Douglas E. Smith

9.2k total citations · 4 hit papers
73 papers, 5.8k citations indexed

About

Douglas E. Smith is a scholar working on Molecular Biology, Ecology and Biomedical Engineering. According to data from OpenAlex, Douglas E. Smith has authored 73 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 34 papers in Ecology and 21 papers in Biomedical Engineering. Recurrent topics in Douglas E. Smith's work include Bacteriophages and microbial interactions (31 papers), DNA and Nucleic Acid Chemistry (18 papers) and RNA and protein synthesis mechanisms (12 papers). Douglas E. Smith is often cited by papers focused on Bacteriophages and microbial interactions (31 papers), DNA and Nucleic Acid Chemistry (18 papers) and RNA and protein synthesis mechanisms (12 papers). Douglas E. Smith collaborates with scholars based in United States, France and Italy. Douglas E. Smith's co-authors include Steven Chu, Thomas T. Perkins, Rae M. Robertson‐Anderson, Hazen P. Babcock, Shelley Grimes, Dwight L. Anderson, Sander J. Tans, Carlos Bustamante, Stephen R. Quake and Derek N. Fuller and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Douglas E. Smith

70 papers receiving 5.6k citations

Hit Papers

The bacteriophage φ29 portal motor can package DNA agains... 1994 2026 2004 2015 2001 1999 1994 1994 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douglas E. Smith United States 36 2.2k 1.9k 1.4k 1.4k 1.0k 73 5.8k
Hazen P. Babcock United States 33 3.7k 1.7× 1.9k 1.0× 1.0k 0.7× 228 0.2× 841 0.8× 38 7.7k
Christoph F. Schmidt Germany 52 4.1k 1.9× 3.3k 1.8× 448 0.3× 827 0.6× 3.7k 3.7× 135 11.8k
Theo Odijk Netherlands 36 1.7k 0.8× 1.8k 1.0× 283 0.2× 545 0.4× 1.1k 1.1× 94 5.6k
John F. Marko United States 60 9.1k 4.2× 2.0k 1.1× 320 0.2× 1.6k 1.1× 2.6k 2.6× 197 12.9k
Shô Asakura Japan 31 1.9k 0.9× 1.8k 1.0× 500 0.3× 348 0.3× 892 0.9× 49 6.8k
Davide Marenduzzo United Kingdom 58 3.9k 1.8× 2.4k 1.3× 177 0.1× 611 0.4× 1.1k 1.1× 252 10.2k
Steven B. Smith United States 30 5.4k 2.5× 3.2k 1.7× 205 0.1× 893 0.6× 5.3k 5.3× 39 10.7k
Thomas T. Perkins United States 32 1.5k 0.7× 1.7k 0.9× 490 0.3× 156 0.1× 2.0k 2.0× 76 4.2k
Pietro Cicuta United Kingdom 42 2.0k 0.9× 1.2k 0.6× 171 0.1× 296 0.2× 619 0.6× 152 5.3k
Andrew J. Spakowitz United States 33 2.4k 1.1× 757 0.4× 99 0.1× 438 0.3× 525 0.5× 100 4.3k

Countries citing papers authored by Douglas E. Smith

Since Specialization
Citations

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

Fields of papers citing papers by Douglas E. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Douglas E. Smith. 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 Douglas E. Smith. The network helps show where Douglas E. Smith may publish in the future.

