Nathan M. Beach

1.3k total citations
35 papers, 992 citations indexed

About

Nathan M. Beach is a scholar working on Animal Science and Zoology, Infectious Diseases and Genetics. According to data from OpenAlex, Nathan M. Beach has authored 35 papers receiving a total of 992 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Animal Science and Zoology, 27 papers in Infectious Diseases and 17 papers in Genetics. Recurrent topics in Nathan M. Beach's work include Viral gastroenteritis research and epidemiology (26 papers), Animal Virus Infections Studies (26 papers) and Virus-based gene therapy research (15 papers). Nathan M. Beach is often cited by papers focused on Viral gastroenteritis research and epidemiology (26 papers), Animal Virus Infections Studies (26 papers) and Virus-based gene therapy research (15 papers). Nathan M. Beach collaborates with scholars based in United States, Spain and United Kingdom. Nathan M. Beach's co-authors include Xiang‐Jin Meng, Tanja Opriessnig, Patrick G. Halbur, Huigang Shen, Yao‐Wei Huang, Sheela Ramamoorthy, Celia Perales, Esteban Domingo, Josep Quer and Laura Córdoba and has published in prestigious journals such as Journal of Virology, Virology and Journal of General Virology.

In The Last Decade

Nathan M. Beach

35 papers receiving 979 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nathan M. Beach United States	20	733	618	526	255	157	35	992
Ana Marek Austria	13	494 0.7×	554 0.9×	620 1.2×	140 0.5×	98 0.6×	16	881
Jay G. Calvert United States	20	1.3k 1.8×	1.2k 1.9×	963 1.8×	174 0.7×	38 0.2×	33	1.6k
Jiexiong Xie China	20	440 0.6×	493 0.8×	287 0.5×	94 0.4×	50 0.3×	47	760
Xinyan Zhai China	14	442 0.6×	350 0.6×	309 0.6×	167 0.7×	72 0.5×	23	706
Eugenio J. Abente United States	17	481 0.7×	859 1.4×	227 0.4×	357 1.4×	102 0.6×	28	1.2k
Elena Canelli Italy	15	304 0.4×	395 0.6×	146 0.3×	151 0.6×	55 0.4×	28	576
Patricia Renson France	16	420 0.6×	411 0.7×	217 0.4×	91 0.4×	42 0.3×	30	579
B. Šmíd Czechia	15	422 0.6×	464 0.8×	149 0.3×	71 0.3×	62 0.4×	51	659
L. Valíček Czechia	14	446 0.6×	464 0.8×	179 0.3×	60 0.2×	55 0.4×	50	637
Catherine Eichwald Switzerland	17	357 0.5×	625 1.0×	292 0.6×	262 1.0×	20 0.1×	30	827

Countries citing papers authored by Nathan M. Beach

Since Specialization

Citations

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

Fields of papers citing papers by Nathan M. Beach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nathan M. Beach. 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 Nathan M. Beach. The network helps show where Nathan M. Beach may publish in the future.

Co-authorship network of co-authors of Nathan M. Beach

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

All Works

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20 of 20 papers shown

Soria, María Eugenia, Josep Gregori, Qian Chen, et al.. (2018). Pipeline for specific subtype amplification and drug resistance detection in hepatitis C virus. BMC Infectious Diseases. 18(1). 446–446. 20 indexed citations

Beach, Nathan M., et al.. (2014). A live-attenuated and an inactivated chimeric porcine circovirus (PCV)1-2 vaccine are both effective at inducing a humoral immune response and reducing PCV2 viremia and intrauterine infection in female swine of breeding age.. Iowa State University Digital Repository (Iowa State University). 15 indexed citations

Perales, Celia, Nathan M. Beach, Julie Sheldon, & Esteban Domingo. (2014). Molecular basis of interferon resistance in hepatitis C virus. Current Opinion in Virology. 8. 38–44. 11 indexed citations

Yin, Shuanghui, Chao‐Ting Xiao, Priscilla F. Gerber, et al.. (2013). Concurrent porcine circovirus type 2a (PCV2a) or PCV2b infection increases the rate of amino acid mutations of porcine reproductive and respiratory syndrome virus (PRRSV) during serial passages in pigs. Virus Research. 178(2). 445–451. 11 indexed citations

Perales, Celia, Nathan M. Beach, Isabel Gallego, et al.. (2013). Response of Hepatitis C Virus to Long-Term Passage in the Presence of Alpha Interferon: Multiple Mutations and a Common Phenotype. Journal of Virology. 87(13). 7593–7607. 59 indexed citations

