Sarah E. Rice

4.2k total citations · 2 hit papers
46 papers, 3.3k citations indexed

About

Sarah E. Rice is a scholar working on Cell Biology, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Sarah E. Rice has authored 46 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Cell Biology, 28 papers in Molecular Biology and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Sarah E. Rice's work include Microtubule and mitosis dynamics (33 papers), Cellular transport and secretion (10 papers) and Photosynthetic Processes and Mechanisms (10 papers). Sarah E. Rice is often cited by papers focused on Microtubule and mitosis dynamics (33 papers), Cellular transport and secretion (10 papers) and Photosynthetic Processes and Mechanisms (10 papers). Sarah E. Rice collaborates with scholars based in United States. Sarah E. Rice's co-authors include Yao Liang Wong, Ghazaleh Ashrafi, Thomas L. Schwarz, Judith A. Steen, Julia S. Schlehe, Dennis J. Selkoe, Xinnan Wang, Dominic Winter, Matthew J. LaVoie and Nariman Naber and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Sarah E. Rice

45 papers receiving 3.2k citations

Hit Papers

PINK1 and Parkin Target M... 1999 2026 2008 2017 2011 1999 250 500 750

Author Peers

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

Author Last Decade Papers Cites
Sarah E. Rice 2.1k 1.8k 560 379 311 46 3.3k
Joseph Albanesi 3.3k 1.6× 2.8k 1.6× 318 0.6× 71 0.2× 633 2.0× 86 4.9k
Kristen J. Verhey 5.1k 2.4× 4.5k 2.6× 350 0.6× 149 0.4× 92 0.3× 95 7.5k
Walter Carrington 3.1k 1.5× 1.1k 0.6× 334 0.6× 89 0.2× 239 0.8× 27 4.3k
Esben Lorentzen 3.9k 1.8× 1.2k 0.7× 239 0.4× 678 1.8× 53 0.2× 72 5.0k
Maria M. Magiera 3.8k 1.8× 2.2k 1.2× 320 0.6× 95 0.3× 132 0.4× 44 4.8k
Naoko Mizuno 1.2k 0.6× 921 0.5× 96 0.2× 304 0.8× 39 0.1× 46 2.3k
Eran Perlson 2.0k 0.9× 984 0.6× 172 0.3× 520 1.4× 34 0.1× 64 3.6k
H. Benjamin Peng 2.6k 1.2× 1.2k 0.7× 52 0.1× 166 0.4× 205 0.7× 90 3.6k
Yoshiyuki Konishi 2.0k 1.0× 846 0.5× 165 0.3× 157 0.4× 26 0.1× 84 3.5k
Fred S. Wouters 2.4k 1.1× 825 0.5× 132 0.2× 162 0.4× 45 0.1× 60 3.7k

