Nicholas M. Shaw

781 total citations
22 papers, 622 citations indexed

About

Nicholas M. Shaw is a scholar working on Molecular Biology, Cell Biology and Organic Chemistry. According to data from OpenAlex, Nicholas M. Shaw has authored 22 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Cell Biology and 3 papers in Organic Chemistry. Recurrent topics in Nicholas M. Shaw's work include Enzyme Catalysis and Immobilization (6 papers), Biotin and Related Studies (5 papers) and Microbial Metabolic Engineering and Bioproduction (4 papers). Nicholas M. Shaw is often cited by papers focused on Enzyme Catalysis and Immobilization (6 papers), Biotin and Related Studies (5 papers) and Microbial Metabolic Engineering and Bioproduction (4 papers). Nicholas M. Shaw collaborates with scholars based in Switzerland, United Kingdom and United States. Nicholas M. Shaw's co-authors include Andreas Kiener, Karen Robins, Martin Fuhrmann, Russell P. Newton, Eric G. Brown, Peter L. Roach, Ricardo B. Ferreira, Kirsty S. Hewitson, Jack E. Baldwin and Jean‐Paul Roduit and has published in prestigious journals such as Journal of Biological Chemistry, PLANT PHYSIOLOGY and Analytical Biochemistry.

In The Last Decade

Nicholas M. Shaw

22 papers receiving 612 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicholas M. Shaw Switzerland 15 425 132 124 115 77 22 622
Melanie S. Rogers United States 17 350 0.8× 79 0.6× 94 0.8× 66 0.6× 298 3.9× 31 682
Ivan M. Turner United States 10 484 1.1× 116 0.9× 55 0.4× 67 0.6× 118 1.5× 11 730
Ian Barr United States 11 557 1.3× 126 1.0× 61 0.5× 57 0.5× 132 1.7× 13 725
John G. Cummings United States 12 332 0.8× 115 0.9× 36 0.3× 72 0.6× 144 1.9× 20 606
Masanari Tsujimura Japan 11 402 0.9× 96 0.7× 18 0.1× 112 1.0× 103 1.3× 14 621
Sa-Ouk Kang South Korea 11 273 0.6× 119 0.9× 43 0.3× 59 0.5× 209 2.7× 19 711
A. Humm Germany 9 232 0.5× 155 1.2× 50 0.4× 39 0.3× 76 1.0× 9 511
R. Coelho Portugal 9 354 0.8× 146 1.1× 28 0.2× 39 0.3× 38 0.5× 17 802
Ronda M. Allen United States 11 364 0.9× 462 3.5× 50 0.4× 42 0.4× 193 2.5× 16 814
D. John Aberhart United States 14 294 0.7× 46 0.3× 26 0.2× 164 1.4× 58 0.8× 58 526

Countries citing papers authored by Nicholas M. Shaw

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas M. Shaw

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas M. Shaw. 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 Nicholas M. Shaw. The network helps show where Nicholas M. Shaw may publish in the future.

