Douglas D. Risser

1.1k total citations
32 papers, 822 citations indexed

About

Douglas D. Risser is a scholar working on Ecology, Evolution, Behavior and Systematics, Renewable Energy, Sustainability and the Environment and Molecular Biology. According to data from OpenAlex, Douglas D. Risser has authored 32 papers receiving a total of 822 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Ecology, Evolution, Behavior and Systematics, 24 papers in Renewable Energy, Sustainability and the Environment and 22 papers in Molecular Biology. Recurrent topics in Douglas D. Risser's work include Biocrusts and Microbial Ecology (24 papers), Algal biology and biofuel production (24 papers) and Photosynthetic Processes and Mechanisms (19 papers). Douglas D. Risser is often cited by papers focused on Biocrusts and Microbial Ecology (24 papers), Algal biology and biofuel production (24 papers) and Photosynthetic Processes and Mechanisms (19 papers). Douglas D. Risser collaborates with scholars based in United States and Germany. Douglas D. Risser's co-authors include Sean M. Callahan, John C. Meeks, Ramya Rajagopalan, Alfonso González, Asha S. Nayar, Christine C. Orozco, Rui Chen, Daniela Ferreira, Kari D. Hagen and Elsie L. Campbell and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Applied and Environmental Microbiology and Biochemistry.

In The Last Decade

Douglas D. Risser

31 papers receiving 822 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douglas D. Risser United States 19 595 413 364 242 80 32 822
Henning Kirst United States 18 920 1.5× 120 0.3× 629 1.7× 92 0.4× 54 0.7× 27 1.1k
Gérard Guglielmi France 14 927 1.6× 283 0.7× 545 1.5× 270 1.1× 101 1.3× 15 1.2k
Shinobu Okamoto Japan 13 548 0.9× 167 0.4× 308 0.8× 213 0.9× 50 0.6× 23 682
Jae‐Hyeok Lee Canada 15 430 0.7× 94 0.2× 247 0.7× 63 0.3× 19 0.2× 26 718
Dennis Dienst Germany 11 695 1.2× 121 0.3× 346 1.0× 256 1.1× 37 0.5× 11 779
Yoon‐Jung Moon South Korea 10 224 0.4× 148 0.4× 114 0.3× 67 0.3× 30 0.4× 14 352
Haim Treves Israel 11 246 0.4× 218 0.5× 258 0.7× 62 0.3× 113 1.4× 16 534
Shinichi Miyamura Japan 14 387 0.7× 181 0.4× 147 0.4× 89 0.4× 24 0.3× 42 689
Sigal Lechno‐Yossef United States 18 603 1.0× 135 0.3× 348 1.0× 267 1.1× 40 0.5× 23 690
Ulf Dühring Germany 13 644 1.1× 71 0.2× 337 0.9× 192 0.8× 42 0.5× 13 783

Countries citing papers authored by Douglas D. Risser

Since Specialization
Citations

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

Fields of papers citing papers by Douglas D. Risser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Douglas D. Risser. 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 Douglas D. Risser. The network helps show where Douglas D. Risser may publish in the future.

Co-authorship network of co-authors of Douglas D. Risser

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas D. Risser. A scholar is included among the top collaborators of Douglas D. Risser 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 Douglas D. Risser. Douglas D. Risser 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
2.
Risser, Douglas D.. (2025). Motility in Filamentous Cyanobacteria. Annual Review of Microbiology. 79(1). 69–85. 1 indexed citations
3.
Maldener, Iris, et al.. (2024). The role of FraI in cell–cell communication and differentiation in the hormogonia-forming cyanobacterium Nostoc punctiforme. mSphere. 9(8). e0051024–e0051024. 2 indexed citations
4.
Glasser, Nathaniel R., Dongtao Cui, Douglas D. Risser, C. Denise Okafor, & Emily P. Balskus. (2024). Accelerating the discovery of alkyl halide-derived natural products using halide depletion. Nature Chemistry. 16(2). 173–182. 8 indexed citations
5.
Risser, Douglas D., et al.. (2024). EbsA is essential for both motility and biofilm formation in the filamentous cyanobacterium Nostoc punctiforme. Microbiology. 170(9). 2 indexed citations
6.
Ferreira, Daniela, et al.. (2022). A regulatory linkage between scytonemin production and hormogonia differentiation in Nostoc punctiforme. iScience. 25(6). 104361–104361. 4 indexed citations
7.
Risser, Douglas D., et al.. (2022). A DnaK(Hsp70) Chaperone System Connects Type IV Pilus Activity to Polysaccharide Secretion in Cyanobacteria. mBio. 13(3). e0051422–e0051422. 6 indexed citations
8.
Risser, Douglas D., et al.. (2021). The cyanobacterial taxis protein HmpF regulates type IV pilus activity in response to light. Proceedings of the National Academy of Sciences. 118(12). 18 indexed citations
9.
Risser, Douglas D., et al.. (2020). Identification of a hormogonium polysaccharide‐specific gene set conserved in filamentous cyanobacteria. Molecular Microbiology. 114(4). 597–608. 19 indexed citations
11.
González, Alfonso, et al.. (2018). A partner‐switching regulatory system controls hormogonium development in the filamentous cyanobacterium Nostoc punctiforme. Molecular Microbiology. 109(4). 555–569. 18 indexed citations
12.
González, Alfonso, Vivian Tam, Jennifer Chang, et al.. (2016). Differential secretion pathways of proteins fused to the Escherichia coli maltose binding protein (MBP) in Pichia pastoris. Protein Expression and Purification. 124. 1–9. 8 indexed citations
13.
Meeks, John C., et al.. (2015). Evidence that a modified type IV pilus‐like system powers gliding motility and polysaccharide secretion in filamentous cyanobacteria. Molecular Microbiology. 98(6). 1021–1036. 74 indexed citations
14.
Risser, Douglas D., et al.. (2015). The non-metabolizable sucrose analog sucralose is a potent inhibitor of hormogonium differentiation in the filamentous cyanobacterium Nostoc punctiforme. Archives of Microbiology. 198(2). 137–147. 26 indexed citations
15.
Campbell, Elsie L., Kari D. Hagen, Rui Chen, et al.. (2014). Genetic Analysis Reveals the Identity of the Photoreceptor for Phototaxis in Hormogonium Filaments of Nostoc punctiforme. Journal of Bacteriology. 197(4). 782–791. 59 indexed citations
16.
17.
Risser, Douglas D. & John C. Meeks. (2012). Comparative transcriptomics with a motility‐deficient mutant leads to identification of a novel polysaccharide secretion system in Nostoc punctiforme. Molecular Microbiology. 87(4). 884–893. 42 indexed citations
18.
Risser, Douglas D. & Sean M. Callahan. (2009). Genetic and cytological evidence that heterocyst patterning is regulated by inhibitor gradients that promote activator decay. Proceedings of the National Academy of Sciences. 106(47). 19884–19888. 65 indexed citations
19.
Risser, Douglas D. & Sean M. Callahan. (2007). Mutagenesis of hetR Reveals Amino Acids Necessary for HetR Function in the Heterocystous Cyanobacterium Anabaena sp. Strain PCC 7120. Journal of Bacteriology. 189(6). 2460–2467. 28 indexed citations
20.
Orozco, Christine C., Douglas D. Risser, & Sean M. Callahan. (2006). Epistasis Analysis of Four Genes from Anabaena sp. Strain PCC 7120 Suggests a Connection between PatA and PatS in Heterocyst Pattern Formation. Journal of Bacteriology. 188(5). 1808–1816. 34 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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