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:

Single cell analysis of PANoptosome cell death complexes through an expansion microscopy method
Yaqiu Wang, Pandian Nagakannan, Joo‐Hui Han, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 10
Open Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Advances in mechanism and regulation of PANoptosis: Prospects in disease treatment
Peng Zhu, Zhuo-Ran Ke, Jing-Xian Chen, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 91

Innate immune inflammatory cell death: PANoptosis and PANoptosomes in host defense and disease
Wen Chen, Jessica M. Gullett, Rebecca E. Tweedell, et al.
European Journal of Immunology (2023) Vol. 53, Iss. 11
Open Access | Times Cited: 64

Therapeutic potential of PANoptosis: innate sensors, inflammasomes, and RIPKs in PANoptosomes
Ankit Pandeya, Thirumala‐Devi Kanneganti
Trends in Molecular Medicine (2023) Vol. 30, Iss. 1, pp. 74-88
Open Access | Times Cited: 63

PANoptosis: Mechanisms, biology, and role in disease
Xu Sun, Yanpeng Yang, Xiaona Meng, et al.
Immunological Reviews (2023) Vol. 321, Iss. 1, pp. 246-262
Open Access | Times Cited: 52

Integrated NLRP3, AIM2, NLRC4, Pyrin inflammasome activation and assembly drive PANoptosis
SuHyeon Oh, Jihye Lee, Ju-Eun Oh, et al.
Cellular and Molecular Immunology (2023) Vol. 20, Iss. 12, pp. 1513-1526
Closed Access | Times Cited: 41

A comparative study of apoptosis, pyroptosis, necroptosis, and PANoptosis components in mouse and human cells
Sk Mohiuddin Choudhury, Roman Sarkar, Rajendra Karki, et al.
PLoS ONE (2024) Vol. 19, Iss. 2, pp. e0299577-e0299577
Open Access | Times Cited: 15

Inflammasome signaling in colorectal cancer
Bhesh Raj Sharma, Thirumala‐Devi Kanneganti
Translational research (2022) Vol. 252, pp. 45-52
Open Access | Times Cited: 52

Mechanisms of PANoptosis and relevant small-molecule compounds for fighting diseases
Lian Wang, Yanghui Zhu, Lu Zhang, et al.
Cell Death and Disease (2023) Vol. 14, Iss. 12
Open Access | Times Cited: 33

PANoptosis-based molecular subtyping and HPAN-index predicts therapeutic response and survival in hepatocellular carcinoma
Fei Song, Chenggui Wang, Jiazhen Mao, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 26

Inflammasome diversity: exploring novel frontiers in the innate immune response
Gyeongju Yu, Young Ki Choi, SangJoon Lee
Trends in Immunology (2024) Vol. 45, Iss. 4, pp. 248-258
Closed Access | Times Cited: 7

Pancancer transcriptomic profiling identifies key PANoptosis markers as therapeutic targets for oncology
Raghvendra Mall, Ratnakar R. Bynigeri, Rajendra Karki, et al.
NAR Cancer (2022) Vol. 4, Iss. 4
Open Access | Times Cited: 33

Comprehensive analysis illustrating the role of PANoptosis-related genes in lung cancer based on bioinformatic algorithms and experiments
Shiyou Wei, Zhigang Chen, Xinyu Ling, et al.
Frontiers in Pharmacology (2023) Vol. 14
Open Access | Times Cited: 20

PANoptosis: Emerging mechanisms and disease implications
Zehong Qi, Lili Zhu, Kangkai Wang, et al.
Life Sciences (2023) Vol. 333, pp. 122158-122158
Closed Access | Times Cited: 16

ZBP1-mediated PANoptosis: A possible novel mechanism underlying the therapeutic effects of penehyclidine hydrochloride on myocardial ischemia–reperfusion injury
Boqun Cui, Zeyou Qi, Wenjun Liu, et al.
International Immunopharmacology (2024) Vol. 137, pp. 112373-112373
Closed Access | Times Cited: 6

Neurotoxic β-amyloid oligomers cause mitochondrial dysfunction—the trigger for PANoptosis in neurons
Xiangyuan Meng, Qi Song, Zinan Liu, et al.
Frontiers in Aging Neuroscience (2024) Vol. 16
Open Access | Times Cited: 5

Korean Red ginseng enhances ZBP1-mediated cell death to suppress viral protein expression in host defense against Influenza A virus
Ju-Eun Oh, Hayeon Kim, Jihye Lee, et al.
The Journal of Microbiology (2025) Vol. 63, Iss. 1, pp. e:2409007-e:2409007
Closed Access

Caspases in PANoptosis
Kaiyuan Song, Yongbin Wu, Sipin Tan
Current Research in Translational Medicine (2025) Vol. 73, Iss. 1, pp. 103502-103502
Closed Access

Engineering materials for pyroptosis induction in cancer treatment
Jiayi Liu, Taili Chen, XianLing Liu, et al.
Bioactive Materials (2023) Vol. 33, pp. 30-45
Open Access | Times Cited: 12

Nuclear Export Inhibitors Selinexor (KPT-330) and Eltanexor (KPT-8602) Provide a Novel Therapy to Reduce Tumor Growth by Induction of PANoptosis
Samuel Camilli, Richard F. Lockey, Narasaiah Kolliputi
Cell Biochemistry and Biophysics (2023) Vol. 81, Iss. 3, pp. 421-426
Closed Access | Times Cited: 10

Implications of inflammatory cell death-PANoptosis in health and disease
Hyun W. Bae, Y.H. Jang, Rajendra Karki, et al.
Archives of Pharmacal Research (2024) Vol. 47, Iss. 7, pp. 617-631
Closed Access | Times Cited: 3

Evaluation of Caspase Activation to Assess Innate Immune Cell Death
Joo‐Hui Han, Rebecca E. Tweedell, Thirumala‐Devi Kanneganti
Journal of Visualized Experiments (2023), Iss. 191
Closed Access | Times Cited: 9

Activation of cytosolic RNA sensors by endogenous ligands: roles in disease pathogenesis
Sarah Straub, Natália G. Sampaio
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 8

Activation of STING by SAMHD1 Deficiency Promotes PANoptosis and Enhances Efficacy of PD-L1 Blockade in Diffuse Large B-cell Lymphoma
Yiqing Cai, Xiaohong Chen, Tiange Lu, et al.
International Journal of Biological Sciences (2023) Vol. 19, Iss. 14, pp. 4627-4643
Open Access | Times Cited: 8

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