Doris J. Bucher

2.3k total citations
55 papers, 1.8k citations indexed

About

Doris J. Bucher is a scholar working on Epidemiology, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Doris J. Bucher has authored 55 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Epidemiology, 18 papers in Molecular Biology and 14 papers in Infectious Diseases. Recurrent topics in Doris J. Bucher's work include Influenza Virus Research Studies (41 papers), Respiratory viral infections research (21 papers) and Monoclonal and Polyclonal Antibodies Research (12 papers). Doris J. Bucher is often cited by papers focused on Influenza Virus Research Studies (41 papers), Respiratory viral infections research (21 papers) and Monoclonal and Polyclonal Antibodies Research (12 papers). Doris J. Bucher collaborates with scholars based in United States, Russia and Australia. Doris J. Bucher's co-authors include Edwin D. Kilbourne, Jianhua Le, Bert E. Johansson, Dennis W. Metzger, Victor C. Huber, Ronald E. Mayner, Francis A. Ennis, Michael A. Phelan, I G Kharitonenkov and Barbara A. Pokorny and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and The Journal of Immunology.

In The Last Decade

Doris J. Bucher

54 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
Doris J. Bucher United States 24 1.3k 555 475 398 283 55 1.8k
Ashley J. Birkett United States 22 1.3k 1.0× 887 1.6× 606 1.3× 443 1.1× 349 1.2× 36 2.3k
Frederick R. Vogel United States 20 569 0.5× 687 1.2× 422 0.9× 289 0.7× 156 0.6× 29 1.4k
Erik de Vries Netherlands 29 1.3k 1.1× 440 0.8× 914 1.9× 551 1.4× 176 0.6× 54 2.3k
Mary Jo Hamilton United States 26 754 0.6× 761 1.4× 399 0.8× 523 1.3× 65 0.2× 54 2.1k
Xiaoping Liang United States 27 1.6k 1.3× 1.1k 1.9× 544 1.1× 530 1.3× 370 1.3× 58 2.5k
Brian A. Crowe Austria 19 723 0.6× 225 0.4× 300 0.6× 331 0.8× 96 0.3× 42 1.3k
Zhirnov Op Russia 24 1.3k 1.0× 624 1.1× 531 1.1× 439 1.1× 71 0.3× 86 1.8k
Debbie Drane Australia 26 473 0.4× 1.1k 2.0× 646 1.4× 256 0.6× 118 0.4× 32 1.7k
Masanobu Ohuchi Japan 16 1.1k 0.8× 274 0.5× 388 0.8× 370 0.9× 106 0.4× 27 1.4k
René Rijnbrand United States 27 768 0.6× 319 0.6× 756 1.6× 567 1.4× 119 0.4× 50 2.2k

Countries citing papers authored by Doris J. Bucher

Since Specialization
Citations

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

Fields of papers citing papers by Doris J. Bucher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Doris J. Bucher. 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 Doris J. Bucher. The network helps show where Doris J. Bucher may publish in the future.

