Jayashree Ray

1.8k total citations
19 papers, 775 citations indexed

About

Jayashree Ray is a scholar working on Molecular Biology, Ecology and Environmental Chemistry. According to data from OpenAlex, Jayashree Ray has authored 19 papers receiving a total of 775 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Ecology and 4 papers in Environmental Chemistry. Recurrent topics in Jayashree Ray's work include Microbial Fuel Cells and Bioremediation (4 papers), Microbial Community Ecology and Physiology (3 papers) and Mine drainage and remediation techniques (3 papers). Jayashree Ray is often cited by papers focused on Microbial Fuel Cells and Bioremediation (4 papers), Microbial Community Ecology and Physiology (3 papers) and Mine drainage and remediation techniques (3 papers). Jayashree Ray collaborates with scholars based in United States, India and France. Jayashree Ray's co-authors include Adam M. Deutschbauer, Adam P. Arkin, Jennifer V. Kuehl, Morgan N. Price, Michael E. Kurczy, Caroline H. Johnson, Gary J. Patti, Junhua Wang, Duane Rinehart and Julijana Ivanišević and has published in prestigious journals such as Analytical Chemistry, Applied and Environmental Microbiology and Biochemistry.

In The Last Decade

Jayashree Ray

19 papers receiving 773 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jayashree Ray United States 12 526 132 131 86 64 19 775
Christopher Bräsen Germany 19 656 1.2× 164 1.2× 152 1.2× 68 0.8× 24 0.4× 34 942
Kazuaki Yoshimune Japan 16 718 1.4× 63 0.5× 113 0.9× 82 1.0× 26 0.4× 53 972
Satoshi Ezaki Japan 15 726 1.4× 121 0.9× 158 1.2× 57 0.7× 26 0.4× 25 974
Shinichi Nagata Japan 18 421 0.8× 79 0.6× 207 1.6× 102 1.2× 25 0.4× 59 866
Akio Tonouchi Japan 15 346 0.7× 84 0.6× 84 0.6× 181 2.1× 34 0.5× 52 658
N. Loffhagen Germany 17 424 0.8× 70 0.5× 91 0.7× 56 0.7× 51 0.8× 39 705
Uta Breuer Germany 15 508 1.0× 185 1.4× 75 0.6× 71 0.8× 18 0.3× 27 778
Takeru Ishige Japan 15 689 1.3× 190 1.4× 92 0.7× 46 0.5× 38 0.6× 17 908
LV Ai-ping China 14 550 1.0× 60 0.5× 131 1.0× 115 1.3× 11 0.2× 56 853

Countries citing papers authored by Jayashree Ray

Since Specialization
Citations

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

Fields of papers citing papers by Jayashree Ray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jayashree Ray

