Soumadwip Ghosh

694 total citations
20 papers, 476 citations indexed

About

Soumadwip Ghosh is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Biomedical Engineering. According to data from OpenAlex, Soumadwip Ghosh has authored 20 papers receiving a total of 476 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Biomedical Engineering. Recurrent topics in Soumadwip Ghosh's work include Receptor Mechanisms and Signaling (7 papers), Protein Structure and Dynamics (4 papers) and Nanopore and Nanochannel Transport Studies (4 papers). Soumadwip Ghosh is often cited by papers focused on Receptor Mechanisms and Signaling (7 papers), Protein Structure and Dynamics (4 papers) and Nanopore and Nanochannel Transport Studies (4 papers). Soumadwip Ghosh collaborates with scholars based in United States, India and United Kingdom. Soumadwip Ghosh's co-authors include Rajarshi Chakrabarti, Nagarajan Vaidehi, Manbir Sandhu, Nevin A. Lambert, Asuka Inoue, Najeah Okashah, Qingwen Wan, Sangbae Lee, Christopher G. Tate and Himanshu Dixit and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Molecular Cell.

In The Last Decade

Soumadwip Ghosh

20 papers receiving 475 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Soumadwip Ghosh United States 13 327 126 72 70 39 20 476
Shailika Nurva United States 5 636 1.9× 192 1.5× 17 0.2× 46 0.7× 22 0.6× 5 714
Luigino Grasso Switzerland 8 476 1.5× 115 0.9× 75 1.0× 17 0.2× 22 0.6× 12 546
R.E. Hubbard United Kingdom 9 199 0.6× 87 0.7× 27 0.4× 32 0.5× 23 0.6× 12 326
Hans‐Joachim Wittmann Germany 15 490 1.5× 215 1.7× 35 0.5× 44 0.6× 21 0.5× 38 737
Julian Thimm Germany 14 363 1.1× 45 0.4× 60 0.8× 23 0.3× 9 0.2× 23 673
James A. R. Dalton Spain 17 591 1.8× 446 3.5× 25 0.3× 217 3.1× 22 0.6× 27 819
You Zhuo United States 11 238 0.7× 76 0.6× 33 0.5× 13 0.2× 12 0.3× 18 340
Maikel Fransen United Kingdom 6 515 1.6× 290 2.3× 105 1.5× 62 0.9× 6 0.2× 7 631
Yuko Kawasaki Japan 14 330 1.0× 42 0.3× 22 0.3× 39 0.6× 21 0.5× 33 510
Alexander Asanov Mexico 15 482 1.5× 125 1.0× 116 1.6× 168 2.4× 195 5.0× 22 810

Countries citing papers authored by Soumadwip Ghosh

Since Specialization
Citations

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

Fields of papers citing papers by Soumadwip Ghosh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Soumadwip Ghosh