Cecere, Thomas E., Xiang‐Jin Meng, Kevin D. Pelzer, et al.. (2012). Co-infection of porcine dendritic cells with porcine circovirus type 2a (PCV2a) and genotype II porcine reproductive and respiratory syndrome virus (PRRSV) induces CD4+CD25+FoxP3+ T cells in vitro. Veterinary Microbiology. 160(1-2). 233–239. 28 indexed citations

Shen, Huigang, et al.. (2012). Expression of human CD46 has no effect on porcine circovirus type 2 infection and shedding in the experimental pig model. Veterinary Research Communications. 36(3). 187–193. 3 indexed citations

Opriessnig, Tanja, Phillip C. Gauger, Kay S. Faaberg, et al.. (2012). Effect of porcine circovirus type 2a or 2b on infection kinetics and pathogenicity of two genetically divergent strains of porcine reproductive and respiratory syndrome virus in the conventional pig model. Veterinary Microbiology. 158(1-2). 69–81. 21 indexed citations

Opriessnig, Tanja, Kevin M. O'neill, Priscilla F. Gerber, et al.. (2012). A PCV2 vaccine based on genotype 2b is more effective than a 2a-based vaccine to protect against PCV2b or combined PCV2a/2b viremia in pigs with concurrent PCV2, PRRSV and PPV infection. Vaccine. 31(3). 487–494. 62 indexed citations

10.

Beach, Nathan M., Seth D. Thompson, Lisa Brown, et al.. (2012). Bordetella avium antibiotic resistance, novel enrichment culture, and antigenic characterization. Veterinary Microbiology. 160(1-2). 189–196. 16 indexed citations

11.

Beach, Nathan M., et al.. (2011). The autotransporter protein from Bordetella avium, Baa1, is involved in host cell attachment. Microbiological Research. 167(1). 55–60. 5 indexed citations

12.

Beach, Nathan M., Laura Córdoba, Scott P. Kenney, & Xiang‐Jin Meng. (2011). Productive infection of human hepatocellular carcinoma cells by porcine circovirus type 1. Vaccine. 29(43). 7303–7306. 21 indexed citations

13.

Sinha, Avanti, Huigang Shen, Nathan M. Beach, et al.. (2011). Porcine reproductive and respiratory syndrome virus (PRRSV) influences infection dynamics of porcine circovirus type 2 (PCV2) subtypes PCV2a and PCV2b by prolonging PCV2 viremia and shedding. Veterinary Microbiology. 152(3-4). 235–246. 47 indexed citations

14.

Kumar, Deepak, Nathan M. Beach, Xiang‐Jin Meng, & Nagendra R. Hegde. (2011). Use of PCR-based assays for the detection of the adventitious agent porcine circovirus type 1 (PCV1) in vaccines, and for confirming the identity of cell substrates and viruses used in vaccine production. Journal of Virological Methods. 179(1). 201–211. 7 indexed citations

15.

Miyamoto, David M., et al.. (2011). Bordetella avium causes induction of apoptosis and nitric oxide synthase in turkey tracheal explant cultures. Microbes and Infection. 13(10). 871–879. 9 indexed citations

16.

Beach, Nathan M. & Xiang‐Jin Meng. (2011). Efficacy and future prospects of commercially available and experimental vaccines against porcine circovirus type 2 (PCV2). Virus Research. 164(1-2). 33–42. 148 indexed citations

17.

Opriessnig, Tanja, Huigang Shen, Narinder Pal, et al.. (2011). A Live-Attenuated Chimeric Porcine Circovirus Type 2 (PCV2) Vaccine Is Transmitted to Contact Pigs but Is Not Upregulated by Concurrent Infection with Porcine Parvovirus (PPV) and Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) and Is Efficacious in a PCV2b-PRRSV-PPV Challenge Model. Clinical and Vaccine Immunology. 18(8). 1261–1268. 31 indexed citations

18.

Beach, Nathan M., et al.. (2010). Novel chimeric porcine circovirus (PCV) with the capsid gene of the emerging PCV2b subtype cloned in the genomic backbone of the non-pathogenic PCV1 is attenuated in vivo and induces protective and cross-protective immunity against PCV2b and PCV2a subtypes in pigs. Vaccine. 29(2). 221–232. 61 indexed citations

19.

Shen, Huigang, Nathan M. Beach, Yao‐Wei Huang, et al.. (2010). Comparison of commercial and experimental porcine circovirus type 2 (PCV2) vaccines using a triple challenge with PCV2, porcine reproductive and respiratory syndrome virus (PRRSV), and porcine parvovirus (PPV). Vaccine. 28(37). 5960–5966. 56 indexed citations

20.

Beach, Nathan M., Robert B. Duncan, C. T. Larsen, et al.. (2009). Persistent Infection of Turkeys with an Avirulent Strain of Turkey Hemorrhagic Enteritis Virus. Avian Diseases. 53(3). 370–375. 17 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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