Chandra Verma

15.8k total citations · 3 hit papers
315 papers, 11.5k citations indexed

About

Chandra Verma is a scholar working on Molecular Biology, Oncology and Organic Chemistry. According to data from OpenAlex, Chandra Verma has authored 315 papers receiving a total of 11.5k indexed citations (citations by other indexed papers that have themselves been cited), including 237 papers in Molecular Biology, 75 papers in Oncology and 44 papers in Organic Chemistry. Recurrent topics in Chandra Verma's work include Protein Structure and Dynamics (59 papers), Cancer-related Molecular Pathways (51 papers) and Chemical Synthesis and Analysis (39 papers). Chandra Verma is often cited by papers focused on Protein Structure and Dynamics (59 papers), Cancer-related Molecular Pathways (51 papers) and Chemical Synthesis and Analysis (39 papers). Chandra Verma collaborates with scholars based in Singapore, United Kingdom and France. Chandra Verma's co-authors include David P. Lane, Christopher J. Brown, Kian Hoe Khoo, Roger W. Beuerman, Rajamani Lakshminarayanan, Shouping Liu, Guy Dodson, Sonia Laı́n, Alan R. Fersht and Chit Fang Cheok and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Chandra Verma

311 papers receiving 11.4k citations

Hit Papers

Awakening guardian angels: drugging the p53 pathway 2009 2026 2014 2020 2009 2014 2017 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chandra Verma Singapore 51 8.0k 2.9k 1.5k 1.3k 1.0k 315 11.5k
Marcel B. Bally Canada 62 9.3k 1.2× 2.4k 0.8× 1.0k 0.7× 286 0.2× 867 0.9× 263 15.3k
Francesc Avilés Spain 52 7.1k 0.9× 2.4k 0.8× 837 0.6× 240 0.2× 1.3k 1.3× 266 9.9k
Tom W. Muir United States 79 20.9k 2.6× 2.8k 1.0× 5.3k 3.5× 1.1k 0.8× 941 0.9× 273 23.7k
Gregory L. Verdine United States 74 18.2k 2.3× 2.3k 0.8× 3.1k 2.1× 595 0.4× 850 0.8× 208 21.3k
James H. Naismith United Kingdom 72 11.1k 1.4× 1.5k 0.5× 2.4k 1.6× 328 0.2× 1.9k 1.8× 292 16.7k
John R. Engen United States 53 7.8k 1.0× 1.4k 0.5× 586 0.4× 256 0.2× 989 1.0× 194 11.3k
K. Ravi Acharya United Kingdom 58 7.1k 0.9× 1.0k 0.4× 1.1k 0.7× 296 0.2× 1.2k 1.2× 272 12.0k
Roman A. Zubarev Sweden 64 8.6k 1.1× 697 0.2× 559 0.4× 434 0.3× 1.1k 1.0× 361 17.1k
Pierre Thibault Canada 72 9.2k 1.2× 1.6k 0.6× 628 0.4× 569 0.4× 243 0.2× 335 15.9k
Nicholas E. Dixon Australia 59 6.8k 0.9× 938 0.3× 677 0.5× 366 0.3× 1.5k 1.5× 193 10.8k

Countries citing papers authored by Chandra Verma

Since Specialization
Citations

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

Fields of papers citing papers by Chandra Verma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chandra Verma

