Songkun Su

2.0k total citations
71 papers, 1.3k citations indexed

About

Songkun Su is a scholar working on Insect Science, Genetics and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Songkun Su has authored 71 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Insect Science, 50 papers in Genetics and 38 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Songkun Su's work include Insect and Pesticide Research (55 papers), Insect and Arachnid Ecology and Behavior (49 papers) and Plant and animal studies (37 papers). Songkun Su is often cited by papers focused on Insect and Pesticide Research (55 papers), Insect and Arachnid Ecology and Behavior (49 papers) and Plant and animal studies (37 papers). Songkun Su collaborates with scholars based in China, Australia and France. Songkun Su's co-authors include Shenglu Chen, Zhiguo Li, Shaowu Zhang, Wenfeng Li, Hongyi Nie, Yanping Chen, Martín Giurfa, María Gabriela de Brito Sanchez, Yan Lin and Limin Yan and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Songkun Su

70 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Songkun Su China 22 1.0k 769 656 180 163 71 1.3k
Aneta Strachecka Poland 20 943 0.9× 753 1.0× 625 1.0× 89 0.5× 132 0.8× 124 1.3k
Julie A. Mustard United States 23 1.0k 1.0× 829 1.1× 881 1.3× 657 3.6× 187 1.1× 33 1.6k
Simona Sagona Italy 19 705 0.7× 460 0.6× 454 0.7× 181 1.0× 77 0.5× 53 922
Morten Schiøtt Denmark 25 1.1k 1.0× 1.2k 1.6× 1.1k 1.6× 177 1.0× 558 3.4× 49 2.2k
Yongyue Lu China 24 1.5k 1.5× 560 0.7× 371 0.6× 281 1.6× 459 2.8× 125 1.9k
Sara Ruschioni Italy 21 1.0k 1.0× 410 0.5× 237 0.4× 147 0.8× 102 0.6× 46 1.3k
Kate Aronstein United States 18 1.8k 1.8× 1.1k 1.4× 934 1.4× 302 1.7× 494 3.0× 25 2.2k
Osman Kaftanoğlu United States 25 1.7k 1.6× 1.3k 1.7× 1.2k 1.9× 138 0.8× 137 0.8× 53 2.0k
Miguel Corona United States 22 1.6k 1.5× 1.8k 2.4× 1.3k 2.0× 392 2.2× 551 3.4× 50 2.4k
Valérie Raymond France 20 980 0.9× 384 0.5× 312 0.5× 387 2.1× 608 3.7× 40 1.5k

Countries citing papers authored by Songkun Su

Since Specialization
Citations

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

Fields of papers citing papers by Songkun Su

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Songkun Su

This figure shows the co-authorship network connecting the top 25 collaborators of Songkun Su. A scholar is included among the top collaborators of Songkun Su 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 Songkun Su. Songkun Su 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.
Nie, Hongyi, et al.. (2023). The association between the hypopharyngeal glands and the molecular mechanism which honey bees secrete royal jelly. Journal of Apicultural Research. 64(1). 281–296. 4 indexed citations
2.
Su, Songkun & Martín Giurfa. (2023). Response to comment on “Food Wanting is Mediated by Transient Activation of Dopaminergic Signaling in the Honeybee Brain”. Science. 381(6657). eadg6207–eadg6207. 1 indexed citations
3.
Nie, Hongyi, et al.. (2023). Discovery of SNP Molecular Markers and Candidate Genes Associated with Sacbrood Virus Resistance in Apis cerana cerana Larvae by Whole-Genome Resequencing. International Journal of Molecular Sciences. 24(7). 6238–6238. 3 indexed citations
4.
Wang, Tianbao, Qiaoling Sun, Xiaomin Ni, et al.. (2023). Differential Brain Expression Patterns of microRNAs Related to Olfactory Performance in Honey Bees (Apis mellifera). Genes. 14(5). 1000–1000. 7 indexed citations
5.
Tang, Jiao, Wei Shi, Songkun Su, et al.. (2023). Survey Results of Honey Bee Colony Losses in Winter in China (2009–2021). Insects. 14(6). 554–554. 11 indexed citations
6.
Chen, Lifu, Yi Zhang, Jiali Yang, et al.. (2022). Lotus Bee Pollen Extract Inhibits Isoproterenol-Induced Hypertrophy via JAK2/STAT3 Signaling Pathway in Rat H9c2 Cells. Antioxidants. 12(1). 88–88. 8 indexed citations
7.
Sanchez, María Gabriela de Brito, Marco Paoli, Zhiguo Li, et al.. (2022). Food wanting is mediated by transient activation of dopaminergic signaling in the honey bee brain. Science. 376(6592). 508–512. 55 indexed citations
8.
Anwar, Muhammad, Zhiguo Li, Hongyi Nie, et al.. (2022). Differential gene expression analysis following olfactory learning in honeybee (Apis mellifera L.). PLoS ONE. 17(2). e0262441–e0262441. 6 indexed citations
9.
Sandoz, Jean‐Christophe, et al.. (2020). Degradation of an appetitive olfactory memory via devaluation of sugar reward is mediated by 5-HT signaling in the honey bee. Neurobiology of Learning and Memory. 173. 107278–107278. 13 indexed citations
10.
11.
Huang, Shaokang, Zhiguo Li, Shahid Mehmood, et al.. (2019). Prevalence of bee viruses in Apis cerana cerana populations from different locations in the Fujian Province of China. MicrobiologyOpen. 8(9). e00830–e00830. 14 indexed citations
12.
Lin, Yan, et al.. (2019). Royal jelly-derived proteins enhance proliferation and migration of human epidermal keratinocytes in an in vitro scratch wound model. BMC Complementary and Alternative Medicine. 19(1). 175–175. 37 indexed citations
13.
14.
Li, Li, et al.. (2012). Dopaminergic pathways and its effects on honeybee behaviors.. Kunchong zhishi. 49(4). 1061–1065. 2 indexed citations
15.
Li, Li, Fang Liu, Wenfeng Li, et al.. (2012). Differences in microRNAs and their expressions between foraging and dancing honey bees, Apis mellifera L.. Journal of Insect Physiology. 58(11). 1438–1443. 22 indexed citations
16.
Li, Zhiguo & Songkun Su. (2010). Advances on Israeli acute paralysis virus of honeybee. Kunchong zhishi. 47(4). 633–637. 1 indexed citations
17.
Su, Songkun, et al.. (2008). East Learns from West: Asiatic Honeybees Can Understand Dance Language of European Honeybees. PLoS ONE. 3(6). e2365–e2365. 32 indexed citations
18.
Chen, Shenglu, Jianke Li, Boxiong Zhong, & Songkun Su. (2005). Microsatellite analysis of royal jelly producing traits of Italian honeybee (Apis mellifera Liguatica).. PubMed. 32(10). 1037–44. 14 indexed citations
19.
Chen, Shenglu, et al.. (2003). [Genetic analysis for developmental behavior of honeybee colony's royal jelly production traits in western honeybees].. PubMed. 30(6). 547–54. 19 indexed citations
20.
Su, Songkun. (2003). Genetic Analysis for Developmental Behavior of Reproductive Ability and HypopheryngealGland in Western Honeybees(Apis melliffera Lingistica). Zhongguo xumu zazhi. 4 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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