Benny J. Evison

826 total citations
17 papers, 663 citations indexed

About

Benny J. Evison is a scholar working on Molecular Biology, Oncology and Organic Chemistry. According to data from OpenAlex, Benny J. Evison has authored 17 papers receiving a total of 663 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 5 papers in Oncology and 4 papers in Organic Chemistry. Recurrent topics in Benny J. Evison's work include Cancer therapeutics and mechanisms (10 papers), DNA and Nucleic Acid Chemistry (4 papers) and DNA Repair Mechanisms (4 papers). Benny J. Evison is often cited by papers focused on Cancer therapeutics and mechanisms (10 papers), DNA and Nucleic Acid Chemistry (4 papers) and DNA Repair Mechanisms (4 papers). Benny J. Evison collaborates with scholars based in Australia, United States and Israel. Benny J. Evison's co-authors include Suzanne M. Cutts, Don R. Phillips, Mas Jaffri Masarudin, Paul J. Pigram, Brad E. Sleebs, Keith G. Watson, Francis C. K. Chiu, Gabriella Pezzoni, Rebecca A. Bilardi and E. MENTA and has published in prestigious journals such as Nucleic Acids Research, Journal of Medicinal Chemistry and Journal of Lipid Research.

In The Last Decade

Benny J. Evison

17 papers receiving 658 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benny J. Evison Australia 9 262 123 102 94 83 17 663
Sheng‐Xue Xie United States 15 446 1.7× 117 1.0× 83 0.8× 97 1.0× 106 1.3× 36 828
Yonghua Liu China 15 190 0.7× 91 0.7× 94 0.9× 106 1.1× 75 0.9× 60 600
Chien‐Ming Hsieh Taiwan 16 185 0.7× 125 1.0× 52 0.5× 58 0.6× 120 1.4× 38 583
Pascal Detampel Switzerland 17 555 2.1× 170 1.4× 65 0.6× 56 0.6× 153 1.8× 35 1.1k
Hashem Khanbabaei Iran 18 583 2.2× 126 1.0× 97 1.0× 40 0.4× 129 1.6× 29 1.1k
Soraya Shahhosseini Iran 16 435 1.7× 126 1.0× 85 0.8× 189 2.0× 143 1.7× 69 981
Abdullah Farooque India 13 332 1.3× 204 1.7× 156 1.5× 88 0.9× 164 2.0× 20 878
Sachin Mittal India 15 243 0.9× 73 0.6× 128 1.3× 80 0.9× 88 1.1× 61 734
L. Grislain France 10 170 0.6× 284 2.3× 92 0.9× 80 0.9× 95 1.1× 17 686

Countries citing papers authored by Benny J. Evison

Since Specialization
Citations

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

Fields of papers citing papers by Benny J. Evison

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benny J. Evison. 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 Benny J. Evison. The network helps show where Benny J. Evison may publish in the future.

