Wouter D. Hoff

5.0k total citations
91 papers, 4.0k citations indexed

About

Wouter D. Hoff is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ecology. According to data from OpenAlex, Wouter D. Hoff has authored 91 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 64 papers in Cellular and Molecular Neuroscience and 15 papers in Ecology. Recurrent topics in Wouter D. Hoff's work include Photoreceptor and optogenetics research (64 papers), Photosynthetic Processes and Mechanisms (31 papers) and Retinal Development and Disorders (27 papers). Wouter D. Hoff is often cited by papers focused on Photoreceptor and optogenetics research (64 papers), Photosynthetic Processes and Mechanisms (31 papers) and Retinal Development and Disorders (27 papers). Wouter D. Hoff collaborates with scholars based in United States, Netherlands and Japan. Wouter D. Hoff's co-authors include Klaas J. Hellingwerf, Aihua Xie, Arthur R. Kroon, Wander W. Sprenger, Kwang-Hwan Jung, John L. Spudich, Judith P. Armitage, Mark Gomelsky, W. Crielaard and Masato Kumauchi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Physical Review Letters.

In The Last Decade

Wouter D. Hoff

88 papers receiving 4.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wouter D. Hoff United States 33 3.0k 2.6k 608 542 357 91 4.0k
Da‐Neng Wang United States 37 4.4k 1.5× 1.1k 0.4× 511 0.8× 718 1.3× 776 2.2× 63 6.1k
Terrance E. Meyer United States 39 3.5k 1.2× 1.1k 0.4× 506 0.8× 434 0.8× 704 2.0× 135 4.9k
Bernd Ludwig Germany 42 6.6k 2.2× 1.8k 0.7× 701 1.2× 248 0.5× 804 2.3× 175 7.8k
Michael I. Verkhovsky Finland 46 5.4k 1.8× 2.6k 1.0× 1.0k 1.7× 234 0.4× 523 1.5× 110 6.4k
Terry E. Meyer United States 32 2.8k 0.9× 1.3k 0.5× 204 0.3× 317 0.6× 303 0.8× 105 4.0k
Jonathan P. Hosler United States 32 3.4k 1.1× 936 0.4× 300 0.5× 317 0.6× 240 0.7× 76 4.1k
Wenrui Chang China 27 4.0k 1.4× 1.1k 0.4× 980 1.6× 1.1k 2.1× 571 1.6× 67 4.8k
Norbert Krauß Germany 36 7.4k 2.5× 3.4k 1.3× 1.7k 2.8× 1.4k 2.6× 1.0k 2.9× 92 9.0k
Armen Y. Mulkidjanian Russia 36 3.2k 1.1× 908 0.3× 642 1.1× 273 0.5× 277 0.8× 114 4.2k
Carola Hunte Germany 41 5.6k 1.9× 502 0.2× 329 0.5× 387 0.7× 444 1.2× 94 6.8k

Countries citing papers authored by Wouter D. Hoff

Since Specialization
Citations

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

Fields of papers citing papers by Wouter D. Hoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wouter D. Hoff

