Both the Hippocampus and Striatum Are Involved in Consolidation of Motor Sequence Memory
Open accessAbstract
Functional magnetic resonance imaging (fMRI) was used to investigate the cerebral correlates of motor sequence memory consolidation. Participants were scanned while training on an implicit oculomotor sequence learning task and during a single testing session taking place 30 min, 5 hr, or 24 hr later. During training, responses observed in hippocampus and striatum were linearly related to the gain in performance observed overnight, but not over the day. Responses in both structures were significantly larger at 24 hr than at 30 min or 5 hr. Additionally, the competitive interaction observed between these structures during training became cooperative overnight. These results stress the importance of both hippocampus and striatum in procedural memory consolidation. Responses in these areas during training seem to condition the overnight memory processing that is associated with a change in their functional interactions. These results show that both structures interact during motor sequence consolidation to optimize subsequent behavior.
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Human fMRI studies provide hints that consolidation of memories during sleep depends on hippocampal activation during prior learning.
“Hints that consolidation of memories during sleep depend on hippocampal activation during prior learning have also been provided by human studies using functional magnetic resonance imaging (fMRI) (16,733,968).”
From About Sleep's Role in Memory (2013) · cites this paper as [16]
In adults, the level of skill performance at learning modulates sleep-dependent memory consolidation, with benefits from sleep most robust at intermediate performance levels.
“In adults, the level of skill performance at learning has repeatedly been demonstrated to modulate sleep-dependent memory consolidation, whereby benefits from sleep appeared to be most robust with intermediate performance levels (16,297,679,1151).”
From About Sleep's Role in Memory (2013) · cites this paper as [16]
Particularly in initial training stages, explicit learning mechanisms involving prefrontal-hippocampal circuitry can be essential for skill acquisition, with parallel storing of procedural and hippocampus-dependent declarative aspects favoring interactions and competitions between memory systems, which can impair implicit task performance.
“Particularly in the initial stages of training, contributions of explicit (i.e., conscious) learning mechanisms involving prefrontal-hippocampal circuitry can be essential for skill acquisition, with the parallel storing of procedural and hippocampus-dependent declarative aspects favoring interactions and competitions between the two memory systems (16,43,937,1042), which can result in an impaired”
From About Sleep's Role in Memory (2013) · cites this paper as [16]
Cites
The assessment and analysis of handedness: The Edinburgh inventory
Oldfield, R. C. (1971) · Neuropsychologia · doi:10.1016/0028-3932(71)90067-4 · Cited by 35,900 · see citing works
The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research
Buysse, D. J., Reynolds, C. F., Monk, T. H., Berman, S. R., & Kupfer, D. J. (1989) · Psychiatry Research · doi:10.1016/0165-1781(89)90047-4 · Cited by 35,234 · see citing works
The Neurology of Eye Movements
Leigh, R. J., & Zee, D. S. (2015) · Oxford University Press eBooks · doi:10.1093/med/9780199969289.001.0001 · Cited by 3,829 · see citing works
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 · see citing works
Sleep function and synaptic homeostasis
Tononi, G., & Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.05.002 · Cited by 2,151 · see citing works
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138 · see citing works
Memory consolidation, retrograde amnesia and the hippocampal complex
Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924 · see citing works
Functional MRI evidence for adult motor cortex plasticity during motor skill learning
Kami, A., Meyer, G., Jezzard, P., Adams, M. M., Turner, R., & Ungerleider, L. G. (1995) · Nature · doi:10.1038/377155a0 · Cited by 1,883 · see citing works
Coordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669 · see citing works
Eichenbaum (2004) · doi:10.1016/j.neuron.2004.08.028 · Cited by 1,464 · see citing works
Practice with Sleep Makes Perfect
Walker, M. P., Brakefield, T., Morgan, A., Hobson, J. A., & Stickgold, R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00746-8 · Cited by 1,307 · see citing works
Odor cues during slow-wave sleep prompt declarative memory consolidation
Rasch, B., Büchel, C., Gais, S., & Born, J. (2007) · Science · doi:10.1126/science.1138581 · Cited by 1,181 · see citing works
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 · see citing works
Memory consolidation and the medial temporal lobe: a simple network model.
