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:

Characterization of Hippo Pathway Components by Gene Inactivation
Steven W. Plouffe, Zhipeng Meng, Kimberly C. Lin, et al.
Molecular Cell (2016) Vol. 64, Iss. 5, pp. 993-1008
Open Access | Times Cited: 248

Showing 1-25 of 248 citing articles:

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: 1042

The Hippo Signaling Pathway in Development and Disease
Yonggang Zheng, Duojia Pan
Developmental Cell (2019) Vol. 50, Iss. 3, pp. 264-282
Open Access | Times Cited: 720

MicroRNA therapy stimulates uncontrolled cardiac repair after myocardial infarction in pigs
Khatia Gabisonia, Giulia Prosdocimo, Giovanni Donato Aquaro, et al.
Nature (2019) Vol. 569, Iss. 7756, pp. 418-422
Open Access | Times Cited: 422

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: 352

The Hippo signalling pathway and its implications in human health and diseases
Minyang Fu, Yuan Hu, Tianxia Lan, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 332

RAP2 mediates mechanoresponses of the Hippo pathway
Zhipeng Meng, Yunjiang Qiu, Kimberly C. Lin, et al.
Nature (2018) Vol. 560, Iss. 7720, pp. 655-660
Open Access | Times Cited: 328

Phase separation of TAZ compartmentalizes the transcription machinery to promote gene expression
Yi Lu, Tiantian Wu, Orit Gutman, et al.
Nature Cell Biology (2020) Vol. 22, Iss. 4, pp. 453-464
Open Access | Times Cited: 293

Control of cellular responses to mechanical cues through YAP/TAZ regulation
Ishani Dasgupta, Dannel McCollum
Journal of Biological Chemistry (2019) Vol. 294, Iss. 46, pp. 17693-17706
Open Access | Times Cited: 265

The Hippo pathway effector proteins YAP and TAZ have both distinct and overlapping functions in the cell
Steven W. Plouffe, Kimberly C. Lin, Jerrell L. Moore, et al.
Journal of Biological Chemistry (2018) Vol. 293, Iss. 28, pp. 11230-11240
Open Access | Times Cited: 208

The Hippo pathway in cancer: YAP/TAZ and TEAD as therapeutic targets in cancer
Richard Cunningham, Carsten Gram Hansen
Clinical Science (2022) Vol. 136, Iss. 3, pp. 197-222
Open Access | Times Cited: 208

CRISPR–Cas: a tool for cancer research and therapeutics
Hao Yin, Wen Xue, Daniel G. Anderson
Nature Reviews Clinical Oncology (2019) Vol. 16, Iss. 5, pp. 281-295
Closed Access | Times Cited: 155

Lats1/2 Sustain Intestinal Stem Cells and Wnt Activation through TEAD-Dependent and Independent Transcription
Qi Li, Yang Sun, Gopala K. Jarugumilli, et al.
Cell stem cell (2020) Vol. 26, Iss. 5, pp. 675-692.e8
Open Access | Times Cited: 153

Genome-wide bidirectional CRISPR screens identify mucins as host factors modulating SARS-CoV-2 infection
Scott B. Biering, Sylvia A. Sarnik, Eleanor Wang, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1078-1089
Open Access | Times Cited: 102

Transcriptional repression of estrogen receptor alpha by YAP reveals the Hippo pathway as therapeutic target for ER+ breast cancer
Shenghong Ma, Tracy Tang, Gary D. Probst, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 96

Hepatocellular carcinoma: signaling pathways, targeted therapy, and immunotherapy
Xiaoting Luo, Xin He, Xingmei Zhang, et al.
MedComm (2024) Vol. 5, Iss. 2
Open Access | Times Cited: 33

SIRT7 promotes Hippo/YAP activation and cancer cell proliferation in hepatocellular carcinoma via suppressing MST1
Yiying Gu, Cong Ding, Tingzi Yu, et al.
Cancer Science (2024) Vol. 115, Iss. 4, pp. 1209-1223
Open Access | Times Cited: 16

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

OTUB2 Promotes Cancer Metastasis via Hippo-Independent Activation of YAP and TAZ
Zhengkui Zhang, Jinjin Du, Shuai Wang, et al.
Molecular Cell (2018) Vol. 73, Iss. 1, pp. 7-21.e7
Open Access | Times Cited: 144

SAV1 promotes Hippo kinase activation through antagonizing the PP2A phosphatase STRIPAK
Sung Jun Bae, Lisheng Ni, Adam Osinski, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 122

Role of the transcriptional coactivators YAP/TAZ in liver cancer
Shihao Zhang, Dawang Zhou
Current Opinion in Cell Biology (2019) Vol. 61, pp. 64-71
Closed Access | Times Cited: 116

Genome-scale screens identify JNK–JUN signaling as a barrier for pluripotency exit and endoderm differentiation
Qing V. Li, Gary Dixon, Nipun Verma, et al.
Nature Genetics (2019) Vol. 51, Iss. 6, pp. 999-1010
Open Access | Times Cited: 112

STRIPAK integrates upstream signals to initiate the Hippo kinase cascade
Rui Chen, Ruiling Xie, Zhipeng Meng, et al.
Nature Cell Biology (2019) Vol. 21, Iss. 12, pp. 1565-1577
Closed Access | Times Cited: 106

Common and Distinctive Functions of the Hippo Effectors Taz and Yap in Skeletal Muscle Stem Cell Function
Congshan Sun, Vanessa D. de Mello, Abdalla D. Mohamed, et al.
Stem Cells (2017) Vol. 35, Iss. 8, pp. 1958-1972
Open Access | Times Cited: 105

Common Regulatory Pathways Mediate Activity of MicroRNAs Inducing Cardiomyocyte Proliferation
Consuelo Torrini, Ryan John Cubero, Ellen Dirkx, et al.
Cell Reports (2019) Vol. 27, Iss. 9, pp. 2759-2771.e5
Open Access | Times Cited: 100

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