Philip G. Kasprzyk

2.2k total citations
50 papers, 1.8k citations indexed

About

Philip G. Kasprzyk is a scholar working on Molecular Biology, Oncology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Philip G. Kasprzyk has authored 50 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 25 papers in Oncology and 9 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Philip G. Kasprzyk's work include Monoclonal and Polyclonal Antibodies Research (9 papers), Cancer therapeutics and mechanisms (8 papers) and HER2/EGFR in Cancer Research (8 papers). Philip G. Kasprzyk is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (9 papers), Cancer therapeutics and mechanisms (8 papers) and HER2/EGFR in Cancer Research (8 papers). Philip G. Kasprzyk collaborates with scholars based in United States, France and United Kingdom. Philip G. Kasprzyk's co-authors include C. Richter King, James L. Mulshine, Anthony M. Treston, Olivier Lavergne, Frank Cuttitta, Ira Pastan, Sun U. Song, Pier Paolo Di Fiore, Grégoire Prévost and Danièle Demarquay and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Philip G. Kasprzyk

50 papers receiving 1.7k citations

Peers

Philip G. Kasprzyk
Jeffrey H. Till United States
Wilma M. McKoy United States
J A Double United Kingdom
Abhijit Bhat United States
Zhong-Yin Zhang United States
Ana M. Tari United States
Aruna Basu United States
Philip G. Kasprzyk
Citations per year, relative to Philip G. Kasprzyk Philip G. Kasprzyk (= 1×) peers Grégoire Prévost

Countries citing papers authored by Philip G. Kasprzyk

Since Specialization
Citations

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

Fields of papers citing papers by Philip G. Kasprzyk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip G. Kasprzyk. 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 Philip G. Kasprzyk. The network helps show where Philip G. Kasprzyk may publish in the future.

