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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:

Interplay of Oxidative Stress and Necrosis-like Cell Death in Cardiac Ischemia/Reperfusion Injury: A Focus on Necroptosis
Adriana Adameová, Csaba Horváth, Safa Abdul‐Ghani, et al.
Biomedicines (2022) Vol. 10, Iss. 1, pp. 127-127
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

ALOX15-launched PUFA-phospholipids peroxidation increases the susceptibility of ferroptosis in ischemia-induced myocardial damage
Xiaohui Ma, Jiang-Han-Zi Liu, Chunyu Liu, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 144
Cardiovascular disease: Mitochondrial dynamics and mitophagy crosstalk mechanisms with novel programmed cell death and macrophage polarisation
Dandan Liu, Hewei Qin, Yang Gao, et al.
Pharmacological Research (2024) Vol. 206, pp. 107258-107258
Open Access | Times Cited: 21
The role of glycolytic metabolic pathways in cardiovascular disease and potential therapeutic approaches
Shuxian Chen, Yuanming Zou, Chunyu Song, et al.
Basic Research in Cardiology (2023) Vol. 118, Iss. 1
Open Access | Times Cited: 23
Endoplasmic reticulum stress-mediated cell death in cardiovascular disease
Yajuan An, Xinshuang Wang, Xiuju Guan, et al.
Cell Stress and Chaperones (2024) Vol. 29, Iss. 1, pp. 158-174
Open Access | Times Cited: 14
Atrial epicardial adipose tissue abundantly secretes myeloperoxidase and activates atrial fibroblasts in patients with atrial fibrillation
Eva R. Meulendijks, Rushd Al‐Shama, Makiri Kawasaki, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 20
Role of RIPK3‑CaMKII‑mPTP signaling pathway‑mediated necroptosis in cardiovascular diseases (Review)
Sheng Chen, Senhong Guan, Zhaohan Yan, et al.
International Journal of Molecular Medicine (2023) Vol. 52, Iss. 4
Open Access | Times Cited: 17
Remodelers of the vascular microenvironment: The effect of biopolymeric hydrogels on vascular diseases
Minhao Li, Meiqi Jin, Huazhe Yang
International Journal of Biological Macromolecules (2024) Vol. 264, pp. 130764-130764
Closed Access | Times Cited: 5
Spotlight on necroptosis: Role in pathogenesis and therapeutic potential of intervertebral disc degeneration
Rui Ran, Shun-Bai Zhang, Yong-Qiang Shi, et al.
International Immunopharmacology (2024) Vol. 138, pp. 112616-112616
Closed Access | Times Cited: 5
Small-Molecule Receptor-Interacting Protein 1 (RIP1) Inhibitors as Therapeutic Agents for Multifaceted Diseases: Current Medicinal Chemistry Insights and Emerging Opportunities
Kunyu Shi, Jifa Zhang, Enda Zhou, et al.
Journal of Medicinal Chemistry (2022) Vol. 65, Iss. 22, pp. 14971-14999
Closed Access | Times Cited: 21
Novel, non-conventional pathways of necroptosis in the heart and other organs: Molecular mechanisms, regulation and inter-organelle interplay
Csaba Horváth, Izabela Jarabicová, Branislav Kura, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2023) Vol. 1870, Iss. 7, pp. 119534-119534
Open Access | Times Cited: 12
Ferroptosis: A New Pathway in the Interaction between Gut Microbiota and Multiple Sclerosis
Junjie Jian, Jun Wei
Frontiers in Bioscience-Landmark (2025) Vol. 30, Iss. 1
Open Access
Impaired RelA signaling and lipid metabolism dysregulation in hepatocytes: driving forces in the progression of metabolic dysfunction-associated steatotic liver disease
Yi-Huai He, Jin-Lian Jiang, Lili Ou, et al.
Cell Death Discovery (2025) Vol. 11, Iss. 1
Open Access
Scutellarin ameliorates ischemia/reperfusion-mediated endothelial dysfunction by upregulating cathepsin D expression to rescue autophagy-lysosomal function
Qi-Zhen Zhuang, Lu Chen, V. Wu, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access
Involvement of Oxidative Stress and Antioxidants in Modification of Cardiac Dysfunction Due to Ischemia–Reperfusion Injury
Naranjan S. Dhalla, Petr Ošťádal, Paramjit S. Tappia
Antioxidants (2025) Vol. 14, Iss. 3, pp. 340-340
Open Access
Necroptosis in myocardial ischaemia-reperfusion injury: current update on mechanisms, therapeutic targets, and translational potential
Siarhei A. Dabravolski, Vladislav Kalmykov, Anastasia O Maksaeva, et al.
APOPTOSIS (2025)
Closed Access
Necroptosis: a significant and promising target for intervention of cardiovascular disease
Yanwei Ji, Xinyu Wen, He-peng Tang, et al.
Biochemical Pharmacology (2025), pp. 116951-116951
Closed Access
Modification of Ischemia/Reperfusion-Induced Alterations in Subcellular Organelles by Ischemic Preconditioning
Paramjit S. Tappia, Anureet K. Shah, Bram Ramjiawan, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3425-3425
Open Access | Times Cited: 18
Analysis of necroptosis and its association with pyroptosis in organ damage in experimental pulmonary arterial hypertension
Izabela Jarabicová, Csaba Horváth, Eva Veľasová, et al.
Journal of Cellular and Molecular Medicine (2022) Vol. 26, Iss. 9, pp. 2633-2645
Open Access | Times Cited: 17
Pharmaceutical Therapies for Necroptosis in Myocardial Ischemia–Reperfusion Injury
Yinchang Zhang, Yantao Zhang, Jinlong Zang, et al.
Journal of Cardiovascular Development and Disease (2023) Vol. 10, Iss. 7, pp. 303-303
Open Access | Times Cited: 9
TRPC6 regulates necroptosis in myocardial ischemia/reperfusion injury via Ca2+/CaMKII signaling pathway
Junhao Li, Zhang Jia-ji, Yunlong Zhong, et al.
Cellular Signalling (2024) Vol. 122, pp. 111344-111344
Closed Access | Times Cited: 3
CaMKII, ‘jack of all trades’ in inflammation during cardiac ischemia/reperfusion injury
Wenjia Zhang, Erdan Dong, Junxia Zhang, et al.
Journal of Molecular and Cellular Cardiology (2023) Vol. 184, pp. 48-60
Closed Access | Times Cited: 7
LGR6 protects against myocardial ischemia-reperfusion injury via suppressing necroptosis
Mengmeng Zhao, Zihui Zheng, Jianfang Liu, et al.
Redox Biology (2024) Vol. 78, pp. 103400-103400
Open Access | Times Cited: 2
N-arachidonoylphenolamine alleviates ischaemia/reperfusion-induced cardiomyocyte necroptosis by restoring proteasomal activity
Jun-Qin Bai, Pang‐Bo Li, Chunmin Li, et al.
European Journal of Pharmacology (2023) Vol. 963, pp. 176235-176235
Closed Access | Times Cited: 6
A bibliometric analysis of myocardial ischemia/reperfusion injury from 2000 to 2023
Yifei Wang, Lijun Guo, Zhibo Zhang, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 5
The involvement of reactive oxygen species in causing chronic cardiovascular and neurodegenerative diseases and some cancers
Jasneet Tiwana, Anureet K. Shah, Naranjan S. Dhalla
SCRIPTA MEDICA (2024) Vol. 55, Iss. 2, pp. 199-217
Open Access | Times Cited: 1
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