Stephen L. Rogers

5.4k total citations
64 papers, 3.9k citations indexed

About

Stephen L. Rogers is a scholar working on Cell Biology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Stephen L. Rogers has authored 64 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Cell Biology, 35 papers in Molecular Biology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Stephen L. Rogers's work include Microtubule and mitosis dynamics (33 papers), Cellular Mechanics and Interactions (25 papers) and Cellular transport and secretion (16 papers). Stephen L. Rogers is often cited by papers focused on Microtubule and mitosis dynamics (33 papers), Cellular Mechanics and Interactions (25 papers) and Cellular transport and secretion (16 papers). Stephen L. Rogers collaborates with scholars based in United States, United Kingdom and Germany. Stephen L. Rogers's co-authors include Gregory C. Rogers, Ronald D. Vale, David Sharp, Vladimir I. Gelfand, Ursula Wiedemann, Nico Stuurman, Mark Peifer, Nasser M. Rusan, R. Horsch and Harry J. Klee and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Stephen L. Rogers

61 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen L. Rogers United States 32 2.9k 2.7k 538 414 224 64 3.9k
Beverly Wendland United States 41 3.4k 1.2× 4.0k 1.5× 343 0.6× 864 2.1× 136 0.6× 69 5.2k
Dannel McCollum United States 37 3.3k 1.2× 4.1k 1.5× 646 1.2× 400 1.0× 171 0.8× 65 5.0k
Damian Brunner Switzerland 25 2.2k 0.8× 2.6k 0.9× 393 0.7× 456 1.1× 147 0.7× 41 3.5k
Michel Labouesse France 42 1.5k 0.5× 3.6k 1.3× 364 0.7× 292 0.7× 376 1.7× 94 5.4k
Arnaud Échard France 36 3.5k 1.2× 2.8k 1.0× 226 0.4× 252 0.6× 307 1.4× 66 4.8k
Koret Hirschberg Israel 25 2.9k 1.0× 3.4k 1.2× 198 0.4× 439 1.1× 227 1.0× 60 5.0k
James B. Moseley United States 28 2.3k 0.8× 2.2k 0.8× 315 0.6× 252 0.6× 138 0.6× 53 3.4k
Thomas E. Kreis Switzerland 37 4.1k 1.4× 3.7k 1.3× 212 0.4× 294 0.7× 343 1.5× 46 5.6k
Kevin T. Vaughan United States 30 2.9k 1.0× 3.0k 1.1× 226 0.4× 335 0.8× 417 1.9× 44 4.1k
Eyal D. Schejter Israel 35 1.6k 0.6× 3.1k 1.1× 177 0.3× 707 1.7× 404 1.8× 69 3.9k

Countries citing papers authored by Stephen L. Rogers

Since Specialization
Citations

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

Fields of papers citing papers by Stephen L. Rogers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen L. Rogers. 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 Stephen L. Rogers. The network helps show where Stephen L. Rogers may publish in the future.