This figure shows the co-authorship network connecting the top 25 collaborators of Wouter D. Hoff. A scholar is included among the top collaborators of Wouter D. Hoff 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 Wouter D. Hoff. Wouter D. Hoff 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.
Hoff, Wouter D., et al.. (2025). The Evolution and Implications of the Inosine tRNA Modification. Journal of Molecular Biology. 437(16). 169187–169187.
2.
Hoff, Wouter D., et al.. (2024). The contours of evolution: In defence of Darwin's tree of life paradigm. BioEssays. 46(5). e2400012–e2400012. 3 indexed citations
3.
Moghadam, Farzaneh, et al.. (2016). Draft genome sequence and detailed analysis of Pantoea eucrina strain Russ and implication for opportunistic pathogenesis. Genomics Data. 10. 63–68. 5 indexed citations
4.
Miller, Neil T., Danny Fuller, Matthew Brian Couger, et al.. (2016). Draft genome sequence of Pseudomonas moraviensis strain Devor implicates metabolic versatility and bioremediation potential. Genomics Data. 9. 154–159. 10 indexed citations
5.
Kumauchi, Masato, et al.. (2015). Experimental Detection of the Intrinsic Difference in Raman Optical Activity of a Photoreceptor Protein under Preresonance and Resonance Conditions. Angewandte Chemie International Edition. 54(39). 11555–11558. 33 indexed citations
6.
Kaledhonkar, Sandip, et al.. (2013). Strong Ionic Hydrogen Bonding Causes a Spectral Isotope Effect in Photoactive Yellow Protein. Biophysical Journal. 105(11). 2577–2585. 17 indexed citations
7.
Challacombe, Jean F., et al.. (2012). An Extremely Halophilic Proteobacterium Combines a Highly Acidic Proteome with a Low Cytoplasmic Potassium Content. Journal of Biological Chemistry. 288(1). 581–588. 58 indexed citations
8.
Kang, Zhouyang, et al.. (2012). Side-chain specific isotopic labeling of proteins for infrared structural biology: The case of ring-D4-tyrosine isotope labeling of photoactive yellow protein. Protein Expression and Purification. 85(1). 125–132. 7 indexed citations
9.
Nome, René A., et al.. (2010). Spectral tuning in photoactive yellow protein by modulation of the shape of the excited state energy surface. Proceedings of the National Academy of Sciences. 107(13). 5821–5826. 28 indexed citations
10.
Kumauchi, Masato, et al.. (2008). Identification of Six New Photoactive Yellow Proteins—Diversity and Structure–Function Relationships in a Bacterial Blue Light Photoreceptor†. Photochemistry and Photobiology. 84(4). 956–969. 53 indexed citations
11.
12.
Pan, Duohai, et al.. (2004). Time-Resolved Resonance Raman Structural Studies of the pB′ Intermediate in the Photocycle of Photoactive Yellow Protein. Biophysical Journal. 86(4). 2374–2382. 37 indexed citations
13.
Lee, Byoung-Chul, Paula Croonquist, Tobin R. Sosnick, & Wouter D. Hoff. (2001). PAS Domain Receptor Photoactive Yellow Protein Is Converted to a Molten Globule State upon Activation. Journal of Biological Chemistry. 276(24). 20821–20823. 46 indexed citations
14.
Lee, Byoung-Chul, Paula Croonquist, & Wouter D. Hoff. (2001). Mimic of Photocycle by a Protein Folding Reaction in Photoactive Yellow Protein. Journal of Biological Chemistry. 276(48). 44481–44487. 9 indexed citations
15.
Hendriks, Johnny, Wouter D. Hoff, Wim Crielaard, & Klaas J. Hellingwerf. (1999). Protonation/Deprotonation Reactions Triggered by Photoactivation of Photoactive Yellow Protein from Ectothiorhodospira halophila. Journal of Biological Chemistry. 274(25). 17655–17660. 63 indexed citations
16.
Aalten, Daan M. F. van, Wouter D. Hoff, J. B. C. Findlay, W. Crielaard, & Klaas J. Hellingwerf. (1998). Concerted motions in the photoactive yellow protein. Protein Engineering Design and Selection. 11(10). 873–879. 22 indexed citations
17.
Hellingwerf, Klaas J., W. Crielaard, M. Joost Teixeira de Mattos, et al.. (1998). Current topics in signal transduction in bacteria. Antonie van Leeuwenhoek. 74(4). 211–227. 20 indexed citations
18.
Hoff, Wouter D., et al.. (1997). Comparison of acid denaturation and light activation in the eubacterial blue-light receptor photoactive yellow protein. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1322(2-3). 151–162. 35 indexed citations
19.
20.
Mathies, Richard A., et al.. (1995). Resonance Raman evidence that the thioester-linked 4-hydroxycinnamyl chromophore of photoactive yellow protein is deprotonated. Biochemistry. 34(39). 12669–12672. 97 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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