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:

Remodeling of ER ‐exit sites initiates a membrane supply pathway for autophagosome biogenesis
Liang Ge, Min Zhang, Samuel J. Kenny, et al.
EMBO Reports (2017) Vol. 18, Iss. 9, pp. 1586-1603
Open Access | Times Cited: 154

Showing 1-25 of 154 citing articles:

Mechanism and medical implications of mammalian autophagy
Ivan Đikić, Zvulun Elazar
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 6, pp. 349-364
Closed Access | Times Cited: 2345

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: 1957

Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 659

Atg2 mediates direct lipid transfer between membranes for autophagosome formation
Takuo Osawa, Tetsuya Kotani, Tatsuya Kawaoka, et al.
Nature Structural & Molecular Biology (2019) Vol. 26, Iss. 4, pp. 281-288
Closed Access | Times Cited: 388

The autophagic membrane tether ATG2A transfers lipids between membranes
Shintaro Maeda, Chinatsu Otomo, Takanori Otomo
eLife (2019) Vol. 8
Open Access | Times Cited: 282

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: 267

ER-Phagy: Quality Control and Turnover of Endoplasmic Reticulum
Haruka Chino, Noboru Mizushima
Trends in Cell Biology (2020) Vol. 30, Iss. 5, pp. 384-398
Open Access | Times Cited: 220

Emerging roles of ATG proteins and membrane lipids in autophagosome formation
Taki Nishimura, Sharon A. Tooze
Cell Discovery (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 215

ER-to-Golgi protein delivery through an interwoven, tubular network extending from ER
Aubrey V. Weigel, Chi‐Lun Chang, Gleb Shtengel, et al.
Cell (2021) Vol. 184, Iss. 9, pp. 2412-2429.e16
Open Access | Times Cited: 212

A Translocation Pathway for Vesicle-Mediated Unconventional Protein Secretion
Min Zhang, Lei Liu, Xubo Lin, et al.
Cell (2020) Vol. 181, Iss. 3, pp. 637-652.e15
Open Access | Times Cited: 204

Local Fatty Acid Channeling into Phospholipid Synthesis Drives Phagophore Expansion during Autophagy
Maximilian Schütter, Patrick Giavalisco, Susanne Brodesser, et al.
Cell (2019) Vol. 180, Iss. 1, pp. 135-149.e14
Open Access | Times Cited: 188

Molecular regulation of autophagosome formation
Yan Hu, Fulvio Reggiori
Biochemical Society Transactions (2022) Vol. 50, Iss. 1, pp. 55-69
Open Access | Times Cited: 69

Recycling of autophagosomal components from autolysosomes by the recycler complex
Chuchu Zhou, Zhe Wu, Wanqing Du, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 4, pp. 497-512
Open Access | Times Cited: 68

Quantitative analysis of autophagy reveals the role of ATG9 and ATG2 in autophagosome formation
David Broadbent, Carlo Barnaba, Gloria I. Perez, et al.
The Journal of Cell Biology (2023) Vol. 222, Iss. 7
Open Access | Times Cited: 46

The Role of ATG9 Vesicles in Autophagosome Biogenesis
Elisabeth Holzer, Sascha Martens, Susanna Tulli
Journal of Molecular Biology (2024) Vol. 436, Iss. 15, pp. 168489-168489
Open Access | Times Cited: 23

Stay in touch with the endoplasmic reticulum
Sha Sun, Zhao Gan, Mingkang Jia, et al.
Science China Life Sciences (2024) Vol. 67, Iss. 2, pp. 230-257
Open Access | Times Cited: 21

Tau fibrils induce nanoscale membrane damage and nucleate cytosolic tau at lysosomes
Kevin Rose, Tyler Jepson, Sankalp Shukla, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 22
Open Access | Times Cited: 20

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: 1

Noncanonical autophagy at ER exit sites regulates procollagen turnover
Shakib Omari, Elena Makareeva, Anna M. Roberts-Pilgrim, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 43
Open Access | Times Cited: 147

ER‐phagy: shaping up and destressing the endoplasmic reticulum
Simon Wilkinson
FEBS Journal (2019) Vol. 286, Iss. 14, pp. 2645-2663
Open Access | Times Cited: 135

COPII vesicles contribute to autophagosomal membranes
Takayuki Shima, Hiromi Kirisako, Hitoshi Nakatogawa
The Journal of Cell Biology (2019) Vol. 218, Iss. 5, pp. 1503-1510
Open Access | Times Cited: 107

Mitochondria-Associated ER Membranes – The Origin Site of Autophagy
Ming Yang, Chenrui Li, Shikun Yang, et al.
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 103

Autophagosomes are formed at a distinct cellular structure
David M. Hollenstein, Claudine Kraft
Current Opinion in Cell Biology (2020) Vol. 65, pp. 50-57
Open Access | Times Cited: 91

Autophagosome biogenesis and human health
Tsuyoshi Kawabata, Tamotsu Yoshimori
Cell Discovery (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 87

Insights into the Pathogenesis of Neurodegenerative Diseases: Focus on Mitochondrial Dysfunction and Oxidative Stress
Anamaria Jurcău
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11847-11847
Open Access | Times Cited: 82

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