Swasti Raychaudhuri

1.2k total citations
26 papers, 933 citations indexed

About

Swasti Raychaudhuri is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Swasti Raychaudhuri has authored 26 papers receiving a total of 933 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Cell Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Swasti Raychaudhuri's work include Mitochondrial Function and Pathology (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Magnetic confinement fusion research (5 papers). Swasti Raychaudhuri is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Magnetic confinement fusion research (5 papers). Swasti Raychaudhuri collaborates with scholars based in India, Germany and United Kingdom. Swasti Raychaudhuri's co-authors include F. Ulrich Hartl, Manajit Hayer‐Hartl, R. Martin Vabulas, Nitai P. Bhattacharyya, Debashis Mukhopadhyay, C. Loew, Dan Garza, Rajat Gupta, Min Zheng and Adriana Villella and has published in prestigious journals such as Cell, Nature Communications and PLoS ONE.

In The Last Decade

Swasti Raychaudhuri

24 papers receiving 919 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Swasti Raychaudhuri India 11 709 264 146 91 87 26 933
Agnieszka Lewandowska Poland 14 873 1.2× 213 0.8× 98 0.7× 103 1.1× 45 0.5× 23 1.1k
Felix Willmund Germany 20 1.2k 1.7× 217 0.8× 60 0.4× 44 0.5× 47 0.5× 30 1.3k
Anne S. Wentink Germany 12 859 1.2× 243 0.9× 63 0.4× 187 2.1× 40 0.5× 19 1.0k
Bohdan J. Soltys Canada 18 1.1k 1.5× 372 1.4× 64 0.4× 96 1.1× 37 0.4× 26 1.4k
Youhei Saito Japan 20 747 1.1× 395 1.5× 101 0.7× 54 0.6× 28 0.3× 76 1.2k
Jorge Cuéllar Spain 17 1.1k 1.5× 256 1.0× 77 0.5× 62 0.7× 28 0.3× 36 1.3k
David Balchin Germany 11 1.2k 1.7× 329 1.2× 62 0.4× 131 1.4× 53 0.6× 17 1.5k
Zsolt Balogi Hungary 15 770 1.1× 257 1.0× 36 0.2× 82 0.9× 23 0.3× 23 1.0k
Julie Grantham Sweden 19 1.4k 2.0× 413 1.6× 130 0.9× 88 1.0× 250 2.9× 33 1.7k
Can Kayatekin United States 15 1.2k 1.7× 215 0.8× 64 0.4× 160 1.8× 25 0.3× 23 1.5k

Countries citing papers authored by Swasti Raychaudhuri

Since Specialization
Citations

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

Fields of papers citing papers by Swasti Raychaudhuri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Swasti Raychaudhuri

This figure shows the co-authorship network connecting the top 25 collaborators of Swasti Raychaudhuri. A scholar is included among the top collaborators of Swasti Raychaudhuri 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 Swasti Raychaudhuri. Swasti Raychaudhuri 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.
2.
Jain, Aanchal, et al.. (2024). Widespread nuclear lamina injuries defeat proteostatic purposes of α-synuclein amyloid inclusions. Journal of Cell Science. 137(7). 2 indexed citations
3.
Raychaudhuri, Swasti, et al.. (2024). Enhanced secretion of promyogenic exosomes by quiescent muscle cells. Frontiers in Cell and Developmental Biology. 12. 1381357–1381357. 1 indexed citations
4.
Kumar, Umesh, Geetika Verma, Nalini Gupta, et al.. (2024). TEX13B is essential for metabolic reprogramming during germ cell differentiation. Human Reproduction. 39(7). 1390–1403.
5.
Pandey, Pratima, et al.. (2022). Stress Responses Elicited by Misfolded Proteins Targeted to Mitochondria. Journal of Molecular Biology. 434(12). 167618–167618. 7 indexed citations
6.
Subramaniam, Gunasekaran, et al.. (2019). Cytoplasmic sequestration of the RhoA effector mDiaphanous1 by Prohibitin2 promotes muscle differentiation. Scientific Reports. 9(1). 8302–8302. 6 indexed citations
7.
Raychaudhuri, Swasti, et al.. (2018). Identification of a splice variant of optineurin which is defective in autophagy and phosphorylation. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1865(11). 1526–1538. 11 indexed citations
8.
Raychaudhuri, Swasti, C. Loew, Roman Körner, et al.. (2014). Interplay of Acetyltransferase EP300 and the Proteasome System in Regulating Heat Shock Transcription Factor 1. Cell. 156(5). 975–985. 123 indexed citations
9.
Raychaudhuri, Swasti, et al.. (2014). Conserved C-terminal nascent peptide binding domain of HYPK facilitates its chaperone-like activity. Journal of Biosciences. 39(4). 659–672. 14 indexed citations
10.
Choudhury, Kamalika Roy, Swasti Raychaudhuri, & Nitai P. Bhattacharyya. (2012). Identification of HYPK-Interacting Proteins Reveals Involvement of HYPK in Regulating Cell Growth, Cell Cycle, Unfolded Protein Response and Cell Death. PLoS ONE. 7(12). e51415–e51415. 29 indexed citations
11.
Raychaudhuri, Swasti, et al.. (2011). Spectroscopic studies reveal conformational flexibility of intrinsically unstructured protein HYPK. 2(4). 434–442. 3 indexed citations
12.
Gupta, Rajat, Prasad Kasturi, Andreas Bracher, et al.. (2011). Firefly luciferase mutants as sensors of proteome stress. Nature Methods. 8(10). 879–884. 173 indexed citations
13.
Vabulas, R. Martin, Swasti Raychaudhuri, Manajit Hayer‐Hartl, & F. Ulrich Hartl. (2010). Protein Folding in the Cytoplasm and the Heat Shock Response. Cold Spring Harbor Perspectives in Biology. 2(12). a004390–a004390. 321 indexed citations
14.
Raychaudhuri, Swasti, Sucharita Dey, Nitai P. Bhattacharyya, & Debashis Mukhopadhyay. (2009). The Role of Intrinsically Unstructured Proteins in Neurodegenerative Diseases. PLoS ONE. 4(5). e5566–e5566. 53 indexed citations
15.
Raychaudhuri, Swasti, et al.. (2007). Huntingtin interacting protein HYPK is intrinsically unstructured. Proteins Structure Function and Bioinformatics. 71(4). 1686–1698. 29 indexed citations
16.
Raychaudhuri, Swasti, Mithun Sinha, Debashis Mukhopadhyay, & Nitai P. Bhattacharyya. (2007). HYPK, a Huntingtin interacting protein, reduces aggregates and apoptosis induced by N-terminal Huntingtin with 40 glutamines in Neuro2a cells and exhibits chaperone-like activity. Human Molecular Genetics. 17(2). 240–255. 70 indexed citations
17.
18.
Raychaudhuri, Swasti. (1999). Ion Temperature Measurement in the Edge Region of SINP Tokamak by a Retarding Field Analyser. Contributions to Plasma Physics. 39(4). 359–365. 5 indexed citations
19.
Raychaudhuri, Swasti. (1996). Studies of Tokamak Plasma from Core to Edge Region by Langmuir Probe. Contributions to Plasma Physics. 36(S1). 125–130. 2 indexed citations
20.
Raychaudhuri, Swasti & Sudip Sengupta. (1992). Study of particle transport to the tokamak edges and the drift-wave-like instability occurring in the SOL region. Plasma Physics and Controlled Fusion. 34(4). 475–486. 7 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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