This figure shows the co-authorship network connecting the top 25 collaborators of Chandra Verma. A scholar is included among the top collaborators of Chandra Verma 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 Chandra Verma. Chandra Verma 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.
Ding, Ke, Barindra Sana, Srinivasaraghavan Kannan, et al.. (2024). Modulation of PETase active site flexibility and activity on morphologically distinct polyethylene terephthalate substrates by surface charge engineering. Biochemical Engineering Journal. 209. 109420–109420. 5 indexed citations
2.
Li, Jianguo, Milad Radiom, Raffaele Mezzenga, et al.. (2024). Phase-separating peptide coacervates with programmable material properties for universal intracellular delivery of macromolecules. Nature Communications. 15(1). 10094–10094. 22 indexed citations
3.
Marzinek, Jan K., et al.. (2024). Coarse-Grained Model of Glycosaminoglycans for Biomolecular Simulations. Journal of Chemical Theory and Computation. 20(8). 3308–3321. 2 indexed citations
4.
Li, Mingyue, Jianguo Li, Xingyu Lu, et al.. (2024). Molecular Mechanism of P53 Peptide Permeation through Lipid Membranes from Solid-State NMR Spectroscopy and Molecular Dynamics Simulations. Journal of the American Chemical Society. 146(33). 23075–23091. 3 indexed citations
5.
Jelinska, Clare, Srinivasaraghavan Kannan, Fernaldo Richtia Winnerdy, et al.. (2023). Stitched peptides as potential cell permeable inhibitors of oncogenic DAXX protein. RSC Chemical Biology. 4(12). 1096–1110. 1 indexed citations
6.
Li, Shuangli, Xue Huang, Yi Yang, et al.. (2023). Design and evaluation of tadpole-like conformational antimicrobial peptides. Communications Biology. 6(1). 1177–1177. 7 indexed citations
7.
Lin, Yen‐Chu, Anil K. Pillai, Tobias Cornvik, et al.. (2022). Engineering an autonomous VH domain to modulate intracellular pathways and to interrogate the eIF4F complex. Nature Communications. 13(1). 4854–4854. 4 indexed citations
8.
Iyengar, Prasanna Vasudevan, Dilraj Lama, Tuan Zea Tan, et al.. (2022). TRAF4 Inhibits Bladder Cancer Progression by Promoting BMP/SMAD Signaling. Molecular Cancer Research. 20(10). 1516–1531. 13 indexed citations
9.
Kumar, Akshita, et al.. (2021). Liquid–Liquid Phase Separation of Short Histidine- and Tyrosine-Rich Peptides: Sequence Specificity and Molecular Topology. The Journal of Physical Chemistry B. 125(25). 6776–6790. 33 indexed citations
10.
Mehta, Sunali, Cushla McKinney, Chandra Verma, et al.. (2020). Dephosphorylation of YB-1 is Required for Nuclear Localisation During G2 Phase of the Cell Cycle. Cancers. 12(2). 315–315. 16 indexed citations
11.
Lim, Xin-Ni, Chao Shan, Jan K. Marzinek, et al.. (2019). Molecular basis of dengue virus serotype 2 morphological switch from 29°C to 37°C. PLoS Pathogens. 15(9). e1007996–e1007996. 24 indexed citations
12.
Tan, Yaw Sing, Jessica Iegre, Stephen J. Walsh, et al.. (2019). Targeted covalent inhibitors of MDM2 using electrophile-bearing stapled peptides. Chemical Communications. 55(55). 7914–7917. 26 indexed citations
13.
Yuen, Tsz Ying, Christopher J. Brown, Yuezhen Xue, et al.. (2019). Stereoisomerism of stapled peptide inhibitors of the p53-Mdm2 interaction: an assessment of synthetic strategies and activity profiles. Chemical Science. 10(26). 6457–6466. 21 indexed citations
14.
Iegre, Jessica, Josephine Gaynord, Yuteng Wu, et al.. (2018). Stapled peptides as a new technology to investigate protein–protein interactions in human platelets. Chemical Science. 9(20). 4638–4643. 27 indexed citations
15.
Marzinek, Jan K., Nirmalya Bag, Roland G. Huber, et al.. (2018). A Funneled Conformational Landscape Governs Flavivirus Fusion Peptide Interaction with Lipid Membranes. Journal of Chemical Theory and Computation. 14(7). 3920–3932. 6 indexed citations
16.
Rout, Bhimsen, et al.. (2017). An intramolecular tryptophan-condensation approach for peptide stapling. Organic & Biomolecular Chemistry. 16(3). 389–392. 16 indexed citations
17.
Lin, Shuimu, Jun-Jie Koh, Thet Tun Aung, et al.. (2017). Symmetrically Substituted Xanthone Amphiphiles Combat Gram-Positive Bacterial Resistance with Enhanced Membrane Selectivity. Journal of Medicinal Chemistry. 60(4). 1362–1378. 72 indexed citations
18.
Wiedmann, Mareike M., Yaw Sing Tan, Yuteng Wu, et al.. (2016). Development of Cell‐Permeable, Non‐Helical Constrained Peptides to Target a Key Protein–Protein Interaction in Ovarian Cancer. Angewandte Chemie. 129(2). 539–544. 6 indexed citations
19.
Wiedmann, Mareike M., Yaw Sing Tan, Yuteng Wu, et al.. (2016). Development of Cell‐Permeable, Non‐Helical Constrained Peptides to Target a Key Protein–Protein Interaction in Ovarian Cancer. Angewandte Chemie International Edition. 56(2). 524–529. 36 indexed citations
20.
Víjayakríshnan, Swetha, Rohini Qamra, Chandra Verma, Ranjan Sen, & Shekhar C. Mande. (2006). Cation-Mediated Interplay of Loops in Chaperonin-10. Journal of Biomolecular Structure and Dynamics. 23(4). 365–375. 1 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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