Adam Zlotnick

11.6k total citations
156 papers, 9.5k citations indexed

About

Adam Zlotnick is a scholar working on Ecology, Epidemiology and Hepatology. According to data from OpenAlex, Adam Zlotnick has authored 156 papers receiving a total of 9.5k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Ecology, 86 papers in Epidemiology and 47 papers in Hepatology. Recurrent topics in Adam Zlotnick's work include Bacteriophages and microbial interactions (112 papers), Hepatitis B Virus Studies (79 papers) and Hepatitis C virus research (46 papers). Adam Zlotnick is often cited by papers focused on Bacteriophages and microbial interactions (112 papers), Hepatitis B Virus Studies (79 papers) and Hepatitis C virus research (46 papers). Adam Zlotnick collaborates with scholars based in United States, Israel and Netherlands. Adam Zlotnick's co-authors include Pablo Ceres, Stephen J. Stray, Paul T. Wingfield, Joseph Che‐Yen Wang, Sarah P. Katen, Jennifer M. Johnson, Stephen J. Stahl, M. G. Finn, Dan Endres and James F. Conway and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Adam Zlotnick

152 papers receiving 9.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adam Zlotnick United States 59 4.8k 4.2k 3.1k 2.7k 1.9k 156 9.5k
Alasdair C. Steven United States 87 5.7k 1.2× 4.8k 1.1× 11.5k 3.7× 656 0.2× 2.5k 1.4× 327 22.1k
Craig E. Cameron United States 59 860 0.2× 2.5k 0.6× 5.3k 1.7× 1.8k 0.7× 4.3k 2.3× 189 12.6k
Paul T. Wingfield United States 67 1.8k 0.4× 2.3k 0.5× 9.8k 3.2× 1.1k 0.4× 2.3k 1.2× 238 16.5k
F.A. Rey France 64 1.1k 0.2× 4.9k 1.2× 3.9k 1.3× 2.0k 0.8× 9.3k 4.9× 202 17.8k
Jonathan M. Grimes United Kingdom 54 2.0k 0.4× 2.1k 0.5× 3.9k 1.3× 265 0.1× 2.9k 1.5× 158 9.4k
C. Cheng Kao United States 49 1.3k 0.3× 833 0.2× 3.0k 1.0× 584 0.2× 1.7k 0.9× 118 7.3k
Stephen J. Stahl United States 48 1.3k 0.3× 1.6k 0.4× 4.2k 1.4× 971 0.4× 1.4k 0.7× 104 7.2k
Hans‐Georg Kräusslich Germany 77 2.1k 0.4× 5.3k 1.3× 9.5k 3.1× 2.9k 1.1× 7.6k 4.0× 300 23.0k
R. Holland Cheng United States 40 842 0.2× 1.0k 0.3× 2.1k 0.7× 638 0.2× 1.8k 0.9× 119 5.8k
James M. Hogle United States 54 1.3k 0.3× 2.2k 0.5× 4.0k 1.3× 225 0.1× 3.4k 1.8× 136 9.7k

Countries citing papers authored by Adam Zlotnick

Since Specialization
Citations

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

Fields of papers citing papers by Adam Zlotnick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adam Zlotnick

