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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:

Extracellular histones, cell-free DNA, or nucleosomes: differences in immunostimulation
Gerben Marsman, Sacha Zeerleder, Brenda M. Luken
Cell Death and Disease (2016) Vol. 7, Iss. 12, pp. e2518-e2518
Open Access | Times Cited: 198

Showing 1-25 of 198 citing articles:

DAMPs and NETs in Sepsis
Naomi‐Liza Denning, Monowar Aziz, Steven D. Gurien, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 472
Life and death of circulating cell-free DNA
Anatoli Kustanovich, Ruth Schwartz, Tamar Peretz, et al.
Cancer Biology & Therapy (2019) Vol. 20, Iss. 8, pp. 1057-1067
Open Access | Times Cited: 451
The role of extracellular histone in organ injury
Eleanor Silk, Hailin Zhao, Hao Weng, et al.
Cell Death and Disease (2017) Vol. 8, Iss. 5, pp. e2812-e2812
Open Access | Times Cited: 273
Toward the Early Detection of Cancer by Decoding the Epigenetic and Environmental Fingerprints of Cell-Free DNA
Ymke van der Pol, Florent Moulière
Cancer Cell (2019) Vol. 36, Iss. 4, pp. 350-368
Open Access | Times Cited: 268
Signaling pathways and intervention therapies in sepsis
Yunyu Zhang, Botao Ning
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 195
A nanoparticulate dual scavenger for targeted therapy of inflammatory bowel disease
Chengxin Shi, Jianati Dawulieti, Feiyu Shi, et al.
Science Advances (2022) Vol. 8, Iss. 4
Open Access | Times Cited: 153
NLRP3 activation induced by neutrophil extracellular traps sustains inflammatory response in the diabetic wound
Dan Liu, Peilang Yang, Min Gao, et al.
Clinical Science (2019) Vol. 133, Iss. 4, pp. 565-582
Closed Access | Times Cited: 152
DNA in extracellular vesicles: biological and clinical aspects
Julia Elzanowska, Christine Semira, Bruno Costa‐Silva
Molecular Oncology (2020) Vol. 15, Iss. 6, pp. 1701-1714
Open Access | Times Cited: 151
The Nexus of cfDNA and Nuclease Biology
Diana Han, Y. M. Dennis Lo
Trends in Genetics (2021) Vol. 37, Iss. 8, pp. 758-770
Open Access | Times Cited: 142
Neutrophil extracellular traps and their histones promote Th17 cell differentiation directly via TLR2
Alicia S. Wilson, Katrina L. Randall, Jessica A. Pettitt, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 122
Cell-free DNA maps COVID-19 tissue injury and risk of death and can cause tissue injury
T. Andargie, Takayuki Tsuji, Fayaz Seifuddin, et al.
JCI Insight (2021) Vol. 6, Iss. 7
Open Access | Times Cited: 118
The emerging roles of neutrophil extracellular traps in wound healing
Shuainan Zhu, Ying Yu, Yun Ren, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 11
Open Access | Times Cited: 106
“The NET effect”: Neutrophil extracellular traps—a potential key component of the dysregulated host immune response in sepsis
Andrew Retter, Mervyn Singer, Djillali Annane
Critical Care (2025) Vol. 29, Iss. 1
Open Access | Times Cited: 3
Neutrophil extracellular traps drive inflammatory pathogenesis in malaria
Sebastian Lorenz Knackstedt, Athina Georgiadou, Falko Apel, et al.
Science Immunology (2019) Vol. 4, Iss. 40
Open Access | Times Cited: 146
Chronic neurodegeneration induces type I interferon synthesis via STING, shaping microglial phenotype and accelerating disease progression
Arshed Nazmi, Robert H. Field, Éadaoin W. Griffin, et al.
Glia (2019) Vol. 67, Iss. 7, pp. 1254-1276
Open Access | Times Cited: 110
Systemic activation of NLRP3 inflammasome in patients with severe primary Sjögren's syndrome fueled by inflammagenic DNA accumulations
Aigli G. Vakrakou, S Boiu, Panayiotis D. Ziakas, et al.
Journal of Autoimmunity (2018) Vol. 91, pp. 23-33
Closed Access | Times Cited: 107
Evidence and impact of neutrophil extracellular traps in malignant melanoma
Fiona Schedel, Sarah Mayer‐Hain, Karin I. Pappelbaum, et al.
Pigment Cell & Melanoma Research (2019) Vol. 33, Iss. 1, pp. 63-73
Closed Access | Times Cited: 97
Neutrophil extracellular traps impair intestinal barrier functions in sepsis by regulating TLR9-mediated endoplasmic reticulum stress pathway
Shilong Sun, Zehua Duan, Xinyu Wang, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 6
Open Access | Times Cited: 91
Circulating mitochondrial DNA is a proinflammatory DAMP in sickle cell disease
Laxminath Tumburu, Shohini Ghosh-Choudhary, Fayaz Seifuddin, et al.
Blood (2021) Vol. 137, Iss. 22, pp. 3116-3126
Open Access | Times Cited: 87
Compromised Anti-inflammatory Action of Neutrophil Extracellular Traps in PAD4-Deficient Mice Contributes to Aggravated Acute Inflammation After Myocardial Infarction
Kaveh Eghbalzadeh, Leena Georgi, Theresa Louis, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 83
Induction of neutrophil extracellular traps during tissue injury: Involvement of STING and Toll‐like receptor 9 pathways
Li Liu, Mao Ye, Bocheng Xu, et al.
Cell Proliferation (2019) Vol. 52, Iss. 3
Open Access | Times Cited: 81
Thrombo-Inflammation in Cardiovascular Disease: An Expert Consensus Document from the Third Maastricht Consensus Conference on Thrombosis
Elisa D’Alessandro, Christian Becker, Wolfgang Bergmeier, et al.
Thrombosis and Haemostasis (2020) Vol. 120, Iss. 04, pp. 538-564
Open Access | Times Cited: 81
Hookworms Evade Host Immunity by Secreting a Deoxyribonuclease to Degrade Neutrophil Extracellular Traps
Tiffany Bouchery, Mati Moyat, Javier Sotillo, et al.
Cell Host & Microbe (2020) Vol. 27, Iss. 2, pp. 277-289.e6
Open Access | Times Cited: 71
Neutrophil Extracellular Traps Delay Diabetic Wound Healing by Inducing Endothelial-to-Mesenchymal Transition via the Hippo pathway
Shuofei Yang, Shuangshuang Wang, Liang Chen, et al.
International Journal of Biological Sciences (2022) Vol. 19, Iss. 1, pp. 347-361
Open Access | Times Cited: 45
Ocular graft-versus-host disease (oGVHD): From A to Z
Mohammad Soleimani, Pouya Mahdavi Sharif, Kasra Cheraqpour, et al.
Survey of Ophthalmology (2023) Vol. 68, Iss. 4, pp. 697-712
Open Access | Times Cited: 27
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