Marybeth Daucher

2.5k total citations
23 papers, 2.0k citations indexed

About

Marybeth Daucher is a scholar working on Virology, Immunology and Infectious Diseases. According to data from OpenAlex, Marybeth Daucher has authored 23 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Virology, 11 papers in Immunology and 10 papers in Infectious Diseases. Recurrent topics in Marybeth Daucher's work include HIV Research and Treatment (15 papers), Immune Cell Function and Interaction (9 papers) and HIV/AIDS Research and Interventions (6 papers). Marybeth Daucher is often cited by papers focused on HIV Research and Treatment (15 papers), Immune Cell Function and Interaction (9 papers) and HIV/AIDS Research and Interventions (6 papers). Marybeth Daucher collaborates with scholars based in United States, Canada and Italy. Marybeth Daucher's co-authors include Anthony S. Fauci, Shyam Kottilil, Audrey Kinter, Domenico Mavilio, Oren J. Cohen, Emanuela Marcenaro, Alessandro Moretta, Gabriella Lombardo, Janet Benjamin and Lin Yin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and The EMBO Journal.

In The Last Decade

Marybeth Daucher

23 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marybeth Daucher United States	21	1.3k	1.2k	534	338	224	23	2.0k
Una O’Doherty United States	19	729 0.6×	1.4k 1.1×	787 1.5×	377 1.1×	391 1.7×	23	1.8k
Shawn P. O’Neil United States	23	1.2k 0.9×	1.3k 1.0×	455 0.9×	529 1.6×	324 1.4×	42	2.1k
Anthony Hoffman United States	10	764 0.6×	1.1k 0.9×	670 1.3×	386 1.1×	293 1.3×	11	1.8k
Alison L. Greenway Australia	14	747 0.6×	1.4k 1.2×	709 1.3×	406 1.2×	401 1.8×	23	1.8k
Benjamin Descours France	12	884 0.7×	959 0.8×	446 0.8×	337 1.0×	254 1.1×	19	1.5k
Annie David France	17	682 0.5×	864 0.7×	482 0.9×	233 0.7×	246 1.1×	22	1.2k
Stanley Kang United States	8	852 0.7×	1.2k 1.0×	599 1.1×	193 0.6×	258 1.2×	8	1.5k
Kristine E. Sheridan United States	7	846 0.7×	1.3k 1.1×	638 1.2×	225 0.7×	253 1.1×	8	1.5k
Eleonora Tresoldi Italy	18	1.2k 1.0×	938 0.8×	461 0.9×	281 0.8×	261 1.2×	27	2.0k
Ioannis Théodorou France	19	1.1k 0.9×	762 0.6×	374 0.7×	280 0.8×	121 0.5×	36	1.6k

Countries citing papers authored by Marybeth Daucher

Since Specialization

Citations

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

Fields of papers citing papers by Marybeth Daucher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marybeth Daucher

This figure shows the co-authorship network connecting the top 25 collaborators of Marybeth Daucher. A scholar is included among the top collaborators of Marybeth Daucher 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 Marybeth Daucher. Marybeth Daucher 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

Zhang, Xiaozhen, Marybeth Daucher, David L. Armistead, Rodney S. Russell, & Shyam Kottilil. (2013). MicroRNA Expression Profiling in HCV-Infected Human Hepatoma Cells Identifies Potential Anti-Viral Targets Induced by Interferon-α. PLoS ONE. 8(2). e55733–e55733. 63 indexed citations

Sherman, Amy C, Nirupama Trehanpati, Marybeth Daucher, et al.. (2012). Augmentation of Hepatitis B Virus-Specific Cellular Immunity with Programmed Death Receptor-1/Programmed Death Receptor-L1 Blockade in Hepatitis B Virus and HIV/Hepatitis B Virus Coinfected Patients Treated with Adefovir. AIDS Research and Human Retroviruses. 29(4). 665–672. 27 indexed citations

Zhang, Xiaozhen, et al.. (2012). Human immunodeficiency virus enhances hepatitis C virus replication by differential regulation of IFN and TGF family genes. Journal of Medical Virology. 84(9). 1344–1352. 7 indexed citations

Reynolds, Steven J., Cissy Kityo, Claire W. Hallahan, et al.. (2010). A Randomized, Controlled, Trial of Short Cycle Intermittent Compared to Continuous Antiretroviral Therapy for the Treatment of HIV Infection in Uganda. PLoS ONE. 5(4). e10307–e10307. 24 indexed citations

Zhang, Xiaozhen, Marybeth Daucher, Juraj Kabát, et al.. (2009). Altered regulation of extrinsic apoptosis pathway in HCV‐infected HCC cells enhances susceptibility to mapatumumab‐induced apoptosis. Hepatology Research. 39(12). 1178–1189. 8 indexed citations

