N. Maltseva

1.5k total citations
20 papers, 651 citations indexed

About

N. Maltseva is a scholar working on Molecular Biology, Epidemiology and Materials Chemistry. According to data from OpenAlex, N. Maltseva has authored 20 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Epidemiology and 5 papers in Materials Chemistry. Recurrent topics in N. Maltseva's work include Biochemical and Molecular Research (6 papers), Enzyme Structure and Function (5 papers) and Antibiotic Resistance in Bacteria (4 papers). N. Maltseva is often cited by papers focused on Biochemical and Molecular Research (6 papers), Enzyme Structure and Function (5 papers) and Antibiotic Resistance in Bacteria (4 papers). N. Maltseva collaborates with scholars based in United States, Poland and India. N. Maltseva's co-authors include Youngchang Kim, A. Joachimiak, Mateusz Wilamowski, R. Jedrzejczak, K. Michalska, M. Endres, Adam Godzik, Jacek Wower, Vlad Nicolaescu and Glenn Randall and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

N. Maltseva

19 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N. Maltseva United States 11 324 315 145 79 61 20 651
Mateusz Wilamowski Poland 14 306 0.9× 310 1.0× 148 1.0× 43 0.5× 120 2.0× 19 694
L. Shuvalova United States 15 377 1.2× 185 0.6× 73 0.5× 73 0.9× 86 1.4× 31 704
Muhammad Junaid China 18 512 1.6× 236 0.7× 173 1.2× 88 1.1× 80 1.3× 34 760
Bharati Pandey India 14 354 1.1× 279 0.9× 97 0.7× 53 0.7× 38 0.6× 33 695
Ekachai Jenwitheesuk Thailand 14 254 0.8× 280 0.9× 165 1.1× 97 1.2× 30 0.5× 24 728
Meliza Talaue United States 10 261 0.8× 235 0.7× 63 0.4× 193 2.4× 80 1.3× 10 544
Shashikant Ray India 12 200 0.6× 237 0.8× 136 0.9× 37 0.5× 32 0.5× 21 540
Olga Riabova Russia 16 316 1.0× 212 0.7× 158 1.1× 224 2.8× 61 1.0× 53 808
Shoaib Saleem Pakistan 11 387 1.2× 261 0.8× 173 1.2× 65 0.8× 86 1.4× 16 573
Lalitha Guruprasad India 14 263 0.8× 233 0.7× 116 0.8× 65 0.8× 45 0.7× 43 624

Countries citing papers authored by N. Maltseva

Since Specialization
Citations

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

Fields of papers citing papers by N. Maltseva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Maltseva

