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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:

Autophagosome maturation: An epic journey from the ER to lysosomes
Yan Zhao, Hong Zhang
The Journal of Cell Biology (2018) Vol. 218, Iss. 3, pp. 757-770
Open Access | Times Cited: 313

Showing 1-25 of 313 citing articles:

Lysosomes as dynamic regulators of cell and organismal homeostasis
Andrea Ballabio, Juan S. Bonifacino
Nature Reviews Molecular Cell Biology (2019) Vol. 21, Iss. 2, pp. 101-118
Closed Access | Times Cited: 1084
Machinery, regulation and pathophysiological implications of autophagosome maturation
Yan Zhao, Patrice Codogno, Hong Zhang
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 11, pp. 733-750
Open Access | Times Cited: 381
Autophagy genes in biology and disease
Hayashi Yamamoto, Sidi Zhang, Noboru Mizushima
Nature Reviews Genetics (2023) Vol. 24, Iss. 6, pp. 382-400
Open Access | Times Cited: 365
Diverse Cellular Roles of Autophagy
Hideaki Morishita, Noboru Mizushima
Annual Review of Cell and Developmental Biology (2019) Vol. 35, Iss. 1, pp. 453-475
Open Access | Times Cited: 325
ORF3a of the COVID-19 virus SARS-CoV-2 blocks HOPS complex-mediated assembly of the SNARE complex required for autolysosome formation
Guangyan Miao, Hongyu Zhao, Yan Li, et al.
Developmental Cell (2020) Vol. 56, Iss. 4, pp. 427-442.e5
Open Access | Times Cited: 309
Lysosome biogenesis: Regulation and functions
Chonglin Yang, Xiaochen Wang
The Journal of Cell Biology (2021) Vol. 220, Iss. 6
Open Access | Times Cited: 308
Autophagosome biogenesis: From membrane growth to closure
Thomas J. Melia, Alf Håkon Lystad, Anne Simonsen
The Journal of Cell Biology (2020) Vol. 219, Iss. 6
Open Access | Times Cited: 269
Liquid-liquid phase separation in biology: mechanisms, physiological functions and human diseases
Hong Zhang, Ji Xiong, Pilong Li, et al.
Science China Life Sciences (2020) Vol. 63, Iss. 7, pp. 953-985
Closed Access | Times Cited: 259
Ubiquitin-mediated regulation of autophagy
Ruey‐Hwa Chen, Yu-Hsuan Chen, Tzu-Yu Huang
Journal of Biomedical Science (2019) Vol. 26, Iss. 1
Open Access | Times Cited: 255
Role of lysosomes in physiological activities, diseases, and therapy
Ziqi Zhang, Pengfei Yue, Tianqi Lu, et al.
Journal of Hematology & Oncology (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 210
The SARS-CoV-2 protein ORF3a inhibits fusion of autophagosomes with lysosomes
Yabin Zhang, Hao Sun, Rongjuan Pei, et al.
Cell Discovery (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 195
Outstanding Questions in Mitophagy: What We Do and Do Not Know
Lambert Montava‐Garriga, Ian G. Ganley
Journal of Molecular Biology (2019) Vol. 432, Iss. 1, pp. 206-230
Open Access | Times Cited: 180
The Structure of the Membrane Protein of SARS-CoV-2 Resembles the Sugar Transporter SemiSWEET
Sunil Thomas
Pathogens and Immunity (2020) Vol. 5, Iss. 1, pp. 342-342
Open Access | Times Cited: 158
New insights regarding SNARE proteins in autophagosome-lysosome fusion
Xiaoyu Tian, Junlin Teng, Jianguo Chen
Autophagy (2020) Vol. 17, Iss. 10, pp. 2680-2688
Open Access | Times Cited: 158
ORF3a of SARS-CoV-2 promotes lysosomal exocytosis-mediated viral egress
Di Chen, Qiaoxia Zheng, Long Sun, et al.
Developmental Cell (2021) Vol. 56, Iss. 23, pp. 3250-3263.e5
Open Access | Times Cited: 156
Autophagy Assays for Biological Discovery and Therapeutic Development
Noboru Mizushima, Leon O. Murphy
Trends in Biochemical Sciences (2020) Vol. 45, Iss. 12, pp. 1080-1093
Open Access | Times Cited: 149
Who’s in control? Principles of Rab GTPase activation in endolysosomal membrane trafficking and beyond
Ann-Christin Borchers, Lars Langemeyer, Christian Ungermann
The Journal of Cell Biology (2021) Vol. 220, Iss. 9
Open Access | Times Cited: 131
VAP-A and its binding partner CERT drive biogenesis of RNA-containing extracellular vesicles at ER membrane contact sites
Bahnisikha Barman, Bong Hwan Sung, Evan Krystofiak, et al.
Developmental Cell (2022) Vol. 57, Iss. 8, pp. 974-994.e8
Open Access | Times Cited: 89
Lysosomes as coordinators of cellular catabolism, metabolic signalling and organ physiology
Carmine Settembre, Rushika M. Perera
Nature Reviews Molecular Cell Biology (2023) Vol. 25, Iss. 3, pp. 223-245
Closed Access | Times Cited: 88
Molecular regulation of autophagosome formation
Yan Hu, Fulvio Reggiori
Biochemical Society Transactions (2022) Vol. 50, Iss. 1, pp. 55-69
Open Access | Times Cited: 70
The chaperone-assisted selective autophagy complex dynamics and dysfunctions
B. Tedesco, Leen Vendredy, Vincent Timmerman, et al.
Autophagy (2023) Vol. 19, Iss. 6, pp. 1619-1641
Open Access | Times Cited: 55
Molecular Mechanisms of Macroautophagy, Microautophagy, and Chaperone-Mediated Autophagy
Hayashi Yamamoto, Takahide Matsui
Journal of Nippon Medical School (2023) Vol. 91, Iss. 1, pp. 2-9
Open Access | Times Cited: 53
Orchestration of MUC2 — The key regulatory target of gut barrier and homeostasis: A review
Yaxin Liu, Zihan Yu, Lanping Zhu, et al.
International Journal of Biological Macromolecules (2023) Vol. 236, pp. 123862-123862
Closed Access | Times Cited: 44
The STX17-SNAP47-VAMP7/VAMP8 complex is the default SNARE complex mediating autophagosome–lysosome fusion
Fenglei Jian, Shen Wang, Rui Tian, et al.
Cell Research (2024) Vol. 34, Iss. 2, pp. 151-168
Closed Access | Times Cited: 18
ATG9A facilitates the closure of mammalian autophagosomes
Ruheena Javed, Muriel Mari, Einar S Trosdal, et al.
The Journal of Cell Biology (2025) Vol. 224, Iss. 2
Closed Access | Times Cited: 2
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