Co-authorship network of co-authors of Douglas E. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas E. Smith. A scholar is included among the top collaborators of Douglas E. Smith 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 Douglas E. Smith. Douglas E. Smith 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.
Jardine, Paul J., et al.. (2023). Role of DNA–DNA sliding friction and nonequilibrium dynamics in viral genome ejection and packaging. Nucleic Acids Research. 51(15). 8060–8069. 1 indexed citations
3.
Sippy, Jean, et al.. (2019). Functional Dissection of a Viral DNA Packaging Machine's Walker B Motif. Journal of Molecular Biology. 431(22). 4455–4474. 11 indexed citations
4.
Berndsen, Zachary T., et al.. (2017). Experimental comparison of forces resisting viral DNA packaging and driving DNA ejection. Physical review. E. 95(5). 52408–52408. 8 indexed citations
5.
Berndsen, Zachary T., et al.. (2015). Continuous Allosteric Regulation of a Viral Packaging Motor by a Sensor that Detects the Density and Conformation of Packaged DNA. Biophysical Journal. 108(2). 315–324. 22 indexed citations
6.
Smith, Douglas E., et al.. (2014). Molecular Interactions and Residues Involved in Force Generation in the T4 Viral DNA Packaging Motor. Journal of Molecular Biology. 426(24). 4002–4017. 7 indexed citations
7.
Alam, Tanfis I., et al.. (2014). Evidence for an electrostatic mechanism of force generation by the bacteriophage T4 DNA packaging motor. Nature Communications. 5(1). 4173–4173. 25 indexed citations
8.
Grimes, Shelley, et al.. (2014). Repulsive DNA-DNA Interactions Accelerate Viral DNA Packaging in Phage Phi29. Physical Review Letters. 112(24). 248101–248101. 34 indexed citations
9.
Smith, Douglas E.. (2011). Single-molecule studies of viral DNA packaging. Current Opinion in Virology. 1(2). 134–141. 54 indexed citations
10.
Torigoe, Sharon E., Debra Urwin, Haruhiko Ishii, Douglas E. Smith, & James T. Kadonaga. (2011). Identification of a Rapidly Formed Nonnucleosomal Histone-DNA Intermediate that Is Converted into Chromatin by ACF. Molecular Cell. 43(4). 638–648. 64 indexed citations
11.
Chemla, Yann R. & Douglas E. Smith. (2011). Single-Molecule Studies of Viral DNA Packaging. Advances in experimental medicine and biology. 726. 549–584. 52 indexed citations
12.
Tsay, James M., Jean Sippy, Benjamin T. Andrews, et al.. (2010). Mutations Altering a Structurally Conserved Loop-Helix-Loop Region of a Viral Packaging Motor Change DNA Translocation Velocity and Processivity. Journal of Biological Chemistry. 285(31). 24282–24289. 25 indexed citations
13.
Robertson‐Anderson, Rae M. & Douglas E. Smith. (2007). Direct Measurement of the Intermolecular Forces Confining a Single Molecule in an Entangled Polymer Solution. Physical Review Letters. 99(12). 126001–126001. 44 indexed citations
14.
Fuller, Derek N., John Peter Rickgauer, Rae M. Robertson‐Anderson, et al.. (2007). Measurements of Single DNA Molecule Packaging Dynamics in Bacteriophage λ Reveal High Forces, High Motor Processivity, and Capsid Transformations. Journal of Molecular Biology. 373(5). 1113–1122. 147 indexed citations
15.
Rickgauer, John Peter, Derek N. Fuller, Shelley Grimes, et al.. (2007). Portal Motor Velocity and Internal Force Resisting Viral DNA Packaging in Bacteriophage ϕ29. Biophysical Journal. 94(1). 159–167. 107 indexed citations
16.
Millin, Rachel, et al.. (2006). Dynamics of Single DNA Looping and Cleavage by Sau3AI and Effect of Tension Applied to the DNA. Biophysical Journal. 91(11). 4154–4165. 12 indexed citations
17.
Smith, Douglas E., et al.. (2001). The bacteriophage φ29 portal motor can package DNA against a large internal force. Nature. 413(6857). 748–752. 820 indexed citations breakdown →
18.
Smith, Douglas E.. (1999). Polymer physics experiments with single DNA molecules. Resuscitation. 96. e3–4. 3 indexed citations
19.
Smith, Douglas E., et al.. (1961). PREPARATION AND EFFECTS OF AN ANTI-MAST CELL SERUM. The Journal of Experimental Medicine. 113(4). 683–692. 10 indexed citations
20.
Smith, Douglas E., G. Svihla, & Harvey M. Patt. (1951). The Effects of X-Radiation on CircuLation in the Wing of the Bat. Physiological Zoology. 24(3). 249–257. 10 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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