David Noble

437 total citations
19 papers, 333 citations indexed

About

David Noble is a scholar working on Molecular Biology, Spectroscopy and Pharmacology. According to data from OpenAlex, David Noble has authored 19 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Spectroscopy and 4 papers in Pharmacology. Recurrent topics in David Noble's work include Plant biochemistry and biosynthesis (5 papers), Microbial Natural Products and Biosynthesis (4 papers) and Natural product bioactivities and synthesis (4 papers). David Noble is often cited by papers focused on Plant biochemistry and biosynthesis (5 papers), Microbial Natural Products and Biosynthesis (4 papers) and Natural product bioactivities and synthesis (4 papers). David Noble collaborates with scholars based in United Kingdom, United States and Germany. David Noble's co-authors include Philip J. Sidebottom, Brian A.M. Rudd, Michael J. Dawson, Richard J. P. Cannell, A.J. Horsewill, Graham Foster, Wen‐Wei Wu, Graham A. Webb, S. J. Lane and Carol Jones and has published in prestigious journals such as Analytical Biochemistry, Chemical Physics Letters and Tetrahedron Letters.

In The Last Decade

David Noble

18 papers receiving 301 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Noble United Kingdom 14 202 94 78 61 39 19 333
Charles N. Tetzlaff United States 11 439 2.2× 171 1.8× 50 0.6× 33 0.5× 26 0.7× 13 502
Peter Merseburger Belgium 4 228 1.1× 95 1.0× 41 0.5× 33 0.5× 15 0.4× 11 377
Jörg Fohrer Germany 13 245 1.2× 102 1.1× 116 1.5× 20 0.3× 37 0.9× 26 377
Tze‐Ming Chan United States 11 131 0.6× 83 0.9× 104 1.3× 11 0.2× 26 0.7× 19 330
Nobuya Tokutake Japan 14 316 1.6× 51 0.5× 104 1.3× 39 0.6× 19 0.5× 23 446
Christopher J. Flynn United States 6 128 0.6× 54 0.6× 103 1.3× 27 0.4× 18 0.5× 6 376
Peter L. Bartner United States 12 350 1.7× 86 0.9× 124 1.6× 286 4.7× 31 0.8× 27 605
О. В. Андреева Russia 14 290 1.4× 44 0.5× 221 2.8× 62 1.0× 15 0.4× 69 656
K.E. Merkel United States 12 153 0.8× 99 1.1× 102 1.3× 50 0.8× 14 0.4× 17 318
Friedrich A. Gollmick Germany 14 322 1.6× 192 2.0× 196 2.5× 44 0.7× 79 2.0× 25 650

