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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:

Location, location, location: A compartmentalized view of TNF-induced necroptotic signaling
André L. Samson, Sarah E. Garnish, Joanne M. Hildebrand, et al.
Science Signaling (2021) Vol. 14, Iss. 668
Closed Access | Times Cited: 68

Showing 26-50 of 68 citing articles:

Surviving death: emerging concepts of RIPK3 and MLKL ubiquitination in the regulation of necroptosis
Rebekka Karlowitz, Sjoerd J. L. van Wijk
FEBS Journal (2021) Vol. 290, Iss. 1, pp. 37-54
Open Access | Times Cited: 27
Dynamics of necroptosis in kidney ischemia-reperfusion injury
Aspasia Pefanis, Anjan K. Bongoni, Jennifer L. McRae, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 12
RIPK3 coordinates RHIM domain–dependent antiviral inflammatory transcription in neurons
Sigal B. Kofman, Lan H. Chu, Joshua Ames, et al.
Science Signaling (2025) Vol. 18, Iss. 880
Closed Access
MLKL activity requires a splicing-regulated, druggable intramolecular interaction
Uris Ros, Veronica Martinez-Osorio, Pedro A. Valiente, et al.
Molecular Cell (2025)
Open Access
Necroptosis: a significant and promising target for intervention of cardiovascular disease
Yanwei Ji, Xinyu Wen, He-peng Tang, et al.
Biochemical Pharmacology (2025), pp. 116951-116951
Closed Access
The Lck inhibitor, AMG-47a, blocks necroptosis and implicates RIPK1 in signalling downstream of MLKL
Annette V. Jacobsen, Catia L. Pierotti, Kym N. Lowes, et al.
Cell Death and Disease (2022) Vol. 13, Iss. 4
Open Access | Times Cited: 17
No Time to Die: How Cytomegaloviruses Suppress Apoptosis, Necroptosis, and Pyroptosis
Y. Deng, Ana Águeda-Pinto, Wolfram Brune
Viruses (2024) Vol. 16, Iss. 8, pp. 1272-1272
Open Access | Times Cited: 3
The Role of the Key Effector of Necroptotic Cell Death, MLKL, in Mouse Models of Disease
Emma C. Tovey Crutchfield, Sarah E. Garnish, Joanne M. Hildebrand
Biomolecules (2021) Vol. 11, Iss. 6, pp. 803-803
Open Access | Times Cited: 21
Ketamine inhibits TNF-α-induced cecal damage by enhancing RIP1 ubiquitination to attenuate lethal SIRS
Bin Deng, Daowei Yang, Huanghui Wu, et al.
Cell Death Discovery (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 15
The VEGFR/PDGFR tyrosine kinase inhibitor, ABT-869, blocks necroptosis by targeting RIPK1 kinase
Catia L. Pierotti, Annette V. Jacobsen, Christoph Grohmann, et al.
Biochemical Journal (2023) Vol. 480, Iss. 9, pp. 665-684
Open Access | Times Cited: 9
Oxidation of caspase-8 by hypothiocyanous acid enables TNF-mediated necroptosis
Stephanie M. Bozonet, Nicholas J. Magon, Abigail J. Schwartfeger, et al.
Journal of Biological Chemistry (2023) Vol. 299, Iss. 6, pp. 104792-104792
Open Access | Times Cited: 8
Regulation of RIP1‐Mediated necroptosis via necrostatin‐1 in periodontitis
Liangyu Tan, Wei‐Cheng Chan, Jing Zhang, et al.
Journal of Periodontal Research (2023) Vol. 58, Iss. 5, pp. 919-931
Closed Access | Times Cited: 8
A common human MLKL polymorphism confers resistance to negative regulation by phosphorylation
Sarah E. Garnish, Katherine R. Martin, Maria Kauppi, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 8
RIPK3 coordinates RHIM domain-dependent inflammatory transcription in neurons
Sigal B. Kofman, Lan H. Chu, Joshua Ames, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Necroptosis in bacterial infections
Xing Yu, Jin Yuan, Lin-xi Shi, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 2
Modulatory effects of necroptosis: A potential preventive approach to control diseases in fish
Xiaojing Xia, Jingjing Li, Jing Yu, et al.
Fish & Shellfish Immunology (2024) Vol. 152, pp. 109802-109802
Closed Access | Times Cited: 2
A new perspective on targeting pulmonary arterial hypertension: Programmed cell death pathways (Autophagy, Pyroptosis, Ferroptosis)
Qingliang Ge, Tianqing Zhang, Jinpu Yu, et al.
Biomedicine & Pharmacotherapy (2024) Vol. 181, pp. 117706-117706
Open Access | Times Cited: 2
Endothelial Caspase-8 prevents fatal necroptotic hemorrhage caused by commensal bacteria
Stefanie M. Bader, Simon Preston, Katie Saliba, et al.
Cell Death and Differentiation (2022) Vol. 30, Iss. 1, pp. 27-36
Open Access | Times Cited: 10
Co-expression of recombinant RIPK3:MLKL complexes using the baculovirus-insect cell system
Cheree Fitzgibbon, Yanxiang Meng, James M. Murphy
Methods in enzymology on CD-ROM/Methods in enzymology (2022), pp. 183-227
Closed Access | Times Cited: 9
Ubiquitylation of RIPK3 beyond-the-RHIM can limit RIPK3 activity and cell death
Daniel Frank, Sarah E. Garnish, Jarrod J. Sandow, et al.
iScience (2022) Vol. 25, Iss. 7, pp. 104632-104632
Open Access | Times Cited: 9
Staphylococcus aureus-Induced Necroptosis Promotes Mitochondrial Damage in Goat Endometrial Epithelial Cells
Yanyan Yi, Kangkang Gao, Pengfei Lin, et al.
Animals (2022) Vol. 12, Iss. 17, pp. 2218-2218
Open Access | Times Cited: 9
MALT1 promotes necroptosis in stroke rat brain via targeting the A20/RIPK3 pathway
Zi-Mei Peng, Yiyue Zhang, Wei Dan, et al.
Archives of Biochemistry and Biophysics (2023) Vol. 735, pp. 109502-109502
Closed Access | Times Cited: 5
A biochemical necroptosis model explains cell-type-specific responses to cell death cues
Geena V. Ildefonso, Marie Oliver Metzig, Alexander Hoffmann, et al.
Biophysical Journal (2023) Vol. 122, Iss. 5, pp. 817-834
Open Access | Times Cited: 5
IFNγ Causes Keratinocyte Necroptosis in Acute Graft-Versus-Host Disease
Lukas Freund, Stephanie Oehrl, Julius Schwingen, et al.
Journal of Investigative Dermatology (2023) Vol. 143, Iss. 9, pp. 1746-1756.e9
Open Access | Times Cited: 5
Human gasdermin D and MLKL disrupt mitochondria, endocytic traffic and TORC1 signalling in budding yeast
Marta Valenti, Marı́a Molina, Vı́ctor J. Cid
Open Biology (2023) Vol. 13, Iss. 5
Open Access | Times Cited: 5

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