Benjamin J. Perrin

3.4k total citations
34 papers, 2.6k citations indexed

About

Benjamin J. Perrin is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Benjamin J. Perrin has authored 34 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 15 papers in Sensory Systems and 15 papers in Cell Biology. Recurrent topics in Benjamin J. Perrin's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Cellular Mechanics and Interactions (11 papers) and Ear Surgery and Otitis Media (6 papers). Benjamin J. Perrin is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), Cellular Mechanics and Interactions (11 papers) and Ear Surgery and Otitis Media (6 papers). Benjamin J. Perrin collaborates with scholars based in United States, Japan and United Kingdom. Benjamin J. Perrin's co-authors include Anna Huttenlocher, James M. Ervasti, Santos J. Franco, David A. Bennin, Tingxi Liu, John P. Kanki, Jonathan R. Mathias, A. Thomas Look, Jaewon Han and David R. Critchley and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Benjamin J. Perrin

33 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benjamin J. Perrin United States 20 1.3k 1.3k 449 444 387 34 2.6k
Andrea Disanza Italy 33 1.7k 1.3× 1.7k 1.4× 218 0.5× 396 0.9× 156 0.4× 47 3.3k
Mark Berryman United States 24 1.8k 1.5× 767 0.6× 221 0.5× 370 0.8× 160 0.4× 34 3.0k
James R. Bartles United States 31 1.5k 1.2× 1.0k 0.8× 177 0.4× 158 0.4× 842 2.2× 54 3.2k
Mark Holt United Kingdom 29 1.7k 1.3× 1.4k 1.1× 230 0.5× 563 1.3× 56 0.1× 44 3.0k
Xufeng Wu United States 39 2.9k 2.3× 3.0k 2.4× 638 1.4× 237 0.5× 88 0.2× 70 5.3k
Folma Buß United Kingdom 38 2.4k 1.9× 1.8k 1.5× 245 0.5× 178 0.4× 53 0.1× 65 4.0k
Noboru Ishiyama Canada 26 1.7k 1.4× 821 0.7× 156 0.3× 148 0.3× 80 0.2× 48 2.4k
Xiaowei Lu United States 33 3.3k 2.6× 881 0.7× 301 0.7× 113 0.3× 305 0.8× 76 4.9k
Mary Anne Conti United States 33 2.9k 2.3× 2.4k 1.9× 294 0.7× 541 1.2× 59 0.2× 50 5.0k
Tong Xiao United States 28 1.6k 1.3× 796 0.6× 487 1.1× 108 0.2× 116 0.3× 37 3.4k

Countries citing papers authored by Benjamin J. Perrin

Since Specialization
Citations

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

Fields of papers citing papers by Benjamin J. Perrin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benjamin J. Perrin. 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 Benjamin J. Perrin. The network helps show where Benjamin J. Perrin may publish in the future.

Co-authorship network of co-authors of Benjamin J. Perrin

This figure shows the co-authorship network connecting the top 25 collaborators of Benjamin J. Perrin. A scholar is included among the top collaborators of Benjamin J. Perrin 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 Benjamin J. Perrin. Benjamin J. Perrin 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.
Krey, Jocelyn F., Ghazaleh Behnammanesh, Christopher M. Yengo, et al.. (2025). Myosin-dependent short actin filaments contribute to peripheral widening in developing stereocilia. Nature Communications. 16(1). 5835–5835. 1 indexed citations
2.
3.
Krey, Jocelyn F., et al.. (2023). Control of stereocilia length during development of hair bundles. PLoS Biology. 21(4). e3001964–e3001964. 18 indexed citations
4.
Southern, William M., et al.. (2022). Nucleotide- and Protein-Dependent Functions of Actg1. Molecular Biology of the Cell. 33(9). ar77–ar77. 8 indexed citations
5.
Miyoshi, Takushi, Qianli Zhang, Shin Watanabe, et al.. (2021). Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures. Cell Reports. 34(5). 108708–108708. 15 indexed citations
6.
Belyantseva, Inna A., Jinan Li, Nicolas F. Berbari, et al.. (2021). Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin. Current Biology. 31(6). 1141–1153.e7. 22 indexed citations
7.
Shimada, Eriko, Fasih M. Ahsan, Mahta Nili, et al.. (2018). PNPase knockout results in mtDNA loss and an altered metabolic gene expression program. PLoS ONE. 13(7). e0200925–e0200925. 15 indexed citations
8.
Lindsay, Angus, Reem Abo‐Zahrah, Kristen A. Baltgalvis, et al.. (2018). Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle. Nature Communications. 9(1). 5104–5104. 30 indexed citations
9.
Perrin, Benjamin J., et al.. (2018). The stable actin core of mechanosensory stereocilia features continuous turnover of actin cross-linkers. Molecular Biology of the Cell. 29(15). 1856–1865. 19 indexed citations
10.
Perrin, Benjamin J., et al.. (2017). Stereocilia morphogenesis and maintenance through regulation of actin stability. PMC. 2 indexed citations
11.
Chamberlain, Christopher M., et al.. (2017). Relative importance of βcyto- and γcyto-actin in primary mouse embryonic fibroblasts. Molecular Biology of the Cell. 28(6). 771–782. 26 indexed citations
12.
Perrin, Benjamin J., et al.. (2016). Stereocilia morphogenesis and maintenance through regulation of actin stability. Seminars in Cell and Developmental Biology. 65. 88–95. 50 indexed citations
13.
Dandapat, Abhijit, Benjamin J. Perrin, Maria Razzoli, et al.. (2016). High Frequency Hearing Loss and Hyperactivity in DUX4 Transgenic Mice. PLoS ONE. 11(3). e0151467–e0151467. 14 indexed citations
14.
Narayanan, Praveena, Paul Chatterton, Akihiro Ikeda, et al.. (2015). Length regulation of mechanosensitive stereocilia depends on very slow actin dynamics and filament-severing proteins. Nature Communications. 6(1). 6855–6855. 75 indexed citations
15.
Piazza, Valeria, Benjamin J. Perrin, Agnieszka Rzadzinska, et al.. (2012). Multi-isotope imaging mass spectrometry reveals slow protein turnover in hair-cell stereocilia. Nature. 481(7382). 520–524. 174 indexed citations
16.
Perrin, Benjamin J. & James M. Ervasti. (2010). The actin gene family: Function follows isoform. Cytoskeleton. 67(10). 630–634. 256 indexed citations
17.
Cortesio, Christa L., Benjamin J. Perrin, David A. Bennin, & Anna Huttenlocher. (2009). Actin-binding Protein-1 Interacts with WASp-interacting Protein to Regulate Growth Factor-induced Dorsal Ruffle Formation. Molecular Biology of the Cell. 21(1). 186–197. 31 indexed citations
18.
Cortesio, Christa L., Keefe T. Chan, Benjamin J. Perrin, et al.. (2008). Calpain 2 and PTP1B function in a novel pathway with Src to regulate invadopodia dynamics and breast cancer cell invasion. The Journal of Cell Biology. 180(5). 957–971. 157 indexed citations
19.
Franco, Santos J., Benjamin J. Perrin, & Anna Huttenlocher. (2004). Isoform specific function of calpain 2 in regulating membrane protrusion. Experimental Cell Research. 299(1). 179–187. 111 indexed citations
20.
Perrin, Benjamin J. & Anna Huttenlocher. (2002). Calpain. The International Journal of Biochemistry & Cell Biology. 34(7). 722–725. 200 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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