Fernando Almazán

5.8k total citations · 1 hit paper
68 papers, 4.2k citations indexed

About

Fernando Almazán is a scholar working on Infectious Diseases, Animal Science and Zoology and Agronomy and Crop Science. According to data from OpenAlex, Fernando Almazán has authored 68 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Infectious Diseases, 36 papers in Animal Science and Zoology and 13 papers in Agronomy and Crop Science. Recurrent topics in Fernando Almazán's work include Viral gastroenteritis research and epidemiology (39 papers), Animal Virus Infections Studies (36 papers) and SARS-CoV-2 and COVID-19 Research (21 papers). Fernando Almazán is often cited by papers focused on Viral gastroenteritis research and epidemiology (39 papers), Animal Virus Infections Studies (36 papers) and SARS-CoV-2 and COVID-19 Research (21 papers). Fernando Almazán collaborates with scholars based in Spain, United States and China. Fernando Almazán's co-authors include Luis Enjuanes, Isabel Sola, Sonia Zúñiga, Eladio Viñuela, Carmen del Arco, José F. Rodrígúez, Silvia Márquez-Jurado, Marta L. DeDiego, Germán Andrés and Javier M. Rodrı́guez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Analytical Chemistry.

In The Last Decade

Fernando Almazán

66 papers receiving 4.2k citations

Hit Papers

Continuous and Discontinuous RNA Synthesis in Coronaviruses 2015 2026 2018 2022 2015 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fernando Almazán Spain 34 2.6k 1.5k 1.0k 749 675 68 4.2k
Rui Luo China 35 1.7k 0.6× 1.4k 0.9× 1.0k 1.0× 533 0.7× 564 0.8× 169 4.1k
Mikael Berg Sweden 32 1.5k 0.6× 1.3k 0.9× 473 0.5× 738 1.0× 400 0.6× 151 3.4k
Hanspeter Stalder Switzerland 21 2.2k 0.8× 450 0.3× 742 0.7× 1.1k 1.5× 564 0.8× 46 3.6k
Fei Gao China 31 1.4k 0.5× 1.1k 0.8× 903 0.9× 265 0.4× 285 0.4× 144 3.0k
Vladimir M. Blinov Russia 28 1.5k 0.6× 566 0.4× 1.9k 1.8× 272 0.4× 935 1.4× 63 4.3k
Peter J. Bredenbeek Netherlands 29 2.8k 1.1× 1.4k 0.9× 1.0k 1.0× 186 0.2× 759 1.1× 49 4.3k
Nanhua Chen China 33 1.9k 0.7× 1.7k 1.1× 455 0.5× 286 0.4× 328 0.5× 133 4.0k
Marco Vignuzzi France 42 2.7k 1.0× 739 0.5× 1.7k 1.7× 298 0.4× 957 1.4× 97 6.0k
Stuart G. Siddell Germany 49 5.8k 2.2× 4.2k 2.8× 1.7k 1.7× 200 0.3× 875 1.3× 131 8.5k
Ding Xiang Liu Singapore 52 5.2k 2.0× 2.7k 1.8× 2.1k 2.0× 211 0.3× 657 1.0× 159 7.9k

