Sandip Basak

1.1k total citations
30 papers, 722 citations indexed

About

Sandip Basak is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Biophysics. According to data from OpenAlex, Sandip Basak has authored 30 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Biophysics. Recurrent topics in Sandip Basak's work include Nicotinic Acetylcholine Receptors Study (9 papers), Ion channel regulation and function (8 papers) and ATP Synthase and ATPases Research (6 papers). Sandip Basak is often cited by papers focused on Nicotinic Acetylcholine Receptors Study (9 papers), Ion channel regulation and function (8 papers) and ATP Synthase and ATPases Research (6 papers). Sandip Basak collaborates with scholars based in United States, Singapore and United Kingdom. Sandip Basak's co-authors include Sudha Chakrapani, Yvonne Gicheru, Shanlin Rao, Mark S.P. Sansom, Gerhard Grüber, Abhijeet Kapoor, Marta Filizola, Malathy Sony Subramanian Manimekalai, Megan L. Mayer and Vera Y. Moiseenkova‐Bell and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Sandip Basak

29 papers receiving 716 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandip Basak United States 12 569 181 90 46 41 30 722
Ben C. Chung United States 8 590 1.0× 124 0.7× 162 1.8× 40 0.9× 74 1.8× 10 791
Thorsten Althoff United States 9 881 1.5× 250 1.4× 75 0.8× 12 0.3× 60 1.5× 13 1.1k
Derek P. Claxton United States 14 806 1.4× 289 1.6× 77 0.9× 15 0.3× 64 1.6× 24 1.1k
Anton O. Chugunov Russia 20 878 1.5× 136 0.8× 44 0.5× 26 0.6× 32 0.8× 54 1.1k
Daohua Jiang China 17 755 1.3× 264 1.5× 42 0.5× 35 0.8× 77 1.9× 34 1.1k
Alex Perálvarez‐Marín Spain 18 588 1.0× 193 1.1× 234 2.6× 28 0.6× 45 1.1× 56 1.1k
Tsukasa Kusakizako Japan 21 878 1.5× 166 0.9× 199 2.2× 10 0.2× 125 3.0× 33 1.3k
Maria Musgaard United Kingdom 16 681 1.2× 261 1.4× 38 0.4× 19 0.4× 33 0.8× 34 876
Mikael C. Bauer Sweden 14 523 0.9× 75 0.4× 53 0.6× 79 1.7× 32 0.8× 22 771
Olga V. Stepanenko Russia 16 567 1.0× 121 0.7× 49 0.5× 8 0.2× 84 2.0× 64 833

Countries citing papers authored by Sandip Basak

Since Specialization
Citations

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

Fields of papers citing papers by Sandip Basak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandip Basak

