Peter B. Berget

1.9k total citations
38 papers, 1.6k citations indexed

About

Peter B. Berget is a scholar working on Molecular Biology, Ecology and Biophysics. According to data from OpenAlex, Peter B. Berget has authored 38 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 15 papers in Ecology and 10 papers in Biophysics. Recurrent topics in Peter B. Berget's work include Bacteriophages and microbial interactions (15 papers), Protein Structure and Dynamics (7 papers) and Advanced Fluorescence Microscopy Techniques (7 papers). Peter B. Berget is often cited by papers focused on Bacteriophages and microbial interactions (15 papers), Protein Structure and Dynamics (7 papers) and Advanced Fluorescence Microscopy Techniques (7 papers). Peter B. Berget collaborates with scholars based in United States. Peter B. Berget's co-authors include Anthony R. Poteete, Jonathan King, James M. Pipas, John H. Wilson, Jonathan W. Jarvik, Alan S. Waggoner, Bruce A. Armitage, Gregory W. Fisher, Sally A. Adler and John J. Schwarz and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Peter B. Berget

38 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter B. Berget United States 21 1.1k 355 347 291 240 38 1.6k
Takahiro Hohsaka Japan 25 1.8k 1.6× 95 0.3× 96 0.3× 402 1.4× 192 0.8× 79 2.0k
Christopher J. Noren United States 24 3.0k 2.6× 122 0.3× 350 1.0× 485 1.7× 200 0.8× 41 3.3k
Thomas J. Magliery United States 22 1.7k 1.5× 127 0.4× 99 0.3× 128 0.4× 255 1.1× 51 2.1k
Natasha Karassina United States 7 1.4k 1.3× 455 1.3× 62 0.2× 459 1.6× 164 0.7× 10 2.0k
Mark G. McDougall United States 13 1.9k 1.6× 476 1.3× 61 0.2× 538 1.8× 189 0.8× 22 2.4k
Rochelle D. Ahmed United Kingdom 22 918 0.8× 167 0.5× 70 0.2× 160 0.5× 273 1.1× 68 1.3k
Jacqui Méndez United States 10 2.4k 2.1× 484 1.4× 69 0.2× 584 2.0× 163 0.7× 14 3.0k
Rachel Friedman Ohana United States 10 1.8k 1.6× 478 1.3× 69 0.2× 551 1.9× 182 0.8× 21 2.4k
Alexandre Juillerat France 25 2.1k 1.9× 336 0.9× 89 0.3× 396 1.4× 91 0.4× 53 3.5k
Marjeta Urh United States 24 3.0k 2.7× 480 1.4× 123 0.4× 615 2.1× 210 0.9× 51 3.8k

Countries citing papers authored by Peter B. Berget

Since Specialization
Citations

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

Fields of papers citing papers by Peter B. Berget

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter B. Berget. 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 Peter B. Berget. The network helps show where Peter B. Berget may publish in the future.

