Robert G. Lloyd

10.6k total citations
134 papers, 9.2k citations indexed

About

Robert G. Lloyd is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Robert G. Lloyd has authored 134 papers receiving a total of 9.2k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Molecular Biology, 102 papers in Genetics and 11 papers in Cancer Research. Recurrent topics in Robert G. Lloyd's work include DNA Repair Mechanisms (109 papers), Bacterial Genetics and Biotechnology (102 papers) and DNA and Nucleic Acid Chemistry (40 papers). Robert G. Lloyd is often cited by papers focused on DNA Repair Mechanisms (109 papers), Bacterial Genetics and Biotechnology (102 papers) and DNA and Nucleic Acid Chemistry (40 papers). Robert G. Lloyd collaborates with scholars based in United Kingdom, United States and Israel. Robert G. Lloyd's co-authors include Gary J. Sharples, Peter McGlynn, Carol Buckman, Akeel A. Mahdi, Matthew C. Whitby, Fiona E. Benson, Christian Rudolph, Stephen C. West, Claire E. Shurvinton and Steven M. Picksley and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert G. Lloyd

134 papers receiving 8.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert G. Lloyd United Kingdom 59 8.4k 5.6k 701 694 638 134 9.2k
Susan T. Lovett United States 51 7.1k 0.8× 4.4k 0.8× 385 0.5× 1.6k 2.3× 710 1.1× 197 8.5k
W. Dean Rupp United States 32 5.0k 0.6× 2.5k 0.4× 815 1.2× 740 1.1× 490 0.8× 67 6.0k
K. Brooks Low United States 28 4.1k 0.5× 3.3k 0.6× 233 0.3× 1.3k 1.9× 299 0.5× 52 6.4k
Murray P. Deutscher United States 61 9.9k 1.2× 3.7k 0.7× 288 0.4× 2.1k 3.0× 445 0.7× 214 10.8k
Roger Woodgate United States 68 12.3k 1.5× 5.0k 0.9× 2.7k 3.8× 794 1.1× 960 1.5× 187 13.6k
Harrison Echols United States 56 8.3k 1.0× 4.8k 0.9× 486 0.7× 2.9k 4.2× 612 1.0× 123 9.8k
Jeffrey W. Roberts United States 44 6.0k 0.7× 4.1k 0.7× 201 0.3× 2.1k 3.0× 223 0.3× 88 6.7k
Steven W. Matson United States 38 3.8k 0.4× 1.9k 0.3× 352 0.5× 555 0.8× 515 0.8× 74 4.4k
Charles S. McHenry United States 46 5.8k 0.7× 3.5k 0.6× 275 0.4× 588 0.8× 248 0.4× 114 6.5k
Jun-ichi Tomizawa Japan 49 7.6k 0.9× 4.1k 0.7× 261 0.4× 2.5k 3.6× 577 0.9× 108 9.0k

Countries citing papers authored by Robert G. Lloyd

Since Specialization
Citations

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

Fields of papers citing papers by Robert G. Lloyd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert G. Lloyd. 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 Robert G. Lloyd. The network helps show where Robert G. Lloyd may publish in the future.

