Thomas E. Carey

71.0k total citations · 3 hit papers
328 papers, 14.1k citations indexed

About

Thomas E. Carey is a scholar working on Molecular Biology, Oncology and Otorhinolaryngology. According to data from OpenAlex, Thomas E. Carey has authored 328 papers receiving a total of 14.1k indexed citations (citations by other indexed papers that have themselves been cited), including 142 papers in Molecular Biology, 125 papers in Oncology and 99 papers in Otorhinolaryngology. Recurrent topics in Thomas E. Carey's work include Head and Neck Cancer Studies (92 papers), Cancer-related Molecular Pathways (33 papers) and Head and Neck Surgical Oncology (33 papers). Thomas E. Carey is often cited by papers focused on Head and Neck Cancer Studies (92 papers), Cancer-related Molecular Pathways (33 papers) and Head and Neck Surgical Oncology (33 papers). Thomas E. Carey collaborates with scholars based in United States, Japan and Finland. Thomas E. Carey's co-authors include Carol R. Bradford, Gregory T. Wolf, Mark E. Prince, Douglas B. Chepeha, Jonathan B. McHugh, Avraham Eisbruch, Francis P. Worden, Kenneth D. McClatchey, Nisha J. D’Silva and Bhavna Kumar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Thomas E. Carey

325 papers receiving 13.8k citations

Hit Papers

Targeted Gold Nanoparticl... 1976 2026 1992 2009 2008 2008 1976 200 400 600

Author Peers

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

Author Last Decade Papers Cites
Thomas E. Carey 6.2k 5.0k 3.6k 2.6k 2.5k 328 14.1k
Jeffrey N. Myers 6.5k 1.1× 6.5k 1.3× 3.6k 1.0× 2.9k 1.1× 2.7k 1.1× 359 15.7k
Reidar Grénman 5.4k 0.9× 5.0k 1.0× 2.5k 0.7× 2.8k 1.1× 3.4k 1.4× 356 13.7k
Ruud H. Brakenhoff 6.2k 1.0× 6.0k 1.2× 5.4k 1.5× 2.9k 1.1× 3.8k 1.5× 242 15.7k
Frans C. S. Ramaekers 7.1k 1.2× 2.4k 0.5× 487 0.1× 1.7k 0.7× 1.1k 0.4× 240 13.4k
Norman J. Maitland 5.2k 0.8× 4.6k 0.9× 270 0.1× 780 0.3× 2.2k 0.9× 214 11.4k
Alan L. Ho 4.2k 0.7× 2.8k 0.6× 494 0.1× 1.7k 0.7× 518 0.2× 191 8.2k
Philippe Birembaut 3.6k 0.6× 3.0k 0.6× 290 0.1× 1.7k 0.7× 2.5k 1.0× 200 9.9k
L. Clifton Stephens 3.5k 0.6× 2.4k 0.5× 319 0.1× 1.3k 0.5× 917 0.4× 192 8.8k
Anil K. Rustgi 9.9k 1.6× 9.6k 1.9× 227 0.1× 4.8k 1.9× 4.1k 1.7× 302 20.2k
Jean A. Laissue 1.7k 0.3× 2.7k 0.5× 443 0.1× 843 0.3× 938 0.4× 194 9.4k

Countries citing papers authored by Thomas E. Carey

Since Specialization
Citations

This map shows the geographic impact of Thomas E. Carey'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 Thomas E. Carey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas E. Carey more than expected).

Fields of papers citing papers by Thomas E. Carey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Carey. 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 Thomas E. Carey. The network helps show where Thomas E. Carey may publish in the future.

