Igor Nabiev

11.0k total citations · 2 hit papers
303 papers, 8.7k citations indexed

About

Igor Nabiev is a scholar working on Molecular Biology, Materials Chemistry and Biomedical Engineering. According to data from OpenAlex, Igor Nabiev has authored 303 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 145 papers in Molecular Biology, 141 papers in Materials Chemistry and 80 papers in Biomedical Engineering. Recurrent topics in Igor Nabiev's work include Quantum Dots Synthesis And Properties (108 papers), Advanced biosensing and bioanalysis techniques (55 papers) and Gold and Silver Nanoparticles Synthesis and Applications (49 papers). Igor Nabiev is often cited by papers focused on Quantum Dots Synthesis And Properties (108 papers), Advanced biosensing and bioanalysis techniques (55 papers) and Gold and Silver Nanoparticles Synthesis and Applications (49 papers). Igor Nabiev collaborates with scholars based in Russia, France and Spain. Igor Nabiev's co-authors include Alyona Sukhanova, Mikhail Artemyev, Yury P. Rakovich, А. В. Караулов, В. А. Олейников, Pavel Samokhvalov, Michel Manfait, Svetlana Bozrova, Pavel Sokolov and M. A. Berestovoy and has published in prestigious journals such as Journal of the American Chemical Society, Advanced Materials and Journal of Biological Chemistry.

In The Last Decade

Igor Nabiev

293 papers receiving 8.5k citations

Hit Papers

Dependence of Nanoparticle ... 2002 2026 2010 2018 2018 2002 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Igor Nabiev Russia 46 4.4k 3.3k 2.6k 1.8k 1.6k 303 8.7k
Stefan Franzen United States 53 2.6k 0.6× 4.4k 1.3× 2.0k 0.8× 2.1k 1.2× 1.7k 1.1× 214 9.6k
Fabien Pinaud United States 29 7.3k 1.7× 4.8k 1.5× 3.0k 1.1× 1.2k 0.7× 2.4k 1.5× 48 10.8k
Yongdong Jin China 49 3.3k 0.8× 2.3k 0.7× 2.5k 1.0× 2.1k 1.2× 2.2k 1.4× 204 7.8k
Thomas Pons France 45 5.4k 1.2× 3.1k 0.9× 2.2k 0.9× 1.1k 0.6× 1.9k 1.2× 107 7.4k
Yoshitaka Ishii United States 35 3.6k 0.8× 3.1k 1.0× 962 0.4× 1.2k 0.7× 2.5k 1.5× 78 10.2k
Hui Zhang China 56 3.2k 0.7× 4.4k 1.3× 4.0k 1.5× 2.4k 1.4× 1.8k 1.1× 218 9.9k
Vasudevanpillai Biju Japan 43 4.5k 1.0× 1.9k 0.6× 2.2k 0.9× 1.4k 0.8× 2.1k 1.3× 154 7.2k
Markus Grabolle Germany 25 3.9k 0.9× 2.5k 0.8× 1.5k 0.6× 584 0.3× 1.4k 0.9× 32 6.7k
W. Russ Algar Canada 49 5.5k 1.2× 5.6k 1.7× 3.2k 1.2× 863 0.5× 1.8k 1.1× 134 9.6k

Countries citing papers authored by Igor Nabiev

Since Specialization
Citations

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

Fields of papers citing papers by Igor Nabiev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Igor Nabiev

