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Post-learning Hippocampal Dynamics Promote Preferential Retention of Rewarding Events
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Reward motivation is known to modulate memory encoding, and this effect depends on interactions between the substantia nigra/ventral tegmental area complex (SN/VTA) and the hippocampus. It is unknown, however, whether these interactions influence offline neural activity in the human brain that is thought to promote memory consolidation. Here we used fMRI to test the effect of reward motivation on post-learning neural dynamics and subsequent memory for objects that were learned in high- and low-reward motivation contexts. We found that post-learning increases in resting-state functional connectivity between the SN/VTA and hippocampus predicted preferential retention of objects that were learned in high-reward contexts. In addition, multivariate pattern classification revealed that hippocampal representations of high-reward contexts were preferentially reactivated during post-learning rest, and the number of hippocampal reactivations was predictive of preferential retention of items learned in high-reward contexts. These findings indicate that reward motivation alters offline post-learning dynamics between the SN/VTA and hippocampus, providing novel evidence for a potential mechanism by which reward could influence memory consolidation.
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“Signs of reward-related biasing of reactivations during sleep and wake have been likewise observed in humans using fMRI.”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [147]
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Cites
AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913
The Nature of Recollection and Familiarity: A Review of 30 Years of Research
Yonelinas, A. P. (2002) · Journal of Memory and Language · doi:10.1006/jmla.2002.2864 · Cited by 3,840
The reward circuit: linking primate anatomy and human imaging
Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718
Large-scale automated synthesis of human functional neuroimaging data.
Yarkoni, T., Poldrack, R. A., Nichols, T. E., Van Essen, D. C., & Wager, T. D. (2011) · Nature Methods · doi:10.1038/nmeth.1635 · Cited by 3,686
The Medial Temporal Lobe and Recognition Memory
Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580
Self-citationAnticipation of Increasing Monetary Reward Selectively Recruits Nucleus Accumbens
Knutson, B., Adams, C. M., Fong, G. W., & Hommer, D. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-16-j0002.2001 · Cited by 2,244
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983
Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759
Reverse replay of behavioural sequences in hippocampal place cells during the awake state
Foster, D. J., & Wilson, M. A. (2006) · Nature · doi:10.1038/nature04587 · Cited by 1,727
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Locus coeruleus and dopaminergic consolidation of everyday memory
Takeuchi, T., Duszkiewicz, A. J., Sonneborn, A., Spooner, P. A., Yamasaki, M., Watanabe, M., Smith, C. C., Fernández, G., Deisseroth, K., Greene, R. W., et al. (2016) · Nature · doi:10.1038/nature19325 · Cited by 827
A contextual binding theory of episodic memory: systems consolidation reconsidered
Yonelinas, A. P., Ranganath, C., Ekstrom, A. D., & Wiltgen, B. J. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0150-4 · Cited by 492
Sleep—A brain-state serving systems memory consolidation
Brodt, S., Inostroza, M., Niethard, N., & Born, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.005 · Cited by 343
Schapiro, A. C., McDevitt, E. A., Rogers, T. T., Mednick, S. C., & Norman, K. A. (2018) · Nature Communications · doi:10.1038/s41467-018-06213-1 · Cited by 282
Mechanisms of Memory Disruption in Depression
Dillon, D. G., & Pizzagalli, D. A. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2017.12.006 · Cited by 292
Transcending time in the brain: How event memories are constructed from experience
