Moritz Kreysing

3.5k total citations · 1 hit paper
36 papers, 2.4k citations indexed

About

Moritz Kreysing is a scholar working on Atomic and Molecular Physics, and Optics, Biomedical Engineering and Molecular Biology. According to data from OpenAlex, Moritz Kreysing has authored 36 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Atomic and Molecular Physics, and Optics, 12 papers in Biomedical Engineering and 11 papers in Molecular Biology. Recurrent topics in Moritz Kreysing's work include Microfluidic and Bio-sensing Technologies (7 papers), Advanced Fluorescence Microscopy Techniques (6 papers) and Orbital Angular Momentum in Optics (6 papers). Moritz Kreysing is often cited by papers focused on Microfluidic and Bio-sensing Technologies (7 papers), Advanced Fluorescence Microscopy Techniques (6 papers) and Orbital Angular Momentum in Optics (6 papers). Moritz Kreysing collaborates with scholars based in Germany, United Kingdom and United States. Moritz Kreysing's co-authors include Jochen Guck, Anatol W. Fritsch, Irina Solovei, Christian Lanctôt, Thomas Cremer, Leo Peichl, Boris Joffe, Mrityunjoy Kar, Mathias Kolle and Juan M. Iglesias‐Artola and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Physical Review Letters.

In The Last Decade

Moritz Kreysing

36 papers receiving 2.4k citations

Hit Papers

Nuclear Architecture of Rod Photoreceptor Cells Adapts to... 2009 2026 2014 2020 2009 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Moritz Kreysing Germany 19 1.4k 464 342 221 188 36 2.4k
Roy Bar‐Ziv Israel 31 1.7k 1.2× 1.0k 2.3× 406 1.2× 229 1.0× 197 1.0× 67 2.9k
Tsvi Tlusty Israel 34 1.2k 0.9× 1.1k 2.4× 459 1.3× 548 2.5× 261 1.4× 98 3.5k
Idán Tuval Spain 22 670 0.5× 989 2.1× 140 0.4× 229 1.0× 373 2.0× 53 2.8k
Christoph A. Weber Germany 25 2.9k 2.0× 704 1.5× 148 0.4× 612 2.8× 592 3.1× 70 4.8k
Akihiro Ikeda Japan 28 1.3k 0.9× 160 0.3× 125 0.4× 178 0.8× 285 1.5× 198 3.0k
David Zwicker Germany 18 891 0.6× 172 0.4× 73 0.2× 185 0.8× 289 1.5× 52 1.6k
David K. Lubensky United States 17 1.1k 0.7× 840 1.8× 311 0.9× 148 0.7× 330 1.8× 30 1.9k
I. E. Spektor Russia 24 779 0.6× 341 0.7× 351 1.0× 224 1.0× 92 0.5× 97 2.1k
Shashi Thutupalli India 19 435 0.3× 679 1.5× 130 0.4× 345 1.6× 140 0.7× 37 2.0k
Allen P. Liu United States 31 2.0k 1.4× 1.0k 2.3× 293 0.9× 127 0.6× 1.3k 6.9× 121 3.6k

