Cited by 329Memory and Neural MechanismsMemory Processes and InfluencesCognitive Functions and Memory

The DOI matches its Crossref record; 92 of the 92 references it cites were found in a registry or an index.

How the hippocampus preserves order: the role of prediction and context

Open access

Davachi, Lila, DuBrow, Sarah·2015·Trends in Cognitive Sciences

DOI 10.1016/j.tics.2014.12.004PMC PMC4380862

Open this paper in CoChat — free account

Abstract

Remembering the sequence of events is critical for deriving meaning from our experiences and guiding behavior. Prior investigations into the function of the human hippocampus have focused on its more general role in associative binding, but recent work has focused on understanding its specific role in encoding and preserving the temporal order of experiences. In this review we summarize recent work in humans examining hippocampal contributions to sequence learning. We distinguish the learning of sequential relationships through repetition from the rapid, episodic acquisition of sequential associations. Taken together, this research begins to clarify the link between hippocampal representations and the preservation of the order of events.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1016/j.tics.2014.12.004

Cites

92 of 92 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Episodic memory: from mind to brain
Tulving, E. (2002) · Annual Review of Psychology · doi:10.1146/annurev.psych.53.100901.135114 · Cited by 4,950
The medial temporal lobe
Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680
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
Interhemispheric differences in the localization of psychological processes in man.
Milner, B. (1971) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a070866 · Cited by 2,405
Memory, navigation and theta rhythm in the hippocampal-entorhinal system
Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847
Modeling hippocampal and neocortical contributions to recognition memory: a complementary-learning-systems approach
Norman, K. A., & O'Reilly, R. C. (2003) · Psychological Review · doi:10.1037/0033-295x.110.4.611 · Cited by 1,312
Hippocampal ‘time cells’ bridge the gap in memory for discontiguous events
MacDonald, C. J., Lepage, K. Q., Eden, U. T., & Eichenbaum, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.012 · Cited by 1,193
A Distributed Representation of Temporal Context
Howard, M. W., & Kahana, M. J. (2002) · Journal of Mathematical Psychology · doi:10.1006/jmps.2001.1388 · Cited by 1,174
Event perception: a mind-brain perspective
Zacks, J. M., Speer, N. K., Swallow, K. M., Braver, T. S., & Reynolds, J. R. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.2.273 · Cited by 1,148
Item, context and relational episodic encoding in humans
Davachi, L. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.10.012 · Cited by 1,138
Self-citation