Clewett, D., DuBrow, S., & Davachi, L. (2019) · Hippocampus · doi:10.1002/hipo.23074 · Cited by 252
Awake Reactivation of Prior Experiences Consolidates Memories and Biases Cognition
Tambini, A., & Davachi, L. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.07.008 · Cited by 190
Reward retroactively enhances memory consolidation for related itemsPreprint
Patil, A., Murty, V. P., Dunsmoor, J. E., Phelps, E. A., & Davachi, L. (2016) · Learning & Memory · doi:10.1101/lm.042978.116 · Cited by 152
Murty, V. P., Tompary, A., Adcock, R. A., & Davachi, L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4032-15.2016 · Cited by 141
What Are Memories For? The Hippocampus Bridges Past Experience with Future Decisions
Biderman, N., Bakkour, A., & Shohamy, D. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.04.004 · Cited by 160
Optimizing motivation and attention for motor performance and learning
Lewthwaite, R., & Wulf, G. (2017) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2017.04.005 · Cited by 137
Memory consolidation as an adaptive process
Cowan, E. T., Schapiro, A. C., Dunsmoor, J. E., & Murty, V. P. (2021) · Psychonomic Bulletin & Review · doi:10.3758/s13423-021-01978-x · Cited by 133
Offline replay supports planning in human reinforcement learning
Momennejad, I., Otto, A. R., Daw, N. D., & Norman, K. A. (2018) · eLife · doi:10.7554/elife.32548 · Cited by 149
Development of Hippocampal–Prefrontal Cortex Interactions through Adolescence
Calabro, F. J., Murty, V. P., Jalbrzikowski, M., Tervo‐Clemmens, B., & Luna, B. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz186 · Cited by 139
Memory and Reward-Based Learning: A Value-Directed Remembering Perspective
Knowlton, B. J., & Castel, A. D. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-032921-050951 · Cited by 115
Integration and differentiation of hippocampal memory traces
Brunec, I. K., Robin, J., Olsen, R. K., Moscovitch, M., & Barense, M. D. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.07.024 · Cited by 122
Replay in Deep Learning: Current Approaches and Missing Biological Elements
Hayes, T. L., Krishnan, G. P., Bazhenov, M., Siegelmann, H. T., Sejnowski, T. J., & Kanan, C. (2021) · Neural Computation · doi:10.1162/neco_a_01433 · Cited by 106
Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction
Gerlicher, A. M. V., Tüscher, O., & Kalisch, R. (2018) · Nature Communications · doi:10.1038/s41467-018-06785-y · Cited by 103
Post-learning hippocampal replay selectively reinforces spatial memory for highly rewarded locations
Michon, F., Sun, J.-J., Kim, C. Y., Ciliberti, D., & Kloosterman, F. (2019) · Current Biology · doi:10.1016/j.cub.2019.03.048 · Cited by 86
Retroactive and graded prioritization of memory by reward
Braun, E. K., Wimmer, G. E., & Shohamy, D. (2018) · Nature Communications · doi:10.1038/s41467-018-07280-0 · Cited by 112
Locus Coeruleus and Dopamine-Dependent Memory Consolidation
Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91
Spontaneous cognitive processes and the behavioral validation of time-varying brain connectivity
Kucyi, A., Tambini, A., Sadaghiani, S., Keilholz, S. D., & Cohen, J. R. (2018) · Network Neuroscience · doi:10.1162/netn_a_00037 · Cited by 95
Motivated misremembering of selfish decisions
Carlson, R. W., Maréchal, M. A., Oud, B., Fehr, E., & Crockett, M. J. (2020) · Nature Communications · doi:10.1038/s41467-020-15602-4 · Cited by 92
Hippocampal representations as a function of time, subregion, and brain state
Duncan, K. D., & Schlichting, M. L. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.03.006 · Cited by 86
Wittkuhn, L., & Schuck, N. W. (2021) · Nature Communications · doi:10.1038/s41467-021-21970-2 · Cited by 77
Reward Prediction Error and Declarative Memory
Ergo, K., Loof, E. D., & Verguts, T. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.02.009 · Cited by 66
Moscovitch, M., & Gilboa, A. (2021) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/yxbrs · Cited by 68
Free recall test experience potentiates strategy-driven effects of value on memory.