Co-authorship network of co-authors of Robert G. Lloyd

This figure shows the co-authorship network connecting the top 25 collaborators of Robert G. Lloyd. A scholar is included among the top collaborators of Robert G. Lloyd 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 Robert G. Lloyd. Robert G. Lloyd 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.
Lloyd, Robert G. & Christian Rudolph. (2016). 25 years on and no end in sight: a perspective on the role of RecG protein. Current Genetics. 62(4). 827–840. 44 indexed citations
2.
Lloyd, Robert G., et al.. (2012). On the viability of Escherichia colicells lacking DNA topoisomerase I. BMC Microbiology. 12(1). 26–26. 30 indexed citations
3.
Atkinson, John D., et al.. (2010). Localization of an accessory helicase at the replisome is critical in sustaining efficient genome duplication. Nucleic Acids Research. 39(3). 949–957. 47 indexed citations
4.
Rudolph, Christian, Amy L. Upton, Lynda K. Harris, & Robert G. Lloyd. (2009). Pathological replication in cells lacking RecG DNA translocase. Molecular Microbiology. 73(3). 352–366. 49 indexed citations
5.
Rudolph, Christian, Amy L. Upton, & Robert G. Lloyd. (2009). Replication fork collisions cause pathological chromosomal amplification in cells lacking RecG DNA translocase. Molecular Microbiology. 74(4). 940–955. 48 indexed citations
6.
Grove, Jane I., et al.. (2005). RecN protein and transcription factor DksA combine to promote faithful recombinational repair of DNA double‐strand breaks. Molecular Microbiology. 57(1). 97–110. 92 indexed citations
7.
Jaktaji, Razieh Pourahmad, et al.. (2005). RNA Polymerase Modulators and DNA Repair Activities Resolve Conflicts between DNA Replication and Transcription. Molecular Cell. 19(2). 247–258. 151 indexed citations
8.
Mahdi, Akeel A., et al.. (2004). Conservation of RecG activity from pathogens to hyperthermophiles. DNA repair. 4(1). 23–31. 14 indexed citations
9.
Muranova, T. A., Svetlana E. Sedelnikova, Philip M. Leonard, et al.. (2003). Crystallization of RusA Holliday junction resolvase fromEscherichia coli. Acta Crystallographica Section D Biological Crystallography. 59(12). 2262–2264. 1 indexed citations
10.
Rafferty, John B., Edward L. Bolt, T. A. Muranova, et al.. (2003). The Structure of Escherichia coli RusA Endonuclease Reveals a New Holliday Junction DNA Binding Fold. Structure. 11(12). 1557–1567. 20 indexed citations
11.
McGlynn, Peter, et al.. (2002). Direct Rescue of Stalled DNA Replication Forks via the Combined Action of PriA and RecG Helicase Activities. Molecular Cell. 9(2). 241–251. 115 indexed citations
12.
McGlynn, Peter & Robert G. Lloyd. (2001). Rescue of stalled replication forks by RecG: Simultaneous translocation on the leading and lagging strand templates supports an active DNA unwinding model of fork reversal and Holliday junction formation. Proceedings of the National Academy of Sciences. 98(15). 8227–8234. 161 indexed citations
13.
McGlynn, Peter & Robert G. Lloyd. (2000). Modulation of RNA Polymerase by (p)ppGpp Reveals a RecG-Dependent Mechanism for Replication Fork Progression. Cell. 101(1). 35–45. 251 indexed citations
14.
Hargreaves, David, David W. Rice, Svetlana E. Sedelnikova, et al.. (1998). Crystal structure of E.coli RuvA with bound DNA Holliday junction at 6 Å resolution. Nature Structural Biology. 5(6). 441–446. 123 indexed citations
15.
Mahdi, Akeel A., et al.. (1996). Holliday Junction Resolvases Encoded by HomologousrusAGenes inEscherichia coliK-12 and Phage 82. Journal of Molecular Biology. 257(3). 561–573. 127 indexed citations
16.
Sharples, Gary J. & Robert G. Lloyd. (1993). AnE.coliRuvC mutant defective in cleavage of synthetic Holliday junctions. Nucleic Acids Research. 21(15). 3359–3364. 12 indexed citations
17.
Leach, David R. F., Robert G. Lloyd, & A. F. W. Coulson. (1992). The SbcCD protein of Escherichia coli is related to two putative nucleases in the UvrA superfamily of nucleotide-binding proteins. Genetica. 87(2). 95–100. 21 indexed citations
18.
19.
Benson, Fiona E., Simon Collier, & Robert G. Lloyd. (1991). Evidence of abortive recombination in ruv mutants of Escherichia coli K12. Molecular and General Genetics MGG. 225(2). 266–272. 60 indexed citations
20.
Mahdi, Akeel A. & Robert G. Lloyd. (1989). Identification of the recR locus of Escherichia coli K-12 and analysis of its role in recombination and DNA repair. Molecular and General Genetics MGG. 216(2-3). 503–510. 98 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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