Iain M. Cheeseman

15.5k total citations · 4 hit papers
109 papers, 11.1k citations indexed

About

Iain M. Cheeseman is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Iain M. Cheeseman has authored 109 papers receiving a total of 11.1k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 84 papers in Cell Biology and 26 papers in Plant Science. Recurrent topics in Iain M. Cheeseman's work include Microtubule and mitosis dynamics (81 papers), Genomics and Chromatin Dynamics (34 papers) and Photosynthetic Processes and Mechanisms (21 papers). Iain M. Cheeseman is often cited by papers focused on Microtubule and mitosis dynamics (81 papers), Genomics and Chromatin Dynamics (34 papers) and Photosynthetic Processes and Mechanisms (21 papers). Iain M. Cheeseman collaborates with scholars based in United States, Japan and France. Iain M. Cheeseman's co-authors include Arshad Desai, Kara L. McKinley, Tatsuo Fukagawa, John R. Yates, Elizabeth M. Wilson-Kubalek, Michael A. Lampson, Tomomi Kiyomitsu, Georjana Barnes, David G. Drubin and Joshua S. Chappie and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Iain M. Cheeseman

105 papers receiving 11.1k citations

Hit Papers

The Conserved KMN Network Constitutes the Core Microtubul... 2002 2026 2010 2018 2006 2007 2002 2015 250 500 750

Peers

Iain M. Cheeseman
Aaron F. Straight United States
Frank Uhlmann United Kingdom
Rebecca Heald United States
Alexey Khodjakov United States
Michael A. Lampson United States
Mark Winey United States
Paul S. Maddox United States
Conly L. Rieder United States
Kerry Bloom United States
Aaron F. Straight United States
Iain M. Cheeseman
Citations per year, relative to Iain M. Cheeseman Iain M. Cheeseman (= 1×) peers Aaron F. Straight

Countries citing papers authored by Iain M. Cheeseman

Since Specialization
Citations

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

Fields of papers citing papers by Iain M. Cheeseman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iain M. Cheeseman

This figure shows the co-authorship network connecting the top 25 collaborators of Iain M. Cheeseman. A scholar is included among the top collaborators of Iain M. Cheeseman 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 Iain M. Cheeseman. Iain M. Cheeseman 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.
Ly, Jimmy, et al.. (2025). RNase MRP subunit composition and role in 40S ribosome biogenesis. Nature Structural & Molecular Biology. 33(1). 20–33.
2.
Su, Kuan-Chung, et al.. (2024). Functional genetics reveals modulators of antimicrotubule drug sensitivity. The Journal of Cell Biology. 224(2). 1 indexed citations
3.
Grishchuk, Ekaterina L., et al.. (2024). Higher-order protein assembly controls kinetochore formation. Nature Cell Biology. 26(1). 45–56. 8 indexed citations
4.
Swartz, S. Zachary, Tzer Han Tan, Margherita Perillo, et al.. (2021). Polarized Dishevelled dissolution and reassembly drives embryonic axis specification in sea star oocytes. Current Biology. 31(24). 5633–5641.e4. 7 indexed citations
5.
Su, Kuan-Chung, et al.. (2018). CRISPR/Cas9-based gene targeting using synthetic guide RNAs enables robust cell biological analyses. Molecular Biology of the Cell. 29(20). 2370–2377. 13 indexed citations
6.
Monda, Julie K. & Iain M. Cheeseman. (2018). Nde1 promotes diverse dynein functions through differential interactions and exhibits an isoform-specific proteasome association. Molecular Biology of the Cell. 29(19). 2336–2345. 15 indexed citations
7.
McKinley, Kara L. & Iain M. Cheeseman. (2017). Large-Scale Analysis of CRISPR/Cas9 Cell-Cycle Knockouts Reveals the Diversity of p53-Dependent Responses to Cell-Cycle Defects. Developmental Cell. 40(4). 405–420.e2. 127 indexed citations
8.
Monnier, Nilah, Zachary Barry, Hye Yoon Park, et al.. (2015). Inferring transient particle transport dynamics in live cells. Nature Methods. 12(9). 838–840. 126 indexed citations
9.
Kiyomitsu, Tomomi & Iain M. Cheeseman. (2013). Cortical Dynein and Asymmetric Membrane Elongation Coordinately Position the Spindle in Anaphase. Cell. 154(2). 391–402. 193 indexed citations
10.
Welburn, Julie P. I. & Iain M. Cheeseman. (2012). The microtubule-binding protein Cep170 promotes the targeting of the kinesin-13 depolymerase Kif2b to the mitotic spindle. Molecular Biology of the Cell. 23(24). 4786–4795. 47 indexed citations
11.
Lorestani, Alexander, F. Douglas Ivey, Sivasakthivel Thirugnanam, et al.. (2012). Targeted proteomic dissection of Toxoplasma cytoskeleton sub‐compartments using MORN1. Cytoskeleton. 69(12). 1069–1085. 41 indexed citations
12.
Backer, Chelsea B., Jennifer H. Gutzman, Chad G. Pearson, & Iain M. Cheeseman. (2012). CSAP localizes to polyglutamylated microtubules and promotes proper cilia function and zebrafish development. Molecular Biology of the Cell. 23(11). 2122–2130. 34 indexed citations
13.
Liu, Dan, Mathijs Vleugel, Chelsea B. Backer, et al.. (2010). Regulated targeting of protein phosphatase 1 to the outer kinetochore by KNL1 opposes Aurora B kinase. The Journal of Cell Biology. 188(6). 809–820. 287 indexed citations
14.
Welburn, Julie P. I., Mathijs Vleugel, Dan Liu, et al.. (2010). Aurora B phosphorylates spatially distinct targets to differentially regulate the kinetochore-microtubule interface. DSpace@MIT (Massachusetts Institute of Technology). 3 indexed citations
15.
Lampson, Michael A. & Iain M. Cheeseman. (2010). Sensing centromere tension: Aurora B and the regulation of kinetochore function. Trends in Cell Biology. 21(3). 133–140. 298 indexed citations
16.
Gascoigne, Karen E. & Iain M. Cheeseman. (2010). Kinetochore assembly: if you build it, they will come. Current Opinion in Cell Biology. 23(1). 102–108. 48 indexed citations
17.
Suzuki, Aussie, Tetsuya Hori, Chelsea B. Backer, et al.. (2009). The CENP-S complex is essential for the stable assembly of outer kinetochore structure. DSpace@MIT (Massachusetts Institute of Technology). 4 indexed citations
18.
Glazer, Andrew M., Alex W. Wilkinson, Chelsea B. Backer, et al.. (2009). The Zn Finger protein Iguana impacts Hedgehog signaling by promoting ciliogenesis. Developmental Biology. 337(1). 148–156. 80 indexed citations
19.
McIntosh, J. Richard, Ekaterina L. Grishchuk, Mary Morphew, et al.. (2008). Fibrils Connect Microtubule Tips with Kinetochores: A Mechanism to Couple Tubulin Dynamics to Chromosome Motion. Cell. 135(2). 322–333. 162 indexed citations
20.
Gassmann, Reto, Anthony Essex, Paul S. Maddox, et al.. (2008). A new mechanism controlling kinetochore–microtubule interactions revealed by comparison of two dynein-targeting components: SPDL-1 and the Rod/Zwilch/Zw10 complex. Genes & Development. 22(17). 2385–2399. 133 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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