Cohen, M. S., Rissman, J., Hovhannisyan, M., Castel, A. D., & Knowlton, B. J. (2017) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0000395 · Cited by 57
Onward and upward: Optimizing motor performance
Chua, L.-K., Wulf, G., & Lewthwaite, R. (2018) · Human Movement Science · doi:10.1016/j.humov.2018.05.006 · Cited by 62
The neuroscience of active learning and direct instruction
Dubinsky, J. M., & Hamid, A. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105737 · Cited by 121
Tambini, A., Berners-Lee, A., & Davachi, L. (2017) · Scientific Reports · doi:10.1038/s41598-017-15608-x · Cited by 55
Causal Contribution of Awake Post-encoding Processes to Episodic Memory Consolidation
Tambini, A., & D’Esposito, M. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.063 · Cited by 54
Distinct Medial Temporal Lobe Network States as Neural Contexts for Motivated Memory Formation
Murty, V. P., & Adcock, R. A. (2017) · Springer eBooks · doi:10.1007/978-3-319-50406-3_15 · Cited by 55
Wittkuhn, L., Chien, S., Hall-McMaster, S., & Schuck, N. W. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.08.002 · Cited by 49
Signed Reward Prediction Errors in the Ventral Striatum Drive Episodic Memory
Calderon, C. B., Loof, E. D., Ergo, K., Snoeck, A., Boehler, C. N., & Verguts, T. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1785-20.2020 · Cited by 49
Motivational Influences on Memory
Murty, V. P., & Dickerson, K. C. (2016) · Advances in motivation and achievement · doi:10.1108/s0749-742320160000019019 · Cited by 49
Reorganization of CA1 dendritic dynamics by hippocampal sharp-wave ripples during learning
Rolotti, S. V., Blockus, H., Sparks, F. T., Priestley, J. B., & Losonczy, A. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.017 · Cited by 50
Liu, Z., Grady, C. L., & Moscovitch, M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.032 · Cited by 52
Neural correlates underlying the effect of reward value on recognition memory
Elliott, B. L., Blais, C., McClure, S. M., & Brewer, G. A. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116296 · Cited by 43
Abstract Representation of Prospective Reward in the Hippocampus
Zeithamová, D., Gelman, B. D., Frank, L. E., & Preston, A. R. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0719-18.2018 · Cited by 40
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DuBrow, S., Eberts, E. A., & Murty, V. P. (2019) · Psychonomic Bulletin & Review · doi:10.3758/s13423-019-01650-5 · Cited by 43
Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
Issa, J. B., Radvansky, B. A., Xuan, F., & Dombeck, D. A. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01557-4 · Cited by 48
Gruber, M. J., Valji, A., & Ranganath, C. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316823279.018 · Cited by 55
Self-citationKing, B. R., Gann, M. A., Mantini, D., Doyon, J., & Albouy, G. (2022) · iScience · doi:10.1016/j.isci.2022.105498 · Cited by 40
Human aging reduces the neurobehavioral influence of motivation on episodic memory
Geddes, M. R., Mattfeld, A. T., Angeles, C. D. L., Keshavan, A., & Gabrieli, J. D. E. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.053 · Cited by 42
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Wang, Y. C., Adcock, R. A., & Egner, T. (2023) · Psychonomic Bulletin & Review · doi:10.3758/s13423-023-02375-2 · Cited by 46
Divided Attention Selectively Impairs Value-Directed Encoding
Elliott, B. L., & Brewer, G. A. (2019) · Collabra Psychology · doi:10.1525/collabra.156 · Cited by 37
Learning offline: memory replay in biological and artificial reinforcement learning
Roscow, E. L., Chua, R., Costa, R. P., Jones, M. W., & Lepora, N. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.07.007 · Cited by 36
Behavioral Modulation by Spontaneous Activity of Dopamine Neurons
Ichinose, T., Tanimoto, H., & Yamagata, N. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00088 · Cited by 37
Halamish, V., Madmon, I., & Moed, A. (2019) · Experimental Psychology (formerly Zeitschrift für Experimentelle Psychologie) · doi:10.1027/1618-3169/a000455 · Cited by 42
Competitive learning modulates memory consolidation during sleep
Antony, J. W., Cheng, L. Y., Brooks, P. P., Paller, K. A., & Norman, K. A. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.08.007 · Cited by 33
