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:

Autosis and autophagic cell death: the dark side of autophagy
Y. Liu, Beth Levine
Cell Death and Differentiation (2014) Vol. 22, Iss. 3, pp. 367-376
Open Access | Times Cited: 657

Showing 1-25 of 657 citing articles:

The molecular machinery of regulated cell death
Daolin Tang, Rui Kang, Tom Vanden Berghe, et al.
Cell Research (2019) Vol. 29, Iss. 5, pp. 347-364
Open Access | Times Cited: 2017

Autophagy promotes ferroptosis by degradation of ferritin
Wen‐Chi Hou, Yangchun Xie, Xinxin Song, et al.
Autophagy (2016) Vol. 12, Iss. 8, pp. 1425-1428
Open Access | Times Cited: 1787

Ferroptosis is an autophagic cell death process
Minghui Gao, Prashant Monian, Qiuhui Pan, et al.
Cell Research (2016) Vol. 26, Iss. 9, pp. 1021-1032
Open Access | Times Cited: 1468

Traumatic Spinal Cord Injury: An Overview of Pathophysiology, Models and Acute Injury Mechanisms
Arsalan Alizadeh, Scott M. Dyck, Soheila Karimi‐Abdolrezaee
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 1075

Neuronal Cell Death
Michael Fricker, Aviva M. Tolkovsky, Vilmantė Borutaitė, et al.
Physiological Reviews (2018) Vol. 98, Iss. 2, pp. 813-880
Open Access | Times Cited: 936

Ferroptosis is a type of autophagy-dependent cell death
Bo Zhou, Jiao Liu, Rui Kang, et al.
Seminars in Cancer Biology (2019) Vol. 66, pp. 89-100
Closed Access | Times Cited: 835

Fundamental Mechanisms of Regulated Cell Death and Implications for Heart Disease
Dominic P. Del Re, Dulguun Amgalan, Andreas Linkermann, et al.
Physiological Reviews (2019) Vol. 99, Iss. 4, pp. 1765-1817
Open Access | Times Cited: 753

AMPK-Mediated BECN1 Phosphorylation Promotes Ferroptosis by Directly Blocking System Xc– Activity
Xinxin Song, Shan Zhu, Pan Chen, et al.
Current Biology (2018) Vol. 28, Iss. 15, pp. 2388-2399.e5
Open Access | Times Cited: 601

Autophagy: machinery and regulation
Zhangyuan Yin, Clarence Pascual, Daniel J. Klionsky
Microbial Cell (2016) Vol. 3, Iss. 12, pp. 588-596
Open Access | Times Cited: 534

Mitochondrial Determinants of Doxorubicin-Induced Cardiomyopathy
Kendall B. Wallace, Vilma A. Sardão, Paulo J. Oliveira
Circulation Research (2020) Vol. 126, Iss. 7, pp. 926-941
Open Access | Times Cited: 429

Lipid storage and lipophagy regulates ferroptosis
Yuansong Bai, Lingjun Meng, Leng Han, et al.
Biochemical and Biophysical Research Communications (2018) Vol. 508, Iss. 4, pp. 997-1003
Closed Access | Times Cited: 393

Autophagy as a molecular target for cancer treatment
Nur Mehpare Kocatürk, Yunus Akkoç, Cenk Kığ, et al.
European Journal of Pharmaceutical Sciences (2019) Vol. 134, pp. 116-137
Closed Access | Times Cited: 338

Cytoplasmic vacuolization in cell death and survival
Andrey V. Shubin, Ilya V. Demidyuk, Alexey A. Komissarov, et al.
Oncotarget (2016) Vol. 7, Iss. 34, pp. 55863-55889
Open Access | Times Cited: 329

SIRT3-SOD2-mROS-dependent autophagy in cadmium-induced hepatotoxicity and salvage by melatonin
Huifeng Pi, Shangcheng Xu, Rüssel J. Reiter, et al.
Autophagy (2015) Vol. 11, Iss. 7, pp. 1037-1051
Open Access | Times Cited: 322

Modulation of inflammation by autophagy: Consequences for human disease
Romana T. Netea‐Maier, Theo S. Plantinga, Frank L. van de Veerdonk, et al.
Autophagy (2015) Vol. 12, Iss. 2, pp. 245-260
Open Access | Times Cited: 321

Oxidative stress and autophagy: Crucial modulators of kidney injury
Angara Sureshbabu, Stefan W. Ryter, Mary E. Choi
Redox Biology (2015) Vol. 4, pp. 208-214
Open Access | Times Cited: 317

Exploiting macrophage autophagy-lysosomal biogenesis as a therapy for atherosclerosis
Ismail Sergin, Trent D. Evans, Xiangyu Zhang, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 310

Targeting autophagy in obesity: from pathophysiology to management
Yingmei Zhang, James R. Sowers, Jun Ren
Nature Reviews Endocrinology (2018) Vol. 14, Iss. 6, pp. 356-376
Closed Access | Times Cited: 304

Arterial ageing: from endothelial dysfunction to vascular calcification
Manfredi Tesauro, Alessandro Mauriello, Valentina Rovella, et al.
Journal of Internal Medicine (2017) Vol. 281, Iss. 5, pp. 471-482
Open Access | Times Cited: 287

Reactive Oxygen Species (ROS) Regulates Different Types of Cell Death by Acting as a Rheostat
Gloria E. Villalpando-Rodriguez, Spencer B. Gibson
Oxidative Medicine and Cellular Longevity (2021) Vol. 2021, Iss. 1
Open Access | Times Cited: 286

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

Glioblastoma and chemoresistance to alkylating agents: Involvement of apoptosis, autophagy, and unfolded protein response
Sabine Hombach‐Klonisch, Maryam Mehrpour, Shahla Shojaei, et al.
Pharmacology & Therapeutics (2017) Vol. 184, pp. 13-41
Closed Access | Times Cited: 255

Therapeutic potential of autophagy-enhancing agents in Parkinson’s disease
Tim E. Moors, Jeroen J.M. Hoozemans, Angela Ingrassia, et al.
Molecular Neurodegeneration (2017) Vol. 12, Iss. 1
Open Access | Times Cited: 249

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