Shari M. Piaskowski

3.0k total citations
38 papers, 1.7k citations indexed

About

Shari M. Piaskowski is a scholar working on Virology, Immunology and Infectious Diseases. According to data from OpenAlex, Shari M. Piaskowski has authored 38 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Virology, 23 papers in Immunology and 13 papers in Infectious Diseases. Recurrent topics in Shari M. Piaskowski's work include HIV Research and Treatment (31 papers), Immune Cell Function and Interaction (19 papers) and HIV/AIDS Research and Interventions (10 papers). Shari M. Piaskowski is often cited by papers focused on HIV Research and Treatment (31 papers), Immune Cell Function and Interaction (19 papers) and HIV/AIDS Research and Interventions (10 papers). Shari M. Piaskowski collaborates with scholars based in United States, Brazil and Switzerland. Shari M. Piaskowski's co-authors include Eva G. Rakasz, David I. Watkins, Nancy A. Wilson, Jessica Furlott, Kimberly L. Weisgrau, John T. Loffredo, David I. Watkins, Thomas C. Friedrich, Dennis R. Burton and Brian Moldt and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and The Journal of Immunology.

In The Last Decade

Shari M. Piaskowski

38 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shari M. Piaskowski United States 22 1.3k 1.0k 441 375 337 38 1.7k
Clarisa M. Buckner United States 19 926 0.7× 848 0.8× 359 0.8× 287 0.8× 336 1.0× 28 1.6k
Jonah B. Sacha United States 25 835 0.7× 981 0.9× 403 0.9× 378 1.0× 352 1.0× 67 1.7k
Heather Knight United States 14 1.2k 1.0× 936 0.9× 533 1.2× 429 1.1× 213 0.6× 38 1.8k
Anita M. Trichel United States 23 926 0.7× 557 0.5× 478 1.1× 456 1.2× 229 0.7× 37 1.4k
Rebecca A. Russell United Kingdom 18 965 0.8× 513 0.5× 602 1.4× 435 1.2× 394 1.2× 26 1.4k
Boris Jülg United States 22 849 0.7× 641 0.6× 549 1.2× 308 0.8× 808 2.4× 48 2.0k
Bruno Vaslin France 24 987 0.8× 897 0.9× 387 0.9× 377 1.0× 133 0.4× 60 1.5k
Béatrice Jacquelin France 20 845 0.7× 746 0.7× 421 1.0× 287 0.8× 297 0.9× 45 1.6k
Jeremy Smedley United States 22 799 0.6× 752 0.7× 517 1.2× 360 1.0× 292 0.9× 56 1.6k
Sanjay V. Joag United States 25 1.5k 1.2× 794 0.8× 686 1.6× 642 1.7× 173 0.5× 57 1.9k

Countries citing papers authored by Shari M. Piaskowski

Since Specialization
Citations

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

Fields of papers citing papers by Shari M. Piaskowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shari M. Piaskowski

