Alexander S. Mankin

12.3k total citations · 1 hit paper
151 papers, 9.1k citations indexed

About

Alexander S. Mankin is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Alexander S. Mankin has authored 151 papers receiving a total of 9.1k indexed citations (citations by other indexed papers that have themselves been cited), including 139 papers in Molecular Biology, 67 papers in Genetics and 24 papers in Ecology. Recurrent topics in Alexander S. Mankin's work include RNA and protein synthesis mechanisms (130 papers), RNA modifications and cancer (76 papers) and Bacterial Genetics and Biotechnology (67 papers). Alexander S. Mankin is often cited by papers focused on RNA and protein synthesis mechanisms (130 papers), RNA modifications and cancer (76 papers) and Bacterial Genetics and Biotechnology (67 papers). Alexander S. Mankin collaborates with scholars based in United States, Russia and Germany. Alexander S. Mankin's co-authors include Nora Vázquez‐Laslop, Liqun Xiong, Tanel Tenson, Dorota Klepacki, Norbert Polacek, Haripriya Ramu, Krishna Kannan, J.A. Dunkle, J.H.D. Cate and Dean L. Shinabarger and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Alexander S. Mankin

151 papers receiving 8.9k citations

Hit Papers

A broad-spectrum lasso pe... 2025 2026 2025 5 10 15 20

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander S. Mankin United States 56 6.9k 2.1k 1.6k 1.2k 985 151 9.1k
Dominique Mengin‐Lecreulx France 59 5.2k 0.7× 3.0k 1.5× 1.1k 0.7× 1.1k 0.9× 1.4k 1.5× 167 10.1k
Andréa Dessen France 47 3.9k 0.6× 1.6k 0.8× 2.3k 1.5× 1.2k 1.0× 749 0.8× 119 8.2k
Daniel N. Wilson Germany 68 10.5k 1.5× 2.9k 1.4× 887 0.6× 1.2k 1.0× 1.5k 1.5× 181 12.6k
Deborah T. Hung United States 42 6.4k 0.9× 957 0.5× 2.2k 1.4× 1.3k 1.1× 732 0.7× 118 10.6k
Thierry Vernet France 48 4.4k 0.6× 1.2k 0.6× 981 0.6× 890 0.7× 566 0.6× 160 7.9k
Bernard Joris Belgium 45 3.9k 0.6× 1.5k 0.7× 1.0k 0.6× 2.8k 2.3× 889 0.9× 186 8.3k
Robert K. Ernst United States 59 6.8k 1.0× 2.1k 1.0× 1.2k 0.7× 2.8k 2.4× 945 1.0× 255 13.3k
Tanel Tenson Estonia 49 4.9k 0.7× 2.5k 1.2× 879 0.6× 1.2k 1.0× 1.1k 1.1× 153 7.5k
David E. Heinrichs Canada 56 3.7k 0.5× 2.2k 1.0× 2.2k 1.4× 1.0k 0.9× 543 0.6× 128 7.0k
Malcolm E. Winkler United States 56 4.6k 0.7× 2.7k 1.3× 900 0.6× 790 0.7× 1.1k 1.1× 140 8.0k

Countries citing papers authored by Alexander S. Mankin

Since Specialization
Citations

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

Fields of papers citing papers by Alexander S. Mankin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander S. Mankin