This figure shows the co-authorship network connecting the top 25 collaborators of Sandip Basak. A scholar is included among the top collaborators of Sandip Basak 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 Sandip Basak. Sandip Basak 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.
Das, Subhadeep, Sandip Basak, & Soumyadev Sarkar. (2025). Decoding Salivary ncRNAomes as Novel Biomarkers for Oral Cancer Detection and Prognosis. Non-Coding RNA. 11(2). 28–28. 1 indexed citations
2.
Biggin, Philip C., et al.. (2024). Cryo-EM structures of prokaryotic ligand-gated ion channel GLIC provide insights into gating in a lipid environment. Nature Communications. 15(1). 2967–2967. 8 indexed citations
3.
Jobichen, Chacko, Sandip Basak, Yeu Khai Choong, et al.. (2023). Bacterioferritin nanocage structures uncover the biomineralization process in ferritins. PNAS Nexus. 2(7). pgad235–pgad235. 8 indexed citations
4.
Zhu, Qiao, Xin‐Fu Yan, Jian Shi, et al.. (2022). Cryo-EM structure of the entire FtsH-HflKC AAA protease complex. Cell Reports. 39(9). 110890–110890. 33 indexed citations
5.
Rao, Shanlin, A. Zaki, Sandip Basak, et al.. (2022). Structural basis for cannabinoid-induced potentiation of alpha1-glycine receptors in lipid nanodiscs. Nature Communications. 13(1). 4862–4862. 13 indexed citations
6.
Basak, Sandip, et al.. (2021). Recombinant expression and purification of pentameric ligand-gated ion channels for Cryo-EM structural studies. Methods in enzymology on CD-ROM/Methods in enzymology. 652. 81–103. 5 indexed citations
7.
Basak, Sandip, et al.. (2020). Elucidate the Binding Mechanism of Various Setrons to 5-HT3AR. Biophysical Journal. 118(3). 190a–190a. 1 indexed citations
8.
Basak, Sandip, Shanlin Rao, Yvonne Gicheru, et al.. (2020). Mechanisms of activation and desensitization of full-length glycine receptor in lipid nanodiscs. Nature Communications. 11(1). 3752–3752. 74 indexed citations
9.
Basak, Sandip, Steven Ramsey, Eric Gibbs, et al.. (2020). High-resolution structures of multiple 5-HT3AR-setron complexes reveal a novel mechanism of competitive inhibition. eLife. 9. 31 indexed citations
10.
Basak, Sandip, Yvonne Gicheru, Shanlin Rao, Mark S.P. Sansom, & Sudha Chakrapani. (2019). Cryo-EM Reveals Two Distinct Serotonin-Bound Conformations of Full-Length 5-HT3A Receptor. Biophysical Journal. 116(3). 37a–37a. 2 indexed citations
11.
Basak, Sandip, Yvonne Gicheru, Amrita Samanta, et al.. (2018). Cryo-EM structure of 5-HT3A receptor in its resting conformation. Nature Communications. 9(1). 514–514. 81 indexed citations
12.
Basak, Sandip, Yvonne Gicheru, Shanlin Rao, Mark S.P. Sansom, & Sudha Chakrapani. (2018). Cryo-EM reveals two distinct serotonin-bound conformations of full-length 5-HT3A receptor. Nature. 563(7730). 270–274. 89 indexed citations
13.
Gicheru, Yvonne, Sandip Basak, & Sudha Chakrapani. (2017). Structural Mechanisms Underlying PUFA Modulation in Pentameric Ligand Gated Ion Channels. Biophysical Journal. 112(3). 320a–320a. 1 indexed citations
14.
Hughes, Taylor, David T. Lodowski, Kevin W. Huynh, et al.. (2017). Structural basis of TRPV5 channel inhibition by econazole revealed by cryo-EM. Nature Structural & Molecular Biology. 25(1). 53–60. 106 indexed citations
15.
Basak, Sandip, et al.. (2016). Site Directed Spin Labeling and EPR Spectroscopic Studies of Pentameric Ligand-Gated Ion Channels. Journal of Visualized Experiments. 6 indexed citations
16.
Basak, Sandip, et al.. (2014). Crystal Structure of Subunits D and F in Complex Gives Insight into Energy Transmission of the Eukaryotic V-ATPase from Saccharomyces cerevisiae. Journal of Biological Chemistry. 290(6). 3183–3196. 34 indexed citations
17.
Basak, Sandip, et al.. (2013). Crystal and NMR Structures Give Insights into the Role and Dynamics of Subunit F of the Eukaryotic V-ATPase from Saccharomyces cerevisiae. Journal of Biological Chemistry. 288(17). 11930–11939. 8 indexed citations
18.
Basak, Sandip, et al.. (2012). Crystallization and preliminary X-ray crystallographic analysis of subunit F (F1–94), an essential coupling subunit of the eukaryotic V1VO-ATPase fromSaccharomyces cerevisiae. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 68(9). 1055–1059. 2 indexed citations
19.
Basak, Sandip, et al.. (2011). NMR solution structure of NBD94483-502 of the nucleotide-binding domain of the Plasmodium yoelii reticulocyte-binding protein Py235. FEMS Microbiology Letters. 318(2). 152–158. 2 indexed citations
20.
Basak, Sandip, Shovanlal Gayen, Youg Raj Thaker, et al.. (2010). Solution structure of subunit F (Vma7p) of the eukaryotic V1VO ATPase from Saccharomyces cerevisiae derived from SAXS and NMR spectroscopy. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1808(1). 360–368. 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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