Alvarez, P., & Squire, L. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.15.7041 · Cited by 1,054 · see citing works
Reorganization and plasticity in the adult brain during learning of motor skills
Doyon, J., & Benali, H. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.004 · Cited by 1,028 · see citing works
Distinct contribution of the cortico-striatal and cortico-cerebellar systems to motor skill learning
Doyon, J., Penhune, V. B., & Ungerleider, L. G. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00158-6 · Cited by 900 · see citing works
Competition among multiple memory systems: converging evidence from animal and human brain studies
Poldrack, R. A., & Packard, M. G. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00157-4 · Cited by 880 · see citing works
Early consolidation in human primary motor cortex
Muellbacher, W., Ziemann, U., Wissel, J., Dang, N., Kofler, M., Facchini, S., Boroojerdi, B., Poewe, W., & Hallett, M. (2002) · Nature · doi:10.1038/nature712 · Cited by 803 · see citing works
Gitelman, D. R., Penny, W. D., Ashburner, J., & Friston, K. J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00058-2 · Cited by 799 · see citing works
Are spatial memories strengthened in the human hippocampus during slow wave sleep?
Peigneux, P., Laureys, S., Fuchs, S., Collette, F., Perrin, F., Reggers, J., Phillips, C., Degueldre, C., Del Fiore, G., Aerts, J., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.007 · Cited by 766 · see citing works
Self-citationExperience-dependent changes in cerebral activation during human REM sleep
Maquet, P., Laureys, S., Peigneux, P., Fuchs, S., Petiau, C., Phillips, C., Aerts, J., Del Fiore, G., Degueldre, C., Meulemans, T., et al. (2000) · Nature Neuroscience · doi:10.1038/77744 · Cited by 747 · see citing works
Self-citationDistinct basal ganglia territories are engaged in early and advanced motor sequence learning
Lehéricy, S., Benali, H., Van de Moortele, P.-F., Pélégrini-Issac, M., Waechter, T., Ugurbil, K., & Doyon, J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502762102 · Cited by 634 · see citing works
An fMRI Study of the Role of the Medial Temporal Lobe in Implicit and Explicit Sequence Learning
Schendan, H. E., Searl, M. M., Melrose, R. J., & Stern, C. E. (2003) · Neuron · doi:10.1016/s0896-6273(03)00123-5 · Cited by 610 · see citing works
Modulation of competing memory systems by distraction
Foerde, K., Knowlton, B. J., & Poldrack, R. A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602659103 · Cited by 600 · see citing works
Sleep forms memory for finger skills
Fischer, S., Hallschmid, M., Elsner, A. L., & Born, J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182178199 · Cited by 589 · see citing works
Memory deficits for implicit contextual information in amnesic subjects with hippocampal damage
Chun, M. M., & Phelps, E. A. (1999) · Nature Neuroscience · doi:10.1038/12222 · Cited by 554 · see citing works
THE NEUROLOGY OF EYE MOVEMENTS
Leigh, R. J., & Zee, D. S. (1984) · Optometry and Vision Science · doi:10.1097/00006324-198402000-00014 · Cited by 501 · see citing works
Experience-dependent changes in cerebellar contributions to motor sequence learning
Doyon, J., Song, A. W., Karni, A., Lalonde, F. M., Adams, M. M., & Ungerleider, L. G. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022615199 · Cited by 478 · see citing works
Sleep and the Time Course of Motor Skill LearningPreprint
Walker, M. P., Brakefield, T., Seidman, J., Morgan, A., Hobson, J. A., & Stickgold, R. (2003) · Learning & Memory · doi:10.1101/lm.58503 · Cited by 457 · see citing works
Awareness Modifies the Skill-Learning Benefits of Sleep
Robertson, E. M., Pascual-Leone, A., & Press, D. Z. (2004) · Current Biology · doi:10.1016/j.cub.2004.01.027 · Cited by 450 · see citing works
Striatal activation during acquisition of a cognitive skill.
Poldrack, R. A., Prabhakaran, V., Seger, C. A., & Gabrieli, J. D. E. (1999) · Neuropsychology · doi:10.1037//0894-4105.13.4.564 · Cited by 428 · see citing works
Striatal activation during acquisition of a cognitive skill.
