The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Implicit Learning–Explicit Knowing: A Role for Sleep in Memory System Interaction
Abstract
There is evidence that sleep supports the enhancement of implicit as well as explicit memories (i.e., two memory systems that during learning normally appear to act together). Here, employing a serial reaction time task (SRTT) paradigm, we examined the question whether sleep can provide explicit knowledge on an implicitly acquired skill. At learning, young healthy subjects (n = 20) were first trained on the SRTT. Then, implicit knowledge was assessed on two test blocks, in which grammatically incorrect target positions were occasionally interspersed by the difference in reaction times between grammatically correct and incorrect target positions. To assess explicit sequence knowledge, thereafter subjects performed on a generation task in which they were explicitly instructed to predict the sequential target positions. In half the subjects, learning took place before a 9-hour retention interval filled with nocturnal sleep (sleep group), in the other half, the retention interval covered a 9-hour period of daytime wakefulness (wake group). At subsequent retesting, both testing on the generation task and the SRTT test blocks was repeated. At learning before the retention interval, subjects displayed significant implicit sequence knowledge which was comparable for the sleep and wake groups. Moreover, both groups did not display any explicit sequence knowledge as indicated by a prediction performance not differing from chance on the generation task. However, at retesting, there was a distinct gain in explicit knowledge in the subjects who had slept in the retention interval, whereas generation task performance in the wake group remained at chance level. SRTT performance in the test blocks at retesting did not indicate any further gain in skill (i.e., unchanged reaction time differences between grammatically correct and incorrect target positions) independently of whether subjects had slept or remained awake after learning. Our results indicate a selective enhancement of explicit memory formation during sleep. Because before sleep subjects only had implicit knowledge on the sequence of target transitions, these data point to an interaction between implicit and explicit memory systems during sleep-dependent off-line learning.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In fact, the latter group at the retest still performed at chance level.”
From System consolidation of memory during sleep (2012) · cites this paper as Fischer et al. 2006
In the citing paper
“At this retest, the subjects who had slept after SRTT training were distinctly more able to deliberately generate the sequence underlying the SRTT than the subjects who had stayed awake after the initial SRTT training.”
From System consolidation of memory during sleep (2012) · cites this paper as Fischer et al. 2006
In the citing paper
“Yet, significant explicit sequence knowledge developed when SRTT training was followed by nocturnal sleep (324,382).”
From About Sleep's Role in Memory (2013) · cites this paper as [382]
In the citing paper
“Sleep deprivation impairs performance on tasks that rely on the explicit memory system (Drosopoulos et al., 2005; Fischer et al., 2006)”
From Dual conception of risk in the Iowa Gambling Task: effects of sleep deprivation and test-retest gap (2013) · cites this paper as Fischer et al., 2006
Citations
Cites
Rechtschaffen, A. (1968) · Medical Entomology and Zoology · Cited by 11,772
Attentional requirements of learning: Evidence from performance measures
Nissen, M. J., & Bullemer, P. (1987) · Cognitive Psychology · doi:10.1016/0010-0285(87)90002-8 · Cited by 2,966
Implicit Learning and Tacit Knowledge
Reber, A. S. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/2834.003.0047 · Cited by 2,013
Huber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854
Declarative and Nondeclarative Memory: Multiple Brain Systems Supporting Learning and Memory
Squire, L. R. (1992) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1992.4.3.232 · Cited by 1,282 · cited 2×
“…takes place without the need of any conscious capacities and without the subject being aware of having acquired or accessed any new information (Destrebecqz & Cleeremans, 2001; Willingham, 2001; Willingham & Goedert-Eschmann, 1999; Seger, 1994; Shanks & John, 1994; Squire, 1992; Reber, 1989).”
BackgroundCharacteristics of dissociable human learning systems
Shanks, D. R., & St. John, M. F. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035032 · Cited by 1,163
Interactive memory systems in the human brain
Poldrack, R. A., Clark, J., Paré-Blagoev, E. J., Shohamy, D., Creso Moyano, J., Myers, C., & Gluck, M. A. (2001) · Nature · doi:10.1038/35107080 · Cited by 1,132
Effects of early and late nocturnal sleep on declarative and procedural memory
Plihal, W., & Born, J. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.4.534 · Cited by 1,026
Wagner, U., Gais, S., Haider, H., Verleger, R., & Born, J. (2004) · Nature · doi:10.1038/nature02223 · Cited by 1,012
Consolidation in human motor memory
Brashers-Krug, T. M., Shadmehr, R., & Bizzi, E. (1996) · Nature · doi:10.1038/382252a0 · Cited by 976
Research works printed but not linked: 1
- Reber A. S., 1989, Journal of Experimental Psychology: General, 120, 112
Cited by
Sorted by citations
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760
Self-citationRasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783
“Yet, significant explicit sequence knowledge developed when SRTT training was followed by nocturnal sleep (324, 382).”
BackgroundSelf-citationHippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759
System consolidation of memory during sleep
Born, J., & Wilhelm, I. (2012) · Psychological Research · doi:10.1007/s00426-011-0335-6 · Cited by 667
Self-citationThe contribution of sleep to hippocampus-dependent memory consolidation
Marshall, L., & Born, J. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.09.001 · Cited by 667
Metadata
- Authors
- Fischer, S., Drosopoulos, S., Tsen, J., & Born, J.
- Affiliations
- University of Lübeck (DE)
- 1University of Lübeck
- Venue
- Journal of Cognitive Neuroscience
- Publisher
- MIT Press - Journals
- Published
- 2006-03-01
- Volume
- 18
- Issue
- 3
- Pages
- 311-319
- ISSN
- 0898-929X (ISSN-L)
- 1530-8898
- OpenAlex
- W2103281316
- Cited by
- 215
- References
- 49
- Citations by year
- 2026: 1 · 2025: 11 · 2024: 9 · 2023: 5 · 2022: 5 · 2021: 12 · 2020: 4 · 2019: 27 · 2018: 9 · 2017: 19 · 2016: 8 · 2015: 14 · 2014: 15 · 2013: 16 · 2012: 9
- FWCI
- 5.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cognitive Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- sleep-dependent memory consolidation, implicit memory, declarative memory, serial reaction time task, sequence learning, retention interval, offline learning
- MeSH terms
- Adolescent, Adult, Female, Humans, Functional Laterality, Learning, Male, Memory, Probability, Reaction Time, Sleep, Wakefulness, Knowledge
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review