Christopher A. Ramsden

5.4k total citations
160 papers, 3.6k citations indexed

About

Christopher A. Ramsden is a scholar working on Organic Chemistry, Molecular Biology and Cell Biology. According to data from OpenAlex, Christopher A. Ramsden has authored 160 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Organic Chemistry, 28 papers in Molecular Biology and 23 papers in Cell Biology. Recurrent topics in Christopher A. Ramsden's work include Synthesis and Characterization of Heterocyclic Compounds (26 papers), Synthesis and Biological Evaluation (23 papers) and melanin and skin pigmentation (22 papers). Christopher A. Ramsden is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (26 papers), Synthesis and Biological Evaluation (23 papers) and melanin and skin pigmentation (22 papers). Christopher A. Ramsden collaborates with scholars based in United Kingdom, Poland and United States. Christopher A. Ramsden's co-authors include Patrick A. Riley, Edward J. Land, W. David Ollis, Christopher G. Newton, Christopher J. Cooksey, Wojciech P. Ozimiński, Michael J. S. Dewar, Peter J. Garratt, Donald H. Lo and Stan Pavel and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Journal of Biological Chemistry.

In The Last Decade

Christopher A. Ramsden

154 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher A. Ramsden United Kingdom 28 1.9k 974 697 635 324 160 3.6k
José Berná Spain 28 2.1k 1.1× 314 0.3× 783 1.1× 238 0.4× 886 2.7× 114 3.2k
Raffaele P. Bonomo Italy 30 649 0.3× 105 0.1× 788 1.1× 317 0.5× 460 1.4× 117 2.8k
Atanu Barik India 23 584 0.3× 88 0.1× 969 1.4× 140 0.2× 322 1.0× 52 2.4k
Timothy E. Machonkin United States 15 493 0.3× 451 0.5× 890 1.3× 376 0.6× 722 2.2× 22 3.8k
Roger H. Bisby United Kingdom 28 685 0.4× 79 0.1× 891 1.3× 135 0.2× 343 1.1× 90 2.3k
Carl H. Schiesser Australia 34 3.6k 1.9× 59 0.1× 557 0.8× 212 0.3× 261 0.8× 194 4.5k
Graziella Vecchio Italy 35 1.4k 0.7× 148 0.2× 949 1.4× 192 0.3× 537 1.7× 152 3.8k
Yehuda Mazur Israel 33 1.3k 0.7× 86 0.1× 993 1.4× 60 0.1× 439 1.4× 164 3.2k
Catherine Belle France 29 651 0.3× 317 0.3× 420 0.6× 263 0.4× 599 1.8× 68 2.6k
Andrea Goti Italy 44 6.4k 3.4× 108 0.1× 2.3k 3.3× 85 0.1× 300 0.9× 210 7.3k

Countries citing papers authored by Christopher A. Ramsden

Since Specialization
Citations

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

Fields of papers citing papers by Christopher A. Ramsden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher A. Ramsden. 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 Christopher A. Ramsden. The network helps show where Christopher A. Ramsden may publish in the future.

