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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:

On the relevance of precision autophagy flux controlin vivo– Points of departure for clinical translation
Ben Loos, Daniel J. Klionsky, André du Toit, et al.
Autophagy (2019) Vol. 16, Iss. 4, pp. 750-762
Open Access | Times Cited: 24

Showing 24 citing articles:

Measurement of autophagic flux in humans: an optimized method for blood samples
Julien Bensalem, Kathryn J. Hattersley, Leanne K. Hein, et al.
Autophagy (2020) Vol. 17, Iss. 10, pp. 3238-3255
Open Access | Times Cited: 40
Autophagie, cellules dendritiques, et maladie de Crohn
Leslie Andromaque, Stéphane Nancey, Mathias Faure, et al.
médecine/sciences (2025) Vol. 41, Iss. 3, pp. 216-219
Open Access
Renoprotective Effect of Isoorientin in Diabetic Nephropathy via Activating Autophagy and Inhibiting the PI3K-AKT-TSC2-mTOR Pathway
Zili Kong, Min Xiao, Bin Wang, et al.
The American Journal of Chinese Medicine (2023) Vol. 51, Iss. 05, pp. 1269-1291
Closed Access | Times Cited: 11
Impaired reprogramming of the autophagy flux in maturing dendritic cells from crohn disease patients with core autophagy gene-related polymorphisms
Gaëlle Quiniou, Leslie Andromaque, Rémi Duclaux‐Loras, et al.
Autophagy (2024) Vol. 20, Iss. 8, pp. 1837-1853
Closed Access | Times Cited: 4
miR-19 Promotes Cell Proliferation, Invasion, Migration, and EMT by Inhibiting SPRED2-mediated Autophagy in Osteosarcoma Cells
Chuhai Xie, Shengyao Liu, Boyi Wu, et al.
Cell Transplantation (2020) Vol. 29, pp. 096368972096246-096368972096246
Open Access | Times Cited: 29
No energy, no autophagy—Mechanisms and therapeutic implications of autophagic response energy requirements
Miloš Mandić, Verica Paunović, Ljubica Vučićević, et al.
Journal of Cellular Physiology (2024) Vol. 239, Iss. 11
Closed Access | Times Cited: 3
Investigating the Role of Spermidine in a Model System of Alzheimer’s Disease Using Correlative Microscopy and Super-resolution Techniques
Dumisile Lumkwana, Christopher J. Peddie, Jurgen Kriel, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 15
Autophagy and podocytopathy
Claudio Ponticelli, Gabriella Moroni, Francesco Reggiani
Nephrology Dialysis Transplantation (2023) Vol. 38, Iss. 9, pp. 1931-1939
Closed Access | Times Cited: 7
Let’s talk about flux: the rising potential of autophagy rate measurements in disease
Nitin Sai Beesabathuni, Matthew W. Kenaston, Ritika Gangaraju, et al.
Autophagy (2024) Vol. 20, Iss. 11, pp. 2574-2580
Closed Access | Times Cited: 2
Quantitative and temporal measurement of dynamic autophagy rates
Nitin Sai Beesabathuni, Soyoon Park, Priya S. Shah
Autophagy (2022) Vol. 19, Iss. 4, pp. 1164-1183
Open Access | Times Cited: 11
Autophagy and Exercise: Current Insights and Future Research Directions
Javier Botella, Christopher S. Shaw, David J. Bishop
International Journal of Sports Medicine (2023) Vol. 45, Iss. 03, pp. 171-182
Closed Access | Times Cited: 6
Spermidine and Rapamycin Reveal Distinct Autophagy Flux Response and Cargo Receptor Clearance Profile
Sholto de Wet, André du Toit, Ben Loos
Cells (2021) Vol. 10, Iss. 1, pp. 95-95
Open Access | Times Cited: 13
Hydroxysafflor Yellow A Exerts Neuroprotective Effects via HIF-1α/BNIP3 Pathway to Activate Neuronal Autophagy after OGD/R
Ruheng Wei, Lijuan Song, Zhuyue Miao, et al.
Cells (2022) Vol. 11, Iss. 23, pp. 3726-3726
Open Access | Times Cited: 7
Exacerbated Age-Related Hippocampal Alterations of Microglia Morphology, β-Amyloid and Lipofuscin Deposition and Presenilin Overexpression in Per1−/−-Mice
Jan Hendrik Börner, Oliver Rawashdeh, Abdelhaq Rami
Antioxidants (2021) Vol. 10, Iss. 9, pp. 1330-1330
Open Access | Times Cited: 8
Autophagy: A Silent Protagonist in Kidney Transplantation
Claudio Ponticelli, Francesco Reggiani, Gabriella Moroni
Transplantation (2023)
Closed Access | Times Cited: 2
The complexity of biological control systems: An autophagy case study
Mariana Pavel, Radu Tanasa, So Jung Park, et al.
BioEssays (2022) Vol. 44, Iss. 3
Open Access | Times Cited: 4
Quantitative and temporal measurement of dynamic autophagy rates
Nitin Sai Beesabathuni, Priya S. Shah
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 5
Monitoring autophagy using super-resolution structured illumination and direct stochastic optical reconstruction microscopy
Dumisile Lumkwana, Lize Engelbrecht, Ben Loos
Methods in cell biology (2021), pp. 139-152
Closed Access | Times Cited: 4
HES1 induces ITPR1-mediated autophagy to exert anti-metastatic effects in pituitary adenomas
Chunjian Qiu, Yao Yao, Suqin Hu, et al.
Translational Cancer Research (2024) Vol. 13, Iss. 2, pp. 661-675
Open Access
Correlative Light and Electron Microscopy (CLEM): Bringing Together the Best of Both Worlds to Study Neuronal Autophagy
Jurgen Kriel, Dumisile Lumkwana, Lydia-Marié Joubert, et al.
Neuromethods (2021), pp. 135-147
Closed Access | Times Cited: 3
Non-invasive monitoring of autophagy
Ben Loos, André du Toit, Jan‐Hendrik S. Hofmeyr
Nature Biomedical Engineering (2022) Vol. 6, Iss. 9, pp. 1015-1016
Closed Access | Times Cited: 1
Nodweddu effaith signalu ghrelin-GHS-R ar awtoffagi niwronaidd
Luke D. Roberts
(2022)
Open Access
Autophagy-dependent cell death; therapeutic target or chance encounter? Recent insights into the mechanisms of death by self-consumption
Jurgen Kriel, Ben Loos
Elsevier eBooks (2021), pp. 93-115
Closed Access
Measuring Autophagosome Flux
André du Toit, Jan‐Hendrik S. Hofmeyr, Ben Loos
Neuromethods (2021), pp. 67-78
Closed Access
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