Sanjeev Narayanan

2.5k total citations
54 papers, 1.8k citations indexed

About

Sanjeev Narayanan is a scholar working on Infectious Diseases, Public Health, Environmental and Occupational Health and Endocrinology. According to data from OpenAlex, Sanjeev Narayanan has authored 54 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Infectious Diseases, 22 papers in Public Health, Environmental and Occupational Health and 11 papers in Endocrinology. Recurrent topics in Sanjeev Narayanan's work include Streptococcal Infections and Treatments (21 papers), Otolaryngology and Infectious Diseases (18 papers) and Clostridium difficile and Clostridium perfringens research (7 papers). Sanjeev Narayanan is often cited by papers focused on Streptococcal Infections and Treatments (21 papers), Otolaryngology and Infectious Diseases (18 papers) and Clostridium difficile and Clostridium perfringens research (7 papers). Sanjeev Narayanan collaborates with scholars based in United States, United Kingdom and Denmark. Sanjeev Narayanan's co-authors include T. G. Nagaraja, George C. Stewart, M. M. Chengappa, Kyeong‐Ok Chang, Yunjeong Kim, Vanessa Sperandio, Meredith M. Curtis, Ralph J. DeBerardinis, Zeping Hu and Greg Peterson and has published in prestigious journals such as PLoS ONE, Journal of Virology and Infection and Immunity.

In The Last Decade

Sanjeev Narayanan

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
Sanjeev Narayanan United States 19 654 587 305 281 254 54 1.8k
Mariano E. Fernández-Miyakawa Argentina 27 978 1.5× 590 1.0× 280 0.9× 417 1.5× 256 1.0× 73 2.5k
Márcia Giambiagi-deMarval Brazil 26 783 1.2× 956 1.6× 149 0.5× 262 0.9× 87 0.3× 82 1.8k
Merja Rantala Finland 21 467 0.7× 357 0.6× 147 0.5× 218 0.8× 136 0.5× 46 1.7k
Petra Lüthje Sweden 19 274 0.4× 490 0.8× 112 0.4× 184 0.7× 251 1.0× 34 1.5k
A. Satyanarayan Naidu Sweden 26 470 0.7× 741 1.3× 217 0.7× 735 2.6× 92 0.4× 54 2.2k
François Lebreton United States 23 947 1.4× 884 1.5× 164 0.5× 337 1.2× 223 0.9× 58 2.1k
Derek J. Fisher United States 24 992 1.5× 544 0.9× 321 1.1× 156 0.6× 112 0.4× 55 1.8k
M. Saminathan India 20 494 0.8× 230 0.4× 127 0.4× 269 1.0× 75 0.3× 84 1.8k
Shana R. Leopold United States 12 624 1.0× 1.2k 2.0× 97 0.3× 410 1.5× 560 2.2× 15 2.5k
Nathan Shankar United States 24 1.7k 2.5× 1.2k 2.1× 486 1.6× 577 2.1× 246 1.0× 44 2.9k

Countries citing papers authored by Sanjeev Narayanan

Since Specialization
Citations

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

Fields of papers citing papers by Sanjeev Narayanan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sanjeev Narayanan

