Martin S. Taylor

18.1k total citations
66 papers, 3.6k citations indexed

About

Martin S. Taylor is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Martin S. Taylor has authored 66 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 26 papers in Genetics and 9 papers in Cancer Research. Recurrent topics in Martin S. Taylor's work include Genomics and Chromatin Dynamics (13 papers), RNA Research and Splicing (10 papers) and RNA and protein synthesis mechanisms (9 papers). Martin S. Taylor is often cited by papers focused on Genomics and Chromatin Dynamics (13 papers), RNA Research and Splicing (10 papers) and RNA and protein synthesis mechanisms (9 papers). Martin S. Taylor collaborates with scholars based in United Kingdom, United States and Australia. Martin S. Taylor's co-authors include Richard Mott, Richard R. Copley, Jonathan Flint, Andrew P. Jackson, Martin A.M. Reijns, Ian J. Jackson, Alison Meynert, William Valdar, David Fitzpatrick and William Cookson and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Martin S. Taylor

66 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin S. Taylor United Kingdom 31 2.2k 1.3k 525 313 249 66 3.6k
Anish Kejariwal United States 7 2.4k 1.1× 1.0k 0.8× 381 0.7× 299 1.0× 353 1.4× 7 3.9k
Edward J. Kulbokas United States 8 2.7k 1.2× 975 0.8× 768 1.5× 329 1.1× 293 1.2× 9 3.7k
Jeffrey G. Reid United States 21 1.7k 0.7× 1.1k 0.9× 642 1.2× 329 1.1× 233 0.9× 33 3.0k
Félix Recillas‐Targa Mexico 31 3.1k 1.4× 898 0.7× 417 0.8× 387 1.2× 210 0.8× 106 3.7k
Khalid Shakir United States 2 2.1k 0.9× 1.8k 1.4× 626 1.2× 612 2.0× 240 1.0× 2 4.3k
Colin A. Semple United Kingdom 32 2.7k 1.2× 827 0.7× 456 0.9× 364 1.2× 366 1.5× 86 3.6k
Emily H. Turner United States 21 2.4k 1.1× 1.6k 1.3× 737 1.4× 353 1.1× 168 0.7× 27 4.2k
Altuna Akalin Germany 30 3.4k 1.5× 746 0.6× 583 1.1× 438 1.4× 254 1.0× 61 4.4k
Gert Jan C. Veenstra Netherlands 32 4.7k 2.1× 1.5k 1.2× 364 0.7× 375 1.2× 240 1.0× 70 5.4k
Ami Levy‐Moonshine United States 5 2.2k 1.0× 1.9k 1.5× 659 1.3× 634 2.0× 256 1.0× 5 4.5k

Countries citing papers authored by Martin S. Taylor

Since Specialization
Citations

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

Fields of papers citing papers by Martin S. Taylor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin S. Taylor. 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 Martin S. Taylor. The network helps show where Martin S. Taylor may publish in the future.

