Cui‐Cui Yin

1.9k total citations
33 papers, 1.4k citations indexed

About

Cui‐Cui Yin is a scholar working on Plant Science, Molecular Biology and Ceramics and Composites. According to data from OpenAlex, Cui‐Cui Yin has authored 33 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Plant Science, 5 papers in Molecular Biology and 2 papers in Ceramics and Composites. Recurrent topics in Cui‐Cui Yin's work include Plant responses to water stress (17 papers), Plant Molecular Biology Research (15 papers) and Postharvest Quality and Shelf Life Management (11 papers). Cui‐Cui Yin is often cited by papers focused on Plant responses to water stress (17 papers), Plant Molecular Biology Research (15 papers) and Postharvest Quality and Shelf Life Management (11 papers). Cui‐Cui Yin collaborates with scholars based in China, United Kingdom and United States. Cui‐Cui Yin's co-authors include Shou‐Yi Chen, Jin‐Song Zhang, Biao Ma, Xiang Lu, Wan‐Ke Zhang, He Zhao, Sijie He, Qing Xiong, Chao Yang and Hui Chen and has published in prestigious journals such as Nature Communications, The Plant Cell and PLANT PHYSIOLOGY.

In The Last Decade

Cui‐Cui Yin

31 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cui‐Cui Yin China 18 1.3k 393 87 57 32 33 1.4k
Poonam Kanwar India 18 897 0.7× 404 1.0× 47 0.5× 26 0.5× 38 1.2× 24 999
Angela Hendrickson Culler United States 11 832 0.6× 402 1.0× 39 0.4× 24 0.4× 51 1.6× 11 922
Peitao Lü China 17 1.4k 1.1× 937 2.4× 56 0.6× 32 0.6× 51 1.6× 45 1.6k
Huilong Hong China 19 955 0.7× 257 0.7× 108 1.2× 37 0.6× 15 0.5× 32 1.1k
Huaxun Ye United States 14 2.1k 1.6× 1.4k 3.5× 82 0.9× 33 0.6× 14 0.4× 17 2.2k
Siddanna Savadi India 15 446 0.3× 191 0.5× 107 1.2× 40 0.7× 25 0.8× 45 544
Cristina Barrero‐Sicilia Spain 14 703 0.5× 467 1.2× 68 0.8× 48 0.8× 8 0.3× 15 808
Akhter Most Sharoni Japan 8 1.5k 1.2× 1.1k 2.7× 81 0.9× 13 0.2× 32 1.0× 8 1.7k
Joon‐Seob Eom South Korea 11 1.3k 1.0× 508 1.3× 89 1.0× 15 0.3× 35 1.1× 13 1.4k
Xiangling Shen China 14 1.0k 0.8× 623 1.6× 57 0.7× 9 0.2× 53 1.7× 30 1.1k

Countries citing papers authored by Cui‐Cui Yin

Since Specialization
Citations

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

Fields of papers citing papers by Cui‐Cui Yin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cui‐Cui Yin. 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 Cui‐Cui Yin. The network helps show where Cui‐Cui Yin may publish in the future.