This figure shows the co-authorship network connecting the top 25 collaborators of Adam Zlotnick. A scholar is included among the top collaborators of Adam Zlotnick 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 Adam Zlotnick. Adam Zlotnick 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.
Patterson, Angela, et al.. (2025). Speed Matters: Directed Assembly of Icosahedral HPV Virus-Like Particles. Journal of the American Chemical Society. 147(28). 24950–24957.
2.
Patterson, Angela, et al.. (2024). Heterogeneity of HPV16 virus-like particles indicates a complex assembly energy surface. Virology. 600. 110211–110211. 2 indexed citations
3.
Hussain, Tariq, Zhongchao Zhao, Lauren F. Barnes, et al.. (2024). Chemically Tagging Cargo for Specific Packaging inside and on the Surface of Virus-like Particles. ACS Nano. 18(32). 21024–21037. 3 indexed citations
4.
González-Gutiérrez, Giovanni, et al.. (2024). A narrow ratio of nucleic acid to SARS-CoV-2 N-protein enables phase separation. Journal of Biological Chemistry. 300(11). 107831–107831.
5.
Hagan, Michael F., et al.. (2023). Engineering Metastability into a Virus-like Particle to Enable Triggered Dissociation. Journal of the American Chemical Society. 145(4). 2322–2331. 6 indexed citations
6.
Maity, Sourav, et al.. (2021). Virus self-assembly proceeds through contact-rich energy minima. Science Advances. 7(45). eabg0811–eabg0811. 25 indexed citations
7.
Zhao, Zhongchao, Joseph Che‐Yen Wang, M. Zhang, et al.. (2021). Asymmetrizing an icosahedral virus capsid by hierarchical assembly of subunits with designed asymmetry. Nature Communications. 12(1). 589–589. 17 indexed citations
8.
Zlotnick, Adam, et al.. (2021). Disassembly of Single Virus Capsids Monitored in Real Time with Multicycle Resistive-Pulse Sensing. Analytical Chemistry. 94(2). 985–992. 13 indexed citations
9.
Barnes, Lauren F., et al.. (2020). Higher Resolution Charge Detection Mass Spectrometry. Analytical Chemistry. 92(16). 11357–11364. 47 indexed citations
10.
Kamsma, Douwe, Andreas S. Biebricher, Chenglei Li, et al.. (2020). Revealing in real-time a multistep assembly mechanism for SV40 virus-like particles. Science Advances. 6(16). eaaz1639–eaaz1639. 24 indexed citations
11.
Shukla, Sourabh, Chao Wang, Veronique Beiss, et al.. (2020). The unique potency of Cowpea mosaic virus (CPMV) in situ cancer vaccine. Biomaterials Science. 8(19). 5489–5503. 58 indexed citations
12.
Glazier, James A., et al.. (2018). Molecular jenga: the percolation phase transition (collapse) in virus capsids. Physical Biology. 15(5). 56005–56005. 12 indexed citations
13.
Schlicksup, Christopher J., et al.. (2018). Competition between Normative and Drug-Induced Virus Self-Assembly Observed with Single-Particle Methods. Journal of the American Chemical Society. 141(3). 1251–1260. 22 indexed citations
14.
Lutomski, Corinne A., et al.. (2018). Multiple Pathways in Capsid Assembly. Journal of the American Chemical Society. 140(17). 5784–5790. 54 indexed citations
15.
Haywood, Daniel G., et al.. (2018). Characterization of Virus Capsids and Their Assembly Intermediates by Multicycle Resistive-Pulse Sensing with Four Pores in Series. Analytical Chemistry. 90(12). 7267–7274. 37 indexed citations
16.
Harms, Zachary D., et al.. (2017). Nanofluidic Devices with 8 Pores in Series for Real-Time, Resistive-Pulse Analysis of Hepatitis B Virus Capsid Assembly. Analytical Chemistry. 89(9). 4855–4862. 38 indexed citations
17.
Belloni, Laura, et al.. (2013). 371 HAPS HEPATITIS B VIRUS (HBV) CAPSID INHIBITORS AFFECT CORE PROTEIN INTERACTION WITH THE MINICHROMOSOME AND TARGET cccDNA FUNCTION. Journal of Hepatology. 58. S153–S153. 3 indexed citations
18.
Bourne, Christina R., M. G. Finn, & Adam Zlotnick. (2006). Global Structural Changes in Hepatitis B Virus Capsids Induced by the Assembly Effector HAP1. Journal of Virology. 80(22). 11055–11061. 148 indexed citations
19.
Stray, Stephen J., Christina R. Bourne, Sreenivas Punna, et al.. (2005). A heteroaryldihydropyrimidine activates and can misdirect hepatitis B virus capsid assembly. Proceedings of the National Academy of Sciences. 102(23). 8138–8143. 216 indexed citations
20.
Muckelbauer, J.K., Monique Kremer, Iwona Minor, et al.. (1995). Structure determination of coxsackievirus B3 to 3.5 Å resolution. Acta Crystallographica Section D Biological Crystallography. 51(6). 871–887. 60 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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