Timothy Hoey

17.2k total citations · 5 hit papers
89 papers, 13.6k citations indexed

About

Timothy Hoey is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Timothy Hoey has authored 89 papers receiving a total of 13.6k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 38 papers in Oncology and 17 papers in Cancer Research. Recurrent topics in Timothy Hoey's work include Genomics and Chromatin Dynamics (16 papers), Cancer Cells and Metastasis (15 papers) and Developmental Biology and Gene Regulation (12 papers). Timothy Hoey is often cited by papers focused on Genomics and Chromatin Dynamics (16 papers), Cancer Cells and Metastasis (15 papers) and Developmental Biology and Gene Regulation (12 papers). Timothy Hoey collaborates with scholars based in United States, France and Italy. Timothy Hoey's co-authors include Michael Levine, Ya‐Lin Sun, Robert Tjian, Michael J. Grusby, Brian David Dynlacht, Austin Gurney, Mark H. Kaplan, Laurie H. Glimcher, Xiang Xu and Michael F. Clarke and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Timothy Hoey

88 papers receiving 13.3k citations

Hit Papers

Phenotypic characterizati... 1991 2026 2002 2014 2007 1996 2007 1991 1993 500 1000 1.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Timothy Hoey 9.1k 4.6k 3.2k 2.0k 1.7k 89 13.6k
Minoru Takata 9.8k 1.1× 3.6k 0.8× 2.2k 0.7× 2.7k 1.3× 1.3k 0.8× 292 14.0k
Bohdan Wasylyk 9.1k 1.0× 3.3k 0.7× 1.6k 0.5× 1.8k 0.9× 2.1k 1.2× 151 12.5k
Bernhard Lüscher 9.1k 1.0× 4.9k 1.1× 3.0k 0.9× 1.1k 0.5× 1.0k 0.6× 191 14.4k
Richard Breathnach 9.2k 1.0× 2.5k 0.6× 2.4k 0.8× 2.1k 1.0× 2.4k 1.4× 81 14.2k
Erwin G. Van Meir 9.2k 1.0× 3.9k 0.8× 2.9k 0.9× 4.7k 2.3× 1.4k 0.8× 171 16.2k
Jonathan D. Licht 14.1k 1.6× 2.4k 0.5× 2.8k 0.9× 1.8k 0.9× 2.1k 1.2× 255 17.9k
Douglas C. Dean 8.4k 0.9× 4.6k 1.0× 1.4k 0.4× 1.9k 0.9× 1.2k 0.7× 107 11.9k
Zora Modrušan 10.6k 1.2× 4.9k 1.1× 5.0k 1.6× 3.6k 1.8× 1.2k 0.7× 166 19.7k
Jun Qin 12.1k 1.3× 3.7k 0.8× 1.4k 0.4× 1.8k 0.9× 1.6k 1.0× 120 14.8k
Scott W. Hiebert 14.1k 1.6× 5.4k 1.2× 2.5k 0.8× 1.8k 0.9× 2.2k 1.4× 176 19.1k

Countries citing papers authored by Timothy Hoey

Since Specialization
Citations

This map shows the geographic impact of Timothy Hoey's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Timothy Hoey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Timothy Hoey more than expected).

Fields of papers citing papers by Timothy Hoey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Timothy Hoey. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Timothy Hoey. The network helps show where Timothy Hoey may publish in the future.

