Kara Anasti

1.6k total citations
18 papers, 390 citations indexed

About

Kara Anasti is a scholar working on Virology, Molecular Biology and Immunology. According to data from OpenAlex, Kara Anasti has authored 18 papers receiving a total of 390 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Virology, 7 papers in Molecular Biology and 7 papers in Immunology. Recurrent topics in Kara Anasti's work include HIV Research and Treatment (16 papers), Immune Cell Function and Interaction (7 papers) and Monoclonal and Polyclonal Antibodies Research (5 papers). Kara Anasti is often cited by papers focused on HIV Research and Treatment (16 papers), Immune Cell Function and Interaction (7 papers) and Monoclonal and Polyclonal Antibodies Research (5 papers). Kara Anasti collaborates with scholars based in United States, Germany and South Korea. Kara Anasti's co-authors include Hua‐Xin Liao, S. Munir Alam, S. Moses Dennison, Frederick H. Jaeger, Barton F. Haynes, Shelley Stewart, Barton F. Haynes, Alberto Fernández‐Tejada, Yusuf Vohra and Baptiste Aussedat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nature Communications.

In The Last Decade

Kara Anasti

18 papers receiving 387 citations

Peers

Kara Anasti
Keiko Kajiwara Japan
Joseph S. Redman United States
Ritu Gaur India
Surya Sankuratri United States
Daniah A. D. Thompson United States
Erica Houthuys Belgium
Marc Potempa United States
Zhi‐Song Qiao China
Keiko Kajiwara Japan
Kara Anasti
Citations per year, relative to Kara Anasti Kara Anasti (= 1×) peers Keiko Kajiwara

Countries citing papers authored by Kara Anasti

Since Specialization
Citations

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

Fields of papers citing papers by Kara Anasti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kara Anasti

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

All Works

18 of 18 papers shown
1.
Ortiz, Yaneth, et al.. (2024). The CH1 domain influences the expression and antigen sensing of the HIV-specific CH31 IgM-BCR and IgG-BCR. Proceedings of the National Academy of Sciences. 121(31). e2404728121–e2404728121. 1 indexed citations
2.
Edwards, Robert J., Irina Kosheleva, Kara Anasti, et al.. (2024). Microsecond dynamics control the HIV-1 Envelope conformation. Science Advances. 10(5). eadj0396–eadj0396. 6 indexed citations
3.
Adams, Lily E., Jaclyn S. Higgins, Kara Anasti, et al.. (2024). Non-neutralizing SARS-CoV-2 N-terminal domain antibodies protect mice against severe disease using Fc-mediated effector functions. PLoS Pathogens. 20(6). e1011569–e1011569. 10 indexed citations
4.
Henderson, Rory, Ye Zhou, Victoria Stalls, et al.. (2023). Structural basis for breadth development in the HIV-1 V3-glycan targeting DH270 antibody clonal lineage. Nature Communications. 14(1). 2782–2782. 7 indexed citations
5.
Hossain, Md. Alamgir, Kara Anasti, Brian Watts, et al.. (2022). B cells expressing IgM B cell receptors of HIV-1 neutralizing antibodies discriminate antigen affinities by sensing binding association rates. Cell Reports. 39(13). 111021–111021. 3 indexed citations
6.
Alam, S. Munir, Kenneth Cronin, Robert Parks, et al.. (2020). Antigenicity and Immunogenicity of HIV-1 Envelope Trimers Complexed to a Small-Molecule Viral Entry Inhibitor. Journal of Virology. 94(21). 3 indexed citations
7.
Henderson, Rory, Brian Watts, Kara Anasti, et al.. (2019). Selection of immunoglobulin elbow region mutations impacts interdomain conformational flexibility in HIV-1 broadly neutralizing antibodies. Nature Communications. 10(1). 654–654. 25 indexed citations
8.
Meyerhoff, Robert, Richard M. Scearce, Joy Pickeral, et al.. (2017). HIV-1 Consensus Envelope-Induced Broadly Binding Antibodies. AIDS Research and Human Retroviruses. 33(8). 859–868. 8 indexed citations
9.
Kahsai, Alem W., James W. Wisler, Jungmin Lee, et al.. (2016). Conformationally selective RNA aptamers allosterically modulate the β2-adrenoceptor. Nature Chemical Biology. 12(9). 709–716. 66 indexed citations
10.
Osuna, Christa E., Ana González, Hsun‐Hsien Chang, et al.. (2014). TCR Affinity Associated with Functional Differences between Dominant and Subdominant SIV Epitope-Specific CD8+ T Cells in Mamu-A*01+ Rhesus Monkeys. PLoS Pathogens. 10(4). e1004069–e1004069. 7 indexed citations
11.
Hardy, Gregory J., Rahul Nayak, Kara Anasti, et al.. (2014). HIV-1 antibodies and vaccine antigen selectively interact with lipid domains. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1838(10). 2662–2669. 4 indexed citations
12.
Aussedat, Baptiste, Yusuf Vohra, Peter K. Park, et al.. (2013). Chemical Synthesis of Highly Congested gp120 V1V2 N-Glycopeptide Antigens for Potential HIV-1-Directed Vaccines. Journal of the American Chemical Society. 135(35). 13113–13120. 44 indexed citations
13.
Fouda, Genevieve G., Frederick H. Jaeger, Joshua D. Amos, et al.. (2013). Tenascin-C is an innate broad-spectrum, HIV-1–neutralizing protein in breast milk. Proceedings of the National Academy of Sciences. 110(45). 18220–18225. 64 indexed citations
14.
Alam, S. Munir, S. Moses Dennison, Baptiste Aussedat, et al.. (2013). Recognition of synthetic glycopeptides by HIV-1 broadly neutralizing antibodies and their unmutated ancestors. Proceedings of the National Academy of Sciences. 110(45). 18214–18219. 56 indexed citations
15.
Alam, S. Munir, Xiaoying Shen, Shi-Mao Xia, et al.. (2012). Isolation of HIV-1-Neutralizing Mucosal Monoclonal Antibodies from Human Colostrum. PLoS ONE. 7(5). e37648–e37648. 20 indexed citations
16.
Hardy, Gregory J., Yee Cheong Lam, Shelley Stewart, et al.. (2011). Screening the interactions between HIV-1 neutralizing antibodies and model lipid surfaces. Journal of Immunological Methods. 376(1-2). 13–19. 3 indexed citations
17.
Alam, S. Munir, Hua‐Xin Liao, S. Moses Dennison, et al.. (2011). Differential Reactivity of Germ Line Allelic Variants of a Broadly Neutralizing HIV-1 Antibody to a gp41 Fusion Intermediate Conformation. Journal of Virology. 85(22). 11725–11731. 36 indexed citations
18.
Dennison, S. Moses, Kara Anasti, Richard M. Scearce, et al.. (2010). Nonneutralizing HIV-1 gp41 Envelope Cluster II Human Monoclonal Antibodies Show Polyreactivity for Binding to Phospholipids and Protein Autoantigens. Journal of Virology. 85(3). 1340–1347. 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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