Seth S. Margolis

2.2k total citations
34 papers, 1.6k citations indexed

About

Seth S. Margolis is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Seth S. Margolis has authored 34 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 14 papers in Cell Biology and 10 papers in Genetics. Recurrent topics in Seth S. Margolis's work include Ubiquitin and proteasome pathways (15 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Endoplasmic Reticulum Stress and Disease (7 papers). Seth S. Margolis is often cited by papers focused on Ubiquitin and proteasome pathways (15 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Endoplasmic Reticulum Stress and Disease (7 papers). Seth S. Margolis collaborates with scholars based in United States, Japan and Türkiye. Seth S. Margolis's co-authors include Sally Kornbluth, Kapil V. Ramachandran, Gabrielle L. Sell, Leta K. Nutt, William G. Dunphy, Christopher D. Freel, Lynne M. Bird, Mette V. Jensen, Jeffrey C. Rathmell and Jennifer A. Perry and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Seth S. Margolis

32 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seth S. Margolis United States 19 1.3k 505 378 237 155 34 1.6k
Makoto Matsuyama Japan 22 1.2k 0.9× 489 1.0× 481 1.3× 164 0.7× 104 0.7× 58 1.8k
Amaris R. Guardiola United States 5 2.1k 1.6× 308 0.6× 191 0.5× 543 2.3× 95 0.6× 6 2.3k
Zhenjie Xu China 10 1.1k 0.8× 823 1.6× 152 0.4× 139 0.6× 69 0.4× 17 1.4k
Stephanie L. Schwartz United States 4 1.3k 1.0× 412 0.8× 192 0.5× 124 0.5× 145 0.9× 5 1.8k
Robert Kopajtich Germany 16 1.4k 1.0× 1.4k 2.7× 132 0.3× 150 0.6× 152 1.0× 30 2.0k
Francesca Cole United States 20 2.2k 1.7× 258 0.5× 636 1.7× 246 1.0× 105 0.7× 30 2.5k
Serge A. Leibovitch France 22 1.4k 1.1× 334 0.7× 209 0.6× 228 1.0× 267 1.7× 57 1.7k
Ryan Schreiner United States 22 847 0.6× 588 1.2× 132 0.3× 93 0.4× 204 1.3× 43 1.5k
Shin‐ichiro Hiraga Japan 24 1.4k 1.1× 295 0.6× 189 0.5× 223 0.9× 212 1.4× 44 1.9k
Muriel Vernet France 15 980 0.8× 407 0.8× 176 0.5× 109 0.5× 61 0.4× 20 1.4k

Countries citing papers authored by Seth S. Margolis

Since Specialization
Citations

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

Fields of papers citing papers by Seth S. Margolis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Seth S. Margolis. 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 Seth S. Margolis. The network helps show where Seth S. Margolis may publish in the future.

