Marie Prewett

3.7k total citations · 2 hit papers
34 papers, 2.9k citations indexed

About

Marie Prewett is a scholar working on Oncology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Marie Prewett has authored 34 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Oncology, 17 papers in Molecular Biology and 14 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Marie Prewett's work include Monoclonal and Polyclonal Antibodies Research (13 papers), HER2/EGFR in Cancer Research (11 papers) and Cancer Treatment and Pharmacology (8 papers). Marie Prewett is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (13 papers), HER2/EGFR in Cancer Research (11 papers) and Cancer Treatment and Pharmacology (8 papers). Marie Prewett collaborates with scholars based in United States, France and Japan. Marie Prewett's co-authors include Neil I. Goldstein, Patricia Rockwell, John Mendelsohn, Andrea T. Hooper, Daniel J. Hicklin, Harlan W. Waksal, Rajiv Bassi, Peter Böhlen, Lee M. Ellis and Yiwen Li and has published in prestigious journals such as Journal of Biological Chemistry, Cancer and Cancer Research.

In The Last Decade

Marie Prewett

33 papers receiving 2.8k citations

Hit Papers

Biological efficacy of a ... 1995 2026 2005 2015 1995 1999 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marie Prewett United States 18 1.7k 1.4k 816 661 509 34 2.9k
Vincenzo Damiano Italy 26 1.9k 1.1× 1.4k 1.0× 1.2k 1.4× 336 0.5× 459 0.9× 62 3.2k
Cammie Rinehart United States 15 1.7k 1.0× 1.7k 1.2× 567 0.7× 719 1.1× 327 0.6× 19 2.8k
Kenneth K. Iwata United States 27 1.8k 1.1× 1.9k 1.4× 976 1.2× 188 0.3× 520 1.0× 50 3.4k
Toru Mukohara Japan 28 2.3k 1.4× 1.7k 1.2× 1.7k 2.0× 448 0.7× 577 1.1× 128 4.1k
Shyhmin Huang United States 23 1.5k 0.9× 1.1k 0.7× 1.0k 1.2× 380 0.6× 291 0.6× 39 2.4k
Gilbert Spizzo Austria 29 1.7k 1.0× 2.1k 1.5× 488 0.6× 351 0.5× 723 1.4× 70 3.8k
John Sarantopoulos United States 28 1.3k 0.8× 1.6k 1.1× 528 0.6× 188 0.3× 382 0.8× 143 3.2k
Helmout Modjtahedi United Kingdom 30 1.4k 0.9× 1.1k 0.7× 548 0.7× 544 0.8× 333 0.7× 81 2.5k
Ralf Brandt United States 18 2.5k 1.5× 1.9k 1.3× 1.1k 1.3× 632 1.0× 381 0.7× 27 4.0k
Rachel Tsan United States 23 1.3k 0.8× 1.3k 0.9× 663 0.8× 184 0.3× 514 1.0× 29 2.5k

Countries citing papers authored by Marie Prewett

Since Specialization
Citations

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

Fields of papers citing papers by Marie Prewett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie Prewett. 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 Marie Prewett. The network helps show where Marie Prewett may publish in the future.

