Richard O. Hynes

99.3k total citations · 36 hit papers
365 papers, 73.6k citations indexed

About

Richard O. Hynes is a scholar working on Immunology and Allergy, Molecular Biology and Cell Biology. According to data from OpenAlex, Richard O. Hynes has authored 365 papers receiving a total of 73.6k indexed citations (citations by other indexed papers that have themselves been cited), including 217 papers in Immunology and Allergy, 172 papers in Molecular Biology and 95 papers in Cell Biology. Recurrent topics in Richard O. Hynes's work include Cell Adhesion Molecules Research (217 papers), Cellular Mechanics and Interactions (66 papers) and Protease and Inhibitor Mechanisms (55 papers). Richard O. Hynes is often cited by papers focused on Cell Adhesion Molecules Research (217 papers), Cellular Mechanics and Interactions (66 papers) and Protease and Inhibitor Mechanisms (55 papers). Richard O. Hynes collaborates with scholars based in United States, United Kingdom and France. Richard O. Hynes's co-authors include Helen Rayburn, Alexandra Naba, Denisa D. Wagner, Jack Lawler, John W. Tamkun, Kenneth M. Yamada, Joy T. Yang, Antonia T. Destree, Charles A. Whittaker and Jun‐Lin Guan and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Richard O. Hynes

362 papers receiving 71.2k citations

Hit Papers

Integrins: Versatility, m... 1973 2026 1990 2008 1992 2002 2005 2000 1982 2.5k 5.0k 7.5k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Richard O. Hynes United States 132 33.4k 31.3k 18.6k 11.8k 11.4k 365 73.6k
Erkki Ruoslahti United States 152 43.8k 1.3× 31.7k 1.0× 18.7k 1.0× 9.2k 0.8× 13.2k 1.2× 466 91.3k
Kenneth M. Yamada United States 140 28.8k 0.9× 24.4k 0.8× 25.4k 1.4× 5.9k 0.5× 9.3k 0.8× 701 71.9k
David A. Cheresh United States 109 28.3k 0.8× 18.3k 0.6× 7.6k 0.4× 6.5k 0.6× 10.6k 0.9× 245 48.7k
Rupert Timpl Germany 124 20.4k 0.6× 22.7k 0.7× 14.4k 0.8× 4.2k 0.4× 8.3k 0.7× 526 49.4k
Timothy A. Springer United States 153 26.0k 0.8× 43.0k 1.4× 10.6k 0.6× 43.4k 3.7× 4.8k 0.4× 536 91.5k
Mark H. Ginsberg United States 108 16.5k 0.5× 21.4k 0.7× 12.8k 0.7× 6.2k 0.5× 3.9k 0.3× 359 41.6k
Judah Folkman United States 141 62.8k 1.9× 10.9k 0.3× 10.0k 0.5× 8.3k 0.7× 29.5k 2.6× 395 105.2k
Zena Werb United States 151 45.6k 1.4× 12.3k 0.4× 11.5k 0.6× 18.5k 1.6× 33.6k 2.9× 416 110.4k
Joan S. Brugge United States 111 25.6k 0.8× 7.4k 0.2× 9.5k 0.5× 5.2k 0.4× 5.1k 0.4× 259 41.9k
Martin A. Schwartz United States 107 22.6k 0.7× 12.4k 0.4× 19.2k 1.0× 4.4k 0.4× 4.0k 0.3× 409 46.8k

Countries citing papers authored by Richard O. Hynes

Since Specialization
Citations

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

Fields of papers citing papers by Richard O. Hynes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard O. Hynes. 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 Richard O. Hynes. The network helps show where Richard O. Hynes may publish in the future.

