Christopher L. Parks

3.4k total citations · 2 hit papers
43 papers, 2.4k citations indexed

About

Christopher L. Parks is a scholar working on Epidemiology, Virology and Genetics. According to data from OpenAlex, Christopher L. Parks has authored 43 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Epidemiology, 16 papers in Virology and 15 papers in Genetics. Recurrent topics in Christopher L. Parks's work include Virology and Viral Diseases (19 papers), Virus-based gene therapy research (15 papers) and HIV Research and Treatment (14 papers). Christopher L. Parks is often cited by papers focused on Virology and Viral Diseases (19 papers), Virus-based gene therapy research (15 papers) and HIV Research and Treatment (14 papers). Christopher L. Parks collaborates with scholars based in United States, Canada and Brazil. Christopher L. Parks's co-authors include Thomas Shenk, Miklós Tóth, Patricia Robinson, Etienne Sibille, Stephen A. Udem, Louis J. Picker, Robert A. Lerch, Marı́a J. Chiuchiolo, Pramila Walpita and Michael Piatak and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Christopher L. Parks

43 papers receiving 2.3k citations

Hit Papers

Profound early control of highly pathogenic SI... 1998 2026 2007 2016 2011 1998 200 400 600

Peers

Christopher L. Parks
Andrew G. MacLean United States
Richard J. O. Barnard United States
Shiu‐Lok Hu United States
Armin Baiker Germany
Edward K. Wagner United States
B Dietzschold United States
Martine Aubert United States
Andrew G. MacLean United States
Christopher L. Parks
Citations per year, relative to Christopher L. Parks Christopher L. Parks (= 1×) peers Andrew G. MacLean

Countries citing papers authored by Christopher L. Parks

Since Specialization
Citations

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

Fields of papers citing papers by Christopher L. Parks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher L. Parks. 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 Christopher L. Parks. The network helps show where Christopher L. Parks may publish in the future.

Co-authorship network of co-authors of Christopher L. Parks

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher L. Parks. A scholar is included among the top collaborators of Christopher L. Parks 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 Christopher L. Parks. Christopher L. Parks 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.
Enriquez, Adrian, Ruben Diaz Avalos, Diptiben Parekh, et al.. (2025). Mapping the antibody response to Lassa virus vaccination of non-human primates. EBioMedicine. 114. 105673–105673. 1 indexed citations
2.
Martins, Maurício A., Lucas Gonzalez-Nieto, Michael J. Ricciardi, et al.. (2020). Rectal Acquisition of Simian Immunodeficiency Virus (SIV) SIVmac239 Infection despite Vaccine-Induced Immune Responses against the Entire SIV Proteome. Journal of Virology. 94(24). 8 indexed citations
3.
Martins, Maurício A., Lucas Gonzalez-Nieto, Young C. Shin, et al.. (2018). The Frequency of Vaccine-Induced T-Cell Responses Does Not Predict the Rate of Acquisition after Repeated Intrarectal SIVmac239 Challenges in Mamu-B*08 + Rhesus Macaques. Journal of Virology. 93(5). 3 indexed citations
4.
Lorenz, Ivo C., Hanh T. Nguyen, Ross Lindsay, et al.. (2014). The Stem of Vesicular Stomatitis Virus G Can Be Replaced With the HIV-1 Env Membrane-Proximal External Region Without Loss of G Function or Membrane-Proximal External Region Antigenic Properties. AIDS Research and Human Retroviruses. 30(11). 1130–1144. 4 indexed citations
6.
Clutton, Genevieve, et al.. (2014). Optimizing parallel induction of HIV type 1-specific antibody and T-cell responses by multicomponent subunit vaccines. AIDS. 28(17). 2495–2504. 9 indexed citations
8.
Parks, Christopher L., Louis J. Picker, & C. Richter King. (2013). Development of replication-competent viral vectors for HIV vaccine delivery. Current Opinion in HIV and AIDS. 8(5). 402–411. 46 indexed citations
9.
Martins, Maurício A., Myrna C. Bonaldo, Richard Rudersdorf, et al.. (2013). Immunogenicity of Seven New Recombinant Yellow Fever Viruses 17D Expressing Fragments of SIVmac239 Gag, Nef, and Vif in Indian Rhesus Macaques. PLoS ONE. 8(1). e54434–e54434. 10 indexed citations
10.
Lindsay, Ross, Heather Arendt, Jennifer Martinez, et al.. (2013). SIV antigen-specific effects on immune responses induced by vaccination with DNA electroporation and plasmid IL-12. Vaccine. 31(42). 4749–4758. 7 indexed citations
11.
Vojnov, Lara, Alexander T. Bean, Eric Peterson, et al.. (2011). DNA/Ad5 vaccination with SIV epitopes induced epitope-specific CD4+ T cells, but few subdominant epitope-specific CD8+ T cells. Vaccine. 29(43). 7483–7490. 6 indexed citations
12.
Witko, Susan E., J. Erik Johnson, Narender K. Kalyan, et al.. (2009). Refined methods for propagating vesicular stomatitis virus vectors that are defective for G protein expression. Journal of Virological Methods. 164(1-2). 43–50. 4 indexed citations
14.
Witko, Susan E., et al.. (2006). Inhibition of measles virus minireplicon-encoded reporter gene expression by V protein. Virology. 348(1). 107–119. 34 indexed citations
15.
Kowalski, Jacek, Karissa Adkins, Heather Arendt, et al.. (2006). Evaluation of neurovirulence and biodistribution of Venezuelan equine encephalitis replicon particles expressing herpes simplex virus type 2 glycoprotein D. Vaccine. 25(12). 2296–2305. 8 indexed citations
16.
Witko, Susan E., J. Erik Johnson, Krista Melville, et al.. (2006). An efficient helper-virus-free method for rescue of recombinant paramyxoviruses and rhadoviruses from a cell line suitable for vaccine development. Journal of Virological Methods. 135(1). 91–101. 53 indexed citations
17.
Clarke, David K., David Cooper, Michael A. Egan, et al.. (2006). Recombinant vesicular stomatitis virus as an HIV-1 vaccine vector. Springer Seminars in Immunopathology. 28(3). 239–253. 57 indexed citations
18.
Parks, Christopher L. & Thomas Shenk. (1996). The Serotonin 1a Receptor Gene Contains a TATA-less Promoter that Responds to MAZ and Sp1. Journal of Biological Chemistry. 271(8). 4417–4430. 199 indexed citations
19.
Spector, David J., et al.. (1993). A Multicomponent cis-Activator of Transcription of the E1b Gene of Adenovirus Type 5. Virology. 194(1). 128–136. 8 indexed citations
20.
Parks, Christopher L., Long‐Sheng Chang, & Thomas Shenk. (1991). A polymerase chain resction mediated by a single primer: cloning of genomic adjacent to a serotonin receptor protein coding region. Nucleic Acids Research. 19(25). 7155–7160. 45 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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