Marc A. Antonyak

5.9k total citations
76 papers, 4.5k citations indexed

About

Marc A. Antonyak is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, Marc A. Antonyak has authored 76 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 27 papers in Pulmonary and Respiratory Medicine and 21 papers in Cancer Research. Recurrent topics in Marc A. Antonyak's work include Extracellular vesicles in disease (29 papers), Blood properties and coagulation (26 papers) and MicroRNA in disease regulation (19 papers). Marc A. Antonyak is often cited by papers focused on Extracellular vesicles in disease (29 papers), Blood properties and coagulation (26 papers) and MicroRNA in disease regulation (19 papers). Marc A. Antonyak collaborates with scholars based in United States, Japan and India. Marc A. Antonyak's co-authors include Richard A. Cerione, Bo Li, Joseph E. Druso, Kristin F. Wilson, Jian Zhang, Lindsey K. Boroughs, Jason E. Boehm, Jared L. Johnson, Arash Latifkar and Kirsten L. Bryant 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

Marc A. Antonyak

75 papers receiving 4.5k citations

Peers

Marc A. Antonyak
Antonino Passaniti United States
Peter Oettgen United States
Balaji Krishnamachary United States
Colin Nixon United Kingdom
Bo Shen United States
Marc A. Antonyak
Citations per year, relative to Marc A. Antonyak Marc A. Antonyak (= 1×) peers Vincenza Dolo

Countries citing papers authored by Marc A. Antonyak

Since Specialization
Citations

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

Fields of papers citing papers by Marc A. Antonyak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc A. Antonyak. 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 Marc A. Antonyak. The network helps show where Marc A. Antonyak may publish in the future.

Co-authorship network of co-authors of Marc A. Antonyak

This figure shows the co-authorship network connecting the top 25 collaborators of Marc A. Antonyak. A scholar is included among the top collaborators of Marc A. Antonyak 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 Marc A. Antonyak. Marc A. Antonyak 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.
Panizza, Elena, Fangyu Wang, Ichiro Nakano, et al.. (2023). Proteomic analysis reveals microvesicles containing NAMPT as mediators of radioresistance in glioma. Life Science Alliance. 6(6). e202201680–e202201680. 15 indexed citations
2.
Latifkar, Arash, Fangyu Wang, Elena Panizza, et al.. (2022). IGF2BP2 promotes cancer progression by degrading the RNA transcript encoding a v-ATPase subunit. Proceedings of the National Academy of Sciences. 119(45). e2200477119–e2200477119. 21 indexed citations
3.
Shi, Feng, et al.. (2020). Embryonic Stem Cell-Derived Extracellular Vesicles Maintain ESC Stemness by Activating FAK. Developmental Cell. 56(3). 277–291.e6. 56 indexed citations
4.
Schwager, Samantha C., François Bordeleau, Jian Zhang, et al.. (2019). Matrix stiffness regulates microvesicle-induced fibroblast activation. American Journal of Physiology-Cell Physiology. 317(1). C82–C92. 41 indexed citations
5.
Katt, William P., Marc A. Antonyak, & Richard A. Cerione. (2018). Opening up about Tissue Transglutaminase: When Conformation Matters More than Enzymatic Activity. SHILAP Revista de lepidopterología. 3(6). 18 indexed citations
6.
Feng, Qiyu, Chengliang Zhang, David H. Lum, et al.. (2017). A class of extracellular vesicles from breast cancer cells activates VEGF receptors and tumour angiogenesis. Nature Communications. 8(1). 14450–14450. 212 indexed citations
7.
Song, Young Hye, Sung Jin Choi, Siyoung Choi, et al.. (2016). Breast cancer-derived extracellular vesicles stimulate myofibroblast differentiation and pro-angiogenic behavior of adipose stem cells. Matrix Biology. 60-61. 190–205. 57 indexed citations
8.
Zhang, Xiaoyu, Saba Khan, Hong Jiang, et al.. (2016). Identifying the functional contribution of the defatty-acylase activity of SIRT6. Nature Chemical Biology. 12(8). 614–620. 74 indexed citations
9.
Druso, Joseph E., Makoto Endo, Xu Peng, et al.. (2016). An Essential Role for Cdc42 in the Functioning of the Adult Mammary Gland. Journal of Biological Chemistry. 291(17). 8886–8895. 13 indexed citations
10.
Bordeleau, François, Bryan Chan, Marc A. Antonyak, et al.. (2015). Microvesicles released from tumor cells disrupt epithelial cell morphology and contractility. Journal of Biomechanics. 49(8). 1272–1279. 17 indexed citations
11.
Santana, Steven M., Marc A. Antonyak, Richard A. Cerione, & Brian J. Kirby. (2014). Microfluidic isolation of cancer-cell-derived microvesicles from hetergeneous extracellular shed vesicle populations. Biomedical Microdevices. 16(6). 869–877. 87 indexed citations
12.
Bryant, Kirsten L., Marc A. Antonyak, Richard A. Cerione, Barbara Baird, & David Holowka. (2013). Mutations in the Polybasic Juxtamembrane Sequence of Both Plasma Membrane- and Endoplasmic Reticulum-localized Epidermal Growth Factor Receptors Confer Ligand-independent Cell Transformation. Journal of Biological Chemistry. 288(48). 34930–34942. 7 indexed citations
13.
Peng, Xu, et al.. (2012). Cardiovascular Development. Methods in molecular biology. 4 indexed citations
14.
Milano, Shawn K., et al.. (2012). Characterization of a Novel Activated Ran GTPase Mutant and Its Ability to Induce Cellular Transformation. Journal of Biological Chemistry. 287(30). 24955–24966. 14 indexed citations
15.
Antonyak, Marc A., Bo Li, Lindsey K. Boroughs, et al.. (2011). Cancer cell-derived microvesicles induce transformation by transferring tissue transglutaminase and fibronectin to recipient cells. Proceedings of the National Academy of Sciences. 108(12). 4852–4857. 412 indexed citations
16.
Li, Bo, Marc A. Antonyak, Joseph E. Druso, et al.. (2010). EGF potentiated oncogenesis requires a tissue transglutaminase-dependent signaling pathway leading to Src activation. Proceedings of the National Academy of Sciences. 107(4). 1408–1413. 43 indexed citations
17.
Wakshlag, Joseph J., et al.. (2006). Effects of Tissue Transglutaminase on β -Amyloid1-42-Induced Apoptosis. The Protein Journal. 25(1). 83–94. 22 indexed citations
18.
Antonyak, Marc A., Jaclyn M. Jansen, Jason E. Boehm, et al.. (2004). Augmentation of Tissue Transglutaminase Expression and Activation by Epidermal Growth Factor Inhibit Doxorubicin-induced Apoptosis in Human Breast Cancer Cells. Journal of Biological Chemistry. 279(40). 41461–41467. 99 indexed citations
19.
Boehm, Jason E., et al.. (2002). Tissue Transglutaminase Protects against Apoptosis by Modifying the Tumor Suppressor Protein p110 Rb. Journal of Biological Chemistry. 277(23). 20127–20130. 100 indexed citations
20.
Mimori, Koshi, Masaki Mori, Yosuke Adachi, et al.. (2000). Analysis of the Genetic Alterations in a Case of Juvenile Multiple Colon Carcinoma With Hypogammaglobulinemia. Annals of Surgical Oncology. 7(9). 692–695. 2 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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