Co-authorship network of co-authors of Marie Prewett

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Prewett. A scholar is included among the top collaborators of Marie Prewett 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 Marie Prewett. Marie Prewett 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.
Forest, Amélie, Dale L. Ludwig, Ying Wang, et al.. (2015). Intrinsic Resistance to Cixutumumab Is Conferred by Distinct Isoforms of the Insulin Receptor. Molecular Cancer Research. 13(12). 1615–1626. 27 indexed citations
2.
Brennan, Laura, Marie Prewett, Inga Duignan, et al.. (2014). A human monoclonal antibody targeting the stem cell factor receptor (c-Kit) blocks tumor cell signaling and inhibits tumor growth. Cancer Biology & Therapy. 15(9). 1208–1218. 11 indexed citations
3.
Prewett, Marie, Rajiv Bassi, Keren Paz, et al.. (2011). Estimating preclinical efficacy targets utilizing cetuximab efficacy in KRAS mutant and wild-type colorectal cancer models.. PubMed. 31(6). 2149–60. 2 indexed citations
4.
Surguladze, David, Mary Jane Plym, Marie Prewett, et al.. (2010). 231 Efficacy of VEGFR2 targeted mAb therapy in preclinical cancer models resistant to antiangiogenic therapy. European Journal of Cancer Supplements. 8(7). 75–75. 1 indexed citations
5.
Prewett, Marie, Rajiv Bassi, Hagop Youssoufian, Eric K. Rowinsky, & James R. Tonra. (2009). Abstract #2774: The fully human EGFR antibody IMC-11F8 significantly increases the antitumor effects of cisplatin+gemcitabine in human non-small cell lung cancer models. Cancer Research. 69. 2774–2774. 3 indexed citations
6.
Surguladze, David, Philipp Steiner, Marie Prewett, & James R. Tonra. (2009). Methods for Evaluating Effects of an Irinotecan + 5-Fluorouracil/Leucovorin (IFL) Regimen in an Orthotopic Metastatic Colorectal Cancer Model Utilizing In Vivo Bioluminescence Imaging. Methods in molecular biology. 602. 235–252. 6 indexed citations
7.
Tonra, James R., Marie Prewett, Erik Corcoran, Daniel J. Hicklin, & Zhenping Zhu. (2008). In Vivo Method for Establishing Synergy Between Antibodies to Epidermal Growth Factor Receptor and Vascular Endothelial Growth Factor Receptor-2. Methods in molecular biology. 525. 545–557. 1 indexed citations
8.
Prewett, Marie, et al.. (2007). IMC-A12 enhances the efficacy of cetuximab + gemcitabine therapy in human pancreatic carcinoma xenografts.. Cancer Research. 67. 652–652. 3 indexed citations
9.
Prewett, Marie, Dhanvanthri S. Deevi, Rajiv Bassi, et al.. (2007). Tumors Established with Cell Lines Selected for Oxaliplatin Resistance Respond to Oxaliplatin if Combined with Cetuximab. Clinical Cancer Research. 13(24). 7432–7440. 43 indexed citations
10.
Shen, Juqun, Haifan Zhang, James R. Tonra, et al.. (2007). An antibody directed against PDGF receptor β enhances the antitumor and the anti-angiogenic activities of an anti-VEGF receptor 2 antibody. Biochemical and Biophysical Research Communications. 357(4). 1142–1147. 32 indexed citations
11.
Rabenau, Karen E., Dan Lu, Paul Balderes, et al.. (2006). Therapeutic Implications of a Human Neutralizing Antibody to the Macrophage-Stimulating Protein Receptor Tyrosine Kinase (RON), a c-MET Family Member. Cancer Research. 66(18). 9162–9170. 105 indexed citations
12.
Lu, Dan, Haifan Zhang, Henry Koo, et al.. (2005). A Fully Human Recombinant IgG-like Bispecific Antibody to Both the Epidermal Growth Factor Receptor and the Insulin-like Growth Factor Receptor for Enhanced Antitumor Activity. Journal of Biological Chemistry. 280(20). 19665–19672. 146 indexed citations
13.
Prewett, Marie, James R. Tonra, Rajiv Bassi, et al.. (2004). Antitumor activity of a novel, human anti-epidermal growth factor receptor (EGFR) monoclonal antibody (IMC-11F8) in human tumor xenograft models. Cancer Research. 64. 1235–1235. 13 indexed citations
14.
Overholser, Jay, Marie Prewett, Andrea T. Hooper, Harlan W. Waksal, & Daniel J. Hicklin. (2000). Epidermal growth factor receptor blockade by antibody IMC‐C225 inhibits growth of a human pancreatic carcinoma xenograft in nude mice. Cancer. 89(1). 74–82. 8 indexed citations
15.
Overholser, Jay, Marie Prewett, Andrea T. Hooper, Harlan W. Waksal, & Daniel J. Hicklin. (2000). Epidermal growth factor receptor blockade by antibody IMC-C225 inhibits growth of a human pancreatic carcinoma xenograft in nude mice. Cancer. 89(1). 74–82. 139 indexed citations
16.
Prewett, Marie, Micol S. Rothman, Harlan W. Waksal, et al.. (1998). Mouse-human chimeric anti-epidermal growth factor receptor antibody C225 inhibits the growth of human renal cell carcinoma xenografts in nude mice.. PubMed. 4(12). 2957–66. 113 indexed citations
17.
Maruyama, Haruhiko, Weiping Li, Jan Žaloudík, et al.. (1996). Monoclonal anti-idiotypic antibody functionally mimics the human gastrointestinal carcinoma epitope GA733. International Journal of Cancer. 65(4). 547–553. 16 indexed citations
18.
Hoxie, James A., et al.. (1994). Polyclonal Antiidiotypic Antibodies Mimicking gp120 of HIV-1. Viral Immunology. 7(2). 61–69. 1 indexed citations
19.
González‐Scarano, Francisco, Shaohong Liang, James A. Hoxie, et al.. (1993). Monoclonal anti-idiotypic antibodies that mimic the epitope on gp120 defined by anti-HIV-1 monoclonal antibody 0.5β. AIDS. 7(12). 1553–1559. 3 indexed citations
20.
Liang, Shaohong, P. Rieber, Marie Prewett, et al.. (1991). Anti-idiotypic Antibodies Against Anti-CD4 Antibodies MT151 and OKT4A. Viral Immunology. 4(2). 83–90.

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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