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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 26-50 of 369 citing articles:

Reconstitution of autophagosome nucleation defines Atg9 vesicles as seeds for membrane formation
Justyna Sawa‐Makarska, Verena Baumann, Nicolas Coudevylle, et al.
Science (2020) Vol. 369, Iss. 6508
Open Access | Times Cited: 222
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: 221
Autophagosome Maturation and Fusion
Fulvio Reggiori, Christian Ungermann
Journal of Molecular Biology (2017) Vol. 429, Iss. 4, pp. 486-496
Open Access | Times Cited: 213
Autophagy signal transduction by ATG proteins: from hierarchies to networks
Sebastian Wesselborg, Björn Stork
Cellular and Molecular Life Sciences (2015) Vol. 72, Iss. 24, pp. 4721-4757
Open Access | Times Cited: 212
Membrane dynamics in autophagosome biogenesis
Sven R. Carlsson, Anne Simonsen
Journal of Cell Science (2015)
Open Access | Times Cited: 204
Mitochondrial ER Contacts Are Crucial for Mitophagy in Yeast
Stefan Böckler, Benedikt Westermann
Developmental Cell (2014) Vol. 28, Iss. 4, pp. 450-458
Open Access | Times Cited: 202
Phosphatidylinositol 3-kinase and COPII generate LC3 lipidation vesicles from the ER-Golgi intermediate compartment
Liang Ge, Min Zhang, Randy Schekman
eLife (2014) Vol. 3
Open Access | Times Cited: 200
Organellophagy: Eliminating cellular building blocks via selective autophagy
Koji Okamoto
The Journal of Cell Biology (2014) Vol. 205, Iss. 4, pp. 435-445
Open Access | Times Cited: 199
The ER-Localized Transmembrane Protein EPG-3/VMP1 Regulates SERCA Activity to Control ER-Isolation Membrane Contacts for Autophagosome Formation
Yan Zhao, Yong Chen, Guangyan Miao, et al.
Molecular Cell (2017) Vol. 67, Iss. 6, pp. 974-989.e6
Open Access | Times Cited: 198
Insights into autophagosome biogenesis from structural and biochemical analyses of the ATG2A-WIPI4 complex
Saikat Chowdhury, Chinatsu Otomo, Alexander Leitner, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 42
Open Access | Times Cited: 192
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: 189
Autophagosome formation is initiated at phosphatidylinositol synthase‐enriched ER subdomains
Taki Nishimura, Norito Tamura, Nozomu Kono, et al.
The EMBO Journal (2017) Vol. 36, Iss. 12, pp. 1719-1735
Open Access | Times Cited: 181
ER –plasma membrane contact sites contribute to autophagosome biogenesis by regulation of local PI 3P synthesis
Anna Chiara Nascimbeni, Francesca Giordano, Nicolas Dupont, et al.
The EMBO Journal (2017) Vol. 36, Iss. 14, pp. 2018-2033
Open Access | Times Cited: 175
Lipid droplet–mediated ER homeostasis regulates autophagy and cell survival during starvation
Ariadna P. Velázquez, Takashi Tatsuta, Ruben Ghillebert, et al.
The Journal of Cell Biology (2016) Vol. 212, Iss. 6, pp. 621-631
Open Access | Times Cited: 174
The Noncanonical Role of ULK/ATG1 in ER-to-Golgi Trafficking Is Essential for Cellular Homeostasis
Joung Hyuck Joo, Bo Wang, Elisa B. Frankel, et al.
Molecular Cell (2016) Vol. 62, Iss. 4, pp. 491-506
Open Access | Times Cited: 171
In situ structural analysis reveals membrane shape transitions during autophagosome formation
Anna Bieber, Cristina Capitanio, Philipp S. Erdmann, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 39
Open Access | Times Cited: 72
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: 25
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: 24
Atomistic Autophagy: The Structures of Cellular Self-Digestion
James H. Hurley, Brenda A. Schulman
Cell (2014) Vol. 157, Iss. 2, pp. 300-311
Open Access | Times Cited: 185
Getting ready for building: signaling and autophagosome biogenesis
Adi Abada, Zvulun Elazar
EMBO Reports (2014) Vol. 15, Iss. 8, pp. 839-852
Open Access | Times Cited: 171
TBC1D14 regulates autophagy via the TRAPP complex and ATG9 traffic
Christopher A. Lamb, Stefanie Nühlen, Delphine Judith, et al.
The EMBO Journal (2015) Vol. 35, Iss. 3, pp. 281-301
Open Access | Times Cited: 168
AMPK and vacuole-associated Atg14p orchestrate μ-lipophagy for energy production and long-term survival under glucose starvation
Arnold Y. Seo, Pick‐Wei Lau, Daniel Feliciano, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 168
The ER Contact Proteins VAPA/B Interact with Multiple Autophagy Proteins to Modulate Autophagosome Biogenesis
Yan Zhao, Nan Liu, Guangyan Miao, et al.
Current Biology (2018) Vol. 28, Iss. 8, pp. 1234-1245.e4
Open Access | Times Cited: 159
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: 158
The EM structure of the TRAPPIII complex leads to the identification of a requirement for COPII vesicles on the macroautophagy pathway
Dongyan Tan, Yiying Cai, Juan Wang, et al.
Proceedings of the National Academy of Sciences (2013) Vol. 110, Iss. 48, pp. 19432-19437
Open Access | Times Cited: 157

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