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

All Works

19 of 19 papers shown
1.
Baudin, Maël, Sébastien Carrère, Olivier Bouchez, et al.. (2022). Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection. New Phytologist. 236(1). 235–248. 14 indexed citations
2.
Sahoo, Rudra Narayan, et al.. (2021). Celecoxib Crystallized from Hydrophilic Polymeric Solutions Showed Modified Crystalline Behavior with an Improved Dissolution Profile. Assay and Drug Development Technologies. 19(4). 237–245. 5 indexed citations
3.
Liu, Hualan, Anthony L. Shiver, Morgan N. Price, et al.. (2021). Functional genetics of human gut commensal Bacteroides thetaiotaomicron reveals metabolic requirements for growth across environments. Cell Reports. 34(9). 108789–108789. 90 indexed citations
4.
Wall, Judy D., Grant M. Zane, Jennifer V. Kuehl, et al.. (2021). Deletion Mutants, Archived Transposon Library, and Tagged Protein Constructs of the Model Sulfate-Reducing Bacterium Desulfovibrio vulgaris Hildenborough. Microbiology Resource Announcements. 10(11). 7 indexed citations
5.
Price, Morgan N., Jayashree Ray, Anthony T. Iavarone, et al.. (2019). Oxidative Pathways of Deoxyribose and Deoxyribonate Catabolism. mSystems. 4(1). 26 indexed citations
6.
Dougherty, Michael J., Adam M. Deutschbauer, Fathi Karouia, et al.. (2019). Results of the Micro-12 Flight Experiment: Effects of Microgravity on Shewanella oneidensis MR-1. NASA Technical Reports Server (NASA). 2 indexed citations
7.
Liu, Hualan, Morgan N. Price, R. Jordan Waters, et al.. (2018). Magic Pools: Parallel Assessment of Transposon Delivery Vectors in Bacteria. mSystems. 3(1). 32 indexed citations
8.
Rand, Jacqueline M., Tippapha Pisithkul, Ryan L. Clark, et al.. (2017). A metabolic pathway for catabolizing levulinic acid in bacteria. Nature Microbiology. 2(12). 1624–1634. 78 indexed citations
9.
Kosina, Suzanne M., M. Danielewicz, Jayashree Ray, et al.. (2016). Exometabolomics Assisted Design and Validation of Synthetic Obligate Mutualism. ACS Synthetic Biology. 5(7). 569–576. 25 indexed citations
10.
Ray, Jayashree, R. Jordan Waters, Jeffrey M. Skerker, et al.. (2015). Complete Genome Sequence of Cupriavidus basilensis 4G11, Isolated from the Oak Ridge Field Research Center Site. Genome Announcements. 3(3). 15 indexed citations
11.
Thorgersen, Michael P., W. Andrew Lancaster, Brian J. Vaccaro, et al.. (2015). Molybdenum Availability Is Key to Nitrate Removal in Contaminated Groundwater Environments. Applied and Environmental Microbiology. 81(15). 4976–4983. 30 indexed citations
12.
Price, Morgan N., Jayashree Ray, Kelly M. Wetmore, et al.. (2014). The genetic basis of energy conservation in the sulfate-reducing bacterium Desulfovibrio alaskensis G20. Frontiers in Microbiology. 5. 577–577. 50 indexed citations
13.
Ray, Jayashree, Kimberly L. Keller, Marcin Zemla, et al.. (2014). Exploring the role of CheA3 in Desulfovibrio vulgaris Hildenborough motility. Frontiers in Microbiology. 5. 77–77. 9 indexed citations
14.
Kuehl, Jennifer V., Morgan N. Price, Jayashree Ray, et al.. (2014). Functional Genomics with a Comprehensive Library of Transposon Mutants for the Sulfate-Reducing Bacterium Desulfovibrio alaskensis G20. mBio. 5(3). e01041–14. 44 indexed citations
16.
Gowda, Harsha, Julijana Ivanišević, Caroline H. Johnson, et al.. (2014). Interactive XCMS Online: Simplifying Advanced Metabolomic Data Processing and Subsequent Statistical Analyses. Analytical Chemistry. 86(14). 6931–6939. 292 indexed citations
17.
Szundi, István, Sylvia K. Choi, William J. McDonald, et al.. (2014). Kinetics and Intermediates of the Reaction of Fully Reduced Escherichia coli bo3 Ubiquinol Oxidase with O2. Biochemistry. 53(33). 5393–5404. 7 indexed citations
18.
Szundi, István, William J. McDonald, Jayashree Ray, et al.. (2012). Spectral Identification of Intermediates Generated during the Reaction of Dioxygen with the Wild-Type and EQ(I-286) Mutant of Rhodobacter sphaeroides Cytochrome c Oxidase. Biochemistry. 51(46). 9302–9311. 7 indexed citations
19.
Szundi, István, Jayashree Ray, Ashtamurthy S. Pawate, Robert B. Gennis, & Ólöf Einarsdóttir. (2007). Flash-Photolysis of Fully Reduced and Mixed-Valence CO-Bound Rhodobacter sphaeroides Cytochrome c Oxidase:  Heme Spectral Shifts. Biochemistry. 46(44). 12568–12578. 10 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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