Robert W. Simons

5.2k total citations · 1 hit paper
49 papers, 4.4k citations indexed

About

Robert W. Simons is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Robert W. Simons has authored 49 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 26 papers in Genetics and 11 papers in Ecology. Recurrent topics in Robert W. Simons's work include RNA and protein synthesis mechanisms (31 papers), Bacterial Genetics and Biotechnology (24 papers) and Bacteriophages and microbial interactions (9 papers). Robert W. Simons is often cited by papers focused on RNA and protein synthesis mechanisms (31 papers), Bacterial Genetics and Biotechnology (24 papers) and Bacteriophages and microbial interactions (9 papers). Robert W. Simons collaborates with scholars based in United States, United Kingdom and Mexico. Robert W. Simons's co-authors include Nancy Kleckner, E. Gerhart H. Wagner, Elizabeth L. Simons, W D Nunn, Rudolf K. Beran, James Matsunaga, Cuiqing Ma, Philip Egan, Stanley Maloy and Sergei Doulatov and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert W. Simons

48 papers receiving 4.3k citations

Hit Papers

Improved single and multicopy lac-based cloning vectors f... 1987 2026 2000 2013 1987 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert W. Simons United States 30 3.5k 2.3k 1.3k 410 343 49 4.4k
Shoshy Altuvia Israel 32 3.5k 1.0× 2.4k 1.0× 1.5k 1.2× 497 1.2× 271 0.8× 50 4.6k
Michael B. Yarmolinsky United States 29 2.3k 0.7× 1.9k 0.8× 1.4k 1.1× 446 1.1× 357 1.0× 51 3.6k
Bert Ely United States 35 2.7k 0.8× 2.2k 0.9× 1.1k 0.9× 335 0.8× 422 1.2× 121 3.8k
Tamás Gaál United States 32 3.5k 1.0× 2.8k 1.2× 1.2k 1.0× 246 0.6× 158 0.5× 43 4.2k
James Erickson United States 26 3.2k 0.9× 2.1k 0.9× 470 0.4× 366 0.9× 337 1.0× 52 4.3k
Lee Kroos United States 35 3.2k 0.9× 3.0k 1.3× 1.5k 1.2× 208 0.5× 449 1.3× 98 4.4k
George B. Spiegelman Canada 35 2.6k 0.7× 1.7k 0.7× 1.3k 1.0× 127 0.3× 444 1.3× 110 4.2k
Bauke Oudega Netherlands 42 3.5k 1.0× 2.9k 1.2× 1.2k 1.0× 1.1k 2.8× 285 0.8× 114 5.1k
M Amemura Japan 25 3.0k 0.9× 1.6k 0.7× 545 0.4× 281 0.7× 528 1.5× 32 3.8k
Sigal Ben‐Yehuda Israel 32 3.1k 0.9× 1.9k 0.8× 1.6k 1.3× 271 0.7× 435 1.3× 54 4.3k

Countries citing papers authored by Robert W. Simons

Since Specialization
Citations

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

Fields of papers citing papers by Robert W. Simons

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert W. Simons

This figure shows the co-authorship network connecting the top 25 collaborators of Robert W. Simons. A scholar is included among the top collaborators of Robert W. Simons 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 W. Simons. Robert W. Simons 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.
Simons, Robert W.. (2021). The Ecology of the Trees, Shrubs, and Woody Vines of Northern Florida. University Press of Florida eBooks.
2.
Liveris, Dionysios, Steven Ringquist, Isabella Moll, et al.. (2008). A Single Mutation in the IF3 N-Terminal Domain Perturbs the Fidelity of Translation Initiation at Three Levels. Journal of Molecular Biology. 383(5). 937–944. 21 indexed citations
3.
Durán‐Figueroa, Noé, et al.. (2006). Polynucleotide phosphorylase interacts with ribonuclease E through a ββαββα domain. Biochimie. 88(6). 725–735. 8 indexed citations
4.
Liu, Minghsun, Rajendar Deora, Sergei Doulatov, et al.. (2002). Reverse Transcriptase-Mediated Tropism Switching in Bordetella Bacteriophage. Science. 295(5562). 2091–2094. 198 indexed citations
5.
Greenberg, Cathryn H. & Robert W. Simons. (1999). Age, composition, and stand structure of old-growth oak sites in the Florida high pine landscape: implications for ecosystem management and restoration. Natural Areas Journal. 34 indexed citations
6.
Johnstone, Brian H., Vi Nguyen, Michael Smith, et al.. (1999). The widely conserved Era G‐protein contains an RNA‐binding domain required for Era function in vivo. Molecular Microbiology. 33(6). 1118–1131. 44 indexed citations
7.
Simons, Robert W., et al.. (1998). Antisense RNA Structure and Function. Cold Spring Harbor Monograph Archive. 35. 437–464. 25 indexed citations
9.
Matsunaga, James, Elizabeth L. Simons, & Robert W. Simons. (1997). Escherichia coli RNase III (rnc) autoregulation occurs independently of rnc gene translation. Molecular Microbiology. 26(5). 1125–1135. 29 indexed citations
10.
Matsunaga, James, Elizabeth L. Simons, & Robert W. Simons. (1996). RNase III autoregulation: structure and function of rncO, the posttranscriptional "operator".. PubMed. 2(12). 1228–40. 54 indexed citations
11.
Matsunaga, James, Michael A. Dyer, Elizabeth L. Simons, & Robert W. Simons. (1996). Expression and regulation of the rnc and pdxJ operons of Escherichia coli. Molecular Microbiology. 22(5). 977–989. 41 indexed citations
12.
Anderson, Paul E., James Matsunaga, Elizabeth L. Simons, & Robert W. Simons. (1996). Structure and regulation of the Salmonella typhimurium rnc-era-recO operon. Biochimie. 78(11-12). 1025–1034. 21 indexed citations
13.
Simons, Elizabeth L., et al.. (1996). Escherichia coli translation initiation factor 3 discriminates the initiation codon in vivo. Molecular Microbiology. 21(2). 347–360. 109 indexed citations
14.
Miller, William G. & Robert W. Simons. (1990). DNA from diverse sources manifests cryptic low‐level transcription in Escherichia coli. Molecular Microbiology. 4(6). 881–893. 5 indexed citations
15.
Simons, Elizabeth L., et al.. (1990). Vectors for constructing kan gene fusions: direct selection of mutations affecting IS10 gene expression. Gene. 90(1). 135–140. 8 indexed citations
16.
Simons, Robert W., Susan W. Vince, & Stephen R. Humphrey. (1989). Hydric hammocks: A guide to management. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 5(2). 4–6. 4 indexed citations
17.
Vince, Susan W., Stephen R. Humphrey, & Robert W. Simons. (1989). The ecology of hydric hammocks: a community profile. 21 indexed citations
18.
Simons, Robert W., et al.. (1989). Insertion sequence IS10 anti-sense pairing initiates by an interaction between the 5′ end of the target RNA and a loop in the anti-sense RNA. Journal of Molecular Biology. 210(3). 561–572. 90 indexed citations
19.
Simons, Robert W. & Nancy Kleckner. (1988). BIOLOGICAL REGULATION BY ANTISENSE RNA IN PROKARYOTES. Annual Review of Genetics. 22(1). 567–600. 148 indexed citations
20.
Simons, Robert W., et al.. (1973). Aseptic Rearing of Anopheles stephensi (Diptera: Culicidae)1. Annals of the Entomological Society of America. 66(5). 949–954. 8 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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