Janet D. Siliciano

25.3k total citations · 9 hit papers
104 papers, 15.9k citations indexed

About

Janet D. Siliciano is a scholar working on Virology, Infectious Diseases and Immunology. According to data from OpenAlex, Janet D. Siliciano has authored 104 papers receiving a total of 15.9k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Virology, 60 papers in Infectious Diseases and 45 papers in Immunology. Recurrent topics in Janet D. Siliciano's work include HIV Research and Treatment (91 papers), HIV/AIDS drug development and treatment (45 papers) and Immune Cell Function and Interaction (42 papers). Janet D. Siliciano is often cited by papers focused on HIV Research and Treatment (91 papers), HIV/AIDS drug development and treatment (45 papers) and Immune Cell Function and Interaction (42 papers). Janet D. Siliciano collaborates with scholars based in United States, Canada and Japan. Janet D. Siliciano's co-authors include Robert F. Siliciano, Daniel A. Goodenough, Bruce R. Stevenson, Mark S. Mooseker, Yoichi Taya, Christine E. Canman, Michael B. Kastan, Kazuyasu Sakaguchi, Ettore Appella and Thomas C. Quinn and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Janet D. Siliciano

101 papers receiving 15.6k citations

Hit Papers

Activation of the ATM Kinase by Ionizing Radiation and Ph... 1986 2026 1999 2012 1998 1999 1986 2003 2013 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janet D. Siliciano United States 53 10.2k 6.9k 5.2k 4.2k 2.0k 104 15.9k
James A. Hoxie United States 74 8.6k 0.8× 3.6k 0.5× 3.2k 0.6× 7.7k 1.8× 2.5k 1.2× 191 16.3k
Stephen C. Peiper United States 59 5.7k 0.6× 2.3k 0.3× 4.3k 0.8× 6.6k 1.6× 4.2k 2.1× 178 14.1k
Lee Ratner United States 64 8.6k 0.8× 5.4k 0.8× 4.9k 0.9× 7.1k 1.7× 2.0k 1.0× 300 17.5k
B. Matija Peterlin United States 72 7.8k 0.8× 3.6k 0.5× 8.3k 1.6× 5.1k 1.2× 1.4k 0.7× 188 15.8k
Frank Kirchhoff Germany 63 8.8k 0.9× 5.1k 0.7× 3.4k 0.7× 5.8k 1.4× 627 0.3× 296 14.0k
Patrice Debré France 69 4.7k 0.5× 3.5k 0.5× 2.5k 0.5× 10.7k 2.6× 2.1k 1.0× 390 18.2k
Jane A. McKeating United Kingdom 73 5.5k 0.5× 3.4k 0.5× 3.6k 0.7× 3.9k 0.9× 654 0.3× 232 21.0k
Mario Stevenson United States 56 8.7k 0.9× 5.2k 0.8× 4.0k 0.8× 3.7k 0.9× 548 0.3× 173 12.4k
Barbara Ensoli Italy 62 5.6k 0.5× 3.0k 0.4× 3.8k 0.7× 4.1k 1.0× 5.4k 2.6× 249 13.8k
John C. Kappes United States 54 8.8k 0.9× 4.9k 0.7× 4.0k 0.8× 4.7k 1.1× 804 0.4× 163 13.8k

Countries citing papers authored by Janet D. Siliciano

Since Specialization
Citations

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

Fields of papers citing papers by Janet D. Siliciano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janet D. Siliciano. 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 Janet D. Siliciano. The network helps show where Janet D. Siliciano may publish in the future.