Countries citing papers authored by Moritz Kreysing

Since Specialization
Citations

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

Fields of papers citing papers by Moritz Kreysing

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moritz Kreysing

This figure shows the co-authorship network connecting the top 25 collaborators of Moritz Kreysing. A scholar is included among the top collaborators of Moritz Kreysing 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 Moritz Kreysing. Moritz Kreysing 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.
Nan, Fan, et al.. (2025). Optical Micromanipulations Based on Model Predictive Control of Thermoviscous Flows. Small. 21(38). e01039–e01039. 1 indexed citations
2.
Minopoli, Antonio, et al.. (2024). Opto-fluidically multiplexed assembly and micro-robotics. Light Science & Applications. 13(1). 59–59. 4 indexed citations
3.
Kreysing, Moritz, et al.. (2023). Theoretical model of confined thermoviscous flows for artificial cytoplasmic streaming. Physical Review Fluids. 8(3). 6 indexed citations
4.
Minopoli, Antonio, et al.. (2023). ISO-FLUCS: symmetrization of optofluidic manipulations in quasi-isothermal micro-environments. PubliCatt (Università Cattolica del Sacro Cuore). 3(1). 17 indexed citations
5.
6.
Iglesias‐Artola, Juan M., Björn Drobot, Mrityunjoy Kar, et al.. (2022). Charge-density reduction promotes ribozyme activity in RNA–peptide coacervates via RNA fluidization and magnesium partitioning. Nature Chemistry. 14(4). 407–416. 81 indexed citations
7.
Fritsch, Anatol W., Omar Adame-Arana, Carsten Hoege, et al.. (2021). Local thermodynamics govern formation and dissolution of Caenorhabditis elegans P granule condensates. Proceedings of the National Academy of Sciences. 118(37). 77 indexed citations
8.
Chartier, Nicolas T., Sebastian Fürthauer, Ben T. Larson, et al.. (2021). A hydraulic instability drives the cell death decision in the nematode germline. Nature Physics. 17(8). 920–925. 40 indexed citations
9.
Roscito, Juliana G., Ronald Naumann, Mihail Sarov, et al.. (2020). Recapitulating Evolutionary Divergence in a Single Cis -Regulatory Element Is Sufficient to Cause Expression Changes of the Lens Gene Tdrd7. Molecular Biology and Evolution. 38(2). 380–392. 5 indexed citations
10.
Mittasch, Matthäus, et al.. (2020). Regulated changes in material properties underlie centrosome disassembly during mitotic exit. The Journal of Cell Biology. 219(4). 38 indexed citations
11.
Iserman, Christiane, Ulrike Friedrich, Taraneh Zarin, et al.. (2020). Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production. Cell. 181(4). 818–831.e19. 156 indexed citations
12.
Drobot, Björn, Juan M. Iglesias‐Artola, Kristian Le Vay, et al.. (2018). Compartmentalised RNA catalysis in membrane-free coacervate protocells. Nature Communications. 9(1). 3643–3643. 268 indexed citations
13.
Saito, Makoto, Daniel Heß, Jan Eglinger, et al.. (2018). Acetylation of intrinsically disordered regions regulates phase separation. Nature Chemical Biology. 15(1). 51–61. 220 indexed citations
14.
Nagelberg, Sara, Lauren D. Zarzar, Natalie J. Nicolas, et al.. (2017). Reconfigurable and responsive droplet-based compound micro-lenses. Nature Communications. 8(1). 14673–14673. 134 indexed citations
15.
Kreysing, Moritz, et al.. (2015). Heat flux across an open pore enables the continuous replication and selection of oligonucleotides towards increasing length. Nature Chemistry. 7(3). 203–208. 127 indexed citations
16.
Kolle, Mathias, et al.. (2013). Bio‐Inspired Band‐Gap Tunable Elastic Optical Multilayer Fibers. Advanced Materials. 25(15). 2239–2245. 178 indexed citations
17.
Francke, Mike, Moritz Kreysing, Andreas F. Mack, et al.. (2013). Grouped retinae and tapetal cups in some Teleostian fish: Occurrence, structure, and function. Progress in Retinal and Eye Research. 38. 43–69. 27 indexed citations
18.
Kreysing, Moritz, et al.. (2010). Physical insight into light scattering by photoreceptor cell nuclei. Optics Letters. 35(15). 2639–2639. 29 indexed citations
19.
Solovei, Irina, Moritz Kreysing, Christian Lanctôt, et al.. (2009). Nuclear Architecture of Rod Photoreceptor Cells Adapts to Vision in Mammalian Evolution. Cell. 137(2). 356–368. 585 indexed citations breakdown →
20.
Kreysing, Moritz, T. Kießling, Anatol W. Fritsch, et al.. (2008). The optical cell rotator. Optics Express. 16(21). 16984–16984. 90 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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