Co-authorship network of co-authors of Peter B. Berget

This figure shows the co-authorship network connecting the top 25 collaborators of Peter B. Berget. A scholar is included among the top collaborators of Peter B. Berget 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 Peter B. Berget. Peter B. Berget 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.
Klase, Zachary, et al.. (2018). A cell surface display fluorescent biosensor for measuring MMP14 activity in real-time. Scientific Reports. 8(1). 5916–5916. 7 indexed citations
2.
Peck, Michelle A., et al.. (2012). Directed Evolution of a Fluorogen-Activating Single Chain Antibody for Function and Enhanced Brightness in the Cytoplasm. Molecular Biotechnology. 54(3). 829–841. 21 indexed citations
3.
Senutovitch, Nina, Robyn L. Stanfield, Gordon S. Rule, et al.. (2012). A Variable Light Domain Fluorogen Activating Protein Homodimerizes To Activate Dimethylindole Red. Biochemistry. 51(12). 2471–2485. 19 indexed citations
4.
Zanotti, Kimberly J., Gloria L. Silva, Yehuda Creeger, et al.. (2010). Blue fluorescent dye-protein complexes based on fluorogenic cyanine dyes and single chain antibody fragments. Organic & Biomolecular Chemistry. 9(4). 1012–1020. 51 indexed citations
5.
Rao, A. Rama Mohan, et al.. (2009). Cell cycle dependence of protein subcellular location inferred from static, asynchronous images. PubMed. 2009. 1016–1019. 7 indexed citations
6.
Fitzpatrick, James A. J., Qi Yan, Jochen J. Sieber, et al.. (2009). STED Nanoscopy in Living Cells Using Fluorogen Activating Proteins. Bioconjugate Chemistry. 20(10). 1843–1847. 66 indexed citations
7.
Szent-Györgyi, Christopher, Brigitte F. Schmidt, Yehuda Creeger, et al.. (2007). Fluorogen-activating single-chain antibodies for imaging cell surface proteins. Nature Biotechnology. 26(2). 235–240. 312 indexed citations
8.
Bateman, Nicholas W., et al.. (2007). Large-Scale Automated Analysis of Location Patterns in Randomly Tagged 3T3 Cells. Annals of Biomedical Engineering. 35(6). 1081–1087. 25 indexed citations
9.
Highlander, Sarah K., et al.. (2006). Complete nucleotide sequence of a P2 family lysogenic bacteriophage, ϕMhaA1-PHL101, from Mannheimia haemolytica serotype A1. Virology. 350(1). 79–89. 14 indexed citations
10.
Banerjee, Deboshri, Andrew L. Markley, Anindya Ghosh, et al.. (2006). “Green” Oxidation Catalysis for Rapid Deactivation of Bacterial Spores. Angewandte Chemie International Edition. 45(24). 3974–3977. 47 indexed citations
11.
Berget, Peter B., et al.. (1993). Sequence of a DNA injection gene from Salmonellatyphimuriumphage P22. Nucleic Acids Research. 21(6). 1499–1499. 6 indexed citations
12.
Schwarz, John J., et al.. (1990). Intragenic suppression of a capsid assembly-defective P22 tailspike mutation.. Genetics. 125(4). 673–681. 22 indexed citations
13.
Berget, Peter B., et al.. (1989). Using Transposon Tn5 Insertions to Sequence Bacteriophage T4 Gene 11. DNA. 8(4). 287–295. 6 indexed citations
14.
Berget, Peter B. & Monjula Chidambaram. (1989). Fine structure genetic and physical map of the phage P22 tail protein gene.. Genetics. 121(1). 13–28. 7 indexed citations
15.
Schwarz, John J. & Peter B. Berget. (1989). The isolation and sequence of missense and nonsense mutations in the cloned bacteriophage P22 tailspike protein gene.. Genetics. 121(4). 635–649. 21 indexed citations
16.
White, Terry B., Peter B. Berget, & Barry T. Nall. (1987). Changes in conformation and slow refolding kinetics in mutant iso-2-cytochrome c with replacement of a conserved proline residue. Biochemistry. 26(14). 4358–4366. 24 indexed citations
17.
Berget, Peter B., Anthony R. Poteete, & Robert T. Sauer. (1983). Control of phage P22 tail protein expression by transcription termination. Journal of Molecular Biology. 164(4). 561–572. 32 indexed citations
18.
Chidambaram, Monjula, et al.. (1983). Isolation and characterization of precursors in bacteriophage T4 baseplate assembly. Journal of Molecular Biology. 170(1). 119–135. 18 indexed citations
19.
Berget, Peter B. & Anthony R. Poteete. (1980). Structure and Functions of the Bacteriophage P22 Tail Protein. Journal of Virology. 34(1). 234–243. 74 indexed citations
20.
Berget, Peter B. & Jonathan King. (1978). Isolation and characterization of precursors in T4 baseplate assembly the complex of gene 10 and gene 11 products. Journal of Molecular Biology. 124(3). 469–486. 17 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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