Countries citing papers authored by Sarah E. Rice

Since Specialization
Citations

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

Fields of papers citing papers by Sarah E. Rice

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah E. Rice

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah E. Rice. A scholar is included among the top collaborators of Sarah E. 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 Sarah E. Rice. Sarah E. 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.
Waitzman, Joshua S., et al.. (2014). SRC Phosphorylation Regulates the Human Kinesin-5, Eg5, and Disrupts the Binding of Eg5 Inhibitors. Biophysical Journal. 106(2). 780a–780a. 1 indexed citations
2.
Focia, Pamela J., et al.. (2014). Structural Coupling of the EF Hand and C-Terminal GTPase Domains in the Mitochondrial Protein Miro. Biophysical Journal. 106(2). 28a–28a. 1 indexed citations
3.
Vinogradova, Maia, et al.. (2013). Plant Kinesin-Like Calmodulin Binding Protein Employs Its Regulatory Domain for Dimerization. PLoS ONE. 8(6). e66669–e66669. 4 indexed citations
4.
Landahl, Eric C. & Sarah E. Rice. (2013). Model-independent decomposition of two-state data. Physical Review E. 88(6). 62713–62713. 2 indexed citations
5.
Waitzman, Joshua S., Adam G. Larson, Jared C. Cochran, et al.. (2012). The Loop 5 Element Structurally and Kinetically Coordinates Dimers of the Human Kinesin-5 Eg5. Biophysical Journal. 102(3). 370a–370a. 3 indexed citations
6.
Seeger, Mark A., Yongbo Zhang, & Sarah E. Rice. (2012). Intrinsic Disorder in the Kinesin Superfamily. Biophysical Journal. 102(3). 368a–368a. 1 indexed citations
7.
Seeger, Mark A., Yongbo Zhang, & Sarah E. Rice. (2012). Kinesin tail domains are intrinsically disordered. Proteins Structure Function and Bioinformatics. 80(10). 2437–2446. 17 indexed citations
8.
Waitzman, Joshua S., Adam G. Larson, Jared C. Cochran, et al.. (2011). The Loop 5 Element Structurally and Kinetically Coordinates Dimers of the Human Kinesin-5, Eg5. Biophysical Journal. 101(11). 2760–2769. 32 indexed citations
9.
Naber, Nariman, Adam G. Larson, Sarah E. Rice, Roger Cooke, & Edward Pate. (2011). Multiple Conformations of the Nucleotide Site of Kinesin Family Motors in the Triphosphate State. Journal of Molecular Biology. 408(4). 628–642. 10 indexed citations
10.
Wang, Xinnan, Dominic Winter, Ghazaleh Ashrafi, et al.. (2011). PINK1 and Parkin Target Miro for Phosphorylation and Degradation to Arrest Mitochondrial Motility. Cell. 147(4). 893–906. 937 indexed citations breakdown →
11.
Seeger, Mark A. & Sarah E. Rice. (2010). The Kinesin-1 Tail Binds to Microtubules in a Manner Similar to Tau. Biophysical Journal. 98(3). 371a–371a. 5 indexed citations
12.
Gelfand, Vladimir I., et al.. (2010). Opposite-Polarity Motors Activate One Another to Trigger Cargo Transport in Live Cells. Biophysical Journal. 98(3). 431a–431a. 3 indexed citations
13.
Wong, Yao Liang & Sarah E. Rice. (2010). Kinesin's Light Chains Inhibit the Head- and Microtubule-Binding Activity of its Tail. Biophysical Journal. 98(3). 371a–371a. 15 indexed citations
14.
Larson, Adam G., Nariman Naber, Roger Cooke, Edward Pate, & Sarah E. Rice. (2010). The Conserved L5 Loop Establishes the Pre-Powerstroke Conformation of the Kinesin-5 Motor, Eg5. Biophysical Journal. 98(11). 2619–2627. 33 indexed citations
15.
Larson, Adam G., Eric C. Landahl, & Sarah E. Rice. (2009). Mechanism of cooperative behaviour in systems of slow and fast molecular motors. Physical Chemistry Chemical Physics. 11(24). 4890–4890. 25 indexed citations
16.
Sindelar, Charles V., et al.. (2008). The kinesin-1 motor protein is regulated by a direct interaction of its head and tail. Proceedings of the National Academy of Sciences. 105(26). 8938–8943. 88 indexed citations
17.
Naber, Nariman, et al.. (2003). EPR Spectroscopy Shows a Microtubule-Dependent Conformational Change in the Kinesin Switch 1 Domain. Biophysical Journal. 84(5). 3190–3196. 26 indexed citations
18.
Rice, Sarah E., Thomas J. Purcell, & James A. Spudich. (2003). [6] Building and using optical traps to study properties of molecular motors. Methods in enzymology on CD-ROM/Methods in enzymology. 361. 112–133. 24 indexed citations
19.
Sindelar, Charles V., et al.. (2002). Two conformations in the human kinesin power stroke defined by X-ray crystallography and EPR spectroscopy. Nature Structural Biology. 9(11). 844–8. 121 indexed citations
20.
Case, Ryan, et al.. (2000). Role of the kinesin neck linker and catalytic core in microtubule-based motility. Current Biology. 10(3). 157–160. 130 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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