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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:

Inflammation in cardiac injury, repair and regeneration
Nikolaos G. Frangogiannis
Current Opinion in Cardiology (2015) Vol. 30, Iss. 3, pp. 240-245
Open Access | Times Cited: 182

Showing 1-25 of 182 citing articles:

The Biological Basis for Cardiac Repair After Myocardial Infarction
Sumanth D. Prabhu, Nikolaos G. Frangogiannis
Circulation Research (2016) Vol. 119, Iss. 1, pp. 91-112
Open Access | Times Cited: 1733
Ischemia/Reperfusion
Theodore J. Kalogeris, Christopher Baines, Maike Krenz, et al.
Comprehensive physiology (2016), pp. 113-170
Open Access | Times Cited: 646
The NLRP3 inflammasome in acute myocardial infarction
Stefano Toldo, Antonio Abbate
Nature Reviews Cardiology (2017) Vol. 15, Iss. 4, pp. 203-214
Closed Access | Times Cited: 540
Guidelines for experimental models of myocardial ischemia and infarction
Merry L. Lindsey, Roberto Bolli, John M. Canty, et al.
AJP Heart and Circulatory Physiology (2018) Vol. 314, Iss. 4, pp. H812-H838
Open Access | Times Cited: 443
IL-10 improves cardiac remodeling after myocardial infarction by stimulating M2 macrophage polarization and fibroblast activation
Mira Jung, Yonggang Ma, Rugmani Padmanabhan Iyer, et al.
Basic Research in Cardiology (2017) Vol. 112, Iss. 3
Open Access | Times Cited: 351
Inflammasome, pyroptosis, and cytokines in myocardial ischemia-reperfusion injury
Stefano Toldo, Adolfo G Mauro, Zachary Cutter, et al.
AJP Heart and Circulatory Physiology (2018) Vol. 315, Iss. 6, pp. H1553-H1568
Open Access | Times Cited: 308
The emerging role of Toll-like receptor 4 in myocardial inflammation
Yongxiang Yang, Jinlei Lv, Shuai Jiang, et al.
Cell Death and Disease (2016) Vol. 7, Iss. 5, pp. e2234-e2234
Open Access | Times Cited: 286
IL-18 cleavage triggers cardiac inflammation and fibrosis upon β-adrenergic insult
Han Xiao, Hao Li, Jingjing Wang, et al.
European Heart Journal (2017) Vol. 39, Iss. 1, pp. 60-69
Open Access | Times Cited: 256
The cardiac lymphatic system stimulates resolution of inflammation following myocardial infarction
Joaquim Miguel Vieira, S. Norman, Cristina Villa del Campo, et al.
Journal of Clinical Investigation (2018) Vol. 128, Iss. 8, pp. 3402-3412
Open Access | Times Cited: 231
Myocardial ischemia-reperfusion injury and the influence of inflammation
Michiel Algoet, Stefan Janssens, Uwe Himmelreich, et al.
Trends in Cardiovascular Medicine (2022) Vol. 33, Iss. 6, pp. 357-366
Closed Access | Times Cited: 231
M1-like macrophage-derived exosomes suppress angiogenesis and exacerbate cardiac dysfunction in a myocardial infarction microenvironment
Shaojun Liu, Jing Chen, Jian Shi, et al.
Basic Research in Cardiology (2020) Vol. 115, Iss. 2
Closed Access | Times Cited: 229
Resolution of Acute Inflammation and the Role of Resolvins in Immunity, Thrombosis, and Vascular Biology
Brian E. Sansbury, Matthew Spite
Circulation Research (2016) Vol. 119, Iss. 1, pp. 113-130
Open Access | Times Cited: 188
IL (Interleukin)-10–STAT3–Galectin-3 Axis Is Essential for Osteopontin-Producing Reparative Macrophage Polarization After Myocardial Infarction
Kohsuke Shirakawa, Jin Endo, Masaharu Kataoka, et al.
Circulation (2018) Vol. 138, Iss. 18, pp. 2021-2035
Open Access | Times Cited: 187
Extracellular vesicle activities regulating macrophage- and tissue-mediated injury and repair responses
Qian Hu, Christopher J. Lyon, Jesse K. Fletcher, et al.
Acta Pharmaceutica Sinica B (2020) Vol. 11, Iss. 6, pp. 1493-1512
Open Access | Times Cited: 179
Inflammation as a therapeutic target in myocardial infarction: learning from past failures to meet future challenges
Amit Saxena, Ilaria Russo, Nikolaos G. Frangogiannis
Translational research (2015) Vol. 167, Iss. 1, pp. 152-166
Open Access | Times Cited: 139
Transition of Macrophages to Fibroblast-Like Cells in Healing Myocardial Infarction
Nezam Haider, Lisardo Boscá, H. Reinier Zandbergen, et al.
Journal of the American College of Cardiology (2019) Vol. 74, Iss. 25, pp. 3124-3135
Open Access | Times Cited: 137
CaMKIIδ-mediated inflammatory gene expression and inflammasome activation in cardiomyocytes initiate inflammation and induce fibrosis
Andrew Willeford, Takeshi Suetomi, Audrey Nickle, et al.
JCI Insight (2018) Vol. 3, Iss. 12
Open Access | Times Cited: 109
Extracellular Vesicles: Immunomodulatory messengers in the context of tissue repair/regeneration
Andreia Silva, José H. Teixeira, Maria Inês Almeida, et al.
European Journal of Pharmaceutical Sciences (2016) Vol. 98, pp. 86-95
Closed Access | Times Cited: 103
The Role of Macrophages in the Infarcted Myocardium: Orchestrators of ECM Remodeling
Sinead A O’Rourke, Aisling Dunne, Michael G. Monaghan
Frontiers in Cardiovascular Medicine (2019) Vol. 6
Open Access | Times Cited: 87
The origins and non-canonical functions of macrophages in development and regeneration
Marine Théret, Rémi Mounier, Fábio Rossi
Development (2019) Vol. 146, Iss. 9
Open Access | Times Cited: 82
Nanosponge for Iron Chelation and Efflux: A Ferroptosis‐Inhibiting Approach for Myocardial Infarction Therapy
Qingbo Lv, Jun Lin, He Huang, et al.
Advanced Science (2024) Vol. 11, Iss. 25
Open Access | Times Cited: 12
Extracellular vesicles from dental pulp mesenchymal stem cells modulate macrophage phenotype during acute and chronic cardiac inflammation in athymic nude rats with myocardial infarction
Elena Amaro-Prellezo, Marta Gómez-Ferrer, Lusine Hakobyan, et al.
Inflammation and Regeneration (2024) Vol. 44, Iss. 1
Open Access | Times Cited: 9
Interleukin-10 exhibit dose-dependent effects on macrophage phenotypes and cardiac remodeling after myocardial infarction
Jing J. Zhang, Rodrigue Rizk, Xiaoping Li, et al.
Frontiers in Physiology (2025) Vol. 15
Open Access | Times Cited: 1
Anti-inflammatory effects of trans-cinnamaldehyde on lipopolysaccharide-stimulated macrophage activation via MAPKs pathway regulation
Mi Eun Kim, Ju Yong Na, Jun Sik Lee
Immunopharmacology and Immunotoxicology (2018) Vol. 40, Iss. 3, pp. 219-224
Closed Access | Times Cited: 76
Myocardial infarction remodeling that progresses to heart failure: a signaling misunderstanding
Alan J. Mouton, Osvaldo J. Rivera, Merry L. Lindsey
AJP Heart and Circulatory Physiology (2018) Vol. 315, Iss. 1, pp. H71-H79
Open Access | Times Cited: 76
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