Li‐Jia Qu

12.4k total citations · 1 hit paper
137 papers, 8.2k citations indexed

About

Li‐Jia Qu is a scholar working on Molecular Biology, Plant Science and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Li‐Jia Qu has authored 137 papers receiving a total of 8.2k indexed citations (citations by other indexed papers that have themselves been cited), including 119 papers in Molecular Biology, 111 papers in Plant Science and 8 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Li‐Jia Qu's work include Plant Molecular Biology Research (90 papers), Plant Reproductive Biology (60 papers) and Photosynthetic Processes and Mechanisms (46 papers). Li‐Jia Qu is often cited by papers focused on Plant Molecular Biology Research (90 papers), Plant Reproductive Biology (60 papers) and Photosynthetic Processes and Mechanisms (46 papers). Li‐Jia Qu collaborates with scholars based in China, United States and Germany. Li‐Jia Qu's co-authors include Hongya Gu, Zhangliang Chen, Genji Qin, Ligeng Ma, Xing Wang Deng, Xing‐Wang Deng, Magnus Holm, Sheng Zhong, Hongyu Zhao and Jinming Li and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Li‐Jia Qu

136 papers receiving 8.0k citations

Hit Papers

Two interacting bZIP proteins are direct targets of COP1-... 2002 2026 2010 2018 2002 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Li‐Jia Qu China 55 6.8k 6.0k 453 257 192 137 8.2k
Hongya Gu China 50 5.6k 0.8× 4.7k 0.8× 411 0.9× 308 1.2× 200 1.0× 119 6.8k
Sean R. Cutler United States 42 9.2k 1.4× 5.0k 0.8× 298 0.7× 188 0.7× 218 1.1× 80 10.8k
Julio Salinas Spain 50 6.3k 0.9× 5.4k 0.9× 272 0.6× 539 2.1× 323 1.7× 113 8.4k
Tetsuya Sakurai Japan 43 5.4k 0.8× 5.0k 0.8× 229 0.5× 464 1.8× 137 0.7× 112 7.7k
Xing‐Wang Deng United States 45 7.6k 1.1× 7.5k 1.2× 187 0.4× 454 1.8× 136 0.7× 90 9.7k
Joshua L. Heazlewood Australia 48 4.1k 0.6× 5.6k 0.9× 211 0.5× 237 0.9× 200 1.0× 117 7.8k
Takeshi Obayashi Japan 27 4.0k 0.6× 5.1k 0.9× 214 0.5× 383 1.5× 158 0.8× 42 7.3k
Catherine Bellini France 47 7.3k 1.1× 6.4k 1.1× 257 0.6× 217 0.8× 193 1.0× 90 9.1k
Nicholas J. Provart Canada 43 6.8k 1.0× 6.3k 1.0× 248 0.5× 736 2.9× 191 1.0× 115 9.3k
Michael P. Timko United States 47 5.2k 0.8× 4.2k 0.7× 938 2.1× 334 1.3× 424 2.2× 198 7.3k

Countries citing papers authored by Li‐Jia Qu

Since Specialization
Citations

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

Fields of papers citing papers by Li‐Jia Qu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Li‐Jia Qu. 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 Li‐Jia Qu. The network helps show where Li‐Jia Qu may publish in the future.

