Wayne S. Sossin

7.9k total citations · 1 hit paper
129 papers, 6.2k citations indexed

About

Wayne S. Sossin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Wayne S. Sossin has authored 129 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Molecular Biology, 84 papers in Cellular and Molecular Neuroscience and 42 papers in Cell Biology. Recurrent topics in Wayne S. Sossin's work include Neurobiology and Insect Physiology Research (49 papers), Neuroscience and Neuropharmacology Research (46 papers) and Protein Kinase Regulation and GTPase Signaling (24 papers). Wayne S. Sossin is often cited by papers focused on Neurobiology and Insect Physiology Research (49 papers), Neuroscience and Neuropharmacology Research (46 papers) and Protein Kinase Regulation and GTPase Signaling (24 papers). Wayne S. Sossin collaborates with scholars based in Canada, United States and United Kingdom. Wayne S. Sossin's co-authors include Mauro Costa‐Mattioli, Nahum Sonenberg, Eric Klann, Jean‐Claude Lacaille, Carole A. Farah, Luc DesGroseillers, Richard H. Scheller, Richard H. Scheller, James H. Schwartz and John R. Dyer and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Wayne S. Sossin

129 papers receiving 6.1k citations

Hit Papers

Translational Control of Long-Lasting Synaptic Plasticity... 2009 2026 2014 2020 2009 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wayne S. Sossin Canada 41 4.0k 3.1k 1.4k 633 600 129 6.2k
Maria Passafaro Italy 36 2.8k 0.7× 2.8k 0.9× 1.0k 0.7× 678 1.1× 586 1.0× 82 4.8k
Michael R. Kreutz Germany 42 3.4k 0.9× 3.1k 1.0× 1.5k 1.0× 999 1.6× 871 1.5× 183 6.2k
Susanne Schoch Germany 43 3.5k 0.9× 3.4k 1.1× 2.1k 1.5× 546 0.9× 984 1.6× 112 6.3k
Alaa El-Husseini Canada 28 2.5k 0.6× 2.2k 0.7× 1.2k 0.8× 399 0.6× 398 0.7× 35 4.3k
Gary A. Wayman United States 41 4.5k 1.1× 3.2k 1.0× 794 0.6× 606 1.0× 599 1.0× 66 7.2k
Andrés Buonanno United States 45 4.3k 1.1× 3.1k 1.0× 604 0.4× 612 1.0× 697 1.2× 95 6.5k
Irm Hermans‐Borgmeyer Germany 42 4.1k 1.0× 2.7k 0.9× 967 0.7× 965 1.5× 366 0.6× 93 6.9k
Daniel T.S. Pak United States 35 3.3k 0.8× 2.0k 0.6× 871 0.6× 522 0.8× 356 0.6× 70 5.1k
Dušan Bartsch Germany 35 3.0k 0.8× 3.3k 1.1× 689 0.5× 665 1.1× 1.2k 1.9× 97 6.4k
Robert Levenson United States 50 5.3k 1.3× 2.6k 0.8× 896 0.6× 461 0.7× 456 0.8× 133 7.5k

Countries citing papers authored by Wayne S. Sossin

Since Specialization
Citations

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

Fields of papers citing papers by Wayne S. Sossin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wayne S. Sossin