Distinct effects of reward and navigation history on hippocampal forward and reverse replays
Bhattarai, B., Lee, J. W., & Jung, M. W. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912533117 · Cited by 37
Individual Differences in Value-Directed Remembering
Elliott, B. L., McClure, S. M., & Brewer, G. A. (2019) · Cognition · doi:10.1016/j.cognition.2020.104275 · Cited by 34
Repetition dynamically and rapidly increases cortical, but not hippocampal, offline reactivation
Yu, W., Zadbood, A., Chanales, A. J. H., & Davachi, L. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2405929121 · Cited by 39
Doss, M. K., de Wit, H., & Gallo, D. A. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105188 · Cited by 37
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Doss, M. K., Samaha, J., Barrett, F. S., Griffiths, R. R., de Wit, H., Gallo, D. A., & Koen, J. D. (2023) · Psychological Review · doi:10.1037/rev0000455 · Cited by 33
Self-citationFrank, L. E., Preston, A. R., & Zeithamová, D. (2019) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-019-00700-8 · Cited by 27
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Schapiro, A. C., McDevitt, E. A., Rogers, T. T., Mednick, S. C., & Norman, K. A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/173021 · Cited by 26
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Chiew, K. S., Stanek, J. K., & Adcock, R. A. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00555 · Cited by 26
Hippocampal signatures of awake targeted memory reactivation
Alm, K. H., Ngo, C. T., & Olson, I. R. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1790-2 · Cited by 26
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Zhu, Y., Zeng, Y., Ren, J., Zhang, L., Chen, C., Fernández, G., & Qin, S. (2022) · eLife · doi:10.7554/elife.60190 · Cited by 25
Wimmer, G. E., & Poldrack, R. A. (2021) · Memory & Cognition · doi:10.3758/s13421-021-01233-7 · Cited by 26
Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
Poh, J.-H., Vu, M.-A. T., Stanek, J. K., Hsiung, A., Egner, T., & Adcock, R. A. (2022) · Nature Communications · doi:10.1038/s41467-022-34459-3 · Cited by 24
Awake Hippocampal–Cortical Co-reactivation Is Associated with Forgetting
Tanrıverdi, B., Cowan, E. T., Metoki, A., Jobson, K. R., Murty, V. P., Chein, J. M., & Olson, I. R. (2023) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02021 · Cited by 21
Cannabinoid disruption of learning mechanisms involved in reward processingPreprint
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Iman, I. N., Ahmad, N. A. Z., Yusof, N. A. M., Talib, U. N., Norazit, A., Kumar, J., Mehat, M. Z., Hassan, Z., Müller, C. P., & Mustapha, M. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.708055 · Cited by 20
Long-term effects of directed forgetting
Hupbach, A. (2017) · Memory · doi:10.1080/09658211.2017.1358748 · Cited by 22
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Sneve, M. H., Grydeland, H., Amlien, I. K., Langnes, E., Walhovd, K. B., & Fjell, A. M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.05.048 · Cited by 20
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Cheng, S., Jiang, T., Xue, J., Wang, S., Chen, C., & Zhang, M. (2020) · Learning & Memory · doi:10.1101/lm.051722.120 · Cited by 19
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Folvik, L., Sneve, M. H., Ness, H. T., Dídac Vidal-piñeiro, A., Raud, L., Geier, O. M., Walhovd, K. B., & Fjell, A. M. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac384 · Cited by 17
Remembering rewarding futures: A simulation‐selection model of the hippocampus
Jung, M. W., Lee, H., Jeong, Y., Lee, J. W., & Lee, I. (2018) · Hippocampus · doi:10.1002/hipo.23023 · Cited by 16
Traces of Semantization, from Episodic to Semantic Memory in a Spiking Cortical Network Model
Chrysanthidis, N., Fiebig, F., Lansner, A., & Herman, P. A. (2022) · eNeuro · doi:10.1523/eneuro.0062-22.2022 · Cited by 14
Gann, M. A., King, B. R., Dolfen, N., Veldman, M. P., Davare, M., Swinnen, S. P., Mantini, D., Robertson, E. M., & Albouy, G. (2021) · Scientific Reports · doi:10.1038/s41598-021-99926-1 · Cited by 14
Chan, J. C. K., O’Donnell, R., & Manley, K. D. (2022) · Journal of Experimental Psychology Applied · doi:10.1037/xap0000394 · Cited by 16
Context and Time Matter: Effects of Emotion and Motivation on Episodic Memory Overtime
