Elena Gustchina

1.1k total citations
19 papers, 869 citations indexed

About

Elena Gustchina is a scholar working on Virology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Elena Gustchina has authored 19 papers receiving a total of 869 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Virology, 10 papers in Molecular Biology and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Elena Gustchina's work include HIV Research and Treatment (13 papers), Monoclonal and Polyclonal Antibodies Research (6 papers) and HIV/AIDS drug development and treatment (5 papers). Elena Gustchina is often cited by papers focused on HIV Research and Treatment (13 papers), Monoclonal and Polyclonal Antibodies Research (6 papers) and HIV/AIDS drug development and treatment (5 papers). Elena Gustchina collaborates with scholars based in United States, Germany and Belarus. Elena Gustchina's co-authors include Carole A. Bewley, G. Marius Clore, John W. Erickson, Sergei Gulnik, Jan Albert, Charles A. Boucher, Monique Nijhuis, Rob Schuurman, Dorien de Jong and P Schipper and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

Elena Gustchina

18 papers receiving 854 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Gustchina United States 15 502 395 317 140 119 19 869
Shigeyoshi Harada Japan 17 467 0.9× 404 1.0× 286 0.9× 72 0.5× 156 1.3× 42 706
Lilia M. Babé United States 16 445 0.9× 467 1.2× 418 1.3× 119 0.8× 83 0.7× 25 964
Joselina Gorniak United States 10 462 0.9× 468 1.2× 404 1.3× 60 0.4× 72 0.6× 10 973
Shilpa R. Shenoy United States 14 282 0.6× 199 0.5× 743 2.3× 147 1.1× 132 1.1× 21 1.2k
Lowri H. Phylip United Kingdom 15 344 0.7× 366 0.9× 437 1.4× 49 0.3× 39 0.3× 23 847
Robert A. Ogert United States 17 737 1.5× 415 1.1× 511 1.6× 129 0.9× 388 3.3× 32 1.4k
Arthur Thornton United States 9 376 0.7× 221 0.6× 324 1.0× 30 0.2× 240 2.0× 11 829
James Merson United States 18 400 0.8× 490 1.2× 638 2.0× 141 1.0× 196 1.6× 27 1.4k
Simon Lister United Kingdom 14 311 0.6× 223 0.6× 236 0.7× 41 0.3× 159 1.3× 23 854
Alison J. Ritchie United Kingdom 9 531 1.1× 597 1.5× 416 1.3× 52 0.4× 61 0.5× 9 1.0k

Countries citing papers authored by Elena Gustchina

Since Specialization
Citations

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

Fields of papers citing papers by Elena Gustchina

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Gustchina

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

All Works

19 of 19 papers shown
1.
Bale, Shridhar, Elena Gustchina, Javier Guenaga, et al.. (2025). Accelerated cGMP production of near-native HIV-1 Env trimers following electroporation transfection and immunogenicity analysis. npj Vaccines. 10(1). 198–198.
2.
Gustchina, Elena, Rodolfo Ghirlando, Peter Schuck, et al.. (2013). Complexes of Neutralizing and Non-Neutralizing Affinity Matured Fabs with a Mimetic of the Internal Trimeric Coiled-Coil of HIV-1 gp41. PLoS ONE. 8(11). e78187–e78187. 19 indexed citations
3.
Dogo‐Isonagie, Cajetan, Son N. Lam, Elena Gustchina, et al.. (2012). Peptides from Second Extracellular Loop of C-C Chemokine Receptor Type 5 (CCR5) Inhibit Diverse Strains of HIV-1. Journal of Biological Chemistry. 287(18). 15076–15086. 22 indexed citations
4.
Shahzad‐ul‐Hussan, Syed, Elena Gustchina, Rodolfo Ghirlando, G. Marius Clore, & Carole A. Bewley. (2011). Solution Structure of the Monovalent Lectin Microvirin in Complex with Manα(1–2)Man Provides a Basis for Anti-HIV Activity with Low Toxicity. Journal of Biological Chemistry. 286(23). 20788–20796. 67 indexed citations
5.
Gustchina, Elena, Mi Li, John M. Louis, et al.. (2010). Structural Basis of HIV-1 Neutralization by Affinity Matured Fabs Directed against the Internal Trimeric Coiled-Coil of gp41. PLoS Pathogens. 6(11). e1001182–e1001182. 38 indexed citations
8.
Plaza, Alberto, Elena Gustchina, Heather L. Baker, Michelle Kelly, & Carole A. Bewley. (2007). Mirabamides A–D, Depsipeptides from the Sponge Siliquariaspongia mirabilis That Inhibit HIV-1 Fusion. Journal of Natural Products. 70(11). 1753–1760. 106 indexed citations
9.
Gustchina, Elena, John M. Louis, Son N. Lam, Carole A. Bewley, & G. Marius Clore. (2007). A Monoclonal Fab Derived from a Human Nonimmune Phage Library Reveals a New Epitope on gp41 and Neutralizes Diverse Human Immunodeficiency Virus Type 1 Strains. Journal of Virology. 81(23). 12946–12953. 33 indexed citations
10.
Gustchina, Elena, John M. Louis, Carole A. Bewley, & G. Marius Clore. (2006). Synergistic Inhibition of HIV-1 Envelope-Mediated Membrane Fusion by Inhibitors Targeting the N and C-Terminal Heptad Repeats of gp41. Journal of Molecular Biology. 364(3). 283–289. 21 indexed citations
11.
Louis, John M., Carole A. Bewley, Elena Gustchina, Annie Aniana, & G. Marius Clore. (2005). Characterization and HIV-1 Fusion Inhibitory Properties of Monoclonal Fabs Obtained From a Human Non-immune Phage Library Selected Against Diverse Epitopes of the Ectodomain of HIV-1 gp41. Journal of Molecular Biology. 353(5). 945–951. 24 indexed citations
12.
Gustchina, Elena, Gerhard Hummer, Carole A. Bewley, & G. Marius Clore. (2005). Differential Inhibition of HIV-1 and SIV Envelope-Mediated Cell Fusion by C34 Peptides Derived from the C-Terminal Heptad Repeat of gp41 from Diverse Strains of HIV-1, HIV-2, and SIV. Journal of Medicinal Chemistry. 48(8). 3036–3044. 27 indexed citations
13.
Gulnik, Sergei, Elena Afonina, Elena Gustchina, et al.. (2002). Utility of (His)6 Tag for Purification and Refolding of Proplasmepsin-2 and Mutants with Altered Activation Properties. Protein Expression and Purification. 24(3). 412–419. 13 indexed citations
14.
Shao, Wei, Angela Lee, Sergei Gulnik, et al.. (2000). A novel putative transcription factor protein MYT2 that preferentially binds supercoiled DNA and induces DNA synthesis in quiescent cells. FEBS Letters. 473(3). 363–369. 2 indexed citations
15.
Nijhuis, Monique, Rob Schuurman, Dorien de Jong, et al.. (1999). Increased fitness of drug resistant HIV-1 protease as a result of acquisition of compensatory mutations during suboptimal therapy. AIDS. 13(17). 2349–2359. 305 indexed citations
16.
Xie, Dong, Sergei Gulnik, Elena Gustchina, et al.. (1999). Drug resistance mutations can affect dimer stability of HIV‐1 protease at neutral pH. Protein Science. 8(8). 1702–1707. 65 indexed citations
17.
Xie, Dong, et al.. (1998). Thermodynamics and Proton Uptake for Pepstatin Binding to Retroviral and Eukaryotic Aspartic Proteases. Advances in experimental medicine and biology. 436. 381–386. 2 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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