Narayanan Veeraraghavan

6.9k total citations · 2 hit papers
40 papers, 2.0k citations indexed

About

Narayanan Veeraraghavan is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Narayanan Veeraraghavan has authored 40 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Epidemiology and 12 papers in Genetics. Recurrent topics in Narayanan Veeraraghavan's work include Rabies epidemiology and control (8 papers), Genomics and Rare Diseases (7 papers) and Virology and Viral Diseases (5 papers). Narayanan Veeraraghavan is often cited by papers focused on Rabies epidemiology and control (8 papers), Genomics and Rare Diseases (7 papers) and Virology and Viral Diseases (5 papers). Narayanan Veeraraghavan collaborates with scholars based in United States, United Kingdom and Netherlands. Narayanan Veeraraghavan's co-authors include Kerry O’Donnell, David M. Geiser, Seogchan Kang, Izabela Makałowska, María del Mar Jiménez-Gasco, Gretchen A. Kuldau, Todd J. Ward, Ning Zhang, Stephen F. Kingsmore and Michelle M. Clark and has published in prestigious journals such as Journal of the American Chemical Society, Nature Genetics and PLoS ONE.

In The Last Decade

Narayanan Veeraraghavan

37 papers receiving 1.9k 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.

FUSARIUM-ID v. 1.0: A DNA Sequence Database for Identifying Fusarium

2004 850 citations Narayanan Veeraraghavan et al. profile →
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

2018 280 citations Lauge Farnaes, Amber Hildreth et al. npj Genomic Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Narayanan Veeraraghavan United States	15	822	810	614	550	119	40	2.0k
Michael Cancilla Australia	15	209 0.3×	637 0.8×	1.3k 2.2×	426 0.8×	155 1.3×	16	1.9k
Genki Kimura Japan	25	181 0.2×	156 0.2×	1.1k 1.7×	492 0.9×	239 2.0×	129	2.2k
Richard Coulson United Kingdom	23	319 0.4×	219 0.3×	1.4k 2.2×	234 0.4×	307 2.6×	30	2.3k
Connie Wong United States	19	257 0.3×	97 0.1×	733 1.2×	230 0.4×	45 0.4×	44	1.4k
Matthew Heidtman United States	14	349 0.4×	172 0.2×	1.6k 2.7×	220 0.4×	210 1.8×	14	2.4k
D.A. Miller United States	29	78 0.1×	1.3k 1.6×	1.8k 2.9×	1.1k 2.0×	74 0.6×	74	2.8k
Simon K. Chan Canada	15	203 0.2×	147 0.2×	762 1.2×	166 0.3×	152 1.3×	24	1.4k
Kira K. Lueders United States	27	93 0.1×	539 0.7×	1.7k 2.8×	506 0.9×	91 0.8×	58	2.3k
S.-H. Yeh Taiwan	10	311 0.4×	160 0.2×	1.3k 2.1×	158 0.3×	659 5.5×	16	2.2k
Xiaofeng Wang China	26	137 0.2×	810 1.0×	985 1.6×	100 0.2×	162 1.4×	91	2.2k

Countries citing papers authored by Narayanan Veeraraghavan

Since Specialization

Citations

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

Fields of papers citing papers by Narayanan Veeraraghavan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Narayanan Veeraraghavan

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

Sweeney, Nathaly M., Shareef Nahas, Shimul Chowdhury, et al.. (2021). Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. npj Genomic Medicine. 6(1). 29–29. 49 indexed citations

James, Kiely N., Michelle M. Clark, Cyrielle Kint, et al.. (2020). Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses. npj Genomic Medicine. 5(1). 33–33. 32 indexed citations

Farnaes, Lauge, Amber Hildreth, Nathaly M. Sweeney, et al.. (2018). Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization. npj Genomic Medicine. 3(1). 10–10. 280 indexed citations breakdown →

