Nasser M. Rusan

3.4k total citations
56 papers, 2.4k citations indexed

About

Nasser M. Rusan is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Nasser M. Rusan has authored 56 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 45 papers in Cell Biology and 13 papers in Plant Science. Recurrent topics in Nasser M. Rusan's work include Microtubule and mitosis dynamics (42 papers), Protist diversity and phylogeny (10 papers) and Ubiquitin and proteasome pathways (7 papers). Nasser M. Rusan is often cited by papers focused on Microtubule and mitosis dynamics (42 papers), Protist diversity and phylogeny (10 papers) and Ubiquitin and proteasome pathways (7 papers). Nasser M. Rusan collaborates with scholars based in United States, Germany and Russia. Nasser M. Rusan's co-authors include Mark Peifer, Patricia Wadsworth, Carey J. Fagerstrom, Gregory C. Rogers, Anne-Marie C. Yvon, Stephen L. Rogers, U. Serdar Tulu, Dorothy A. Lerit, Brian J. Galletta and David M. Roberts and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Nasser M. Rusan

53 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nasser M. Rusan United States 27 1.8k 1.7k 385 342 307 56 2.4k
Douglas R. Kellogg United States 34 3.4k 1.9× 2.0k 1.2× 600 1.6× 267 0.8× 289 0.9× 65 3.9k
Jens Lüders Spain 24 2.3k 1.3× 1.8k 1.1× 239 0.6× 344 1.0× 145 0.5× 38 2.7k
Sophie G. Martin Switzerland 33 3.4k 1.9× 1.7k 1.0× 538 1.4× 230 0.7× 153 0.5× 85 4.0k
Aaron C. Groen United States 28 2.0k 1.1× 2.0k 1.2× 292 0.8× 182 0.5× 189 0.6× 38 2.6k
Valérie Doye France 39 5.2k 2.9× 1.9k 1.2× 262 0.7× 268 0.8× 168 0.5× 60 5.9k
Antonina Roll‐Mecak United States 32 2.7k 1.5× 2.0k 1.2× 185 0.5× 356 1.0× 125 0.4× 54 3.6k
Sebastian A. Leidel Germany 33 3.4k 1.9× 1.0k 0.6× 308 0.8× 391 1.1× 426 1.4× 61 3.9k
Dae In Kim United States 15 2.7k 1.5× 2.1k 1.2× 229 0.6× 263 0.8× 181 0.6× 29 3.9k
Akatsuki Kimura Japan 28 2.0k 1.1× 935 0.6× 357 0.9× 217 0.6× 120 0.4× 60 2.6k
Sue L. Jaspersen United States 32 3.5k 1.9× 1.9k 1.1× 703 1.8× 215 0.6× 171 0.6× 69 3.8k

Countries citing papers authored by Nasser M. Rusan

Since Specialization
Citations

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

Fields of papers citing papers by Nasser M. Rusan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nasser M. Rusan. 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 Nasser M. Rusan. The network helps show where Nasser M. Rusan may publish in the future.

