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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:

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: 158

Showing 1-25 of 158 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: 1988
Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 669
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: 554
ATG2 transports lipids to promote autophagosome biogenesis
Diana P. Valverde, Shenliang Yu, Rajendra Boggavarapu, et al.
The Journal of Cell Biology (2019) Vol. 218, Iss. 6, pp. 1787-1798
Open Access | Times Cited: 457
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: 312
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: 285
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
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: 218
Calcium transients on the ER surface trigger liquid-liquid phase separation of FIP200 to specify autophagosome initiation sites
Qiaoxia Zheng, Yong Chen, Di Chen, et al.
Cell (2022) Vol. 185, Iss. 22, pp. 4082-4098.e22
Open Access | Times Cited: 108
ER ‐phagy: selective autophagy of the endoplasmic reticulum
Keisuke Mochida, Hitoshi Nakatogawa
EMBO Reports (2022) Vol. 23, Iss. 8
Open Access | Times Cited: 83
Molecular regulation of autophagosome formation
Yan Hu, Fulvio Reggiori
Biochemical Society Transactions (2022) Vol. 50, Iss. 1, pp. 55-69
Open Access | Times Cited: 70
Autophagy in health and disease: From molecular mechanisms to therapeutic target
Guang Lu, Yu Wang, Yin Shi, et al.
MedComm (2022) Vol. 3, Iss. 3
Open Access | Times Cited: 70
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
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: 22
CALCOCO 1 acts with VAMP ‐associated proteins to mediate ER ‐phagy
Thaddaeus Mutugi Nthiga, Birendra Kumar Shrestha, Eva Sjøttem, et al.
The EMBO Journal (2020) Vol. 39, Iss. 15
Open Access | Times Cited: 121
Upregulation of Rubicon promotes autosis during myocardial ischemia/reperfusion injury
Jihoon Nah, Peiyong Zhai, Chun-Yang Huang, et al.
Journal of Clinical Investigation (2020) Vol. 130, Iss. 6, pp. 2978-2991
Open Access | Times Cited: 113
FFAT motif phosphorylation controls formation and lipid transfer function of inter‐organelle contacts
Thomas Di Mattia, Arthur Martinet, Souade Ikhlef, et al.
The EMBO Journal (2020) Vol. 39, Iss. 23
Open Access | Times Cited: 107
The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
Meng Lü, Francesca W. van Tartwijk, Julie Qiaojin Lin, et al.
Science Advances (2020) Vol. 6, Iss. 51
Open Access | Times Cited: 81
A UPR-Induced Soluble ER-Phagy Receptor Acts with VAPs to Confer ER Stress Resistance
Dan Zhao, Chenxi Zou, Xiao‐Man Liu, et al.
Molecular Cell (2020) Vol. 79, Iss. 6, pp. 963-977.e3
Open Access | Times Cited: 72
Membrane supply and remodeling during autophagosome biogenesis
Rubén Gómez‐Sánchez, Sharon A. Tooze, Fulvio Reggiori
Current Opinion in Cell Biology (2021) Vol. 71, pp. 112-119
Open Access | Times Cited: 72
A new type of ERGIC–ERES membrane contact mediated by TMED9 and SEC12 is required for autophagosome biogenesis
Shulin Li, Rui Yan, Jialu Xu, et al.
Cell Research (2021) Vol. 32, Iss. 2, pp. 119-138
Open Access | Times Cited: 57
TraB family proteins are components of ER-mitochondrial contact sites and regulate ER-mitochondrial interactions and mitophagy
Chengyang Li, Patrick Duckney, Tong Zhang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 43
Mitochondria associated ER membranes and cerebral ischemia: Molecular mechanisms and therapeutic strategies
Ruiqi Jiang, Qiqi Li, Rui Sheng
Pharmacological Research (2023) Vol. 191, pp. 106761-106761
Open Access | Times Cited: 24
Membrane remodeling and trafficking piloted by SARS-CoV-2
Maria Concetta Sergio, Simona Ricciardi, Andrea Maria Guarino, et al.
Trends in Cell Biology (2024) Vol. 34, Iss. 9, pp. 785-800
Open Access | Times Cited: 12
Rickettsia parkeri forms extensive, stable contacts with the rough endoplasmic reticulum
Yamilex Acevedo‐Sánchez, Patrick J. Woida, Caroline Anderson, et al.
The Journal of Cell Biology (2025) Vol. 224, Iss. 3
Closed Access | Times Cited: 1
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