Co-authorship network of co-authors of Stephen L. Rogers

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen L. Rogers. A scholar is included among the top collaborators of Stephen L. Rogers 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 Stephen L. Rogers. Stephen L. Rogers 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.
Kim, Sun K., et al.. (2024). EB-SUN, a new microtubule plus-end tracking protein in Drosophila. Molecular Biology of the Cell. 35(12). ar147–ar147.
2.
Rogers, Stephen L., et al.. (2023). CryoET shows cofilactin filaments inside the microtubule lumen. EMBO Reports. 24(11). e57264–e57264. 6 indexed citations
3.
4.
Rogers, Stephen L., et al.. (2015). TOG Proteins Are Spatially Regulated by Rac-GSK3β to Control Interphase Microtubule Dynamics. PLoS ONE. 10(9). e0138966–e0138966. 9 indexed citations
5.
6.
Applewhite, Derek A., et al.. (2013). The actin-microtubule cross-linking activity ofDrosophilaShort stop is regulated by intramolecular inhibition. Molecular Biology of the Cell. 24(18). 2885–2893. 37 indexed citations
7.
Zhang, Dong, Shannon F. Stewman, Juan Daniel Díaz‐Valencia, et al.. (2011). Drosophila katanin is a microtubule depolymerase that regulates cortical-microtubule plus-end interactions and cell migration. Nature Cell Biology. 13(4). 361–369. 86 indexed citations
8.
Banerjee, Swati, et al.. (2010). Drosophila Neurexin IV Interacts with Roundabout and Is Required for Repulsive Midline Axon Guidance. Journal of Neuroscience. 30(16). 5653–5667. 31 indexed citations
9.
Schimizzi, Gregory V., Joshua D. Currie, & Stephen L. Rogers. (2010). Expression Levels of a Kinesin-13 Microtubule Depolymerase Modulates the Effectiveness of Anti-Microtubule Agents. PLoS ONE. 5(6). e11381–e11381. 12 indexed citations
10.
Applewhite, Derek A., et al.. (2010). The Spectraplakin Short Stop Is an Actin–Microtubule Cross-Linker That Contributes to Organization of the Microtubule Network. Molecular Biology of the Cell. 21(10). 1714–1724. 83 indexed citations
11.
Rogers, Gregory C., Nasser M. Rusan, Mark Peifer, & Stephen L. Rogers. (2008). A Multicomponent Assembly Pathway Contributes to the Formation of Acentrosomal Microtubule Arrays in Interphase Drosophila Cells. Molecular Biology of the Cell. 19(7). 3163–3178. 112 indexed citations
12.
Gates, Julie, James P. Mahaffey, Stephen L. Rogers, et al.. (2007). Enabled plays key roles in embryonic epithelial morphogenesis in Drosophila. Development. 134(11). 2027–2039. 105 indexed citations
13.
Jiang, Lan, Stephen L. Rogers, & Stephen T. Crews. (2007). The Drosophila Dead end Arf-like3 GTPase controls vesicle trafficking during tracheal fusion cell morphogenesis. Developmental Biology. 311(2). 487–499. 37 indexed citations
14.
Dzhindzhev, Nikola S., Stephen L. Rogers, Ronald D. Vale, & Hiroyuki Ohkura. (2005). Distinct mechanisms govern the localisation of Drosophila CLIP-190 to unattached kinetochores and microtubule plus-ends. Journal of Cell Science. 118(16). 3781–3790. 35 indexed citations
15.
Rogers, Stephen L., Ursula Wiedemann, Nico Stuurman, & Ronald D. Vale. (2003). Molecular requirements for actin-based lamella formation in Drosophila S2 cells. The Journal of Cell Biology. 162(6). 1079–1088. 350 indexed citations
16.
Rothenberg, Michael E., Stephen L. Rogers, Ronald D. Vale, Lily Yeh Jan, & Yuh Nung Jan. (2003). Drosophila Pod-1 Crosslinks Both Actin and Microtubules and Controls the Targeting of Axons. Neuron. 39(5). 779–791. 56 indexed citations
17.
Rogers, Stephen L., Gregory C. Rogers, David Sharp, & Ronald D. Vale. (2002). Drosophila EB1 is important for proper assembly, dynamics, and positioning of the mitotic spindle. The Journal of Cell Biology. 158(5). 873–884. 337 indexed citations
18.
Rogers, Stephen L. & Vladimir I. Gelfand. (2000). Membrane trafficking, organelle transport, and the cytoskeleton. Current Opinion in Cell Biology. 12(1). 57–62. 160 indexed citations
19.
Rogers, Stephen L., et al.. (1993). Shade levels for taro cropping systems. 5(2). 9–12. 3 indexed citations
20.
Rogers, Stephen L. & R.C. Rosecrance. (1992). Coppice management of Paraserianthes falcataria in Western Samoa.. 10. 178–179. 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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