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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:

Regulation of the Hippo–YAP pathway by protease-activated receptors (PARs)
Jung‐Soon Mo, Fa‐Xing Yu, Rui Gong, et al.
Genes & Development (2012) Vol. 26, Iss. 19, pp. 2138-2143
Open Access | Times Cited: 267

Showing 1-25 of 267 citing articles:

Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer
Fa‐Xing Yu, Bin Zhao, Kun‐Liang Guan
Cell (2015) Vol. 163, Iss. 4, pp. 811-828
Open Access | Times Cited: 1944
The Biology of YAP/TAZ: Hippo Signaling and Beyond
Stefano Piccolo, Sirio Dupont, Michelangelo Cordenonsi
Physiological Reviews (2014) Vol. 94, Iss. 4, pp. 1287-1312
Closed Access | Times Cited: 1547
A Mechanical Checkpoint Controls Multicellular Growth through YAP/TAZ Regulation by Actin-Processing Factors
Mariaceleste Aragona, Tito Panciera, Andrea Manfrin, et al.
Cell (2013) Vol. 154, Iss. 5, pp. 1047-1059
Closed Access | Times Cited: 1481
Mechanisms of Hippo pathway regulation
Zhipeng Meng, Toshiro Moroishi, Kun‐Liang Guan
Genes & Development (2016) Vol. 30, Iss. 1, pp. 1-17
Open Access | Times Cited: 1447
The Hippo pathway: regulators and regulations
Fa‐Xing Yu, Kun‐Liang Guan
Genes & Development (2013) Vol. 27, Iss. 4, pp. 355-371
Open Access | Times Cited: 1154
The Hippo Pathway: Biology and Pathophysiology
Shenghong Ma, Zhipeng Meng, Rui Chen, et al.
Annual Review of Biochemistry (2018) Vol. 88, Iss. 1, pp. 577-604
Closed Access | Times Cited: 1029
The two faces of Hippo: targeting the Hippo pathway for regenerative medicine and cancer treatment
Randy L. Johnson, Georg Halder
Nature Reviews Drug Discovery (2013) Vol. 13, Iss. 1, pp. 63-79
Open Access | Times Cited: 839
Cellular Mechanotransduction: From Tension to Function
Fabiana De Martino, Ana Rubina Perestrelo, Vladimír Vinarský, et al.
Frontiers in Physiology (2018) Vol. 9
Open Access | Times Cited: 755
Alternative Wnt Signaling Activates YAP/TAZ
Hyun Woo Park, Young Chul Kim, Bo Yu, et al.
Cell (2015) Vol. 162, Iss. 4, pp. 780-794
Open Access | Times Cited: 616
The Hippo pathway effectors TAZ and YAP in development, homeostasis and disease
Xaralabos Varelas
Development (2014) Vol. 141, Iss. 8, pp. 1614-1626
Open Access | Times Cited: 600
The Hippo signaling pathway in stem cell biology and cancer
Jung‐Soon Mo, Hyun Woo Park, Kun‐Liang Guan
EMBO Reports (2014) Vol. 15, Iss. 6, pp. 642-656
Open Access | Times Cited: 598
Intraovarian Control of Early Folliculogenesis
Aaron J.W. Hsueh, Kazuhiro Kawamura, Yuan Cheng, et al.
Endocrine Reviews (2014) Vol. 36, Iss. 1, pp. 1-24
Open Access | Times Cited: 594
YAP regulates cell mechanics by controlling focal adhesion assembly
Giorgia Nardone, Jorge Oliver‐De La Cruz, Jan Vrbský, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 530
Hippo-Independent Activation of YAP by the GNAQ Uveal Melanoma Oncogene through a Trio-Regulated Rho GTPase Signaling Circuitry
Xiaodong Feng, María Sol Degese, Ramiro Iglesias‐Bartolomé, et al.
Cancer Cell (2014) Vol. 25, Iss. 6, pp. 831-845
Open Access | Times Cited: 519
YAP and TAZ: a nexus for Hippo signaling and beyond
Carsten Gram Hansen, Toshiro Moroishi, Kun‐Liang Guan
Trends in Cell Biology (2015) Vol. 25, Iss. 9, pp. 499-513
Open Access | Times Cited: 508
Cellular energy stress induces AMPK-mediated regulation of YAP and the Hippo pathway
Jung-Soon Mo, Zhipeng Meng, Young Chul Kim, et al.
Nature Cell Biology (2015) Vol. 17, Iss. 4, pp. 500-510
Open Access | Times Cited: 489
YAP mediates crosstalk between the Hippo and PI(3)K–TOR pathways by suppressing PTEN via miR-29
Karen Tumaneng, Karin Schlegelmilch, Ryan C. Russell, et al.
Nature Cell Biology (2012) Vol. 14, Iss. 12, pp. 1322-1329
Open Access | Times Cited: 425
Mutant Gq/11 Promote Uveal Melanoma Tumorigenesis by Activating YAP
Fa‐Xing Yu, Jing Luo, Jung‐Soon Mo, et al.
Cancer Cell (2014) Vol. 25, Iss. 6, pp. 822-830
Open Access | Times Cited: 415
Adhesion to fibronectin regulates Hippo signaling via the FAK–Src–PI3K pathway
Nam‐Gyun Kim, Barry M. Gumbiner
The Journal of Cell Biology (2015) Vol. 210, Iss. 3, pp. 503-515
Open Access | Times Cited: 376
Interplay between YAP/TAZ and Metabolism
Ja Hyun Koo, Kun‐Liang Guan
Cell Metabolism (2018) Vol. 28, Iss. 2, pp. 196-206
Open Access | Times Cited: 349
Cytokinesis Failure Triggers Hippo Tumor Suppressor Pathway Activation
Neil J. Ganem, Hauke Cornils, Shang-Yi Chiu, et al.
Cell (2014) Vol. 158, Iss. 4, pp. 833-848
Open Access | Times Cited: 348
Downstream of Mutant KRAS, the Transcription Regulator YAP Is Essential for Neoplastic Progression to Pancreatic Ductal Adenocarcinoma
Weiying Zhang, Nivedita Nandakumar, Yuhao Shi, et al.
Science Signaling (2014) Vol. 7, Iss. 324
Open Access | Times Cited: 334
Protein kinase A activates the Hippo pathway to modulate cell proliferation and differentiation
Fa‐Xing Yu, Yifan Zhang, Hyun Woo Park, et al.
Genes & Development (2013) Vol. 27, Iss. 11, pp. 1223-1232
Open Access | Times Cited: 305
Mechanical regulation of bone remodeling
Lijun Wang, Xiuling You, Lingli Zhang, et al.
Bone Research (2022) Vol. 10, Iss. 1
Open Access | Times Cited: 281
Integrin signalling regulates YAP/TAZ to control skin homeostasis
Ahmed Elbediwy, Zoé I. Vincent‐Mistiaen, Bradley Spencer‐Dene, et al.
Development (2016)
Open Access | Times Cited: 273
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