OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Selenium-Encoded Isotopic Signature Targeted Profiling
Jinjun Gao, Fan Yang, Jinteng Che, et al.
ACS Central Science (2018) Vol. 4, Iss. 8, pp. 960-970
Open Access | Times Cited: 63

Showing 1-25 of 63 citing articles:

Ferroptosis: machinery and regulation
Xin Chen, Jingbo Li, Rui Kang, et al.
Autophagy (2020) Vol. 17, Iss. 9, pp. 2054-2081
Open Access | Times Cited: 1318

The Metabolic Underpinnings of Ferroptosis
Jiashuo Zheng, Marcus Conrad
Cell Metabolism (2020) Vol. 32, Iss. 6, pp. 920-937
Open Access | Times Cited: 941

Ferroptosis: mechanisms and links with diseases
Hong-Fa Yan, Ting Zou, Qing‐zhang Tuo, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 899

GPX4 at the Crossroads of Lipid Homeostasis and Ferroptosis
Giovanni C. Forcina, Scott J. Dixon
PROTEOMICS (2019) Vol. 19, Iss. 18
Closed Access | Times Cited: 745

The chemical basis of ferroptosis
Marcus Conrad, Derek A. Pratt
Nature Chemical Biology (2019) Vol. 15, Iss. 12, pp. 1137-1147
Closed Access | Times Cited: 710

The multifaceted role of ferroptosis in liver disease
Junyi Chen, Xiaopeng Li, Chaodong Ge, et al.
Cell Death and Differentiation (2022) Vol. 29, Iss. 3, pp. 467-480
Open Access | Times Cited: 412

Selective covalent targeting of GPX4 using masked nitrile-oxide electrophiles
John K. Eaton, Laura Furst, Richard A. Ruberto, et al.
Nature Chemical Biology (2020) Vol. 16, Iss. 5, pp. 497-506
Open Access | Times Cited: 333

Redox homeostasis maintained by GPX4 facilitates STING activation
Mutian Jia, Danhui Qin, Chunyuan Zhao, et al.
Nature Immunology (2020) Vol. 21, Iss. 7, pp. 727-735
Closed Access | Times Cited: 289

Ferroptosis Affects the Progression of Nonalcoholic Steatohepatitis via the Modulation of Lipid Peroxidation–Mediated Cell Death in Mice
Jing Qi, Jong-Won Kim, Zixiong Zhou, et al.
American Journal Of Pathology (2019) Vol. 190, Iss. 1, pp. 68-81
Open Access | Times Cited: 250

Emerging mechanisms and targeted therapy of ferroptosis in cancer
Haiyan Wang, Yan Cheng, Chao Mao, et al.
Molecular Therapy (2021) Vol. 29, Iss. 7, pp. 2185-2208
Open Access | Times Cited: 223

The ferroptosis inducing compounds RSL3 and ML162 are not direct inhibitors of GPX4 but of TXNRD1
Dorian M. Cheff, Chuying Huang, Karoline Scholzen, et al.
Redox Biology (2023) Vol. 62, pp. 102703-102703
Open Access | Times Cited: 93

Exploiting ferroptosis vulnerabilities in cancer
Toshitaka Nakamura, Marcus Conrad
Nature Cell Biology (2024) Vol. 26, Iss. 9, pp. 1407-1419
Closed Access | Times Cited: 21

Rare codon recoding for efficient noncanonical amino acid incorporation in mammalian cells
Wenlong Ding, Wei Yu, Yulin Chen, et al.
Science (2024) Vol. 384, Iss. 6700, pp. 1134-1142
Closed Access | Times Cited: 20

Selenium: Tracing Another Essential Element of Ferroptotic Cell Death
Marcus Conrad, Bettina Proneth
Cell chemical biology (2020) Vol. 27, Iss. 4, pp. 409-419
Open Access | Times Cited: 106

Diacylfuroxans Are Masked Nitrile Oxides That Inhibit GPX4 Covalently
John K. Eaton, Richard A. Ruberto, Anneke Kramm, et al.
Journal of the American Chemical Society (2019) Vol. 141, Iss. 51, pp. 20407-20415
Open Access | Times Cited: 102

Using the Oxytosis/Ferroptosis Pathway to Understand and Treat Age-Associated Neurodegenerative Diseases
Pamela Maher, António Currais, David Schubert
Cell chemical biology (2020) Vol. 27, Iss. 12, pp. 1456-1471
Open Access | Times Cited: 78

Regulation of ferroptosis by bioactive phytochemicals: Implications for medical nutritional therapy
Kai Zheng, Yun Dong, Rong Yang, et al.
Pharmacological Research (2021) Vol. 168, pp. 105580-105580
Closed Access | Times Cited: 56

Ferroptosis and Its Multifaceted Role in Cancer: Mechanisms and Therapeutic Approach
Heshu Chen, Chenyu Wang, Zemin Liu, et al.
Antioxidants (2022) Vol. 11, Iss. 8, pp. 1504-1504
Open Access | Times Cited: 56

Small-molecule allosteric inhibitors of GPX4
Hengrui Liu, F. Forouhar, Annie Lin, et al.
Cell chemical biology (2022) Vol. 29, Iss. 12, pp. 1680-1693.e9
Open Access | Times Cited: 51

Interplay of Nrf2 and BACH1 in inducing ferroportin expression and enhancing resistance of human macrophages towards ferroptosis
Dmitry Namgaladze, Dominik C. Fuhrmann, Bernhard Brüne
Cell Death Discovery (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 36

Targeting lipid metabolism for ferroptotic cancer therapy
Minhua Luo, Jiajing Yan, Xinyu Hu, et al.
APOPTOSIS (2022) Vol. 28, Iss. 1-2, pp. 81-107
Closed Access | Times Cited: 28

Chemical Biology Approaches to Interrogate the Selenoproteome
Jennifer C. Peeler, Eranthie Weerapana
Accounts of Chemical Research (2019) Vol. 52, Iss. 10, pp. 2832-2840
Open Access | Times Cited: 44

The selenocysteine toolbox: A guide to studying the 21st amino acid
Christina Z. Chung, Natalie Krahn
Archives of Biochemistry and Biophysics (2022) Vol. 730, pp. 109421-109421
Closed Access | Times Cited: 25

Ferroptosis and Its Emerging Role in Pre-Eclampsia
Zhixian Chen, Jianfeng Gan, Mo Zhang, et al.
Antioxidants (2022) Vol. 11, Iss. 7, pp. 1282-1282
Open Access | Times Cited: 24

A new era of cysteine proteomics – Technological advances in thiol biology
Nils Burger, Edward T. Chouchani
Current Opinion in Chemical Biology (2024) Vol. 79, pp. 102435-102435
Closed Access | Times Cited: 5

Page 1 - Next Page

Scroll to top