Cyril H. Benes

31.0k total citations · 4 hit papers
123 papers, 10.9k citations indexed

About

Cyril H. Benes is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Cyril H. Benes has authored 123 papers receiving a total of 10.9k indexed citations (citations by other indexed papers that have themselves been cited), including 92 papers in Molecular Biology, 49 papers in Oncology and 21 papers in Cancer Research. Recurrent topics in Cyril H. Benes's work include Cancer-related Molecular Pathways (14 papers), Cancer therapeutics and mechanisms (14 papers) and DNA Repair Mechanisms (13 papers). Cyril H. Benes is often cited by papers focused on Cancer-related Molecular Pathways (14 papers), Cancer therapeutics and mechanisms (14 papers) and DNA Repair Mechanisms (13 papers). Cyril H. Benes collaborates with scholars based in United States, United Kingdom and Germany. Cyril H. Benes's co-authors include Patricia Greninger, Ultan McDermott, Daniel A. Haber, Mathew J. Garnett, Jeffrey A. Engelman, Sridhar Ramaswamy, Lee Zou, Michael R. Stratton, Wanjuan Yang and Howard Lightfoot and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Cyril H. Benes

120 papers receiving 10.8k citations

Hit Papers

Genomics of Drug Sensitiv... 2012 2026 2016 2021 2012 2012 2013 2015 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cyril H. Benes United States 49 7.4k 4.0k 2.9k 2.5k 906 123 10.9k
Ultan McDermott United Kingdom 39 8.2k 1.1× 4.8k 1.2× 3.9k 1.3× 3.6k 1.5× 1.1k 1.2× 94 13.0k
Aik Choon Tan United States 56 6.8k 0.9× 4.5k 1.1× 2.0k 0.7× 2.8k 1.1× 430 0.5× 262 12.1k
Mathew J. Garnett United Kingdom 38 7.1k 1.0× 3.1k 0.8× 1.7k 0.6× 1.9k 0.8× 1.5k 1.6× 85 9.8k
Simon Forbes United Kingdom 21 7.6k 1.0× 2.8k 0.7× 2.2k 0.7× 4.0k 1.6× 798 0.9× 46 11.2k
Julien Sage United States 64 8.9k 1.2× 6.7k 1.6× 1.8k 0.6× 2.0k 0.8× 418 0.5× 150 14.2k
Michael A. Davies United States 57 7.4k 1.0× 6.9k 1.7× 2.6k 0.9× 1.9k 0.8× 661 0.7× 325 12.3k
Barry S. Taylor United States 46 5.5k 0.7× 3.3k 0.8× 2.7k 0.9× 3.0k 1.2× 370 0.4× 118 9.9k
Jeffrey R. Infante United States 63 6.9k 0.9× 9.0k 2.2× 3.5k 1.2× 2.5k 1.0× 491 0.5× 343 14.8k
Sarat Chandarlapaty United States 51 6.3k 0.9× 6.0k 1.5× 4.1k 1.4× 2.9k 1.2× 454 0.5× 205 12.6k
Kevin B. Kim United States 38 5.4k 0.7× 5.1k 1.3× 1.5k 0.5× 970 0.4× 854 0.9× 116 8.2k

Countries citing papers authored by Cyril H. Benes

Since Specialization
Citations

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

Fields of papers citing papers by Cyril H. Benes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cyril H. Benes. 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 Cyril H. Benes. The network helps show where Cyril H. Benes may publish in the future.

