Lois Pollack

6.8k total citations
117 papers, 4.6k citations indexed

About

Lois Pollack is a scholar working on Molecular Biology, Materials Chemistry and Biomedical Engineering. According to data from OpenAlex, Lois Pollack has authored 117 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 35 papers in Materials Chemistry and 16 papers in Biomedical Engineering. Recurrent topics in Lois Pollack's work include RNA and protein synthesis mechanisms (40 papers), DNA and Nucleic Acid Chemistry (38 papers) and Enzyme Structure and Function (28 papers). Lois Pollack is often cited by papers focused on RNA and protein synthesis mechanisms (40 papers), DNA and Nucleic Acid Chemistry (38 papers) and Enzyme Structure and Function (28 papers). Lois Pollack collaborates with scholars based in United States, United Arab Emirates and Canada. Lois Pollack's co-authors include Suzette A. Pabit, Steve P. Meisburger, Lisa W. Kwok, Jessica S. Lamb, Gerard C. L. Wong, Hye Yoon Park, Kurt Andresen, Julie L. Sutton, Watt W. Webb and Xiangyun Qiu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Physical Review Letters.

In The Last Decade

Lois Pollack

114 papers receiving 4.6k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Lois Pollack 3.1k 992 951 503 502 117 4.6k
Mathias Lösche 3.1k 1.0× 1.0k 1.1× 1.1k 1.1× 427 0.8× 1.7k 3.4× 105 5.8k
Jan Lipfert 3.6k 1.2× 574 0.6× 1.1k 1.2× 327 0.7× 1.0k 2.1× 115 5.0k
Don C. Lamb 4.1k 1.3× 1.1k 1.1× 882 0.9× 226 0.4× 567 1.1× 153 6.6k
Marc Adrian 3.2k 1.0× 930 0.9× 358 0.4× 70 0.1× 588 1.2× 38 5.9k
Dominique Bourgeois 3.1k 1.0× 1.6k 1.6× 293 0.3× 171 0.3× 513 1.0× 116 5.1k
Stéphanie Finet 1.5k 0.5× 1.1k 1.1× 318 0.3× 201 0.4× 420 0.8× 61 2.8k
Simon Ebbinghaus 2.1k 0.7× 695 0.7× 302 0.3× 209 0.4× 783 1.6× 80 3.4k
Edward A. Lemke 5.9k 1.9× 948 1.0× 643 0.7× 84 0.2× 344 0.7× 114 7.9k
Paul R. Selvin 5.5k 1.8× 2.5k 2.5× 1.7k 1.8× 339 0.7× 1.5k 2.9× 91 10.6k
A. Rupprecht 2.2k 0.7× 429 0.4× 582 0.6× 651 1.3× 868 1.7× 139 3.4k

Countries citing papers authored by Lois Pollack

Since Specialization
Citations

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

Fields of papers citing papers by Lois Pollack

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lois Pollack. 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 Lois Pollack. The network helps show where Lois Pollack may publish in the future.