Co-authorship network of co-authors of Cui‐Cui Yin

This figure shows the co-authorship network connecting the top 25 collaborators of Cui‐Cui Yin. A scholar is included among the top collaborators of Cui‐Cui Yin 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 Cui‐Cui Yin. Cui‐Cui Yin 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.
Zhou, Bin, Jingjing Liang, Yanbao Tian, et al.. (2025). A single‐MYB transcription factor GmMYB331 regulates seed oil accumulation and seed size/weight in soybean. Journal of Integrative Plant Biology. 68(2). 470–485.
2.
Zhou, Yang, Yihong Gao, Baocai Zhang, et al.. (2024). CELLULOSE SYNTHASE-LIKE C proteins modulate cell wall establishment during ethylene-mediated root growth inhibition in rice. The Plant Cell. 36(9). 3751–3769. 8 indexed citations
3.
Li, Xinkai, Yi‐Hua Huang, Rui Zhao, et al.. (2024). Membrane protein MHZ3 regulates the on-off switch of ethylene signaling in rice. Nature Communications. 15(1). 5987–5987. 6 indexed citations
4.
Tao, Jian‐Jun, Cui‐Cui Yin, Yang Zhou, et al.. (2023). The universal and divergent roles of ethylene in rice and some other crop plants under salt stress. Environmental and Experimental Botany. 217. 105555–105555. 2 indexed citations
5.
Hu, Yang, Jian‐Jun Tao, Lu Long, et al.. (2023). GmJAZ3 interacts with GmRR18a and GmMYC2a to regulate seed traits in soybean. Journal of Integrative Plant Biology. 65(8). 1983–2000. 33 indexed citations
6.
Wei, Wei, Lu Long, Xiao‐Hua Bian, et al.. (2023). Zinc‐finger protein GmZF351 improves both salt and drought stress tolerance in soybean. Journal of Integrative Plant Biology. 65(7). 1636–1650. 40 indexed citations
7.
Huang, Yi‐Hua, Jiaqi Han, Biao Ma, et al.. (2023). A translational regulator MHZ9 modulates ethylene signaling in rice. Nature Communications. 14(1). 4674–4674. 16 indexed citations
8.
Zhou, Yang, Biao Ma, Jian‐Jun Tao, et al.. (2022). Rice EIL1 interacts with OsIAAs to regulate auxin biosynthesis mediated by the tryptophan aminotransferase MHZ10/OsTAR2 during root ethylene responses. The Plant Cell. 34(11). 4366–4387. 29 indexed citations
9.
Wei, Wei, Jian‐Jun Tao, Cui‐Cui Yin, et al.. (2022). Melatonin regulates gene expressions through activating auxin synthesis and signaling pathways. Frontiers in Plant Science. 13. 1057993–1057993. 20 indexed citations
10.
Long, Lu, Wei Wei, Jian‐Jun Tao, et al.. (2021). Nuclear factor Y subunit GmNFYA competes with GmHDA13 for interaction with GmFVE to positively regulate salt tolerance in soybean. Plant Biotechnology Journal. 19(11). 2362–2379. 65 indexed citations
11.
12.
Zhao, He, Biao Ma, Xinkai Li, et al.. (2020). The GDSL Lipase MHZ11 Modulates Ethylene Signaling in Rice Roots. The Plant Cell. 32(5). 1626–1643. 45 indexed citations
13.
Zhao, He, Biao Ma, Cui‐Cui Yin, et al.. (2020). Histidine kinase MHZ1/OsHK1 interacts with ethylene receptors to regulate root growth in rice. Nature Communications. 11(1). 518–518. 52 indexed citations
14.
Zheng, Hongyuan, Lingli Dong, Huaibing Jin, et al.. (2019). The TuMYB46L‐TuACO3 module regulates ethylene biosynthesis in einkorn wheat defense to powdery mildew. New Phytologist. 225(6). 2526–2541. 50 indexed citations
15.
Liang, Shanshan, Cui‐Cui Yin, Xiaodong Xie, et al.. (2019). Overexpression of OsARD1 Improves Submergence, Drought, and Salt Tolerances of Seedling Through the Enhancement of Ethylene Synthesis in Rice. Frontiers in Plant Science. 10. 1088–1088. 56 indexed citations
16.
Yin, Cui‐Cui, He Zhao, Biao Ma, Shou‐Yi Chen, & Jinsong Zhang. (2017). Diverse Roles of Ethylene in Regulating Agronomic Traits in Rice. Frontiers in Plant Science. 8. 1676–1676. 48 indexed citations
17.
Yin, Cui‐Cui, Biao Ma, Wei Wang, et al.. (2016). RNA Extraction and Preparation in Rice (Oryza sativa). PubMed. 1(2). 411–418. 6 indexed citations
18.
19.
Yin, Cui‐Cui, et al.. (2014). Cloning and analysis of anti-stress transcription factor gene HhDREB2 from Halimodendron halodendron Voss.. Zhongguo nongye ke-ji daobao. 16(4). 71–78. 1 indexed citations
20.
Ma, Biao, Sijie He, Cui‐Cui Yin, et al.. (2013). Identification of Rice Ethylene-Response Mutants and Characterization of MHZ7/OsEIN2 in Distinct Ethylene Response and Yield Trait Regulation. Molecular Plant. 6(6). 1830–1848. 121 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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