This figure shows the co-authorship network connecting the top 25 collaborators of Soumadwip Ghosh. A scholar is included among the top collaborators of Soumadwip Ghosh 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 Soumadwip Ghosh. Soumadwip Ghosh 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.
Ma, Ning, S. Bhattacharya, Zuzana Jandová, et al.. (2025). Frustration in the protein-protein interface plays a central role in the cooperativity of PROTAC ternary complexes. Nature Communications. 16(1). 8595–8595. 2 indexed citations
2.
Ma, Ning, Nadia Arang, Ajit Prakash, et al.. (2023). Catalytic site mutations confer multiple states of G protein activation. Science Signaling. 16(772). eabq7842–eabq7842. 11 indexed citations
3.
Sandhu, Manbir, Ning Ma, Yoon Namkung, et al.. (2022). Dynamic spatiotemporal determinants modulate GPCR:G protein coupling selectivity and promiscuity. Nature Communications. 13(1). 7428–7428. 32 indexed citations
4.
Ghosh, Soumadwip, et al.. (2022). Sequence coevolution and structure stabilization modulate olfactory receptor expression. Biophysical Journal. 121(5). 830–840. 6 indexed citations
5.
Ghosh, Soumadwip, Sharon L. Campbell, Reid H. J. Olsen, et al.. (2021). A universal allosteric mechanism for G protein activation. Molecular Cell. 81(7). 1384–1396.e6. 41 indexed citations
6.
Ikegami, Kentaro, Claire A. de March, Soumadwip Ghosh, et al.. (2020). Structural instability and divergence from conserved residues underlie intracellular retention of mammalian odorant receptors. Proceedings of the National Academy of Sciences. 117(6). 2957–2967. 34 indexed citations
7.
Lee, Sangbae, et al.. (2020). How Do Branched Detergents Stabilize GPCRs in Micelles?. Biochemistry. 59(23). 2125–2134. 42 indexed citations
8.
Okashah, Najeah, Qingwen Wan, Soumadwip Ghosh, et al.. (2019). Variable G protein determinants of GPCR coupling selectivity. Proceedings of the National Academy of Sciences. 116(24). 12054–12059. 100 indexed citations
9.
Ghosh, Soumadwip, Srisairam Achuthan, Xiaohong Chen, et al.. (2019). Machine Learning for Prioritization of Thermostabilizing Mutations for G-Protein Coupled Receptors. Biophysical Journal. 117(11). 2228–2239. 12 indexed citations
10.
Dubey, Richa, Jhankar Acharya, Soumadwip Ghosh, et al.. (2019). Azadirachtin inhibits amyloid formation, disaggregates pre-formed fibrils and protects pancreatic β-cells from human islet amyloid polypeptide/amylin-induced cytotoxicity. Biochemical Journal. 476(5). 889–907. 32 indexed citations
11.
Ghosh, Soumadwip, et al.. (2019). Prediction of Conformation Specific Thermostabilizing Mutations for Class A G Protein-Coupled Receptors. Journal of Chemical Information and Modeling. 59(9). 3744–3754. 4 indexed citations
12.
Ghosh, Soumadwip, et al.. (2018). Engineering Salt Bridge Networks between Transmembrane Helices Confers Thermostability in G-Protein-Coupled Receptors. Journal of Chemical Theory and Computation. 14(12). 6574–6585. 8 indexed citations
13.
Maity, Atanu, et al.. (2018). Salt Induced Structural Collapse, Swelling, and Signature of Aggregation of Two ssDNA Strands: Insights from Molecular Dynamics Simulation. The Journal of Physical Chemistry B. 123(1). 47–56. 16 indexed citations
14.
15.
Ghosh, Soumadwip, et al.. (2017). Can an ammonium-based room temperature ionic liquid counteract the urea-induced denaturation of a small peptide?. Physical Chemistry Chemical Physics. 19(11). 7772–7787. 21 indexed citations
16.
Ghosh, Soumadwip & Rajarshi Chakrabarti. (2016). Unzipping of Double-Stranded Ribonucleic Acids by Graphene and Single-Walled Carbon Nanotube: Helix Geometry versus Surface Curvature. The Journal of Physical Chemistry C. 120(39). 22681–22693. 22 indexed citations
17.
Ghosh, Soumadwip & Rajarshi Chakrabarti. (2016). Spontaneous Unzipping of Xylonucleic Acid Assisted by a Single-Walled Carbon Nanotube: A Computational Study. The Journal of Physical Chemistry B. 120(15). 3642–3652. 15 indexed citations
18.
19.
Ghosh, Soumadwip, et al.. (2015). Probing the Salt Concentration Dependent Nucleobase Distribution in a Single-Stranded DNA–Single-Walled Carbon Nanotube Hybrid with Molecular Dynamics. The Journal of Physical Chemistry B. 120(3). 455–466. 24 indexed citations
20.
Ghosh, Soumadwip, Himanshu Dixit, & Rajarshi Chakrabarti. (2015). Ion assisted structural collapse of a single stranded DNA: A molecular dynamics approach. Chemical Physics. 459. 137–147. 22 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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