Co-authorship network of co-authors of Cyril H. Benes

This figure shows the co-authorship network connecting the top 25 collaborators of Cyril H. Benes. A scholar is included among the top collaborators of Cyril H. Benes 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 Cyril H. Benes. Cyril H. Benes 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.
Jacob, Sheeba, Jinyang Cai, Konstantinos V. Floros, et al.. (2022). Genomic screening reveals ubiquitin-like modifier activating enzyme 1 as a potent and druggable target in c-MYC-high triple negative breast cancer models. PNAS Nexus. 1(5). pgac232–pgac232. 6 indexed citations
2.
Krytska, Kateryna, Timothy L. Lochmann, Renata Sano, et al.. (2021). Venetoclax-based Rational Combinations are Effective in Models of MYCN -amplified Neuroblastoma. Molecular Cancer Therapeutics. 20(8). 1400–1411. 13 indexed citations
3.
Heisey, Daniel A.R., Sheeba Jacob, Timothy L. Lochmann, et al.. (2021). Pharmaceutical Interference of the EWS-FLI1–driven Transcriptome By Cotargeting H3K27ac and RNA Polymerase Activity in Ewing Sarcoma. Molecular Cancer Therapeutics. 20(10). 1868–1879. 11 indexed citations
4.
Ben‐Hamo, Rotem, A. Berger, Nancy Gavert, et al.. (2020). Predicting and affecting response to cancer therapy based on pathway-level biomarkers. Nature Communications. 11(1). 3296–3296. 52 indexed citations
5.
Lochmann, Timothy L., Konstantinos V. Floros, Mitra Naseri, et al.. (2017). Venetoclax Is Effective in Small-Cell Lung Cancers with High BCL-2 Expression. Clinical Cancer Research. 24(2). 360–369. 93 indexed citations
6.
Buisson, Rémi, Michael S. Lawrence, Cyril H. Benes, & Lee Zou. (2017). APOBEC3A and APOBEC3B Activities Render Cancer Cells Susceptible to ATR Inhibition. Cancer Research. 77(17). 4567–4578. 95 indexed citations
7.
Ember, S.W., Que T. Lambert, Norbert Berndt, et al.. (2017). Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics. Molecular Cancer Therapeutics. 16(6). 1054–1067. 41 indexed citations
8.
Han, Jing, Lynnette Marcar, Joshua C. Black, et al.. (2017). Radiation Resistance in KRAS-Mutated Lung Cancer Is Enabled by Stem-like Properties Mediated by an Osteopontin–EGFR Pathway. Cancer Research. 77(8). 2018–2028. 77 indexed citations
9.
Liu, Yan, Yuyang Li, Xiaoen Wang, et al.. (2017). Gemcitabine and Chk1 Inhibitor AZD7762 Synergistically Suppress the Growth of Lkb1-Deficient Lung Adenocarcinoma. Cancer Research. 77(18). 5068–5076. 25 indexed citations
10.
Conery, Andrew R., Richard C. Centore, Archana Bommi‐Reddy, et al.. (2016). Preclinical Anticancer Efficacy of BET Bromodomain Inhibitors Is Determined by the Apoptotic Response. Cancer Research. 76(6). 1313–1319. 23 indexed citations
11.
Liu, Qi, Meng Wang, Jing Han, et al.. (2015). Adapting a Drug Screening Platform to Discover Associations of Molecular Targeted Radiosensitizers with Genomic Biomarkers. Molecular Cancer Research. 13(4). 713–720. 29 indexed citations
12.
Rechem, Capucine Van, Joshua C. Black, Myriam Boukhali, et al.. (2015). Lysine Demethylase KDM4A Associates with Translation Machinery and Regulates Protein Synthesis. Cancer Discovery. 5(3). 255–263. 51 indexed citations
13.
Flynn, Rachel Litman, Maya Jeitany, Hiroaki Wakimoto, et al.. (2015). Alternative lengthening of telomeres renders cancer cells hypersensitive to ATR inhibitors. Science. 347(6219). 273–277. 376 indexed citations breakdown →
14.
Rechem, Capucine Van, Joshua C. Black, Patricia Greninger, et al.. (2015). A Coding Single-Nucleotide Polymorphism in Lysine Demethylase KDM4A Associates with Increased Sensitivity to mTOR Inhibitors. Cancer Discovery. 5(3). 245–254. 22 indexed citations
15.
Alagesan, Brinda, Gianmarco Contino, Alexander R. Guimarães, et al.. (2014). Combined MEK and PI3K Inhibition in a Mouse Model of Pancreatic Cancer. Clinical Cancer Research. 21(2). 396–404. 103 indexed citations
16.
Wang, Meng, Patricia Greninger, Anurag Singh, et al.. (2014). EGFR-Mediated Chromatin Condensation Protects KRAS-Mutant Cancer Cells against Ionizing Radiation. Cancer Research. 74(10). 2825–2834. 55 indexed citations
17.
Heilmann, Andreas, Rushika M. Perera, Veronika Ecker, et al.. (2014). CDK4/6 and IGF1 Receptor Inhibitors Synergize to Suppress the Growth of p16INK4A-Deficient Pancreatic Cancers. Cancer Research. 74(14). 3947–3958. 90 indexed citations
18.
Emerling, Brooke M., Cyril H. Benes, George Poulogiannis, et al.. (2013). Identification of CDCP1 as a hypoxia-inducible factor 2α (HIF-2α) target gene that is associated with survival in clear cell renal cell carcinoma patients. Proceedings of the National Academy of Sciences. 110(9). 3483–3488. 49 indexed citations
19.
Puissant, Alexandre, Stacey M. Frumm, Gabriela Alexe, et al.. (2013). Targeting MYCN in Neuroblastoma by BET Bromodomain Inhibition. Cancer Discovery. 3(3). 308–323. 457 indexed citations breakdown →
20.
Wang, Meng, Liliana Gheorghiu, Patricia Greninger, et al.. (2013). EGFR-Activating Mutations Correlate with a Fanconi Anemia–like Cellular Phenotype That Includes PARP Inhibitor Sensitivity. Cancer Research. 73(20). 6254–6263. 35 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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