Countries citing papers authored by Fernando Almazán

Since Specialization
Citations

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

Fields of papers citing papers by Fernando Almazán

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fernando Almazán

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando Almazán. A scholar is included among the top collaborators of Fernando Almazán 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 Fernando Almazán. Fernando Almazán 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.
Chiem, Kevin, Aitor Nogales, Fernando Almazán, Chengjin Ye, & Luis Martínez‐Sobrido. (2023). Bacterial Artificial Chromosome Reverse Genetics Approaches for SARS-CoV-2. Methods in molecular biology. 2733. 133–153.
2.
Meseguer, Salvador, Mari‐Paz Rubio, Begoña Lainez, et al.. (2023). SARS-CoV-2-encoded small RNAs are able to repress the host expression of SERINC5 to facilitate viral replication. Frontiers in Microbiology. 14. 6 indexed citations
3.
Ye, Chengjin, Kevin Chiem, Jun‐Gyu Park, et al.. (2020). Rescue of SARS-CoV-2 from a Single Bacterial Artificial Chromosome. mBio. 11(5). 83 indexed citations
4.
Ávila‐Pérez, Ginés, Aitor Nogales, J. Park, et al.. (2019). A natural polymorphism in Zika virus NS2A protein responsible of virulence in mice. Scientific Reports. 9(1). 19968–19968. 20 indexed citations
5.
Ávila‐Pérez, Ginés, Jun‐Gyu Park, Aitor Nogales, Fernando Almazán, & Luis Martínez‐Sobrido. (2019). Rescue of Recombinant Zika Virus from a Bacterial Artificial Chromosome cDNA Clone. Journal of Visualized Experiments. 13 indexed citations
6.
Usme-Ciro, José A., et al.. (2016). Generation of a DNA-Launched Reporter Replicon Based on Dengue Virus Type 2 as a Multipurpose Platform. Intervirology. 59(5-6). 275–282. 1 indexed citations
7.
Almazán, Fernando, Isabel Sola, Sonia Zúñiga, et al.. (2014). Coronavirus reverse genetic systems: Infectious clones and replicons. Virus Research. 189. 262–270. 110 indexed citations
8.
Wang, Chengbao, Baicheng Huang, Ning Kong, et al.. (2013). A novel porcine reproductive and respiratory syndrome virus vector system that stably expresses enhanced green fluorescent protein as a separate transcription unit. Veterinary Research. 44(1). 104–104. 55 indexed citations
9.
Usme-Ciro, José A., Jaime Lopera-Madrid, Luis Enjuanes, Fernando Almazán, & Juan Carlos Gallego-Gómez. (2013). Development of a novel DNA-launched dengue virus type 2 infectious clone assembled in a bacterial artificial chromosome. Virus Research. 180. 12–22. 28 indexed citations
10.
Usme-Ciro, José A., et al.. (2013). Cytoplasmic RNA viruses as potential vehicles for the delivery of therapeutic small RNAs. Virology Journal. 10(1). 185–185. 32 indexed citations
11.
Wang, Chengbao, Jianfei Chen, Hongyan Shi, et al.. (2010). Rapid differentiation of vaccine strain and Chinese field strains of transmissible gastroenteritis virus by restriction fragment length polymorphism of the N gene. Virus Genes. 41(1). 47–58. 6 indexed citations
12.
Arco, Carmen del, Isabel Sola, Aitor Nogales, et al.. (2009). Host cell proteins interacting with the 3′ end of TGEV coronavirus genome influence virus replication. Virology. 391(2). 304–314. 60 indexed citations
13.
Ortego, Javier, Isabel Sola, Fernando Almazán, et al.. (2003). Transmissible gastroenteritis coronavirus gene 7 is not essential but influences in vivo virus replication and virulence. Virology. 308(1). 13–22. 89 indexed citations
14.
González, José M., Fernando Almazán, Zoltán Pénzes, Enrique Calvo, & Luis Enjuanes. (2001). Cloning Of A Transmissible Gastroenteritis Coronavirus Full-Length cDNA. Advances in experimental medicine and biology. 494. 533–536. 5 indexed citations
15.
González‐Aseguinolaza, Gloria, et al.. (1997). Cloning of the gp63 surface protease of Leishmania infantum. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1361(1). 92–102. 15 indexed citations
16.
Garcı́a-Escudero, Ramón, Fernando Almazán, Javier M. Rodrı́guez, et al.. (1995). Vectors for the genetic manipulation of African swine fever virus. Journal of Biotechnology. 40(2). 121–131. 28 indexed citations
17.
Almazán, Fernando, et al.. (1995). A set of African swine fever virus tandem repeats shares similarities with SAR-like sequences. Journal of General Virology. 76(4). 729–740. 8 indexed citations
18.
Chacón, Matilde R., Fernando Almazán, Marı́a L. Nogal, Eladio Viñuela, & José F. Rodrígúez. (1995). The African Swine Fever Virus IAP Homolog Is a Late Structural Polypeptide. Virology. 214(2). 670–674. 64 indexed citations
19.
Rodrı́guez, Javier M., Fernando Almazán, Eladio Viñuela, & José F. Rodrígúez. (1992). Genetic manipulation of African swine fever virus: Construction of recombinant viruses expressing the β-galactosidase gene. Virology. 188(1). 67–76. 45 indexed citations
20.
Reaven, Peter D., Sampath Parthasarathy, Elizabeth R. Miller, et al.. (1991). Feasibility of using an oleate-rich diet to reduce the susceptibility of low-density lipoprotein to oxidative modification in humans. American Journal of Clinical Nutrition. 54(4). 701–706. 268 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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