John R. Vance

640 total citations
13 papers, 549 citations indexed

About

John R. Vance is a scholar working on Molecular Biology, Oncology and Organic Chemistry. According to data from OpenAlex, John R. Vance has authored 13 papers receiving a total of 549 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Oncology and 4 papers in Organic Chemistry. Recurrent topics in John R. Vance's work include Cancer therapeutics and mechanisms (11 papers), DNA Repair Mechanisms (4 papers) and Bioactive Compounds and Antitumor Agents (3 papers). John R. Vance is often cited by papers focused on Cancer therapeutics and mechanisms (11 papers), DNA Repair Mechanisms (4 papers) and Bioactive Compounds and Antitumor Agents (3 papers). John R. Vance collaborates with scholars based in United States, Poland and Canada. John R. Vance's co-authors include Thomas E. Wilson, Kenneth F. Bastow, Mary‐Ann Bjornsti, Zhiyan Xiao, Kuo‐Hsiung Lee, Hui-Kang Wang, Christian Bailly, Yves Pommier, Michael H. Woo and Dindial Ramotar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Molecular and Cellular Biology.

In The Last Decade

John R. Vance

13 papers receiving 538 citations

Peers

John R. Vance

MB

ONCOL

OC

TOXIC

PS

Mary M. McHugh United States

Julie T. Millard United States

Peter B. Sampson Canada

Ivo Frydrych Czechia

Monica Abdelmalak United States

S.F. Bellon United States

Ekaterina S. Ilina Russia

Qiuping Wang China

Nancy A. Wicnienski United States

Pranati Samadder Canada

Mary M. McHugh United States

John R. Vance

411 ×0.8

MB

107 ×0.8

ONCOL

141 ×1.4

OC

69 ×1.1

TOXIC

8 ×0.2

PS

Citations per year, relative to John R. Vance John R. Vance (= 1×) peers Mary M. McHugh

Countries citing papers authored by John R. Vance

Since Specialization

Citations

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

Fields of papers citing papers by John R. Vance

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John R. Vance. 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 John R. Vance. The network helps show where John R. Vance may publish in the future.

Co-authorship network of co-authors of John R. Vance

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

All Works

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13 of 13 papers shown

1.

Merwe, Mariè van der, et al.. (2004). Substitution of Conserved Residues within the Active Site Alters the Cleavage Religation Equilibrium of DNA Topoisomerase I. Journal of Biological Chemistry. 279(52). 54069–54078. 17 indexed citations

2.

Xiao, Zhiyan, John R. Vance, Kenneth F. Bastow, et al.. (2004). Antitumor agents. Part 235: Novel 4′-ester etoposide analogues as potent DNA topoisomerase II inhibitors with improved therapeutic potential. Bioorganic & Medicinal Chemistry. 12(12). 3363–3369. 18 indexed citations

3.

Xiao, Zhiyan, Kenneth F. Bastow, John R. Vance, & Kuo‐Hsiung Lee. (2004). Antitumor agents. Part 227: Studies on novel 4′-O-demethyl-epipodophyllotoxins as antitumor agents targeting topoisomerase II. Bioorganic & Medicinal Chemistry. 12(12). 3339–3344. 25 indexed citations

4.

Xiao, Zhiyan, Kenneth F. Bastow, John R. Vance, et al.. (2004). Antitumor Agents. 234. Design, Synthesis, and Biological Evaluation of Novel 4β-[(4‘ ‘-Benzamido)-Amino]-4‘-O-Demethyl-Epipodophyllotoxin Derivatives. Journal of Medicinal Chemistry. 47(21). 5140–5148. 41 indexed citations

5.

Deshpande, Rajashree A., et al.. (2003). The Role of Yeast DNA 3′-Phosphatase Tpp1 and Rad1/Rad10 Endonuclease in Processing Spontaneous and Induced Base Lesions. Journal of Biological Chemistry. 278(33). 31434–31443. 35 indexed citations

6.

Woo, Michael H., et al.. (2002). Active Site Mutations in DNA Topoisomerase I Distinguish the Cytotoxic Activities of Camptothecin and the Indolocarbazole, Rebeccamycin. Journal of Biological Chemistry. 277(6). 3813–3822. 31 indexed citations

7.

Vance, John R. & Thomas E. Wilson. (2002). Yeast Tdp1 and Rad1-Rad10 function as redundant pathways for repairing Top1 replicative damage. Proceedings of the National Academy of Sciences. 99(21). 13669–13674. 179 indexed citations

8.

Vance, John R. & Thomas E. Wilson. (2001). Uncoupling of 3′-Phosphatase and 5′-Kinase Functions in Budding Yeast. Journal of Biological Chemistry. 276(18). 15073–15081. 49 indexed citations

9.

Vance, John R. & Thomas E. Wilson. (2001). Repair of DNA Strand Breaks by the Overlapping Functions of Lesion-Specific and Non-Lesion-Specific DNA 3′ Phosphatases. Molecular and Cellular Biology. 21(21). 7191–7198. 68 indexed citations

10.

Fertala, Jolanta, John R. Vance, Philippe Pourquier, Yves Pommier, & Mary‐Ann Bjornsti. (2000). Substitutions of Asn-726 in the Active Site of Yeast DNA Topoisomerase I Define Novel Mechanisms of Stabilizing the Covalent Enzyme-DNA Intermediate. Journal of Biological Chemistry. 275(20). 15246–15253. 31 indexed citations

11.

Vance, John R. & Kenneth F. Bastow. (1999). Inhibition of DNA topoisomerase II catalytic activity by the antiviral agents 7-chloro-1,3-dihydroxyacridone and 1,3,7-trihydroxyacridone∗∗A preliminary account of this work was presented at the 89th AACR meeting held in New Orleans, LA, March 28-April 1, 1998.. Biochemical Pharmacology. 58(4). 703–708. 21 indexed citations

12.

Bastow, Kenneth F., et al.. (1998). The Cytotoxicity of 2-Formyl and 2-Acetyl-(6-picolyl)-4N-Substituted Thiosemicarbazones and Their Copper(II) Complexes. Archiv der Pharmazie. 331(4). 121–127. 33 indexed citations

13.

Bastow, Kenneth F., et al.. (1998). The Cytotoxicity of 2-Formyl and 2-Acetyl-(6-picolyl)-4N-Substituted Thiosemicarbazones and Their Copper(II) Complexes. Archiv der Pharmazie. 331(4). 121–127. 1 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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