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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:

Functions of NOD-Like Receptors in Human Diseases
Yifei Zhong, Anna Kinio, Maya Saleh
Frontiers in Immunology (2013) Vol. 4
Open Access | Times Cited: 286

Showing 1-25 of 286 citing articles:

NLRP3 inflammasome and its inhibitors: a review
Bo‐Zong Shao, Zhe‐Qi Xu, Han Bin-Ze, et al.
Frontiers in Pharmacology (2015) Vol. 6
Open Access | Times Cited: 749
Pharmacological Inhibitors of the NLRP3 Inflammasome
Ayesha Zahid, Bofeng Li, Arnaud John Kombe Kombe, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 563
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
Innate immunity in diabetes and diabetic nephropathy
Jun Wada, Hirofumi Makino
Nature Reviews Nephrology (2015) Vol. 12, Iss. 1, pp. 13-26
Closed Access | Times Cited: 371
Role of the NLRP3 inflammasome in cancer
Maryam Moossavi, Negin Parsamanesh, Afsane Bahrami, et al.
Molecular Cancer (2018) Vol. 17, Iss. 1
Open Access | Times Cited: 367
SARS-CoV-2 proteases PLpro and 3CLpro cleave IRF3 and critical modulators of inflammatory pathways (NLRP12 and TAB1): implications for disease presentation across species
Mehdi Moustaqil, Emma Ollivier, Hsin-Ping Chiu, et al.
Emerging Microbes & Infections (2020) Vol. 10, Iss. 1, pp. 178-195
Open Access | Times Cited: 239
Current role of the NLRP3 inflammasome on obesity and insulin resistance: A systematic review
Jakeline Rheinheimer, Bianca Marmontel de Souza, Natali S. Cardoso, et al.
Metabolism (2017) Vol. 74, pp. 1-9
Open Access | Times Cited: 237
The porcine innate immune system: An update
Kerstin H. Mair, Corinna Sedlak, Tobias Käser, et al.
Developmental & Comparative Immunology (2014) Vol. 45, Iss. 2, pp. 321-343
Open Access | Times Cited: 224
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
Pattern recognition receptors in fungal immunity
Emmanuel C. Patin, Aiysha Thompson, Selinda J. Orr
Seminars in Cell and Developmental Biology (2018) Vol. 89, pp. 24-33
Open Access | Times Cited: 183
Origin and Consequences of Necroinflammation
Maysa Sarhan, W. Land, Wulf Tonnus, et al.
Physiological Reviews (2018) Vol. 98, Iss. 2, pp. 727-780
Open Access | Times Cited: 179
The metabolic nature of inflammatory bowel diseases
Timon E. Adolph, Moritz Meyer, Julian Schwärzler, et al.
Nature Reviews Gastroenterology & Hepatology (2022) Vol. 19, Iss. 12, pp. 753-767
Closed Access | Times Cited: 177
Bacterial NLR-related proteins protect against phage
Emily M. Kibby, Amy N. Conte, A. Maxwell Burroughs, et al.
Cell (2023) Vol. 186, Iss. 11, pp. 2410-2424.e18
Open Access | Times Cited: 89
The role of NOD-like receptors in innate immunity
Cássio Luiz Coutinho Almeida-da-Silva, Luiz Eduardo Baggio Savio, Robson Coutinho‐Silva, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 68
Inhibitors of the NLRP3 inflammasome pathway as promising therapeutic candidates for inflammatory diseases (Review)
Xiaolu Zhang, Ziyu Wang, Yujia Zheng, et al.
International Journal of Molecular Medicine (2023) Vol. 51, Iss. 4
Open Access | Times Cited: 59
The NF-κB signaling system in the immunopathogenesis of inflammatory bowel disease
Tapas Mukherjee, Naveen Kumar, M. L. Chawla, et al.
Science Signaling (2024) Vol. 17, Iss. 818
Closed Access | Times Cited: 43
NLRP inflammasomes in health and disease
Zhihao Xu, Arnaud John Kombe Kombe, Shasha Deng, et al.
Molecular Biomedicine (2024) Vol. 5, Iss. 1
Open Access | Times Cited: 29
Exercise mimetics: a novel strategy to combat neuroinflammation and Alzheimer’s disease
Renqing Zhao
Journal of Neuroinflammation (2024) Vol. 21, Iss. 1
Open Access | Times Cited: 20
Blau Syndrome, the prototypic auto-inflammatory granulomatous disease
Carine Wouters, Anne Maes, Kevin P. Foley, et al.
Pediatric Rheumatology (2014) Vol. 12, Iss. 1
Open Access | Times Cited: 186
Danger signals – damaged-self recognition across the tree of life
Martin Heil, W. Land
Frontiers in Plant Science (2014) Vol. 5
Open Access | Times Cited: 180
Transplantation and Damage-Associated Molecular Patterns (DAMPs)
W. Land, Patrizia Agostinis, Stephan Gasser, et al.
American Journal of Transplantation (2016) Vol. 16, Iss. 12, pp. 3338-3361
Open Access | Times Cited: 143
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
Red cell DAMPs and inflammation
Rafaela Mendonça, Angélica Aparecida Antoniellis Silveira, Nicola Conran
Inflammation Research (2016) Vol. 65, Iss. 9, pp. 665-678
Closed Access | Times Cited: 138
NOD-like receptor signaling in inflammation-associated cancers: From functions to targeted therapies
Peng Liu, Ziwen Lu, Lanlan Liu, et al.
Phytomedicine (2019) Vol. 64, pp. 152925-152925
Closed Access | Times Cited: 134
The Role of Damage-Associated Molecular Patterns (DAMPs) in Human Diseases: Part II: DAMPs as diagnostics, prognostics and therapeutics in clinical medicine.
W. Land
DOAJ (DOAJ: Directory of Open Access Journals) (2015) Vol. 15, Iss. 2, pp. e157-70
Closed Access | Times Cited: 134
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