Co-authorship network of co-authors of Nasser M. Rusan

This figure shows the co-authorship network connecting the top 25 collaborators of Nasser M. Rusan. A scholar is included among the top collaborators of Nasser M. Rusan 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 Nasser M. Rusan. Nasser M. Rusan 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.
2.
Galletta, Brian J., Carey J. Fagerstrom, Bing Yang, et al.. (2023). The E3 ligase Poe promotes Pericentrin degradation. Molecular Biology of the Cell. 34(9). br15–br15. 1 indexed citations
3.
Liu, Rong, Neil Billington, Brian J. Galletta, et al.. (2022). Pericentrin interacts with Kinesin-1 to drive centriole motility. The Journal of Cell Biology. 221(9). 6 indexed citations
4.
Galletta, Brian J., Carey J. Fagerstrom, Justin M. Fear, et al.. (2020). Sperm Head-Tail Linkage Requires Restriction of Pericentriolar Material to the Proximal Centriole End. Developmental Cell. 53(1). 86–101.e7. 18 indexed citations
5.
Fagerstrom, Carey J., et al.. (2019). Fascetto interacting protein ensures proper cytokinesis and ploidy. Molecular Biology of the Cell. 30(8). 992–1007. 4 indexed citations
6.
Buster, Daniel W., et al.. (2018). Asterless is a Polo-like kinase 4 substrate that both activates and inhibits kinase activity depending on its phosphorylation state. Molecular Biology of the Cell. 29(23). 2874–2886. 18 indexed citations
7.
Hammer, John A., et al.. (2017). A centrosomal scaffold shows some self-control. Journal of Biological Chemistry. 292(50). 20410–20411. 4 indexed citations
8.
Plevock, Karen M., Rebecca C. Adikes, Julian Haase, et al.. (2017). Stu2 uses a 15-nm parallel coiled coil for kinetochore localization and concomitant regulation of the mitotic spindle. Molecular Biology of the Cell. 29(3). 285–294. 4 indexed citations
9.
Galletta, Brian J. & Nasser M. Rusan. (2015). A yeast two-hybrid approach for probing protein–protein interactions at the centrosome. Methods in cell biology. 129. 251–277. 23 indexed citations
10.
Lerit, Dorothy A., Joanna Poulton, Carey J. Fagerstrom, et al.. (2015). Interphase centrosome organization by the PLP-Cnn scaffold is required for centrosome function. The Journal of Cell Biology. 210(1). 79–97. 50 indexed citations
11.
Lerit, Dorothy A., Karen M. Plevock, & Nasser M. Rusan. (2014). Live Imaging of <em>Drosophila</em> Larval Neuroblasts. Journal of Visualized Experiments. 23 indexed citations
12.
Lerit, Dorothy A., Jeremy T. Smyth, & Nasser M. Rusan. (2013). Organelle asymmetry for proper fitness, function, and fate. Chromosome Research. 21(3). 271–286. 17 indexed citations
13.
Klebba, Joseph E., Daniel W. Buster, Annie L. Nguyen, et al.. (2013). Polo-like Kinase 4 Autodestructs by Generating Its Slimb-Binding Phosphodegron. Current Biology. 23(22). 2255–2261. 65 indexed citations
14.
Ahmad, Shaad M., Terese R. Tansey, Brian W. Busser, et al.. (2012). Two Forkhead Transcription Factors Regulate the Division of Cardiac Progenitor Cells by a Polo-Dependent Pathway. Developmental Cell. 23(1). 97–111. 24 indexed citations
15.
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
16.
Rusan, Nasser M. & Mark Peifer. (2007). A role for a novel centrosome cycle in asymmetric cell division. The Journal of Cell Biology. 177(1). 13–20. 194 indexed citations
17.
Daniels, Robert, et al.. (2006). Simian Virus 40 Late Proteins Possess Lytic Properties That Render Them Capable of Permeabilizing Cellular Membranes. Journal of Virology. 80(13). 6575–6587. 37 indexed citations
18.
Wadsworth, Patricia, Nasser M. Rusan, U. Serdar Tulu, & Carey J. Fagerstrom. (2005). Stable expression of fluorescently tagged proteins for studies of mitosis in mammalian cells. Nature Methods. 2(12). 981–987. 15 indexed citations
19.
Tulu, U. Serdar, Nasser M. Rusan, & Patricia Wadsworth. (2003). Peripheral, Non-Centrosome-Associated Microtubules Contribute to Spindle Formation in Centrosome-Containing Cells. Current Biology. 13(21). 1894–1899. 89 indexed citations
20.
Rusan, Nasser M., U. Serdar Tulu, Carey J. Fagerstrom, & Patricia Wadsworth. (2002). Reorganization of the microtubule array in prophase/prometaphase requires cytoplasmic dynein-dependent microtubule transport. The Journal of Cell Biology. 158(6). 997–1003. 102 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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