Subash C. Das

3.2k total citations · 1 hit paper
30 papers, 2.4k citations indexed

About

Subash C. Das is a scholar working on Epidemiology, Infectious Diseases and Genetics. According to data from OpenAlex, Subash C. Das has authored 30 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Epidemiology, 10 papers in Infectious Diseases and 8 papers in Genetics. Recurrent topics in Subash C. Das's work include Virology and Viral Diseases (10 papers), Influenza Virus Research Studies (8 papers) and Virus-based gene therapy research (8 papers). Subash C. Das is often cited by papers focused on Virology and Viral Diseases (10 papers), Influenza Virus Research Studies (8 papers) and Virus-based gene therapy research (8 papers). Subash C. Das collaborates with scholars based in United States, Japan and United Kingdom. Subash C. Das's co-authors include Asit K. Pattnaik, Yoshihiro Kawaoka, Masato Hatta, Kyoko Shinya, Makoto Ozawa, Chengjun Li, S. Yamada, Gabriele Neumann, Eileen A. Maher and Shinji Watanabe and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Subash C. Das

29 papers receiving 2.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Experimental adaptation of an influenza H5 HA confers respiratory droplet transmission to a reassortant H5 HA/H1N1 virus in ferrets

2012 1.1k citations Masaki Imai, Tokiko Watanabe et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Subash C. Das United States	20	1.5k	795	651	538	513	30	2.4k
Glenn A. Marsh Australia	36	2.1k 1.4×	2.2k 2.8×	590 0.9×	370 0.7×	328 0.6×	99	3.4k
Bin Zhou United States	30	1.7k 1.1×	1.1k 1.4×	855 1.3×	529 1.0×	461 0.9×	72	2.8k
Xiangjie Sun United States	26	1.6k 1.1×	759 1.0×	573 0.9×	458 0.9×	603 1.2×	71	2.3k
Erik de Vries Netherlands	29	1.3k 0.9×	551 0.7×	914 1.4×	440 0.8×	297 0.6×	54	2.3k
Neal Van Hoeven United States	25	1.7k 1.2×	814 1.0×	570 0.9×	852 1.6×	647 1.3×	43	2.5k
Shunlin Hu China	27	1.9k 1.3×	803 1.0×	390 0.6×	365 0.7×	864 1.7×	150	2.4k
Tokiko Watanabe Japan	19	2.0k 1.4×	823 1.0×	757 1.2×	682 1.3×	495 1.0×	30	2.6k
Ronald N. Harty United States	38	1.9k 1.3×	2.1k 2.7×	830 1.3×	785 1.5×	205 0.4×	87	4.2k
Stéphane Hausmann Switzerland	29	916 0.6×	581 0.7×	1.2k 1.8×	648 1.2×	100 0.2×	47	2.5k
Nadia Naffakh France	36	2.7k 1.8×	885 1.1×	1.4k 2.2×	898 1.7×	770 1.5×	83	3.7k

Countries citing papers authored by Subash C. Das

Since Specialization

Citations

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

Fields of papers citing papers by Subash C. Das

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Subash C. Das. 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 Subash C. Das. The network helps show where Subash C. Das may publish in the future.

Co-authorship network of co-authors of Subash C. Das

This figure shows the co-authorship network connecting the top 25 collaborators of Subash C. Das. A scholar is included among the top collaborators of Subash C. Das 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 Subash C. Das. Subash C. Das is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bell, Callum J., Nicholas P. Devitt, Faye Schilkey, et al.. (2024). Identification and quantitation of multiple variants in RNA virus genomes. Biology Methods and Protocols. 9(1). bpae004–bpae004.

Tsuji, Isamu, Fue Vang, Jill A. Livengood, et al.. (2022). Somatic Hypermutation and Framework Mutations of Variable Region Contribute to Anti-Zika Virus-Specific Monoclonal Antibody Binding and Function. Journal of Virology. 96(11). e0007122–e0007122. 5 indexed citations

DeMaso, Christina R., et al.. (2022). Specificity and Breadth of the Neutralizing Antibody Response to a Live-Attenuated Tetravalent Dengue Vaccine. The Journal of Infectious Diseases. 226(11). 1959–1963. 8 indexed citations

Raju, Nagarajan, Xiaoyan Zhan, Subash C. Das, et al.. (2022). Neutralization fingerprinting technology for characterizing polyclonal antibody responses to dengue vaccines. Cell Reports. 41(11). 111807–111807. 1 indexed citations

Kobayashi, Kyousuke, et al.. (2022). TAK − 021, an inactivated Enterovirus 71 vaccine candidate, provides cross-protection against heterologous sub-genogroups in human scavenger receptor B2 transgenic mice. Vaccine. 40(24). 3330–3337. 2 indexed citations