This figure shows the co-authorship network connecting the top 25 collaborators of Sanjeev Narayanan. A scholar is included among the top collaborators of Sanjeev Narayanan 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 Sanjeev Narayanan. Sanjeev Narayanan 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.
AbdelKhalek, Ahmed, et al.. (2023). Cdc14 phosphatase contributes to cell wall integrity and pathogenesis in Candida albicans. Frontiers in Microbiology. 14. 1129155–1129155. 4 indexed citations
2.
Narayanan, Sanjeev, et al.. (2023). Albumin Deficiency Reduces Hepatic Steatosis and Improves Glucose Metabolism in a Mouse Model of Diet-Induced Obesity. Nutrients. 15(9). 2060–2060. 10 indexed citations
3.
Narayanan, Sanjeev, et al.. (2023). Outer-Membrane Vesicles of Fusobacterium necrophorum: A Proteomic, Lipidomic, and Functional Characterization. Microorganisms. 11(8). 2082–2082. 6 indexed citations
4.
Amachawadi, Raghavendra G., et al.. (2021). Leukotoxin production by Fusobacterium necrophorum strains in relation to severity of liver abscesses in cattle. Anaerobe. 69. 102344–102344. 11 indexed citations
5.
Kumar, Aman, Regan M. Russell, Reed Pifer, et al.. (2020). The Serotonin Neurotransmitter Modulates Virulence of Enteric Pathogens. Cell Host & Microbe. 28(1). 41–53.e8. 91 indexed citations
6.
Amachawadi, Raghavendra G., et al.. (2019). Leukotoxic activity of Fusobacterium necrophorum of cattle origin. Anaerobe. 56. 51–56. 14 indexed citations
7.
Menon, Swapna, et al.. (2018). Characterization of Fusobacterium necrophorum subsp. necrophorum outer membrane proteins. Anaerobe. 50. 101–105. 3 indexed citations
8.
Basel, Matthew T., Sanjeev Narayanan, Chanran Ganta, et al.. (2017). Developing a xenograft human tumor model in immunocompetent mice. Cancer Letters. 412. 256–263. 14 indexed citations
9.
Wendel, Sebastian O., Hamad Alshetaiwi, Tej B. Shrestha, et al.. (2015). Cell Based Drug Delivery: Micrococcus luteus Loaded Neutrophils as Chlorhexidine Delivery Vehicles in a Mouse Model of Liver Abscesses in Cattle. PLoS ONE. 10(5). e0128144–e0128144. 26 indexed citations
10.
11.
Curtis, Meredith M., et al.. (2014). The Gut Commensal Bacteroides thetaiotaomicron Exacerbates Enteric Infection through Modification of the Metabolic Landscape. Cell Host & Microbe. 16(6). 759–769. 231 indexed citations
12.
Lawrence, Mark L., Kate S. KuKanich, Butch KuKanich, et al.. (2013). Effect of cefovecin on the fecal flora of healthy dogs. The Veterinary Journal. 198(1). 259–266. 23 indexed citations
13.
Kumar, Amit, et al.. (2012). Adhesion of Fusobacterium necrophorum to bovine endothelial cells is mediated by outer membrane proteins. Veterinary Microbiology. 162(2-4). 813–818. 14 indexed citations
14.
Peterson, Greg, et al.. (2011). Catecholamines increase conjugative gene transfer between enteric bacteria. Microbial Pathogenesis. 51(1-2). 1–8. 49 indexed citations
15.
Jacob, Megan E., J. T. Fox, T. G. Nagaraja, et al.. (2010). Effects of Feeding Elevated Concentrations of Copper and Zinc on the Antimicrobial Susceptibilities of Fecal Bacteria in Feedlot Cattle. Foodborne Pathogens and Disease. 7(6). 643–648. 39 indexed citations
16.
Amachawadi, Raghavendra G., Megan E. Jacob, Xiaorong Shi, et al.. (2010). Occurrence of tcrB , a Transferable Copper Resistance Gene, in Fecal Enterococci of Swine. Foodborne Pathogens and Disease. 7(9). 1089–1097. 26 indexed citations
17.
18.
Stewart, George C., et al.. (2007). Leukotoxin operon and differential expressions of the leukotoxin gene in bovine Fusobacterium necrophorum subspecies. Anaerobe. 14(1). 13–18. 16 indexed citations
19.
Narayanan, Sanjeev, M. M. Chengappa, George C. Stewart, & T. G. Nagaraja. (2003). Immunogenicity and protective effects of truncated recombinant leukotoxin proteins of Fusobacterium necrophorum in mice. Veterinary Microbiology. 93(4). 335–347. 21 indexed citations
20.
Narayanan, Sanjeev, T. G. Nagaraja, M. M. Chengappa, & George C. Stewart. (2001). Electrophoretic mobility anomalies associated with PCR amplification of the intergenic spacer region between 16S and 23S ribosomal RNA genes of Fusobacterium necrophorum. Journal of Microbiological Methods. 46(2). 165–169. 8 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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