Flagged first, then by citations

Show all 90 references

Sorted by citations

Items 201–300 of 329

Consolidation Enhances Sequential Multistep Anticipation but Diminishes Access to Perceptual Features
Tarder-Stoll, H., Baldassano, C. A., & Aly, M. (2024) · Psychological Science · doi:10.1177/09567976241256617 · Cited by 7
Changes in the experience of time: The impact of spatial information on the perception and memory of duration
Fenerci, C., Castanheira, K. D. S., LoParco, M., & Sheldon, S. (2020) · Quarterly Journal of Experimental Psychology · doi:10.1177/1747021820968492 · Cited by 6
Temporal and spatial selectivity of hippocampal connectivity with sensorimotor cortex during individual finger movementsPreprint
Miller, M. J., & Burman, D. D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/479436 · Cited by 8
Generating event boundaries in memory without prediction errorPreprint
Shim, S., Mugisho, F., Davachi, L., & Baldassano, C. A. (2024) · doi:10.31234/osf.io/4bdp6 · Cited by 9
Self-citation
Cerebellar Direct Current Stimulation Reveals the Causal Role of the Cerebellum in Temporal Prediction
Terranova, S., Botta, A., Putzolu, M., Bonassi, G., Cosentino, C., Mezzarobba, S., Ravizzotti, E., Pelosin, E., & Avanzino, L. (2023) · The Cerebellum · doi:10.1007/s12311-023-01649-8 · Cited by 5
The well‐worn route revisited: Striatal and hippocampal system contributions to familiar route navigation
Buckley, M. G., McGregor, A., Ihssen, N., Austen, J. M., Thurlbeck, S., Smith, S. P., Heinecke, A., & Lew, A. R. (2024) · Hippocampus · doi:10.1002/hipo.23607 · Cited by 5
Time-dependent neural arbitration between cue associative and episodic fear memories
Cortese, A., Ohata, R., Alemany-González, M., Kitagawa, N., Imamizu, H., & Koizumi, A. (2024) · Nature Communications · doi:10.1038/s41467-024-52733-4 · Cited by 5
Neurotypical subjective experience is caused by a hippocampal simulation
Faw, M., & Faw, B. (2016) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1412 · Cited by 7
Associative binding in early childhood: Evidence from a preferential looking paradigm
Johnson, E. G., Leckey, S., Davinson, K., & Ghetti, S. (2019) · Developmental Psychobiology · doi:10.1002/dev.21904 · Cited by 5
The impact of encoding scenarios on different forms of temporal order memory
Sheldon, S. (2020) · Psychological Research · doi:10.1007/s00426-020-01440-y · Cited by 4
Events and Boundaries
DuBrow, S. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.18 · Cited by 4
Self-citation
Event memory uniquely predicts memory for large-scale space
Sargent, J. Q., Zacks, J. M., Hambrick, D. Z., & Lin, N. (2018) · Memory & Cognition · doi:10.3758/s13421-018-0860-2 · Cited by 6
Anticipatory reinstatement of expected perceptual events during visual sequence learningPreprint
Senoussi, M., VanRullen, R., & Reddy, L. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.28.402123 · Cited by 5
A Review of Short-Term, Long-Term, and Memory Consolidation Mechanisms in the Hippocampus and Cerebral Cortex
Yang, Z., Khairuddin, A. S. M., Chuah, J. H., Wong, W. R., Noman, H. M. F., Putri, T. W. O., Xu, X., & Haq, M. M. (2025) · IEEE Access · doi:10.1109/access.2025.3555539 · Cited by 4
Sequence as output, not limitation
Shi, E. R. (2026) · Evolutionary Linguistic Theory · doi:10.1075/elt.25002.shi · Cited by 4
Visual Statistical Learning Alters Low-Dimensional Cortical Architecture
Rowchan, K., Gale, D. J., Nick, Q., Gallivan, J. P., & Wammes, J. D. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1932-24.2025 · Cited by 4
Retracted
Neural population dynamics and temporal context cells in macaque medial parietal cortex support temporal order memory
Zuo, S., Wang, C., Wang, L., Jin, Z., Zhou, X., 苏宁, Liu, J., McHugh, T. J., Kusunoki, M., & Kwok, S. C. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003759 · Cited by 14
The Effect of Abstract Inter-Chunk Relationships on Serial-Order Control
Moss, M. E., Zhang, M., & Mayr, U. (2022) · Cognition · doi:10.1016/j.cognition.2023.105578 · Cited by 4
A bio-inspired method of autonomous positioning using spatial association based on place cells firing
Li, W., Wu, D., Zhou, Y., & Du, J. Y. (2017) · International Journal of Advanced Robotic Systems · doi:10.1177/1729881417728015 · Cited by 3
Long-term memory of real-world episodes is independent of recency effects: magic tricks as ecological tasks