Co-authorship network of co-authors of Timothy Hoey

This figure shows the co-authorship network connecting the top 25 collaborators of Timothy Hoey. A scholar is included among the top collaborators of Timothy Hoey based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Timothy Hoey. Timothy Hoey is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ranjbarvaziri, Sara, Amara Greer-Short, Farshad Farshidfar, et al.. (2024). Targeting HDAC6 to treat heart failure with preserved ejection fraction in mice. Nature Communications. 15(1). 1352–1352. 24 indexed citations
2.
Farshidfar, Farshad, Sara Ranjbarvaziri, Amara Greer-Short, et al.. (2024). Co-Administration of Inhibitors of HDAC6 and SGLT2 in Murine HFpEF Models Results in Additive Improvements in Cardiac Structural and Functional Measures. Journal of Cardiac Failure. 30(1). 164–164. 1 indexed citations
3.
Lim, Gah‐Hyun, Timothy Hoey, Shifeng Zhu, et al.. (2018). COP1, a negative regulator of photomorphogenesis, positively regulates plant disease resistance via double-stranded RNA binding proteins. PLoS Pathogens. 14(3). e1006894–e1006894. 28 indexed citations
4.
Fischer, Marcus, Vincent Yeung, Fiore Cattaruzza, et al.. (2017). RSPO3 antagonism inhibits growth and tumorigenicity in colorectal tumors harboring common Wnt pathway mutations. Scientific Reports. 7(1). 15270–15270. 37 indexed citations
5.
Lim, Jing Shan, Alvaro Ibaseta, Marcus Fischer, et al.. (2017). Intratumoural heterogeneity generated by Notch signalling promotes small-cell lung cancer. Nature. 545(7654). 360–364. 311 indexed citations
6.
Yen, Wan-Ching, Marcus Fischer, Fumiko Axelrod, et al.. (2015). Targeting Notch Signaling with a Notch2/Notch3 Antagonist (Tarextumab) Inhibits Tumor Growth and Decreases Tumor-Initiating Cell Frequency. Clinical Cancer Research. 21(9). 2084–2095. 195 indexed citations
7.
Pastò, Anna, Valentina Serafin, Giorgia Pilotto, et al.. (2014). NOTCH3 Signaling Regulates MUSASHI-1 Expression in Metastatic Colorectal Cancer Cells. Cancer Research. 74(7). 2106–2118. 49 indexed citations
8.
Minuzzo, Sonia, Valentina Agnusdei, Irene Pusceddu, et al.. (2014). DLL4 regulates NOTCH signaling and growth of T acute lymphoblastic leukemia cells in NOD/SCID mice. Carcinogenesis. 36(1). 115–121. 28 indexed citations
9.
Zhang, Yaqing, John P. Morris, Wei Yan, et al.. (2013). Canonical Wnt Signaling Is Required for Pancreatic Carcinogenesis. Cancer Research. 73(15). 4909–4922. 152 indexed citations
10.
Fischer, Marcus, Mark J. Hynes, Jingjiang Wu, et al.. (2012). Anti-DLL4 Has Broad Spectrum Activity in Pancreatic Cancer Dependent on Targeting DLL4-Notch Signaling in Both Tumor and Vasculature Cells. Clinical Cancer Research. 18(19). 5374–5386. 58 indexed citations
11.
Gurney, Austin & Timothy Hoey. (2011). Anti-DLL4, a cancer therapeutic with multiple mechanisms of action. PubMed. 3(1). 18–18. 29 indexed citations
12.
Fischer, Marcus, Wan-Ching Yen, Ann M. Kapoun, et al.. (2010). Anti-DLL4 Inhibits Growth and Reduces Tumor-Initiating Cell Frequency in Colorectal Tumors with Oncogenic KRAS Mutations. Cancer Research. 71(5). 1520–1525. 100 indexed citations
13.
Hoey, Timothy, Wan-Ching Yen, Fumiko Axelrod, et al.. (2009). DLL4 Blockade Inhibits Tumor Growth and Reduces Tumor-Initiating Cell Frequency. Cell stem cell. 5(2). 168–177. 318 indexed citations
14.
Horst, Edward H. van der, Lawrence Chinn, Min Wang, et al.. (2009). Discovery of Fully Human Anti-MET Monoclonal Antibodies with Antitumor Activity against Colon Cancer Tumor Models In Vivo. Neoplasia. 11(4). 355–IN5. 48 indexed citations
15.
Harrison, Martin, Jing Li, Yan Degenhardt, Timothy Hoey, & Scott Powers. (2004). Wip1-deficient mice are resistant to common cancer genes. Trends in Molecular Medicine. 10(8). 359–361. 47 indexed citations
16.
Mu, David, Liyun Chen, Xiping Zhang, et al.. (2003). Genomic amplification and oncogenic properties of the KCNK9 potassium channel gene. Cancer Cell. 3(3). 297–302. 208 indexed citations
17.
Broxmeyer, Hal E., Heather A. Bruns, Shangming Zhang, et al.. (2002). Th1 Cells Regulate Hematopoietic Progenitor Cell Homeostasis by Production of Oncostatin M. Immunity. 16(6). 815–825. 72 indexed citations
18.
Li, Jing, Ying Yang, Peng Yue, et al.. (2002). Oncogenic properties of PPM1D located within a breast cancer amplification epicenter at 17q23. Nature Genetics. 31(2). 133–134. 207 indexed citations
19.
Ranger, Ann, Martin R. Hodge, Ellen M. Gravallese, et al.. (1998). Delayed Lymphoid Repopulation with Defects in IL-4–Driven Responses Produced by Inactivation of NF-ATc. Immunity. 8(1). 125–134. 253 indexed citations
20.
Dynlacht, Brian David, Timothy Hoey, & Robert Tjian. (1991). Isolation of coactivators associated with the TATA-binding protein that mediate transcriptional activation. Cell. 66(3). 563–576. 625 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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