Paul W. Doetsch

1.7k total citations
29 papers, 1.3k citations indexed

About

Paul W. Doetsch is a scholar working on Molecular Biology, Cancer Research and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Paul W. Doetsch has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 6 papers in Cancer Research and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Paul W. Doetsch's work include DNA Repair Mechanisms (18 papers), Carcinogens and Genotoxicity Assessment (4 papers) and Mitochondrial Function and Pathology (4 papers). Paul W. Doetsch is often cited by papers focused on DNA Repair Mechanisms (18 papers), Carcinogens and Genotoxicity Assessment (4 papers) and Mitochondrial Function and Pathology (4 papers). Paul W. Doetsch collaborates with scholars based in United States, France and India. Paul W. Doetsch's co-authors include Anita H. Corbett, Nicholas C. Bauer, Tina T. Saxowsky, Erica Werner, Huichen Wang, Walter Deutsch, Gerald S. Shadel, Thomas W. O’Rourke, Adly Yacoub and Mark R. Kelley and has published in prestigious journals such as Chemical Reviews, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Paul W. Doetsch

29 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul W. Doetsch United States 15 1.0k 269 113 109 95 29 1.3k
Stanislav Naryzhny Russia 19 857 0.8× 157 0.6× 145 1.3× 49 0.4× 26 0.3× 64 1.1k
Lei Tang China 20 503 0.5× 173 0.6× 109 1.0× 83 0.8× 48 0.5× 64 979
Matthew J. McKay Australia 23 606 0.6× 83 0.3× 110 1.0× 76 0.7× 52 0.5× 55 1.2k
Charles Vidair United States 17 823 0.8× 91 0.3× 182 1.6× 59 0.5× 88 0.9× 31 1.2k
Shuai Guo China 19 967 1.0× 259 1.0× 65 0.6× 29 0.3× 106 1.1× 53 1.3k
Frank Dolbeare United States 18 506 0.5× 380 1.4× 169 1.5× 57 0.5× 85 0.9× 25 1.2k
Pavel Spirin Russia 18 644 0.6× 142 0.5× 109 1.0× 77 0.7× 23 0.2× 90 1.0k
Georg H. Lüers Germany 23 1.4k 1.4× 133 0.5× 120 1.1× 37 0.3× 46 0.5× 47 1.8k
Praveen Kumar United States 20 652 0.6× 112 0.4× 137 1.2× 51 0.5× 37 0.4× 56 1.2k

Countries citing papers authored by Paul W. Doetsch

Since Specialization
Citations

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

Fields of papers citing papers by Paul W. Doetsch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul W. Doetsch. 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 Paul W. Doetsch. The network helps show where Paul W. Doetsch may publish in the future.

