Vijay Chudasama

6.2k total citations · 2 hit papers
111 papers, 5.0k citations indexed

About

Vijay Chudasama is a scholar working on Molecular Biology, Organic Chemistry and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Vijay Chudasama has authored 111 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 59 papers in Organic Chemistry and 51 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Vijay Chudasama's work include Monoclonal and Polyclonal Antibodies Research (49 papers), Chemical Synthesis and Analysis (39 papers) and Click Chemistry and Applications (37 papers). Vijay Chudasama is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (49 papers), Chemical Synthesis and Analysis (39 papers) and Click Chemistry and Applications (37 papers). Vijay Chudasama collaborates with scholars based in United Kingdom, Portugal and Argentina. Vijay Chudasama's co-authors include Stephen Caddick, Antoine Maruani, James R. Baker, Marcos Fernández, Faiza Javaid, Daniel A. Richards, Mark E. B. Smith, Richard J. Fitzmaurice, Péter A. Szijj and Nafsika Forte and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Chemical Society Reviews.

In The Last Decade

Vijay Chudasama

110 papers receiving 4.9k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Advances in targeting the folate receptor in the treatment/imaging of cancers

2017 459 citations Vijay Chudasama et al. Chemical Science profile →
Antibody–PROTAC Conjugates Enable HER2-Dependent Targeted Protein Degradation of BRD4

2020 242 citations Marı́a Maneiro, Nafsika Forte et al. ACS Chemical Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vijay Chudasama United Kingdom	38	2.6k	1.9k	1.6k	1.5k	943	111	5.0k
Pascal Dumy France	47	5.4k 2.1×	3.1k 1.6×	1.1k 0.7×	855 0.6×	593 0.6×	252	7.4k
Christopher P. Leamon United States	43	3.2k 1.2×	921 0.5×	1.1k 0.7×	1.7k 1.2×	1.3k 1.3×	94	6.6k
Nicholas J. Agard United States	17	4.2k 1.6×	3.9k 2.0×	1.6k 1.0×	542 0.4×	505 0.5×	24	5.9k
David Rabuka United States	32	2.2k 0.8×	1.2k 0.6×	1.2k 0.8×	1.0k 0.7×	337 0.4×	58	3.3k
Didier Boturyn France	31	1.8k 0.7×	684 0.4×	732 0.5×	463 0.3×	526 0.6×	111	3.0k
Ravi Chari United States	30	2.6k 1.0×	808 0.4×	3.4k 2.1×	3.7k 2.5×	532 0.6×	76	6.3k
Mark D. Bednarski United States	41	3.3k 1.3×	2.5k 1.3×	1.1k 0.7×	415 0.3×	1.1k 1.2×	95	6.8k
Floris L. van Delft Netherlands	46	4.8k 1.9×	6.2k 3.2×	1.8k 1.1×	771 0.5×	422 0.4×	174	8.2k
J. Strohalm Czechia	40	2.2k 0.8×	1.0k 0.5×	762 0.5×	868 0.6×	1.3k 1.4×	90	5.2k
Christian P. R. Hackenberger Germany	40	4.2k 1.6×	3.0k 1.6×	1.3k 0.8×	860 0.6×	285 0.3×	162	5.6k

Countries citing papers authored by Vijay Chudasama

Since Specialization

Citations

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

Fields of papers citing papers by Vijay Chudasama

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vijay Chudasama

This figure shows the co-authorship network connecting the top 25 collaborators of Vijay Chudasama. A scholar is included among the top collaborators of Vijay Chudasama 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 Vijay Chudasama. Vijay Chudasama is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Bouloc, Nathalie, Ning Wang, Péter A. Szijj, et al.. (2025). Formation of mono- and dual-labelled antibody fragment conjugates via reversible site-selective disulfide modification and proximity induced lysine reactivity. Chemical Science. 16(6). 2763–2776. 1 indexed citations

Hernandez‐Alba, Oscar, Sarah Cianférani, Christopher J. Scott, et al.. (2024). Modular Semisynthetic Approach to Generate T Cell-Dependent Bispecific Constructs from Recombinant IgG1 Antibodies. Bioconjugate Chemistry. 1 indexed citations

Coelho, Jaime A. S., et al.. (2024). Macrocyclic Dual‐Locked “Turn‐On” Drug for Selective and Traceless Release in Cancer Cells. Angewandte Chemie. 136(18). 2 indexed citations

Coelho, Jaime A. S., et al.. (2024). Macrocyclic Dual‐Locked “Turn‐On” Drug for Selective and Traceless Release in Cancer Cells. Angewandte Chemie International Edition. 63(18). e202314143–e202314143. 6 indexed citations

