Valorie D. Bowman

3.5k total citations
39 papers, 2.8k citations indexed

About

Valorie D. Bowman is a scholar working on Molecular Biology, Ecology and Genetics. According to data from OpenAlex, Valorie D. Bowman has authored 39 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 19 papers in Ecology and 15 papers in Genetics. Recurrent topics in Valorie D. Bowman's work include Bacteriophages and microbial interactions (19 papers), Viral gastroenteritis research and epidemiology (9 papers) and Virus-based gene therapy research (9 papers). Valorie D. Bowman is often cited by papers focused on Bacteriophages and microbial interactions (19 papers), Viral gastroenteritis research and epidemiology (9 papers) and Virus-based gene therapy research (9 papers). Valorie D. Bowman collaborates with scholars based in United States, Russia and Japan. Valorie D. Bowman's co-authors include Michael G. Rossmann, Paul R. Chipman, Timothy S. Baker, Anthony J. Battisti, Andrei Fokine, Carol M. Bator, Venigalla B. Rao, Marc C. Morais, Richard Kühn and Susan Hafenstein and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nano Letters.

In The Last Decade

Valorie D. Bowman

39 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valorie D. Bowman United States 32 1.4k 1.3k 787 737 419 39 2.8k
Nicola J. Stonehouse United Kingdom 31 1.6k 1.2× 1.1k 0.8× 399 0.5× 752 1.0× 371 0.9× 102 3.1k
Terje Dokland United States 31 2.3k 1.6× 1.5k 1.1× 1.1k 1.4× 1.5k 2.1× 456 1.1× 80 4.6k
Nicola G. A. Abrescia Spain 25 1.2k 0.9× 809 0.6× 473 0.6× 463 0.6× 332 0.8× 72 2.5k
José R. Castón Spain 37 1.2k 0.8× 1.3k 1.0× 607 0.8× 732 1.0× 1.3k 3.2× 97 3.9k
David S. Peabody United States 39 2.7k 1.9× 1.4k 1.1× 697 0.9× 480 0.7× 346 0.8× 79 4.4k
Naiqian Cheng United States 46 2.7k 1.9× 2.0k 1.5× 884 1.1× 925 1.3× 611 1.5× 86 5.7k
Alan Rein United States 42 2.9k 2.1× 595 0.5× 967 1.2× 1.5k 2.1× 380 0.9× 98 5.3k
Juha T. Huiskonen United Kingdom 37 1.3k 0.9× 863 0.7× 459 0.6× 1.6k 2.1× 381 0.9× 85 3.6k
Jacomine Krijnse Locker Germany 27 727 0.5× 519 0.4× 570 0.7× 870 1.2× 361 0.9× 36 2.4k
Jeffrey A. Speir United States 25 1.3k 0.9× 1.1k 0.8× 321 0.4× 430 0.6× 623 1.5× 42 2.9k

Countries citing papers authored by Valorie D. Bowman

Since Specialization
Citations

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

Fields of papers citing papers by Valorie D. Bowman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Valorie D. Bowman. 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 Valorie D. Bowman. The network helps show where Valorie D. Bowman may publish in the future.