Co-authorship network of co-authors of Li‐Jia Qu

This figure shows the co-authorship network connecting the top 25 collaborators of Li‐Jia Qu. A scholar is included among the top collaborators of Li‐Jia Qu 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 Li‐Jia Qu. Li‐Jia Qu 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.
Baillie, Alice L., Jen Sloan, Li‐Jia Qu, & Lisa M. Smith. (2023). Signalling between the sexes during pollen tube reception. Trends in Plant Science. 29(3). 343–354. 10 indexed citations
2.
Song, Zihan, et al.. (2023). The central cell: another opportunity for fertilization recovery in plants. 2(1). 0–0. 6 indexed citations
3.
Kato, Mariko, Tomohiko Tsuge, Sheng Zhong, et al.. (2023). Redundant function of the Arabidopsis phosphatidylinositol 4‐phosphate 5‐kinase genes PIP5K4–6 is essential for pollen germination. The Plant Journal. 117(1). 212–225. 9 indexed citations
4.
Zhu, Danling, Yi Wen, Haiyan Zheng, et al.. (2023). Distinct chromatin signatures in the Arabidopsis male gametophyte. Nature Genetics. 55(4). 706–720. 26 indexed citations
5.
Shen, Manman, Zhen Chen, Taocun Dou, et al.. (2022). Exploring the expression and preliminary function of chicken regulator of G protein signalling 3 (RGS3) gene in follicular development. British Poultry Science. 63(5). 613–620. 1 indexed citations
6.
Zhao, Fengli, Danling Zhu, Xi Chen, et al.. (2022). Progressive chromatin silencing of ABA biosynthesis genes permits seed germination in Arabidopsis. The Plant Cell. 34(8). 2871–2891. 25 indexed citations
7.
Liu, Meiling, Zhijuan Wang, Saiying Hou, et al.. (2021). AtLURE1/PRK6-mediated signaling promotes conspecific micropylar pollen tube guidance. PLANT PHYSIOLOGY. 186(2). 865–873. 13 indexed citations
8.
Li, Wenhao, Qiyun Li, Zhijuan Wang, et al.. (2021). Lack of ethylene does not affect reproductive success and synergid cell death in Arabidopsis. Molecular Plant. 15(2). 354–362. 28 indexed citations
9.
Zhong, Sheng, Meiling Liu, Zhijuan Wang, et al.. (2019). Cysteine-rich peptides promote interspecific genetic isolation in Arabidopsis. Science. 364(6443). 105 indexed citations
10.
Ge, Zengxiang, Alice Y. Cheung, & Li‐Jia Qu. (2018). Pollen tube integrity regulation in flowering plants: insights from molecular assemblies on the pollen tube surface. New Phytologist. 222(2). 687–693. 63 indexed citations
11.
He, Shan, Yan Sun, Qian Yang, et al.. (2017). A Novel Imprinted Gene NUWA Controls Mitochondrial Function in Early Seed Development in Arabidopsis. PLoS Genetics. 13(1). e1006553–e1006553. 28 indexed citations
12.
Hao, Lihong, Xiaolin Wei, Jingjing Liu, et al.. (2017). SNAIL1 is essential for female gametogenesis in Arabidopsis thaliana. Journal of Integrative Plant Biology. 59(9). 629–641. 11 indexed citations
13.
Hao, Lihong, Jingjing Liu, Sheng Zhong, Hongya Gu, & Li‐Jia Qu. (2016). AtVPS41-mediated endocytic pathway is essential for pollen tube–stigma interaction in Arabidopsis. Proceedings of the National Academy of Sciences. 113(22). 6307–6312. 71 indexed citations
14.
Yan, Yang, Ling Li, & Li‐Jia Qu. (2015). Plant Mediator complex and its critical functions in transcription regulation. Journal of Integrative Plant Biology. 58(2). 106–118. 68 indexed citations
15.
Lin, Qing, Yohei Ohashi, Mariko Kato, et al.. (2015). GLABRA2 Directly Suppresses Basic Helix-Loop-Helix Transcription Factor Genes with Diverse Functions in Root Hair Development. The Plant Cell. 27(10). tpc.15.00607–tpc.15.00607. 115 indexed citations
16.
Meng, Liqiang, Yinghui Wang, Ming‐Ying Shang, et al.. (2011). Astragaloside IV synergizes with ferulic acid to inhibit renal tubulointerstitial fibrosis in rats with obstructive nephropathy. British Journal of Pharmacology. 162(8). 1805–1818. 65 indexed citations
17.
Zhang, Yunfei, et al.. (2009). Characterization of Arabidopsis MYB transcription factor gene AtMYB17 and its possible regulation by LEAFY and AGL15. Journal of genetics and genomics. 36(2). 99–107. 64 indexed citations
19.
Wang, Zhe, Xinlei Wang, Jin Miao, et al.. (2007). Identification and characterization of COI1-dependent transcription factor genes involved in JA-mediated response to wounding in Arabidopsis plants. Plant Cell Reports. 27(1). 125–135. 56 indexed citations
20.
Qin, Genji, Hongya Gu, Yunde Zhao, et al.. (2005). An Indole-3-Acetic Acid Carboxyl Methyltransferase Regulates Arabidopsis Leaf Development. The Plant Cell. 17(10). 2693–2704. 251 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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