Colin Jaques

650 total citations
16 papers, 550 citations indexed

About

Colin Jaques is a scholar working on Molecular Biology, Physical and Theoretical Chemistry and Atmospheric Science. According to data from OpenAlex, Colin Jaques has authored 16 papers receiving a total of 550 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Physical and Theoretical Chemistry and 3 papers in Atmospheric Science. Recurrent topics in Colin Jaques's work include Viral Infectious Diseases and Gene Expression in Insects (10 papers), Protein purification and stability (7 papers) and Microbial Metabolic Engineering and Bioproduction (3 papers). Colin Jaques is often cited by papers focused on Viral Infectious Diseases and Gene Expression in Insects (10 papers), Protein purification and stability (7 papers) and Microbial Metabolic Engineering and Bioproduction (3 papers). Colin Jaques collaborates with scholars based in United Kingdom, Switzerland and United States. Colin Jaques's co-authors include S. I. Ionov, C. Wittig, G. A. Brucker, Andrew J. Racher, Brian C. Hadley, Thaddaeus A. Webster, C. Mark Smales, Sarah J. Turner, Elaine Martin and Y. Wen and has published in prestigious journals such as The Journal of Chemical Physics, SHILAP Revista de lepidopterología and Biotechnology and Bioengineering.

In The Last Decade

Colin Jaques

16 papers receiving 517 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Colin Jaques United Kingdom 12 280 222 214 119 73 16 550
T. R. Hays United States 10 340 1.2× 173 0.8× 210 1.0× 57 0.5× 66 0.9× 19 598
Alexandra Nemeth Austria 17 663 2.4× 288 1.3× 295 1.4× 11 0.1× 28 0.4× 22 847
Takuhiro Otosu Japan 11 157 0.6× 173 0.8× 69 0.3× 18 0.2× 80 1.1× 29 348
Young D. Park United States 9 301 1.1× 61 0.3× 366 1.7× 26 0.2× 46 0.6× 10 600
Yukio Adachi Japan 13 215 0.8× 95 0.4× 112 0.5× 22 0.2× 44 0.6× 44 496
T. Winkler Germany 8 65 0.2× 219 1.0× 43 0.2× 7 0.1× 115 1.6× 12 349
Albert P. Zens United States 12 62 0.2× 117 0.5× 190 0.9× 10 0.1× 35 0.5× 23 329
Stephen Parus United States 10 88 0.3× 105 0.5× 125 0.6× 6 0.1× 18 0.2× 14 440
Elizabeth L. Forsythe United States 16 35 0.1× 399 1.8× 42 0.2× 123 1.0× 13 0.2× 27 739
Deon S. Anex United States 15 108 0.4× 187 0.8× 425 2.0× 36 0.3× 3 0.0× 23 807

Countries citing papers authored by Colin Jaques

Since Specialization
Citations

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

Fields of papers citing papers by Colin Jaques

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Colin Jaques

This figure shows the co-authorship network connecting the top 25 collaborators of Colin Jaques. A scholar is included among the top collaborators of Colin Jaques 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 Colin Jaques. Colin Jaques 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.
Kontoravdi, Cleo, et al.. (2023). Elucidating lactate metabolism in industrial CHO cultures through the combined use of flux balance and principal component analyses. Biochemical Engineering Journal. 202. 109184–109184. 7 indexed citations
2.
Povey, Jane F., et al.. (2022). Manipulation of mRNA translation elongation influences the fragmentation of a biotherapeutic Fc‐fusion protein produced in CHO cells. Biotechnology and Bioengineering. 119(12). 3408–3420. 5 indexed citations
3.
4.
Povey, Jane F., Andrew P. Dean, Sarah J. Turner, et al.. (2021). A proline metabolism selection system and its application to the engineering of lipid biosynthesis in Chinese hamster ovary cells. Metabolic Engineering Communications. 13. e00179–e00179. 14 indexed citations
5.
Webster, Thaddaeus A., et al.. (2020). Feedback control of two supplemental feeds during fed-batch culture on a platform process using inline Raman models for glucose and phenylalanine concentration. Bioprocess and Biosystems Engineering. 44(1). 127–140. 22 indexed citations
6.
Povey, Jane F., Ian R. Brown, Andrew P. Dean, et al.. (2020). Data for engineering lipid metabolism of Chinese hamster ovary (CHO) cells for enhanced recombinant protein production. SHILAP Revista de lepidopterología. 29. 105217–105217. 5 indexed citations
7.
Povey, Jane F., Ian R. Brown, Andrew P. Dean, et al.. (2019). Engineering of Chinese hamster ovary cell lipid metabolism results in an expanded ER and enhanced recombinant biotherapeutic protein production. Metabolic Engineering. 57. 203–216. 41 indexed citations
8.
Racher, Andrew J., et al.. (2019). Improving the accuracy of flux balance analysis through the implementation of carbon availability constraints for intracellular reactions. Biotechnology and Bioengineering. 116(9). 2339–2352. 21 indexed citations
9.
Jaques, Colin, et al.. (2018). At‐line raman spectroscopy and design of experiments for robust monitoring and control of miniature bioreactor cultures. Biotechnology Progress. 35(2). e2740–e2740. 23 indexed citations
10.
Webster, Thaddaeus A., et al.. (2018). Development of generic raman models for a GS‐KO TM CHO platform process. Biotechnology Progress. 34(3). 730–737. 55 indexed citations
11.
Martin, Elaine, et al.. (2017). Extraction of indirectly captured information for use in a comparison of offline pH measurement technologies. Journal of Biotechnology. 251. 160–165. 2 indexed citations
12.
Berg, Frans van den, et al.. (2017). Comparison of spectroscopy technologies for improved monitoring of cell culture processes in miniature bioreactors. Biotechnology Progress. 33(2). 337–346. 37 indexed citations
13.
Ionov, S. I., et al.. (1993). Subpicosecond resolution studies of the H+CO2→CO+OH reaction photoinitiated in CO2–HI complexes. The Journal of Chemical Physics. 99(9). 6553–6561. 92 indexed citations
14.
Ionov, S. I., et al.. (1993). Probing the NO2→NO+O transition state via time resolved unimolecular decomposition. The Journal of Chemical Physics. 99(5). 3420–3435. 103 indexed citations
15.
Jaques, Colin, et al.. (1993). Photoinitiated processes in complexes: subpicosecond studies of CO2—Hl and stereospecificity in Ar—HX. Journal of the Chemical Society Faraday Transactions. 89(10). 1419–1425. 52 indexed citations
16.
Ionov, S. I., et al.. (1992). Subpicosecond OH production from photoexcited CO2–HI complexes. The Journal of Chemical Physics. 97(12). 9486–9489. 60 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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