Co-authorship network of co-authors of Lois Pollack

This figure shows the co-authorship network connecting the top 25 collaborators of Lois Pollack. A scholar is included among the top collaborators of Lois Pollack 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 Lois Pollack. Lois Pollack 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.
Badiee, Mohsen, et al.. (2024). Cation-induced intramolecular coil-to-globule transition in poly(ADP-ribose). Nature Communications. 15(1). 7901–7901. 3 indexed citations
2.
Henning, Robert, Mark A. Wilson, Lois Pollack, et al.. (2024). Scaling and merging time-resolved pink-beam diffraction with variational inference. Structural Dynamics. 11(6). 64301–64301.
3.
Olson, Wilma K., John H. Maddocks, Pablo D. Dans, et al.. (2023). An open call for contributions to a special issue of Biophysical Reviews focused on multiscale simulations of DNA from electrons to nucleosomes. Biophysical Reviews. 15(6). 1901–1902. 1 indexed citations
4.
Woodside, Michael T., et al.. (2023). Atomistic structure of the SARS-CoV-2 pseudoknot in solution from SAXS-driven molecular dynamics. Nucleic Acids Research. 51(20). 11332–11344. 11 indexed citations
5.
Katz, Andrea M., George D. Calvey, Suzette A. Pabit, et al.. (2023). Chaotic advection mixer for capturing transient states of diverse biological macromolecular systems with time-resolved small-angle X-ray scattering. IUCrJ. 10(3). 363–375. 5 indexed citations
6.
Pollack, Lois, et al.. (2021). The structural plasticity of nucleic acid duplexes revealed by WAXS and MD. Science Advances. 7(17). 25 indexed citations
7.
Zhang, Kaiming, Jimin Wang, Suzanne J. DeGregorio, et al.. (2021). Structural analyses of an RNA stability element interacting with poly(A). Proceedings of the National Academy of Sciences. 118(14). 16 indexed citations
8.
Pabit, Suzette A., et al.. (2020). Elucidating the Role of Microprocessor Protein DGCR8 in Bending RNA Structures. Biophysical Journal. 119(12). 2524–2536. 4 indexed citations
9.
Pollack, Lois, et al.. (2020). Visualizing a viral genome with contrast variation small angle X-ray scattering. Journal of Biological Chemistry. 295(47). 15923–15932. 8 indexed citations
10.
Tokuda, Joshua M., et al.. (2018). Local DNA Sequence Controls Asymmetry of DNA Unwrapping from Nucleosome Core Particles. Biophysical Journal. 115(5). 773–781. 32 indexed citations
11.
Elber, Ron, et al.. (2018). Conformations of an RNA Helix-Junction-Helix Construct Revealed by SAXS Refinement of MD Simulations. Biophysical Journal. 116(1). 19–30. 17 indexed citations
12.
Pabit, Suzette A., et al.. (2018). Divalent ions tune the kinetics of a bacterial GTPase center rRNA folding transition from secondary to tertiary structure. RNA. 24(12). 1828–1838. 15 indexed citations
13.
Chen, Yujie, Joshua M. Tokuda, Traci Topping, et al.. (2016). Asymmetric unwrapping of nucleosomal DNA propagates asymmetric opening and dissociation of the histone core. Proceedings of the National Academy of Sciences. 114(2). 334–339. 82 indexed citations
14.
Wang, Juan, et al.. (2014). Fast Binding Kinetics of RNA Aptamers Measured using a Novel Microfluidic Mixer. Biophysical Journal. 106(2). 796a–796a. 1 indexed citations
15.
Tokuda, Joshua M., Traci Topping, Julie L. Sutton, et al.. (2014). Revealing transient structures of nucleosomes as DNA unwinds. Nucleic Acids Research. 42(13). 8767–8776. 60 indexed citations
16.
Chen, Huimin, Steve P. Meisburger, Suzette A. Pabit, et al.. (2011). Ionic strength-dependent persistence lengths of single-stranded RNA and DNA. Proceedings of the National Academy of Sciences. 109(3). 799–804. 309 indexed citations
17.
Lamb, Jessica S., et al.. (2009). Dimer formation in the blue light sensing protein Vivid. Biophysical Journal. 96(3). 524a–524a. 1 indexed citations
18.
Li, Li, Suzette A. Pabit, Jessica S. Lamb, Hye Yoon Park, & Lois Pollack. (2009). Closing The Lid On Dna End-to-end Stacking Interactions. Biophysical Journal. 96(3). 346a–346a. 2 indexed citations
19.
Russell, Rick, Ian S. Millett, Mark W. Täte, et al.. (2002). Rapid compaction during RNA folding. Proceedings of the National Academy of Sciences. 99(7). 4266–4271. 173 indexed citations
20.
Pollack, Lois. (1965). RECOMMENDED DELAY IN COUNTING AFTER NEUTRON ACTIVATION. Transactions of the American Nuclear Society. 1 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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