Co-authorship network of co-authors of Benny J. Evison

This figure shows the co-authorship network connecting the top 25 collaborators of Benny J. Evison. A scholar is included among the top collaborators of Benny J. Evison 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 Benny J. Evison. Benny J. Evison is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Lee, Joung-Hyun, Kevin L. Shores, Jennifer B. Kwon, et al.. (2023). PCSK9 activation promotes early atherosclerosis in a vascular microphysiological system. APL Bioengineering. 7(4). 46103–46103. 7 indexed citations
2.
Nudelman, Abraham, et al.. (2022). An evaluation of the interaction of pixantrone with formaldehyde-releasing drugs in cancer cells. Cancer Chemotherapy and Pharmacology. 89(6). 773–784. 2 indexed citations
3.
Suchowerska, Alexandra K., Geurt Stokman, James T. Palmer, et al.. (2022). A Novel, Orally Bioavailable, Small-Molecule Inhibitor of PCSK9 With Significant Cholesterol-Lowering Properties In Vivo. Journal of Lipid Research. 63(11). 100293–100293. 15 indexed citations
4.
Sleebs, Brad E., Kurt Lackovic, Keith G. Watson, et al.. (2021). Development of an automated assay for accelerated in vitro detection of DNA adduct-inducing and crosslinking agents. Bioorganic & Medicinal Chemistry Letters. 35. 127813–127813. 2 indexed citations
5.
Evison, Benny J., James T. Palmer, Gilles Lambert, et al.. (2020). A small molecule inhibitor of PCSK9 that antagonizes LDL receptor binding via interaction with a cryptic PCSK9 binding groove. Bioorganic & Medicinal Chemistry. 28(6). 115344–115344. 36 indexed citations
6.
Evison, Benny J., J. Grant Collins, Céline Kelso, et al.. (2019). Formaldehyde-activated WEHI-150 induces DNA interstrand crosslinks with unique structural features. Bioorganic & Medicinal Chemistry. 28(3). 115260–115260. 4 indexed citations
8.
Evison, Benny J., Brad E. Sleebs, Keith G. Watson, Don R. Phillips, & Suzanne M. Cutts. (2015). Mitoxantrone, More than Just Another Topoisomerase II Poison. Medicinal Research Reviews. 36(2). 248–299. 182 indexed citations
9.
Evison, Benny J., et al.. (2014). Design, synthesis, and DNA sequence selectivity of formaldehyde-mediated DNA-adducts of the novel N-(4-aminobutyl) acridine-4-carboxamide. Bioorganic & Medicinal Chemistry Letters. 24(24). 5710–5715. 2 indexed citations
10.
Swift, Lonnie P., Benny J. Evison, Ada Rephaeli, et al.. (2012). The hydroxyl epimer of doxorubicin controls the rate of formation of cytotoxic anthracycline-DNA adducts. Cancer Chemotherapy and Pharmacology. 71(3). 809–816. 8 indexed citations
11.
Evison, Benny J., Rebecca A. Bilardi, Brad E. Sleebs, et al.. (2011). M2, a novel anthracenedione, elicits a potent DNA damage response that can be subverted through checkpoint kinase inhibition to generate mitotic catastrophe. Biochemical Pharmacology. 82(11). 1604–1618. 8 indexed citations
12.
Buck, Damian P., et al.. (2010). DNA binding by pixantrone. Organic & Biomolecular Chemistry. 8(23). 5359–5359. 12 indexed citations
13.
Evison, Benny J., Brad E. Sleebs, Keith G. Watson, et al.. (2010). New Anthracenedione Derivatives with Improved Biological Activity by Virtue of Stable Drug−DNA Adduct Formation. Journal of Medicinal Chemistry. 53(19). 6851–6866. 19 indexed citations
14.
Evison, Benny J., Rebecca A. Bilardi, Francis C. K. Chiu, et al.. (2009). CpG methylation potentiates pixantrone and doxorubicin-induced DNA damage and is a marker of drug sensitivity. Nucleic Acids Research. 37(19). 6355–6370. 29 indexed citations
15.
Evison, Benny J., Don R. Phillips, & Suzanne M. Cutts. (2009). In vitro Transcription Assay for Resolution of Drug-DNA Interactions at Defined DNA Sequences. Methods in molecular biology. 613. 207–222. 2 indexed citations
16.
Evison, Benny J., Francis C. K. Chiu, Gabriella Pezzoni, Don R. Phillips, & Suzanne M. Cutts. (2008). Formaldehyde-Activated Pixantrone Is a Monofunctional DNA Alkylator That Binds Selectively to CpG and CpA Doublets. Molecular Pharmacology. 74(1). 184–194. 22 indexed citations
17.
Evison, Benny J., et al.. (2007). Pixantrone can be activated by formaldehyde to generate a potent DNA adduct forming agent. Nucleic Acids Research. 35(11). 3581–3589. 36 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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