Bram Prevo

1.5k total citations
25 papers, 947 citations indexed

About

Bram Prevo is a scholar working on Molecular Biology, Cell Biology and Biophysics. According to data from OpenAlex, Bram Prevo has authored 25 papers receiving a total of 947 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Cell Biology and 7 papers in Biophysics. Recurrent topics in Bram Prevo's work include Microtubule and mitosis dynamics (15 papers), Genetic and Kidney Cyst Diseases (6 papers) and Genetics, Aging, and Longevity in Model Organisms (6 papers). Bram Prevo is often cited by papers focused on Microtubule and mitosis dynamics (15 papers), Genetic and Kidney Cyst Diseases (6 papers) and Genetics, Aging, and Longevity in Model Organisms (6 papers). Bram Prevo collaborates with scholars based in United States, Netherlands and United Kingdom. Bram Prevo's co-authors include Erwin J.G. Peterman, Jonathan M. Scholey, Pierre Mangeol, Felix Oswald, Dhanya K. Cheerambathur, Karen Oegema, Arshad Desai, Şeyda Açar, Pablo Lara-González and Ingrid Brust‐Mascher and has published in prestigious journals such as Chemical Society Reviews, Nature Communications and Genes & Development.

In The Last Decade

Bram Prevo

24 papers receiving 946 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bram Prevo United States 12 693 480 443 111 64 25 947
Benjamin Lacroix France 14 915 1.3× 846 1.8× 181 0.4× 127 1.1× 106 1.7× 27 1.3k
Walter Huynh United States 11 730 1.1× 588 1.2× 80 0.2× 51 0.5× 90 1.4× 14 1.1k
Isabelle Flückiger Switzerland 12 734 1.1× 735 1.5× 238 0.5× 61 0.5× 14 0.2× 15 910
Elif Nur Firat‐Karalar Türkiye 18 743 1.1× 662 1.4× 372 0.8× 14 0.1× 51 0.8× 34 1.1k
Manuel Hilbert Switzerland 14 777 1.1× 537 1.1× 137 0.3× 32 0.3× 80 1.3× 17 1.1k
Didier Portran France 10 1.0k 1.5× 781 1.6× 291 0.7× 16 0.1× 102 1.6× 13 1.5k
Morgan E. DeSantis United States 15 890 1.3× 479 1.0× 86 0.2× 126 1.1× 92 1.4× 27 1.1k
Shunya Hozumi Japan 11 396 0.6× 212 0.4× 84 0.2× 41 0.4× 78 1.2× 17 599
Paul T. Conduit United Kingdom 14 1.1k 1.7× 1.1k 2.4× 212 0.5× 49 0.4× 25 0.4× 22 1.4k
Malan Silva United States 13 542 0.8× 224 0.5× 405 0.9× 149 1.3× 30 0.5× 18 734

Countries citing papers authored by Bram Prevo

Since Specialization
Citations

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

Fields of papers citing papers by Bram Prevo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bram Prevo. 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 Bram Prevo. The network helps show where Bram Prevo may publish in the future.

