Kausik Si

4.0k total citations
33 papers, 2.9k citations indexed

About

Kausik Si is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Kausik Si has authored 33 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 5 papers in Cell Biology. Recurrent topics in Kausik Si's work include RNA Research and Splicing (16 papers), Prion Diseases and Protein Misfolding (9 papers) and Neurobiology and Insect Physiology Research (8 papers). Kausik Si is often cited by papers focused on RNA Research and Splicing (16 papers), Prion Diseases and Protein Misfolding (9 papers) and Neurobiology and Insect Physiology Research (8 papers). Kausik Si collaborates with scholars based in United States, United Kingdom and South Korea. Kausik Si's co-authors include Eric R. Kandel, Susan Lindquist, Umadas Maitra, Craig H. Bailey, Amitabha Majumdar, Yun‐Beom Choi, Martin Theis, Huixiang Zhu, Joung‐Hun Kim and Maria Concetta Miniaci and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Kausik Si

32 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kausik Si United States 24 2.4k 753 547 340 233 33 2.9k
Paul Skehel United Kingdom 26 2.0k 0.9× 1.3k 1.7× 463 0.8× 317 0.9× 253 1.1× 43 3.6k
Mazahir T. Hasan Germany 27 1.9k 0.8× 1.2k 1.6× 338 0.6× 291 0.9× 586 2.5× 44 3.9k
Kristin Baer United Kingdom 28 1.3k 0.5× 1.1k 1.5× 287 0.5× 266 0.8× 327 1.4× 40 2.4k
Stephanie M. Hughes New Zealand 24 988 0.4× 529 0.7× 509 0.9× 224 0.7× 367 1.6× 55 1.9k
Huidy Shu United States 9 1.1k 0.5× 857 1.1× 402 0.7× 170 0.5× 260 1.1× 10 2.5k
JoAnn Buchanan United States 17 1.4k 0.6× 1.1k 1.5× 418 0.8× 156 0.5× 129 0.6× 24 3.0k
Roberto Jappelli United States 11 1.2k 0.5× 576 0.8× 648 1.2× 236 0.7× 110 0.5× 20 2.4k
Takayuki Sassa Japan 22 1.5k 0.6× 399 0.5× 256 0.5× 131 0.4× 216 0.9× 44 2.5k
Julie Perroy France 30 1.6k 0.7× 1.5k 2.0× 169 0.3× 163 0.5× 361 1.5× 63 2.6k
Tudor A. Fulga United States 32 2.1k 0.9× 703 0.9× 886 1.6× 223 0.7× 304 1.3× 51 3.5k