Co-authorship network of co-authors of Valorie D. Bowman

This figure shows the co-authorship network connecting the top 25 collaborators of Valorie D. Bowman. A scholar is included among the top collaborators of Valorie D. Bowman 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 Valorie D. Bowman. Valorie D. Bowman 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.
Timm, David E., et al.. (2018). Cryo-electron microscopy structure of a human PRMT5:MEP50 complex. PLoS ONE. 13(3). e0193205–e0193205. 12 indexed citations
2.
3.
Fokine, Andrei, Zhihong Zhang, Shuji Kanamaru, et al.. (2013). The Molecular Architecture of the Bacteriophage T4 Neck. Journal of Molecular Biology. 425(10). 1731–1744. 64 indexed citations
4.
Browning, Christopher R., Mikhail M. Shneider, Valorie D. Bowman, David Schwarzer, & P.G. Leiman. (2012). Phage Pierces the Host Cell Membrane with the Iron-Loaded Spike. Structure. 20(2). 326–339. 73 indexed citations
5.
Schwarzer, David, Falk F. R. Buettner, Christopher R. Browning, et al.. (2012). A Multivalent Adsorption Apparatus Explains the Broad Host Range of Phage phi92: a Comprehensive Genomic and Structural Analysis. Journal of Virology. 86(19). 10384–10398. 98 indexed citations
6.
Lee, Hoyoung, Rahul Sharma, Jae‐Sung Lee, et al.. (2011). Influence of Nano-Carrier Architecture onin VitrosiRNA Delivery Performance andin VivoBiodistribution: PolyplexesvsMicelleplexes. ACS Nano. 5(5). 3493–3505. 96 indexed citations
7.
Kaufmann, Bärbel, Valorie D. Bowman, Yi Li, et al.. (2010). Structure of Penaeus stylirostris Densovirus, a Shrimp Pathogen. Journal of Virology. 84(21). 11289–11296. 42 indexed citations
8.
Cherrier, Mickaël V., V.A. Kostyuchenko, Chuan Xiao, et al.. (2009). An icosahedral algal virus has a complex unique vertex decorated by a spike. Proceedings of the National Academy of Sciences. 106(27). 11085–11089. 69 indexed citations
9.
Morais, Marc C., et al.. (2008). Defining Molecular and Domain Boundaries in the Bacteriophage ϕ29 DNA Packaging Motor. Structure. 16(8). 1267–1274. 89 indexed citations
10.
Choi, Kyung H., et al.. (2008). Insight into DNA and Protein Transport in Double-Stranded DNA Viruses: The Structure of Bacteriophage N4. Journal of Molecular Biology. 378(3). 726–736. 93 indexed citations
11.
Sun, Siyang, Kiran Kondabagil, Bonnie Draper, et al.. (2008). The Structure of the Phage T4 DNA Packaging Motor Suggests a Mechanism Dependent on Electrostatic Forces. Cell. 135(7). 1251–1262. 200 indexed citations
12.
Levy, Hazel C., Valorie D. Bowman, L. Govindasamy, et al.. (2008). Heparin binding induces conformational changes in Adeno-associated virus serotype 2. Journal of Structural Biology. 165(3). 146–156. 90 indexed citations
13.
Fokine, Andrei, Valorie D. Bowman, Anthony J. Battisti, et al.. (2007). Cryo-electron microscopy study of bacteriophage T4 displaying anthrax toxin proteins. Virology. 367(2). 422–427. 18 indexed citations
14.
Fokine, Andrei, Anthony J. Battisti, Valorie D. Bowman, et al.. (2007). Cryo-EM Study of the Pseudomonas Bacteriophage φKZ. Structure. 15(9). 1099–1104. 62 indexed citations
15.
Hafenstein, Susan, Laura M Palermo, V.A. Kostyuchenko, et al.. (2007). Asymmetric binding of transferrin receptor to parvovirus capsids. Proceedings of the National Academy of Sciences. 104(16). 6585–6589. 81 indexed citations
16.
Rossmann, Michael G., Fumio Arisaka, Anthony J. Battisti, et al.. (2006). From structure of the complex to understanding of the biology. Acta Crystallographica Section D Biological Crystallography. 63(1). 9–16. 15 indexed citations
17.
Xiao, Chuan, Paul R. Chipman, Anthony J. Battisti, et al.. (2005). Cryo-electron Microscopy of the Giant Mimivirus. Journal of Molecular Biology. 353(3). 493–496. 98 indexed citations
18.
Luongo, Cindy, Xing Zhang, Stephen B. Walker, et al.. (2002). Loss of Activities for mRNA Synthesis Accompanies Loss of λ2 Spikes from Reovirus Cores: An Effect of λ2 on λ1 Shell Structure. Virology. 296(1). 24–38. 14 indexed citations
19.
Bernal, Ricardo A., Susan Hafenstein, Norman H. Olson, et al.. (2002). Structural Studies of Bacteriophage α3 Assembly. Journal of Molecular Biology. 325(1). 11–24. 51 indexed citations
20.
Bowman, Valorie D., et al.. (1992). Degeneration of photoreceptors in rhodopsin mutants of Drosophila. Journal of Neurobiology. 23(6). 605–626. 81 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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