Kottilil, Shyam, Xiaozhen Zhang, Richard A. Lempicki, et al.. (2009). Human immunodeficiency virus and hepatitis C infections induce distinct immunologic imprints in peripheral mononuclear cells # †. Hepatology. 50(1). 34–45. 42 indexed citations

Daucher, Marybeth, David A. Price, Jason M. Brenchley, et al.. (2008). Virological Outcome after Structured Interruption of Antiretroviral Therapy for Human Immunodeficiency Virus Infection Is Associated with the Functional Profile of Virus-Specific CD8⁺T Cells. Journal of Virology. 82(8). 4102–4114. 48 indexed citations

Gupta, Neil, James Arthos, Prateeti Khazanie, et al.. (2005). Targeted lysis of HIV-infected cells by natural killer cells armed and triggered by a recombinant immunoglobulin fusion protein: implications for immunotherapy. Virology. 332(2). 491–497. 30 indexed citations

Cicala, Claudia, James Arthos, Nina Censoplano, et al.. (2005). HIV-1 gp120 induces NFAT nuclear translocation in resting CD4+ T-cells. Virology. 345(1). 105–114. 39 indexed citations

10.

Kinter, Audrey, Sarah Kern, Lin Yin, et al.. (2004). CD25+CD4+ Regulatory T Cells from the Peripheral Blood of Asymptomatic HIV-infected Individuals Regulate CD4+ and CD8+ HIV-specific T Cell Immune Responses In Vitro and Are Associated with Favorable Clinical Markers of Disease Status. The Journal of Experimental Medicine. 200(3). 331–343. 365 indexed citations

11.

Dybul, Mark, Robin Dewar, Frank Maldarelli, et al.. (2004). A Proof‐of‐Concept Study of Short‐Cycle Intermittent Antiretroviral Therapy with a Once‐Daily Regimen of Didanosine, Lamivudine, and Efavirenz for the Treatment of Chronic HIV Infection. The Journal of Infectious Diseases. 189(11). 1974–1982. 44 indexed citations

12.

Dybul, Mark, Marybeth Daucher, Kurt Hertogs, et al.. (2003). Long‐Cycle Structured Intermittent versus Continuous Highly Active Antiretroviral Therapy for the Treatment of Chronic Infection with Human Immunodeficiency Virus: Effects on Drug Toxicity and on Immunologic and Virologic Parameters. The Journal of Infectious Diseases. 188(3). 388–396. 62 indexed citations

13.

Mavilio, Domenico, Janet Benjamin, Marybeth Daucher, et al.. (2003). Natural killer cells in HIV-1 infection: Dichotomous effects of viremia on inhibitory and activating receptors and their functional correlates. Proceedings of the National Academy of Sciences. 100(25). 15011–15016. 306 indexed citations

14.

Dybul, Mark, Tae‐Wook Chun, Christian Yoder, et al.. (2001). Short-cycle structured intermittent treatment of chronic HIV infection with highly active antiretroviral therapy: Effects on virologic, immunologic, and toxicity parameters. Proceedings of the National Academy of Sciences. 98(26). 15161–15166. 111 indexed citations

15.

Cohen, Oren J., Stefania Paolucci, Marybeth Daucher, et al.. (1998). CXCR4 and CCR5 Genetic Polymorphisms in Long-Term Nonprogressive Human Immunodeficiency Virus Infection: Lack of Association with Mutations other than CCR5-Δ32. Journal of Virology. 72(7). 6215–6217. 53 indexed citations

16.

Pantaleo, Giuseppe, Hugo Soudeyns, James F. Demarest, et al.. (1997). Accumulation of human immunodeficiency virus‐specific cytotoxic T lymphocytes away from the predominant site of virus replication during primary infection. European Journal of Immunology. 27(12). 3166–3173. 35 indexed citations

17.

Pantaleo, Giuseppe, James F. Demarest, Timothy W. Schacker, et al.. (1997). The qualitative nature of the primary immune response to HIV infection is a prognosticator of disease progression independent of the initial level of plasma viremia. Proceedings of the National Academy of Sciences. 94(1). 254–258. 219 indexed citations

18.

Pantaleo, Giuseppe, Hugo Soudeyns, James F. Demarest, et al.. (1997). Evidence for rapid disappearance of initially expanded HIV-specific CD8⁺T cell clones during primary HIV infection. Proceedings of the National Academy of Sciences. 94(18). 9848–9853. 165 indexed citations

19.

Franzoso, Guido, Louise Carlson, Keith Brown, et al.. (1996). Activation of the serum response factor by p65/NF-kappaB.. The EMBO Journal. 15(13). 3403–3412. 58 indexed citations

20.

Ragheb, Jack A., Peter Bressler, Marybeth Daucher, et al.. (1995). Analysis of trans -Dominant Mutants of the HIV Type 1 Rev Protein for Their Ability to Inhibit Rev Function, HIV Type 1 Replication, and Their Use as Anti-HIV Gene Therapeutics. AIDS Research and Human Retroviruses. 11(11). 1343–1353. 24 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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