Robert C. Bast

76.6k total citations · 15 hit papers
608 papers, 44.8k citations indexed

About

Robert C. Bast is a scholar working on Molecular Biology, Reproductive Medicine and Oncology. According to data from OpenAlex, Robert C. Bast has authored 608 papers receiving a total of 44.8k indexed citations (citations by other indexed papers that have themselves been cited), including 231 papers in Molecular Biology, 195 papers in Reproductive Medicine and 182 papers in Oncology. Recurrent topics in Robert C. Bast's work include Ovarian cancer diagnosis and treatment (193 papers), Monoclonal and Polyclonal Antibodies Research (91 papers) and HER2/EGFR in Cancer Research (49 papers). Robert C. Bast is often cited by papers focused on Ovarian cancer diagnosis and treatment (193 papers), Monoclonal and Polyclonal Antibodies Research (91 papers) and HER2/EGFR in Cancer Research (49 papers). Robert C. Bast collaborates with scholars based in United States, United Kingdom and China. Robert C. Bast's co-authors include Gordon B. Mills, Robert C. Knapp, Ian Jacobs, Andrew Berchuck, Daniel F. Hayes, Jonathan M. Niloff, Mark R. Somerfield, Bryan T. Hennessy, Robert Mennel and Robert B. Colvin and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Robert C. Bast

599 papers receiving 43.3k citations

Hit Papers

A Radioimmunoassay Using a Monoclonal Antibody to Monitor... 1981 2026 1996 2011 1983 2007 1981 2006 2009 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert C. Bast United States 105 17.8k 13.7k 13.7k 9.6k 6.9k 608 44.8k
Giovanni Scambia Italy 89 11.1k 0.6× 16.5k 1.2× 12.4k 0.9× 4.3k 0.4× 4.2k 0.6× 2.0k 49.2k
Martin Gore United Kingdom 78 12.9k 0.7× 4.9k 0.4× 14.4k 1.0× 4.9k 0.5× 3.6k 0.5× 382 29.5k
Ignace Vergote Belgium 89 7.3k 0.4× 21.6k 1.6× 13.5k 1.0× 5.2k 0.5× 2.6k 0.4× 899 38.3k
Elizabeth A. Eisenhauer Canada 61 12.0k 0.7× 2.9k 0.2× 15.2k 1.1× 7.3k 0.8× 3.2k 0.5× 213 41.9k
Elisabeth G.E. de Vries Netherlands 102 14.3k 0.8× 2.2k 0.2× 24.1k 1.8× 6.4k 0.7× 4.3k 0.6× 1.0k 47.8k
Ursula A. Matulonis United States 77 7.9k 0.4× 8.2k 0.6× 13.4k 1.0× 3.1k 0.3× 3.3k 0.5× 443 23.1k
Robert L. Coleman United States 72 7.7k 0.4× 9.5k 0.7× 7.7k 0.6× 3.5k 0.4× 1.7k 0.3× 690 23.3k
Michael Friedländer Australia 73 7.5k 0.4× 9.8k 0.7× 15.7k 1.1× 4.6k 0.5× 1.6k 0.2× 493 27.5k
Andrew Berchuck United States 73 8.1k 0.5× 6.9k 0.5× 5.8k 0.4× 3.8k 0.4× 1.7k 0.2× 358 19.9k
Amit M. Oza Canada 72 7.4k 0.4× 7.0k 0.5× 10.8k 0.8× 3.5k 0.4× 1.7k 0.2× 599 21.7k

Countries citing papers authored by Robert C. Bast

Since Specialization
Citations

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

Fields of papers citing papers by Robert C. Bast

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert C. Bast. 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 Robert C. Bast. The network helps show where Robert C. Bast may publish in the future.

