Norbert J. Roberts

3.5k total citations
88 papers, 2.7k citations indexed

About

Norbert J. Roberts is a scholar working on Epidemiology, Immunology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Norbert J. Roberts has authored 88 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Epidemiology, 33 papers in Immunology and 15 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Norbert J. Roberts's work include Respiratory viral infections research (28 papers), Influenza Virus Research Studies (26 papers) and Immune Cell Function and Interaction (16 papers). Norbert J. Roberts is often cited by papers focused on Respiratory viral infections research (28 papers), Influenza Virus Research Studies (26 papers) and Immune Cell Function and Interaction (16 papers). Norbert J. Roberts collaborates with scholars based in United States, Canada and Italy. Norbert J. Roberts's co-authors include Joan E. Nichols, David B. Ettensohn, Roy T. Steigbigel, R. Gordon Douglas, Mark W. Frampton, Mark J. Utell, Paul E. Morrow, Kathryn Sandberg, Jean A. Niles and Sol M. Michaelson and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Norbert J. Roberts

85 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Norbert J. Roberts United States 33 1.2k 918 486 422 322 88 2.7k
Elliot Goldstein United States 28 1.0k 0.9× 277 0.3× 605 1.2× 436 1.0× 220 0.7× 104 2.4k
P Pinkston United States 19 748 0.6× 427 0.5× 406 0.8× 988 2.3× 210 0.7× 23 2.3k
Sture Löfgren Sweden 28 878 0.7× 957 1.0× 591 1.2× 117 0.3× 808 2.5× 90 3.1k
Paul Andersen Denmark 25 1.1k 1.0× 306 0.3× 738 1.5× 279 0.7× 220 0.7× 88 2.5k
Carolina Scagnolari Italy 32 1.6k 1.3× 646 0.7× 1.1k 2.3× 658 1.6× 523 1.6× 169 3.3k
Svend Ellermann‐Eriksen Denmark 27 700 0.6× 516 0.6× 565 1.2× 152 0.4× 286 0.9× 99 2.0k
C. O. Solberg Norway 27 629 0.5× 553 0.6× 476 1.0× 230 0.5× 372 1.2× 116 2.2k
Denise Lecossier France 25 1.5k 1.2× 577 0.6× 1.5k 3.1× 711 1.7× 537 1.7× 38 3.5k
Leah A. Cohn United States 33 440 0.4× 224 0.2× 780 1.6× 700 1.7× 428 1.3× 146 3.3k
Eric J. Hansen United States 36 1.3k 1.1× 345 0.4× 426 0.9× 253 0.6× 822 2.6× 96 3.5k

Countries citing papers authored by Norbert J. Roberts

Since Specialization
Citations

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

Fields of papers citing papers by Norbert J. Roberts

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Norbert J. Roberts. 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 Norbert J. Roberts. The network helps show where Norbert J. Roberts may publish in the future.

