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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:

Autophagy in the immune system
Daniel J. Puleston, Anna Katharina Simon
Immunology (2013) Vol. 141, Iss. 1, pp. 1-8
Open Access | Times Cited: 157

Showing 1-25 of 157 citing articles:

Phagocytosis: An Immunobiologic Process
Siamon Gordon
Immunity (2016) Vol. 44, Iss. 3, pp. 463-475
Open Access | Times Cited: 747
Photodynamic therapy (PDT) of cancer: from local to systemic treatment
J. Dąbrowski, Luı́s G. Arnaut
Photochemical & Photobiological Sciences (2015) Vol. 14, Iss. 10, pp. 1765-1780
Open Access | Times Cited: 448
TFEB and TFE3: Linking Lysosomes to Cellular Adaptation to Stress
Nina Raben, Rosa Puertollano
Annual Review of Cell and Developmental Biology (2016) Vol. 32, Iss. 1, pp. 255-278
Open Access | Times Cited: 372
Autophagy as a molecular target for cancer treatment
Nur Mehpare Kocatürk, Yunus Akkoç, Cenk Kığ, et al.
European Journal of Pharmaceutical Sciences (2019) Vol. 134, pp. 116-137
Closed Access | Times Cited: 337
Autophagy is a critical regulator of memory CD8+ T cell formation
Daniel J. Puleston, Hanlin Zhang, Timothy J. Powell, et al.
eLife (2014) Vol. 3
Open Access | Times Cited: 321
Autophagy in the renewal, differentiation and homeostasis of immune cells
Alexander J. Clarke, Anna Katharina Simon
Nature reviews. Immunology (2018) Vol. 19, Iss. 3, pp. 170-183
Closed Access | Times Cited: 301
TFEB and TFE3 cooperate in the regulation of the innate immune response in activated macrophages
Nunzia Pastore, Owen A. Brady, Heba I. Diab, et al.
Autophagy (2016) Vol. 12, Iss. 8, pp. 1240-1258
Open Access | Times Cited: 289
Phospholipase D Signaling Pathways and Phosphatidic Acid as Therapeutic Targets in Cancer
Ronald C. Bruntz, Craig W. Lindsley, H. Alex Brown
Pharmacological Reviews (2014) Vol. 66, Iss. 4, pp. 1033-1079
Open Access | Times Cited: 245
Role of microglia in stroke
Anna M. Planas
Glia (2024) Vol. 72, Iss. 6, pp. 1016-1053
Open Access | Times Cited: 29
Pro-survival autophagy and cancer cell resistance to therapy
Chandan Kanta Das, Mahitosh Mandal, Donat Kögel
Cancer and Metastasis Reviews (2018) Vol. 37, Iss. 4, pp. 749-766
Open Access | Times Cited: 145
Suppressing glucose metabolism with epigallocatechin-3-gallate (EGCG) reduces breast cancer cell growth in preclinical models
Ran Wei, Limin Mao, Ping Xu, et al.
Food & Function (2018) Vol. 9, Iss. 11, pp. 5682-5696
Open Access | Times Cited: 145
Taurine attenuates arsenic-induced pyroptosis and nonalcoholic steatohepatitis by inhibiting the autophagic-inflammasomal pathway
Tianming Qiu, Pei Pei, Xiaofeng Yao, et al.
Cell Death and Disease (2018) Vol. 9, Iss. 10
Open Access | Times Cited: 137
Binding of the pathogen receptor HSP90AA1 to avibirnavirus VP2 induces autophagy by inactivating the AKT-MTOR pathway
Boli Hu, Yina Zhang, Jia Lu, et al.
Autophagy (2015) Vol. 11, Iss. 3, pp. 503-515
Open Access | Times Cited: 129
Long-term live imaging reveals cytosolic immune responses of host hepatocytes againstPlasmodiuminfection and parasite escape mechanisms
Mónica Prado, Nina Eickel, Mariana De Niz, et al.
Autophagy (2015) Vol. 11, Iss. 9, pp. 1561-1579
Open Access | Times Cited: 129
ATG16L1: A multifunctional susceptibility factor in Crohn disease
Mohammad Salem, Mette Ammitzboell, Kris Nys, et al.
Autophagy (2015) Vol. 11, Iss. 4, pp. 585-594
Open Access | Times Cited: 127
Autophagy and Non-Alcoholic Fatty Liver Disease
Vanessa Lavallard, Philippe Gual
BioMed Research International (2014) Vol. 2014, pp. 1-13
Open Access | Times Cited: 125
Influenza M2 protein regulates MAVS-mediated signaling pathway through interacting with MAVS and increasing ROS production
Ruifang Wang, Yinxing Zhu, Xian Lin, et al.
Autophagy (2019) Vol. 15, Iss. 7, pp. 1163-1181
Open Access | Times Cited: 96
Autophagy and the Immune Response
Bing Cui, Heng Lin, Jinmei Yu, et al.
Advances in experimental medicine and biology (2019), pp. 595-634
Open Access | Times Cited: 88
Transcriptomic and metabolomic analysis revealed potential mechanisms of growth and disease resistance dimorphism in male and female common carp (Cyprinus carpio)
Chang Cai, Peng Yang, Yong Shi, et al.
Fish & Shellfish Immunology (2025) Vol. 158, pp. 110150-110150
Closed Access | Times Cited: 1
Autophagy in airway diseases: a new frontier in human asthma?
A.A. Zeki, Behzad Yeganeh, Nicholas J. Kenyon, et al.
Allergy (2015) Vol. 71, Iss. 1, pp. 5-14
Open Access | Times Cited: 85
Repurposing Drugs in Oncology (ReDO)—clarithromycin as an anti-cancer agent
An M. T. Van Nuffel, Vidula Sukhatme, Pan Pantziarka, et al.
ecancermedicalscience (2015) Vol. 9
Open Access | Times Cited: 80
Infectious bursal disease virus in poultry: current status and future prospects
Silke Rautenschlein, Tamiru N. Alkie
Veterinary Medicine Research and Reports (2016), pp. 9-9
Open Access | Times Cited: 72
Regulation of B cell fate, survival, and function by mitochondria and autophagy
Héctor Sandoval, Srikanth Kodali, Jin Wang
Mitochondrion (2017) Vol. 41, pp. 58-65
Open Access | Times Cited: 69
Streptococcus pneumoniae Induces Autophagy through the Inhibition of the PI3K-I/Akt/mTOR Pathway and ROS Hypergeneration in A549 Cells
Pu Li, Jing Shi, Qiao He, et al.
PLoS ONE (2015) Vol. 10, Iss. 3, pp. e0122753-e0122753
Open Access | Times Cited: 67
Infectious Bursal Disease Virus-Host Interactions: Multifunctional Viral Proteins that Perform Multiple and Differing Jobs
Yao Qin, Shijun J. Zheng
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 1, pp. 161-161
Open Access | Times Cited: 66
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