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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:

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: 156

Showing 1-25 of 156 citing articles:

Molecular mechanisms and physiological functions of mitophagy
Mashun Onishi, Koji Yamano, Miyuki Sato, et al.
The EMBO Journal (2021) Vol. 40, Iss. 3
Open Access | Times Cited: 944
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 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
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: 291
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
Mitochondria in health, disease, and aging
John S. Harrington, Stefan W. Ryter, Maria Plataki, et al.
Physiological Reviews (2023) Vol. 103, Iss. 4, pp. 2349-2422
Open Access | Times Cited: 281
Mitochondrial autophagy: molecular mechanisms and implications for cardiovascular disease
Anqi Li, Meng Gao, Bilin Liu, et al.
Cell Death and Disease (2022) Vol. 13, Iss. 5
Open Access | Times Cited: 224
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: 220
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: 158
PINK1/Parkin-mediated mitophagy in neurodegenerative diseases
Jie Li, Dongming Yang, Zhiping Li, et al.
Ageing Research Reviews (2022) Vol. 84, pp. 101817-101817
Closed Access | Times Cited: 145
Regulation of PRKN-independent mitophagy
Petra Terešak, Ana Lapao, Nemanja Subic, et al.
Autophagy (2021) Vol. 18, Iss. 1, pp. 24-39
Open Access | Times Cited: 142
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
Mitophagy in cardiovascular diseases: molecular mechanisms, pathogenesis, and treatment
Amir Ajoolabady, Mario Chiong, Sergio Lavandero, et al.
Trends in Molecular Medicine (2022) Vol. 28, Iss. 10, pp. 836-849
Open Access | Times Cited: 125
Mitophagy: Molecular Mechanisms, New Concepts on Parkin Activation and the Emerging Role of AMPK/ULK1 Axis
Roberto Iorio, Giuseppe Celenza, Sabrina Petricca
Cells (2021) Vol. 11, Iss. 1, pp. 30-30
Open Access | Times Cited: 122
Mitochondrial degradation: Mitophagy and beyond
Louise Uoselis, Thanh Ngoc Nguyen, Michael Lazarou
Molecular Cell (2023) Vol. 83, Iss. 19, pp. 3404-3420
Open Access | Times Cited: 113
Crosstalk between mitochondrial biogenesis and mitophagy to maintain mitochondrial homeostasis
Lei Liu, Yanjun Li, Guo Chen, et al.
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 80
A degradative to secretory autophagy switch mediates mitochondria clearance in the absence of the mATG8-conjugation machinery
Hayden Weng Siong Tan, Guang Lu, Han Dong, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 78
Mechanisms underlying ubiquitin-driven selective mitochondrial and bacterial autophagy
Ellen A. Goodall, Felix Kraus, J. Wade Harper
Molecular Cell (2022) Vol. 82, Iss. 8, pp. 1501-1513
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
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
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
Structural basis for ATG9A recruitment to the ULK1 complex in mitophagy initiation
Xuefeng Ren, Thanh Ngoc Nguyen, Wai Kit Lam, et al.
Science Advances (2023) Vol. 9, Iss. 7
Open Access | Times Cited: 44
The role of PINK1–Parkin in mitochondrial quality control
Derek P. Narendra, Richard J. Youle
Nature Cell Biology (2024) Vol. 26, Iss. 10, pp. 1639-1651
Closed Access | Times Cited: 42
Optineurin provides a mitophagy contact site for TBK1 activation
Koji Yamano, Momoha Sawada, Reika Kikuchi, et al.
The EMBO Journal (2024) Vol. 43, Iss. 5, pp. 754-779
Open Access | Times Cited: 26
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
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