Björn Rasch

12.6k total citations · 2 hit papers
126 papers, 8.0k citations indexed

About

Björn Rasch is a scholar working on Cognitive Neuroscience, Experimental and Cognitive Psychology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Björn Rasch has authored 126 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Cognitive Neuroscience, 56 papers in Experimental and Cognitive Psychology and 19 papers in Cellular and Molecular Neuroscience. Recurrent topics in Björn Rasch's work include Sleep and Wakefulness Research (81 papers), Memory and Neural Mechanisms (55 papers) and Sleep and related disorders (49 papers). Björn Rasch is often cited by papers focused on Sleep and Wakefulness Research (81 papers), Memory and Neural Mechanisms (55 papers) and Sleep and related disorders (49 papers). Björn Rasch collaborates with scholars based in Switzerland, Germany and United States. Björn Rasch's co-authors include Jan Born, Steffen Gais, Christian Büchel, Thomas Schreiner, Susanne Diekelmann, Maren Jasmin Cordi, Sandra Ackermann, Dominique J.‐F. de Quervain, Ewald Naumann and Erich Seifritz and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Björn Rasch

124 papers receiving 7.9k citations

Hit Papers

About Sleep's Role in Memory 2007 2026 2013 2019 2013 2007 500 1000 1.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Björn Rasch 6.5k 3.6k 1.3k 1.1k 385 126 8.0k
Steffen Gais 7.6k 1.2× 3.4k 0.9× 2.0k 1.5× 1.2k 1.1× 250 0.6× 77 8.7k
Robert Stickgold 6.2k 1.0× 3.1k 0.9× 1.0k 0.8× 708 0.6× 567 1.5× 60 7.2k
Susanne Diekelmann 5.1k 0.8× 2.7k 0.8× 1.1k 0.9× 916 0.8× 163 0.4× 51 5.8k
Evelyne Balteau 4.8k 0.7× 1.8k 0.5× 916 0.7× 1.2k 1.1× 626 1.6× 87 6.7k
Gilles Vandewalle 4.8k 0.7× 2.4k 0.7× 1.1k 0.9× 2.1k 2.0× 478 1.2× 121 7.1k
Sophie Schwartz 7.0k 1.1× 2.5k 0.7× 500 0.4× 618 0.6× 772 2.0× 140 8.4k
Virginie Sterpenich 3.5k 0.5× 1.6k 0.5× 715 0.5× 837 0.8× 271 0.7× 63 4.4k
Matthias Mölle 7.1k 1.1× 2.8k 0.8× 2.0k 1.5× 1.4k 1.3× 130 0.3× 81 8.2k
Philippe Peigneux 8.1k 1.2× 3.4k 0.9× 1.4k 1.0× 1.4k 1.2× 874 2.3× 230 11.0k
Ken A. Paller 10.1k 1.6× 3.1k 0.9× 953 0.7× 424 0.4× 1.2k 3.2× 204 11.2k

Countries citing papers authored by Björn Rasch

Since Specialization
Citations

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

Fields of papers citing papers by Björn Rasch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Björn Rasch

This figure shows the co-authorship network connecting the top 25 collaborators of Björn Rasch. A scholar is included among the top collaborators of Björn Rasch 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 Björn Rasch. Björn Rasch 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.
Adelhöfer, Nico, Alejandra Alonso, Luciana Besedovsky, et al.. (2025). Hacking the functions of sleep: noninvasive approaches to stimulate sleep neurophysiology. Physiological Reviews. 106(2). 675–749. 1 indexed citations
3.
Kasten, Florian H., et al.. (2024). No Benefit in Memory Performance after Nocturnal Memory Reactivation Coupled with Theta-tACS. SHILAP Revista de lepidopterología. 6(2). 211–233. 1 indexed citations
4.
Cordi, Maren Jasmin, Thomas Schreiner, & Björn Rasch. (2023). Is prior knowledge essential? Additional training opportunities restore sleep‐associated memory benefits under conditions of low prior knowledge. Journal of Sleep Research. 32(4). 3 indexed citations
5.
Schoch, Sarah F., et al.. (2023). Neural correlates of sleep‐induced benefits on traumatic memory processing. Human Brain Mapping. 44(9). 3506–3518. 9 indexed citations
6.
Weber, Frederik D., Zsófia Zavecz, Björn Rasch, et al.. (2023). Sustained polyphasic sleep restriction abolishes human growth hormone release. SLEEP. 47(2). 3 indexed citations
7.
Revenstorf, Dirk, et al.. (2023). Hypnose in Psychotherapie, Psychosomatik und Medizin.
8.
Rasch, Björn, et al.. (2023). Targeted memory reactivation during slow-wave sleep vs. sleep stage N2: no significant differences in a vocabulary task. Learning & Memory. 30(9). 192–200. 8 indexed citations
9.
Loretz, Erna, et al.. (2021). Exposure to relaxing words during sleep promotes slow-wave sleep and subjective sleep quality. SLEEP. 44(11). 12 indexed citations
10.
Rasch, Björn, et al.. (2021). Embodiment of sleep‐related words: Evidence from event‐related potentials. Psychophysiology. 58(8). e13824–e13824. 3 indexed citations
11.
Schoch, Sarah F., Maren Jasmin Cordi, Michael Schredl, & Björn Rasch. (2018). The effect of dream report collection and dream incorporation on memory consolidation during sleep. Journal of Sleep Research. 28(1). e12754–e12754. 21 indexed citations
12.
Schreiner, Thomas & Björn Rasch. (2014). Boosting Vocabulary Learning by Verbal Cueing During Sleep. Cerebral Cortex. 25(11). 4169–4179. 139 indexed citations
13.
Ackermann, Sandra, David Coynel, Matthias Fastenrath, et al.. (2014). BAIAP2 Is Related to Emotional Modulation of Human Memory Strength. PLoS ONE. 9(1). e83707–e83707. 13 indexed citations
14.
Bosch, Oliver G., Julia S. Rihm, Milan Scheidegger, et al.. (2013). Sleep deprivation increases dorsal nexus connectivity to the dorsolateral prefrontal cortex in humans. Proceedings of the National Academy of Sciences. 110(48). 19597–19602. 77 indexed citations
15.
Papassotiropoulos, Andreas, Elka Stefanova, Christian Vogler, et al.. (2011). A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. Molecular Psychiatry. 18(2). 255–263. 29 indexed citations
16.
Rasch, Björn, Andreas Papassotiropoulos, & Dominique J.‐F. de Quervain. (2010). Imaging genetics of cognitive functions: Focus on episodic memory. NeuroImage. 53(3). 870–877. 41 indexed citations
17.
Rasch, Björn, Klara Spalek, Roger Luechinger, et al.. (2009). A genetic variation of the noradrenergic system is related to differential amygdala activation during encoding of emotional memories. Proceedings of the National Academy of Sciences. 106(45). 19191–19196. 109 indexed citations
18.
Gais, Steffen, Björn Rasch, Ullrich Wagner, & Jan Born. (2008). Visual–Procedural Memory Consolidation during Sleep Blocked by Glutamatergic Receptor Antagonists. Journal of Neuroscience. 28(21). 5513–5518. 35 indexed citations
19.
Rasch, Björn & Jan Born. (2007). Maintaining memories by reactivation. Current Opinion in Neurobiology. 17(6). 698–703. 171 indexed citations
20.
Rasch, Björn, Jan Born, & Steffen Gais. (2006). Combined Blockade of Cholinergic Receptors Shifts the Brain from Stimulus Encoding to Memory Consolidation. Journal of Cognitive Neuroscience. 18(5). 793–802. 105 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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