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:

YAP/TAZ as therapeutic targets in cancer
Francesca Zanconato, Giusy Battilana, Michelangelo Cordenonsi, et al.
Current Opinion in Pharmacology (2016) Vol. 29, pp. 26-33
Open Access | Times Cited: 204

Showing 1-25 of 204 citing articles:

Mechanobiology of YAP and TAZ in physiology and disease
Tito Panciera, Luca Azzolin, Michelangelo Cordenonsi, et al.
Nature Reviews Molecular Cell Biology (2017) Vol. 18, Iss. 12, pp. 758-770
Open Access | Times Cited: 1096

Signaling pathways in cancer-associated fibroblasts and targeted therapy for cancer
Fanglong Wu, Jin Yang, Junjiang Liu, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 459

The Hippo Signaling Network and Its Biological Functions
Jyoti R. Misra, Kenneth D. Irvine
Annual Review of Genetics (2018) Vol. 52, Iss. 1, pp. 65-87
Open Access | Times Cited: 400

Hippo Pathway in Cancer: Aberrant Regulation and Therapeutic Opportunities
Philamer Calses, James J. Crawford, Jennie R. Lill, et al.
Trends in cancer (2019) Vol. 5, Iss. 5, pp. 297-307
Open Access | Times Cited: 375

YAP and TAZ: a signalling hub of the tumour microenvironment
Francesca Zanconato, Michelangelo Cordenonsi, Stefano Piccolo
Nature reviews. Cancer (2019) Vol. 19, Iss. 8, pp. 454-464
Closed Access | Times Cited: 315

Mechanotransduction in tumor progression: The dark side of the force
Florence Broders‐Bondon, Thanh Huong Nguyen Ho-Bouldoires, Manuel Fernández Sánchez, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 5, pp. 1571-1587
Open Access | Times Cited: 281

Targeting FAK in anticancer combination therapies
John C. Dawson, Alan Serrels, Dwayne G. Stupack, et al.
Nature reviews. Cancer (2021) Vol. 21, Iss. 5, pp. 313-324
Open Access | Times Cited: 263

Analysis of the role of the Hippo pathway in cancer
Yanyan Han
Journal of Translational Medicine (2019) Vol. 17, Iss. 1
Open Access | Times Cited: 260

WNT Signaling in Tumors: The Way to Evade Drugs and Immunity
Elena Martín‐Orozco, Ana Sanchez-Fernandez, Irene Ortiz-Parra, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 237

Regulation of heterogeneous cancer-associated fibroblasts: the molecular pathology of activated signaling pathways
Go J. Yoshida
Journal of Experimental & Clinical Cancer Research (2020) Vol. 39, Iss. 1
Open Access | Times Cited: 222

Platelets reduce anoikis and promote metastasis by activating YAP1 signaling
Monika Haemmerle, Morgan Taylor, Tony Gutschner, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 214

Phenotypic Plasticity of Invasive Edge Glioma Stem-like Cells in Response to Ionizing Radiation
Mutsuko Minata, Alessandra Audia, Junfeng Shi, et al.
Cell Reports (2019) Vol. 26, Iss. 7, pp. 1893-1905.e7
Open Access | Times Cited: 193

Cell plasticity in epithelial homeostasis and tumorigenesis
Júlia Varga, Florian R. Greten
Nature Cell Biology (2017) Vol. 19, Iss. 10, pp. 1133-1141
Closed Access | Times Cited: 188

Melatonin and Hippo Pathway: Is There Existing Cross-Talk?
Federica Lo Sardo, Paola Muti, Giovanni Blandino, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 9, pp. 1913-1913
Open Access | Times Cited: 177

Cancer cell plasticity: Impact on tumor progression and therapy response
Victoria da Silva-Diz, Laura Lorenzo-Sanz, Adrià Bernat-Peguera, et al.
Seminars in Cancer Biology (2018) Vol. 53, pp. 48-58
Closed Access | Times Cited: 175

Selective YAP/TAZ inhibition in fibroblasts via dopamine receptor D1 agonism reverses fibrosis
Andrew J. Haak, Enis Kostallari, Delphine Sicard, et al.
Science Translational Medicine (2019) Vol. 11, Iss. 516
Open Access | Times Cited: 175

Systems biology-based investigation of cooperating microRNAs as monotherapy or adjuvant therapy in cancer
Xin Lai, Martin Eberhardt, Ulf Schmitz, et al.
Nucleic Acids Research (2019) Vol. 47, Iss. 15, pp. 7753-7766
Open Access | Times Cited: 159

The Extracellular Matrix: Its Composition, Function, Remodeling, and Role in Tumorigenesis
Kevin Dzobo, Collet Dandara
Biomimetics (2023) Vol. 8, Iss. 2, pp. 146-146
Open Access | Times Cited: 76

Drugs Targeting p53 Mutations with FDA Approval and in Clinical Trials
Shigeto Nishikawa, Tomoo Iwakuma
Cancers (2023) Vol. 15, Iss. 2, pp. 429-429
Open Access | Times Cited: 64

A p53 Super-tumor Suppressor Reveals a Tumor Suppressive p53-Ptpn14-Yap Axis in Pancreatic Cancer
Stephano S. Mello, Liz J. Valente, Nitin Raj, et al.
Cancer Cell (2017) Vol. 32, Iss. 4, pp. 460-473.e6
Open Access | Times Cited: 165

YAP/TAZ Activation as a Target for Treating Metastatic Cancer
Janine Warren, Yuxuan Xiao, John M. Lamar
Cancers (2018) Vol. 10, Iss. 4, pp. 115-115
Open Access | Times Cited: 151

Cancer-associated adipocytes: emerging supporters in breast cancer
Chongru Zhao, Min Wu, Ning Zeng, et al.
Journal of Experimental & Clinical Cancer Research (2020) Vol. 39, Iss. 1
Open Access | Times Cited: 130

Matrix stiffness modulates the activity of MMP-9 and TIMP-1 in hepatic stellate cells to perpetuate fibrosis
Dariusz Lachowski, Ernesto Cortés, Alistair Rice, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 125

Insight into Mechanobiology: How Stem Cells Feel Mechanical Forces and Orchestrate Biological Functions
Chiara Argentati, Francesco Morena, Ilaria Tortorella, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 21, pp. 5337-5337
Open Access | Times Cited: 110

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