Countries citing papers authored by David Noble

Since Specialization
Citations

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

Fields of papers citing papers by David Noble

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Noble

This figure shows the co-authorship network connecting the top 25 collaborators of David Noble. A scholar is included among the top collaborators of David Noble 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 David Noble. David Noble 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.
Noble, David, Joan E. Adamo, Oliver Serang, et al.. (2025). AlphaBind, a domain-specific model to predict and optimize antibody–antigen binding affinity. mAbs. 17(1). 2534626–2534626.
2.
Noble, David, et al.. (2009). 1H–19F spin–lattice relaxation spectroscopy: Proton tunnelling in the hydrogen bond studied by field-cycling NMR. Journal of Magnetic Resonance. 201(2). 157–164. 3 indexed citations
3.
Noble, David, et al.. (2008). Field-cycling NMR investigations of 13C–1H cross-relaxation and cross-polarisation: The nuclear solid effect and dynamic nuclear polarisation. Solid State Nuclear Magnetic Resonance. 34(1-2). 110–117. 4 indexed citations
4.
Wu, Wen‐Wei, David Noble, J. R. Owers-Bradley, & A.J. Horsewill. (2005). A 13C field-cycling NMR relaxometry investigation of proton tunnelling in the hydrogen bond: Dynamic isotope effects, the influence of heteronuclear interactions and coupled relaxation. Journal of Magnetic Resonance. 175(2). 210–221. 14 indexed citations
5.
Wu, Wen‐Wei, David Noble, & A.J. Horsewill. (2005). The correspondence between quantum and classical mechanics: an experimental demonstration of the smooth transition between the two regimes. Chemical Physics Letters. 402(4-6). 519–523. 15 indexed citations
6.
7.
O’Neill, Melanie J., Jane A. Lewis, S. Holland, et al.. (1998). Isolation of Translactone-containing Triterpenes with Thrombin Inhibitory Activities from the Leaves of Lantana camara. Journal of Natural Products. 61(11). 1328–1331. 33 indexed citations
8.
Stead, Paul, Brian A.M. Rudd, Helen Bradshaw, David Noble, & Michael J. Dawson. (1996). Induction of phenazine biosynthesis in cultures ofPseudomonas aeruginosaby L-N-(3-oxohexanoyl) homoserine lactone. FEMS Microbiology Letters. 140(1). 15–22. 18 indexed citations
9.
Stead, Paul, Mahmoud Mahmoudian, Graham A. Webb, et al.. (1996). Efficient procedures for the large-scale preparation of (1S,2S)-trans-2-methoxycyclohexanol, a key chiral intermediate in the synthesis of tricyclic β-lactam antibiotics. Tetrahedron Asymmetry. 7(8). 2247–2250. 25 indexed citations
10.
Middleton, Robert F., Graham Foster, Richard J. P. Cannell, et al.. (1995). Novel Squalestatins Produced by Biotransformation.. The Journal of Antibiotics. 48(4). 311–316. 15 indexed citations
11.
Starkey, Ian D., Mahmoud Mahmoudian, David Noble, et al.. (1995). Synthesis and influenza virus sialidase inhibitory activity of the 5-desacetamido analogue of 2,3-didehydro-2,4-dideoxy-4-guanidinyl-N-acetylneuraminic acid (GG167). Tetrahedron Letters. 36(2). 299–302. 22 indexed citations
12.
Herbert, Richard B., S. Baumberg, Jonathan H. Cove, et al.. (1995). The biosynthesis of nikkomycin X from histidine in Streptomyces tendae. Tetrahedron Letters. 36(13). 2351–2354. 13 indexed citations
13.
Foster, Graham, et al.. (1994). The squalestatins, novel inhibitors of squalene synthase produced by a species of Phoma. V. Minor metabolites.. The Journal of Antibiotics. 47(7). 740–754. 39 indexed citations
14.
Cannell, Richard J. P., Michael J. Dawson, Richard Hale, et al.. (1994). Production of additional squalestatin analogues by directed biosynthesis.. The Journal of Antibiotics. 47(2). 247–249. 10 indexed citations
15.
Cannell, Richard J. P., Michael J. Dawson, Richard Hale, et al.. (1993). The squalestatins, novel inhibitors of squalene synthase produced by a species of Phoma. IV. Preparation of fluorinated squalestatins by directed biosynthesis.. The Journal of Antibiotics. 46(9). 1381–1389. 21 indexed citations
16.
Roberts, Stanley M., Andrew Thorpe, Nicholas J. Turner, et al.. (1993). The isolation and absolute configuration of (1S,2S,3R)-4- Hydroxymethylcyclopent-4-ene-1,2,3-triol: A putative intermediate in the biosynthesis of aristeromycin by Streptomyces citricolor. Tetrahedron Letters. 34(25). 4083–4086. 11 indexed citations
17.
Jones, Carol, Philip J. Sidebottom, Richard J. P. Cannell, David Noble, & Brian A.M. Rudd. (1992). The squalestatins, novel inhibitors of squalene synthase produced by a species of Phoma. III. Biosynthesis.. The Journal of Antibiotics. 45(9). 1492–1498. 37 indexed citations
18.
DAVIES, H. G., et al.. (1986). Microbial hydroxylation of cyclohexylcyclohexane:Synthesis of an analogue of leukotriene-B3. Tetrahedron Letters. 27(9). 1089–1092. 13 indexed citations
19.
Dawson, Michael J., David Noble, Susan M. Green, et al.. (1983). Reduction of bicyclo [3.2.0] hept-2-en-6-one with dehydrogenase enzymes in whole cell preparations of some fungi and yeasts. Journal of the Chemical Society Perkin Transactions 1. 2119–2119. 14 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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