Herman F. Staats

7.0k total citations · 1 hit paper
109 papers, 5.5k citations indexed

About

Herman F. Staats is a scholar working on Immunology, Epidemiology and Molecular Biology. According to data from OpenAlex, Herman F. Staats has authored 109 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Immunology, 35 papers in Epidemiology and 24 papers in Molecular Biology. Recurrent topics in Herman F. Staats's work include Immunotherapy and Immune Responses (29 papers), HIV Research and Treatment (18 papers) and Mast cells and histamine (17 papers). Herman F. Staats is often cited by papers focused on Immunotherapy and Immune Responses (29 papers), HIV Research and Treatment (18 papers) and Mast cells and histamine (17 papers). Herman F. Staats collaborates with scholars based in United States, Singapore and Japan. Herman F. Staats's co-authors include Soman N. Abraham, Jerry R. McGhee, Hiroshi Kiyono, Kohtaro Fujihashi, Barton F. Haynes, T J Palker, Christopher P. Shelburne, Robert N. Lausch, R J Jackson and James B. McLachlan and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Herman F. Staats

105 papers receiving 5.4k citations

Hit Papers

Cardiolipin Polyspecific Autoreactivity in Two Broadly Ne... 2005 2026 2012 2019 2005 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Herman F. Staats United States 39 3.2k 1.2k 1.1k 970 961 109 5.5k
Kohtaro Fujihashi United States 53 5.0k 1.6× 1.5k 1.2× 1.5k 1.4× 1.3k 1.3× 377 0.4× 169 8.3k
Brian L. Kelsall United States 51 6.6k 2.1× 1.8k 1.4× 1.3k 1.2× 1.1k 1.2× 633 0.7× 107 9.8k
Hiroshi Kiyono United States 37 2.8k 0.9× 776 0.6× 1.0k 0.9× 922 1.0× 455 0.5× 88 4.9k
John H. Eldridge United States 40 3.1k 1.0× 1.5k 1.2× 1.7k 1.6× 1.4k 1.5× 832 0.9× 101 6.5k
Erik P. Lillehoj United States 53 1.6k 0.5× 2.1k 1.7× 687 0.6× 874 0.9× 376 0.4× 172 8.0k
Cécil Czerkinsky Sweden 51 5.2k 1.6× 1.9k 1.5× 1.9k 1.7× 2.2k 2.3× 620 0.6× 162 10.2k
Alistair J. Ramsay Australia 37 3.4k 1.1× 992 0.8× 1.3k 1.2× 850 0.9× 620 0.6× 81 6.3k
S E Macatonia United Kingdom 27 6.2k 1.9× 901 0.7× 1.1k 1.0× 532 0.5× 627 0.7× 38 7.9k
Hiroshi Kiyono Japan 66 7.8k 2.5× 2.7k 2.1× 1.7k 1.6× 1.6k 1.6× 278 0.3× 232 12.6k
Malcolm Turner United Kingdom 41 4.1k 1.3× 1.3k 1.0× 1.2k 1.1× 815 0.8× 183 0.2× 136 7.2k

Countries citing papers authored by Herman F. Staats

Since Specialization
Citations

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

Fields of papers citing papers by Herman F. Staats

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Herman F. Staats. 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 Herman F. Staats. The network helps show where Herman F. Staats may publish in the future.

