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:

Rab5-dependent autophagosome closure by ESCRT
Fan Zhou, Zulin Wu, Mengzhu Zhao, et al.
The Journal of Cell Biology (2019) Vol. 218, Iss. 6, pp. 1908-1927
Open Access | Times Cited: 156

Showing 1-25 of 156 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: 1984

The many functions of ESCRTs
Marina Vietri, Maja Radulovic, Harald Stenmark
Nature Reviews Molecular Cell Biology (2019) Vol. 21, Iss. 1, pp. 25-42
Closed Access | Times Cited: 767

Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 669

A Diversity of Selective Autophagy Receptors Determines the Specificity of the Autophagy Pathway
Vladimir Kirkin, Vladimir V. Rogov
Molecular Cell (2019) Vol. 76, Iss. 2, pp. 268-285
Open Access | Times Cited: 459

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: 359

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

Autophagosome-Lysosome Fusion
Péter Lőrincz, Gábor Juhász
Journal of Molecular Biology (2019) Vol. 432, Iss. 8, pp. 2462-2482
Open Access | Times Cited: 248

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: 220

Autophagy and Macrophage Functions: Inflammatory Response and Phagocytosis
Ming-Yue Wu, Jiahong Lu
Cells (2019) Vol. 9, Iss. 1, pp. 70-70
Open Access | Times Cited: 199

ESCRT-mediated phagophore sealing during mitophagy
Zhen Yan, Hélène Spangenberg, Michael J. Munson, et al.
Autophagy (2019) Vol. 16, Iss. 5, pp. 826-841
Open Access | Times Cited: 165

Acetylated tau inhibits chaperone-mediated autophagy and promotes tau pathology propagation in mice
Benjamı́n Caballero, Mathieu Bourdenx, Enrique Luengo, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 146

Autophagosome biogenesis comes out of the black box
Chunmei Chang, Liv Jensen, James H. Hurley
Nature Cell Biology (2021) Vol. 23, Iss. 5, pp. 450-456
Open Access | Times Cited: 135

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: 129

ER-phagy: mechanisms, regulation, and diseases connected to the lysosomal clearance of the endoplasmic reticulum
Fulvio Reggiori, Maurizio Molinari
Physiological Reviews (2022) Vol. 102, Iss. 3, pp. 1393-1448
Open Access | Times Cited: 109

An ESCRT-dependent step in fatty acid transfer from lipid droplets to mitochondria through VPS13D−TSG101 interactions
Jingru Wang, Na Fang, Juan Xiong, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 104

Orchestration of selective autophagy by cargo receptors
Elias Adriaenssens, Luca Ferrari, Sascha Martens
Current Biology (2022) Vol. 32, Iss. 24, pp. R1357-R1371
Open Access | Times Cited: 77

Asgard archaea shed light on the evolutionary origins of the eukaryotic ubiquitin-ESCRT machinery
Tomoyuki Hatano, Saravanan Palani, Dimitra Papatziamou, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 76

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: 70

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

Lysosomal quality control: molecular mechanisms and therapeutic implications
Haoxiang Yang, Xiaojun Tan
Trends in Cell Biology (2023) Vol. 33, Iss. 9, pp. 749-764
Open Access | Times Cited: 45

Neuronal Autophagy: Regulations and Implications in Health and Disease
Caroline Liénard, Alexandre Pintart, Pascale Bomont
Cells (2024) Vol. 13, Iss. 1, pp. 103-103
Open Access | Times Cited: 19

ESCRT machinery mediates selective microautophagy of endoplasmic reticulum in yeast
Jasmin Schäfer, Julia P. Schessner, Peter W. Bircham, et al.
The EMBO Journal (2019) Vol. 39, Iss. 2
Open Access | Times Cited: 110

VPS37A directs ESCRT recruitment for phagophore closure
Yoshinori Takahashi, Xinwen Liang, Tatsuya Hattori, et al.
The Journal of Cell Biology (2019) Vol. 218, Iss. 10, pp. 3336-3354
Open Access | Times Cited: 108

Pexophagy: A Model for Selective Autophagy
Kyla Germain, Peter K. Kim
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 2, pp. 578-578
Open Access | Times Cited: 98

Sealing holes in cellular membranes
Yan Zhen, Maja Radulovic, Marina Vietri, et al.
The EMBO Journal (2021) Vol. 40, Iss. 7
Open Access | Times Cited: 97

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