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:

p62-mediated phase separation at the intersection of the ubiquitin-proteasome system and autophagy
Alberto Danieli, Sascha Martens
Journal of Cell Science (2018) Vol. 131, Iss. 19
Open Access | Times Cited: 129

Showing 1-25 of 129 citing articles:

Autophagy in Neurons
Andrea KH Stavoe, Erika L.F. Holzbaur
Annual Review of Cell and Developmental Biology (2019) Vol. 35, Iss. 1, pp. 477-500
Open Access | Times Cited: 264

Liquid-liquid phase separation in biology: mechanisms, physiological functions and human diseases
Hong Zhang, Ji Xiong, Pilong Li, et al.
Science China Life Sciences (2020) Vol. 63, Iss. 7, pp. 953-985
Closed Access | Times Cited: 254

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

Autophagy in aging and longevity
Shi Quan Wong, Anita Kumar, Joslyn Mills, et al.
Human Genetics (2019) Vol. 139, Iss. 3, pp. 277-290
Open Access | Times Cited: 185

Mechanisms for Active Regulation of Biomolecular Condensates
Johannes Söding, David Zwicker, Salma Sohrabi-Jahromi, et al.
Trends in Cell Biology (2019) Vol. 30, Iss. 1, pp. 4-14
Open Access | Times Cited: 167

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

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: 155

Liquid Biomolecular Condensates and Viral Lifecycles: Review and Perspectives
Temitope Akhigbe Etibor, Yohei Yamauchi, Maria João Amorim
Viruses (2021) Vol. 13, Iss. 3, pp. 366-366
Open Access | Times Cited: 110

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

Liquid–liquid phase separation in autophagy
Nobuo N. Noda, Zheng Wang, Hong Zhang
The Journal of Cell Biology (2020) Vol. 219, Iss. 8
Open Access | Times Cited: 136

Lysosomal Dysfunction at the Centre of Parkinson’s Disease and Frontotemporal Dementia/Amyotrophic Lateral Sclerosis
Rebecca L. Wallings, Stewart W. Humble, Michael E. Ward, et al.
Trends in Neurosciences (2019) Vol. 42, Iss. 12, pp. 899-912
Open Access | Times Cited: 117

Phase Separation, Transition, and Autophagic Degradation of Proteins in Development and Pathogenesis
Zheng Wang, Hong Zhang
Trends in Cell Biology (2019) Vol. 29, Iss. 5, pp. 417-427
Closed Access | Times Cited: 97

Recruitment and Activation of the ULK1/Atg1 Kinase Complex in Selective Autophagy
Eleonora Turco, Dorotea Fracchiolla, Sascha Martens
Journal of Molecular Biology (2019) Vol. 432, Iss. 1, pp. 123-134
Open Access | Times Cited: 96

C9orf72 ALS-FTD: recent evidence for dysregulation of the autophagy-lysosome pathway at multiple levels
Jimmy Beckers, Arun Kumar Tharkeshwar, Philip Van Damme
Autophagy (2021) Vol. 17, Iss. 11, pp. 3306-3322
Open Access | Times Cited: 85

Plant Selective Autophagy—Still an Uncharted Territory With a Lot of Hidden Gems
Madlen Stephani, Yasin Dagdas
Journal of Molecular Biology (2019) Vol. 432, Iss. 1, pp. 63-79
Open Access | Times Cited: 78

Alternative systems for misfolded protein clearance: life beyond the proteasome
Harvey E. Johnston, Rahul S. Samant
FEBS Journal (2020) Vol. 288, Iss. 15, pp. 4464-4487
Open Access | Times Cited: 73

TXNIP positively regulates the autophagy and apoptosis in the rat müller cell of diabetic retinopathy
Haocheng Ao, Haichun Li, Xiujuan Zhao, et al.
Life Sciences (2021) Vol. 267, pp. 118988-118988
Open Access | Times Cited: 60

Phase separation of Nur77 mediates celastrol-induced mitophagy by promoting the liquidity of p62/SQSTM1 condensates
Shuangzhou Peng, Xiaohong Chen, Sijie Chen, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 58

De novo lipogenesis fuels adipocyte autophagosome and lysosome membrane dynamics
Leslie A. Rowland, Adı́lson Guilherme, Felipe Henriques, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 32

S-acylation of p62 promotes p62 droplet recruitment into autophagosomes in mammalian autophagy
Xue Huang, Jia Yao, Lu Liu, et al.
Molecular Cell (2023) Vol. 83, Iss. 19, pp. 3485-3501.e11
Open Access | Times Cited: 29

MCC950 reduces autophagy and improves cognitive function by inhibiting NLRP3-dependent neuroinflammation in a rat model of Alzheimer's disease
Abdul Naeem, Ravi Prakash, Neha Kumari, et al.
Brain Behavior and Immunity (2023) Vol. 116, pp. 70-84
Closed Access | Times Cited: 28

Linear ubiquitination induces NEMO phase separation to activate NF-κB signaling
Simran Goel, Rosario Oliva, Sadasivam Jeganathan�, et al.
Life Science Alliance (2023) Vol. 6, Iss. 4, pp. e202201607-e202201607
Open Access | Times Cited: 26

Tianxiangdan suppresses foam cell formation by enhancing lipophagy and reduces the progression of atherosclerosis
Yajie Zhang, Huan He, Guligena Sawuer, et al.
In Vitro Cellular & Developmental Biology - Animal (2025)
Closed Access | Times Cited: 1

Phase separation of p62: roles and regulations in autophagy
Xue Huang, Jinpei Zhang, Jia Yao, et al.
Trends in Cell Biology (2025)
Closed Access | Times Cited: 1

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