Douwe Molenaar

13.9k total citations · 2 hit papers
131 papers, 10.5k citations indexed

About

Douwe Molenaar is a scholar working on Molecular Biology, Food Science and Genetics. According to data from OpenAlex, Douwe Molenaar has authored 131 papers receiving a total of 10.5k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Molecular Biology, 57 papers in Food Science and 32 papers in Genetics. Recurrent topics in Douwe Molenaar's work include Probiotics and Fermented Foods (51 papers), Microbial Metabolic Engineering and Bioproduction (29 papers) and Bacterial Genetics and Biotechnology (24 papers). Douwe Molenaar is often cited by papers focused on Probiotics and Fermented Foods (51 papers), Microbial Metabolic Engineering and Bioproduction (29 papers) and Bacterial Genetics and Biotechnology (24 papers). Douwe Molenaar collaborates with scholars based in Netherlands, Germany and United States. Douwe Molenaar's co-authors include Bas Teusink, Willem M. de Vos, Michiel Kleerebezem, Michel E. van der Rest, Roland J. Siezen, Johan E. T. van Hylckama Vlieg, Peter A. Bron, Tjakko Abee, Christian Lange and Arnold J. M. Driessen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Douwe Molenaar

130 papers receiving 10.2k citations

Hit Papers

Complete genome sequence of Lactobacillus plantarum WCFS1 2003 2026 2010 2018 2003 2018 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douwe Molenaar Netherlands 56 7.1k 4.5k 2.0k 1.6k 975 131 10.5k
Wil N. Konings Netherlands 69 9.8k 1.4× 5.0k 1.1× 2.1k 1.1× 2.7k 1.7× 743 0.8× 318 16.0k
Jan Kok Netherlands 69 10.1k 1.4× 7.3k 1.6× 2.5k 1.3× 3.0k 1.9× 519 0.5× 251 15.5k
Roland J. Siezen Netherlands 69 10.8k 1.5× 7.7k 1.7× 2.9k 1.5× 1.8k 1.1× 683 0.7× 227 16.2k
Tjakko Abee Netherlands 74 8.3k 1.2× 7.0k 1.5× 1.6k 0.8× 1.9k 1.2× 1.1k 1.2× 339 16.2k
Bart C. Weimer United States 43 3.9k 0.6× 2.5k 0.6× 1.2k 0.6× 553 0.3× 372 0.4× 178 7.1k
Dmitry A. Rodionov United States 57 7.1k 1.0× 918 0.2× 1.4k 0.7× 2.1k 1.3× 856 0.9× 168 11.3k
Paul L.H. McSweeney Ireland 55 6.6k 0.9× 10.2k 2.3× 3.0k 1.5× 732 0.5× 580 0.6× 217 14.2k
Bart Devreese Belgium 57 5.8k 0.8× 1.1k 0.2× 622 0.3× 1.2k 0.7× 822 0.8× 306 10.9k
Jos Vanderleyden Belgium 69 8.6k 1.2× 4.2k 0.9× 1.5k 0.8× 1.5k 1.0× 834 0.9× 224 18.1k
Ian R. Booth United Kingdom 58 6.6k 0.9× 1.4k 0.3× 408 0.2× 2.8k 1.8× 980 1.0× 166 10.9k

Countries citing papers authored by Douwe Molenaar

Since Specialization
Citations

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

Fields of papers citing papers by Douwe Molenaar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Douwe Molenaar

