D. Noah Sather

4.8k total citations
70 papers, 2.4k citations indexed

About

D. Noah Sather is a scholar working on Immunology, Virology and Molecular Biology. According to data from OpenAlex, D. Noah Sather has authored 70 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Immunology, 33 papers in Virology and 19 papers in Molecular Biology. Recurrent topics in D. Noah Sather's work include HIV Research and Treatment (33 papers), Immune Cell Function and Interaction (17 papers) and Malaria Research and Control (17 papers). D. Noah Sather is often cited by papers focused on HIV Research and Treatment (33 papers), Immune Cell Function and Interaction (17 papers) and Malaria Research and Control (17 papers). D. Noah Sather collaborates with scholars based in United States, Germany and United Kingdom. D. Noah Sather's co-authors include Leonidas Stamatatos, Spyros A. Kalams, Iliyana Mikell, Edward M. Golenberg, Galit Alter, Marcus Altfeld, Stefan H. I. Kappe, George Sellhorn, Blake Wood and Zachary Caldwell and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Communications.

In The Last Decade

D. Noah Sather

68 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. Noah Sather United States 27 1.3k 1.1k 768 557 428 70 2.4k
Evelien M. Bunnik United States 25 790 0.6× 652 0.6× 697 0.9× 467 0.8× 97 0.2× 53 2.0k
Mangala Rao United States 27 542 0.4× 1.1k 0.9× 889 1.2× 489 0.9× 342 0.8× 87 2.2k
Min Tang China 15 1.4k 1.1× 845 0.8× 874 1.1× 571 1.0× 509 1.2× 36 2.3k
Carol D. Weiss United States 27 1.6k 1.2× 756 0.7× 669 0.9× 1.2k 2.2× 398 0.9× 65 2.6k
Udy Olshevsky Israel 22 1.4k 1.1× 770 0.7× 744 1.0× 1.1k 1.9× 441 1.0× 38 2.5k
Sanjay Phogat United States 24 1.6k 1.2× 1.2k 1.0× 751 1.0× 668 1.2× 688 1.6× 41 2.3k
Ruben M. Markosyan United States 19 797 0.6× 517 0.5× 585 0.8× 624 1.1× 146 0.3× 24 1.7k
Robert Parks United States 23 1.0k 0.8× 885 0.8× 675 0.9× 839 1.5× 352 0.8× 45 2.1k
Jason T. Kimata United States 26 963 0.7× 1.1k 0.9× 481 0.6× 678 1.2× 68 0.2× 81 2.1k
Herbert Kuster Switzerland 27 1.5k 1.1× 661 0.6× 390 0.5× 1.1k 2.0× 216 0.5× 59 2.4k

Countries citing papers authored by D. Noah Sather

Since Specialization
Citations

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

Fields of papers citing papers by D. Noah Sather

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. Noah Sather. 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 D. Noah Sather. The network helps show where D. Noah Sather may publish in the future.