Bestue, D., Martı́nez, L. M., Gómez-Marín, À., Gea, M. Á., & Camı́, J. (2020) · Heliyon · doi:10.1016/j.heliyon.2020.e05260 · Cited by 4
Cortical semantization of autobiographical memory over subjective chronological time: An fMRI study
McWilliams, K., Kaplan, A., Eline, E. E., Kaminer, I., Zodrow, S., Petersen, J., Williams, J. M., & Osipowicz, K. Z. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15652 · Cited by 6
The medial temporal lobe is critical for spatial relational perceptionPreprint
Ruiz, N. A., Meager, M. R., Agarwal, S., & Aly, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/765222 · Cited by 4
Prediction error is out of context: The dominance of contextual stability in segmenting episodic eventsPreprint
Güler, B., Serin, F., & Günseli, E. (2023) · doi:10.31234/osf.io/jgq64 · Cited by 5
Emotional learning selectively distorts the temporal organization of memory: A quantitative synthesis
Laing, P. A. F., Hennings, A. C., Cooper, S. E., & Dunsmoor, J. E. (2025) · Cognition · doi:10.1016/j.cognition.2025.106382 · Cited by 3
Offline contributions to early skill learning
Brooks, E., Hendrikse, J. J., Buch, E. R., Censor, N., Cohen, L. G., & Coxon, J. D. (2026) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2026.02.006 · Cited by 6
Towards a conflict account of déjà vu: The role of memory errors and memory expectation conflict in the experience of déjà vu
Aitken, C. B. A., Jentzsch, I., & O’Connor, A. R. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105467 · Cited by 4
Recall as a Window into Hippocampally Defined Events
Rait, L. I., & Hutchinson, J. B. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02198 · Cited by 3
Time after Time: Preserving Temporal Memories When Experiences Repeat
Zou, F., & Kuhl, B. A. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02212 · Cited by 3
Personalized Neural State Segmentation: Validating the Greedy State Boundary Search Algorithm for Individual-level Functional Magnetic Resonance Imaging Data
Wilford, R., Chen, H., Wharton-Shukster, E., Finn, A. S., & Duncan, K. D. (2025) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02345 · Cited by 5
Differential patterns of contextual organization of memory in first-episode psychosis
Murty, V. P., McKinney, R. A., DuBrow, S., Jalbrzikowski, M., Haas, G. L., & Luna, B. (2018) · Schizophrenia · doi:10.1038/s41537-018-0046-8 · Cited by 3
Self-citation
Memory for Space, Time, and Episodes ☆
Asem, J. S. A., & Fortin, N. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21015-8 · Cited by 5
Hippocampal-neocortical interactions sharpen over time for predictive actionsPreprint
Hindy, N. C., Avery, E. W., & Turk‐Browne, N. B. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/483115 · Cited by 3
Dynamic arousal signals construct memories of time and eventsPreprint
Clewett, D., Gasser, C., & Davachi, L. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/765214 · Cited by 3
Self-citation
Hippocampal spatial and sequential representations of event structure scaffold precise episodic temporal order memoryPreprint
Liu, C., Ye, Z., Chen, C., Axmacher, N., & Xue, G. (2020) · doi:10.21203/rs.3.rs-40727/v1 · Cited by 3
Hippocampal representations switch from errors to predictions during acquisition of predictive associationsPreprint
Aitken, F., & Kok, P. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.21.461228 · Cited by 3
Consolidation enhances multistep anticipatory judgements but diminishes access to perceptual featuresPreprint
Tarder-Stoll, H., Baldassano, C. A., & Aly, M. (2023) · doi:10.31234/osf.io/x2f7s · Cited by 3
REMI: Reconstructing Episodic Memory During Internally Driven Path PlanningPreprint
Wang, Z., Morris, G., Derdikman, D., Chaudhari, P., & Balasubramanian, V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.02.662824 · Cited by 4
Investigating the impact of healthy aging on memory for temporal duration and order
Thavabalasingam, S., Aashat, S., Palombo, D. J., Verfaellie, M. H., & Lee, A. C. H. (2022) · Aging Neuropsychology and Cognition · doi:10.1080/13825585.2022.2120178 · Cited by 3
Shared spectral fingerprints of temporal memory precision and representation of the temporal structure of complex narratives
Frisoni, M., Croce, P., Tosoni, A., Zappasodi, F., & Sestieri, C. (2025) · iScience · doi:10.1016/j.isci.2025.112132 · Cited by 3
Sequencing thought into speech: Hippocampal functions in linguistic linearization