Co-authorship network of co-authors of Thomas E. Carey

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Carey. A scholar is included among the top collaborators of Thomas E. Carey 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 Thomas E. Carey. Thomas E. Carey 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.
Koehl, Bérengère, Cédric Vrignaud, Thankam Nair, et al.. (2023). Lack of the human choline transporter‐like protein SLC44A2 causes hearing impairment and a rare red blood phenotype. EMBO Molecular Medicine. 15(3). e16320–e16320. 6 indexed citations
2.
Brouwer, Andrew F., Heather M. Walline, Yan Kwan Lau, et al.. (2022). Incidence and clearance of oral and cervicogenital HPV infection: longitudinal analysis of the MHOC cohort study. BMJ Open. 12(1). e056502–e056502. 12 indexed citations
3.
Brouwer, Andrew F., Heather M. Walline, Thomas E. Carey, et al.. (2022). Understanding the mechanisms of HPV-related carcinogenesis: Implications for cell cycle dynamics. Journal of Theoretical Biology. 551-552. 111235–111235. 5 indexed citations
4.
Mastrangelo, Michael A., Sara Ture, Charles O. Smith, et al.. (2020). The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function. Nature Communications. 11(1). 3479–3479. 56 indexed citations
5.
Nisa, Lluís, Paola Francica, Roland Giger, et al.. (2019). Targeting the MET Receptor Tyrosine Kinase as a Strategy for Radiosensitization in Locoregionally Advanced Head and Neck Squamous Cell Carcinoma. Molecular Cancer Therapeutics. 19(2). 614–626. 11 indexed citations
6.
Tan, Yee Sun, Kanokwan Sansanaphongpricha, Yuying Xie, et al.. (2018). Mitigating SOX2-potentiated Immune Escape of Head and Neck Squamous Cell Carcinoma with a STING-inducing Nanosatellite Vaccine. Clinical Cancer Research. 24(17). 4242–4255. 124 indexed citations
7.
Nisa, Lluís, David Barras, Michaela Medová, et al.. (2018). Comprehensive Genomic Profiling of Patient-matched Head and Neck Cancer Cells: A Preclinical Pipeline for Metastatic and Recurrent Disease. Molecular Cancer Research. 16(12). 1912–1926. 23 indexed citations
8.
Eisenberg, Marisa C., Andrew F. Brouwer, Heather M. Walline, et al.. (2018). Dynamics and Determinants of HPV Infection: The Michigan HPV and Oropharyngeal Cancer (M-HOC) Study. BMJ Open. 8(10). e021618–e021618. 9 indexed citations
9.
Koneva, Lada A., Yanxiao Zhang, Shama Virani, et al.. (2017). HPV Integration in HNSCC Correlates with Survival Outcomes, Immune Response Signatures, and Candidate Drivers. Molecular Cancer Research. 16(1). 90–102. 147 indexed citations
10.
Gleber‐Netto, Frederico O., Mei Zhao, Sanchit Trivedi, et al.. (2017). Distinct pattern of TP53 mutations in human immunodeficiency virus–related head and neck squamous cell carcinoma. Cancer. 124(1). 84–94. 18 indexed citations
11.
Zhang, Yanxiao, Lada A. Koneva, Shama Virani, et al.. (2016). Subtypes of HPV-Positive Head and Neck Cancers Are Associated with HPV Characteristics, Copy Number Alterations, PIK3CA Mutation, and Pathway Signatures. Clinical Cancer Research. 22(18). 4735–4745. 110 indexed citations
12.
Walline, Heather M., Christine M. Komarck, Jonathan B. McHugh, et al.. (2016). Genomic Integration of High-Risk HPV Alters Gene Expression in Oropharyngeal Squamous Cell Carcinoma. Molecular Cancer Research. 14(10). 941–952. 41 indexed citations
13.
Vitale‐Cross, Lynn, Daniel Martı́n, Abraham Schneider, et al.. (2015). Prevention of Tumor Growth Driven by PIK3CA and HPV Oncogenes by Targeting mTOR Signaling with Metformin in Oral Squamous Carcinomas Expressing OCT3. Cancer Prevention Research. 8(3). 197–207. 48 indexed citations
14.
Udager, Aaron M., Delphine Rolland, Jonathan B. McHugh, et al.. (2015). High-Frequency Targetable EGFR Mutations in Sinonasal Squamous Cell Carcinomas Arising from Inverted Sinonasal Papilloma. Cancer Research. 75(13). 2600–2606. 97 indexed citations
15.
Zhao, Mei, Daisuke Sano, Curtis R. Pickering, et al.. (2011). Assembly and Initial Characterization of a Panel of 85 Genomically Validated Cell Lines from Diverse Head and Neck Tumor Sites. Clinical Cancer Research. 17(23). 7248–7264. 224 indexed citations
16.
Feng, Felix Y., Hyungjin Myra Kim, Teresa Lyden, et al.. (2010). Intensity-Modulated Chemoradiotherapy Aiming to Reduce Dysphagia in Patients With Oropharyngeal Cancer: Clinical and Functional Results. Journal of Clinical Oncology. 28(16). 2732–2738. 261 indexed citations
17.
Misawa, Kiyoshi, Yo Ueda, Takeharu Kanazawa, et al.. (2008). Epigenetic Inactivation of Galanin Receptor 1 in Head and Neck Cancer. Clinical Cancer Research. 14(23). 7604–7613. 56 indexed citations
18.
Shangary, Sanjeev, Ke Ding, Su Qiu, et al.. (2008). Reactivation of p53 by a specific MDM2 antagonist (MI-43) leads to p21-mediated cell cycle arrest and selective cell death in colon cancer. Molecular Cancer Therapeutics. 7(6). 1533–1542. 75 indexed citations
19.
Verhaegen, Monique, Joshua A. Bauer, Cristina Martín de la Vega, et al.. (2006). A Novel BH3 Mimetic Reveals a Mitogen-Activated Protein Kinase–Dependent Mechanism of Melanoma Cell Death Controlled by p53 and Reactive Oxygen Species. Cancer Research. 66(23). 11348–11359. 117 indexed citations
20.
Wahl, Richard L., Kathryn A. Kimmel, William H. Beierwaltes, & Thomas E. Carey. (1987). Radioimmunodiagnosis of Human-Derived Squamous Cell Carcinoma. Hybridoma. 6(2). 111–119. 14 indexed citations

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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