Poldrack, R. A., Prabhakaran, V., Seger, C. A., & Gabrieli, J. D. E. (1999) · Neuropsychology · doi:10.1037/0894-4105.13.4.564 · Cited by 428 · see citing works
The Time Course of Changes during Motor Sequence Learning: A Whole-Brain fMRI Study
Toni, I., Krams, M., Turner, R., & Passingham, R. E. (1998) · NeuroImage · doi:10.1006/nimg.1998.0349 · Cited by 411 · see citing works
Korman, M., Raz, N., Flash, T., & Karni, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2035019100 · Cited by 378 · see citing works
Doyon, J., Owen, A. M., Petrides, M., Sziklas, V., & Evans, A. C. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01249.x · Cited by 326 · see citing works
Peigneux, P., Laureys, S., Fuchs, S., Destrebecqz, A., Collette, F., Delbeuck, X., Phillips, C. L. M., Aerts, J. J., Fiore, G. D., Degueldre, C., et al. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00278-7 · Cited by 309 · see citing works
Self-citationSleep-dependent motor memory plasticity in the human brain
Walker, M. P., Stickgold, R., Alsop, D., Gaab, N., & Schlaug, G. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.007 · Cited by 308 · see citing works
Parallel brain systems for learning with and without awareness.Preprint
Reber, P. J., & Squire, L. R. (1994) · Learning & Memory · doi:10.1101/lm.1.4.217 · Cited by 266 · see citing works
Motor Memory Consolidation in Sleep Shapes More Effective Neuronal Representations
Fischer, S., Nitschke, M. F., Melchert, U. H., Erdmann, C., & Born, J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1743-05.2005 · Cited by 255 · see citing works
Gabrieli, J. D. E., Corkin, S., Mickel, S. F., & Growdon, J. H. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.6.899 · Cited by 234 · see citing works
Dynamics of Frontal, Striatal, and Hippocampal Systems during Rule Learning
Seger, C. A. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj092 · Cited by 222 · see citing works
Basal ganglia and dopamine contributions to probabilistic category learning
Daphna Shohamy, A., Myers, C. E., Kalanithi, J., & Gluck, M. A. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.07.008 · Cited by 216 · see citing works
Functional Anatomy of a Prelearned Sequence of Horizontal Saccades in Humans
Petit, L., Orssaud, C., Tzourio‐Mazoyer, N., Crivello, F., Berthoz, A., & Mazoyer, B. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-11-03714.1996 · Cited by 214 · see citing works
Maquet, P., Schwartz, S., Passingham, R. E., & Frith, C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-04-01432.2003 · Cited by 199 · see citing works
Self-citationThe basal ganglia in human learning
Seger, C. A. (2006) · The Neuroscientist · doi:10.1177/1073858405285632 · Cited by 182 · see citing works
Striatum forever, despite sequence learning variability: A random effect analysis of PET data
Peigneux, P., Maquet, P., Meulemans, T., Destrebecqz, A., Laureys, S., Degueldre, C., Delfiore, G., Aerts, J. J., Luxen, A., Franck, G., et al. (2000) · Human Brain Mapping · doi:10.1002/1097-0193(200008)10:4 · Cited by 172 · see citing works
Self-citationFrom primed to learn: the saturation of repetition priming and the induction of long-term memory
Hauptmann, B., & Karni, A. (2002) · Cognitive Brain Research · doi:10.1016/s0926-6410(01)00124-0 · Cited by 166 · see citing works
Gabrieli, J. D. E., Corkin, S., Mickel, S. F., et al. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.6.899 · Cited by 166 · see citing works
Fletcher, P. C., Zafiris, O., Frith, C., Honey, R. A. E., Corlett, P. R., Zilles, K., & Fink, G. R. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh201 · Cited by 156 · see citing works
Higher-Order Associative Learning in Amnesia: Evidence from the Serial Reaction Time Task
Curran, T. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.4.522 · Cited by 149 · see citing works
Degonda, N., Mondadori, C. R. A., Bosshardt, S., Schmidt, C. F., Boesiger, P., Nitsch, R. M., Höck, C., & Henke, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.030 · Cited by 147 · see citing works
How do memory systems interact? Evidence from human classification learning
Poldrack, R. A., & Rodriguez, P. F. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.05.003 · Cited by 145 · see citing works
Sleep-Dependent Consolidation of Contextual Learning
Spencer, R. M. C., Sunm, M., & Ivry, R. B. (2006) · Current Biology · doi:10.1016/j.cub.2006.03.094 · Cited by 138 · see citing works
