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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:

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: 268

Showing 1-25 of 268 citing articles:

Autophagy in inflammation, infection, and immunometabolism
Vojo Deretić
Immunity (2021) Vol. 54, Iss. 3, pp. 437-453
Open Access | Times Cited: 576
The autophagic membrane tether ATG2A transfers lipids between membranes
Shintaro Maeda, Chinatsu Otomo, Takanori Otomo
eLife (2019) Vol. 8
Open Access | Times Cited: 286
Autophagy in metabolic disease and ageing
Munehiro Kitada, Daisuke Koya
Nature Reviews Endocrinology (2021) Vol. 17, Iss. 11, pp. 647-661
Closed Access | Times Cited: 286
Mechanisms of Selective Autophagy
Trond Lamark, Terje Johansen
Annual Review of Cell and Developmental Biology (2021) Vol. 37, Iss. 1, pp. 143-169
Open Access | Times Cited: 281
The Cargo Receptor NDP52 Initiates Selective Autophagy by Recruiting the ULK Complex to Cytosol-Invading Bacteria
Benjamin J. Ravenhill, Keith B. Boyle, Natalia von Muhlinen, et al.
Molecular Cell (2019) Vol. 74, Iss. 2, pp. 320-329.e6
Open Access | Times Cited: 268
STING induces LC3B lipidation onto single-membrane vesicles via the V-ATPase and ATG16L1-WD40 domain
Tara D. Fischer, Chunxin Wang, Benjamin Scott Padman, et al.
The Journal of Cell Biology (2020) Vol. 219, Iss. 12
Open Access | Times Cited: 149
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
Mechanisms of nonvesicular lipid transport
Karin M. Reinisch, William A. Prinz
The Journal of Cell Biology (2021) Vol. 220, Iss. 3
Open Access | Times Cited: 128
Beyond autophagy: LC3-associated phagocytosis and endocytosis
Carolina Peña-Martinez, Alexis Rickman, Bradlee L. Heckmann
Science Advances (2022) Vol. 8, Iss. 43
Open Access | Times Cited: 114
ATG9A and ATG2A form a heteromeric complex essential for autophagosome formation
Alexander R. van Vliet, George N. Chiduza, Sarah Maslen, et al.
Molecular Cell (2022) Vol. 82, Iss. 22, pp. 4324-4339.e8
Open Access | Times Cited: 91
Emerging degrader technologies engaging lysosomal pathways
Yu Ding, Dong Xing, Yiyan Fei, et al.
Chemical Society Reviews (2022) Vol. 51, Iss. 21, pp. 8832-8876
Open Access | Times Cited: 77
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
ER as master regulator of membrane trafficking and organelle function
Eva M. Wenzel, Liv Anker Elfmark, Harald Stenmark, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 10
Open Access | Times Cited: 70
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
Recent advances in targeting autophagy in cancer
Vaibhav Jain, Mahendra Pal Singh, Ravi K. Amaravadi
Trends in Pharmacological Sciences (2023) Vol. 44, Iss. 5, pp. 290-302
Closed Access | Times Cited: 57
Unconventional initiation of PINK1/Parkin mitophagy by Optineurin
Thanh Ngoc Nguyen, Justyna Sawa‐Makarska, Grace Khuu, et al.
Molecular Cell (2023) Vol. 83, Iss. 10, pp. 1693-1709.e9
Open Access | Times Cited: 54
RBG Motif Bridge-Like Lipid Transport Proteins: Structure, Functions, and Open Questions
Michael G. Hanna, Andrés Guillén-Samander, Pietro De Camilli
Annual Review of Cell and Developmental Biology (2023) Vol. 39, Iss. 1, pp. 409-434
Open Access | Times Cited: 53
Liquid–liquid phase separation in autophagy
Nobuo N. Noda, Zheng Wang, Hong Zhang
The Journal of Cell Biology (2020) Vol. 219, Iss. 8
Open Access | Times Cited: 135
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
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
Mammalian hybrid pre-autophagosomal structure HyPAS generates autophagosomes
Suresh Kumar, Ruheena Javed, Michal Mudd, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5950-5969.e22
Open Access | Times Cited: 83
The autophagy protein ATG9A enables lipid mobilization from lipid droplets
Élodie Mailler, Carlos M. Guardia, Xiaofei Bai, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 81
The role of autophagy in death of cardiomyocytes
Shohei Ikeda, Daniela Zablocki, Junichi Sadoshima
Journal of Molecular and Cellular Cardiology (2021) Vol. 165, pp. 1-8
Open Access | Times Cited: 78
AMPK: a key regulator of energy stress and calcium-induced autophagy
Rimpi Saikia, Jomon Joseph
Journal of Molecular Medicine (2021) Vol. 99, Iss. 11, pp. 1539-1551
Closed Access | Times Cited: 77
A Sonication‐Activated Valence‐Variable Sono‐Sensitizer/Catalyst for Autography Inhibition/Ferroptosis‐Induced Tumor Nanotherapy
Wei Feng, Zhonglong Liu, Lili Xia, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 48
Closed Access | Times Cited: 61
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