James E. H. Day

522 total citations
9 papers, 251 citations indexed

About

James E. H. Day is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, James E. H. Day has authored 9 papers receiving a total of 251 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Organic Chemistry and 2 papers in Pharmacology. Recurrent topics in James E. H. Day's work include Heat shock proteins research (3 papers), Cell death mechanisms and regulation (2 papers) and Catalytic C–H Functionalization Methods (2 papers). James E. H. Day is often cited by papers focused on Heat shock proteins research (3 papers), Cell death mechanisms and regulation (2 papers) and Catalytic C–H Functionalization Methods (2 papers). James E. H. Day collaborates with scholars based in United Kingdom, Brazil and Germany. James E. H. Day's co-authors include Paul Workman, Christopher J. Moody, Swee Y. Sharp, Wynne Aherne, Martin Rowlands, Nicola E. Wilsher, Pamela A. Williams, George A. Ward, Christopher N. Johnson and Aman Iqbal and has published in prestigious journals such as Journal of Medicinal Chemistry, Chemistry - A European Journal and Bioorganic & Medicinal Chemistry.

In The Last Decade

James E. H. Day

9 papers receiving 238 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James E. H. Day United Kingdom	7	167	88	42	32	27	9	251
Rebecca A. Gallego United States	4	157 0.9×	94 1.1×	59 1.4×	18 0.6×	46 1.7×	5	267
Divya Pingili India	6	169 1.0×	114 1.3×	54 1.3×	25 0.8×	59 2.2×	21	299
Yoshiaki Washio United Kingdom	8	192 1.1×	215 2.4×	51 1.2×	30 0.9×	50 1.9×	11	373
Aman Iqbal United Kingdom	8	199 1.2×	40 0.5×	28 0.7×	41 1.3×	25 0.9×	9	242
Tatiana McHardy United Kingdom	8	281 1.7×	148 1.7×	72 1.7×	26 0.8×	62 2.3×	11	389
Jon J. Hangeland United States	10	241 1.4×	163 1.9×	22 0.5×	33 1.0×	25 0.9×	17	396
Theresa R. Phillips United Kingdom	5	159 1.0×	76 0.9×	80 1.9×	19 0.6×	10 0.4×	6	224
Anke Mueller‐Fahrnow France	6	138 0.8×	53 0.6×	45 1.1×	20 0.6×	25 0.9×	8	219
Jesús Vázquez Spain	10	265 1.6×	100 1.1×	54 1.3×	21 0.7×	65 2.4×	12	368
Y. Carrasco United States	7	225 1.3×	91 1.0×	15 0.4×	39 1.2×	56 2.1×	10	336

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-authorship network of co-authors of James E. H. Day

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

All Works

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9 of 9 papers shown

Vessecchi, Ricardo, et al.. (2022). Growth vector elaboration of fragments: regioselective functionalization of 5-hydroxy-6-azaindazole and 3-hydroxy-2,6-naphthyridine. Organic & Biomolecular Chemistry. 20(37). 7483–7490. 3 indexed citations

Tamanini, Emiliano, Ildiko M. Buck, Gianni Chessari, et al.. (2017). Discovery of a Potent Nonpeptidomimetic, Small-Molecule Antagonist of Cellular Inhibitor of Apoptosis Protein 1 (cIAP1) and X-Linked Inhibitor of Apoptosis Protein (XIAP). Journal of Medicinal Chemistry. 60(11). 4611–4625. 57 indexed citations

Chessari, Gianni, Ildiko M. Buck, James E. H. Day, et al.. (2015). Fragment-Based Drug Discovery Targeting Inhibitor of Apoptosis Proteins: Discovery of a Non-Alanine Lead Series with Dual Activity Against cIAP1 and XIAP. Journal of Medicinal Chemistry. 58(16). 6574–6588. 67 indexed citations

Day, James E. H., et al.. (2015). The Synthesis of 3,3-Dimethyl Aza- and Diazaindolines Using a Palladium-Catalysed Intramolecular Reductive Cyclisation. Synlett. 26(18). 2570–2574. 7 indexed citations

Day, James E. H., Swee Y. Sharp, Martin Rowlands, et al.. (2011). Targeting the Hsp90 Molecular Chaperone with Novel Macrolactams. Synthesis, Structural, Binding, and Cellular Studies. ACS Chemical Biology. 6(12). 1339–1347. 16 indexed citations

Day, James E. H., Swee Y. Sharp, Martin Rowlands, et al.. (2010). Inhibition of Hsp90 with Resorcylic Acid Macrolactones: Synthesis and Binding Studies. Chemistry - A European Journal. 16(34). 10366–10372. 21 indexed citations

Day, James E. H., Swee Y. Sharp, Martin Rowlands, et al.. (2010). Targeting the Hsp90 Chaperone: Synthesis of Novel Resorcylic Acid Macrolactone Inhibitors of Hsp90. Chemistry - A European Journal. 16(9). 2758–2763. 30 indexed citations

Reynisson, Jóhannes, William Court, James E. H. Day, et al.. (2009). The identification of novel PLC-γ inhibitors using virtual high throughput screening. Bioorganic & Medicinal Chemistry. 17(8). 3169–3176. 49 indexed citations

Moody, Christopher J., James E. H. Day, & Alexander J. Blake. (2009). An Improved Synthesis of ResorcylicAcid Macrolactone Inhibitors of Hsp90. Synlett. 2009(10). 1567–1570. 1 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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