Phoebe A. Rice

7.3k total citations · 3 hit papers
86 papers, 5.5k citations indexed

About

Phoebe A. Rice is a scholar working on Molecular Biology, Genetics and Materials Chemistry. According to data from OpenAlex, Phoebe A. Rice has authored 86 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 26 papers in Genetics and 16 papers in Materials Chemistry. Recurrent topics in Phoebe A. Rice's work include DNA and Nucleic Acid Chemistry (31 papers), RNA and protein synthesis mechanisms (28 papers) and DNA Repair Mechanisms (26 papers). Phoebe A. Rice is often cited by papers focused on DNA and Nucleic Acid Chemistry (31 papers), RNA and protein synthesis mechanisms (28 papers) and DNA Repair Mechanisms (26 papers). Phoebe A. Rice collaborates with scholars based in United States, United Kingdom and China. Phoebe A. Rice's co-authors include Nigel D. F. Grindley, Kiyoshi Mizuuchi, Katrine Whiteson, Kerren K. Swinger, Shuwei Yang, Howard A. Nash, Thomas A. Steitz, Chuan He, E.M. Duguid and Ying Z. Pigli and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Phoebe A. Rice

85 papers receiving 5.4k citations

Hit Papers

Crystal Structure of an IHF-DNA Complex: A Protein-Induce... 1994 2026 2004 2015 1996 2006 1994 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Phoebe A. Rice United States 35 4.6k 1.5k 944 773 478 86 5.5k
Robert J. Crouch United States 41 5.5k 1.2× 1.2k 0.8× 668 0.7× 712 0.9× 466 1.0× 86 6.4k
Henri Buc France 36 4.0k 0.9× 2.2k 1.5× 708 0.8× 503 0.7× 262 0.5× 79 4.9k
Nigel D. F. Grindley United States 49 5.7k 1.3× 2.6k 1.7× 1.4k 1.5× 535 0.7× 761 1.6× 108 6.8k
Sylvie Doublié United States 36 5.0k 1.1× 997 0.7× 394 0.4× 549 0.7× 284 0.6× 91 5.7k
David S. Waugh United States 48 5.8k 1.3× 1.8k 1.2× 834 0.9× 448 0.6× 550 1.2× 140 7.7k
Charles S. McHenry United States 46 5.8k 1.3× 3.5k 2.4× 588 0.6× 374 0.5× 248 0.5× 114 6.5k
Daniel Ladant France 47 4.8k 1.1× 2.8k 1.9× 831 0.9× 667 0.9× 275 0.6× 144 7.6k
Luis Blanco Spain 47 6.3k 1.4× 2.0k 1.4× 1.4k 1.5× 565 0.7× 595 1.2× 146 7.4k
Jacob Lebowitz United States 32 2.8k 0.6× 618 0.4× 688 0.7× 350 0.5× 254 0.5× 74 4.3k
Muriel Delepierre France 40 3.5k 0.8× 922 0.6× 268 0.3× 689 0.9× 737 1.5× 158 5.4k

Countries citing papers authored by Phoebe A. Rice

Since Specialization
Citations

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

Fields of papers citing papers by Phoebe A. Rice

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Phoebe A. Rice. 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 Phoebe A. Rice. The network helps show where Phoebe A. Rice may publish in the future.

