays a Key Role in Uric Acid Metabolism of Bombyx mori. Cells. 10(9). 2243–2243. 12 indexed citations

10.

Chen, Kai, Ye Yu, Dehong Yang, et al.. (2021). Correction: Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori. PLoS Genetics. 17(5). e1009572–e1009572. 11 indexed citations

11.

Chen, Kai, Ye Yu, Dehong Yang, et al.. (2020). Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori. PLoS Genetics. 16(11). e1009194–e1009194. 23 indexed citations

12.

Zhang, Sufang, Xin Zhou, Xiangbo Kong, et al.. (2020). Chromosome‐level genome assembly of an important pine defoliator, Dendrolimus punctatus (Lepidoptera; Lasiocampidae). Molecular Ecology Resources. 20(4). 1023–1037. 22 indexed citations

13.

Huang, Yongping, et al.. (2019). Optimization of extraction process of peptidoglycan from cell wall of Bacillus natto and preliminary identification of its structure.. ACTA AGRICULTURAE UNIVERSITATIS JIANGXIENSIS. 41(1). 174–185. 1 indexed citations

14.

Xu, Jun, Qinglin Dong, Ye Yu, et al.. (2018). Mass spider silk production through targeted gene replacement in Bombyx mori. Proceedings of the National Academy of Sciences. 115(35). 8757–8762. 115 indexed citations

15.

Xie, Lei, Ning Liu, Yongping Huang, & Qian Wang. (2011). Flagellate community structure in Coptotermes formosanus (Isoptera: Rhinotermitidae) and a comparison of three study methods.. Acta Entomologica Sinica. 54(10). 1140–1146. 3 indexed citations

16.

Li, Muwang, et al.. (2007). Detection of homozygosity in near isogenic Lines of non-susceptible to Zhenjiang strain of densonucleosis virus in silkworm. AFRICAN JOURNAL OF BIOTECHNOLOGY. 6(14). 1629–1633. 8 indexed citations

17.

Huang, Yongping. (2006). The Polymorphism of Silkworm, Bombyx mori (L.) Amylase Gene. Zhongguo nongye Kexue. 1 indexed citations

18.

Huang, Yongping. (2006). Bernoulli's Equation in the Non-inertia Frame of Reference. 1 indexed citations

19.

Fang, Shou‐Min, et al.. (2005). Application of SSR marker to analysis of genetic polymorphism in Bombyx mori and Bombyx mandarina. 31(3). 251–256. 1 indexed citations

20.

Zhao, Weiguo, et al.. (2005). Phylogeny of the genus Morus (Urticales: Moraceae) inferred from ITS and trnL-F sequences. AFRICAN JOURNAL OF BIOTECHNOLOGY. 4(6). 563–569. 31 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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