Co-authorship network of co-authors of Robert C. Bast

This figure shows the co-authorship network connecting the top 25 collaborators of Robert C. Bast. A scholar is included among the top collaborators of Robert C. Bast 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 Robert C. Bast. Robert C. Bast 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.
Zhang, Xudong, et al.. (2024). Crizotinib Enhances PARP Inhibitor Efficacy in Ovarian Cancer Cells and Xenograft Models by Inducing Autophagy. Molecular Cancer Research. 22(9). 840–851. 4 indexed citations
2.
Irajizad, Ehsan, Chae Young Han, Joseph Celestino, et al.. (2022). A Blood-Based Metabolite Panel for Distinguishing Ovarian Cancer from Benign Pelvic Masses. Clinical Cancer Research. 28(21). 4669–4676. 10 indexed citations
3.
Gray, Joshua P., Rajan Chaudhari, Margie N. Sutton, et al.. (2021). Directed evolution of cyclic peptides for inhibition of autophagy. Chemical Science. 12(10). 3526–3543. 27 indexed citations
4.
Lytle, Nikki K., Seth T. Gammon, Tikvah K. Hayes, et al.. (2020). Analysis of RAS protein interactions in living cells reveals a mechanism for pan-RAS depletion by membrane-targeted RAS binders. Proceedings of the National Academy of Sciences. 117(22). 12121–12130. 12 indexed citations
5.
Gentry‐Maharaj, Aleksandra, Oleg Blyuss, Andy Ryan, et al.. (2020). Multi-Marker Longitudinal Algorithms Incorporating HE4 and CA125 in Ovarian Cancer Screening of Postmenopausal Women. Cancers. 12(7). 1931–1931. 22 indexed citations
6.
Kobayashi, Makoto, Hiroyuki Katayama, Ehsan Irajizad, et al.. (2020). Proteome Profiling Uncovers an Autoimmune Response Signature That Reflects Ovarian Cancer Pathogenesis. Cancers. 12(2). 485–485. 7 indexed citations
7.
Skubitz, Amy P.N., Qing Cao, Timothy K. Starr, et al.. (2019). Simultaneous Measurement of 92 Serum Protein Biomarkers for the Development of a Multiprotein Classifier for Ovarian Cancer Detection. Cancer Prevention Research. 12(3). 171–184. 14 indexed citations
8.
Yang, Hailing, Weiqun Mao, Cristian Rodriguez‐Aguayo, et al.. (2018). Paclitaxel Sensitivity of Ovarian Cancer Can be Enhanced by Knocking Down Pairs of Kinases that Regulate MAP4 Phosphorylation and Microtubule Stability. Clinical Cancer Research. 24(20). 5072–5084. 32 indexed citations
9.
Yang, Wei-Lei, Aleksandra Gentry‐Maharaj, Andy Ryan, et al.. (2017). Elevation of TP53 Autoantibody Before CA125 in Preclinical Invasive Epithelial Ovarian Cancer. Clinical Cancer Research. 23(19). 5912–5922. 44 indexed citations
10.
Zhou, Jinhua, Shu Zhang, Abdulkhaliq Alsaadi, et al.. (2016). A Novel Compound ARN-3236 Inhibits Salt-Inducible Kinase 2 and Sensitizes Ovarian Cancer Cell Lines and Xenografts to Paclitaxel. Clinical Cancer Research. 23(8). 1945–1954. 48 indexed citations
11.
Deniger, Drew C., Sourindra N. Maiti, Tiejuan Mi, et al.. (2014). Activating and Propagating Polyclonal Gamma Delta T Cells with Broad Specificity for Malignancies. Clinical Cancer Research. 20(22). 5708–5719. 104 indexed citations
12.
Zhang, Shu, Zhen Lü, Anna K. Unruh, et al.. (2014). Clinically Relevant microRNAs in Ovarian Cancer. Molecular Cancer Research. 13(3). 393–401. 70 indexed citations
13.
Su, Jen-Liang, Xiaoyun Cheng, Hirohito Yamaguchi, et al.. (2011). FOXO3a-Dependent Mechanism of E1A-Induced Chemosensitization. Cancer Research. 71(21). 6878–6887. 39 indexed citations
14.
Ahmed, Ahmed A., Xiaoyan Wang, Zhen Lü, et al.. (2011). Modulating Microtubule Stability Enhances the Cytotoxic Response of Cancer Cells to Paclitaxel. Cancer Research. 71(17). 5806–5817. 45 indexed citations
15.
Landen, Charles N., Blake W. Goodman, Ashwini A. Katre, et al.. (2010). Targeting Aldehyde Dehydrogenase Cancer Stem Cells in Ovarian Cancer. Molecular Cancer Therapeutics. 9(12). 3186–3199. 322 indexed citations
16.
Xie, Xiaoming, Jennifer L. Hsu, Min Gew Choi, et al.. (2009). A novel hTERT promoter–driven E1A therapeutic for ovarian cancer. Molecular Cancer Therapeutics. 8(8). 2375–2382. 30 indexed citations
17.
Bast, Robert C., Lajos Pusztai, Billie‐Jo Kerns, et al.. (1998). Coexpression of the HER-2 Gene Product, pl85 HER-2 , and Epidermal Growth Factor Receptor, pl70 EGF-R , on Epithelial Ovarian Cancers and Normal Tissues. Hybridoma. 17(4). 313–321. 32 indexed citations
18.
Xu, Fengfeng, C. Boyer, Kathy O'Briant, et al.. (1997). Heregulin and agonistic anti-p185(c-erbB2) antibodies inhibit proliferation but increase invasiveness of breast cancer cells that overexpress p185(c-erbB2): increased invasiveness may contribute to poor prognosis.. PubMed. 3(9). 1629–34. 61 indexed citations
20.
Jacobs, Ian, et al.. (1996). High sensitivity and specificity of screening for ovarian cancer with the risk of ovarian cancer (ROC) algorithm based on rising CA125 levels.. UCL Discovery (University College London). 4 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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