Co-authorship network of co-authors of Nicholas M. Shaw

This figure shows the co-authorship network connecting the top 25 collaborators of Nicholas M. Shaw. A scholar is included among the top collaborators of Nicholas M. Shaw 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 Nicholas M. Shaw. Nicholas M. Shaw 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.
Shaw, Nicholas M., et al.. (2022). Effects of mutant lamins on nucleo-cytoskeletal coupling in Drosophila models of LMNA muscular dystrophy. Frontiers in Cell and Developmental Biology. 10. 934586–934586. 15 indexed citations
2.
Challand, Martin R., et al.. (2009). Product inhibition in the radical S‐adenosylmethionine family. FEBS Letters. 583(8). 1358–1362. 35 indexed citations
3.
Shaw, Nicholas M., Karen Robins, & Andreas Kiener. (2003). Lonza: 20 Years of Biotransformations. ChemInform. 34(27). 1 indexed citations
4.
Shaw, Nicholas M. & Andrew B. Naughton. (2003). The substrate specificity of the heat-stable stereospecific amidase from Klebsiella oxytoca. Tetrahedron. 60(3). 747–752. 18 indexed citations
5.
6.
Hewitson, Kirsty S., Sandrine Ollagnier de Choudens, Yiannis Sanakis, et al.. (2001). The iron-sulfur center of biotin synthase: site-directed mutants. JBIC Journal of Biological Inorganic Chemistry. 7(1-2). 83–93. 42 indexed citations
7.
Hewitson, Kirsty S., Jack E. Baldwin, Nicholas M. Shaw, & Peter L. Roach. (2000). Mutagenesis of the proposed iron‐sulfur cluster binding ligands in Escherichia coli biotin synthase. FEBS Letters. 466(2-3). 372–376. 29 indexed citations
8.
Hewitson, Kirsty S., et al.. (2000). MioC Is an FMN-binding Protein That Is Essential forEscherichia coli Biotin Synthase Activity in Vitro. Journal of Biological Chemistry. 275(41). 32277–32280. 27 indexed citations
9.
Fuhrmann, Martin, et al.. (1999). Purification, characterization, DNA sequence and cloning of a pimeloyl-CoA synthetase from Pseudomonas mendocina 35. Biochemical Journal. 340(3). 793–793. 3 indexed citations
10.
Fuhrmann, Martin, et al.. (1999). Purification, characterization, DNA sequence and cloning of a pimeloyl-CoA synthetase from Pseudomonas mendocina 35. Biochemical Journal. 340(3). 793–801. 17 indexed citations
11.
Meyer, Hans‐Peter, et al.. (1997). Biotransformations for Fine Chemical Production. CHIMIA International Journal for Chemistry. 51(6). 287–287. 10 indexed citations
12.
Fuhrmann, Martin, et al.. (1995). Biotin Synthase from Escherichiacoli, an Investigation of the Low Molecular Weight and Protein Components Required for Activity inVitro. Journal of Biological Chemistry. 270(32). 19158–19165. 87 indexed citations
13.
Baxter, Robert L., et al.. (1992). Synthesis and biological activity of 9-mercaptodethiobiotin—a putative biotin precursor in Escherichia coli. Journal of the Chemical Society Perkin Transactions 1. 255–258. 14 indexed citations
14.
Ferreira, Ricardo B. & Nicholas M. Shaw. (1989). Effect of osmotic stress on protein turnover in Lemna minor fronds. Planta. 179(4). 456–465. 33 indexed citations
15.
Shaw, Nicholas M. & Roy W. Harding. (1988). Heat-stable, calcium-inhibited cyclic nucleotide phosphodiesterase from Neurospora crassa. Phytochemistry. 27(5). 1281–1288. 1 indexed citations
16.
Shaw, Nicholas M. & Roy W. Harding. (1987). Intracellular and Extracellular Cyclic Nucleotides in Wild-Type and White Collar Mutant Strains of Neurospora crassa. PLANT PHYSIOLOGY. 83(2). 377–383. 14 indexed citations
17.
Shaw, Nicholas M. & David D. Davies. (1985). Tritium labelling of the amino acids of Sinapis alba is identical in darkness and far-red light. Phytochemistry. 24(9). 1891–1894. 1 indexed citations
18.
Shaw, Nicholas M. & Roy W. Harding. (1983). Calcium inhibition of a heat‐stable cyclic nucleotide phosphodiesterase from Neurospora crassa. FEBS Letters. 152(2). 295–299. 4 indexed citations
19.
Brown, Eric G., Russell P. Newton, & Nicholas M. Shaw. (1982). Analysis of the free nucleotide pools of mammalian tissues by high-pressure liquid chromatography. Analytical Biochemistry. 123(2). 378–388. 66 indexed citations
20.
Shaw, Nicholas M., Eric G. Brown, & Russell P. Newton. (1979). Analysis by High-Pressure Liquid Chromatography of the Free Nucleotide Pools of Rat Tissues. Biochemical Society Transactions. 7(6). 1250–1251. 5 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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