This figure shows the co-authorship network connecting the top 25 collaborators of Douwe Molenaar. A scholar is included among the top collaborators of Douwe Molenaar 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 Douwe Molenaar. Douwe Molenaar 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.
Hertzberger, Rosanne, et al.. (2025). Insights into host dependency from a chemically defined medium for the human vaginal bacterium Lactobacillus crispatus. Archives of Microbiology. 207(9). 212–212.
2.
Breur, Marjolein, Douwe Molenaar, Sophie van der Sluis, et al.. (2022). Cortical Pathology in Vanishing White Matter. Cells. 11(22). 3581–3581. 6 indexed citations
3.
Battjes, J.A., Chrats Melkonian, Sebastián N. Mendoza, et al.. (2022). Ethanol-lactate transition of Lachancea thermotolerans is linked to nitrogen metabolism. Food Microbiology. 110. 104167–104167. 21 indexed citations
4.
Hertzberger, Rosanne, et al.. (2022). Genetic Elements Orchestrating Lactobacillus crispatus Glycogen Metabolism in the Vagina. International Journal of Molecular Sciences. 23(10). 5590–5590. 19 indexed citations
5.
Brenzinger, Kristof, Ohana Y. A. Costa, Adrian Ho, et al.. (2021). Steering microbiomes by organic amendments towards climate-smart agricultural soils. Biology and Fertility of Soils. 57(8). 1053–1074. 20 indexed citations
6.
Chen, Yu, Sjef Boeren, Herwig Bachmann, et al.. (2021). Proteome constraints reveal targets for improving microbial fitness in nutrient‐rich environments. Molecular Systems Biology. 17(4). e10093–e10093. 33 indexed citations
7.
Lara, Elena Garcia, et al.. (2021). Using Functional Annotations to Study Pairwise Interactions in Urinary Tract Infection Communities. Genes. 12(8). 1221–1221. 5 indexed citations
8.
Veer, Charlotte van der, Rosanne Hertzberger, Sylvia M. Bruisten, et al.. (2019). Comparative genomics of human Lactobacillus crispatus isolates reveals genes for glycosylation and glycogen degradation: implications for in vivo dominance of the vaginal microbiota. Microbiome. 7(1). 49–49. 100 indexed citations
9.
Mendoza, Sebastián N., Brett G. Olivier, Douwe Molenaar, & Bas Teusink. (2019). A systematic assessment of current genome-scale metabolic reconstruction tools. Genome biology. 20(1). 158–158. 150 indexed citations
10.
Eckhardt, Thomas, Anne de Jong, Filipe Branco dos Santos, et al.. (2015). Protein costs do not explain evolution of metabolic strategies and regulation of ribosomal content: does protein investment explain an anaerobic bacterial C rabtree effect?. Molecular Microbiology. 97(1). 77–92. 49 indexed citations
11.
Siezen, Roland J., Jumamurat R. Bayjanov, Giovanna E. Felis, et al.. (2011). Genome‐scale diversity and niche adaptation analysis of Lactococcus lactis by comparative genome hybridization using multi‐strain arrays. Microbial Biotechnology. 4(3). 383–402. 67 indexed citations
12.
Saulnier, Delphine, Filipe Duarte Santos, Stefan Roos, et al.. (2011). Exploring Metabolic Pathway Reconstruction and Genome-Wide Expression Profiling in Lactobacillus reuteri to Define Functional Probiotic Features. PLoS ONE. 6(4). e18783–e18783. 146 indexed citations
13.
Rud, Ida, Kristine Naterstad, Roger S. Bongers, et al.. (2010). Functional analysis of the role of CggR (central glycolytic gene regulator) in Lactobacillus plantarum by transcriptome analysis. Microbial Biotechnology. 4(3). 345–356. 10 indexed citations
14.
Hemert, Saskia van, Marjolein Meijerink, Douwe Molenaar, et al.. (2010). Identification of Lactobacillus plantarum genes modulating the cytokine response of human peripheral blood mononuclear cells. BMC Microbiology. 10(1). 293–293. 163 indexed citations
15.
Derrien, Muriel, Sahar El Aidy, Mirjana Rajilić–Stojanović, et al.. (2009). Spatial And Temporal Analysis Of Intestinal Microbiota In Conventionalized Germ Free Mice In Correlation With The Host Responses, Using A High-Throughput Phylogenetic Microarray.. Microbial Ecology. 57(3). 566–567. 2 indexed citations
16.
Wels, Michiel, Roger S. Bongers, Jos Boekhorst, et al.. (2009). Large Intergenic Cruciform-Like Supermotifs in the Lactobacillus plantarum Genome. Journal of Bacteriology. 191(10). 3420–3423. 4 indexed citations
17.
Stevens, Marc J. A., Douwe Molenaar, Anne de Jong, Willem M. de Vos, & Michiel Kleerebezem. (2009). σ 54-mediated control of the mannose phosphotransferase sytem in Lactobacillus plantarum impacts on carbohydrate metabolism. Microbiology. 156(3). 695–707. 25 indexed citations
18.
Ingham, Colin J., A.J. Sprenkels, Johan G. Bomer, et al.. (2007). The micro-Petri dish, a million-well growth chip for the culture and high-throughput screening of microorganisms. Proceedings of the National Academy of Sciences. 104(46). 18217–18222. 192 indexed citations
19.
Siezen, Roland J., et al.. (2007). Genome-scale genotype-phenotype matching of two Lactococcus lactis plant isolates identifies adaptation mechanisms to the plant niche. Applied and Environmental Microbiology. 424–436. 1 indexed citations
20.
Rademaker, J. L. W., et al.. (2006). Natural diversity and adaptive responses of Lactococcus lactis. Current Opinion in Biotechnology. 17(2). 183–190. 94 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026