Sun, Q. Y., Gu, S., & Yang, J. (2018) · Neural Plasticity · doi:10.1155/2018/7051925 · Cited by 17
Selective memory disrupted in intra-modal dual-task encoding conditions
Siegel, A. L. M., Schwartz, S. T., & Castel, A. D. (2021) · Memory & Cognition · doi:10.3758/s13421-021-01166-1 · Cited by 15
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Krishnan, S., & Sheffield, M. E. J. (2023) · SSRN Electronic Journal · doi:10.1101/2023.12.21.572809 · Cited by 16
Iyer, S., Collier, E., Broom, T. W., Finn, E. S., & Meyer, M. L. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2306295121 · Cited by 16
Tompary, A., & Davachi, L. (2024) · eLife · doi:10.7554/elife.84359 · Cited by 17
Neuronal Oscillations and Reactivation Subserving Memory Consolidation
Bergmann, T. O., & Staresina, B. P. (2017) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-319-45066-7_12 · Cited by 14
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Bang, J. W., Hamilton-Fletcher, G., & Chan, K. C. (2021) · The Neuroscientist · doi:10.1177/10738584211037619 · Cited by 17
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Willems, T., & Henke, K. (2021) · Hippocampus · doi:10.1002/hipo.23391 · Cited by 13
Pu, Y., Cornwell, B. R., Cheyne, D., & Johnson, B. W. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.05.029 · Cited by 14
Barr, J. L., Bray, B., & Forster, G. L. (2018) · InTech eBooks · doi:10.5772/intechopen.70854 · Cited by 13
Murty, V. P., Tompary, A., Adcock, R. A., & Davachi, L. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.4032-15.2017 · Cited by 18
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Motivated misremembering of selfish decisionsPreprint
Carlson, R. W., Maréchal, M. A., Oud, B., Fehr, E., & Crockett, M. J. (2018) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/7ck25 · Cited by 14
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Hilaire, K. J. S., Chan, J. C. K., & Ahn, D. (2023) · Psychonomic Bulletin & Review · doi:10.3758/s13423-023-02353-8 · Cited by 16
Meliß, S., Tsuchiyagaito, A., Byrne, P., van Reekum, C. M., & Murayama, K. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00134 · Cited by 15
Reactivation and consolidation of memory traces during post‐encoding rest across the adult lifespan
Mekbib, D. B., & McDonough, I. M. (2025) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.52290 · Cited by 11
Evolutionary monkey oscillomics: Generating linking hypotheses from preserved brain rhythms
Murphy, E. (2016) · Theoretical Linguistics · doi:10.1515/tl-2016-0005 · Cited by 11
Chiew, K. S., Hashemi, J., Gans, L. K., Lerebours, L., Clement, N. J., Vu, M.-A. T., Sapiro, G., Heller, N. E., & Adcock, R. A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193506 · Cited by 10
Dickerson, K. C., & Adcock, R. A. (2018) · Wiley eBooks · doi:10.1002/9781119170174.epcn107 · Cited by 13
Metadata
- Authors
- Gruber, M. J., Ritchey, M., Wang, S.-F., Doss, M. K., & Ranganath, C.
- Affiliations
- University of California, Davis (US)
- Corresponding author
- Gruber, Matthias J.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2016-03
- Volume
- 89
- Issue
- 5
- Pages
- 1110-1120
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC4777629
- OpenAlex
- W2257753958
- Cited by
- 212
- References
- 67
- Citations by year
- 2026: 10 · 2025: 19 · 2024: 27 · 2023: 18 · 2022: 25 · 2021: 28 · 2020: 17 · 2019: 21 · 2018: 24 · 2017: 16 · 2016: 7
- FWCI
- 14.41
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Office of Naval Research (N00014-15-1-0033)
- Guggenheim Fellowship
- Parke-Davis Exchange Fellowship from the University of Cambridge
- Visiting Professorship from the Leverhulme Trust
- K99 NIH Pathway to Independence Award (K99MH103401)
- German Academic Exchange Service
- German Research Foundation
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- reward motivation, memory consolidation, hippocampus, substantia nigra/ventral tegmental area, resting-state functional connectivity, hippocampal reactivation, object memory, reward context
- MeSH terms
- Adult, Brain Mapping, Female, Hippocampus, Humans, Image Processing, Computer-Assisted, Learning, Magnetic Resonance Imaging, Male, Oxygen, Reaction Time, Retention, Psychology, Reward, Young Adult
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.
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