Shi, E. R. (2026) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2026.101376 · Cited by 2
The striatum in time production: The model of Huntington's disease in longitudinal study
Lemoine, L., Lunven, M., Fraisse, N., Youssov, K., Bapst, B., Morgado, G., Reilmann, R., Busse, M. E., Craufurd, D., Rosser, A., et al. (2022) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2022.108459 · Cited by 2
The Effect of Facial Expressions on the Process of Learning, and Memory of Face Images among Healthy Participants and Individuals with Traumatic Brain Injury (TBI): Examination Using Eye Movements
Lugasi, N., Sachar, Y., & Vakil, E. (2023) · Psychology · doi:10.4236/psych.2023.148077 · Cited by 2
Temporal context-guided memory capabilities in rodents
Slater, B., Petkov, C. I., & Easton, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-95410-2 · Cited by 2
Threat Impairs the Organization of Memory Around Motivational Context
Horwath, E. A., Katerman, B. S., Biju, M., DuBrow, S., & Murty, V. P. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02242 · Cited by 2
Self-citation
Neural evidence for representationally specific prediction in language processingPreprint
Wang, L., Kuperberg, G. R., & Jensen, O. B. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/243667 · Cited by 2
Content-based dissociation of hippocampal involvement in predictionPreprint
Kok, P., Rait, L. I., & Turk‐Browne, N. B. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/568303 · Cited by 2
Metric and chronological time in human episodic memoryPreprint
Evensmoen, H. R., Rimol, L. M., Rise, H. H., Hansen, T. I., Nili, H., Winkler, A. M., & Haberg, A. K. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.11.084202 · Cited by 2
Mnemonic content and hippocampal patterns shape judgments of timePreprint
Sherman, B. E., DuBrow, S., Winawer, J. A., & Davachi, L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.03.454949 · Cited by 2
Self-citation
Goal shifts structure memories and prioritize event-defining information in long- term memoryPreprint
Cowan, E. T., Chanales, A. J. H., Davachi, L., & Clewett, D. (2024) · doi:10.31234/osf.io/ejsrf · Cited by 2
Self-citation
Pattern integration and differentiation: Dual process model of episodic memory
Evensmoen, H. R., Rimol, L. M., Rise, H. S., Hansen, T. I., Nili, H., Winkler, A. M., & Haberg, A. K. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00433 · Cited by 1
Melody for a memory: sleep boosts the brain’s representation of sequential events
Aton, S. J. (2025) · SLEEP · doi:10.1093/sleep/zsae316 · Cited by 1
Manners Matter: Action History Guides Attention and Repair Choices During Interaction
Singh, A., Wrede, B., Richter, B., Groß, A., & Rohlfing, K. J. (2025) · IEEE International Conference on Development and Learning (ICDL) · doi:10.1109/icdl63968.2025.11204385 · Cited by 1
CA2/3-dependent stability of frontal mnemonic representations predict episodic deficits in human amnesia
Miller, T. D., Hickling, A. L., Wu, Y. I., Zhou, J. H., Handel, A. E., Coutinho, E., Pollak, T. A., Zandi, M. S., Maguire, E. A., & Rosenthal, C. R. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116527 · Cited by 2
Behavioral and neural mechanisms underlying contextual processing in naturalistic short video viewing
Cao, Z., Xiao, X., Wang, Y., Li, R., Xie, Y., Wu, L., Bi, S., Yang, F., & Wang, Y. (2025) · iScience · doi:10.1016/j.isci.2025.114269 · Cited by 3
Simultaneous manipulation of emotion and working memory load distorts temporal distance memory
Kim, G., Ye, Q., & Lee, A. C. H. (2026) · Memory & Cognition · doi:10.3758/s13421-026-01865-7 · Cited by 1
Adaptive processing of predictions and prediction errors in hippocampal subregions
Bein, O., & Davachi, L. (2026) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2025.0239 · Cited by 4
Self-citation
The role of hippocampal predictions in cognition: bridging perception and memory
Aly, M., Barense, M. D., & Kok, P. (2026) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2025.0236 · Cited by 1
Non-spatial similarity can bias spatial distances in a cognitive map
Xing, X., & Saunders, J. A. (2022) · Cognition · doi:10.1016/j.cognition.2022.105251 · Cited by 2
Modulation of Spectral Representation and Connectivity Patterns in Response to Visual Narrative in the Human Brain
Sabra, Z., Alawieh, A. M., Bonilha, L., Naselaris, T., & AuYong, N. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.886938 · Cited by 1
