Alex B. Kleinpeter

672 total citations
16 papers, 443 citations indexed

About

Alex B. Kleinpeter is a scholar working on Virology, Infectious Diseases and Epidemiology. According to data from OpenAlex, Alex B. Kleinpeter has authored 16 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Virology, 9 papers in Infectious Diseases and 9 papers in Epidemiology. Recurrent topics in Alex B. Kleinpeter's work include HIV Research and Treatment (11 papers), HIV/AIDS drug development and treatment (9 papers) and interferon and immune responses (5 papers). Alex B. Kleinpeter is often cited by papers focused on HIV Research and Treatment (11 papers), HIV/AIDS drug development and treatment (9 papers) and interferon and immune responses (5 papers). Alex B. Kleinpeter collaborates with scholars based in United States, United Kingdom and Australia. Alex B. Kleinpeter's co-authors include Eric O. Freed, Chad M. Petit, Alexander S. Jureka, Kevin S. Harrod, Leo C. James, Adolfo Saiardi, Donna L. Mallery, Jennifer L. Tipper, Till Böcking and K. M. Rifat Faysal and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Journal of Molecular Biology.

In The Last Decade

Alex B. Kleinpeter

16 papers receiving 440 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alex B. Kleinpeter United States 11 228 195 159 147 137 16 443
Jonathan Rawson United States 13 325 1.4× 242 1.2× 112 0.7× 261 1.8× 102 0.7× 23 559
Pheroze Joshi United States 13 352 1.5× 290 1.5× 69 0.4× 303 2.1× 120 0.9× 16 584
Yasuyuki Miyazaki Japan 13 199 0.9× 112 0.6× 78 0.5× 305 2.1× 80 0.6× 25 507
Clifton Ricana United States 6 209 0.9× 219 1.1× 54 0.3× 142 1.0× 33 0.2× 8 398
Naoya Doi Japan 11 265 1.2× 196 1.0× 56 0.4× 93 0.6× 94 0.7× 41 332
Mayra L. Garcia United States 11 178 0.8× 170 0.9× 218 1.4× 188 1.3× 148 1.1× 11 561
Maria Anders Germany 9 303 1.3× 162 0.8× 106 0.7× 148 1.0× 72 0.5× 9 451
Valérie Vivet‐Boudou France 13 266 1.2× 192 1.0× 86 0.5× 370 2.5× 38 0.3× 27 595
Sheikh Abdul Rahman United States 9 137 0.6× 155 0.8× 68 0.4× 138 0.9× 59 0.4× 10 380
Amelia Still United States 9 232 1.0× 119 0.6× 63 0.4× 320 2.2× 44 0.3× 10 523

Countries citing papers authored by Alex B. Kleinpeter

Since Specialization
Citations

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

Fields of papers citing papers by Alex B. Kleinpeter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alex B. Kleinpeter. 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 Alex B. Kleinpeter. The network helps show where Alex B. Kleinpeter may publish in the future.

Co-authorship network of co-authors of Alex B. Kleinpeter

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

All Works

16 of 16 papers shown
1.
Zhu, Yanan, Alex B. Kleinpeter, Juan Shen, et al.. (2025). Structural basis for HIV-1 capsid adaption to a deficiency in IP6 packaging. Nature Communications. 16(1). 8152–8152. 1 indexed citations
2.
Annamalai, Arun S., S.M. Bester, Guochao Wei, et al.. (2025). Structural and mechanistic bases for resistance of the M66I capsid variant to lenacapavir. mBio. 16(5). e0361324–e0361324. 6 indexed citations
3.
Kleinpeter, Alex B., Donna L. Mallery, Nadine Renner, et al.. (2024). HIV-1 adapts to lost IP6 coordination through second-site mutations that restore conical capsid assembly. Nature Communications. 15(1). 8017–8017. 5 indexed citations
4.
Zadrozny, Kaneil K., Caitlin M. Quinn, Alex B. Kleinpeter, et al.. (2023). Structural basis of HIV-1 maturation inhibitor binding and activity. Nature Communications. 14(1). 1237–1237. 16 indexed citations
5.
Kleinpeter, Alex B., Yanan Zhu, Donna L. Mallery, et al.. (2023). The Effect of Inositol Hexakisphosphate on HIV-1 Particle Production and Infectivity can be Modulated by Mutations that Affect the Stability of the Immature Gag Lattice. Journal of Molecular Biology. 435(11). 168037–168037. 9 indexed citations
6.
Kleinpeter, Alex B., et al.. (2023). Structural Investigations of Interactions between the Influenza a Virus NS1 and Host Cellular Proteins. Viruses. 15(10). 2063–2063. 6 indexed citations
7.
Renner, Nadine, Alex B. Kleinpeter, Donna L. Mallery, et al.. (2023). HIV-1 is dependent on its immature lattice to recruit IP6 for mature capsid assembly. Nature Structural & Molecular Biology. 30(3). 370–382. 36 indexed citations
8.
Yan, Huanchang, Qingmei Li, Sherimay D. Ablan, et al.. (2022). Enhanced Transmissibility and Decreased Virulence of HIV-1 CRF07_BC May Explain Its Rapid Expansion in China. Microbiology Spectrum. 10(4). e0014622–e0014622. 20 indexed citations
9.
Mendonça, Luiza, Dapeng Sun, Jiying Ning, et al.. (2021). CryoET structures of immature HIV Gag reveal six-helix bundle. Communications Biology. 4(1). 481–481. 32 indexed citations
10.
Mallery, Donna L., Alex B. Kleinpeter, Nadine Renner, et al.. (2021). A stable immature lattice packages IP 6 for HIV capsid maturation. Science Advances. 7(11). 42 indexed citations
11.
Kleinpeter, Alex B. & Eric O. Freed. (2020). HIV-1 Maturation: Lessons Learned from Inhibitors. Viruses. 12(9). 940–940. 68 indexed citations
12.
Jureka, Alexander S., Alex B. Kleinpeter, Jennifer L. Tipper, Kevin S. Harrod, & Chad M. Petit. (2020). The influenza NS1 protein modulates RIG-I activation via a strain-specific direct interaction with the second CARD of RIG-I. Journal of Biological Chemistry. 295(4). 1153–1164. 36 indexed citations
13.
Jureka, Alexander S., Alex B. Kleinpeter, Jennifer L. Tipper, Kevin S. Harrod, & Chad M. Petit. (2019). The influenza NS1 protein modulates RIG-I activation via a strain-specific direct interaction with the second CARD of RIG-I. Journal of Biological Chemistry. 295(4). 1153–1164. 32 indexed citations
14.
Mallery, Donna L., K. M. Rifat Faysal, Alex B. Kleinpeter, et al.. (2019). Cellular IP6 Levels Limit HIV Production while Viruses that Cannot Efficiently Package IP6 Are Attenuated for Infection and Replication. Cell Reports. 29(12). 3983–3996.e4. 64 indexed citations
15.
Kleinpeter, Alex B., et al.. (2018). Structural analyses reveal the mechanism of inhibition of influenza virus NS1 by two antiviral compounds. Journal of Biological Chemistry. 293(38). 14659–14668. 23 indexed citations
16.
Jureka, Alexander S., Alex B. Kleinpeter, Gabriel Cornilescu, Claudia C. Cornilescu, & Chad M. Petit. (2015). Structural Basis for a Novel Interaction between the NS1 Protein Derived from the 1918 Influenza Virus and RIG-I. Structure. 23(11). 2001–2010. 47 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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