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:

PAMPs and DAMPs: signal 0s that spur autophagy and immunity
Daolin Tang, Rui Kang, Carolyn B. Coyne, et al.
Immunological Reviews (2012) Vol. 249, Iss. 1, pp. 158-175
Open Access | Times Cited: 1061

Showing 1-25 of 1061 citing articles:

Broadening horizons: the role of ferroptosis in cancer
Xin Chen, Rui Kang, Guido Kroemer, et al.
Nature Reviews Clinical Oncology (2021) Vol. 18, Iss. 5, pp. 280-296
Closed Access | Times Cited: 2070

The molecular machinery of regulated cell death
Daolin Tang, Rui Kang, Tom Vanden Berghe, et al.
Cell Research (2019) Vol. 29, Iss. 5, pp. 347-364
Open Access | Times Cited: 2017

Self-consumption: the interplay of autophagy and apoptosis
Guillermo Mariño, Mireia Niso‐Santano, Eric H. Baehrecke, et al.
Nature Reviews Molecular Cell Biology (2014) Vol. 15, Iss. 2, pp. 81-94
Open Access | Times Cited: 2003

Ferroptosis: machinery and regulation
Xin Chen, Jingbo Li, Rui Kang, et al.
Autophagy (2020) Vol. 17, Iss. 9, pp. 2054-2081
Open Access | Times Cited: 1366

Sepsis and septic shock
Richard S. Hotchkiss, Lyle L. Moldawer, Steven M. Opal, et al.
Nature Reviews Disease Primers (2016) Vol. 2, Iss. 1
Open Access | Times Cited: 1287

Cancer cell–autonomous contribution of type I interferon signaling to the efficacy of chemotherapy
Antonella Sistigu, Takahiro Yamazaki, Erika Vacchelli, et al.
Nature Medicine (2014) Vol. 20, Iss. 11, pp. 1301-1309
Closed Access | Times Cited: 936

Consensus guidelines for the definition, detection and interpretation of immunogenic cell death
Lorenzo Galluzzi, Ilio Vitale, Sarah H. Warren, et al.
Journal for ImmunoTherapy of Cancer (2020) Vol. 8, Iss. 1, pp. e000337-e000337
Open Access | Times Cited: 855

Neuroinflammation and depression: A review
Romain Troubat, Pascal Barone, Samuel Leman, et al.
European Journal of Neuroscience (2020) Vol. 53, Iss. 1, pp. 151-171
Closed Access | Times Cited: 765

Fundamental Mechanisms of Regulated Cell Death and Implications for Heart Disease
Dominic P. Del Re, Dulguun Amgalan, Andreas Linkermann, et al.
Physiological Reviews (2019) Vol. 99, Iss. 4, pp. 1765-1817
Open Access | Times Cited: 753

Limiting inflammation—the negative regulation of NF-κB and the NLRP3 inflammasome
Inna S. Afonina, Zhenyu Zhong, Michael Karin, et al.
Nature Immunology (2017) Vol. 18, Iss. 8, pp. 861-869
Closed Access | Times Cited: 666

The role of oxidative stress during inflammatory processes
Jérôme Lugrin, Nathalie Rosenblatt‐Velin, Roumen Parapanov, et al.
Biological Chemistry (2013) Vol. 395, Iss. 2, pp. 203-230
Open Access | Times Cited: 631

Autophagy, ferroptosis, pyroptosis, and necroptosis in tumor immunotherapy
Weitong Gao, Yuqin Wang, Yang Zhou, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 612

The clearance of dead cells by efferocytosis
Emilio Boada-Romero, Jennifer Martinez, Bradlee L. Heckmann, et al.
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 7, pp. 398-414
Open Access | Times Cited: 585

Toll-like receptors in immunity and inflammatory diseases: Past, present, and future
Vijay Kumar
International Immunopharmacology (2018) Vol. 59, pp. 391-412
Open Access | Times Cited: 576

Ferroptosis in infection, inflammation, and immunity
Xin Chen, Rui Kang, Guido Kroemer, et al.
The Journal of Experimental Medicine (2021) Vol. 218, Iss. 6
Open Access | Times Cited: 541

The role of mitochondrial dysfunction in sepsis-induced multi-organ failure
Mervyn Singer
Virulence (2013) Vol. 5, Iss. 1, pp. 66-72
Open Access | Times Cited: 522

The release and activity of HMGB1 in ferroptosis
Qirong Wen, Jiao Liu, Rui Kang, et al.
Biochemical and Biophysical Research Communications (2019) Vol. 510, Iss. 2, pp. 278-283
Closed Access | Times Cited: 497

HMGB1 in Cancer: Good, Bad, or Both?
Rui Kang, Qiuhong Zhang, Herbert J. Zeh, et al.
Clinical Cancer Research (2013) Vol. 19, Iss. 15, pp. 4046-4057
Open Access | Times Cited: 452

The hallmarks of COVID-19 disease
Daolin Tang, Paul B. Comish, Rui Kang
PLoS Pathogens (2020) Vol. 16, Iss. 5, pp. e1008536-e1008536
Open Access | Times Cited: 452

Pattern recognition receptors and central nervous system repair
Kristina A. Kigerl, Juan Pablo de Rivero Vaccari, W. Dalton Dietrich, et al.
Experimental Neurology (2014) Vol. 258, pp. 5-16
Open Access | Times Cited: 429

Maternal immune activation and neuroinflammation in human neurodevelopmental disorders
Velda X. Han, Shrujna Patel, Hannah Jones, et al.
Nature Reviews Neurology (2021) Vol. 17, Iss. 9, pp. 564-579
Closed Access | Times Cited: 422

Autophagy and Cellular Immune Responses
Yuting Ma, Lorenzo Galluzzi, Laurence Zitvogel, et al.
Immunity (2013) Vol. 39, Iss. 2, pp. 211-227
Open Access | Times Cited: 420

Oxidative Damage of DNA Confers Resistance to Cytosolic Nuclease TREX1 Degradation and Potentiates STING-Dependent Immune Sensing
Nadine Gehrke, Christina Mertens, Thomas Zillinger, et al.
Immunity (2013) Vol. 39, Iss. 3, pp. 482-495
Open Access | Times Cited: 402

The lncRNA Neat1 promotes activation of inflammasomes in macrophages
Pengfei Zhang, Limian Cao, Rongbin Zhou, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 393

Release and activity of histone in diseases
R Chen, Rui Kang, X-G Fan, et al.
Cell Death and Disease (2014) Vol. 5, Iss. 8, pp. e1370-e1370
Open Access | Times Cited: 381

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