Kim, Jihoon, Chisato Shimizu, Stephen F. Kingsmore, et al.. (2017). Whole genome sequencing of an African American family highlights toll like receptor 6 variants in Kawasaki disease susceptibility. PLoS ONE. 12(2). e0170977–e0170977. 13 indexed citations

Eicher, John D., Ming‐Huei Chen, Achilleas Pitsillides, et al.. (2017). Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation. Thrombosis and Haemostasis. 117(6). 1083–1092. 8 indexed citations

Huang, Zhuoyi, Navin Rustagi, Narayanan Veeraraghavan, et al.. (2016). A hybrid computational strategy to address WGS variant analysis in >5000 samples. BMC Bioinformatics. 17(1). 361–361. 5 indexed citations

Polfus, Linda M., Eric Boerwinkle, Richard A. Gibbs, et al.. (2016). Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome. Molecular Case Studies. 2(6). a001255–a001255. 9 indexed citations

Li, Alexander, Alanna C. Morrison, Christie Kovar, et al.. (2015). Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease. Nature Genetics. 47(6). 640–642. 33 indexed citations

Campbell, Ian M., Tomasz Gambin, Shalini N. Jhangiani, et al.. (2015). Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses. Human Mutation. 37(3). 231–234. 12 indexed citations

10.

Reid, Jeffrey G., Andrew Carroll, Narayanan Veeraraghavan, et al.. (2014). Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline. BMC Bioinformatics. 15(1). 30–30. 111 indexed citations

11.

Swei, Andrea, Brandy J. Russell, Samia N. Naccache, et al.. (2013). The Genome Sequence of Lone Star Virus, a Highly Divergent Bunyavirus Found in the Amblyomma americanum Tick. PLoS ONE. 8(4). e62083–e62083. 40 indexed citations

12.

Veeraraghavan, Narayanan, et al.. (2011). Metal Binding Motif in the Active Site of the HDV Ribozyme Binds Divalent and Monovalent Ions. Biochemistry. 50(13). 2672–2682. 44 indexed citations

13.

Veeraraghavan, Narayanan, Abir Ganguly, Barbara L. Golden, Philip C. Bevilacqua, & Sharon Hammes‐Schiffer. (2011). Mechanistic Strategies in the HDV Ribozyme: Chelated and Diffuse Metal Ion Interactions and Active Site Protonation. The Journal of Physical Chemistry B. 115(25). 8346–8357. 31 indexed citations

14.

Veeraraghavan, Narayanan, Philip C. Bevilacqua, & Sharon Hammes‐Schiffer. (2010). Long-Distance Communication in the HDV Ribozyme: Insights from Molecular Dynamics and Experiments. Journal of Molecular Biology. 402(1). 278–291. 22 indexed citations

15.

Veeraraghavan, Narayanan. (1961). Influenza virus isolations at the Government of India Influenza Centre, Coonoor, during 1950-60.. PubMed. 24. 679–86. 3 indexed citations

16.

Veeraraghavan, Narayanan, et al.. (1961). Antigenic value of lyophilized phenolized antirabies vaccine.. PubMed. 25. 115–7. 1 indexed citations

17.

Veeraraghavan, Narayanan. (1959). Improvement of the antigenicity of antirabies vaccine by pooling checked by post-challenge vaccination of guinea-pigs.. PubMed. 20(1). 121–31. 5 indexed citations

18.

Veeraraghavan, Narayanan, et al.. (1958). Virus content of brains and submaxillary glands and occurrence of Negri bodies in animals suspected of having died of natural rabies infection.. PubMed. 18(3). 469–71. 2 indexed citations

19.

Veeraraghavan, Narayanan & P. K. Sukumaran. (1954). Q fever survey in the Nilgiris and coimbatore districts of the Madras State.. PubMed. 42(1). 5–7. 1 indexed citations

20.

Veeraraghavan, Narayanan. (1954). Phenolized vaccine treatment of people exposed to rabies in Southern India.. PubMed. 10(5). 789–96. 11 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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