The Dynamics of Hippocampal Activation during Encoding of Overlapping Sequences
Kumaran, D., & Maguire, E. A. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.024 · Cited by 120 · see citing works
The time course of off-line motor sequence learning
Press, D. Z., Casement, M. D., Pascual‐Leone, Á., & Robertson, E. M. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2005.05.010 · Cited by 103 · see citing works
Human Cortical Networks for New and Familiar Sequences of Saccades
Grosbras, M. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.10.936 · Cited by 93 · see citing works
Implicit oculomotor sequence learning in humans: Time course of offline processing
Albouy, G., Ruby, P. M., Phillips, C. L. M., Luxen, A., Peigneux, P., & Maquet, P. (2006) · Brain Research · doi:10.1016/j.brainres.2006.03.076 · Cited by 82 · see citing works
Self-citationLeconte, P., Hennevin, E., & Bloch, V. (1973) · Brain Research · doi:10.1016/0006-8993(73)90428-9 · Cited by 77 · see citing works
Active hippocampus during nonconscious memories
Henke, K., Treyer, V., Nagy, E. T., Kneifel, S., Dürsteler, M., Nitsch, R. M., & Buck, A. (2003) · Consciousness and Cognition · doi:10.1016/s1053-8100(02)00006-5 · Cited by 74 · see citing works
Circadian modulation of sequence learning under high and low sleep pressure conditions
Cajochen, C., Knoblauch, V., Wirz‐Justice, A., Kräuchi, K., Graw, P., & Wallach, D. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.08.013 · Cited by 70 · see citing works
Oculomotor sequence learning: a positron emission tomography study
Kawashima, R., Tanji, J., Okada, K., Sugiura, M., Sato, K., Kinomura, S., Inoue, K., Ogawa, A., & Fukuda, H. (1998) · Experimental Brain Research · doi:10.1007/s002210050485 · Cited by 56 · see citing works
Ambrosini, M. V., LANGELLA, M., GIRONICARNEVALE, U., & Giuditta, A. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90134-n · Cited by 40 · see citing works
Nagy, H., Kéri, S., Myers, C. E., Benedek, G., Daphna Shohamy, A., & Gluck, M. A. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.10.017 · Cited by 40 · see citing works
Involvement of the medial temporal lobe in priming for new associations
Yang, J., Weng, X., Guan, L., et al. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00289-0 · Cited by 28 · see citing works
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Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works
Neuroplasticity Subserving Motor Skill Learning
Dayan, E., & Cohen, L. G. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.008 · Cited by 1,408 · see citing works
Functional Neuroimaging Insights into the Physiology of Human Sleep.
Dang-Vu, T. T., Schabus, M., Desseilles, M., Sterpenich, V., Bonjean, M., & Maquet, P. (2010) · SLEEP · doi:10.1093/sleep/33.12.1589 · Cited by 284 · see citing works
Self-citationPromoting memory consolidation during sleep: A meta-analysis of targeted memory reactivation
Hu, X., Cheng, L. Y., Chiu, M. H., & Paller, K. A. (2020) · Psychological Bulletin · doi:10.1037/bul0000223 · Cited by 232 · see citing works
From Creation to Consolidation: A Novel Framework for Memory Processing
Robertson, E. M. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000019 · Cited by 236 · see citing works
Niemann, C., Godde, B., & Voelcker-Rehage, C. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00170 · Cited by 190 · see citing works
McMorris, T. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.08.011 · Cited by 188 · see citing works
The sleeping child outplays the adult's capacity to convert implicit into explicit knowledge
Wilhelm, I., Rose, M., Imhof, K. I., Rasch, B., Büchel, C., & Born, J. (2013) · Nature Neuroscience · doi:10.1038/nn.3343 · Cited by 170 · see citing works
Sleep and memory in mammals, birds and invertebrates
Vorster, A. P., & Born, J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.09.020 · Cited by 169 · see citing works
New Insights in Human Memory Interference and Consolidation
Robertson, E. M. (2012) · Current Biology · doi:10.1016/j.cub.2011.11.051 · Cited by 168 · see citing works
The role of rapid eye movement sleep for amygdala-related memory processing
Genzel, L., Spoormaker, V. I., Konrad, B. N., & Dresler, M. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.01.008 · Cited by 161 · see citing works
Sleep-dependent memory consolidation – What can be learnt from children?