Tambyah, Paul Anantharajah, Jolene Oon, Shi-Hsia Hwa, et al.. (2019). An inactivated enterovirus 71 vaccine is safe and immunogenic in healthy adults: A phase I, double blind, randomized, placebo-controlled, study of two dosages. Vaccine. 37(31). 4344–4353. 14 indexed citations

Fuchs, Jeremy F., et al.. (2015). Efficacy of a Trivalent Hand, Foot, and Mouth Disease Vaccine against Enterovirus 71 and Coxsackieviruses A16 and A6 in Mice. Viruses. 7(11). 5919–5932. 42 indexed citations

Uraki, Ryuta, Subash C. Das, Masato Hatta, et al.. (2014). Hemozoin as a novel adjuvant for inactivated whole virion influenza vaccine. Vaccine. 32(41). 5295–5300. 12 indexed citations

Florek, Kelsey R., Jason T. Weinfurter, Sinthujan Jegaskanda, et al.. (2014). Modified Vaccinia Virus Ankara Encoding Influenza Virus Hemagglutinin Induces Heterosubtypic Immunity in Macaques. Journal of Virology. 88(22). 13418–13428. 38 indexed citations

10.

Das, Subash C., Jeremy F. Fuchs, M. Suresh, et al.. (2013). Deciphering the protective role of adaptive immunity to CHIKV/IRES a novel candidate vaccine against Chikungunya in the A129 mouse model. Vaccine. 31(33). 3353–3360. 69 indexed citations

11.

Brewoo, Joseph N., Tim D. Powell, Jeremy C. Jones, et al.. (2013). Cross-protective immunity against multiple influenza virus subtypes by a novel modified vaccinia Ankara (MVA) vectored vaccine in mice. Vaccine. 31(14). 1848–1855. 28 indexed citations

12.

Das, Subash C., Masato Hatta, Peter R. Wilker, et al.. (2012). Nanoemulsion W805EC improves immune responses upon intranasal delivery of an inactivated pandemic H1N1 influenza vaccine. Vaccine. 30(48). 6871–6877. 31 indexed citations

13.

Dinh, Phat X., Debasis Panda, Phani B. Das, et al.. (2012). A single amino acid change resulting in loss of fluorescence of eGFP in a viral fusion protein confers fitness and growth advantage to the recombinant vesicular stomatitis virus. Virology. 432(2). 460–469. 8 indexed citations

14.

Imai, Masaki, Tokiko Watanabe, Masato Hatta, et al.. (2012). Experimental adaptation of an influenza H5 HA confers respiratory droplet transmission to a reassortant H5 HA/H1N1 virus in ferrets. Nature. 486(7403). 420–428. 1090 indexed citations breakdown →

15.

Walsh, Kevin B., John R. Teijaro, Peter R. Wilker, et al.. (2011). Suppression of cytokine storm with a sphingosine analog provides protection against pathogenic influenza virus. Proceedings of the National Academy of Sciences. 108(29). 12018–12023. 195 indexed citations

16.

Otsuka, Motoyuki, Qing Jing, Philippe Georgel, et al.. (2007). Hypersusceptibility to Vesicular Stomatitis Virus Infection in Dicer1-Deficient Mice Is Due to Impaired miR24 and miR93 Expression. Immunity. 27(1). 123–134. 293 indexed citations

17.

Parida, Satya, Mana Mahapatra, Kumar Sai Sailesh, et al.. (2007). Rescue of a chimeric rinderpest virus with the nucleocapsid protein derived from peste-des-petits-ruminants virus: use as a marker vaccine. Journal of General Virology. 88(7). 2019–2027. 23 indexed citations

18.

Liu, Shuanghu, Israr-ul H. Ansari, Subash C. Das, & Asit K. Pattnaik. (2006). Insertion and deletion analyses identify regions of non-structural protein 5A of Hepatitis C virus that are dispensable for viral genome replication. Journal of General Virology. 87(2). 323–327. 27 indexed citations

19.

Zhang, Jun, et al.. (2004). The Latent Membrane Protein 1 of Epstein-Barr Virus Establishes an Antiviral State via Induction of Interferon-stimulated Genes. Journal of Biological Chemistry. 279(44). 46335–46342. 48 indexed citations

20.

Das, Subash C., Michael D. Baron, Michael A. Skinner, & Thomas Barrett. (2000). Improved technique for transient expression and negative strand virus rescue using fowlpox T7 recombinant virus in mammalian cells. Journal of Virological Methods. 89(1-2). 119–127. 19 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