Anthony M.C. Brown

7.9k total citations
66 papers, 6.3k citations indexed

About

Anthony M.C. Brown is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Anthony M.C. Brown has authored 66 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 14 papers in Genetics and 13 papers in Oncology. Recurrent topics in Anthony M.C. Brown's work include Wnt/β-catenin signaling in development and cancer (35 papers), Cancer-related gene regulation (26 papers) and Epigenetics and DNA Methylation (11 papers). Anthony M.C. Brown is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (35 papers), Cancer-related gene regulation (26 papers) and Epigenetics and DNA Methylation (11 papers). Anthony M.C. Brown collaborates with scholars based in United States, United Kingdom and Sweden. Anthony M.C. Brown's co-authors include Louise R. Howe, Roger Bradley, Keith Brennan, Andrew J. Dannenberg, Kotha Subbaramaiah, Jan Kitajewski, Harold Varmus, Marianna Giarrè, Martin A. Julius and José Manuel González‐Sancho and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Anthony M.C. Brown

66 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anthony M.C. Brown United States 41 4.7k 1.3k 1.1k 698 555 66 6.3k
Chunming Liu United States 32 5.2k 1.1× 765 0.6× 887 0.8× 569 0.8× 242 0.4× 87 6.4k
Claudio Sette Italy 54 6.5k 1.4× 797 0.6× 858 0.8× 1.3k 1.9× 654 1.2× 179 8.9k
Angie Rizzino United States 43 4.3k 0.9× 740 0.6× 896 0.8× 751 1.1× 240 0.4× 140 5.7k
Guntram Suske Germany 42 5.8k 1.2× 1.2k 0.9× 1.0k 0.9× 820 1.2× 166 0.3× 89 7.8k
Roshantha A.S. Chandraratna United States 49 5.4k 1.1× 2.0k 1.5× 731 0.6× 597 0.9× 206 0.4× 155 7.7k
Tung O. Chan United States 31 4.7k 1.0× 445 0.3× 1.2k 1.1× 667 1.0× 161 0.3× 51 6.6k
Anna Bagnato Italy 46 3.3k 0.7× 459 0.4× 1.4k 1.3× 1.0k 1.5× 185 0.3× 124 6.2k
Phyllis Ponte United States 22 3.9k 0.8× 746 0.6× 574 0.5× 436 0.6× 251 0.5× 27 5.8k
Susan E. Crawford United States 31 3.7k 0.8× 659 0.5× 832 0.7× 1.1k 1.6× 148 0.3× 92 5.9k
Motoyasu Saji United States 48 3.6k 0.8× 1.2k 0.9× 1.7k 1.5× 782 1.1× 106 0.2× 133 7.0k

Countries citing papers authored by Anthony M.C. Brown

Since Specialization
Citations

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

Fields of papers citing papers by Anthony M.C. Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anthony M.C. Brown. 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 Anthony M.C. Brown. The network helps show where Anthony M.C. Brown may publish in the future.