Co-authorship network of co-authors of D. Noah Sather

This figure shows the co-authorship network connecting the top 25 collaborators of D. Noah Sather. A scholar is included among the top collaborators of D. Noah Sather 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 D. Noah Sather. D. Noah Sather 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.
Logue, Jennifer K., Helen Y. Chu, Janet A. Englund, et al.. (2025). Infant CD4 T-Cell Response to SARS-CoV-2 mRNA Vaccination Is Restricted in Cytokine Production and Modified by Vaccine Manufacturer. Open Forum Infectious Diseases. 12(10). ofaf599–ofaf599.
2.
Vigdorovich, Vladimir, et al.. (2023). Coimmunization with Preerythrocytic Antigens alongside Circumsporozoite Protein Can Enhance Sterile Protection against Plasmodium Sporozoite Infection. Microbiology Spectrum. 11(2). e0379122–e0379122. 4 indexed citations
3.
Vigdorovich, Vladimir, Sara Carbonetti, Nana Minkah, et al.. (2022). Anti-TRAP/SSP2 monoclonal antibodies can inhibit sporozoite infection and may enhance protection of anti-CSP monoclonal antibodies. npj Vaccines. 7(1). 58–58. 6 indexed citations
4.
Vijayan, Kamalakannan, Ramyavardhanee Chandrasekaran, Vladimir Vigdorovich, et al.. (2022). Germinal center activity and B cell maturation are associated with protective antibody responses against Plasmodium pre-erythrocytic infection. PLoS Pathogens. 18(7). e1010671–e1010671. 5 indexed citations
5.
Spencer, David A., Delphine C. Malherbe, Néstor Vázquez Bernat, et al.. (2021). Polyfunctional Tier 2–Neutralizing Antibodies Cloned following HIV-1 Env Macaque Immunization Mirror Native Antibodies in a Human Donor. The Journal of Immunology. 206(5). 999–1012. 4 indexed citations
6.
Lippy, Adriana, Brian G. Oliver, James T. Fuller, et al.. (2021). Rapid progression is associated with lymphoid follicle dysfunction in SIV-infected infant rhesus macaques. PLoS Pathogens. 17(5). e1009575–e1009575. 5 indexed citations
7.
Amanat, Fatima, Shirin Strohmeier, Philip Meade, et al.. (2021). Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus. PLoS Biology. 19(12). e3001384–e3001384. 10 indexed citations
8.
Carreño, Juan Manuel, Hala Alshammary, Gagandeep Singh, et al.. (2021). Evidence for retained spike-binding and neutralizing activity against emerging SARS-CoV-2 variants in serum of COVID-19 mRNA vaccine recipients. EBioMedicine. 73. 103626–103626. 18 indexed citations
9.
Schäfer, Carola, Nicholas Dambrauskas, Erika L. Flannery, et al.. (2021). Partial protection against P. vivax infection diminishes hypnozoite burden and blood-stage relapses. Cell Host & Microbe. 29(5). 752–756.e4. 15 indexed citations
10.
Vigdorovich, Vladimir, Diana Kouiavskaia, Jiangyang Zhao, et al.. (2020). Human IgA Monoclonal Antibodies That Neutralize Poliovirus, Produced by Hybridomas and Recombinant Expression. SHILAP Revista de lepidopterología. 9(1). 5–5. 10 indexed citations
11.
Dambrauskas, Nicholas, et al.. (2020). Oral Immunization with HIV-1 Envelope SOSIP trimers elicits systemic immune responses and cross-reactive anti-V1V2 antibodies in non-human primates. PLoS ONE. 15(5). e0233577–e0233577. 8 indexed citations
12.
Harrington, Whitney E., Nicholas Dambrauskas, Yonghou Jiang, et al.. (2020). Plasma From Recovered COVID-19 Patients Inhibits Spike Protein Binding to ACE2 in a Microsphere-Based Inhibition Assay. The Journal of Infectious Diseases. 222(12). 1965–1973. 13 indexed citations
13.
Schäfer, Carola, Nicholas Dambrauskas, Ryan Steel, et al.. (2018). A recombinant antibody against Plasmodium vivax UIS4 for distinguishing replicating from dormant liver stages. Malaria Journal. 17(1). 370–370. 23 indexed citations
14.
Carbonetti, Sara, Brian G. Oliver, Vladimir Vigdorovich, et al.. (2017). A method for the isolation and characterization of functional murine monoclonal antibodies by single B cell cloning. Journal of Immunological Methods. 448. 66–73. 34 indexed citations
15.
Hessell, Ann J., Delphine C. Malherbe, Franco Pissani, et al.. (2016). Achieving Potent Autologous Neutralizing Antibody Responses against Tier 2 HIV-1 Viruses by Strategic Selection of Envelope Immunogens. The Journal of Immunology. 196(7). 3064–3078. 34 indexed citations
16.
Keitany, Gladys J., Karen S. Kim Guisbert, Akshay T. Krishnamurty, et al.. (2016). Blood Stage Malaria Disrupts Humoral Immunity to the Pre-erythrocytic Stage Circumsporozoite Protein. Cell Reports. 17(12). 3193–3205. 50 indexed citations
17.
Sather, D. Noah, Sara Carbonetti, Delphine C. Malherbe, et al.. (2014). Development of Broadly Neutralizing Anti-HIV-1 Antibodies during Natural Infection through Early Epitope Acquisition and Subsequent Maturation. AIDS Research and Human Retroviruses. 30(S1). A35–A35. 1 indexed citations
18.
Sather, D. Noah, et al.. (2010). Functional analysis of B and C class floral organ genes in spinach demonstrates their role in sexual dimorphism. BMC Plant Biology. 10(1). 46–46. 53 indexed citations
19.
Sather, D. Noah & Leonidas Stamatatos. (2010). Epitope specificities of broadly neutralizing plasmas from HIV-1 infected subjects. Vaccine. 28. B8–B12. 34 indexed citations
20.
Sather, D. Noah, Jakob Armann, Lance Ching, et al.. (2008). Factors Associated with the Development of Cross-Reactive Neutralizing Antibodies during Human Immunodeficiency Virus Type 1 Infection. Journal of Virology. 83(2). 757–769. 402 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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