David M. Kehoe

3.2k total citations
52 papers, 2.3k citations indexed

About

David M. Kehoe is a scholar working on Molecular Biology, Plant Science and Renewable Energy, Sustainability and the Environment. According to data from OpenAlex, David M. Kehoe has authored 52 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 30 papers in Plant Science and 15 papers in Renewable Energy, Sustainability and the Environment. Recurrent topics in David M. Kehoe's work include Photosynthetic Processes and Mechanisms (44 papers), Light effects on plants (27 papers) and Algal biology and biofuel production (14 papers). David M. Kehoe is often cited by papers focused on Photosynthetic Processes and Mechanisms (44 papers), Light effects on plants (27 papers) and Algal biology and biofuel production (14 papers). David M. Kehoe collaborates with scholars based in United States, France and United Kingdom. David M. Kehoe's co-authors include Arthur Grossman, Andrian Gutu, Devaki Bhaya, Kirk E. Apt, Laurence Garczarek, Frédéric Partensky, Alyssa Grossman, Elaine M. Tobin, Joseph E. Sanfilippo and Beronda L. Montgomery and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

David M. Kehoe

51 papers receiving 2.3k 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 M. Kehoe United States 25 1.8k 1.0k 934 658 385 52 2.3k
Taina Tyystjärvi Finland 25 1.5k 0.8× 607 0.6× 724 0.8× 295 0.4× 260 0.7× 49 1.8k
Yukako Hihara Japan 29 2.2k 1.2× 453 0.4× 1.4k 1.5× 421 0.6× 516 1.3× 64 2.4k
Mitsunori Katayama Japan 24 1.7k 0.9× 1.1k 1.1× 627 0.7× 406 0.6× 249 0.6× 40 2.1k
Hualing Mi China 24 1.8k 1.0× 727 0.7× 717 0.8× 150 0.2× 168 0.4× 67 2.2k
Maria Mittag Germany 33 1.8k 1.0× 1.2k 1.1× 1.1k 1.2× 144 0.2× 385 1.0× 88 3.0k
Rei Narikawa Japan 30 2.2k 1.2× 1.7k 1.7× 811 0.9× 614 0.9× 198 0.5× 73 2.7k
Natalia Battchikova Finland 25 2.0k 1.1× 566 0.6× 794 0.9× 112 0.2× 389 1.0× 43 2.3k
Xenie Johnson France 22 1.3k 0.7× 709 0.7× 798 0.9× 223 0.3× 102 0.3× 30 1.8k
Jerry J. Brand United States 24 1.0k 0.6× 293 0.3× 682 0.7× 306 0.5× 458 1.2× 51 1.7k
Ivar Virgin Sweden 10 2.2k 1.2× 1.2k 1.2× 562 0.6× 209 0.3× 145 0.4× 22 2.6k

Countries citing papers authored by David M. Kehoe

Since Specialization
Citations

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

Fields of papers citing papers by David M. Kehoe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David M. Kehoe