Remembering Sarah DuBrow across All Contexts
Tompary, A., deBettencourt, M. T., & Rouhani, N. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02189 · Cited by 1
Event Memory in Fact and Fiction
Bezdek, M. A., Butler, A. C., & Zacks, J. M. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.76 · Cited by 1
Rapid Learning of Temporal Dependencies at Multiple Timescales
Smith, C. M., Thompson‐Schill, S. L., & Schapiro, A. C. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02232 · Cited by 2
The effect of alcohol on brain structures involved in the formation of addiction
Chaikovska, V. R., & Pershyn, M. (2024) · Reports of Vinnytsia National Medical University · doi:10.31393/reports-vnmedical-2024-28(3)-27 · Cited by 1
Sequence learning recodes cortical representations instead of strengthening initial ones
Kalm, K., & Norris, D. G. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008969 · Cited by 1
Explicit Sequence Memory in Recall of Temporally-structured Episodes
Stern, Y., Katz, R., & Sadeh, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-59472-8 · Cited by 3
Candidate Neural Activity for the Encoding of Temporal Content in Memory
Jayachandran, M., & Allen, T. A. (2022) · Neuromethods · doi:10.1007/978-1-0716-2631-3_7 · Cited by 1
Hippocampal overshadowing : exploring the underlying mechanisms
Gulbrandsen, T. L. (2015) · Open ULeth Scholarship (OPUS) (University of Lethbridge) · Cited by 1
The psychological arrow of time and the human brain dynamics of event orderingPreprint
Gauthier, B., Pestke, K., & van Wassenhove, V. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/180711 · Cited by 1
Editorial overview: Memory in time and space
Davachi, L., & Burgess, N. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.10.009 · Cited by 1
Self-citation
How emotional memory affects face remembering: an ERP investigationPreprint
Proverbio, A., Vanutelli, M. E., & Viganò, S. (2017) · bioRxiv · doi:10.1101/208256 · Cited by 1
Does a turn in the road mark a turn of events? Turns along travelled routes provide contextual boundaries during navigationPreprint
Brunec, I. K., Ozubko, J. D., Ander, T., Moscovitch, M., & Barense, M. D. (2018) · OSF Preprints (OSF Preprints) · doi:10.31219/osf.io/g6dp3 · Cited by 2
Cross-modal facilitation of memory through actionsPreprint
Gasser, C., & Davachi, L. (2022) · Research Square · doi:10.21203/rs.3.rs-1466467/v1 · Cited by 1
Self-citation
Long-term memory of real-world episodes is independent of recency effects: magic tricks as ecological tasks.Preprint
Bestue, D., Martı́nez, L. M., Gómez-Marín, À., Gea, M. Á., & Camı́, J. (2020) · doi:10.31234/osf.io/pq4b3 · Cited by 1
A Locus Coeruleus- Dorsal CA1 Dopaminergic Circuit Modulates Memory LinkingPreprint
Chowdhury, A., Luchetti, A., Fernandes, G., Filho, D. A., Kastellakis, G., Tzilivaki, A., Ramirez, E. M., Tran, M. Y., Poirazi, P., & Silva, A. J. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3985190 · Cited by 1
Dual-stream cortical feedbacks mediate sensory predictionPreprint
Chu, Q., Ma, O., Hang, Y., & Tian, X. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.12.499695 · Cited by 1
The hippocampus binds movements to their temporal position in a motor sequencePreprint
Dolfen, N., Reverberi, S., de Beeck, H. O., King, B. R., & Albouy, G. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.20.521084 · Cited by 1
The multifaceted nature of self-generation effects: Independent and interactive effects of actions, predictability, and delay on sensory processing and memory encoding of sounds.Preprint
Paraskevoudi, N., & SanMiguel, I. (2023) · doi:10.22541/au.168322155.53723594/v1 · Cited by 2
The speed of detection vs. segmentation from continuous sequences: Evidence for an anticipation mechanism for detection through a computational modelPreprint
Luo, M., Cao, R., & Wang, F. H. (2024) · eLife · doi:10.7554/elife.95761.1 · Cited by 1
The influence of categorical stimuli on relational memory bindingPreprint
Schwarb, H. D., Dulas, M. R., & Cohen, N. J. (2024) · Learning & Memory · doi:10.1101/lm.054006.124 · Cited by 1
Hippocampus responds to mismatches with predictions based on episodic memories but not generalised knowledgePreprint
Varga, D., Raykov, P., Jefferies, E., Ben-Yakov, A., & Bird, C. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.04.636427 · Cited by 1
