James E. H. Day

527 citations
9 papers · 255 · h-index 7

Impact in

Papers in

    • Heat shock proteins research 3
    • Plant biochemistry and biosynthesis 2
    • Cell death mechanisms and regulation 2
    • ATP Synthase and ATPases Research 2
    • Catalytic C–H Functionalization Methods 2
    • Cyclopropane Reaction Mechanisms 1

James E. H. Day

9 papers receiving 242 citations

Peers

James E. H. Day
Comparison fields: 5 of 45
  • Toxicology 17
  • Organic Chemistry 89
  • Computational Theory and Mathematics 43
  • Molecular Biology 166
  • Pharmacology 32
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Aijun Lu China
Dušan Ružić Serbia
Tatiana McHardy United Kingdom
Jon J. Hangeland United States
Christine Kaiser United States
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Jean‐Michel Robert France
Rebecca A. Gallego United States
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Citations per field
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Citations per year

Countries citing papers authored by James E. H. Day

Since Specialization
Citations

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

Fields of papers citing papers by James E. H. Day

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James E. H. Day. 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 James E. H. Day. The network helps show where James E. H. Day may publish in the future.

Co-authors

The 25 scholars most cited alongside James E. H. Day, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with James E. H. Day Line = papers co-authored together James E. H. Day links everyone, so they are left out of the graph.

All Works

9 of 9 papers shown
#Work
1 201569
2 201757
3 200951
4 201030
5 201021
6 201116
7 20157
8 20223
9 20091

About James E. H. Day

James E. H. Day is a scholar working on Molecular Biology, Organic Chemistry, Pharmacology, Computational Theory and Mathematics and Cancer Research, having authored 9 papers that have together received 255 indexed citations. Recurring topics across this work include Heat shock proteins research (3 papers), Plant biochemistry and biosynthesis (2 papers), Cell death mechanisms and regulation (2 papers), Catalytic C–H Functionalization Methods (2 papers), Computational Drug Discovery Methods (2 papers), Microbial Natural Products and Biosynthesis (2 papers), ATP Synthase and ATPases Research (2 papers) and Cyclopropane Reaction Mechanisms (1 paper). The work is most often cited by research in Toxicology (17 citations), Organic Chemistry (89 citations), Computational Theory and Mathematics (43 citations), Molecular Biology (166 citations) and Pharmacology (32 citations). James E. H. Day has collaborated with scholars based in United Kingdom, Germany and Brazil. Frequent co-authors include Paul Workman, Christopher J. Moody, Michael Reader, Swee Y. Sharp, Wynne Aherne, Martin Rowlands, Pamela A. Williams, Christopher N. Johnson, Edward J. Lewis and Emiliano Tamanini. Their work appears in journals such as Journal of Medicinal Chemistry, Synlett, Chemistry - A European Journal, Organic & Biomolecular Chemistry and Bioorganic & Medicinal Chemistry.

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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