Co-authorship network of co-authors of Paul W. Doetsch

This figure shows the co-authorship network connecting the top 25 collaborators of Paul W. Doetsch. A scholar is included among the top collaborators of Paul W. Doetsch 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 Paul W. Doetsch. Paul W. Doetsch 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.
Kar, Anirban, Natalya Degtyareva, & Paul W. Doetsch. (2024). Human NTHL1 expression and subcellular distribution determines cisplatin sensitivity in human lung epithelial and non-small cell lung cancer cells. NAR Cancer. 6(1). zcae006–zcae006. 2 indexed citations
2.
Werner, Erica, Qiudong Deng, Eric B. Dammer, et al.. (2019). Ionizing Radiation induction of cholesterol biosynthesis in Lung tissue. Scientific Reports. 9(1). 12546–12546. 18 indexed citations
3.
Swartzlander, Daniel B., H. R. Powers, Emily G. Kuiper, et al.. (2016). Identification of SUMO modification sites in the base excision repair protein, Ntg1. DNA repair. 48. 51–62. 7 indexed citations
4.
Sridharan, Deepa, Aroumougame Asaithamby, Steve R. Blattnig, et al.. (2016). Evaluating biomarkers to model cancer risk post cosmic ray exposure. Life Sciences in Space Research. 9. 19–47. 34 indexed citations
5.
Liu, Bingchen, Xiaoyu Lu, Yujia Zhai, et al.. (2016). Inhibition of TRPC6 reduces non-small cell lung cancer cell proliferation and invasion. Oncotarget. 8(3). 5123–5134. 28 indexed citations
6.
Bauer, Nicholas C., Paul W. Doetsch, & Anita H. Corbett. (2015). Mechanisms Regulating Protein Localization. Traffic. 16(10). 1039–1061. 115 indexed citations
7.
Sridharan, Deepa, Aroumougame Asaithamby, Susan M. Bailey, et al.. (2015). Understanding Cancer Development Processes after HZE-Particle Exposure: Roles of ROS, DNA Damage Repair and Inflammation. Radiation Research. 183(1). 1–26. 93 indexed citations
8.
Bauer, Nicholas C., Anita H. Corbett, & Paul W. Doetsch. (2015). The current state of eukaryotic DNA base damage and repair. Nucleic Acids Research. 43(21). gkv1136–gkv1136. 170 indexed citations
9.
Xie, Maohua, Paul W. Doetsch, & Xingming Deng. (2015). Bcl2 inhibition of mitochondrial DNA repair. BMC Cancer. 15(1). 586–586. 9 indexed citations
10.
Kow, Yoke W., et al.. (2014). Inactivation of a common OGG1 variant by TNF-alpha in mammalian cells. DNA repair. 26. 15–22. 33 indexed citations
11.
Zhang, Xiangming, Wooi Loon Ng, Ping Wang, et al.. (2012). MicroRNA-21 Modulates the Levels of Reactive Oxygen Species by Targeting SOD3 and TNF α . Cancer Research. 72(18). 4707–4713. 153 indexed citations
12.
Swartzlander, Dan, Lyra Griffiths, Joon Lee, et al.. (2010). Regulation of base excision repair: Ntg1 nuclear and mitochondrial dynamic localization in response to genotoxic stress. Nucleic Acids Research. 38(12). 3963–3974. 30 indexed citations
13.
Griffiths, Lyra, Dan Swartzlander, Kellen L. Meadows, et al.. (2008). Dynamic Compartmentalization of Base Excision Repair Proteins in Response to Nuclear and Mitochondrial Oxidative Stress. Molecular and Cellular Biology. 29(3). 794–807. 37 indexed citations
14.
Saxowsky, Tina T. & Paul W. Doetsch. (2006). RNA Polymerase Encounters with DNA Damage:  Transcription-Coupled Repair or Transcriptional Mutagenesis?. Chemical Reviews. 106(2). 474–488. 144 indexed citations
15.
O’Rourke, Thomas W., et al.. (2002). Mitochondrial Dysfunction Due to Oxidative Mitochondrial DNA Damage Is Reduced through Cooperative Actions of Diverse Proteins. Molecular and Cellular Biology. 22(12). 4086–4093. 107 indexed citations
16.
Viswanathan, Anand, et al.. (1999). E. coli RNA Polymerase Bypass of DNA Base Damage: Mutagenesis at the Level of Transcription. Annals of the New York Academy of Sciences. 870(1). 386–388. 11 indexed citations
17.
18.
Yacoub, Adly, et al.. (1996). A Drosophila ribosomal protein contains 8-oxoguanine and abasic site DNA repair activities.. The EMBO Journal. 15(9). 2306–2312. 106 indexed citations
19.
Hamilton, Krista K., et al.. (1994). [10] Purification and properties of yeast redoxyendonuclease. Methods in enzymology on CD-ROM/Methods in enzymology. 234. 102–115. 4 indexed citations
20.
Doetsch, Paul W., et al.. (1988). Nuclease SP: a novel enzyme from spinach that incises damaged duplex DNA preferentially at sites of adenine. Nucleic Acids Research. 16(14). 6935–6952. 10 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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