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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:

NOD-Like Receptors: Versatile Cytosolic Sentinels
Vinicius N. Motta, Fraser Soares, Tian Sun, et al.
Physiological Reviews (2014) Vol. 95, Iss. 1, pp. 149-178
Closed Access | Times Cited: 312

Showing 1-25 of 312 citing articles:

Pattern recognition receptors in health and diseases
Danyang Li, Minghua Wu
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 1077
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
NOD-Like Receptors in Infection, Immunity, and Diseases
Young Keun Kim, Jeon‐Soo Shin, Moon H. Nahm
Yonsei Medical Journal (2015) Vol. 57, Iss. 1, pp. 5-5
Open Access | Times Cited: 393
Epithelial Toll-like receptors and their role in gut homeostasis and disease
Juan F. Burgueño, María T. Abreu
Nature Reviews Gastroenterology & Hepatology (2020) Vol. 17, Iss. 5, pp. 263-278
Closed Access | Times Cited: 316
STING: a master regulator in the cancer-immunity cycle
Yuanyuan Zhu, Xiang An, Xiao Zhang, et al.
Molecular Cancer (2019) Vol. 18, Iss. 1
Open Access | Times Cited: 309
Toll-Like Receptors (TLRs), NOD-Like Receptors (NLRs), and RIG-I-Like Receptors (RLRs) in Innate Immunity. TLRs, NLRs, and RLRs Ligands as Immunotherapeutic Agents for Hematopoietic Diseases
Katarzyna Wicherska‐Pawłowska, Tomasz Wróbel, Justyna Rybka
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13397-13397
Open Access | Times Cited: 211
Targeting the NLRP3 inflammasome in cardiovascular diseases
Stefano Toldo, Eleonora Mezzaroma, Leo F. Buckley, et al.
Pharmacology & Therapeutics (2021) Vol. 236, pp. 108053-108053
Open Access | Times Cited: 198
Inflammatory and fibrotic responses of cardiac fibroblasts to myocardial damage associated molecular patterns (DAMPs)
Neil A. Turner
Journal of Molecular and Cellular Cardiology (2015) Vol. 94, pp. 189-200
Open Access | Times Cited: 185
Butyrate, a metabolite of intestinal bacteria, enhances sleep
Éva Szentirmai, Nicklaus S. Millican, Ashley R. Massie, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 178
PTX3, a Humoral Pattern Recognition Molecule, in Innate Immunity, Tissue Repair, and Cancer
Cecília Garlanda, Barbara Bottazzi, Elena Magrini, et al.
Physiological Reviews (2018) Vol. 98, Iss. 2, pp. 623-639
Open Access | Times Cited: 174
Pathogenesis of allergic diseases and implications for therapeutic interventions
Ji Wang, Yumei Zhou, Honglei Zhang, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 151
Targeting nucleotide metabolism: a promising approach to enhance cancer immunotherapy
Huailiang Wu, Yue Gong, Peng Ji, et al.
Journal of Hematology & Oncology (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 111
The role of animal hosts in shaping gut microbiome variation
Elisa Maritan, Andrea Quagliariello, Enric Frago, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2024) Vol. 379, Iss. 1901
Open Access | Times Cited: 23
The innate immune system in chronic cardiomyopathy: a European Society of Cardiology (ESC) scientific statement from the Working Group on Myocardial Function of the ESC
Stefan Frantz, Inês Falcão‐Pires, Jean‐Luc Balligand, et al.
European Journal of Heart Failure (2018) Vol. 20, Iss. 3, pp. 445-459
Open Access | Times Cited: 154
Cellular and Molecular Connections between Autophagy and Inflammation
Pierre Lapaquette, Jean Guzzo, Lionel Brétillon, et al.
Mediators of Inflammation (2015) Vol. 2015, Iss. 1
Open Access | Times Cited: 142
Nod2: The intestinal gate keeper
Ziad Al Nabhani, Gilles Dietrich, Jean‐Pierre Hugot, et al.
PLoS Pathogens (2017) Vol. 13, Iss. 3, pp. e1006177-e1006177
Open Access | Times Cited: 141
TLRs/NLRs: Shaping the landscape of host immunity
Komal Dolasia, Manoj Kumar Bisht, Gourango Pradhan, et al.
International Reviews of Immunology (2017) Vol. 37, Iss. 1, pp. 3-19
Closed Access | Times Cited: 134
Evolutionary Convergence and Divergence in NLR Function and Structure
Étienne Meunier, Petr Brož
Trends in Immunology (2017) Vol. 38, Iss. 10, pp. 744-757
Closed Access | Times Cited: 131
Macropinocytosis: New Insights Into Its Underappreciated Role in Innate Immune Cell Surveillance
Johnathan Canton
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 124
NOD-like receptors: major players (and targets) in the interface between innate immunity and cancer
Fernando Janczur Velloso, Marina Trombetta-Lima, Valesca Anschau, et al.
Bioscience Reports (2019) Vol. 39, Iss. 4
Open Access | Times Cited: 119
Zoonotic Potential of Emerging Paramyxoviruses
Patricia A. Thibault, Ruth Watkinson, Andrés Moreira‐Soto, et al.
Advances in virus research (2017), pp. 1-55
Open Access | Times Cited: 109
Role of inflammasomes in inflammatory autoimmune rheumatic diseases
Young‐Su Yi
Korean Journal of Physiology and Pharmacology (2017) Vol. 22, Iss. 1, pp. 1-1
Open Access | Times Cited: 102
NOD-like receptors in autoimmune diseases
Li Chen, Shiqi Cao, Zemin Lin, et al.
Acta Pharmacologica Sinica (2021) Vol. 42, Iss. 11, pp. 1742-1756
Open Access | Times Cited: 97
Roles of PRR-Mediated Signaling Pathways in the Regulation of Oxidative Stress and Inflammatory Diseases
Pengwei Li, Mingxian Chang
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 14, pp. 7688-7688
Open Access | Times Cited: 90
Staphylococcus aureus modulation of innate immune responses through Toll-like (TLR), (NOD)-like (NLR) and C-type lectin (CLR) receptors
Fatemeh Askarian, Theresa Wagner, Mona Johannessen, et al.
FEMS Microbiology Reviews (2018) Vol. 42, Iss. 5, pp. 656-671
Open Access | Times Cited: 88
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