Cai, Yunpeng, Jesper S. Nielsen, Vijay Chudasama, et al.. (2024). An Albumin-Holliday Junction Biomolecular Modular Design for Programmable Multifunctionality and Prolonged Circulation. Bioconjugate Chemistry. 35(2). 214–222. 3 indexed citations

Bahou, Calise, Richard J. Spears, Ksenia S. Stankevich, et al.. (2023). Hydrogel Cross-Linking via Thiol-Reactive Pyridazinediones. Biomacromolecules. 24(11). 4646–4652. 4 indexed citations

Hernandez‐Alba, Oscar, Sarah Cianférani, Christopher J. Scott, et al.. (2023). Rapid Access to Potent Bispecific T Cell Engagers Using Biogenic Tyrosine Click Chemistry. Bioconjugate Chemistry. 34(12). 2215–2220. 6 indexed citations

Bahou, Calise, Jonathan P. Wojciechowski, Richard J. Spears, et al.. (2023). Use of pyridazinediones for tuneable and reversible covalent cysteine modification applied to peptides, proteins and hydrogels. Chemical Science. 14(47). 13743–13754. 7 indexed citations

Szijj, Péter A., et al.. (2023). Chemical generation of checkpoint inhibitory T cell engagers for the treatment of cancer. Nature Chemistry. 15(11). 1636–1647. 22 indexed citations

10.

Parkes, Michael A., Michael Staniforth, Jack M. Woolley, et al.. (2022). Intramolecular thiomaleimide [2 + 2] photocycloadditions: stereoselective control for disulfide stapling and observation of excited state intermediates by transient absorption spectroscopy. Chemical Science. 13(10). 2909–2918. 5 indexed citations

11.

Palmfeldt, Johan, Vijay Chudasama, Jesper Wengel, et al.. (2022). Albumin Biomolecular Drug Designs Stabilized through Improved Thiol Conjugation and a Modular Locked Nucleic Acid Functionalized Assembly. Bioconjugate Chemistry. 33(2). 333–342. 7 indexed citations

12.

Yu, Zilin, Jana Kim, Kavitha Sunassee, et al.. (2021). New Bifunctional Chelators Incorporating Dibromomaleimide Groups for Radiolabeling of Antibodies with Positron Emission Tomography Imaging Radioisotopes. Bioconjugate Chemistry. 32(7). 1214–1222. 12 indexed citations

13.

Richards, Daniel A., Michael R. Thomas, Péter A. Szijj, et al.. (2021). Employing defined bioconjugates to generate chemically functionalised gold nanoparticles for in vitro diagnostic applications. Nanoscale. 13(27). 11921–11931. 11 indexed citations

14.

Forte, Nafsika, et al.. (2020). One-pot thiol–amine bioconjugation to maleimides: simultaneous stabilisation and dual functionalisation. Chemical Science. 11(42). 11455–11460. 24 indexed citations

15.

Maneiro, Marı́a, Nafsika Forte, Maria M. Shchepinova, et al.. (2020). Antibody–PROTAC Conjugates Enable HER2-Dependent Targeted Protein Degradation of BRD4. ACS Chemical Biology. 15(6). 1306–1312. 242 indexed citations breakdown →

16.

Forte, Nafsika, et al.. (2019). Cysteine-to-lysine transfer antibody fragment conjugation. Chemical Science. 10(47). 10919–10924. 19 indexed citations

17.

Galan, Sébastien R. G., James R. Wickens, Jitka Daďová, et al.. (2018). Post-translational site-selective protein backbone α-deuteration. Nature Chemical Biology. 14(10). 955–963. 25 indexed citations

18.

Loynachan, Colleen N., Michael R. Thomas, Eleanor R. Gray, et al.. (2017). Platinum Nanocatalyst Amplification: Redefining the Gold Standard for Lateral Flow Immunoassays with Ultrabroad Dynamic Range. ACS Nano. 12(1). 279–288. 336 indexed citations

19.

Pye, Hayley, Antoine Maruani, João P. M. Nunes, et al.. (2016). A HER2 selective theranostic agent for surgical resection guidance and photodynamic therapy. Photochemical & Photobiological Sciences. 15(10). 1227–1238. 16 indexed citations

20.

Bryden, Francesca, Antoine Maruani, Huguette Savoie, et al.. (2014). Regioselective and Stoichiometrically Controlled Conjugation of Photodynamic Sensitizers to a HER2 Targeting Antibody Fragment. Bioconjugate Chemistry. 25(3). 611–617. 60 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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