Simon H. Reed

1.9k total citations
53 papers, 1.4k citations indexed

About

Simon H. Reed is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Simon H. Reed has authored 53 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 7 papers in Genetics and 7 papers in Cancer Research. Recurrent topics in Simon H. Reed's work include DNA Repair Mechanisms (38 papers), Genomics and Chromatin Dynamics (27 papers) and CRISPR and Genetic Engineering (20 papers). Simon H. Reed is often cited by papers focused on DNA Repair Mechanisms (38 papers), Genomics and Chromatin Dynamics (27 papers) and CRISPR and Genetic Engineering (20 papers). Simon H. Reed collaborates with scholars based in United Kingdom, United States and China. Simon H. Reed's co-authors include Raymond Waters, Errol C. Friedberg, Yumin Teng, Stephen Albert Johnston, Wenya Huang, Shirong Yu, Thomas G. Gillette, Yachuan Yu, Hairong Liu and Zheng Zhou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Simon H. Reed

53 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simon H. Reed United Kingdom 23 1.3k 168 154 150 120 53 1.4k
Marcin Pacek United States 11 1.5k 1.1× 281 1.7× 212 1.4× 239 1.6× 282 2.4× 11 1.6k
Emmanuelle Martini France 16 1.7k 1.3× 151 0.9× 157 1.0× 213 1.4× 142 1.2× 25 1.8k
Michał R. Gdula United Kingdom 14 964 0.7× 83 0.5× 167 1.1× 173 1.2× 109 0.9× 16 1.1k
Robert J. Kokoska United States 19 1.6k 1.2× 114 0.7× 352 2.3× 360 2.4× 71 0.6× 31 1.7k
Igor Chesnokov United States 19 1.3k 0.9× 140 0.8× 66 0.4× 226 1.5× 227 1.9× 32 1.4k
Oliver Fleck Switzerland 18 1.1k 0.8× 116 0.7× 149 1.0× 120 0.8× 93 0.8× 37 1.2k
Veronika Altmannová Czechia 15 1.0k 0.8× 249 1.5× 138 0.9× 142 0.9× 107 0.9× 23 1.1k
François Dragon Canada 15 1.5k 1.1× 72 0.4× 80 0.5× 86 0.6× 25 0.2× 20 1.6k
Julian Stingele Germany 15 1.0k 0.8× 252 1.5× 129 0.8× 52 0.3× 156 1.3× 25 1.1k
Benjamin Pardo France 14 841 0.6× 116 0.7× 103 0.7× 83 0.6× 91 0.8× 19 921

Countries citing papers authored by Simon H. Reed

Since Specialization
Citations

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

Fields of papers citing papers by Simon H. Reed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon H. Reed

This figure shows the co-authorship network connecting the top 25 collaborators of Simon H. Reed. A scholar is included among the top collaborators of Simon H. Reed 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 Simon H. Reed. Simon H. Reed 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.
Zhou, Zheng, et al.. (2024). Long non-coding RNA LIP interacts with PARP-1 influencing the efficiency of base excision repair. Non-coding RNA Research. 9(3). 649–658. 5 indexed citations
2.
Salk, Jesse J., Iñigo Martincorena, Robert R. Young, et al.. (2023). Next Generation Sequencing Workshop at the Royal Society of Medicine (London, May 2022): how genomics is on the path to modernizing genetic toxicology. Mutagenesis. 38(4). 192–200. 3 indexed citations
3.
Reed, Simon H., et al.. (2022). To incise or not and where: SET-domain methyltransferases know. Trends in Biochemical Sciences. 48(4). 321–330. 7 indexed citations
4.
Murat, Pierre, et al.. (2022). DNA replication initiation shapes the mutational landscape and expression of the human genome. Science Advances. 8(45). eadd3686–eadd3686. 13 indexed citations
5.
Fellows, Mick D., et al.. (2022). Precision digital mapping of endogenous and induced genomic DNA breaks by INDUCE-seq. Nature Communications. 13(1). 3989–3989. 20 indexed citations
6.
Menzies, Georgina, Ian A. Prior, Andrea Brancale, Simon H. Reed, & Paul D. Lewis. (2021). Carcinogen-induced DNA structural distortion differences in the RAS gene isoforms; the importance of local sequence. BMC Chemistry. 15(1). 51–51. 6 indexed citations
7.
8.
Teng, Yumin, et al.. (2017). Integrated Microarray-based Tools for Detection of Genomic DNA Damage and Repair Mechanisms. Methods in molecular biology. 1672. 77–99. 1 indexed citations
9.
Yu, Shirong, Katie Evans, Mark K. Bennett, et al.. (2016). Global genome nucleotide excision repair is organized into domains that promote efficient DNA repair in chromatin. Genome Research. 26(10). 1376–1387. 24 indexed citations
10.
Waters, Raymond, et al.. (2015). Histone modification and chromatin remodeling during NER. DNA repair. 36. 105–113. 45 indexed citations
11.
Powell, J.R., Mark R. Bennett, Katie Evans, et al.. (2015). 3D-DIP-Chip: a microarray-based method to measure genomic DNA damage. Scientific Reports. 5(1). 7975–7975. 30 indexed citations
12.
Powell, James, Mark K. Bennett, Raymond Waters, Nigel Skinner, & Simon H. Reed. (2013). Functional Genome-wide Analysis: a Technical Review, Its Developments and Its Relevance to Cancer Research. PubMed. 7(2). 157–166. 3 indexed citations
13.
Yu, Yachuan, et al.. (2013). Histone variant Htz1 promotes histone H3 acetylation to enhance nucleotide excision repair in Htz1 nucleosomes. Nucleic Acids Research. 41(19). 9006–9019. 24 indexed citations
14.
Reed, Simon H.. (2011). Nucleotide excision repair in chromatin: Damage removal at the drop of a HAT. DNA repair. 10(7). 734–742. 19 indexed citations
15.
Reed, Simon H., et al.. (2010). Silenced yeast chromatin is maintained by Sir2 in preference to permitting histone acetylations for efficient NER. Nucleic Acids Research. 38(14). 4675–4686. 11 indexed citations
16.
Yu, Shirong, Tom Owen‐Hughes, Errol C. Friedberg, Raymond Waters, & Simon H. Reed. (2003). The yeast Rad7/Rad16/Abf1 complex generates superhelical torsion in DNA that is required for nucleotide excision repair. DNA repair. 3(3). 277–287. 42 indexed citations
17.
Reed, Simon H., et al.. (1999). The 19S Regulatory Complex of the Proteasome Functions Independently of Proteolysis in Nucleotide Excision Repair. Molecular Cell. 3(6). 687–695. 169 indexed citations
18.
Reed, Simon H., et al.. (1998). The Yeast RAD7 and RAD16 Genes Are Required for Postincision Events during Nucleotide Excision Repair. Journal of Biological Chemistry. 273(45). 29481–29488. 42 indexed citations
19.
Wang, Zhigang, Shuguang Wei, Simon H. Reed, et al.. (1997). The RAD7 , RAD16 , and RAD23 Genes of Saccharomyces cerevisiae : Requirement for Transcription-Independent Nucleotide Excision Repair In Vitro and Interactions between the Gene Products. Molecular and Cellular Biology. 17(2). 635–643. 70 indexed citations
20.
Jones, Gary W., Simon H. Reed, & Raymond Waters. (1997). Characterization of therad14-2 Mutant ofSaccharomyces cerevisiae: Implications for the Recognition of UV Photoproducts by the Rad14 Protein. Yeast. 13(1). 31–36. 2 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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