Countries citing papers authored by Kausik Si

Since Specialization
Citations

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

Fields of papers citing papers by Kausik Si

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kausik Si

This figure shows the co-authorship network connecting the top 25 collaborators of Kausik Si. A scholar is included among the top collaborators of Kausik Si 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 Kausik Si. Kausik Si 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.
Zheng, Fan, Liying Li, Yanxiao Zhang, et al.. (2021). Proteome plasticity in response to persistent environmental change. Molecular Cell. 81(16). 3294–3309.e12. 13 indexed citations
2.
Hervás, Rubén, Michael Rau, Wenjuan Zhang, et al.. (2020). Cryo-EM structure of a neuronal functional amyloid implicated in memory persistence in Drosophila. Science. 367(6483). 1230–1234. 133 indexed citations
3.
Singh, Narendra Pratap, Bony De Kumar, Ariel Paulson, et al.. (2020). A six-amino-acid motif is a major determinant in functional evolution of HOX1 proteins. Genes & Development. 34(23-24). 1680–1696. 13 indexed citations
4.
Hervás, Rubén, Therese M. Gerbich, Paulo César Leal, et al.. (2019). Amyloid-like Assembly Activates a Phosphatase in the Developing Drosophila Embryo. Cell. 178(6). 1403–1420.e21. 10 indexed citations
5.
Li, Liying, et al.. (2018). Translational Control by Prion-like Proteins. Trends in Cell Biology. 28(6). 494–505. 21 indexed citations
6.
Wu, Jianping, et al.. (2018). Antimicrobial peptides modulate long-term memory. PLoS Genetics. 14(10). e1007440–e1007440. 51 indexed citations
7.
Blanchette, Marco, et al.. (2017). Regulated Intron Removal Integrates Motivational State and Experience. Cell. 169(5). 836–848.e15. 30 indexed citations
8.
Lee, Seung‐Hee, Jaehoon Shim, Sue‐Hyun Lee, et al.. (2016). ApCPEB4, a non-prion domain containing homolog of ApCPEB, is involved in the initiation of long-term facilitation. Molecular Brain. 9(1). 91–91. 4 indexed citations
9.
Khan, Mohammed Repon, Liying Li, Anita Saraf, et al.. (2015). Amyloidogenic Oligomerization Transforms Drosophila Orb2 from a Translation Repressor to an Activator. Cell. 163(6). 1468–1483. 86 indexed citations
10.
Li, Liying, et al.. (2014). Contribution of Orb2A Stability in Regulated Amyloid-Like Oligomerization of Drosophila Orb2. PLoS Biology. 12(2). e1001786–e1001786. 43 indexed citations
11.
Majumdar, Amitabha, Huoqing Jiang, Mohammed Repon Khan, et al.. (2012). Critical Role of Amyloid-like Oligomers of Drosophila Orb2 in the Persistence of Memory. Cell. 148(3). 515–529. 214 indexed citations
12.
Si, Kausik, et al.. (2010). Aplysia CPEB Can Form Prion-like Multimers in Sensory Neurons that Contribute to Long-Term Facilitation. Cell. 140(3). 421–435. 278 indexed citations
13.
Miniaci, Maria Concetta, Joung‐Hun Kim, Sathyanarayanan V. Puthanveettil, et al.. (2008). Sustained CPEB-Dependent Local Protein Synthesis Is Required to Stabilize Synaptic Growth for Persistence of Long-Term Facilitation in Aplysia. Neuron. 59(6). 1024–1036. 111 indexed citations
14.
Bailey, Craig H., Eric R. Kandel, & Kausik Si. (2004). The Persistence of Long-Term Memory. Neuron. 44(1). 49–57. 205 indexed citations
15.
Si, Kausik, Maurizio Giustetto, Amit Etkin, et al.. (2003). A Neuronal Isoform of CPEB Regulates Local Protein Synthesis and Stabilizes Synapse-Specific Long-Term Facilitation in Aplysia. Cell. 115(7). 893–904. 324 indexed citations
16.
Si, Kausik, Susan Lindquist, & Eric R. Kandel. (2003). A Neuronal Isoform of the Aplysia CPEB Has Prion-Like Properties. Cell. 115(7). 879–891. 439 indexed citations
17.
Giustetto, Maurizio, Ashok N. Hegde, Kausik Si, et al.. (2003). Axonal transport of eukaryotic translation elongation factor 1α mRNA couples transcription in the nucleus to long-term facilitation at the synapse. Proceedings of the National Academy of Sciences. 100(23). 13680–13685. 70 indexed citations
18.
Theis, Martin, Kausik Si, & Eric R. Kandel. (2003). Two previously undescribed members of the mouse CPEB family of genes and their inducible expression in the principal cell layers of the hippocampus. Proceedings of the National Academy of Sciences. 100(16). 9602–9607. 158 indexed citations
19.
Chaudhuri, Jayanta, Kausik Si, & Umadas Maitra. (1997). Function of Eukaryotic Translation Initiation Factor 1A (eIF1A) (Formerly Called eIF-4C) in Initiation of Protein Synthesis. Journal of Biological Chemistry. 272(12). 7883–7891. 81 indexed citations
20.
Si, Kausik, Kallol Das, & Umadas Maitra. (1996). Characterization of Multiple mRNAs That Encode Mammalian Translation Initiation Factor 5 (eIF-5). Journal of Biological Chemistry. 271(28). 16934–16938. 57 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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