Wilhelm, I., Prehn-Kristensen, A., & Born, J. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.002 · Cited by 161 · see citing works
Wilhelm, I., Metzkow‐Mészàros, M., Knapp, S., & Born, J. (2012) · Developmental Science · doi:10.1111/j.1467-7687.2012.01146.x · Cited by 143 · see citing works
Durrant, S. J., Cairney, S. A., & Lewis, P. A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs244 · Cited by 124 · see citing works
Cerebellar contributions to visuomotor adaptation and motor sequence learning: an ALE meta-analysis
Bernard, J. A., & Seidler, R. D. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00027 · Cited by 122 · see citing works
Rauchs, G., Feyers, D., Landeau, B., Bastin, C., Luxen, A., Maquet, P., & Collette, F. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3972-10.2011 · Cited by 121 · see citing works
Self-citationThe role of sleep in motor sequence consolidation: stabilization rather than enhancement
Nettersheim, A., Hallschmid, M., Born, J., & Diekelmann, S. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1236-14.2015 · Cited by 104 · see citing works
Cooperation between the hippocampus and the striatum during episodic encoding
Sadeh, T., Shohamy, D., Levy, D. R., Reggev, N., & Maril, A. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21549 · Cited by 104 · see citing works
Schapiro, A. C., Reid, A. G., Morgan, A., Manoach, D. S., Verfaellie, M., & Stickgold, R. (2019) · Hippocampus · doi:10.1002/hipo.23101 · Cited by 94 · see citing works
At least eighty percent of brain grey matter is modifiable by physical activity: A review study
Batouli, S. A. H., & Saba, V. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.06.002 · Cited by 92 · see citing works
Cortical–hippocampal coupling during manifold exploration in motor cortex
Kim, J., Joshi, A., Frank, L., & Ganguly, K. (2023) · Nature · doi:10.1038/s41586-022-05533-z · Cited by 77 · see citing works
The impact of overnight consolidation upon memory for emotional and neutral encoding contexts
Lewis, P. A., Cairney, S., Manning, L., & Critchley, H. D. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.05.009 · Cited by 79 · see citing works
Evidence for two distinct sleep-related long-term memory consolidation processes
Schönauer, M., Grätsch, M., & Gais, S. (2015) · Cortex · doi:10.1016/j.cortex.2014.08.005 · Cited by 73 · see citing works
Concurrent TMS to the primary motor cortex augments slow motor learning
Narayana, S., Zhang, W., Rogers, W., Strickland, C., Franklin, C., Lancaster, J. L., & Fox, P. T. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.024 · Cited by 41 · see citing works
Keeping time in your sleep: Overnight consolidation of temporal rhythm
Lewis, P. A., Couch, T. J., & Walker, M. P. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.10.025 · Cited by 38 · see citing works
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Nicolas, J., King, B. R., Levesque, D., Lazzouni, L., Coffey, E., Swinnen, S., Doyon, J., Carrier, J., & Albouy, G. (2022) · eLife · doi:10.7554/elife.73930 · Cited by 28 · see citing works
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Sawangjit, A., Harkotte, M., Oyanedel, C. N., Niethard, N., Born, J., & Inostroza, M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2203165119 · Cited by 28 · see citing works
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Debarnot, U., Castellani, E., Guillot, A., Giannotti, V., Dimarco, M., & Sebastiani, L. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.10.009 · Cited by 17 · see citing works
- Authors
- Albouy, G., Sterpenich, V., Balteau, E., Vandewalle, G., Desseilles, M., Dang-Vu, T., Darsaud, A., Ruby, P., Luppi, P.-H., Degueldre, C., Peigneux, P., Luxen, A., & Maquet, P.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- University of Liège (BE)
- Inserm (FR)
- Corresponding author
- Maquet, Pierre
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2008-04
- Volume
- 58
- Issue
- 2
- Pages
- 261-272
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2078889033
- Cited by
- 463
- References
- 64
- Citations by year
- 2026: 12 · 2025: 28 · 2024: 30 · 2023: 26 · 2022: 32 · 2021: 27 · 2020: 25 · 2019: 29 · 2018: 16 · 2017: 24 · 2016: 35 · 2015: 22 · 2014: 25 · 2013: 39 · 2012: 25
- FWCI
- 11.71
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Repository of the University of Namur (publishedVersion)
- Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
- Lirias (KU Leuven) (submittedVersion)
- ORBi (University of Liège) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- memory consolidation, hippocampus, striatum, procedural memory, implicit learning
- MeSH terms
- Adult, Analysis of Variance, Brain Mapping, Corpus Striatum, Eye Movements, Female, Hippocampus, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Memory, Oxygen, Reaction Time, Serial Learning, Task Performance and Analysis
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 ›
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