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 between Metabolism Reprogramming and Epithelial-to-Mesenchymal Transition in Cancer Stem Cells
Yoann Daniel, Elise Lelou, Caroline Aninat, et al.
Cancers (2021) Vol. 13, Iss. 8, pp. 1973-1973
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

The Epithelial–Mesenchymal Transition at the Crossroads between Metabolism and Tumor Progression
Monica Fedele, Riccardo Sgarra, Sabrina Battista, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 2, pp. 800-800
Open Access | Times Cited: 123

Mitochondrial metabolism: a predictive biomarker of radiotherapy efficacy and toxicity
Farzad Taghizadeh‐Hesary, Mohammad Houshyari, Mohammad Farhadi
Journal of Cancer Research and Clinical Oncology (2023) Vol. 149, Iss. 9, pp. 6719-6741
Closed Access | Times Cited: 29

Ginsenosides in cancer: A focus on the regulation of cell metabolism
Yao Wang, Yunfeng Guan
Biomedicine & Pharmacotherapy (2022) Vol. 156, pp. 113756-113756
Open Access | Times Cited: 33

Inside the stemness engine: Mechanistic links between deregulated transcription factors and stemness in cancer
Egle-Helene Ervin, Rhiannon French, Chao‐Hui Chang, et al.
Seminars in Cancer Biology (2022) Vol. 87, pp. 48-83
Open Access | Times Cited: 31

Targeting autophagy and lipid metabolism in cancer stem cells
Bandana Chakravarti, Jawed A. Siddiqui, Rohit A. Sinha, et al.
Biochemical Pharmacology (2023) Vol. 212, pp. 115550-115550
Closed Access | Times Cited: 17

The multifaceted roles of mitochondria at the crossroads of cell life and death in cancer
Fabrizio Fontana, Patrízia Limonta
Free Radical Biology and Medicine (2021) Vol. 176, pp. 203-221
Closed Access | Times Cited: 33

Tolerable glycometabolic stress boosts cancer cell resilience through altered N-glycosylation and Notch signaling activation
Shungo Iwamoto, Takashi Kobayashi, Hisatoshi Hanamatsu, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4

Epithelial-to-Mesenchymal Transition-Derived Heterogeneity in Head and Neck Squamous Cell Carcinomas
Philipp Baumeister, Jiefu Zhou, Martin Canis, et al.
Cancers (2021) Vol. 13, Iss. 21, pp. 5355-5355
Open Access | Times Cited: 24

Escape From Cisplatin-Induced Senescence of Hypoxic Lung Cancer Cells Can Be Overcome by Hydroxychloroquine
Aleksandra Olszewska, Agata Borkowska, Monika Granica, et al.
Frontiers in Oncology (2022) Vol. 11
Open Access | Times Cited: 17

Roadmap on plasticity and epigenetics in cancer
Jasmine Foo, David Basanta, Russell C. Rockne, et al.
Physical Biology (2022) Vol. 19, Iss. 3, pp. 031501-031501
Open Access | Times Cited: 17

Twist-Induced Epithelial-to-Mesenchymal Transition Confers Specific Metabolic and Mitochondrial Alterations
H. M. Parker, Kayla Haberman, Tolulope Ojo, et al.
Cells (2025) Vol. 14, Iss. 2, pp. 80-80
Open Access

Endoplasmic Reticulum Stress and Its Role in Metabolic Reprogramming of Cancer
Salvatore Zarrella, Maria Rosaria Miranda, Verdiana Covelli, et al.
Metabolites (2025) Vol. 15, Iss. 4, pp. 221-221
Open Access

Irradiation Activates MZF1 to Inhibit miR-541-5p Expression and Promote Epithelial-Mesenchymal Transition (EMT) in Radiation-Induced Pulmonary Fibrosis (RIPF) by Upregulating Slug
Xinxin Liang, Ziyan Yan, Ping Wang, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11309-11309
Open Access | Times Cited: 23

Shooting at Moving and Hidden Targets—Tumour Cell Plasticity and the Notch Signalling Pathway in Head and Neck Squamous Cell Carcinomas
Joanna Kałafut, Arkadiusz Czerwonka, Alinda Anameriç, et al.
Cancers (2021) Vol. 13, Iss. 24, pp. 6219-6219
Open Access | Times Cited: 23

USP22 Contributes to Chemoresistance, Stemness, and EMT Phenotype of Triple-Negative Breast Cancer Cells by egulating the Warburg Effect via c-Myc Deubiquitination
Jie Li, Runfang Gao, Jing Zhang
Clinical Breast Cancer (2022) Vol. 23, Iss. 2, pp. 162-175
Closed Access | Times Cited: 12

Fatty Acid Metabolites and the Tumor Microenvironment as Potent Regulators of Cancer Stem Cell Signaling
Toshiyuki Murai, Satoru Matsuda
Metabolites (2023) Vol. 13, Iss. 6, pp. 709-709
Open Access | Times Cited: 7

Analysis and experimental validation of fatty acid metabolism-related genes prostacyclin synthase (PTGIS) in endometrial cancer
Bo Wang, Shuwen Ge, Zihao Wang, et al.
Aging (2023) Vol. 15, Iss. 19, pp. 10322-10346
Open Access | Times Cited: 7

Prolyl 4-hydroxylase P4HA1 Mediates the Interplay Between Glucose Metabolism and Stemness in Pancreatic Cancer Cells
Xiaopeng Cao, Yi Cao, Hui Zhao, et al.
Current Stem Cell Research & Therapy (2022) Vol. 18, Iss. 5, pp. 712-719
Closed Access | Times Cited: 11

Role of Intra- and Extracellular Lipid Signals in Cancer Stemness and Potential Therapeutic Strategy
Jianming Hu, Leyi Zhang, Wuzhen Chen, et al.
Frontiers in Pharmacology (2021) Vol. 12
Open Access | Times Cited: 11

Transcriptomics and Metabolomics Identify Drug Resistance of Dormant Cell in Colorectal Cancer
Lang Xie, Renli Huang, Hongyun Huang, et al.
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 7

Exosomal noncoding RNAs: decoding their role in thyroid cancer progression
Weiming Sun, Chenjun Jiang, Qianqian Liu, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 1

Glioblastoma Stem-Like Cells (GSCs) with Mesenchymal Signature: Lipid Profiles of Mobile Lipids Obtained with MRS before and after Radio/Chemical Treatments
Sveva Grande, Alessandra Palma, Anna Maria Luciani, et al.
Biomolecules (2022) Vol. 12, Iss. 8, pp. 1051-1051
Open Access | Times Cited: 3

Long-term 1,2-dimethylhydrazine triggers pathological remodeling of colon mucosa through repression of sestrin2, nuclear factor (erythroid-derived 2)-like 2, and sirtuin4 stimulating mitochondrial stress and metabolic reprogramming
Bader-Edine Allal, Abdelkader Bounaama, Dany Silva, et al.
Naunyn-Schmiedeberg s Archives of Pharmacology (2023) Vol. 396, Iss. 6, pp. 1291-1307
Closed Access | Times Cited: 1

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