This figure shows the co-authorship network connecting the top 25 collaborators of Shari M. Piaskowski. A scholar is included among the top collaborators of Shari M. Piaskowski 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 Shari M. Piaskowski. Shari M. Piaskowski 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
2.
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
3.
Bimber, Benjamin N., Arpita Das, Shari M. Piaskowski, et al.. (2013). Acute Phase CD8+ T Lymphocytes against Alternate Reading Frame Epitopes Select for Rapid Viral Escape during SIV Infection. PLoS ONE. 8(5). e61383–e61383. 6 indexed citations
4.
Reynolds, Matthew R., Andrea M. Weiler, Shari M. Piaskowski, et al.. (2012). A trivalent recombinant Ad5 gag/pol/nef vaccine fails to protect rhesus macaques from infection or control virus replication after a limiting-dose heterologous SIV challenge. Vaccine. 30(30). 4465–4475. 28 indexed citations
5.
Piaskowski, Shari M., Richard Rudersdorf, Kim L. Weisgrau, et al.. (2011). Dengue virus-specific CD4+ and CD8+ T lymphocytes target NS1, NS3 and NS5 in infected Indian rhesus macaques. Immunogenetics. 64(2). 111–121. 24 indexed citations
7.
Bonaldo, Myrna C., Maurício A. Martins, Richard Rudersdorf, et al.. (2010). Recombinant Yellow Fever Vaccine Virus 17D Expressing Simian Immunodeficiency Virus SIVmac239 Gag Induces SIV-Specific CD8 + T-Cell Responses in Rhesus Macaques. Journal of Virology. 84(7). 3699–3706. 40 indexed citations
8.
Mudd, Philip A., Shari M. Piaskowski, Patrícia Neves, et al.. (2010). The live-attenuated yellow fever vaccine 17D induces broad and potent T cell responses against several viral proteins in Indian rhesus macaques—implications for recombinant vaccine design. Immunogenetics. 62(9). 593–600. 12 indexed citations
9.
Reynolds, Matthew R., Shari M. Piaskowski, Kimberly L. Weisgrau, et al.. (2010). Ex vivo analysis of SIV‐infected cells by flow cytometry. Cytometry Part A. 77A(11). 1059–1066. 6 indexed citations
10.
Sauer, Mariana M., Sabri Saeed Sanabani, Helena Tomiyama, et al.. (2010). Unexpected Diversity of Cellular Immune Responses against Nef and Vif in HIV-1-Infected Patients Who Spontaneously Control Viral Replication. PLoS ONE. 5(7). e11436–e11436. 10 indexed citations
11.
Maness, Nicholas J., Shari M. Piaskowski, Jessica Furlott, et al.. (2010). CD8 + T Cell Recognition of Cryptic Epitopes Is a Ubiquitous Feature of AIDS Virus Infection. Journal of Virology. 84(21). 11569–11574. 18 indexed citations
12.
Vojnov, Lara, Jason S. Reed, Kim L. Weisgrau, et al.. (2009). Effective Simian Immunodeficiency Virus-Specific CD8 + T Cells Lack an Easily Detectable, Shared Characteristic. Journal of Virology. 84(2). 753–764. 17 indexed citations
13.
Burwitz, Benjamin J., Justin Greene, Ann Detmer, et al.. (2009). Mauritian Cynomolgus Macaques Share Two Exceptionally Common Major Histocompatibility Complex Class I Alleles That Restrict Simian Immunodeficiency Virus-Specific CD8+T Cells. Journal of Virology. 83(12). 6011–6019. 61 indexed citations
14.
Sacha, Jonah B., Matthew R. Reynolds, Matthew B. Buechler, et al.. (2008). Differential Antigen Presentation Kinetics of CD8 + T-Cell Epitopes Derived from the Same Viral Protein. Journal of Virology. 82(18). 9293–9298. 22 indexed citations
15.
Maness, Nicholas J., Laura Valentine, Gemma E. May, et al.. (2007). AIDS virus–specific CD8+ T lymphocytes against an immunodominant cryptic epitope select for viral escape. The Journal of Experimental Medicine. 204(11). 2505–2512. 43 indexed citations
16.
Loffredo, John T., Benjamin J. Burwitz, Eva G. Rakasz, et al.. (2006). The Antiviral Efficacy of Simian Immunodeficiency Virus-Specific CD8 + T Cells Is Unrelated to Epitope Specificity and Is Abrogated by Viral Escape. Journal of Virology. 81(6). 2624–2634. 57 indexed citations
17.
Kaizu, Masahiko, Andrea M. Weiler, Kim L. Weisgrau, et al.. (2006). Repeated Intravaginal Inoculation with Cell‐Associated Simian Immunodeficiency Virus Results in Persistent Infection of Nonhuman Primates. The Journal of Infectious Diseases. 194(7). 912–916. 44 indexed citations
18.
Loffredo, John T., John Sidney, Shari M. Piaskowski, et al.. (2005). The High Frequency Indian Rhesus Macaque MHC Class I Molecule, Mamu-B*01, Does Not Appear to Be Involved in CD8+ T Lymphocyte Responses to SIVmac239. The Journal of Immunology. 175(9). 5986–5997. 34 indexed citations
19.
Fee, Dominic B., et al.. (2004). Traumatic brain injury increases TGFβRII expression on endothelial cells. Brain Research. 1012(1-2). 52–59. 21 indexed citations
20.
Fee, Dominic B., Benjamin J. Herdrich, Diane Sewell, et al.. (2003). Activated/effector CD4+ T cells exacerbate acute damage in the central nervous system following traumatic injury. Journal of Neuroimmunology. 136(1-2). 54–66. 112 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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