This figure shows the co-authorship network connecting the top 25 collaborators of Igor Nabiev. A scholar is included among the top collaborators of Igor Nabiev 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 Igor Nabiev. Igor Nabiev 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.
Charlier, Cathy, et al.. (2024). Photonic Crystal Surface Mode Real-Time Imaging of RAD51 DNA Repair Protein Interaction with the ssDNA Substrate. Biosensors. 14(1). 43–43. 2 indexed citations
2.
Караулов, А. В., et al.. (2024). Cytotoxic Effects of Doxorubicin on Cancer Cells and Macrophages Depend Differently on the Microcarrier Structure. Pharmaceutics. 16(6). 785–785. 3 indexed citations
3.
Караулов, А. В., et al.. (2024). Functionalized Calcium Carbonate-Based Microparticles as a Versatile Tool for Targeted Drug Delivery and Cancer Treatment. Pharmaceutics. 16(5). 653–653. 3 indexed citations
5.
Terryn, Christine, et al.. (2023). Impact of Macrophages on the Interaction of Cetuximab-Functionalized Polyelectrolyte Capsules with EGFR-Expressing Cancer Cells. ACS Applied Materials & Interfaces. 15(45). 52137–52149. 4 indexed citations
6.
Krivenkov, Victor, Pavel Samokhvalov, Igor Nabiev, & Yury P. Rakovich. (2021). pH-Sensing Platform Based on Light–Matter Coupling in Colloidal Complexes of Silver Nanoplates and J-Aggregates. The Journal of Physical Chemistry C. 125(3). 1972–1979. 14 indexed citations
7.
Melnikau, Dzmitry, Pavel Samokhvalov, Ana Sánchez‐Iglesias, et al.. (2021). Strong coupling effects in a plexciton system of gold nanostars and J-aggregates. Journal of Luminescence. 242. 118557–118557. 19 indexed citations
8.
Караулов, А. В., et al.. (2021). Designing Functionalized Polyelectrolyte Microcapsules for Cancer Treatment. Nanomaterials. 11(11). 3055–3055. 14 indexed citations
9.
Krivenkov, Victor, А. Е. Efimov, Е. В. Коростылев, et al.. (2021). Nanoparticle-Doped Hybrid Polyelectrolyte Microcapsules with Controlled Photoluminescence for Potential Bioimaging Applications. Polymers. 13(23). 4076–4076. 3 indexed citations
11.
Dovzhenko, Dmitriy, et al.. (2021). Strong exciton−photon coupling with colloidal quantum dots in a tunable microcavity. Applied Physics Letters. 119(1). 6 indexed citations
12.
Krivenkov, Victor, Pavel Samokhvalov, Ana Sánchez‐Iglesias, et al.. (2021). Strong increase in the effective two-photon absorption cross-section of excitons in quantum dots due to the nonlinear interaction with localized plasmons in gold nanorods. Nanoscale. 13(8). 4614–4623. 11 indexed citations
13.
Charlier, Cathy, Milena Popova, Pierre Weigel, et al.. (2019). Interactions of the Rad51 inhibitor DIDS with human and bovine serum albumins: Optical spectroscopy and isothermal calorimetry approaches. Biochimie. 167. 187–197. 3 indexed citations
14.
Мартынов, И. Л., et al.. (2018). Сравнение режимов возбуждения флуоресценции полупроводниковых квантовых точек на основе селенида кадмия для биомедицинских приложений. Вестник Российского государственного медицинского университета. 45–52.
15.
Mochalov, Konstantin, et al.. (2018). A versatile tunable microcavity for investigation of light–matter interaction. Review of Scientific Instruments. 89(5). 53105–53105. 10 indexed citations
16.
Charlier, Cathy, et al.. (2018). Assessment of DNA-PKcs kinase activity by quantum dot–based microarray. Scientific Reports. 8(1). 10968–10968. 4 indexed citations
17.
Nabiev, Igor, et al.. (2016). Charge transfer and separation in photoexcited quantum dot-based systems. Nano Today. 11(2). 189–211. 100 indexed citations
18.
Feofanov, Alexey V., et al.. (1998). [Surface enhanced Raman spectroscopy for characterization of structural characteristics of carbon chains in alpha1-acid glycoprotein and pseudoglycoproteins].. PubMed. 24(6). 412–21. 1 indexed citations
19.
Feofanov, Alexey V., et al.. (1997). [Study of sialated neoglycoconjugates by surface enhanced Raman scattering spectroscopy].. PubMed. 23(11). 910–8. 1 indexed citations
20.
Modyanov, N.N., Elena Arystarkhova, Karine N. Dzhandzhugazyan, et al.. (1987). Transmembrane organization of Na,K-ATPase: secondary structure of hydrophilic and hydrophobic regions in a- and b-subunits of enzyme as probed by optical spectroscopy. Биологические мембраны Журнал мембранной и клеточной биологии. 4(12). 1244–1253. 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026