John W. Copeland

2.3k total citations · 1 hit paper
30 papers, 2.0k citations indexed

About

John W. Copeland is a scholar working on Molecular Biology, Cell Biology and Immunology and Allergy. According to data from OpenAlex, John W. Copeland has authored 30 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 20 papers in Cell Biology and 6 papers in Immunology and Allergy. Recurrent topics in John W. Copeland's work include Cellular Mechanics and Interactions (17 papers), Microtubule and mitosis dynamics (7 papers) and Cell Adhesion Molecules Research (6 papers). John W. Copeland is often cited by papers focused on Cellular Mechanics and Interactions (17 papers), Microtubule and mitosis dynamics (7 papers) and Cell Adhesion Molecules Research (6 papers). John W. Copeland collaborates with scholars based in Canada, United States and United Kingdom. John W. Copeland's co-authors include Richard Treisman, Athanassia Sotiropoulos, Olivier Geneste, Kevin G. Young, Henry M. Krause, Thomas Kitzing, Ying Wang, Olivier Pertz, Robert Grosse and Andrzej Nasiadka and has published in prestigious journals such as Nature, Cell and Journal of Biological Chemistry.

In The Last Decade

John W. Copeland

30 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Signal-Regulated Activation of Serum Response Factor Is Mediated by Changes in Actin Dynamics

1999 572 citations Athanassia Sotiropoulos, John W. Copeland et al. Cell profile →

Peers

John W. Copeland

MB

CB

IA

GENET

CCM

Anika Steffen Germany

Christof Haffner Germany

Emmanuel Vignal France

Geri Kreitzer United States

Metello Innocenti Italy

Eugen Kerkhoff Germany

Sven Bogdan Germany

Steven J. Winder United Kingdom

Russell E. McConnell United States

Marianne Martin France

Anika Steffen Germany

John W. Copeland

1.0k ×0.8

MB

1.4k ×1.6

CB

452 ×1.6

IA

165 ×0.6

GENET

136 ×0.7

CCM

Citations per year, relative to John W. Copeland John W. Copeland (= 1×) peers Anika Steffen

Countries citing papers authored by John W. Copeland

Since Specialization

Citations

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

Fields of papers citing papers by John W. Copeland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John W. Copeland. 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 John W. Copeland. The network helps show where John W. Copeland may publish in the future.

Co-authorship network of co-authors of John W. Copeland

This figure shows the co-authorship network connecting the top 25 collaborators of John W. Copeland. A scholar is included among the top collaborators of John W. Copeland 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 John W. Copeland. John W. Copeland is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Copeland, John W., et al.. (2023). SPECC1L binds the myosin phosphatase complex MYPT1/PP1β and can regulate its distribution between microtubules and filamentous actin. Journal of Biological Chemistry. 299(2). 102893–102893. 4 indexed citations

2.

Fox, Sarah, Amanda Tran, Laura Trinkle‐Mulcahy, & John W. Copeland. (2022). Cooperative assembly of filopodia by the formin FMNL2 and I-BAR domain protein IRTKS. Journal of Biological Chemistry. 298(11). 102512–102512. 8 indexed citations

3.

Lai, Christine Chieh-Lin, John W. Copeland, Trevor F. Moraes, et al.. (2020). The scaffold-protein IQGAP1 enhances and spatially restricts the actin-nucleating activity of Diaphanous-related formin 1 (DIAPH1). Journal of Biological Chemistry. 295(10). 3134–3147. 11 indexed citations

4.

Copeland, John W.. (2019). Formins, Golgi, and the Centriole. Results and problems in cell differentiation. 67. 27–48. 3 indexed citations

5.

Copeland, John W.. (2019). Actin-based regulation of ciliogenesis – The long and the short of it. Seminars in Cell and Developmental Biology. 102. 132–138. 20 indexed citations

6.

Guarguaglini, Giulia, et al.. (2018). Actin-dependent regulation of cilia length by the inverted formin FHDC1. Molecular Biology of the Cell. 29(13). 1611–1627. 31 indexed citations

7.

Copeland, John W., et al.. (2016). A specific FMNL2 isoform is up-regulated in invasive cells. BMC Cell Biology. 17(1). 32–32. 12 indexed citations

8.

Copeland, John W., et al.. (2015). Actin- and microtubule-dependent regulation of Golgi morphology by FHDC1. Molecular Biology of the Cell. 27(2). 260–276. 32 indexed citations

9.

Fattouh, Ramzi, Hyunwoo Kwon, John W. Copeland, et al.. (2014). The Diaphanous-Related Formins Promote Protrusion Formation and Cell-to-Cell Spread of Listeria monocytogenes. The Journal of Infectious Diseases. 211(7). 1185–1195. 34 indexed citations

10.

Lynch, Jennifer, Maria Meehan, John Crean, et al.. (2013). Metastasis Suppressor microRNA-335 Targets the Formin Family of Actin Nucleators. PLoS ONE. 8(11). e78428–e78428. 30 indexed citations

11.

Lee, Jonathan M., et al.. (2012). The Ability to Induce Microtubule Acetylation Is a General Feature of Formin Proteins. PLoS ONE. 7(10). e48041–e48041. 57 indexed citations

12.

Chan, Matthew W. C., et al.. (2010). Force-induced Myofibroblast Differentiation through Collagen Receptors Is Dependent on Mammalian Diaphanous (mDia). Journal of Biological Chemistry. 285(12). 9273–9281. 46 indexed citations

13.

Young, Kevin G. & John W. Copeland. (2008). Formins in cell signaling. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1803(2). 183–190. 93 indexed citations

14.

Abdennur, Nezar, et al.. (2008). Interaction of the N- and C-terminal Autoregulatory Domains of FRL2 Does Not Inhibit FRL2 Activity. Journal of Biological Chemistry. 283(48). 33750–33762. 48 indexed citations

15.

Young, Kevin G., et al.. (2008). INF1 Is a Novel Microtubule-associated Formin. Molecular Biology of the Cell. 19(12). 5168–5180. 53 indexed citations

16.

Green, Brenda J., et al.. (2007). The Diaphanous Inhibitory Domain/Diaphanous Autoregulatory Domain Interaction Is Able to Mediate Heterodimerization between mDia1 and mDia2. Journal of Biological Chemistry. 282(41). 30120–30130. 38 indexed citations

17.

Copeland, John W., et al.. (2004). Homo-oligomerization Is Essential for F-actin Assembly by the Formin Family FH2 Domain. Journal of Biological Chemistry. 279(48). 50250–50256. 53 indexed citations

18.

Copeland, John W. & Richard Treisman. (2002). The Diaphanous-related Formin mDia1 Controls Serum Response Factor Activity through its Effects on Actin Polymerization. Molecular Biology of the Cell. 13(11). 4088–4099. 157 indexed citations

19.

Sotiropoulos, Athanassia, et al.. (1999). Signal-Regulated Activation of Serum Response Factor Is Mediated by Changes in Actin Dynamics. Cell. 98(2). 159–169. 572 indexed citations breakdown →

20.

Copeland, John W., et al.. (1996). Patterning of the Drosophila embryo by a homeodomain-deleted Ftz polypeptide. Nature. 379(6561). 162–165. 77 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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