Ralph Feuer

12.7k total citations
34 papers, 2.1k citations indexed

About

Ralph Feuer is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, Ralph Feuer has authored 34 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Cardiology and Cardiovascular Medicine, 18 papers in Molecular Biology and 12 papers in Epidemiology. Recurrent topics in Ralph Feuer's work include Viral Infections and Immunology Research (20 papers), RNA regulation and disease (10 papers) and interferon and immune responses (9 papers). Ralph Feuer is often cited by papers focused on Viral Infections and Immunology Research (20 papers), RNA regulation and disease (10 papers) and interferon and immune responses (9 papers). Ralph Feuer collaborates with scholars based in United States, Canada and Australia. Ralph Feuer's co-authors include J. Lindsay Whitton, Christopher T. Cornell, Robb R. Pagarigan, Ignacio Mena, Roberta A. Gottlieb, Ginger Tsueng, Jenna M. Tabor-Godwin, Jon Sin, Stephanie Harkins and Mark K. Slifka and has published in prestigious journals such as Nature Communications, Journal of Neuroscience and The Journal of Immunology.

In The Last Decade

Ralph Feuer

34 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ralph Feuer United States	26	967	783	605	596	495	34	2.1k
Penny Clarke United States	30	436 0.5×	797 1.0×	432 0.7×	1000 1.7×	502 1.0×	56	2.3k
Jeroen R. P. M. Strating Netherlands	23	765 0.8×	952 1.2×	326 0.5×	506 0.8×	276 0.6×	38	1.8k
Florence Colbère-Garapin France	25	837 0.9×	975 1.2×	425 0.7×	682 1.1×	269 0.5×	58	2.2k
Leena Kinnunen Finland	26	1.1k 1.1×	854 1.1×	834 1.4×	1.0k 1.7×	595 1.2×	54	3.0k
Kyoko Tsukiyama–Kohara Japan	34	743 0.8×	1.7k 2.2×	2.4k 3.9×	704 1.2×	575 1.2×	153	5.1k
Glenn F. Rall United States	26	252 0.3×	845 1.1×	913 1.5×	765 1.3×	870 1.8×	67	2.5k
Zheng Xing United States	30	264 0.3×	895 1.1×	891 1.5×	1.2k 2.0×	934 1.9×	81	3.3k
Iván Ventoso Spain	19	355 0.4×	982 1.3×	265 0.4×	389 0.7×	493 1.0×	33	1.7k
Eugene Agapov United States	27	206 0.2×	522 0.7×	1.2k 2.0×	615 1.0×	1.1k 2.1×	49	3.1k
Jung‐Hyang Sur South Korea	27	459 0.5×	491 0.6×	579 1.0×	592 1.0×	318 0.6×	125	2.8k

Countries citing papers authored by Ralph Feuer

Since Specialization

Citations

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

Fields of papers citing papers by Ralph Feuer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph Feuer

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Piplani, Honit, Deepti Lall, Elizabeth L. McCabe, et al.. (2022). TBK1 and GABARAP family members suppress Coxsackievirus B infection by limiting viral production and promoting autophagic degradation of viral extracellular vesicles. PLoS Pathogens. 18(8). e1010350–e1010350. 10 indexed citations

Thoman, Marilyn L., Dale A. Chatfield, Kent G. Osborn, et al.. (2020). <p>Acetylcholine Regulates Pulmonary Pathology During Viral Infection and Recovery</p>. ImmunoTargets and Therapy. Volume 9. 333–350. 18 indexed citations

Andres, Allen M., et al.. (2019). Coxsackievirus B infection induces the extracellular release of miR-590-5p, a proviral microRNA. Virology. 529. 169–176. 32 indexed citations

Xue, Yuan Chao, Ralph Feuer, Neil R. Cashman, & Honglin Luo. (2018). Enteroviral Infection: The Forgotten Link to Amyotrophic Lateral Sclerosis?. Frontiers in Molecular Neuroscience. 11. 63–63. 67 indexed citations

Xue, Yuan Chao, Chelsea M. Ruller, Gabriel Fung, et al.. (2018). Enteroviral Infection Leads to Transactive Response DNA-Binding Protein 43 Pathology in Vivo. American Journal Of Pathology. 188(12). 2853–2862. 21 indexed citations