Co-authorship network of co-authors of Bram Prevo

This figure shows the co-authorship network connecting the top 25 collaborators of Bram Prevo. A scholar is included among the top collaborators of Bram Prevo 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 Bram Prevo. Bram Prevo 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.
Mitra, Aniruddha, et al.. (2025). DYF-5 regulates intraflagellar transport by affecting train turnaround. Molecular Biology of the Cell. 36(5). ar53–ar53. 2 indexed citations
2.
Blow, Frances, Kate L. Jeffrey, Franklin Wang‐Ngai Chow, et al.. (2024). SID-2 is a conserved extracellular vesicle protein that is not associated with environmental RNAi in parasitic nematodes. Open Biology. 14(11). 240190–240190. 1 indexed citations
3.
Prevo, Bram, et al.. (2024). The kinetochore protein KNL-1 regulates the actin cytoskeleton to control dendrite branching. The Journal of Cell Biology. 224(2). 3 indexed citations
4.
Prevo, Bram, et al.. (2024). The outer kinetochore components KNL-1 and Ndc80 complex regulate axon and neuronal cell body positioning in the C. elegans nervous system. Molecular Biology of the Cell. 35(6). ar83–ar83. 1 indexed citations
5.
Prevo, Bram & William C. Earnshaw. (2024). DNA packaging by molecular motors: from bacteriophage to human chromosomes. Nature Reviews Genetics. 25(11). 785–802. 5 indexed citations
6.
Prevo, Bram, et al.. (2023). Sculpting the dendritic landscape: Actin, microtubules, and the art of arborization. Current Opinion in Cell Biology. 84. 102214–102214. 2 indexed citations
7.
Cheerambathur, Dhanya K., Bram Prevo, Neil Hattersley, et al.. (2019). The Kinetochore-Microtubule Coupling Machinery Is Repurposed in Sensory Nervous System Morphogenesis. Developmental Cell. 48(6). 864–872.e7. 33 indexed citations
8.
Hattersley, Neil, Pablo Lara-González, Dhanya K. Cheerambathur, et al.. (2018). Employing the one-cell C. elegans embryo to study cell division processes. Methods in cell biology. 144. 185–231. 7 indexed citations
9.
Oswald, Felix, Bram Prevo, Şeyda Açar, & Erwin J.G. Peterman. (2018). Interplay between Ciliary Ultrastructure and IFT-Train Dynamics Revealed by Single-Molecule Super-resolution Imaging. Cell Reports. 25(1). 224–235. 20 indexed citations
10.
Wang, Shaohe, Ngang Heok Tang, Pablo Lara-González, et al.. (2017). A toolkit for GFP-mediated tissue-specific protein degradation in C. elegans. Development. 144(14). 2694–2701. 81 indexed citations
11.
Cheerambathur, Dhanya K., Bram Prevo, Neil Hattersley, et al.. (2017). Dephosphorylation of the Ndc80 Tail Stabilizes Kinetochore-Microtubule Attachments via the Ska Complex. Developmental Cell. 41(4). 424–437.e4. 45 indexed citations
12.
Barbosa, Daniel José, et al.. (2017). Dynactin binding to tyrosinated microtubules promotes centrosome centration in C. elegans by enhancing dynein-mediated organelle transport. PLoS Genetics. 13(7). e1006941–e1006941. 34 indexed citations
13.
Prevo, Bram, et al.. (2017). Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia. Nature Communications. 8(1). 14591–14591. 36 indexed citations
14.
Kim, Tae-Kyung, Pablo Lara-González, Bram Prevo, et al.. (2017). Kinetochores accelerate or delay APC/C activation by directing Cdc20 to opposing fates. Genes & Development. 31(11). 1089–1094. 47 indexed citations
15.
Prevo, Bram, Pierre Mangeol, Felix Oswald, Jonathan M. Scholey, & Erwin J.G. Peterman. (2015). Functional differentiation of cooperating kinesin-2 motors orchestrates cargo import and transport in C. elegans cilia. Nature Cell Biology. 17(12). 1536–1545. 123 indexed citations
16.
Slabodnick, Mark M., et al.. (2013). Visualizing Cytoplasmic Flow During Single-cell Wound Healing in <em>Stentor coeruleus</em>. Journal of Visualized Experiments.
17.
Prevo, Bram & Erwin J.G. Peterman. (2013). Förster resonance energy transfer and kinesin motor proteins. Chemical Society Reviews. 43(4). 1144–1155. 56 indexed citations
18.
Slabodnick, Mark M., et al.. (2013). Visualizing Cytoplasmic Flow During Single-cell Wound Healing in <em>Stentor coeruleus</em>. Journal of Visualized Experiments. e50848–e50848. 10 indexed citations
19.
Wildenberg, Siet van den, Bram Prevo, & Erwin J.G. Peterman. (2011). A Brief Introduction to Single-Molecule Fluorescence Methods. Methods in molecular biology. 783. 81–99. 9 indexed citations
20.
Hao, Limin, Ingrid Brust‐Mascher, Gul Civelekoglu‐Scholey, et al.. (2011). Intraflagellar transport delivers tubulin isotypes to sensory cilium middle and distal segments. Nature Cell Biology. 13(7). 790–798. 143 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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