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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:

Autophagosomal YKT6 is required for fusion with lysosomes independently of syntaxin 17
Takahide Matsui, Peidu Jiang, Saori Nakano, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 8, pp. 2633-2645
Open Access | Times Cited: 214

Showing 1-25 of 214 citing articles:

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Daniel J. Klionsky, Amal Kamal Abdel‐Aziz, Sara Abdelfatah, et al.
Autophagy (2021) Vol. 17, Iss. 1, pp. 1-382
Open Access | Times Cited: 1998
Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 677
Lysosome biology in autophagy
Willa Wen‐You Yim, Noboru Mizushima
Cell Discovery (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 632
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: 384
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: 366
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
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
Autophagy and Autophagy-Related Diseases: A Review
Tadashi Ichimiya, Tsukasa Yamakawa, Takehiro Hirano, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 23, pp. 8974-8974
Open Access | Times Cited: 252
Autophagosome-Lysosome Fusion
Péter Lőrincz, Gábor Juhász
Journal of Molecular Biology (2019) Vol. 432, Iss. 8, pp. 2462-2482
Open Access | Times Cited: 249
Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration
Tara E. Tracy, Jesús Madero‐Pérez, Danielle L. Swaney, et al.
Cell (2022) Vol. 185, Iss. 4, pp. 712-728.e14
Open Access | Times Cited: 212
Genome-wide CRISPR screen identifies TMEM41B as a gene required for autophagosome formation
Keigo Morita, Yutaro Hama, Tamaki Izume, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 11, pp. 3817-3828
Open Access | Times Cited: 202
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: 196
Autophagy: A Key Regulator of Homeostasis and Disease: An Overview of Molecular Mechanisms and Modulators
Laura Gómez-Virgilio, Maria‐del‐Carmen Silva‐Lucero, Diego-Salvador Flores-Morelos, et al.
Cells (2022) Vol. 11, Iss. 15, pp. 2262-2262
Open Access | Times Cited: 164
Autophagy in Neurodegenerative Diseases: A Hunter for Aggregates
Hyungsun Park, Ju‐Hee Kang, Seongju Lee
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 9, pp. 3369-3369
Open Access | Times Cited: 161
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: 160
The role of autophagy in viral infections
Tong Chen, Shaoyu Tu, Ling Ding, et al.
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 105
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: 54
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: 19
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
TRIM proteins in autophagy: selective sensors in cell damage and innate immune responses
Martina Di Rienzo, Alessandra Romagnoli, Manuela Antonioli, et al.
Cell Death and Differentiation (2020) Vol. 27, Iss. 3, pp. 887-902
Open Access | Times Cited: 136
Autophagy and endocytosis – interconnections and interdependencies
Åsa Birna Birgisdottir, Terje Johansen
Journal of Cell Science (2020) Vol. 133, Iss. 10
Open Access | Times Cited: 132
p62-mediated phase separation at the intersection of the ubiquitin-proteasome system and autophagy
Alberto Danieli, Sascha Martens
Journal of Cell Science (2018) Vol. 131, Iss. 19
Open Access | Times Cited: 130
ESCRT-III-driven piecemeal micro-ER-phagy remodels the ER during recovery from ER stress
Marisa Loi, Andrea Raimondi, Diego Morone, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 126
Phosphorylation of Syntaxin 17 by TBK1 Controls Autophagy Initiation
Suresh Kumar, Yuexi Gu, Yakubu Princely Abudu, et al.
Developmental Cell (2019) Vol. 49, Iss. 1, pp. 130-144.e6
Open Access | Times Cited: 120
Reconstitution reveals Ykt6 as the autophagosomal SNARE in autophagosome–vacuole fusion
Levent Bas, Daniel Papinski, Mariya Licheva, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 10, pp. 3656-3669
Open Access | Times Cited: 110
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