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander S. Mankin. A scholar is included among the top collaborators of Alexander S. Mankin 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 S. Mankin. Alexander S. Mankin 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.
Jangra, Manoj, Dmitrii Y. Travin, Elena V. Aleksandrova, et al.. (2025). A broad-spectrum lasso peptide antibiotic targeting the bacterial ribosome. Nature. 640(8060). 1022–1030. 24 indexed citations breakdown →
2.
Aleksandrova, Elena V., Dorota Klepacki, Nora Vázquez‐Laslop, et al.. (2024). Macrolones target bacterial ribosomes and DNA gyrase and can evade resistance mechanisms. Nature Chemical Biology. 20(12). 1680–1690. 14 indexed citations
3.
Huang, Weiping, et al.. (2024). Sequence diversity of apidaecin-like peptides arresting the terminating ribosome. Nucleic Acids Research. 52(15). 8967–8978. 2 indexed citations
4.
Wu, Kelvin J. Y., Dorota Klepacki, Alexander S. Mankin, & Andrew G. Myers. (2023). A method for tritiation of iboxamycin permits measurement of its ribosomal binding. Bioorganic & Medicinal Chemistry Letters. 91. 129364–129364. 3 indexed citations
5.
Johnson, T., A’Lester C. Allen, Elena V. Aleksandrova, et al.. (2023). Structure–Activity Relationships of the Antimicrobial Peptide Natural Product Apidaecin. Journal of Medicinal Chemistry. 66(17). 11831–11842. 15 indexed citations
6.
Shao, Xinhao, Adam J. Hockenberry, Yu Gao, et al.. (2022). Discovery of Unannotated Small Open Reading Frames in Streptococcus pneumoniae D39 Involved in Quorum Sensing and Virulence Using Ribosome Profiling. mBio. 13(4). e0124722–e0124722. 13 indexed citations
7.
Zhang, Yan, Nikolay A. Aleksashin, Dorota Klepacki, et al.. (2022). The context of the ribosome binding site in mRNAs defines specificity of action of kasugamycin, an inhibitor of translation initiation. Proceedings of the National Academy of Sciences. 119(4). 15 indexed citations
8.
Beckert, Bertrand, Shanmugapriya Sothiselvam, Lars V. Bock, et al.. (2021). Structural and mechanistic basis for translation inhibition by macrolide and ketolide antibiotics. Nature Communications. 12(1). 4466–4466. 58 indexed citations
9.
Svetlov, Maxim S., Egor A. Syroegin, Elena V. Aleksandrova, et al.. (2021). Structure of Erm-modified 70S ribosome reveals the mechanism of macrolide resistance. Nature Chemical Biology. 17(4). 412–420. 90 indexed citations
10.
Huang, Shijie, Nikolay A. Aleksashin, A.B. Loveland, et al.. (2020). Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly. Nature Communications. 11(1). 2900–2900. 25 indexed citations
11.
Svetlov, Maxim S., et al.. (2020). A long-distance rRNA base pair impacts the ability of macrolide antibiotics to kill bacteria. Proceedings of the National Academy of Sciences. 117(4). 1971–1975. 12 indexed citations
12.
Florin, Tanja, Xinhao Shao, Dorota Klepacki, et al.. (2020). Genome-wide effects of the antimicrobial peptide apidaecin on translation termination in bacteria. eLife. 9. 31 indexed citations
13.
Carlson, Erik D., Anne E. d’Aquino, Do Soon Kim, et al.. (2019). Engineered ribosomes with tethered subunits for expanding biological function. Nature Communications. 10(1). 3920–3920. 55 indexed citations
14.
Choi, Junhong, James Marks, Jingji Zhang, et al.. (2019). Dynamics of the context-specific translation arrest by chloramphenicol and linezolid. Nature Chemical Biology. 16(3). 310–317. 34 indexed citations
15.
Svetlov, Maxim S., Nora Vázquez‐Laslop, & Alexander S. Mankin. (2017). Kinetics of drug–ribosome interactions defines the cidality of macrolide antibiotics. Proceedings of the National Academy of Sciences. 114(52). 13673–13678. 54 indexed citations
16.
Florin, Tanja, Cristina Maracci, Michael Graf, et al.. (2017). An antimicrobial peptide that inhibits translation by trapping release factors on the ribosome. Nature Structural & Molecular Biology. 24(9). 752–757. 133 indexed citations
17.
LaMarre, Jacqueline M., Benjamin P. Howden, & Alexander S. Mankin. (2011). Inactivation of the Indigenous Methyltransferase RlmN in Staphylococcus aureus Increases Linezolid Resistance. Antimicrobial Agents and Chemotherapy. 55(6). 2989–2991. 39 indexed citations
18.
Kannan, Krishna & Alexander S. Mankin. (2011). Macrolide antibiotics in the ribosome exit tunnel: species‐specific binding and action. Annals of the New York Academy of Sciences. 1241(1). 33–47. 88 indexed citations
19.
Siibak, Triinu, Lauri Peil, Liqun Xiong, et al.. (2008). Erythromycin- and Chloramphenicol-Induced Ribosomal Assembly Defects Are Secondary Effects of Protein Synthesis Inhibition. Antimicrobial Agents and Chemotherapy. 53(2). 563–571. 62 indexed citations
20.
Tenson, Tanel & Alexander S. Mankin. (1995). Comparison of functional peptide encoded in the Escherichia coli 23S rRNA with other peptides involved in cis-regulation of translation. Biochemistry and Cell Biology. 73(11-12). 1061–1070. 16 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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