Co-authorship network of co-authors of Seth S. Margolis

This figure shows the co-authorship network connecting the top 25 collaborators of Seth S. Margolis. A scholar is included among the top collaborators of Seth S. Margolis 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 Seth S. Margolis. Seth S. Margolis 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.
Tippens, Nathaniel D., Ahmed Mohyeldin, Shuyan Wang, et al.. (2025). YAP controls cell migration and invasion through a Rho GTPase switch.. PubMed. 18(888). eadu3794–eadu3794. 2 indexed citations
2.
Margolis, Seth S., et al.. (2025). Mechanisms of ubiquitin-independent proteasomal degradation and their roles in age-related neurodegenerative disease. Frontiers in Cell and Developmental Biology. 12. 1531797–1531797. 3 indexed citations
3.
Delannoy, Michael, et al.. (2024). The nociceptive activity of peripheral sensory neurons is modulated by the neuronal membrane proteasome. Cell Reports. 43(4). 114058–114058. 4 indexed citations
4.
He, Hai‐yan, et al.. (2023). Neuronal membrane proteasomes regulate neuronal circuit activity in vivo and are required for learning-induced behavioral plasticity. Proceedings of the National Academy of Sciences. 120(3). e2216537120–e2216537120. 19 indexed citations
5.
Margolis, Seth S., et al.. (2023). Proteasome cap particle regulates synapses. Science. 380(6647). 795–796. 1 indexed citations
6.
Bharadwaj, Rahul, Joel E. Kleinman, Daniel R. Weinberger, et al.. (2023). Orthogonal approaches required to measure proteasome composition and activity in mammalian brain tissue. Journal of Biological Chemistry. 299(6). 104811–104811. 10 indexed citations
7.
Margolis, Seth S., et al.. (2021). The proteasome and its role in the nervous system. Cell chemical biology. 28(7). 903–917. 58 indexed citations
8.
Ramachandran, Kapil V., Jack Fu, Thomas Schaffer, et al.. (2018). Activity-Dependent Degradation of the Nascentome by the Neuronal Membrane Proteasome. Molecular Cell. 71(1). 169–177.e6. 58 indexed citations
9.
Schaffer, Thomas, et al.. (2018). PKCε Inhibits Neuronal Dendritic Spine Development through Dual Phosphorylation of Ephexin5. Cell Reports. 25(9). 2470–2483.e8. 13 indexed citations
10.
Hamilton, Andrew M., Laxmi Kumar Parajuli, Oscar Vivas, et al.. (2017). A dual role for the RhoGEF Ephexin5 in regulation of dendritic spine outgrowth. Molecular and Cellular Neuroscience. 80. 66–74. 16 indexed citations
11.
Ramachandran, Kapil V. & Seth S. Margolis. (2017). A mammalian nervous-system-specific plasma membrane proteasome complex that modulates neuronal function. Nature Structural & Molecular Biology. 24(4). 419–430. 99 indexed citations
12.
Sell, Gabrielle L. & Seth S. Margolis. (2015). From UBE3A to Angelman syndrome: a substrate perspective. Frontiers in Neuroscience. 9. 322–322. 54 indexed citations
13.
Margolis, Seth S., et al.. (2015). Angelman Syndrome. Neurotherapeutics. 12(3). 641–650. 110 indexed citations
14.
Nutt, Leta K., Marisa R. Buchakjian, Eugene Gan, et al.. (2009). Metabolic Control of Oocyte Apoptosis Mediated by 14-3-3ζ-Regulated Dephosphorylation of Caspase-2. Developmental Cell. 16(6). 856–866. 81 indexed citations
15.
Guo, Jessie Yanxiang, Ayumi Yamada, Taisuke Kajino, et al.. (2008). Aven-Dependent Activation of ATM Following DNA Damage. Current Biology. 18(13). 933–942. 41 indexed citations
16.
Guo, Yanxiang, Ayumi Yamada, Jennifer A. Perry, et al.. (2007). A Role for Cdc2- and PP2A-Mediated Regulation of Emi2 in the Maintenance of CSF Arrest. Current Biology. 17(3). 213–224. 40 indexed citations
17.
Margolis, Seth S., Jennifer A. Perry, Craig M. Forester, et al.. (2006). Role for the PP2A/B56δ Phosphatase in Regulating 14-3-3 Release from Cdc25 to Control Mitosis. Cell. 127(4). 759–773. 163 indexed citations
18.
Margolis, Seth S., et al.. (2003). Phosphorylation of the cyclin b1 cytoplasmic retention sequence by mitogen-activated protein kinase and Plx.. PubMed. 1(4). 280–9. 46 indexed citations
19.
Margolis, Seth S.. (2003). PP1 control of M phase entry exerted through 14-3-3-regulated Cdc25 dephosphorylation. The EMBO Journal. 22(21). 5734–5745. 117 indexed citations
20.
Banik, Soma S. R., et al.. (2002). C-Terminal Regions of the Human Telomerase Catalytic Subunit Essential for In Vivo Enzyme Activity. Molecular and Cellular Biology. 22(17). 6234–6246. 83 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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