Co-authorship network of co-authors of Janet D. Siliciano

This figure shows the co-authorship network connecting the top 25 collaborators of Janet D. Siliciano. A scholar is included among the top collaborators of Janet D. Siliciano 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 Janet D. Siliciano. Janet D. Siliciano 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.
White, Jennifer A., Filippo Dragoni, Emily J. Fray, et al.. (2025). Superinfection promotes replication and diversification of defective HIV-1 proviruses in people with non-suppressible viraemia. Nature Microbiology. 10(11). 2736–2748.
2.
Wu, Fengting, Srona Sengupta, Francesco R. Simonetti, et al.. (2024). Bispecific antibodies promote natural killer cell-mediated elimination of HIV-1 reservoir cells. Nature Immunology. 25(3). 462–470. 17 indexed citations
3.
Dragoni, Filippo, Fengting Wu, Jun Lai, et al.. (2024). Cognate antigen engagement induces HIV-1 expression in latently infected CD4+ T cells from people on long-term antiretroviral therapy. Immunity. 57(12). 2928–2944.e6. 1 indexed citations
4.
Wu, Fengting, et al.. (2024). CD4+ T cells with latent HIV-1 have reduced proliferative responses to T cell receptor stimulation. The Journal of Experimental Medicine. 221(3). 7 indexed citations
5.
Sengupta, Srona, AeRyon Kim, Tatiana Boronina, et al.. (2023). A cell-free antigen processing system informs HIV-1 epitope selection and vaccine design. The Journal of Experimental Medicine. 220(7). 3 indexed citations
6.
Fray, Emily J., Fengting Wu, Francesco R. Simonetti, et al.. (2023). Antiretroviral therapy reveals triphasic decay of intact SIV genomes and persistence of ancestral variants. Cell Host & Microbe. 31(3). 356–372.e5. 12 indexed citations
7.
White, Jennifer A., Francesco R. Simonetti, Subul Beg, et al.. (2022). Complex decay dynamics of HIV virions, intact and defective proviruses, and 2LTR circles following initiation of antiretroviral therapy. Proceedings of the National Academy of Sciences. 119(6). 52 indexed citations
8.
Kwon, Kyungyoon J., Andrew E. Timmons, Srona Sengupta, et al.. (2020). Different human resting memory CD4 + T cell subsets show similar low inducibility of latent HIV-1 proviruses. Science Translational Medicine. 12(528). 69 indexed citations
9.
Timmons, Andrew E., Emily J. Fray, Mithra R. Kumar, et al.. (2020). HSF1 inhibition attenuates HIV-1 latency reversal mediated by several candidate LRAs In Vitro and Ex Vivo. Proceedings of the National Academy of Sciences. 117(27). 15763–15771. 25 indexed citations
10.
Simonetti, Francesco R., Jennifer A. White, Camille Tumiotto, et al.. (2020). Intact proviral DNA assay analysis of large cohorts of people with HIV provides a benchmark for the frequency and composition of persistent proviral DNA. Proceedings of the National Academy of Sciences. 117(31). 18692–18700. 60 indexed citations
11.
Antar, Annukka A.R., Katharine M. Jenike, Sunyoung Jang, et al.. (2020). Longitudinal study reveals HIV-1–infected CD4+ T cell dynamics during long-term antiretroviral therapy. Journal of Clinical Investigation. 130(7). 3543–3559. 54 indexed citations
12.
Peluso, Michael J., Peter Bacchetti, Kristen D. Ritter, et al.. (2020). Differential decay of intact and defective proviral DNA in HIV-1–infected individuals on suppressive antiretroviral therapy. JCI Insight. 5(4). 124 indexed citations
13.
Simonetti, Francesco R., Hao Zhang, Kyle Rhodehouse, et al.. (2020). Antigen-driven clonal selection shapes the persistence of HIV-1–infected CD4+ T cells in vivo. Journal of Clinical Investigation. 131(3). 100 indexed citations
14.
Bertagnolli, Lynn N., Joseph Varriale, Francesco R. Simonetti, et al.. (2020). Autologous IgG antibodies block outgrowth of a substantial but variable fraction of viruses in the latent reservoir for HIV-1. Proceedings of the National Academy of Sciences. 117(50). 32066–32077. 46 indexed citations
15.
Rosenbloom, Daniel I. S., Peter Bacchetti, Mars Stone, et al.. (2019). Assessing intra-lab precision and inter-lab repeatability of outgrowth assays of HIV-1 latent reservoir size. PLoS Computational Biology. 15(4). e1006849–e1006849. 17 indexed citations
16.
Bruner, Katherine M., Alexandra J. Murray, Ross A. Pollack, et al.. (2016). Defective proviruses rapidly accumulate during acute HIV-1 infection. Nature Medicine. 22(9). 1043–1049. 515 indexed citations breakdown →
17.
Rosenbloom, Daniel I. S., Oliver Elliott, Alison L. Hill, et al.. (2015). Designing and Interpreting Limiting Dilution Assays: General Principles and Applications to the Latent Reservoir for Human Immunodeficiency Virus-1. Open Forum Infectious Diseases. 2(4). ofv123–ofv123. 94 indexed citations
18.
Siliciano, Janet D. & Robert F. Siliciano. (2013). Recent trends in HIV-1 drug resistance. Current Opinion in Virology. 3(5). 487–494. 36 indexed citations
19.
Brennan, Timothy, John O. Woods, Ahmad R. Sedaghat, et al.. (2009). Analysis of Human Immunodeficiency Virus Type 1 Viremia and Provirus in Resting CD4 + T Cells Reveals a Novel Source of Residual Viremia in Patients on Antiretroviral Therapy. Journal of Virology. 83(17). 8470–8481. 103 indexed citations
20.
Saavedra‐Lozano, Jesús, Cynthia McCoig, Jinbo Xu, et al.. (2002). An Anti‐CD45RO Immunotoxin Kills Latently Infected Human Immunodeficiency Virus (HIV) CD4 T Cells in the Blood of HIV‐Positive Persons. The Journal of Infectious Diseases. 185(3). 306–314. 12 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

Rankless by CCL
2026