Co-authorship network of co-authors of Martin S. Taylor

This figure shows the co-authorship network connecting the top 25 collaborators of Martin S. Taylor. A scholar is included among the top collaborators of Martin S. Taylor 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 Martin S. Taylor. Martin S. Taylor 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.
Nielsen, Mathias I., Justina C. Wolters, Hua Jiang, et al.. (2025). Targeted detection of endogenous LINE-1 proteins and ORF2p interactions. Mobile DNA. 16(1). 3–3. 1 indexed citations
2.
Anderson, Craig, et al.. (2024). DNA lesion bypass and the stochastic dynamics of transcription-coupled repair. Proceedings of the National Academy of Sciences. 121(20). e2403871121–e2403871121. 3 indexed citations
3.
Ginno, Paul A., Christina Ernst, Mikaela Behm, et al.. (2024). Single-mitosis dissection of acute and chronic DNA mutagenesis and repair. Nature Genetics. 56(5). 913–924. 1 indexed citations
4.
Jarman, Edward J., Alison Meynert, Graeme R. Grimes, et al.. (2022). In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma. Cancer Research. 82(8). 1548–1559. 7 indexed citations
5.
Young, Robert S., et al.. (2022). The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation. Genome biology. 23(1). 89–89. 3 indexed citations
6.
Kaiser, Vera B., Yatendra Kumar, Fiona Semple, et al.. (2021). Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome. Genome Research. 31(11). 1994–2007. 4 indexed citations
7.
Longman, Dáša, Magdalena M. Maslon, Laura C. Murphy, et al.. (2020). Identification of a localized nonsense-mediated decay pathway at the endoplasmic reticulum. Genes & Development. 34(15-16). 1075–1088. 39 indexed citations
8.
Halachev, Mihail, Alison Meynert, Martin S. Taylor, et al.. (2019). Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. PLoS Genetics. 15(11). e1008480–e1008480. 14 indexed citations
9.
Kaiser, Vera B., Martin S. Taylor, & Colin A. Semple. (2016). Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types. PLoS Genetics. 12(8). e1006207–e1006207. 58 indexed citations
10.
Luciano, Michelle, Victoria Svinti, Archie Campbell, et al.. (2015). Exome Sequencing to Detect Rare Variants Associated With General Cognitive Ability: A Pilot Study. Twin Research and Human Genetics. 18(2). 117–125. 7 indexed citations
11.
Rooms, Liesbeth, Jacqueline K. Rainger, Martin S. Taylor, et al.. (2014). FRA2A Is a CGG Repeat Expansion Associated with Silencing of AFF3. PLoS Genetics. 10(4). e1004242–e1004242. 29 indexed citations
12.
Huang, Guo‐Jen, Sagiv Shifman, William Valdar, et al.. (2009). High resolution mapping of expression QTLs in heterogeneous stock mice in multiple tissues. Genome Research. 19(6). 1133–1140. 60 indexed citations
13.
Ke, Xiayi, Martin S. Taylor, & Lon R. Cardon. (2008). Singleton SNPs in the human genome and implications for genome-wide association studies. European Journal of Human Genetics. 16(4). 506–515. 28 indexed citations
14.
Elliott, Susan J., Sarah Wakefield, Martin S. Taylor, et al.. (2004). A comparative analysis of the psychosocial impacts of waste disposal facilities. Journal of Environmental Planning and Management. 47(3). 351–363. 13 indexed citations
15.
Logan, Darren W., et al.. (2003). The structure and evolution of the melanocortin and MCH receptors in fish and mammals. Genomics. 81(2). 184–191. 129 indexed citations
16.
Logan, Darren W., Robert J. Bryson‐Richardson, Martin S. Taylor, Peter D. Currie, & Ian J. Jackson. (2003). Sequence Characterization of Teleost Fish Melanocortin Receptors. Annals of the New York Academy of Sciences. 994(1). 319–330. 25 indexed citations
17.
Taylor, Martin S., et al.. (1997). Co-amplification of the Amelogenin and HLA DQα Genes: Optimization and Validation. Journal of Forensic Sciences. 42(1). 130–136. 2 indexed citations
18.
Taylor, Martin S., et al.. (1997). Co-amplification of the amelogenin and HLA DQ alpha genes: optimization and validation.. PubMed. 42(1). 130–6. 1 indexed citations
19.
DeMarini, David M., Ron Williams, Lance R. Brooks, & Martin S. Taylor. (1992). Use of Cyanopropyl-Bonded HPLC Column for Bioassay-Directed Fractionation of Organic Extracts from Incinerator Emissions. International Journal of Environmental & Analytical Chemistry. 48(3-4). 187–199. 13 indexed citations
20.
Holmes, M, et al.. (1991). Intussusception in cystic fibrosis.. Archives of Disease in Childhood. 66(6). 726–727. 24 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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