Separating Patterns of Space and Time: Differences in Memory for Event Duration and Sequential Order
Brunec, I. K. (2015) · TSpace (University of Toronto)
Situating mental time travel in the broad context of temporal cognition: A neural systems approach
Carvalho, F. M. (2018) · Filosofia Unisinos · doi:10.4013/fsu.2018.191.09
Time, Body, Memory: The Staged Moment in Posttraumatic Letters, Journals, Essays, and Memoirs
Jensen, M. (2019) · Palgrave studies in life writing · doi:10.1007/978-3-030-06106-7_3
ATTENTIONAL MODULATION OF THE MEDIAL TEMPORAL LOBE
Córdova, N. I. (2017)
Using movies to assess cognitive and neural functioning in temporal lobe epilepsy
Ladowski, D. (2019) · Scholarship@Western (Western University)
Weaving a story: narrative formation over prolonged time scales relies on cortical cohesiveness of distributed brain networksPreprint
Assouline, A., & Mendelsohn, A. (2021) · Research Square · doi:10.21203/rs.3.rs-155155/v1
Hippocampal Contributions to Structuring and Segmenting Experience
Brunec, I. K. (2019) · TSpace (University of Toronto)
Az aktuális teljesítmény és a mögötte álló tudás disszociációja: az idői tényezők szerepének áttekintése a procedurális tanulás példáján keresztül
Kiss, M. M., Németh, D., & Janacsek, K. (2020) · Magyar Pszichológiai Szemle · doi:10.1556/0016.2020.00027 · Cited by 1
「カナダの染織工芸・キルトとフットラグ」展によせて (〔日本博物館協会〕支部が推薦する博物館情報-2-東北支部)
飯田, 美. (1993) · 博物館研究
Neuro-electronic Hybrid Systems
George, J. B. (2021)
Sensory suppression and increased neuromodulation during actions disrupt memory encoding of unpredictable self-initiated stimuliPreprint
Paraskevoudi, N., & SanMiguel, I. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.15.472750
Long-term memory of real-world episodes is independent of recency effects: magic tricks as ecological tasksPreprint
Bestue, D., Martínez, L. M., Gómez-Marín, À., & Camı́, J. (2020) · doi:10.31234/osf.io/np4t5
Linear Order in Language
Hoppe, D. B. (2022) · doi:10.33612/diss.238906691
The Role of the Hippocampus in Detecting the Novelty of Impressions: A Literature Review
Kaverina, M. Y., Kuleva, A. Y., & Андреевна, К. О. (2022) · The Russian Journal of Cognitive Science · doi:10.47010/22.1-2.2
Online abstraction during statistical learning revealed by neural entrainment from intracranial recordingsPreprint
Sherman, B. E., Aljishi, A., Graves, K. N., Quraishi, I. H., Sivaraju, A., Damisah, E. C., & Turk‐Browne, N. B. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.11.523605
The neural representations underlying asymmetric cross‐modal prediction of words
Shi, L., Liu, C., Peng, X., Cao, Y., Levy, D. A., & Xue, G. (2023) · Human Brain Mapping · doi:10.1002/hbm.26219
The effect of reward prediction errors on temporal order and source memory
ZHANG, H., CHENG, X., & Weibin, M. A. O. (2023) · Acta Psychologica Sinica · doi:10.3724/sp.j.1041.2023.01049
Retrieval of temporal structure at recall can occur automatically
Sadeh, T., & Moscovitch, M. (2023) · Cognition · doi:10.1016/j.cognition.2023.105647
Events and Weak Narrativity
Miller, B. (2023) · Springer eBooks · doi:10.1007/978-3-031-40349-1_6
Statistical learning of uniform- and mixed-length artificial languages: Different computational mechanisms support different task demandsPreprint
Luo, M., Cao, R., & Wang, F. H. (2024) · eLife · doi:10.7554/elife.95761

Authors: Davachi, L., & DuBrow, S.
Affiliations: New York University (US)
ORCID: Davachi, Lila
DuBrow, Sarah
Venue: Trends in Cognitive Sciences
Publisher: Elsevier BV
Published: 2015-02
Volume: 19
Issue: 2
Pages: 92-99
ISSN: 1364-6613 (ISSN-L)
DOI: 10.1016/j.tics.2014.12.004
PMC: PMC4380862
OpenAlex: W2039772527
Cited by: 328
References: 90
Citations by year: 2026: 23 · 2025: 29 · 2024: 33 · 2023: 29 · 2022: 34 · 2021: 23 · 2020: 27 · 2019: 29 · 2018: 27 · 2017: 33 · 2016: 26 · 2015: 12
FWCI: 3.25
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Trends in Cognitive Sciences (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute of Mental Health (R01MH074692)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
Keywords: hippocampus, temporal order, sequence learning, prediction, context, episodic memory, memory encoding
MeSH terms: Animals, Hippocampus, Humans, Learning, Memory, Anticipation, Psychological

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

How the hippocampus preserves order: the role of prediction and context

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks