Alexander Grishaev

4.2k total citations · 1 hit paper
77 papers, 3.2k citations indexed

About

Alexander Grishaev is a scholar working on Molecular Biology, Materials Chemistry and Spectroscopy. According to data from OpenAlex, Alexander Grishaev has authored 77 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 35 papers in Materials Chemistry and 25 papers in Spectroscopy. Recurrent topics in Alexander Grishaev's work include Protein Structure and Dynamics (46 papers), Enzyme Structure and Function (34 papers) and Advanced NMR Techniques and Applications (19 papers). Alexander Grishaev is often cited by papers focused on Protein Structure and Dynamics (46 papers), Enzyme Structure and Function (34 papers) and Advanced NMR Techniques and Applications (19 papers). Alexander Grishaev collaborates with scholars based in United States, Canada and Switzerland. Alexander Grishaev's co-authors include Ad Bax, Jinfa Ying, Miguel Llinás, G. Marius Clore, Jill Trewhella, Charles D. Schwieters, Rodolfo Ghirlando, Lishan Yao, Gabriel Cornilescu and Wenwei Zheng and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Alexander Grishaev

75 papers receiving 3.1k citations

Hit Papers

align trajectories

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.

Ionization and structural properties of mRNA lipid nanoparticles influence expression in intramuscular and intravascular administration

2021 291 citations Manuel Carrasco, Suman Alishetty et al. Communications Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexander Grishaev United States	29	2.6k	1.2k	758	177	172	77	3.2k
Florence Cordier France	28	1.8k 0.7×	544 0.5×	908 1.2×	166 0.9×	109 0.6×	53	2.6k
Remco Sprangers Germany	28	3.0k 1.1×	680 0.6×	647 0.9×	201 1.1×	128 0.7×	60	3.4k
Nils‐Alexander Lakomek Germany	19	1.7k 0.6×	647 0.6×	804 1.1×	154 0.9×	156 0.9×	39	2.1k
Ananya Majumdar United States	36	3.0k 1.2×	462 0.4×	554 0.7×	283 1.6×	171 1.0×	121	3.5k
Loïc Salmon France	23	1.8k 0.7×	732 0.6×	645 0.9×	145 0.8×	106 0.6×	46	2.1k
Steven M. Pascal United States	19	2.6k 1.0×	569 0.5×	486 0.6×	331 1.9×	125 0.7×	44	3.2k
Robert M. Vernon Canada	27	4.0k 1.6×	852 0.7×	427 0.6×	293 1.7×	123 0.7×	36	4.6k
Marcel Ottiger United States	21	2.8k 1.1×	1.1k 0.9×	1.4k 1.8×	223 1.3×	234 1.4×	29	3.5k
Magnus Wolf‐Watz Sweden	24	2.9k 1.1×	1.3k 1.1×	522 0.7×	401 2.3×	204 1.2×	56	3.6k
Türkan Haliloǧlu Türkiye	30	2.3k 0.9×	882 0.8×	256 0.3×	183 1.0×	66 0.4×	100	3.1k

Countries citing papers authored by Alexander Grishaev

Since Specialization

Citations

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

Fields of papers citing papers by Alexander Grishaev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Grishaev

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Grishaev. A scholar is included among the top collaborators of Alexander Grishaev 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 Alexander Grishaev. Alexander Grishaev 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

Szalai, Veronika A., et al.. (2025). Structure and Dynamics of Monoclonal Antibody Domains Using Spins, Scattering, and Simulations. ChemMedChem. 20(8). e202400917–e202400917.

Bergonzo, Christina & Alexander Grishaev. (2025). Critical Assessment of RNA and DNA Structure Predictions via Artificial Intelligence: The Imitation Game. Journal of Chemical Information and Modeling. 65(7). 3544–3554. 4 indexed citations

Hatch, Harold W., Christina Bergonzo, Marco A. Blanco, et al.. (2024). Anisotropic coarse-grain Monte Carlo simulations of lysozyme, lactoferrin, and NISTmAb by precomputing atomistic models. The Journal of Chemical Physics. 161(9). 3 indexed citations

Thelen, Jacob L., Volker S. Urban, Hugh O’Neill, et al.. (2024). Morphological Characterization of Self-Amplifying mRNA Lipid Nanoparticles. ACS Nano. 18(2). 1464–1476. 24 indexed citations

Chen, Jiahui, Olaf J. Borkiewicz, Alexander Grishaev, et al.. (2023). Extended q‐Range X‐Ray Scattering Reveals High‐Resolution Structural Details of Biomacromolecules in Aqueous Solutions. Chemistry - A European Journal. 29(31). e202203551–e202203551. 1 indexed citations

Lorimer, Ellen, et al.. (2022). Structural and biophysical properties of farnesylated KRas interacting with the chaperone SmgGDS-558. Biophysical Journal. 121(19). 3684–3697. 1 indexed citations

Bergonzo, Christina, Alexander Grishaev, & Sandro Bottaro. (2022). Conformational heterogeneity of UCAAUC RNA oligonucleotide from molecular dynamics simulations, SAXS, and NMR experiments. RNA. 28(7). 937–946. 16 indexed citations

Carrasco, Manuel, Suman Alishetty, Mohamad‐Gabriel Alameh, et al.. (2021). Ionization and structural properties of mRNA lipid nanoparticles influence expression in intramuscular and intravascular administration. Communications Biology. 4(1). 956–956. 291 indexed citations breakdown →

Galkin, Andrey, Javier Guenaga, Sijy O’Dell, et al.. (2020). HIV-1 gp120–CD4-Induced Antibody Complex Elicits CD4 Binding Site–Specific Antibody Response in Mice. The Journal of Immunology. 204(6). 1543–1561. 4 indexed citations

10.

Debnath, Subrata, Dalibor Košek, Stewart R. Durell, et al.. (2018). A trapped human PPM1A–phosphopeptide complex reveals structural features critical for regulation of PPM protein phosphatase activity. Journal of Biological Chemistry. 293(21). 7993–8008. 18 indexed citations

11.

Zheng, Wenwei, Alessandro Borgia, Alexander Grishaev, Benjamin Schuler, & Robert B. Best. (2017). Resolving the Controversy between SAXS and FRET Measurements on Unfolded Proteins. Biophysical Journal. 112(3). 315a–315a. 1 indexed citations

12.

Maltsev, Alexander S., Alexander Grishaev, Julien Roche, Michael Zasloff, & Ad Bax. (2014). Improved Cross Validation of a Static Ubiquitin Structure Derived from High Precision Residual Dipolar Couplings Measured in a Drug-Based Liquid Crystalline Phase. Journal of the American Chemical Society. 136(10). 3752–3755. 64 indexed citations

13.

Hickman, Alison B., Hosam E. Ewis, Xianghong Li, et al.. (2014). Structural Basis of hAT Transposon End Recognition by Hermes, an Octameric DNA Transposase from Musca domestica. Cell. 158(2). 353–367. 53 indexed citations

14.

Li, Fang, Jung Ho Lee, Alexander Grishaev, Jinfa Ying, & Ad Bax. (2014). High Accuracy of Karplus Equations for Relating Three‐Bond J Couplings to Protein Backbone Torsion Angles. ChemPhysChem. 16(3). 572–578. 30 indexed citations

15.

Deshmukh, Lalit, Charles D. Schwieters, Alexander Grishaev, et al.. (2013). Structure and Dynamics of Full-Length HIV-1 Capsid Protein in Solution. Journal of the American Chemical Society. 135(43). 16133–16147. 98 indexed citations

16.

Lakomek, Nils‐Alexander, Joshua D. Kaufman, Stephen J. Stahl, et al.. (2013). Internal Dynamics of the Homotrimeric HIV‐1 Viral Coat Protein gp41 on Multiple Time Scales. Angewandte Chemie International Edition. 52(14). 3911–3915. 55 indexed citations

17.

Grishaev, Alexander, Jinfa Ying, & Ad Bax. (2012). Imino Hydrogen Positions in Nucleic Acids from Density Functional Theory Validated by NMR Residual Dipolar Couplings. Journal of the American Chemical Society. 134(16). 6956–6959. 2 indexed citations

18.

Schwieters, Charles D., Jeong‐Yong Suh, Alexander Grishaev, et al.. (2010). Solution Structure of the 128 kDa Enzyme I Dimer from Escherichia coli and Its 146 kDa Complex with HPr Using Residual Dipolar Couplings and Small- and Wide-Angle X-ray Scattering. Journal of the American Chemical Society. 132(37). 13026–13045. 92 indexed citations

19.

Comoletti, Davide, Alexander Grishaev, Andrew E. Whitten, Palmer Taylor, & Jill Trewhella. (2008). Characterization of the solution structure of a neuroligin/β-neurexin complex. Chemico-Biological Interactions. 175(1-3). 150–155. 8 indexed citations

20.

Grishaev, Alexander & Miguel Llinás. (2002). Protein structure elucidation from NMR proton densities. Proceedings of the National Academy of Sciences. 99(10). 6713–6718. 27 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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