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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:

ER exit sites are physical and functional core autophagosome biogenesis components
Martin Graef, Jonathan R. Friedman, Christopher I. Graham, et al.
Molecular Biology of the Cell (2013) Vol. 24, Iss. 18, pp. 2918-2931
Open Access | Times Cited: 369

Showing 1-25 of 369 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: 2382
The autophagosome: origins unknown, biogenesis complex
Christopher A. Lamb, Tamotsu Yoshimori, Sharon A. Tooze
Nature Reviews Molecular Cell Biology (2013) Vol. 14, Iss. 12, pp. 759-774
Closed Access | Times Cited: 1234
Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 677
A brief history of autophagy from cell biology to physiology and disease
Noboru Mizushima
Nature Cell Biology (2018) Vol. 20, Iss. 5, pp. 521-527
Closed Access | Times Cited: 607
Mechanisms of Autophagy Initiation
James H. Hurley, Lindsey N. Young
Annual Review of Biochemistry (2017) Vol. 86, Iss. 1, pp. 225-244
Open Access | Times Cited: 589
The functional universe of membrane contact sites
William A. Prinz, Alexandre Toulmay, Tamás Balla
Nature Reviews Molecular Cell Biology (2019) Vol. 21, Iss. 1, pp. 7-24
Open Access | Times Cited: 562
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: 400
Atg9 is a lipid scramblase that mediates autophagosomal membrane expansion
Kazuaki Matoba, Tetsuya Kotani, Akihisa Tsutsumi, et al.
Nature Structural & Molecular Biology (2020) Vol. 27, Iss. 12, pp. 1185-1193
Closed Access | Times Cited: 352
A current perspective of autophagosome biogenesis
Shusaku Shibutani, Tamotsu Yoshimori
Cell Research (2013) Vol. 24, Iss. 1, pp. 58-68
Open Access | Times Cited: 343
Autophagosome Biogenesis in Primary Neurons Follows an Ordered and Spatially Regulated Pathway
Sandra Maday, Erika L.F. Holzbaur
Developmental Cell (2014) Vol. 30, Iss. 1, pp. 71-85
Open Access | Times Cited: 340
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
Determinants and Functions of Mitochondrial Behavior
Katherine Labbè, Andrew Murley, Jodi Nunnari
Annual Review of Cell and Developmental Biology (2014) Vol. 30, Iss. 1, pp. 357-391
Open Access | Times Cited: 311
Autophagy initiation by ULK complex assembly on ER tubulovesicular regions marked by ATG9 vesicles
Eleftherios Karanasios, Simon Walker, Hanneke Okkenhaug, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 295
The autophagic membrane tether ATG2A transfers lipids between membranes
Shintaro Maeda, Chinatsu Otomo, Takanori Otomo
eLife (2019) Vol. 8
Open Access | Times Cited: 289
Ltc1 is an ER-localized sterol transporter and a component of ER–mitochondria and ER–vacuole contacts
Andrew Murley, Reta D. Sarsam, Alexandre Toulmay, et al.
The Journal of Cell Biology (2015) Vol. 209, Iss. 4, pp. 539-548
Open Access | Times Cited: 277
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: 270
ER-phagy mediates selective degradation of endoplasmic reticulum independently of the core autophagy machinery
Sebastian Schuck, Ciara M Gallagher, Peter Walter
Journal of Cell Science (2014)
Open Access | Times Cited: 266
MICOS coordinates with respiratory complexes and lipids to establish mitochondrial inner membrane architecture
Jonathan R. Friedman, Arnaud Mourier, Justin Yamada, et al.
eLife (2015) Vol. 4
Open Access | Times Cited: 263
The Atg2-Atg18 complex tethers pre-autophagosomal membranes to the endoplasmic reticulum for autophagosome formation
Tetsuya Kotani, Hiromi Kirisako, Michiko Koizumi, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 41, pp. 10363-10368
Open Access | Times Cited: 257
Structure, lipid scrambling activity and role in autophagosome formation of ATG9A
Shintaro Maeda, Hayashi Yamamoto, Lisa N. Kinch, et al.
Nature Structural & Molecular Biology (2020) Vol. 27, Iss. 12, pp. 1194-1201
Open Access | Times Cited: 252
An overview of macroautophagy in yeast
Xin Wen, Daniel J. Klionsky
Journal of Molecular Biology (2016) Vol. 428, Iss. 9, pp. 1681-1699
Open Access | Times Cited: 251
Atg9 establishes Atg2-dependent contact sites between the endoplasmic reticulum and phagophores
Rubén Gómez‐Sánchez, Jaqueline Rose, Rodrigo Soares Guimarães, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 8, pp. 2743-2763
Open Access | Times Cited: 247
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: 229
Structure and function of the ULK1 complex in autophagy
Mary Grace Lin, James H. Hurley
Current Opinion in Cell Biology (2016) Vol. 39, pp. 61-68
Open Access | Times Cited: 228
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: 223
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