Yuan Qin

8.1k total citations · 1 hit paper
166 papers, 4.7k citations indexed

About

Yuan Qin is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Yuan Qin has authored 166 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 130 papers in Plant Science, 121 papers in Molecular Biology and 12 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Yuan Qin's work include Plant Molecular Biology Research (90 papers), Plant Reproductive Biology (61 papers) and Photosynthetic Processes and Mechanisms (26 papers). Yuan Qin is often cited by papers focused on Plant Molecular Biology Research (90 papers), Plant Reproductive Biology (61 papers) and Photosynthetic Processes and Mechanisms (26 papers). Yuan Qin collaborates with scholars based in China, United States and Taiwan. Yuan Qin's co-authors include Hanyang Cai, Mohammad Aslam, Zhilin Yuan, Xueyu Pan, Lihua Zhao, Zhenbiao Yang, Ravishankar Palanivelu, Irina S. Druzhinina, Yanhui Liu and Yan Cheng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

Yuan Qin

157 papers receiving 4.7k citations

Hit Papers

Microbially Mediated Plant Salt Tolerance and Microbiome-... 2016 2026 2019 2022 2016 50 100 150 200 250
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.

  1. Microbially Mediated Plant Salt Tolerance and Microbiome-based Solutions for Saline Agriculture
    2016 275 citations Yuan Qin et al. profile →

Peers

Yuan Qin
Ji‐Young Lee South Korea
Gunnar Wingsle Sweden
Yang Zhao China
Brendan J. McConkey Canada
Hiroaki Shimada Japan
José R. Dinneny United States
Bo Zhang China
Hitoshi Mori Japan
Marcin Rapacz Poland
Maurice S. B. Ku United States
Ji‐Young Lee South Korea
Yuan Qin
Citations per year, relative to Yuan Qin Yuan Qin (= 1×) peers Ji‐Young Lee

Countries citing papers authored by Yuan Qin

Since Specialization
Citations

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

Fields of papers citing papers by Yuan Qin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuan Qin

This figure shows the co-authorship network connecting the top 25 collaborators of Yuan Qin. A scholar is included among the top collaborators of Yuan Qin 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 Yuan Qin. Yuan Qin 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.
Huang, Youmei, Yunlong Zhang, Jiahong Yang, et al.. (2025). Revisiting the female germline cell development. Frontiers in Plant Science. 15. 1525729–1525729. 2 indexed citations
2.
Liu, Liping, Yuan Qin, & Hanyang Cai. (2025). Understanding the Functional Megaspore Development: Current Status/Progress, Perspectives. Plant Cell & Environment. 48(7). 4921–4927. 2 indexed citations
3.
Luo, Tiantian, S. V. G. N. Priyadarshani, Han Cheng, et al.. (2024). Overexpression of AcWRKY31 Increases Sensitivity to Salt and Drought and Improves Tolerance to Mealybugs in Pineapple. Plants. 13(13). 1850–1850. 1 indexed citations
4.
Qin, Yuan, et al.. (2024). Rubus tingzhouensis (Rosaceae), a new species from Fujian, China. PhytoKeys. 249. 251–267.
5.
Huang, Youmei, Mengnan Chai, Han Su, et al.. (2023). Chromatin Remodeling Complex SWR1 Regulates Root Development by Affecting the Accumulation of Reactive Oxygen Species (ROS). Plants. 12(4). 940–940. 2 indexed citations
6.
Cai, Hanyang, Youmei Huang, Liping Liu, et al.. (2023). Signaling by the EPFL-ERECTA family coordinates female germline specification through the BZR1 family in Arabidopsis. The Plant Cell. 35(5). 1455–1473. 18 indexed citations
7.
Huang, Youmei, Liping Liu, Mengnan Chai, et al.. (2023). Epigenetic regulation of female germline development through ERECTA signaling pathway. New Phytologist. 240(3). 1015–1033. 6 indexed citations
8.
Cheng, Yan, Yu Wang, Zhenyang Liao, et al.. (2023). Unveiling the genomic blueprint of salt stress: insights from <i>Ipomoea pes-caprae</i> L.. 2(1). 0–0. 5 indexed citations
9.
10.
Chen, Binqing, Xie Dang, Yanqiu Yang, et al.. (2022). The IPGA1‐ANGUSTIFOLIA module regulates microtubule organisation and pavement cell shape in Arabidopsis. New Phytologist. 236(4). 1310–1325. 8 indexed citations
11.
Cai, Hanyang, Liping Liu, Man Zhang, et al.. (2021). Spatiotemporal control of miR398 biogenesis, via chromatin remodeling and kinase signaling, ensures proper ovule development. The Plant Cell. 33(5). 1530–1553. 24 indexed citations
12.
Shi, Yan, Xingtan Zhang, Xiaojun Chang, et al.. (2021). Integrated analysis of DNA methylome and transcriptome reveals epigenetic regulation of CAM photosynthesis in pineapple. BMC Plant Biology. 21(1). 19–19. 18 indexed citations
13.
Liu, Yanhui, Man Zhang, Liping Liu, et al.. (2021). High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana. Communications Biology. 4(1). 1149–1149. 26 indexed citations
14.
Rathor, Pramod, Tudor Borza, Yanhui Liu, et al.. (2020). Low Mannitol Concentrations in Arabidopsis thaliana Expressing Ectocarpus Genes Improve Salt Tolerance. Plants. 9(11). 1508–1508. 18 indexed citations
15.
Chen, Huihuang, Lanxin Li, Liping Liu, et al.. (2020). AcoMYB4, an Ananas comosus L. MYB Transcription Factor, Functions in Osmotic Stress through Negative Regulation of ABA Signaling. International Journal of Molecular Sciences. 21(16). 5727–5727. 31 indexed citations
16.
Cai, Hanyang, Mengnan Chai, Fangqian Chen, et al.. (2020). HBI1 acts downstream of ERECTA and SWR1 in regulating inflorescence architecture through the activation of the brassinosteroid and auxin signaling pathways. New Phytologist. 229(1). 414–428. 22 indexed citations
17.
Su, Zhenxia, et al.. (2020). Regulation of Female Germline Specification via Small RNA Mobility in Arabidopsis. The Plant Cell. 32(9). 2842–2854. 48 indexed citations
18.
Priyadarshani, S. V. G. N., Hanyang Cai, Qiao Zhou, et al.. (2019). An Efficient Agrobacterium Mediated Transformation of Pineapple with GFP-Tagged Protein Allows Easy, Non-Destructive Screening of Transgenic Pineapple Plants. Biomolecules. 9(10). 617–617. 21 indexed citations
19.
Yang, Yanqiu, Xie Dang, Huibo Ren, et al.. (2019). Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis. Journal of Experimental Botany. 70(19). 5231–5243. 14 indexed citations
20.
Qin, Yuan, Lihua Zhao, Megan I. Skaggs, et al.. (2014). ACTIN-RELATED PROTEIN6 Regulates Female Meiosis by Modulating Meiotic Gene Expression in Arabidopsis. The Plant Cell. 26(4). 1612–1628. 65 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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