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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 regulatory role of autophagy for resetting the memory of heat stress in plants
Mastoureh Sedaghatmehr, Venkatesh P. Thirumalaikumar, Iman Kamranfar, et al.
Plant Cell & Environment (2018) Vol. 42, Iss. 3, pp. 1054-1064
Open Access | Times Cited: 107

Showing 26-50 of 107 citing articles:

Decoding the molecular mechanism underlying salicylic acid (SA)‐mediated plant immunity: an integrated overview from its biosynthesis to the mode of action
Rajib Roychowdhury, Sapna Mishra, Gautam Anand, et al.
Physiologia Plantarum (2024) Vol. 176, Iss. 3
Open Access | Times Cited: 12
Unraveling the role of autophagy and antioxidants in anther and pistil responses to heat stress in rapeseed (Brassica napus L.)
Valiollah Mohammadi, Ahmad rezaeizadeh, Behnam Mondak, et al.
Plant Cell Reports (2025) Vol. 44, Iss. 2
Open Access | Times Cited: 1
The Adaptation and Tolerance of Major Cereals and Legumes to Important Abiotic Stresses
Jagadish Rane, Ajay Kumar Singh, Mahesh Kumar, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 23, pp. 12970-12970
Open Access | Times Cited: 49
Autophagy during drought: function, regulation, and potential application
Jie Tang, Diane C. Bassham
The Plant Journal (2021) Vol. 109, Iss. 2, pp. 390-401
Closed Access | Times Cited: 45
Transcriptional Regulators of Plant Adaptation to Heat Stress
Xuejing Wang, Nicholas Wui Kiat Tan, Fong Yi Chung, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 17, pp. 13297-13297
Open Access | Times Cited: 18
Autophagy: a key player in the recovery of plants from heat stress
Mastoureh Sedaghatmehr, Salma Balazadeh
Journal of Experimental Botany (2024) Vol. 75, Iss. 8, pp. 2246-2255
Open Access | Times Cited: 7
Yes, plants do have memory
Yutcelia Carolina Galviz-Fajardo, Rafael Vasconcelos Ribeiro, Gustavo Maia Souza
Theoretical and Experimental Plant Physiology (2020) Vol. 32, Iss. 3, pp. 195-202
Closed Access | Times Cited: 50
Target of Rapamycin in Control of Autophagy: Puppet Master and Signal Integrator
Yosia Mugume, Zakayo Kazibwe, Diane C. Bassham
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 21, pp. 8259-8259
Open Access | Times Cited: 43
Plant Autophagy: An Intricate Process Controlled by Various Signaling Pathways
Pingping Wang, Tongtong Wang, Jingyi Han, et al.
Frontiers in Plant Science (2021) Vol. 12
Open Access | Times Cited: 41
A ‘hot’ cocktail: The multiple layers of thermomemory in plants
Salma Balazadeh
Current Opinion in Plant Biology (2021) Vol. 65, pp. 102147-102147
Open Access | Times Cited: 40
Autophagy in Plant Abiotic Stress Management
Hong Chen, Jiangli Dong, Tao Wang
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4075-4075
Open Access | Times Cited: 39
Degradation Mechanism of Autophagy-Related Proteins and Research Progress
Yanhui Zhou, Hakim Manghwar, Weiming Hu, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 13, pp. 7301-7301
Open Access | Times Cited: 25
Mechanisms of autophagy function and regulation in plant growth, development, and response to abiotic stress
Yongbo Li, Xiang-Min Xu, Guang Qi, et al.
The Crop Journal (2023) Vol. 11, Iss. 6, pp. 1611-1625
Open Access | Times Cited: 16
NBR1-mediated selective autophagy of ARF7 modulates root branching
Elise Nagel Ebstrup, Jeppe Ansbøl, Ana Páez-García, et al.
EMBO Reports (2024) Vol. 25, Iss. 6, pp. 2571-2591
Open Access | Times Cited: 6
Autophagy in plants
Morten Petersen, Tamar Avin‐Wittenberg, Diane C. Bassham, et al.
Autophagy Reports (2024) Vol. 3, Iss. 1
Open Access | Times Cited: 5
Drought stress memory and subsequent drought stress tolerance in plants
Łukasz Wojtyla, Ewelina Paluch-Lubawa, Ewa Sobieszczuk‐Nowicka, et al.
Elsevier eBooks (2020), pp. 115-131
Closed Access | Times Cited: 36
Broad and Complex Roles of NBR1-Mediated Selective Autophagy in Plant Stress Responses
Yan Zhang, Zhixiang Chen
Cells (2020) Vol. 9, Iss. 12, pp. 2562-2562
Open Access | Times Cited: 36
Autophagy is responsible for the accumulation of proteogenic dipeptides in response to heat stress in Arabidopsis thaliana
Venkatesh P. Thirumalaikumar, Mateusz Wagner, Salma Balazadeh, et al.
FEBS Journal (2020) Vol. 288, Iss. 1, pp. 281-292
Open Access | Times Cited: 34
The epigenetic chromatin-based regulation of somatic heat stress memory in plants
Saqlain Haider, Javed Iqbal, Muzaffar Shaukat, et al.
Plant Gene (2021) Vol. 27, pp. 100318-100318
Closed Access | Times Cited: 29
Priming by High Temperature Stress Induces MicroRNA Regulated Heat Shock Modules Indicating Their Involvement in Thermopriming Response in Rice
Akhilesh Kumar Kushawaha, Ambreen Khan, Sudhir K. Sopory, et al.
Life (2021) Vol. 11, Iss. 4, pp. 291-291
Open Access | Times Cited: 28
Carbon starvation, senescence and specific mitochondrial stresses, but not nitrogen starvation and general stresses, are major triggers for mitophagy in Arabidopsis
Sylwia Kacprzak, Olivier Van Aken
Autophagy (2022) Vol. 18, Iss. 12, pp. 2894-2912
Open Access | Times Cited: 22
A glucose–target of rapamycin signaling axis integrates environmental history of heat stress through maintenance of transcription-associated epigenetic memory in Arabidopsis
Mohan Sharma, Manvi Sharma, Muhammed Jamsheer K, et al.
Journal of Experimental Botany (2022) Vol. 73, Iss. 20, pp. 7083-7102
Closed Access | Times Cited: 21
Echoes of a Stressful Past: Abiotic Stress Memory in Crop Plants towards Enhanced Adaptation
Georgios Lagiotis, Panagiotis Madesis, Evangelia Stavridou
Agriculture (2023) Vol. 13, Iss. 11, pp. 2090-2090
Open Access | Times Cited: 13
PeHSFA3 is essential for the heat-stress response of Populus × euramericana
Shixiong Ren, Hongyan Zou, Jiawen Cui, et al.
Industrial Crops and Products (2024) Vol. 219, pp. 119054-119054
Closed Access | Times Cited: 4
Induction of Radiata Pine Somatic Embryogenesis at High Temperatures Provokes a Long-Term Decrease in DNA Methylation/Hydroxymethylation and Differential Expression of Stress-Related Genes
Ander Castander-Olarieta, Cátia Pereira, Ester Sales, et al.
Plants (2020) Vol. 9, Iss. 12, pp. 1762-1762
Open Access | Times Cited: 30

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