Co-authorship network of co-authors of Doris J. Bucher

This figure shows the co-authorship network connecting the top 25 collaborators of Doris J. Bucher. A scholar is included among the top collaborators of Doris J. Bucher 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 Doris J. Bucher. Doris J. Bucher 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.
Wang, Jiong, Shannon P. Hilchey, Ollivier Hyrien, et al.. (2015). Multi-Dimensional Measurement of Antibody-Mediated Heterosubtypic Immunity to Influenza. PLoS ONE. 10(6). e0129858–e0129858. 23 indexed citations
3.
Le, Jianhua, et al.. (2014). Development of high yield reassortants for influenza type B viruses and analysis of their gene compositions. Vaccine. 33(7). 879–884. 9 indexed citations
4.
Wei, Hui, William J. Rice, Doris J. Bucher, et al.. (2014). Morphology of Influenza B/Lee/40 Determined by Cryo-Electron Microscopy. PLoS ONE. 9(2). e88288–e88288. 21 indexed citations
5.
Doyle, Tracey M., Changgui Li, Doris J. Bucher, et al.. (2013). A monoclonal antibody targeting a highly conserved epitope in influenza B neuraminidase provides protection against drug resistant strains. Biochemical and Biophysical Research Communications. 441(1). 226–229. 43 indexed citations
6.
Le, Jianhua, Shiroh Onodera, Barbara A. Pokorny, et al.. (2013). Molecular Signature of High Yield (Growth) Influenza A Virus Reassortants Prepared as Candidate Vaccine Seeds. PLoS ONE. 8(6). e65955–e65955. 12 indexed citations
7.
Stöhr, Klaus, et al.. (2012). Influenza Virus Surveillance, Vaccine Strain Selection, and Manufacture. Methods in molecular biology. 865. 147–162. 62 indexed citations
8.
9.
Bucher, Doris J., Terrence M. Tumpey, Anice C. Lowen, et al.. (2010). 2009 H1N1 swine flu: the 2010 perspective. Annals of the New York Academy of Sciences. 1205(s1). E10–20. 1 indexed citations
10.
Stevens, James, Li‐Mei Chen, P.J. Carney, et al.. (2010). Receptor Specificity of Influenza A H3N2 Viruses Isolated in Mammalian Cells and Embryonated Chicken Eggs. Journal of Virology. 84(21). 11599–11600. 1 indexed citations
11.
Seligman, Stephen & Doris J. Bucher. (2003). The importance of being outer: consequences of the distinction between the outer and inner surfaces of flavivirus glycoprotein E. Trends in Microbiology. 11(3). 108–110. 15 indexed citations
12.
Baum, Ellen Z., Pamela C. Wagaman, Ignatius J. Turchi, et al.. (2003). A point mutation in influenza B neuraminidase confers resistance to peramivir and loss of slow binding. Antiviral Research. 59(1). 13–22. 39 indexed citations
14.
Daniels, Thomas J., Shobha Varde, Jianhua Le, et al.. (1998). Geographic Risk for Lyme Disease and Human Granulocytic Ehrlichiosis in Southern New York State. Applied and Environmental Microbiology. 64(12). 4663–4669. 85 indexed citations
15.
Milstein, Sam, et al.. (1993). Oral Immunization of Rats with Proteinoid Microspheres Encapsulating Influenza Virus Antigens. Pharmaceutical Research. 10(8). 1243–1247. 48 indexed citations
16.
Dourmashkin, R. R., Doris J. Bucher, & John Oxford. (1993). Small virus‐like particles bud from the cell membranes of normal as well as HIV‐infected human lymphoid cells. Journal of Medical Virology. 39(3). 229–232. 8 indexed citations
17.
Klimov, Alexander, et al.. (1992). Subtype H7 influenza viruses: comparative antigenic and molecular analysis of the HA-, M-, and NS-genes. Archives of Virology. 122(1-2). 143–161. 9 indexed citations
18.
Herlocher, M. Louise, Doris J. Bucher, & Robert G. Webster. (1992). Host range determination and functional mapping of the nucleoprotein and matrix genes of influenza viruses using monoclonal antibodies. Virus Research. 22(3). 281–293. 10 indexed citations
19.
Bucher, Doris J., А. Михаил, Patricia M. Graves, et al.. (1991). Rapid detection of type A influenza viruses with monoclonal antibodies to the M protein (M1) by enzyme-linked immunosorbent assay and time-resolved fluoroimmunoassay. Journal of Clinical Microbiology. 29(11). 2484–2488. 24 indexed citations
20.
Johansson, Bert E., Doris J. Bucher, Barbara A. Pokorny, А. Михаил, & Edwin D. Kilbourne. (1989). Identification of PR8 M1 protein in influenza virus high-yield reassortants by M1-specific monoclonal antibodies. Virology. 171(2). 634–636. 22 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