Colette Matthewman

1.4k total citations
12 papers, 730 citations indexed

About

Colette Matthewman is a scholar working on Molecular Biology, Plant Science and Biochemistry. According to data from OpenAlex, Colette Matthewman has authored 12 papers receiving a total of 730 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Plant Science and 3 papers in Biochemistry. Recurrent topics in Colette Matthewman's work include Nitrogen and Sulfur Effects on Brassica (8 papers), Genomics, phytochemicals, and oxidative stress (4 papers) and CRISPR and Genetic Engineering (3 papers). Colette Matthewman is often cited by papers focused on Nitrogen and Sulfur Effects on Brassica (8 papers), Genomics, phytochemicals, and oxidative stress (4 papers) and CRISPR and Genetic Engineering (3 papers). Colette Matthewman collaborates with scholars based in United Kingdom, Germany and United States. Colette Matthewman's co-authors include Stanislav Kopřiva, Anna Kopřivová, Sarah G. Mugford, Bok‐Rye Lee, Cintia Goulart Kawashima, Tamás Dalmay, Dalibor Húska, Tibor Csorba, Ulf‐Ingo Flügge and Ruslan Yatusevich and has published in prestigious journals such as Nature Biotechnology, FEBS Letters and New Phytologist.

In The Last Decade

Colette Matthewman

12 papers receiving 719 citations

Peers

Colette Matthewman

MB

PS

BIOCH

EC

ND

Ana M. Laureano‐Marín Spain

J. John Vidmar Canada

Jens Freitag Germany

Cordula Kruse Germany

Chao Yu China

Bożena Szal Poland

Bernadette Gambonnet France

Deepa Khare South Korea

Dirk Büssis Germany

Szymon Kubala Poland

Ana M. Laureano‐Marín Spain

Colette Matthewman

309 ×0.5

MB

412 ×0.8

PS

184 ×1.4

BIOCH

8 ×0.2

EC

33 ×1.3

ND

Citations per year, relative to Colette Matthewman Colette Matthewman (= 1×) peers Ana M. Laureano‐Marín

Countries citing papers authored by Colette Matthewman

Since Specialization

Citations

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

Fields of papers citing papers by Colette Matthewman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Colette Matthewman

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

All Works

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12 of 12 papers shown

1.

Molloy, Jenny, Nicola J. Patron, Colette Matthewman, et al.. (2018). Opening options for material transfer. Nature Biotechnology. 36(10). 923–927. 39 indexed citations

2.

Parry, Geraint, Nicola J. Patron, Ruth Bastow, & Colette Matthewman. (2016). Meeting report: GARNet/OpenPlant CRISPR-Cas workshop. Plant Methods. 12(1). 6–6. 9 indexed citations

3.

Christiansen, Michael W., Colette Matthewman, Charlotte O’Shea, et al.. (2016). Barley plants over-expressing the NAC transcription factor geneHvNAC005show stunting and delay in development combined with early senescence. Journal of Experimental Botany. 67(17). 5259–5273. 31 indexed citations

4.

Carmichael, Ruth E., et al.. (2015). An introduction to synthetic biology in plant systems. New Phytologist. 208(1). 20–22. 2 indexed citations

5.

Kopřiva, Stanislav, et al.. (2012). Control of sulfur partitioning between primary and secondary metabolism in Arabidopsis. Frontiers in Plant Science. 3. 163–163. 69 indexed citations

6.

Matthewman, Colette, Cintia Goulart Kawashima, Dalibor Húska, et al.. (2012). miR395 is a general component of the sulfate assimilation regulatory network in Arabidopsis. FEBS Letters. 586(19). 3242–3248. 84 indexed citations

7.

Kawashima, Cintia Goulart, Colette Matthewman, Siqi Huang, et al.. (2011). Interplay of SLIM1 and miR395 in the regulation of sulfate assimilation in Arabidopsis. The Plant Journal. 66(5). 863–876. 157 indexed citations

8.

Mugford, Sarah G., Bok‐Rye Lee, Anna Kopřivová, Colette Matthewman, & Stanislav Kopřiva. (2010). Control of sulfur partitioning between primary and secondary metabolism. The Plant Journal. 65(1). 96–105. 105 indexed citations

9.

Kopřivová, Anna, et al.. (2010). Regulation of sulfate assimilation in Physcomitrella patens: mosses are different!. Planta. 232(2). 461–470. 12 indexed citations

10.

Yatusevich, Ruslan, Sarah G. Mugford, Colette Matthewman, et al.. (2009). Genes of primary sulfate assimilation are part of the glucosinolate biosynthetic network inArabidopsis thaliana. The Plant Journal. 62(1). 1–11. 113 indexed citations

11.

Kopřiva, Stanislav, Sarah G. Mugford, Colette Matthewman, & Anna Kopřivová. (2009). Plant sulfate assimilation genes: redundancy versus specialization. Plant Cell Reports. 28(12). 1769–1780. 71 indexed citations

12.

Mugford, Sarah G., Colette Matthewman, Lionel Hill, & Stanislav Kopřiva. (2009). Adenosine‐5′‐phosphosulfate kinase is essential for Arabidopsis viability. FEBS Letters. 584(1). 119–123. 38 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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