Co-authorship network of co-authors of Christopher A. Ramsden

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher A. Ramsden. A scholar is included among the top collaborators of Christopher A. Ramsden 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 Christopher A. Ramsden. Christopher A. Ramsden 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.
Ozimiński, Wojciech P. & Christopher A. Ramsden. (2024). A DFT study of mono-, bi- and tricyclic examples ofsemi-conjugated heterocyclic mesomeric betaines. ARKIVOC. 2024(1). 1 indexed citations
2.
Ramsden, Christopher A. & Patrick A. Riley. (2014). Mechanistic aspects of the tyrosinase oxidation of hydroquinone. Bioorganic & Medicinal Chemistry Letters. 24(11). 2463–2464. 13 indexed citations
3.
Stratford, Michael R.L., Christopher A. Ramsden, & Patrick A. Riley. (2012). The influence of hydroquinone on tyrosinase kinetics. Bioorganic & Medicinal Chemistry. 20(14). 4364–4370. 29 indexed citations
4.
Krygowski, Tadeusz M., Wojciech P. Ozimiński, & Christopher A. Ramsden. (2010). Sigma- and pi- electron structure of aza-azoles. Journal of Molecular Modeling. 17(6). 1427–1433. 18 indexed citations
5.
Ramsden, Christopher A., Michael R.L. Stratford, & Patrick A. Riley. (2009). The influence of catechol structure on the suicide-inactivation of tyrosinase. Organic & Biomolecular Chemistry. 7(17). 3388–3388. 24 indexed citations
6.
Land, Edward J., Almudena Perona, Christopher A. Ramsden, & Patrick A. Riley. (2009). Dopamine quinone chemistry: a study of the influence of amide, amidine and guanidine substituents [-NH-CX-Y] on the mode of reaction. Organic & Biomolecular Chemistry. 7(5). 944–944. 11 indexed citations
7.
Jones, Gurnos & Christopher A. Ramsden. (2008). Five-membered rings with one heteroatom together with their benzo and other carbocyclic-fused derivatives. Elsevier eBooks. 2 indexed citations
8.
Borovanský, J, Ruth Edge, Edward J. Land, et al.. (2006). Mechanistic studies of melanogenesis: the influence of N‐substitution on dopamine quinone cyclization. Pigment Cell Research. 19(2). 170–178. 25 indexed citations
9.
Land, Edward J., Almudena Perona, Christopher A. Ramsden, & Patrick A. Riley. (2005). Oxidation of N-substituted dopamine derivatives: irreversible formation of a spirocyclic product. Organic & Biomolecular Chemistry. 3(13). 2387–2387. 9 indexed citations
10.
Land, Edward J., Christopher A. Ramsden, & Patrick A. Riley. (2004). Quinone Chemistry and Melanogenesis. Methods in enzymology on CD-ROM/Methods in enzymology. 378. 88–109. 95 indexed citations
11.
Land, Edward J., et al.. (2003). Formation of para-quinomethanes via 4-aminobutylcatechol oxidation and ortho-quinone tautomerism. Organic & Biomolecular Chemistry. 1(17). 3120–3120. 12 indexed citations
12.
Land, Edward J., et al.. (2003). Mechanistic Studies of Catechol Generation from Secondary Quinone Amines Relevant to Indole Formation and Tyrosinase Activation. Pigment Cell Research. 16(4). 397–406. 12 indexed citations
13.
Ramsden, Christopher A., et al.. (2002). Synthesis of Pyridine-stretched 2′-Deoxynucleosides. Synlett. 2002(9). 1483–1486. 2 indexed citations
14.
Land, Edward J., Christopher A. Ramsden, & Patrick A. Riley. (2001). Pulse radiolysis studies of ortho-quinone chemistry relevant to melanogenesis. Journal of Photochemistry and Photobiology B Biology. 64(2-3). 123–135. 25 indexed citations
15.
Morgan, Noel G., et al.. (1999). Imidazolines and Pancreatic Hormone Secretiona. Annals of the New York Academy of Sciences. 881(1). 217–228. 54 indexed citations
16.
Chan, Susan L.F., et al.. (1997). Evidence that the ability of imidazoline compounds to stimulate insulin secretion is not due to interaction with σ receptors. European Journal of Pharmacology. 323(2-3). 241–244. 20 indexed citations
18.
Ramsden, Christopher A.. (1996). Fused five- and six-membered rings without ring junction heteroatoms. Pergamon eBooks. 1 indexed citations
19.
Ramsden, Christopher A., et al.. (1995). Rearrangement and cyclo-α-elimination of N-substituted amidines using (diacetoxyiodo)benzene. Journal of the Chemical Society Perkin Transactions 1. 615–617. 30 indexed citations
20.
Ollis, W. David & Christopher A. Ramsden. (1974). Cyclic meso-ionic compounds. Part XII. Synthesis, spectroscopic properties, and chemistry of 1,3,4-oxadiazolium-2-aminides. Journal of the Chemical Society Perkin Transactions 1. 642–642. 4 indexed citations

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