This figure shows the co-authorship network connecting the top 25 collaborators of Wayne S. Sossin. A scholar is included among the top collaborators of Wayne S. Sossin 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 Wayne S. Sossin. Wayne S. Sossin 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.
Mahmood, Niaz, Jung‐Hyun Choi, Sean W. Dooling, et al.. (2024). The ISR downstream target ATF4 represses long-term memory in a cell type–specific manner. Proceedings of the National Academy of Sciences. 121(31). e2407472121–e2407472121. 5 indexed citations
2.
Graber, Tyson E., et al.. (2024). Puromycin reveals a distinct conformation of neuronal ribosomes. Proceedings of the National Academy of Sciences. 121(7). e2306993121–e2306993121. 2 indexed citations
3.
Jafarnejad, Seyed Mehdi, et al.. (2023). Ribosomes in RNA Granules Are Stalled on mRNA Sequences That Are Consensus Sites for FMRP Association. Journal of Neuroscience. 43(14). 2440–2459. 14 indexed citations
4.
Fan, Xiaotang, et al.. (2023). The role of specific isoforms of CaV2 and the common C-terminal of CaV2 in calcium channel function in sensory neurons of Aplysia. Scientific Reports. 13(1). 20216–20216. 1 indexed citations
5.
Farah, Carole A., et al.. (2021). MRI of Capn15 Knockout Mice and Analysis of Capn 15 Distribution Reveal Possible Roles in Brain Development and Plasticity. Neuroscience. 465. 128–141. 7 indexed citations
6.
Farah, Carole A., Richard Holt, Fabiola Ceroni, et al.. (2020). Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits. Human Molecular Genetics. 29(18). 3054–3063. 17 indexed citations
7.
Hastings, Margaret H., et al.. (2018). The zinc fingers of the small optic lobes calpain bind polyubiquitin. Journal of Neurochemistry. 146(4). 429–445. 11 indexed citations
8.
Graber, Tyson E., Arkady Khoutorsky, Alexandre David, et al.. (2013). Reactivation of stalled polyribosomes in synaptic plasticity. Proceedings of the National Academy of Sciences. 110(40). 16205–16210. 126 indexed citations
9.
Dyer, John R. & Wayne S. Sossin. (2013). Characterization of the Role of eIF4G in Stimulating Cap- and IRES-Dependent Translation in Aplysia Neurons. PLoS ONE. 8(9). e74085–e74085. 5 indexed citations
10.
Dyer, John R., et al.. (2012). Rictor regulates phosphorylation of the novel protein kinase C Apl II in Aplysia sensory neurons. Journal of Neurochemistry. 122(6). 1108–1117. 1 indexed citations
11.
Sossin, Wayne S., et al.. (2010). Translation of 5′ terminal oligopyrimidine tract (5′TOP) mRNAs in Aplysia Californica is regulated by the target of rapamycin (TOR). Biochemical and Biophysical Research Communications. 404(3). 816–821. 5 indexed citations
12.
Wang, Dan Ohtan, et al.. (2009). Synapse- and Stimulus-Specific Local Translation During Long-Term Neuronal Plasticity. Science. 324(5934). 1536–1540. 160 indexed citations
13.
Li, Quan, Diancai Cai, Ann E. Fink, et al.. (2009). Role of Protein Kinase C in the Induction and Maintenance of Serotonin-Dependent Enhancement of the Glutamate Response in Isolated Siphon Motor Neurons ofAplysia californica. Journal of Neuroscience. 29(16). 5100–5107. 42 indexed citations
14.
Costa‐Mattioli, Mauro, Wayne S. Sossin, Eric Klann, & Nahum Sonenberg. (2009). Translational Control of Long-Lasting Synaptic Plasticity and Memory. Neuron. 61(1). 10–26. 750 indexed citations breakdown →
15.
Dyer, John R., et al.. (2006). Mnk is a negative regulator of cap‐dependent translation in Aplysia neurons. Journal of Neurochemistry. 97(1). 79–91. 20 indexed citations
16.
Nakhost, Arash, et al.. (2006). PKC Modulation of Transmitter Release by SNAP-25 at Sensory-to-Motor Synapses in Aplysia. Journal of Neurophysiology. 97(1). 134–143. 22 indexed citations
17.
Fan, Xiaotang, et al.. (2004). 5‐HT stimulates eEF2 dephosphorylation in a rapamycin‐sensitive manner in Aplysia neurites. Journal of Neurochemistry. 90(6). 1464–1476. 42 indexed citations
18.
Wayne, Nancy L., et al.. (2004). Activity-Dependent Regulation of Neurohormone Synthesis and Its Impact on Reproductive Behavior in Aplysia1. Biology of Reproduction. 70(2). 277–281. 14 indexed citations
19.
Dyer, John R., et al.. (2004). Characterization of a novel molluskan tyrosine kinase receptor that inhibits neurite regeneration. Journal of Neurobiology. 60(2). 127–136. 4 indexed citations
20.
Nakhost, Arash, et al.. (1999). Protein Kinase C Phosphorylated at a Conserved Threonine Is Retained in the Cytoplasm. Journal of Biological Chemistry. 274(41). 28944–28949. 25 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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