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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:

Full length RTN3 regulates turnover of tubular endoplasmic reticulum via selective autophagy
Paolo Grumati, Giulio Morozzi, Soraya Hölper, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 373

Showing 1-25 of 373 citing articles:

Biological Functions of Autophagy Genes: A Disease Perspective
Beth Levine, Guido Kroemer
Cell (2019) Vol. 176, Iss. 1-2, pp. 11-42
Open Access | Times Cited: 2281
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
Emerging functions of the EGFR in cancer
Sara Sigismund, Daniele Avanzato, Letizia Lanzetti
Molecular Oncology (2017) Vol. 12, Iss. 1, pp. 3-20
Open Access | Times Cited: 1191
Unsolved mysteries: How does lipid peroxidation cause ferroptosis?
Huizhong Feng, Brent R. Stockwell
PLoS Biology (2018) Vol. 16, Iss. 5, pp. e2006203-e2006203
Open Access | Times Cited: 636
Regulation of selective autophagy: the p62/SQSTM1 paradigm
Trond Lamark, Steingrim Svenning, Terje Johansen
Essays in Biochemistry (2017) Vol. 61, Iss. 6, pp. 609-624
Closed Access | Times Cited: 621
Autophagy-Dependent Ferroptosis: Machinery and Regulation
Jiao Liu, Feimei Kuang, Guido Kroemer, et al.
Cell chemical biology (2020) Vol. 27, Iss. 4, pp. 420-435
Open Access | Times Cited: 597
Selective Autophagy: ATG8 Family Proteins, LIR Motifs and Cargo Receptors
Terje Johansen, Trond Lamark
Journal of Molecular Biology (2019) Vol. 432, Iss. 1, pp. 80-103
Open Access | Times Cited: 580
The mechanisms and roles of selective autophagy in mammals
Jose Norberto S. Vargas, Maho Hamasaki, Tsuyoshi Kawabata, et al.
Nature Reviews Molecular Cell Biology (2022) Vol. 24, Iss. 3, pp. 167-185
Closed Access | Times Cited: 569
Autophagy: The Master of Bulk and Selective Recycling
Richard S. Marshall, Richard D. Vierstra
Annual Review of Plant Biology (2018) Vol. 69, Iss. 1, pp. 173-208
Open Access | Times Cited: 491
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: 460
CCPG1 Is a Non-canonical Autophagy Cargo Receptor Essential for ER-Phagy and Pancreatic ER Proteostasis
Matthew D. Smith, Margaret E Harley, Alain J. Kemp, et al.
Developmental Cell (2017) Vol. 44, Iss. 2, pp. 217-232.e11
Open Access | Times Cited: 385
Crosstalk Between Mammalian Autophagy and the Ubiquitin-Proteasome System
Nur Mehpare Kocatürk, Devrim Gözüaçık
Frontiers in Cell and Developmental Biology (2018) Vol. 6
Open Access | Times Cited: 356
Selective autophagy of intracellular organelles: Recent research advances
Wen Li, Pengcheng He, Yuge Huang, et al.
Theranostics (2020) Vol. 11, Iss. 1, pp. 222-256
Open Access | Times Cited: 343
Protein quality control in the secretory pathway
Zhihao Sun, Jeffrey L. Brodsky
The Journal of Cell Biology (2019) Vol. 218, Iss. 10, pp. 3171-3187
Open Access | Times Cited: 330
Diverse Cellular Roles of Autophagy
Hideaki Morishita, Noboru Mizushima
Annual Review of Cell and Developmental Biology (2019) Vol. 35, Iss. 1, pp. 453-475
Open Access | Times Cited: 325
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles
Ren-qi Yao, Chao Ren, Zhaofan Xia, et al.
Autophagy (2020) Vol. 17, Iss. 2, pp. 385-401
Open Access | Times Cited: 313
The different autophagy degradation pathways and neurodegeneration
Angeleen Fleming, Mathieu Bourdenx, Motoki Fujimaki, et al.
Neuron (2022) Vol. 110, Iss. 6, pp. 935-966
Open Access | Times Cited: 302
Intrinsically Disordered Protein TEX264 Mediates ER-phagy
Haruka Chino, Tomohisa Hatta, Tohru Natsume, et al.
Molecular Cell (2019) Vol. 74, Iss. 5, pp. 909-921.e6
Open Access | Times Cited: 297
Autophagy in tumour immunity and therapy
Houjun Xia, Douglas R. Green, Weiping Zou
Nature reviews. Cancer (2021) Vol. 21, Iss. 5, pp. 281-297
Open Access | Times Cited: 293
Ubiquitin signaling and autophagy
Paolo Grumati, Ivan Đikić
Journal of Biological Chemistry (2017) Vol. 293, Iss. 15, pp. 5404-5413
Open Access | Times Cited: 287
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
The Unfolded Protein Response: Detecting and Responding to Fluctuations in the Protein-Folding Capacity of the Endoplasmic Reticulum
G Elif Karagöz, Diego Acosta‐Alvear, Peter Walter
Cold Spring Harbor Perspectives in Biology (2019) Vol. 11, Iss. 9, pp. a033886-a033886
Open Access | Times Cited: 266
ATL3 Is a Tubular ER-Phagy Receptor for GABARAP-Mediated Selective Autophagy
Qingzhou Chen, Ya Ting Xiao, Peiyuan Chai, et al.
Current Biology (2019) Vol. 29, Iss. 5, pp. 846-855.e6
Closed Access | Times Cited: 252
TEX264 Is an Endoplasmic Reticulum-Resident ATG8-Interacting Protein Critical for ER Remodeling during Nutrient Stress
Heeseon An, Alban Ordureau, João A. Paulo, et al.
Molecular Cell (2019) Vol. 74, Iss. 5, pp. 891-908.e10
Open Access | Times Cited: 250
Autophagy in liver diseases: A review
Hui Qian, Xiaojuan Chao, Jessica A. Williams, et al.
Molecular Aspects of Medicine (2021) Vol. 82, pp. 100973-100973
Open Access | Times Cited: 250
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