Co-authorship network of co-authors of Philip G. Kasprzyk

This figure shows the co-authorship network connecting the top 25 collaborators of Philip G. Kasprzyk. A scholar is included among the top collaborators of Philip G. Kasprzyk 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 Philip G. Kasprzyk. Philip G. Kasprzyk 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.
Kasprzyk, Philip G., Larry M. Tremaine, Odette A. Fahmi, & Jing‐Ke Weng. (2023). In Vitro Evaluation of the Potential for Drug Interactions by Salidroside. Nutrients. 15(17). 3723–3723. 4 indexed citations
2.
Döhle, Wolfgang, Mathew P. Leese, Fabrice Jourdan, et al.. (2014). Synthesis, Antitubulin, and Antiproliferative SAR of C3/C1‐Substituted Tetrahydroisoquinolines. ChemMedChem. 9(2). 350–370. 15 indexed citations
3.
Brézak, Marie-Christine, Annie Valette, Muriel Quaranta, et al.. (2008). IRC‐083864, a novel bis quinone inhibitor of CDC25 phosphatases active against human cancer cells. International Journal of Cancer. 124(6). 1449–1456. 42 indexed citations
4.
Prévost, Grégoire, Muriel Quaranta, Céline Frongia, et al.. (2007). A novel synthetic CDC25 phosphatase inhibitor inhibits human cancer growth in vitro and in vivo. Cancer Research. 67. 3228–3228. 1 indexed citations
5.
Foster, Paul, Simon P. Newman, Philip G. Kasprzyk, et al.. (2007). 2-MeOE2bisMATE and 2-EtE2bisMATE induce cell cycle arrest and apoptosis in breast cancer xenografts as shown by a novel ex vivo technique. Breast Cancer Research and Treatment. 111(2). 251–260. 30 indexed citations
6.
Newman, Stephen T., Paul Foster, Joanna M. Day, et al.. (2007). The therapeutic potential of a series of orally bioavailable anti-angiogenic microtubule disruptors as therapy for hormone-independent prostate and breast cancers. British Journal of Cancer. 97(12). 1673–1682. 25 indexed citations
7.
Prévost, Grégoire, Anne Pradines, Marie-Christine Brézak, et al.. (2001). Inhibition of human tumor cell growthin vivo by an orally bioavailable inhibitor of human farnesyltransferase, BIM-46228. International Journal of Cancer. 91(5). 718–722. 23 indexed citations
8.
Demarquay, Danièle, Marion Huchet, Hélène Coulomb, et al.. (2001). The homocamptothecin BN 80915 is a highly potent orally active topoisomerase I poison. Anti-Cancer Drugs. 12(1). 9–19. 24 indexed citations
9.
Papadopoulos, Vassilios, Hua Li, Hakima Amri, et al.. (2000). Drug-induced inhibition of the peripheral-type benzodiazepine receptor expression and cell proliferation in human breast cancer cells.. PubMed. 20(5A). 2835–47. 50 indexed citations
10.
Huchet, Marion, Danièle Demarquay, Hélène Coulomb, et al.. (2000). The Dual Topoisomerase Inhibitor, BN 80927, Is Highly Potent against Cell Proliferation and Tumor Growth. Annals of the New York Academy of Sciences. 922(1). 303–305. 13 indexed citations
11.
Lavergne, Olivier, Danièle Demarquay, Philip G. Kasprzyk, & Dennis Bigg. (2000). Homocamptothecins: E‐Ring Modified CPT Analogues. Annals of the New York Academy of Sciences. 922(1). 100–111. 20 indexed citations
12.
King, C. Richter, Philip G. Kasprzyk, Paul H. Fischer, Robert E. Bird, & Nancy A. Turner. (1996). Preclinical testing of an anti-erbB-2 recombinant toxin. Breast Cancer Research and Treatment. 38(1). 19–25. 9 indexed citations
13.
Reiter, Yoram, Ulrich Brinkmann, B. Lee, et al.. (1994). Improved binding and antitumor activity of a recombinant anti-erbB2 immunotoxin by disulfide stabilization of the Fv fragment. Journal of Biological Chemistry. 269(28). 18327–18331. 81 indexed citations
14.
Avis, Ingalill, Frank Cuttitta, Anthony M. Treston, et al.. (1993). Effect of gastrin‐releasing peptide on the pancreatic tumor cell line (capan). Molecular Carcinogenesis. 8(4). 214–220. 16 indexed citations
15.
Kasprzyk, Philip G., Sun U. Song, Pier Paolo Di Fiore, & C. Richter King. (1992). Therapy of an animal model of human gastric cancer using a combination of anti-erbB-2 monoclonal antibodies.. PubMed. 52(10). 2771–6. 135 indexed citations
16.
Kovacs, T. O. G., Philip G. Kasprzyk, Anthony M. Treston, et al.. (1991). Preclinical Evaluation of an Anti-Autocrine Growth Factor Monoclonal Antibody for Treatment of Patients With Small-Cell Lung Cancer. JNCI Journal of the National Cancer Institute. 83(20). 1470–1476. 30 indexed citations
17.
Mulshine, James L., Anthony M. Treston, Ronald B. Natale, et al.. (1989). Autocrine Growth Factors as Therapeutic Targets in Lung Cancer. CHEST Journal. 96(1). 31S–34S. 6 indexed citations
18.
Kasprzyk, Philip G., Ingalill Avis, Yoichi Nakanishi, et al.. (1988). Solid-phase peptide quantitation assay using labeled monoclonal antibody and glutaraldehyde fixation. Analytical Biochemistry. 174(1). 224–234. 11 indexed citations
19.
20.
Kasprzyk, Philip G., Frank Cuttitta, Anthony M. Treston, et al.. (1988). Consideration of the Chemistry of Solid‐Phase Matrix Interactions Leads to Improved Quantitation of Neuropeptidesa,b. Annals of the New York Academy of Sciences. 547(1). 41–53. 3 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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