This figure shows the co-authorship network connecting the top 25 collaborators of David M. Kehoe. A scholar is included among the top collaborators of David M. Kehoe 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 M. Kehoe. David M. Kehoe 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.
Kehoe, David M., Avijit Biswas, Bo Chen, et al.. (2024). Light Color Regulation of Photosynthetic Antennae Biogenesis in Marine Phytoplankton. Plant and Cell Physiology. 66(2). 168–180.
2.
Capovilla, Giovanna, et al.. (2023). Chitin degradation by Synechococcus WH7803. Scientific Reports. 13(1). 19944–19944. 1 indexed citations
3.
Grébert, Théophile, Laurence Garczarek, Vincent Daubin, et al.. (2022). Diversity and Evolution of Pigment Types in MarineSynechococcusCyanobacteria. Genome Biology and Evolution. 14(4). 16 indexed citations
4.
Grébert, Théophile, Suman Pokhrel, Morgane Ratin, et al.. (2021). Molecular bases of an alternative dual-enzyme system for light color acclimation of marineSynechococcuscyanobacteria. Proceedings of the National Academy of Sciences. 118(9). 17 indexed citations
5.
Sanfilippo, Joseph E., et al.. (2020). CpeY is a phycoerythrobilin lyase for cysteine 82 of the phycoerythrin I α-subunit in marine Synechococcus. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1861(8). 148215–148215. 5 indexed citations
6.
Pokhrel, Suman, et al.. (2020). CpeT is the phycoerythrobilin lyase for Cys-165 on β-phycoerythrin from Fremyella diplosiphon and the chaperone-like protein CpeZ greatly improves its activity. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1861(12). 148284–148284. 6 indexed citations
7.
Gutu, Andrian, et al.. (2019). CpeF is the bilin lyase that ligates the doubly linked phycoerythrobilin on β-phycoerythrin in the cyanobacterium Fremyella diplosiphon. Journal of Biological Chemistry. 294(11). 3987–3999. 15 indexed citations
8.
Kehoe, David M., et al.. (2018). Diverse light responses of cyanobacteria mediated by phytochrome superfamily photoreceptors. Nature Reviews Microbiology. 17(1). 37–50. 105 indexed citations
9.
Sanfilippo, Joseph E., et al.. (2017). Adaptation to Blue Light in Marine Synechococcus Requires MpeU, an Enzyme with Similarity to Phycoerythrobilin Lyase Isomerases. Frontiers in Microbiology. 8. 243–243. 19 indexed citations
10.
Whippo, Craig W., et al.. (2015). Translation initiation factor 3 families: what are their roles in regulating cyanobacterial and chloroplast gene expression?. Photosynthesis Research. 126(1). 147–159. 9 indexed citations
11.
Gutu, Andrian & David M. Kehoe. (2011). Emerging Perspectives on the Mechanisms, Regulation, and Distribution of Light Color Acclimation in Cyanobacteria. Molecular Plant. 5(1). 1–13. 121 indexed citations
12.
Partensky, Frédéric, Daniella Mella–Flores, Gildas Le Corguillé, et al.. (2010). Ultraviolet stress delays chromosome replication in light/dark synchronized cells of the marine cyanobacterium Prochlorococcus marinus PCC9511. BMC Microbiology. 10(1). 204–204. 24 indexed citations
13.
14.
Stowe-Evans, Emily L. & David M. Kehoe. (2004). Signal transduction during light-quality acclimation in cyanobacteria: a model system for understanding phytochrome-response pathways in prokaryotes. Photochemical & Photobiological Sciences. 3(6). 495–502. 19 indexed citations
15.
Terauchi, Kazuki, Beronda L. Montgomery, Arthur Grossman, J. Clark Lagarias, & David M. Kehoe. (2004). RcaE is a complementary chromatic adaptation photoreceptor required for green and red light responsiveness. Molecular Microbiology. 51(2). 567–577. 104 indexed citations
16.
Montgomery, Beronda L., et al.. (2003). CotB is essential for complete activation of green light‐induced genes during complementary chromatic adaptation in Fremyella diplosiphon. Molecular Microbiology. 50(3). 781–793. 17 indexed citations
17.
Kehoe, David M., et al.. (1999). DNA microarrays for studies of higher plants and other photosynthetic organisms. Trends in Plant Science. 4(1). 38–41. 60 indexed citations
18.
Tobin, Elaine M. & David M. Kehoe. (1994). Phytochrome regulated gene expression. PubMed. 5(5). 335–346. 54 indexed citations
19.
Kehoe, David M. & Arthur Grossman. (1994). Complementary chromatic adaptation: photoperception to gene regulation. PubMed. 5(5). 303–313. 37 indexed citations
20.
Kehoe, David M., J. Degenhardt, Ilga Winicov, & Elaine M. Tobin. (1994). Two 10-bp regions are critical for phytochrome regulation of a Lemna gibba Lhcb gene promoter.. The Plant Cell. 6(8). 1123–1134. 46 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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