Co-authorship network of co-authors of Herman F. Staats

This figure shows the co-authorship network connecting the top 25 collaborators of Herman F. Staats. A scholar is included among the top collaborators of Herman F. Staats 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 Herman F. Staats. Herman F. Staats 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
2.
Batty, Cole J., John A. Roque, Michael A. Carlock, et al.. (2023). Development of a broadly active influenza intranasal vaccine adjuvanted with self-assembled particles composed of mastoparan-7 and CpG. Frontiers in Immunology. 14. 1103765–1103765. 7 indexed citations
3.
Cui, Zhifen, Cong Zeng, Furong Huang, et al.. (2022). Cas13d knockdown of lung protease Ctsl prevents and treats SARS-CoV-2 infection. Nature Chemical Biology. 18(10). 1056–1064. 39 indexed citations
4.
Choi, Hae Woong, Jutamas Suwanpradid, Il Hwan Kim, et al.. (2018). Perivascular dendritic cells elicit anaphylaxis by relaying allergens to mast cells via microvesicles. Science. 362(6415). 58 indexed citations
5.
Zaccaro, Daniel J., et al.. (2013). Evaluation of vaccine-induced antibody responses: Impact of new technologies. Vaccine. 31(25). 2756–2761. 14 indexed citations
6.
Městecký, Jiří, Peter F. Wright, Lucia Lopalco, et al.. (2010). Scarcity or Absence of Humoral Immune Responses in the Plasma and Cervicovaginal Lavage Fluids of Heavily HIV-1-Exposed But Persistently Seronegative Women. AIDS Research and Human Retroviruses. 27(5). 469–486. 35 indexed citations
7.
Clapp, Beata, Sarah Golden, Massimo Maddaloni, Herman F. Staats, & David W. Pascual. (2010). Adenovirus F protein as a delivery vehicle for botulinum B. BMC Immunology. 11(1). 36–36. 4 indexed citations
8.
Kunder, Christian A., Ashley L. St. John, Guojie Li, et al.. (2009). Mast cell–derived particles deliver peripheral signals to remote lymph nodes. The Journal of Experimental Medicine. 206(11). 2455–2467. 140 indexed citations
9.
Moyes, David L., Manohursingh Runglall, Stephen Challacombe, et al.. (2009). NALT / BALT and Oral Cavity. Mucosal Immunology. 2. 20–20.
10.
Hofmann, Alison, Herman F. Staats, & Soman N. Abraham. (2009). Use of a Mast Cell Activator as a Mucosal Adjuvant for Pertussis Vaccines. Journal of Allergy and Clinical Immunology. 123(2). S164–S164. 1 indexed citations
12.
Thompson, Joseph M., Michael G. Nicholson, Alan C. Whitmore, et al.. (2008). Nonmucosal Alphavirus Vaccination Stimulates a Mucosal Inductive Environment in the Peripheral Draining Lymph Node. The Journal of Immunology. 181(1). 574–585. 21 indexed citations
13.
Peacock, James W., et al.. (2006). Capric Acid and Hydroxypropylmethylcellulose Increase the Immunogenicity of Nasally Administered Peptide Vaccines. AIDS Research and Human Retroviruses. 22(6). 558–568. 13 indexed citations
14.
Maddaloni, Massimo, Herman F. Staats, Gayle Callis, et al.. (2006). Mucosal Vaccine Targeting Improves Onset of Mucosal and Systemic Immunity to Botulinum Neurotoxin A. The Journal of Immunology. 177(8). 5524–5532. 27 indexed citations
15.
Hale, Laura P., David J. Fitzhugh, & Herman F. Staats. (2006). Oral immunogenicity of the plant proteinase bromelain. International Immunopharmacology. 6(13-14). 2038–2046. 17 indexed citations
16.
Kobayashi, Ryoki, Tomoko Kohda, Kosuke Kataoka, et al.. (2005). A Novel Neurotoxoid Vaccine Prevents Mucosal Botulism. The Journal of Immunology. 174(4). 2190–2195. 28 indexed citations
17.
Wright, Peter F., Pamela A. Kozlowski, Paul A. Goepfert, et al.. (2002). Detection of Mucosal Antibodies in HIV Type 1-Infected Individuals. AIDS Research and Human Retroviruses. 18(17). 1291–1300. 51 indexed citations
18.
Staats, Herman F., William M. Gwinn, Shawn S. Jackson, et al.. (2001). Cytokine Requirements for Induction of Systemic and Mucosal CTL After Nasal Immunization. The Journal of Immunology. 167(9). 5386–5394. 81 indexed citations
19.
Laskowitz, Daniel T., et al.. (2000). Altered immune responses in apolipoprotein E-deficient mice. Journal of Lipid Research. 41(4). 613–620. 129 indexed citations
20.
Xu-Amano, J, et al.. (1994). The common mucosal immune system: from basic principles to enteric vaccines with relevance for the female reproductive tract. Reproduction Fertility and Development. 6(3). 369–379. 36 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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