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:

Autophagy in acute kidney injury
Gur P. Kaushal, Sudhir V. Shah
Kidney International (2016) Vol. 89, Iss. 4, pp. 779-791
Open Access | Times Cited: 354

Showing 1-25 of 354 citing articles:

Autophagy in major human diseases
Daniel J. Klionsky, Giulia Petroni, Ravi K. Amaravadi, et al.
The EMBO Journal (2021) Vol. 40, Iss. 19
Open Access | Times Cited: 1092

Endoplasmic reticulum stress, the unfolded protein response and autophagy in kidney diseases
Andrey V. Cybulsky
Nature Reviews Nephrology (2017) Vol. 13, Iss. 11, pp. 681-696
Closed Access | Times Cited: 442

Mitochondria ROS and mitophagy in acute kidney injury
L. Joseph Su, Jiahao Zhang, Candelaria Gomez‐Manzano, et al.
Autophagy (2022) Vol. 19, Iss. 2, pp. 401-414
Open Access | Times Cited: 407

Autophagy in kidney homeostasis and disease
Chengyuan Tang, Man J. Livingston, Zhiwen Liu, et al.
Nature Reviews Nephrology (2020) Vol. 16, Iss. 9, pp. 489-508
Open Access | Times Cited: 367

AKI on CKD: heightened injury, suppressed repair, and the underlying mechanisms
Liyu He, Qingqing Wei, Jing Liu, et al.
Kidney International (2017) Vol. 92, Iss. 5, pp. 1071-1083
Open Access | Times Cited: 349

Recent Advances in Models, Mechanisms, Biomarkers, and Interventions in Cisplatin-Induced Acute Kidney Injury
Sara J. Holditch, Carolyn N. Brown, Andrew M. Lombardi, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 12, pp. 3011-3011
Open Access | Times Cited: 304

Mitochondrial quality control mechanisms as molecular targets in cardiac ischemia–reperfusion injury
Jin Wang, Hao Zhou
Acta Pharmaceutica Sinica B (2020) Vol. 10, Iss. 10, pp. 1866-1879
Open Access | Times Cited: 260

PINK1-PRKN/PARK2 pathway of mitophagy is activated to protect against renal ischemia-reperfusion injury
Chengyuan Tang, Hailong Han, Mingjuan Yan, et al.
Autophagy (2017) Vol. 14, Iss. 5, pp. 880-897
Open Access | Times Cited: 249

HIF-1α-BNIP3-mediated mitophagy in tubular cells protects against renal ischemia/reperfusion injury
Zongjie Fu, Zhiyu Wang, Lian Xu, et al.
Redox Biology (2020) Vol. 36, pp. 101671-101671
Open Access | Times Cited: 245

Ischemia and Reperfusion Injury in Kidney Transplantation: Relevant Mechanisms in Injury and Repair
Gertrude J. Nieuwenhuijs‐Moeke, Søren Erik Pischke, Stefan P. Berger, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 1, pp. 253-253
Open Access | Times Cited: 233

Legumain promotes tubular ferroptosis by facilitating chaperone-mediated autophagy of GPX4 in AKI
Chuan’ai Chen, Dekun Wang, Yangyang Yu, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 228

Clearance of damaged mitochondria via mitophagy is important to the protective effect of ischemic preconditioning in kidneys
Man J. Livingston, Jinghong Wang, Jiliang Zhou, et al.
Autophagy (2019) Vol. 15, Iss. 12, pp. 2142-2162
Open Access | Times Cited: 205

Nephrotoxicity and Renal Pathophysiology: A Contemporary Perspective
Lillie Marie A. Barnett, Brian S. Cummings
Toxicological Sciences (2018) Vol. 164, Iss. 2, pp. 379-390
Open Access | Times Cited: 197

Review: the Role and Mechanisms of Macrophage Autophagy in Sepsis
Peng Qiu, Yang Liu, Jin Zhang
Inflammation (2018) Vol. 42, Iss. 1, pp. 6-19
Closed Access | Times Cited: 191

Supramolecular Nanofibers Containing Arginine-Glycine-Aspartate (RGD) Peptides Boost Therapeutic Efficacy of Extracellular Vesicles in Kidney Repair
Chuyue Zhang, Yuna Shang, Xiaoniao Chen, et al.
ACS Nano (2020) Vol. 14, Iss. 9, pp. 12133-12147
Closed Access | Times Cited: 175

Autophagy in Chronic Kidney Diseases
Tien‐An Lin, Victor Chien‐Chia Wu, Chao‐Yung Wang
Cells (2019) Vol. 8, Iss. 1, pp. 61-61
Open Access | Times Cited: 152

Epigenetic regulator BRD4 is involved in cadmium-induced acute kidney injury via contributing to lysosomal dysfunction, autophagy blockade and oxidative stress
Zhonggui Gong, Yuan Zhao, Zhen‐Yong Wang, et al.
Journal of Hazardous Materials (2021) Vol. 423, pp. 127110-127110
Closed Access | Times Cited: 132

Tubular cells produce FGF2 via autophagy after acute kidney injury leading to fibroblast activation and renal fibrosis
Man J. Livingston, Shaoqun Shu, Ying Fan, et al.
Autophagy (2022) Vol. 19, Iss. 1, pp. 256-277
Open Access | Times Cited: 124

SIRT1 attenuates sepsis-induced acute kidney injury via Beclin1 deacetylation-mediated autophagy activation
Zhiya Deng, Maomao Sun, Jie Wu, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 2
Open Access | Times Cited: 117

The Effect of Oxidative Stress-Induced Autophagy by Cadmium Exposure in Kidney, Liver, and Bone Damage, and Neurotoxicity
Yonggang Ma, Qunchao Su, Chengguang Yue, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13491-13491
Open Access | Times Cited: 105

The Pathophysiology of Sepsis-Associated AKI
Shuhei Kuwabara, Eibhlin Goggins, Mark D. Okusa
Clinical Journal of the American Society of Nephrology (2022) Vol. 17, Iss. 7, pp. 1050-1069
Open Access | Times Cited: 98

NADPH oxidase 4 promotes cisplatin-induced acute kidney injury via ROS-mediated programmed cell death and inflammation
Xiao‐Ming Meng, Gui‐Ling Ren, Li Gao, et al.
Laboratory Investigation (2017) Vol. 98, Iss. 1, pp. 63-78
Open Access | Times Cited: 171

Autophagy blockade and lysosomal membrane permeabilization contribute to lead-induced nephrotoxicity in primary rat proximal tubular cells
Xiang-Bin Song, Gang Liu, Fei Liu, et al.
Cell Death and Disease (2017) Vol. 8, Iss. 6, pp. e2863-e2863
Open Access | Times Cited: 162

Mitophagy-dependent macrophage reprogramming protects against kidney fibrosis
Divya Bhatia, Kuei‐Pin Chung, Kiichi Nakahira, et al.
JCI Insight (2019) Vol. 4, Iss. 23
Open Access | Times Cited: 139

Oxidative Stress and Acute Kidney Injury in Critical Illness: Pathophysiologic Mechanisms—Biomarkers—Interventions, and Future Perspectives
Paraskevi Pavlakou, Vassilios Liakopoulos, Theodoros Eleftheriadis, et al.
Oxidative Medicine and Cellular Longevity (2017) Vol. 2017, Iss. 1
Open Access | Times Cited: 135

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