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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:

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: 553

Showing 1-25 of 553 citing articles:

Autophagy in healthy aging and disease
Yahyah Aman, Tomas Schmauck‐Medina, Malene Hansen, et al.
Nature Aging (2021) Vol. 1, Iss. 8, pp. 634-650
Open Access | Times Cited: 805
Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 640
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: 559
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: 477
The ATG conjugation systems in autophagy
Noboru Mizushima
Current Opinion in Cell Biology (2019) Vol. 63, pp. 1-10
Open Access | Times Cited: 366
Mechanisms of mitochondrial dysfunction and their impact on age-related macular degeneration
Kai Kaarniranta, Hannu Uusitalo, Janusz Błasiak, et al.
Progress in Retinal and Eye Research (2020) Vol. 79, pp. 100858-100858
Open Access | Times Cited: 338
Quality control of the mitochondrion
Matthew Yoke Wui Ng, Timothy Wai, Anne Simonsen
Developmental Cell (2021) Vol. 56, Iss. 7, pp. 881-905
Open Access | Times Cited: 268
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: 258
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: 254
Wetting regulates autophagy of phase-separated compartments and the cytosol
Jaime Agudo‐Canalejo, Sebastian W. Schultz, Haruka Chino, et al.
Nature (2021) Vol. 591, Iss. 7848, pp. 142-146
Closed Access | Times Cited: 198
Mitochondria as a Cellular Hub in Infection and Inflammation
Pauline Andrieux, Christophe Chevillard, Edécio Cunha‐Neto, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11338-11338
Open Access | Times Cited: 196
Role and Mechanisms of Mitophagy in Liver Diseases
Xiaowen Ma, Tara McKeen, Jianhua Zhang, et al.
Cells (2020) Vol. 9, Iss. 4, pp. 837-837
Open Access | Times Cited: 191
p62/SQSTM1-droplet serves as a platform for autophagosome formation and anti-oxidative stress response
Shun Kageyama, Sigurður Guðmundsson, Yu‐shin Sou, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 189
A cross-kingdom conserved ER-phagy receptor maintains endoplasmic reticulum homeostasis during stress
Madlen Stephani, Lorenzo Picchianti, Alexander Gajic, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 188
The mitophagy pathway and its implications in human diseases
Shouliang Wang, Haijiao Long, Lianjie Hou, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 167
Mitophagy in Human Diseases
Laura Doblado, Claudia Lueck, Claudia Rey, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 3903-3903
Open Access | Times Cited: 156
Dimerization of mitophagy receptor BNIP3L/NIX is essential for recruitment of autophagic machinery
Mija Marinković, Matilda Šprung, Ivana Novak
Autophagy (2020) Vol. 17, Iss. 5, pp. 1232-1243
Open Access | Times Cited: 155
Activation and targeting of ATG8 protein lipidation
Sascha Martens, Dorotea Fracchiolla
Cell Discovery (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 151
A guide to the regulation of selective autophagy receptors
Andrea Gubaš, Ivan Đikić
FEBS Journal (2021) Vol. 289, Iss. 1, pp. 75-89
Open Access | Times Cited: 148
Amyloid-type Protein Aggregation and Prion-like Properties of Amyloids
Dieter Willbold, Birgit Strodel, Gunnar F. Schröder, et al.
Chemical Reviews (2021) Vol. 121, Iss. 13, pp. 8285-8307
Open Access | Times Cited: 147
Critical role of mitochondrial ubiquitination and the OPTN–ATG9A axis in mitophagy
Koji Yamano, Reika Kikuchi, Waka Kojima, et al.
The Journal of Cell Biology (2020) Vol. 219, Iss. 9
Open Access | Times Cited: 145
Reconstitution defines the roles of p62, NBR1 and TAX1BP1 in ubiquitin condensate formation and autophagy initiation
Eleonora Turco, Adriana Savova, Flora Gere, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 143
Non-canonical autophagy drives alternative ATG8 conjugation to phosphatidylserine
Joanne Durgan, Alf Håkon Lystad, Katherine E. Sloan, et al.
Molecular Cell (2021) Vol. 81, Iss. 9, pp. 2031-2040.e8
Open Access | Times Cited: 141
Emerging roles of ATG7 in human health and disease
Jack J. Collier, Fumi Suomi, Monika Oláhová, et al.
EMBO Molecular Medicine (2021) Vol. 13, Iss. 12
Open Access | Times Cited: 119
The multifaceted role of autophagy in cancer
Ryan C. Russell, Kun‐Liang Guan
The EMBO Journal (2022) Vol. 41, Iss. 13
Open Access | Times Cited: 119
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