This figure shows the co-authorship network connecting the top 25 collaborators of N. Maltseva. A scholar is included among the top collaborators of N. Maltseva 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 N. Maltseva. N. Maltseva 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.
Wang, Xingyou, Masha M. Rosenberg, Youngchang Kim, et al.. (2025). Role of the Mobile Active Site Flap in IMP Dehydrogenase Inhibitor Binding. ACS Infectious Diseases. 11(2). 442–452. 1 indexed citations
2.
Kim, Youngchang, N. Maltseva, C. Tesar, et al.. (2024). Epitopes recognition of SARS-CoV-2 nucleocapsid RNA binding domain by human monoclonal antibodies. iScience. 27(2). 108976–108976. 1 indexed citations
3.
Kim, Youngchang, Seung Hwan Lee, Maren Nattermann, et al.. (2024). Revealing reaction intermediates in one-carbon elongation by thiamine diphosphate/CoA-dependent enzyme family. Communications Chemistry. 7(1). 160–160. 5 indexed citations
4.
5.
Mullowney, Michael W., N. Maltseva, M. Endres, et al.. (2022). Functional and Structural Characterization of Diverse NfsB Chloramphenicol Reductase Enzymes from Human Pathogens. Microbiology Spectrum. 10(2). e0013922–e0013922. 7 indexed citations
6.
Wilamowski, Mateusz, D.A. Sherrell, Youngchang Kim, et al.. (2022). Time-resolved β-lactam cleavage by L1 metallo-β-lactamase. Nature Communications. 13(1). 7379–7379. 15 indexed citations
7.
Kim, Youngchang, Jacek Wower, N. Maltseva, et al.. (2021). Tipiracil binds to uridine site and inhibits Nsp15 endoribonuclease NendoU from SARS-CoV-2. Communications Biology. 4(1). 193–193. 86 indexed citations
8.
Wilamowski, Mateusz, D.A. Sherrell, G. Minasov, et al.. (2021). 2′-O methylation of RNA cap in SARS-CoV-2 captured by serial crystallography. Proceedings of the National Academy of Sciences. 118(21). 52 indexed citations
9.
Michalska, K., Samantha Wellington, N. Maltseva, et al.. (2021). Catalytically impaired TrpA subunit of tryptophan synthase from Chlamydia trachomatis is an allosteric regulator of TrpB. Protein Science. 30(9). 1904–1918. 8 indexed citations
10.
Kim, Youngchang, R. Jedrzejczak, N. Maltseva, et al.. (2020). Crystal structure of Nsp15 endoribonuclease NendoU from SARS‐CoV ‐2. Protein Science. 29(7). 1596–1605. 269 indexed citations
11.
Kim, Youngchang, Kemin Tan, Karen Nguyen, et al.. (2019). Structural and functional characterization of three Type B and C chloramphenicol acetyltransferases from Vibrio species. Protein Science. 29(3). 695–710. 14 indexed citations
12.
13.
Kim, Youngchang, et al.. (2019). Oxanosine Monophosphate Is a Covalent Inhibitor of Inosine 5′-Monophosphate Dehydrogenase. Chemical Research in Toxicology. 32(3). 456–466. 1 indexed citations
14.
Makowska-Grzyska, M., Youngchang Kim, N. Maltseva, et al.. (2015). A Novel Cofactor-binding Mode in Bacterial IMP Dehydrogenases Explains Inhibitor Selectivity. Journal of Biological Chemistry. 290(9). 5893–5911. 33 indexed citations
15.
Makowska-Grzyska, M., Youngchang Kim, Suresh Kumar Gorla, et al.. (2015). Mycobacterium tuberculosis IMPDH in Complexes with Substrates, Products and Antitubercular Compounds. PLoS ONE. 10(10). e0138976–e0138976. 35 indexed citations
16.
Murzin, Dmitry Yu., et al.. (2014). CATALYTIC CONVERSION OF n-HEPTANE. 26(52). 13–19. 1 indexed citations
17.
Nusca, Tyler D., Youngchang Kim, N. Maltseva, et al.. (2012). Functional and Structural Analysis of the Siderophore Synthetase AsbB through Reconstitution of the Petrobactin Biosynthetic Pathway from Bacillus anthracis. Journal of Biological Chemistry. 287(19). 16058–16072. 34 indexed citations
18.
Makowska-Grzyska, M., Youngchang Kim, Ruiying Wu, et al.. (2012). Bacillus anthracis Inosine 5′-Monophosphate Dehydrogenase in Action: The First Bacterial Series of Structures of Phosphate Ion-, Substrate-, and Product-Bound Complexes. Biochemistry. 51(31). 6148–6163. 29 indexed citations
19.
Kim, Youngchang, L. Bigelow, Irina Dementieva, et al.. (2008). High-Throughput Protein Purification for X-Ray Crystallography and NMR. Advances in protein chemistry and structural biology. 75. 85–105. 36 indexed citations
20.
Hatzos, C., et al.. (2005). Use of reductive methylation of proteins to increase crystallization efficiency at the Midwest Center for Structural Genomics. Acta Crystallographica Section A Foundations of Crystallography. 61(a1). c437–c437. 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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