Sin, Jon, Vrushali Mangale, Wdee Thienphrapa, Roberta A. Gottlieb, & Ralph Feuer. (2015). Recent progress in understanding coxsackievirus replication, dissemination, and pathogenesis. Virology. 484. 288–304. 86 indexed citations

Robinson, Scott M., Ginger Tsueng, Jon Sin, et al.. (2014). Coxsackievirus B Exits the Host Cell in Shed Microvesicles Displaying Autophagosomal Markers. PLoS Pathogens. 10(4). e1004045–e1004045. 256 indexed citations

Mendez, Natalie, Lingzhi Zhang, Farah Hedjran, et al.. (2014). Encapsulation of adenovirus serotype 5 in anionic lecithin liposomes using a bead-based immunoprecipitation technique enhances transfection efficiency. Biomaterials. 35(35). 9554–9561. 45 indexed citations

Sin, Jon, Chengqun Huang, Mathias H. Konstandin, et al.. (2014). The Impact of Juvenile Coxsackievirus Infection on Cardiac Progenitor Cells and Postnatal Heart Development. PLoS Pathogens. 10(7). e1004249–e1004249. 13 indexed citations

10.

Ruller, Chelsea M., Scott M. Robinson, Kristeene A. Knopp, et al.. (2013). Distinct neural stem cell tropism, early immune activation, and choroid plexus pathology following coxsackievirus infection in the neonatal central nervous system. Laboratory Investigation. 94(2). 161–181. 18 indexed citations

11.

Ruller, Chelsea M., Jenna M. Tabor-Godwin, Scott M. Robinson, et al.. (2011). Neural Stem Cell Depletion and CNS Developmental Defects After Enteroviral Infection. American Journal Of Pathology. 180(3). 1107–1120. 28 indexed citations

12.

Banerjee, Anirban, Brandon J. Kim, Andrew S. Cutting, et al.. (2011). Bacterial Pili exploit integrin machinery to promote immune activation and efficient blood-brain barrier penetration. Nature Communications. 2(1). 462–462. 105 indexed citations

13.

Tabor-Godwin, Jenna M., Chelsea M. Ruller, Stephen W. Harkins, et al.. (2010). A Novel Population of Myeloid Cells Responding to Coxsackievirus Infection Assists in the Dissemination of Virus within the Neonatal CNS. Journal of Neuroscience. 30(25). 8676–8691. 66 indexed citations

14.

Kemball, Christopher C., Stephanie Harkins, Jason K. Whitmire, et al.. (2009). Coxsackievirus B3 Inhibits Antigen Presentation In Vivo, Exerting a Profound and Selective Effect on the MHC Class I Pathway. PLoS Pathogens. 5(10). e1000618–e1000618. 40 indexed citations

15.

Feuer, Ralph & J. Lindsay Whitton. (2008). Preferential Coxsackievirus Replication in Proliferating/Activated Cells: Implications for Virus Tropism, Persistence, and Pathogenesis. Current topics in microbiology and immunology. 323. 149–173. 22 indexed citations

16.

Buchmeier, Michael J., Tom Wolfe, Joey Ting, et al.. (2007). Exacerbated Pathology of Viral Encephalitis in Mice with Central Nervous System-Specific Autoantibodies. American Journal Of Pathology. 170(2). 557–566. 17 indexed citations

17.

Feuer, Ralph, Robb R. Pagarigan, Stephanie Harkins, et al.. (2005). Coxsackievirus Targets Proliferating Neuronal Progenitor Cells in the Neonatal CNS. Journal of Neuroscience. 25(9). 2434–2444. 67 indexed citations

18.

Whitton, J. Lindsay, Christopher T. Cornell, & Ralph Feuer. (2005). Host and virus determinants of picornavirus pathogenesis and tropism. Nature Reviews Microbiology. 3(10). 765–776. 200 indexed citations

19.

Hunziker, Isabelle P., Stephanie Harkins, Ralph Feuer, Christopher T. Cornell, & J. Lindsay Whitton. (2004). Generation and analysis of an RNA vaccine that protects against coxsackievirus B3 challenge. Virology. 330(1). 196–208. 25 indexed citations

20.

Feuer, Ralph, Ignacio Mena, Robb R. Pagarigan, Daniel E. Hassett, & J. Lindsay Whitton. (2004). Coxsackievirus replication and the cell cycle: a potential regulatory mechanism for viral persistence/latency. Medical Microbiology and Immunology. 193(2-3). 83–90. 30 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.

Explore authors with similar magnitude of impact