Co-authorship network of co-authors of Richard O. Hynes

This figure shows the co-authorship network connecting the top 25 collaborators of Richard O. Hynes. A scholar is included among the top collaborators of Richard O. Hynes 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 Richard O. Hynes. Richard O. Hynes 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.
Tian, Chenxi, Daniel Öhlund, Steffen Rickelt, et al.. (2020). Cancer Cell–Derived Matrisome Proteins Promote Metastasis in Pancreatic Ductal Adenocarcinoma. Cancer Research. 80(7). 1461–1474. 128 indexed citations
2.
Hebert, Jess D., Samuel A. Myers, Alexandra Naba, et al.. (2020). Proteomic Profiling of the ECM of Xenograft Breast Cancer Metastases in Different Organs Reveals Distinct Metastatic Niches. Cancer Research. 80(7). 1475–1485. 90 indexed citations
3.
Rickelt, Steffen, Miyeko Mana, Charles A. Whittaker, et al.. (2019). Agrin in the Muscularis Mucosa Serves as a Biomarker Distinguishing Hyperplastic Polyps from Sessile Serrated Lesions. Clinical Cancer Research. 26(6). 1277–1287. 11 indexed citations
4.
Li, Ran, Jess D. Hebert, Hao Xing, et al.. (2016). Macrophage-Secreted TNFα and TGFβ1 Influence Migration Speed and Persistence of Cancer Cells in 3D Tissue Culture via Independent Pathways. Cancer Research. 77(2). 279–290. 78 indexed citations
5.
Oudin, Madeleine J., Oliver Jonas, Tatsiana Kosciuk, et al.. (2016). Tumor Cell–Driven Extracellular Matrix Remodeling Drives Haptotaxis during Metastatic Progression. Cancer Discovery. 6(5). 516–531. 155 indexed citations
6.
Chen, Michelle B., John M. Lamar, Ran Li, Richard O. Hynes, & Roger D. Kamm. (2016). Elucidation of the Roles of Tumor Integrin β1 in the Extravasation Stage of the Metastasis Cascade. Cancer Research. 76(9). 2513–2524. 133 indexed citations
7.
Hebert, Jess D., Alexandra Boussommier-Calleja, Richard O. Hynes, et al.. (2016). Macrophage-Secreted TNFα and TGFβ1 Influence Migration Speed and Persistence of Cancer Cells in 3D Tissue Culture via Independent Pathways. DSpace@MIT (Massachusetts Institute of Technology). 22 indexed citations
8.
Heilmann, Silja, Kajan Ratnakumar, Erin M. Langdon, et al.. (2015). A Quantitative System for Studying Metastasis Using Transparent Zebrafish. Cancer Research. 75(20). 4272–4282. 84 indexed citations
9.
Yang, Liquan, Guangchun Chen, Glynis Scott, et al.. (2011). GPR56 Regulates VEGF Production and Angiogenesis during Melanoma Progression. Cancer Research. 71(16). 5558–5568. 3 indexed citations
10.
Liu, Hui, Shao‐En Ong, Kwabena Badu-Nkansah, et al.. (2011). CUB-domain–containing protein 1 (CDCP1) activates Src to promote melanoma metastasis. Proceedings of the National Academy of Sciences. 108(4). 1379–1384. 79 indexed citations
11.
Xu, Lei, Shahinoor Begum, Marc Barry, et al.. (2010). GPR56 Plays varying roles in endogenous cancer progression. Clinical & Experimental Metastasis. 27(4). 241–249. 2 indexed citations
12.
Sobolev, Olga, Patrick Stern, Adam Lacy‐Hulbert, & Richard O. Hynes. (2009). Natural Killer Cells Require Selectins for Suppression of Subcutaneous Tumors. Cancer Research. 69(6). 2531–2539. 14 indexed citations
13.
Xu, Lei, Steven S. Shen, Yujin Hoshida, et al.. (2008). Gene Expression Changes in an Animal Melanoma Model Correlate with Aggressiveness of Human Melanoma Metastases. Molecular Cancer Research. 6(5). 760–769. 195 indexed citations
14.
Hynes, Richard O.. (2007). Abstract. Journal of Thrombosis and Haemostasis. 5. PLEN–M3.
15.
Lacy‐Hulbert, Adam, Aileen M. Smith, Hamid Tissire, et al.. (2007). Ulcerative colitis and autoimmunity induced by loss of myeloid αv integrins. Proceedings of the National Academy of Sciences. 104(40). 15823–15828. 181 indexed citations
16.
Xu, Lei & Richard O. Hynes. (2007). GPR56 and TG2: Possible Roles in Suppression of Tumor Growth by the Microenvironment. Cell Cycle. 6(2). 160–165. 45 indexed citations
17.
Xu, Lei, et al.. (2006). GPR56, an atypical G protein-coupled receptor, binds tissue transglutaminase, TG2, and inhibits melanoma tumor growth and metastasis. Proceedings of the National Academy of Sciences. 103(24). 9023–9028. 227 indexed citations
18.
Lindenbach, Brett D., Matthew J. Evans, Andrew J. Syder, et al.. (2005). Complete Replication of Hepatitis C Virus in Cell Culture. Science. 309(5734). 623–626. 1850 indexed citations breakdown →
19.
Wong, Sunny Y., Herbert Haack, Denise Crowley, et al.. (2005). Tumor-Secreted Vascular Endothelial Growth Factor-C Is Necessary for Prostate Cancer Lymphangiogenesis, but Lymphangiogenesis Is Unnecessary for Lymph Node Metastasis. Cancer Research. 65(21). 9789–9798. 129 indexed citations
20.
Ni, Heyu, Peter S.T. Yuen, Jane E. Trevithick, et al.. (2003). Plasma fibronectin promotes thrombus growth and stability in injured arterioles. Proceedings of the National Academy of Sciences. 100(5). 2415–2419. 165 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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