Louise Edwards

1.0k total citations
16 papers, 434 citations indexed

About

Louise Edwards is a scholar working on Organic Chemistry, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Louise Edwards has authored 16 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 4 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Louise Edwards's work include Asymmetric Synthesis and Catalysis (6 papers), Migraine and Headache Studies (3 papers) and Synthetic Organic Chemistry Methods (3 papers). Louise Edwards is often cited by papers focused on Asymmetric Synthesis and Catalysis (6 papers), Migraine and Headache Studies (3 papers) and Synthetic Organic Chemistry Methods (3 papers). Louise Edwards collaborates with scholars based in Canada and Sweden. Louise Edwards's co-authors include Mark Lautens, William Tam, Charles E. Loader, Hugh J. Anderson, Alan J. Lough, Robert McDonald, Niall J. Gogan, Abdelmalik Slassi, Methvin Isaac and Sengen Sun and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Louise Edwards

16 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louise Edwards Canada 12 319 77 64 60 34 16 434
Ramazan Altundaş Türkiye 12 247 0.8× 124 1.6× 49 0.8× 56 0.9× 40 1.2× 45 384
Felice Liberatore Italy 14 233 0.7× 177 2.3× 51 0.8× 86 1.4× 47 1.4× 35 476
W. R. TULLY New Zealand 10 464 1.5× 161 2.1× 72 1.1× 32 0.5× 22 0.6× 18 622
L. Mark Hodges United States 16 410 1.3× 133 1.7× 135 2.1× 78 1.3× 40 1.2× 19 606
Anne G. Glenn United States 8 312 1.0× 50 0.6× 24 0.4× 41 0.7× 35 1.0× 12 395
Junichi Hibino Japan 8 273 0.9× 61 0.8× 48 0.8× 55 0.9× 80 2.4× 13 373
Anthony P. Guzikowski United States 11 148 0.5× 143 1.9× 81 1.3× 23 0.4× 79 2.3× 15 367
J. Lucchetti Belgium 11 466 1.5× 121 1.6× 110 1.7× 55 0.9× 66 1.9× 16 674
Sreeletha B. Panicker India 11 534 1.7× 84 1.1× 35 0.5× 87 1.4× 104 3.1× 15 579
Ren Nakao Japan 12 213 0.7× 54 0.7× 61 1.0× 82 1.4× 149 4.4× 33 343

Countries citing papers authored by Louise Edwards

Since Specialization
Citations

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

Fields of papers citing papers by Louise Edwards

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Edwards

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

All Works

16 of 16 papers shown
1.
Raboisson, Patrick, Anna Breitholtz‐Emanuelsson, Louise Edwards, et al.. (2012). Discovery and characterization of AZD9272 and AZD6538—Two novel mGluR5 negative allosteric modulators selected for clinical development. Bioorganic & Medicinal Chemistry Letters. 22(22). 6974–6979. 29 indexed citations
2.
Slassi, Abdelmalik, Methvin Isaac, Louise Edwards, et al.. (2005). Recent Advances in Non-Competitive mGlu5 Receptor Antagonists and their Potential Therapeutic Applications. Current Topics in Medicinal Chemistry. 5(9). 897–911. 42 indexed citations
3.
Demchyshyn, Lidia, et al.. (2003). 3-(2-Pyrrolidin-1-ylethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives as high affinity human 5-HT1B/1D ligands. Bioorganic & Medicinal Chemistry Letters. 14(3). 727–729. 1 indexed citations
4.
Isaac, Methvin, Louise Edwards, Julie M. Wilson, et al.. (2003). Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-Bioavailable 5-HT 1D agonists. Bioorganic & Medicinal Chemistry Letters. 13(24). 4409–4413. 5 indexed citations
5.
Demchyshyn, Lidia, et al.. (2003). (R)-3-(N-Methylpyrrolidin-2-ylmethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives as high affinity h5-HT1B/1D ligands. Bioorganic & Medicinal Chemistry Letters. 13(20). 3419–3421. 4 indexed citations
6.
Isaac, Methvin, Abdelmalik Slassi, Louise Edwards, et al.. (2000). Pyrrolo[3,2,1- ij ]quinoline derivatives, a 5-HT 2c receptor agonist with selectivity over the 5-HT 2a receptor: potential therapeutic applications for epilepsy and obesity. Bioorganic & Medicinal Chemistry Letters. 10(9). 919–921. 37 indexed citations
7.
Slassi, Abdelmalik, Louise Edwards, Charles Q. Meng, et al.. (2000). 5-Alkyltryptamine derivatives as highly selective and potent 5-HT1D receptor agonists. Bioorganic & Medicinal Chemistry Letters. 10(15). 1707–1709. 12 indexed citations
8.
Sun, Sengen, Louise Edwards, & Paul Harrison. (1998). Glycoluril † as an efficient molecular template for intramolecular Claisen-type condensations. Journal of the Chemical Society Perkin Transactions 1. 437–448. 19 indexed citations
9.
Edwards, Louise, Mark Lautens, & Alan J. Lough. (1997). The crystal structure and absolute configuration ofexo- 0130 0138 V 2 Rc,Ss)-(−)-8-p-tolylsulfinyltetracyclo[4.3.0.02,4.03,7]nonane. Journal of Chemical Crystallography. 27(8). 471–474. 2 indexed citations
10.
Lautens, Mark, Louise Edwards, William Tam, & Alan J. Lough. (1995). Nickel-catalyzed [2.pi. + 2.pi. + 2.pi.] (homo-Diels-Alder) and [2.pi. + 2.pi.] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes.. Journal of the American Chemical Society. 117(41). 10276–10291. 46 indexed citations
11.
Lautens, Mark, et al.. (1995). Cobalt-Catalyzed [2.pi. + 2.pi. + 2.pi.] (Homo-Diels-Alder) and [2.pi. + 2.pi. + 4.pi.] Cycloadditions of Bicyclo[2.2.1]hepta-2,5-dienes. Journal of the American Chemical Society. 117(26). 6863–6879. 76 indexed citations
12.
Lautens, Mark, William Tam, & Louise Edwards. (1994). Stereoselectivity in the homo-Diels–Alder reaction: effect of a remote 7-substituent on nickel-catalysed cycloadditions. Journal of the Chemical Society Perkin Transactions 1. 2143–2150. 17 indexed citations
13.
Lautens, Mark, William Tam, & Louise Edwards. (1992). Cobalt-catalyzed intramolecular homo Diels-Alder reactions. The Journal of Organic Chemistry. 57(1). 8–9. 24 indexed citations
14.
Lautens, Mark & Louise Edwards. (1991). Regiochemical control in the homo-Diels-Alder reaction: substituent effects. The Journal of Organic Chemistry. 56(12). 3761–3763. 19 indexed citations
15.
Lautens, Mark & Louise Edwards. (1989). Stereoselectivity in the Homo Diels-Alder Reaction. Tetrahedron Letters. 30(49). 6813–6816. 14 indexed citations
16.
Anderson, Hugh J., et al.. (1985). Pyrrole chemistry. XXVIII. Substitution reactions of 1-(phenylsulfonyl)pyrrole and some derivatives. Canadian Journal of Chemistry. 63(4). 896–902. 87 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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