Co-authorship network of co-authors of Norbert J. Roberts

This figure shows the co-authorship network connecting the top 25 collaborators of Norbert J. Roberts. A scholar is included among the top collaborators of Norbert J. Roberts 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 Norbert J. Roberts. Norbert J. Roberts 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.
Roberts, Norbert J.. (2023). The Enigma of Lymphocyte Apoptosis in the Response to Influenza Virus Infection. Viruses. 15(3). 759–759. 11 indexed citations
2.
Nichols, Joan E., et al.. (2019). The role of cell surface expression of influenza virus neuraminidase in induction of human lymphocyte apoptosis. Virology. 534. 80–86. 6 indexed citations
3.
Patel, Janak A., et al.. (2010). Interleukin-6 −174 and Tumor Necrosis Factor α −308 Polymorphisms Enhance Cytokine Production by Human Macrophages Exposed to Respiratory Viruses. Journal of Interferon & Cytokine Research. 30(12). 917–921. 19 indexed citations
4.
Schürmann, Wolfgang, Mark W. Frampton, Norbert J. Roberts, et al.. (1997). A Flow Cytometric Assay of Fc Receptor-Mediated Phagocytosis. Journal of Aerosol Medicine. 10(1). 1–12. 5 indexed citations
5.
Santis, C. De, Piera Robbioni, Renato Longhi, et al.. (1993). Cross-Reactive Response to Human Immunodeficiency Virus Type 1 (HIV-l) gp120 and HLA Class I Heavy Chains Induced by Receipt of HIV-1-Derived Envelope Vaccines. The Journal of Infectious Diseases. 168(6). 1396–1403. 23 indexed citations
6.
Daher, N, M. C. Keefer, Richard C. Reichman, Raphael Dolin, & Norbert J. Roberts. (1993). Persisting Human Immunodeficiency Virus Type 1 gp160-Specific Human T Lymphocyte Responses Including CD8+ Cytotoxic Activity after Receipt of Envelope Vaccines. The Journal of Infectious Diseases. 168(2). 306–313. 33 indexed citations
7.
8.
Nichols, Joan E., David J. Mock, & Norbert J. Roberts. (1993). Use of FITC-labeled influenza virus and flow cytometry to assess binding and internalization of virus by monocytes-macrophages and lymphocytes. Archives of Virology. 130(3-4). 441–455. 29 indexed citations
9.
Roberts, Norbert J., et al.. (1992). The limited role of the human interferon system response to respiratory syncytial virus challenge: analysis and comparison to influenza virus challenge. Microbial Pathogenesis. 12(6). 409–414. 26 indexed citations
10.
Salkind, Alan R. & Norbert J. Roberts. (1992). Recent observations regarding the pathogenesis of recurrent respiratory syncytial virus infections: implications for vaccine development. Vaccine. 10(8). 519–523. 11 indexed citations
11.
Frampton, Mark W., Karen Z. Voter, Paul E. Morrow, et al.. (1992). Sulfuric Acid Aerosol Exposure in Humans Assessed by Bronchoalveolar Lavage. American Review of Respiratory Disease. 146(3). 626–632. 28 indexed citations
12.
Levy, Paul C., Mark J. Utell, Howard B. Fleit, et al.. (1991). Characterization of Human Alveolar Macrophage Fcγ Receptor III: A Transmembrane Glycoprotein that is Shed under In Vitro Culture Conditions. American Journal of Respiratory Cell and Molecular Biology. 5(4). 307–314. 19 indexed citations
13.
Bonnez, William, Richard C. Reichman, Joanne Strussenberg, & Norbert J. Roberts. (1991). In vitro Interactions between Bovine Papillomavirus and Human Monocytes and Macrophages. Intervirology. 32(4). 246–252. 5 indexed citations
14.
Mock, David J. & Norbert J. Roberts. (1990). Role of the Monocyte-Macrophage in Influenza Virus Infection of Lymphocytes: Implications for HIV Infection. AIDS Research and Human Retroviruses. 6(8). 965–966. 3 indexed citations
15.
16.
Frampton, Mark W., et al.. (1989). Effects of Nitrogen Dioxide Exposure on Bronchoalveolar Lavage Proteins in Humans. American Journal of Respiratory Cell and Molecular Biology. 1(6). 499–505. 38 indexed citations
17.
Frampton, Mark W., et al.. (1989). Nitrogen dioxide exposure in vivo and human alveolar macrophage inactivation of influenza virus in vitro. Environmental Research. 48(2). 179–192. 90 indexed citations
18.
Roberts, Norbert J.. (1988). The Concept of Immunofocusing Illustrated by Influenza Virus Infection. Clinical Infectious Diseases. 10(6). 1071–1074. 7 indexed citations
19.
Pinkston, P, et al.. (1988). Effects of in vitro exposure to nitrogen dioxide on human alveolar macrophage release of neutrophil chemotactic factor and interleukin-1. Environmental Research. 47(1). 48–58. 10 indexed citations
20.

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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