Co-authorship network of co-authors of Anthony M.C. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony M.C. Brown. A scholar is included among the top collaborators of Anthony M.C. Brown 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 Anthony M.C. Brown. Anthony M.C. Brown 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.
Marchal, Juan Antonio, Francisca E. Cara, Anthony M.C. Brown, et al.. (2018). Hydroxytyrosol inhibits cancer stem cells and the metastatic capacity of triple-negative breast cancer cell lines by the simultaneous targeting of epithelial-to-mesenchymal transition, Wnt/β-catenin and TGFβ signaling pathways. European Journal of Nutrition. 58(8). 3207–3219. 48 indexed citations
2.
Stadler, Sonja C., C. Vincent, V D Fedorov, et al.. (2013). Correction for Stadler et al., Dysregulation of PAD4-mediated citrullination of nuclear GSK3β activates TGF-β signaling and induces epithelial-to-mesenchymal transition in breast cancer cells. Proceedings of the National Academy of Sciences. 110(40). 16283–16283. 3 indexed citations
3.
Brown, Anthony M.C., et al.. (2010). Mammary stem cells and cancer: roles of Wnt signaling in plain view. Breast Cancer Research. 12(5). 313–313. 9 indexed citations
4.
Brown, Anthony M.C., et al.. (2007). GRB10 binds to LRP6, the Wnt co-receptor and inhibits canonical Wnt signaling pathway. Biochemical and Biophysical Research Communications. 356(3). 648–654. 16 indexed citations
5.
Agalliu, Dritan, Marina Vorontchikhina, Audrey Ahn, et al.. (2006). Wnt5a Signaling Induces Proliferation and Survival of Endothelial Cells In Vitro and Expression of MMP-1 and Tie-2. Molecular Biology of the Cell. 17(12). 5163–5172. 185 indexed citations
6.
Howe, Louise R., Rachelle L. Dillon, Lawrence J.T. Young, et al.. (2005). HER2/neu-Induced Mammary Tumorigenesis and Angiogenesis Are Reduced in Cyclooxygenase-2 Knockout Mice. Cancer Research. 65(21). 10113–10119. 114 indexed citations
7.
González‐Sancho, José Manuel, Keith Brennan, Leslie Castelo‐Soccio, & Anthony M.C. Brown. (2004). Wnt Proteins Induce Dishevelled Phosphorylation via an LRP5/6- Independent Mechanism, Irrespective of Their Ability To Stabilize β-Catenin. Molecular and Cellular Biology. 24(11). 4757–4768. 142 indexed citations
8.
Brennan, Keith, José Manuel González‐Sancho, Leslie Castelo‐Soccio, Louise R. Howe, & Anthony M.C. Brown. (2004). Truncated mutants of the putative Wnt receptor LRP6/Arrow can stabilize β-catenin independently of Frizzled proteins. Oncogene. 23(28). 4873–4884. 87 indexed citations
9.
Howe, Louise R. & Anthony M.C. Brown. (2004). Wnt Signaling and Breast Cancer. Cancer Biology & Therapy. 3(1). 36–41. 272 indexed citations
10.
Brennan, Keith & Anthony M.C. Brown. (2004). Wnt Proteins in Mammary Development and Cancer. Journal of Mammary Gland Biology and Neoplasia. 9(2). 119–131. 206 indexed citations
11.
Howe, Louise R., Kotha Subbaramaiah, Jay Patel, et al.. (2002). Celecoxib, a selective cyclooxygenase 2 inhibitor, protects against human epidermal growth factor receptor 2 (HER-2)/neu-induced breast cancer.. PubMed. 62(19). 5405–7. 177 indexed citations
12.
Howe, Louise R., Howard C. Crawford, Kotha Subbaramaiah, et al.. (2001). PEA3 Is Up-regulated in Response to Wnt1 and Activates the Expression of Cyclooxygenase-2. Journal of Biological Chemistry. 276(23). 20108–20115. 112 indexed citations
13.
Robbins, Melanie J., Andrew D. Medhurst, David A. Campbell, et al.. (2000). Cloning and Characterization of Human NTT5 and v7-3: Two Orphan Transporters of the Na+/Cl−-Dependent Neurotransmitter Transporter Gene Family. Genomics. 70(2). 241–252. 38 indexed citations
14.
Bergstein, Ivan, Leonard M. Eisenberg, Jayant Bhalerao, et al.. (1997). Isolation of Two Novel WNT Genes, WNT14 and WNT15, One of Which (WNT15) Is Closely Linked to WNT3 on Human Chromosome 17q21. Genomics. 46(3). 450–458. 43 indexed citations
15.
16.
Bergstein, Ivan, Roger A. Schultz, Michael P. Osborne, et al.. (1995). Investigation of the Possible Role of WNT Genes in Human Breast Cancer. Annals of the New York Academy of Sciences. 768(1). 257–257. 5 indexed citations
17.
Herzlinger, Doris, Jizeng Qiao, David Cohen, Naren Ramakrishna, & Anthony M.C. Brown. (1994). Induction of Kidney Epithelial Morphogenesis by Cells Expressing Wnt-1. Developmental Biology. 166(2). 815–818. 117 indexed citations
18.
Eisenberg, Leonard M., Philip W. Ingham, & Anthony M.C. Brown. (1992). Cloning and characterization of a novel Drosophila Wnt gene, Dwnt-5, a putative downstream target of the homeobox gene Distal-less. Developmental Biology. 154(1). 73–83. 40 indexed citations
19.
Koo, Han‐Mo, et al.. (1992). A spleen necrosis virus-based retroviral vector which expresses two genes from a dicistronic mRNA. Virology. 186(2). 669–675. 34 indexed citations
20.
Birnbaumer, Lutz, Juan Codina, Rafael Mattera, et al.. (1988). Receptor-Effector Coupling by G Proteins: Purification of Human Erythrocyte Gi-2 and Gi-3 and Analysis of Effector Regulation Using Recombinant   Subunits Synthesized in Escherichia coli. Cold Spring Harbor Symposia on Quantitative Biology. 53(0). 229–239. 12 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Chunming Liu Breakdown of academic impact, for papers by Claudio Sette Breakdown of academic impact, for papers by Angie Rizzino Breakdown of academic impact, for papers by Guntram Suske Breakdown of academic impact, for papers by Roshantha A.S. Chandraratna Breakdown of academic impact, for papers by Tung O. Chan Breakdown of academic impact, for papers by Anna Bagnato Breakdown of academic impact, for papers by Phyllis Ponte Breakdown of academic impact, for papers by Susan E. Crawford Breakdown of academic impact, for papers by Motoyasu Saji
Rankless by CCL
2026