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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

A transcriptome analysis uncovers Panax notoginseng resistance to Fusarium solani induced by methyl jasmonate
Diqiu Liu, Qin Zhao, Xiuming Cui, et al.
Genes & Genomics (2019) Vol. 41, Iss. 12, pp. 1383-1396
Closed Access | Times Cited: 49

Showing 1-25 of 49 citing articles:

Function and Mechanism of Jasmonic Acid in Plant Responses to Abiotic and Biotic Stresses
Yun Wang, Salma Mostafa, Wen Zeng, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8568-8568
Open Access | Times Cited: 368
Multilayered regulation of secondary metabolism in medicinal plants
Yan Zhao, Guanze Liu, Feng Yang, et al.
Molecular Horticulture (2023) Vol. 3, Iss. 1
Open Access | Times Cited: 46
Jasmonic Acid (JA) in Plant Immune Response: Unravelling Complex Molecular Mechanisms and Networking of Defence Signalling Against Pathogens
Rajib Roychowdhury, Alkesh Hada, Sabarni Biswas, et al.
Journal of Plant Growth Regulation (2024)
Closed Access | Times Cited: 15
Role of secondary metabolites in plant defense mechanisms: a molecular and biotechnological insights
R. C. Upadhyay, Rajesh K. Saini, P. K. Shukla, et al.
Phytochemistry Reviews (2024)
Closed Access | Times Cited: 15
Discovery of plant chemical defence mediated by a two-component system involving β-glucosidase in Panax species
Lijuan Ma, Xiao Liu, Liwei Guo, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
Exploring the role of jasmonic acid in boosting the production of secondary metabolites in medicinal plants: Pathway for future research
Varisha Khan, Anshu Jha, Princi, et al.
Industrial Crops and Products (2024) Vol. 220, pp. 119227-119227
Closed Access | Times Cited: 9
Genome-wide identification and characterization of WRKYs family involved in responses to Cylindrocarpon destructans in Panax notoginseng
Manqiao Li, Xingliang Che, Qiwen Liang, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 1
Plant–pathogen interaction with root rot of Panax notoginseng as a model: Insight into pathogen pathogenesis, plant defence response and biological control
Jianbin Li, Mingtao Ai, Jiae Hou, et al.
Molecular Plant Pathology (2024) Vol. 25, Iss. 2
Open Access | Times Cited: 7
Proline‐rich protein PRPL1 enhances Panax notoginseng defence against Fusarium solani by regulating reactive oxygen species balance and strengthening the cell wall barrier
Linlin Su, Wenyun Li, Xiaohua Chen, et al.
Plant Cell & Environment (2024) Vol. 47, Iss. 7, pp. 2375-2393
Closed Access | Times Cited: 7
A Pathogenesis-Related Protein-Like Gene Is Involved in the Panax notoginseng Defense Response to the Root Rot Pathogen
Shan Li, Zie Wang, Bifeng Tang, et al.
Frontiers in Plant Science (2021) Vol. 11
Open Access | Times Cited: 33
Cucumber mosaic virus impairs the physiological homeostasis of Panax notoginseng and induces saponin-mediated resistance
Yongchao Cheng, Tianrui Zheng, Daoyong Yang, et al.
Virology (2024) Vol. 591, pp. 109983-109983
Closed Access | Times Cited: 5
Transcriptome analysis reveals ethylene-mediated defense responses to Fusarium oxysporum f. sp. cucumerinum infection in Cucumis sativus L.
Jingping Dong, Yuean Wang, Qianqian Xian, et al.
BMC Plant Biology (2020) Vol. 20, Iss. 1
Open Access | Times Cited: 33
Research progress in diseases of Panax notoginseng
Jianbin Li, Yongli Bao, Z. Wang, et al.
Physiological and Molecular Plant Pathology (2022) Vol. 121, pp. 101878-101878
Closed Access | Times Cited: 21
Panax notoginseng WRKY Transcription Factor 9 Is a Positive Regulator in Responding to Root Rot Pathogen Fusarium solani
Lilei Zheng, Bingling Qiu, Linlin Su, et al.
Frontiers in Plant Science (2022) Vol. 13
Open Access | Times Cited: 20
Dirigent gene family is involved in the molecular interaction between Panax notoginseng and root rot pathogen Fusarium solani
Jie Deng, Ruipan Guan, Tingting Liang, et al.
Industrial Crops and Products (2022) Vol. 178, pp. 114544-114544
Closed Access | Times Cited: 19
Panax notoginseng transcription factor WRKY15 modulates resistance to Fusarium solani by up-regulating osmotin-like protein expression and inducing JA/SA signaling pathways
Linlin Su, Lilei Zheng, Hanlin Wang, et al.
BMC Plant Biology (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 11
Function and regulation of a chitinase gene during Panax notoginseng defense response to root rot
Hanlin Wang, Jun Hai, Yuan Qu, et al.
Journal of Applied Research on Medicinal and Aromatic Plants (2024) Vol. 39, pp. 100533-100533
Closed Access | Times Cited: 4
The EIN3 transcription factor GmEIL1 improves soybean resistance to Phytophthora sojae
Xi Chen, Yan Sun, Yu Yang, et al.
Molecular Plant Pathology (2024) Vol. 25, Iss. 4
Open Access | Times Cited: 4
Biocontrol effects and underlying mechanism of Bacillus subtilis Pn1 on Panax notoginseng root rot caused by Fusarium solani
Gan Kunfa, Meng Chen, Liang Tingting, et al.
Industrial Crops and Products (2025) Vol. 229, pp. 120963-120963
Open Access
Transcriptomic and Metabolomic Changes Triggered by Fusarium solani in Common Bean (Phaseolus vulgaris L.)
Limin Chen, Quancong Wu, Tianjun He, et al.
Genes (2020) Vol. 11, Iss. 2, pp. 177-177
Open Access | Times Cited: 31
Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid
Han Li, Xuan Zhou, Yiting Zhao, et al.
Journal of Integrative Plant Biology (2020) Vol. 62, Iss. 9, pp. 1433-1451
Closed Access | Times Cited: 28
WRKY11 up-regulated dirigent expression to enhance lignin/lignans accumulation in Lilium regale Wilson during response to Fusarium wilt
Jie Deng, Zie Wang, Wanyi Li, et al.
Journal of Integrative Agriculture (2023) Vol. 23, Iss. 8, pp. 2703-2722
Open Access | Times Cited: 9
The Chalcone Isomerase Family in Cotton: Whole-Genome Bioinformatic and Expression Analyses of the Gossypium barbadense L. Response to Fusarium Wilt Infection
Qianli Zu, Yanying Qu, Zhiyong Ni, et al.
Genes (2019) Vol. 10, Iss. 12, pp. 1006-1006
Open Access | Times Cited: 20
WRKY Transcription Factors Actively Respond to Fusarium oxysporum in Lilium regale
Shan Li, Guanze Liu, Limei Pu, et al.
Phytopathology (2021) Vol. 111, Iss. 9, pp. 1625-1637
Open Access | Times Cited: 16
Lilium regale Wilson WRKY3 modulates an antimicrobial peptide gene, LrDef1, during response to Fusarium oxysporum
Zie Wang, Jie Deng, Tingting Liang, et al.
BMC Plant Biology (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 11
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