Co-authorship network of co-authors of Phoebe A. Rice

This figure shows the co-authorship network connecting the top 25 collaborators of Phoebe A. Rice. A scholar is included among the top collaborators of Phoebe A. Rice 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 Phoebe A. Rice. Phoebe A. Rice 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.
Ruppel, Hans Georg, Evan S. Snitkin, Vincent B. Young, et al.. (2025). Flagellar switch inverted repeats impact heterogeneity in flagellar gene expression and thus C. difficile RT027/MLST1 virulence. Cell Reports. 44(6). 115830–115830. 1 indexed citations
2.
Pigli, Ying Z., et al.. (2025). Large serine integrases utilise scavenged phage proteins as directionality cofactors. Nucleic Acids Research. 53(3).
3.
Pigli, Ying Z., Søren Heissel, Vincent Libis, et al.. (2024). DNA glycosylases provide antiviral defence in prokaryotes. Nature. 629(8011). 410–416. 10 indexed citations
4.
Rice, Phoebe A., et al.. (2023). Crystal structure of a cap-independent translation enhancer RNA. Nucleic Acids Research. 51(16). 8891–8907. 6 indexed citations
5.
Montaño, Sherwin P., Sally‐J. Rowland, James R. Fuller, et al.. (2022). Structural basis for topological regulation of Tn3 resolvase. Nucleic Acids Research. 51(3). 1001–1018. 2 indexed citations
6.
Mir‐Sanchis, Ignacio, et al.. (2020). A novel DNA primase-helicase pair encoded by SCCmec elements. eLife. 9. 7 indexed citations
7.
Koirala, Deepak, Yaming Shao, Yelena Koldobskaya, et al.. (2019). A conserved RNA structural motif for organizing topology within picornaviral internal ribosome entry sites. Nature Communications. 10(1). 3629–3629. 18 indexed citations
8.
Rice, Phoebe A.. (2019). Structure of the P element transpososome reveals new twists on the DD(E/D) theme. Nature Structural & Molecular Biology. 26(11). 989–990. 1 indexed citations
9.
Trejo, Stephen J., Ronald S. Rock, W. Marshall Stark, Martin R. Boocock, & Phoebe A. Rice. (2017). Snapshots of a molecular swivel in action. Nucleic Acids Research. 46(10). 5286–5296. 7 indexed citations
10.
Fuller, James R. & Phoebe A. Rice. (2017). Target DNA bending by the Mu transpososome promotes careful transposition and prevents its reversal. eLife. 6. 20 indexed citations
11.
Kuznetsov, Serguei V., et al.. (2017). Two-step interrogation then recognition of DNA binding site by Integration Host Factor: an architectural DNA-bending protein. Nucleic Acids Research. 46(4). 1741–1755. 13 indexed citations
12.
Kiljunen, Saija, Saija Haapa-Paananen, Maria I. Pajunen, et al.. (2017). Mu transpososome activity-profiling yields hyperactive MuA variants for highly efficient genetic and genome engineering. Nucleic Acids Research. 46(9). 4649–4661. 3 indexed citations
13.
Rowland, Sally‐J., et al.. (2011). Structural Basis for Catalytic Activation of a Serine Recombinase. Structure. 19(6). 799–809. 37 indexed citations
14.
Haddadian, Esmael J., Haipeng Gong, Abhishek Jha, et al.. (2011). Automated Real-Space Refinement of Protein Structures Using a Realistic Backbone Move Set. Biophysical Journal. 101(4). 899–909. 22 indexed citations
15.
Yang, Cai‐Guang, Chengqi Yi, E.M. Duguid, et al.. (2008). Crystal structures of DNA/RNA repair enzymes AlkB and ABH2 bound to dsDNA. Nature. 452(7190). 961–965. 202 indexed citations
16.
Mouw, Kent W. & Phoebe A. Rice. (2007). Shaping the Borrelia burgdorferi genome: crystal structure and binding properties of the DNA‐bending protein Hbb. Molecular Microbiology. 63(5). 1319–1330. 56 indexed citations
17.
Lu, Ping, Héctor Sandoval, Phoebe A. Rice, & David B. Roth. (2007). Amino acid residues in Rag1 crucial for DNA hairpin formation (35.12). The Journal of Immunology. 178(1_Supplement). S3–S3. 1 indexed citations
18.
Lu, Ping, Héctor Sandoval, Vicky Brandt, Phoebe A. Rice, & David B. Roth. (2006). Amino acid residues in Rag1 crucial for DNA hairpin formation. Nature Structural & Molecular Biology. 13(11). 1010–1015. 31 indexed citations
19.
Kohlstaedt, Lori A., Jimin Wang, Phoebe A. Rice, Jonathan M. Friedman, & Thomas A. Steitz. (1993). 12 The Structure of HIV-1 Reverse Transcriptase. Cold Spring Harbor Monograph Archive. 23. 223–249. 27 indexed citations
20.
Rice, Phoebe A. & Thomas A. Steitz. (1993). MODEL FOR A DNA MEDIATED SYNAPTIC COMPLEX SUGGESTED BY CRYSTAL PACKING OF GAMMA DELTA RESOLVASE SUBUNITS. PubMed. 13(7). 1514–24. 53 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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