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:

Spatiotemporal Control of ULK1 Activation by NDP52 and TBK1 during Selective Autophagy
Jose Norberto S. Vargas, Chunxin Wang, Eric Bunker, et al.
Molecular Cell (2019) Vol. 74, Iss. 2, pp. 347-362.e6
Open Access | Times Cited: 385

Showing 1-25 of 385 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: 1976

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

Cellular quality control by the ubiquitin-proteasome system and autophagy
Christian Pohl, Ivan Đikić
Science (2019) Vol. 366, Iss. 6467, pp. 818-822
Closed Access | Times Cited: 888

Mechanisms governing autophagosome biogenesis
Hitoshi Nakatogawa
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 8, pp. 439-458
Closed Access | Times Cited: 669

Lysosome biology in autophagy
Willa Wen‐You Yim, Noboru Mizushima
Cell Discovery (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 615

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: 579

Autophagy in inflammation, infection, and immunometabolism
Vojo Deretić
Immunity (2021) Vol. 54, Iss. 3, pp. 437-453
Open Access | Times Cited: 565

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: 558

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: 457

The ATG conjugation systems in autophagy
Noboru Mizushima
Current Opinion in Cell Biology (2019) Vol. 63, pp. 1-10
Open Access | Times Cited: 386

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

PINK1/PARKIN signalling in neurodegeneration and neuroinflammation
Peter M. J. Quinn, Paula I. Moreira, António Francisco Ambrósio, et al.
Acta Neuropathologica Communications (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 322

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: 318

ALS Genetics: Gains, Losses, and Implications for Future Therapies
Garam Kım, Olivia Gautier, Eduardo Tassoni-Tsuchida, et al.
Neuron (2020) Vol. 108, Iss. 5, pp. 822-842
Open Access | Times Cited: 292

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

Mitophagy: An Emerging Role in Aging and Age-Associated Diseases
Guo Chen, Guido Kroemer, Oliver Kepp
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 289

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

Ubiquitin signalling in neurodegeneration: mechanisms and therapeutic opportunities
Marlene F. Schmidt, Zhong Yan Gan, David Komander, et al.
Cell Death and Differentiation (2021) Vol. 28, Iss. 2, pp. 570-590
Open Access | Times Cited: 280

Cellular mitophagy: Mechanism, roles in diseases and small molecule pharmacological regulation
Yingying Lü, Zhijia Li, Shuangqian Zhang, et al.
Theranostics (2023) Vol. 13, Iss. 2, pp. 736-766
Open Access | Times Cited: 272

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: 267

AMPK: restoring metabolic homeostasis over space and time
Elijah Trefts, Reuben J. Shaw
Molecular Cell (2021) Vol. 81, Iss. 18, pp. 3677-3690
Open Access | Times Cited: 263

Ubiquitin-mediated regulation of autophagy
Ruey‐Hwa Chen, Yu-Hsuan Chen, Tzu-Yu Huang
Journal of Biomedical Science (2019) Vol. 26, Iss. 1
Open Access | Times Cited: 254

ER-Phagy: Quality Control and Turnover of Endoplasmic Reticulum
Haruka Chino, Noboru Mizushima
Trends in Cell Biology (2020) Vol. 30, Iss. 5, pp. 384-398
Open Access | Times Cited: 224

Reconstitution of autophagosome nucleation defines Atg9 vesicles as seeds for membrane formation
Justyna Sawa‐Makarska, Verena Baumann, Nicolas Coudevylle, et al.
Science (2020) Vol. 369, Iss. 6508
Open Access | Times Cited: 220

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: 197

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