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 accessAbstract
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.
Overview
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
Cites
Statistics
Verification
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.
Citations
Cites
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
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
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
Cited by
Sorted by citations
The theory of constructed emotion: an active inference account of interoception and categorization
Barrett, L. F. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw154 · Cited by 1,426
“…are responsible for implementing allostasis, and that are usually assigned an emotional function, are ‘driving’ the perception signals, i.e. the ‘concepts’, that constitute the brain’s internal model, in conjunction with the hippocampus (e.g. see Davachi and DuBrow, 2015; Hasson et al. , 2015).”
How Do Expectations Shape Perception?
de Lange, F. P., Heilbron, M., & Kok, P. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.06.002 · Cited by 975
Consolidation alters motor sequence-specific distributed representations
Pinsard, B., Boutin, A., Gabitov, E., Lungu, O., Benali, H., & Doyon, J. (2019) · eLife · doi:10.7554/elife.39324 · Cited by 1,066
Episodic memory and beyond: the hippocampus and neocortex in transformation
Moscovitch, M., Cabeza, R., Winocur, G., & Nadel, L. (2016) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143733 · Cited by 1,062
The theory of constructed emotion: an active inference account of interoception and categorization
Barrett, L. F. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx060 · Cited by 950
“…that are responsible for implementing allostasis, and that are usually assigned an emotional function, are ‘driving’ the perception signals, i.e. the ‘concepts’, that constitute the brain’s internal model, in conjunction with the hippocampus (e.g. see Davachi and DuBrow, 2015; Hasson et al., 2015).”
An active inference theory of allostasis and interoception in depression
Barrett, L. F., Quigley, K. S., & Hamilton, P. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0011 · Cited by 554
Space and Time: The Hippocampus as a Sequence Generator
Buzsáki, G., & Tingley, D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.07.006 · Cited by 461
Prior expectations induce prestimulus sensory templates
Kok, P., Mostert, P., & de Lange, F. P. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1705652114 · Cited by 340
The Necessity of the Medial Temporal Lobe for Statistical Learning
Schapiro, A. C., Gregory, E., Landau, B., McCloskey, M. E., & Turk‐Browne, N. B. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00578 · Cited by 328
Memory and Space: Towards an Understanding of the Cognitive Map
Schiller, D., Eichenbaum, H., Buffalo, E. A., Davachi, L., Foster, D. J., Leutgeb, S., & Ranganath, C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2618-15.2015 · Cited by 340
Self-citationStatistical learning of temporal community structure in the hippocampus
Schapiro, A. C., Turk‐Browne, N. B., Norman, K. A., & Botvinick, M. (2015) · Hippocampus · doi:10.1002/hipo.22523 · Cited by 306
Episodic sequence memory is supported by a theta-gamma phase code
Heusser, A. C., Poeppel, D., Ezzyat, Y., & Davachi, L. (2016) · Nature Neuroscience · doi:10.1038/nn.4374 · Cited by 290
Self-citationHippocampal ensemble dynamics timestamp events in long-term memory
Rubin, A., Geva, N., Sheintuch, L., & Ziv, Y. (2015) · eLife · doi:10.7554/elife.12247 · Cited by 275
Hippocampal contributions to social and cognitive deficits in autism spectrum disorder
Banker, S. M., Gu, X., Schiller, D., & Foss‐Feig, J. H. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.08.005 · Cited by 291
Memory: organization and control.
Eichenbaum, H. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044131 · Cited by 257
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
Self-citationAn event map of memory space in the hippocampus
Deuker, L., Bellmund, J. L. S., Schröder, T. N., & Doeller, C. F. (2016) · eLife · doi:10.7554/elife.16534 · Cited by 243
Temporal binding within and across events
DuBrow, S., & Davachi, L. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.011 · Cited by 226
Self-citationMontagrin, A., Saiote, C., & Schiller, D. (2017) · Hippocampus · doi:10.1002/hipo.22797 · Cited by 211
The role of spatial boundaries in shaping long-term event representations
Horner, A. J., Bisby, J. A., Wang, A., Bogus, K., & Burgess, N. (2016) · Cognition · doi:10.1016/j.cognition.2016.05.013 · Cited by 175
Mau, W., Sullivan, D. W., Kinsky, N. R., Hasselmo, M. E., Howard, M. W., & Eichenbaum, H. (2018) · Current Biology · doi:10.1016/j.cub.2018.03.051 · Cited by 191
Temporal Memory Is Shaped by Encoding Stability and Intervening Item Reactivation
DuBrow, S., & Davachi, L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2535-14.2014 · Cited by 203
Self-citationSchafer, M., & Schiller, D. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.006 · Cited by 186
Overlap among Spatial Memories Triggers Repulsion of Hippocampal Representations
Chanales, A. J. H., Oza, A., Favila, S. E., & Kuhl, B. A. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.057 · Cited by 180
Pupil-linked arousal signals track the temporal organization of events in memory
Clewett, D., Gasser, C., & Davachi, L. (2020) · Nature Communications · doi:10.1038/s41467-020-17851-9 · Cited by 154
Self-citationNonspatial Sequence Coding in CA1 Neurons
Allen, T. A., Salz, D. M., McKenzie, S., & Fortin, N. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2874-15.2016 · Cited by 156
The hippocampus: a special place for time
Ranganath, C., & Hsieh, L.-T. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13043 · Cited by 120
Sols, I., DuBrow, S., Davachi, L., & Fuentemilla, L. (2017) · Current Biology · doi:10.1016/j.cub.2017.09.057 · Cited by 140
Self-citationBoundaries Shape Cognitive Representations of Spaces and Events
Brunec, I. K., Moscovitch, M., & Barense, M. D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.03.013 · 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
Episodic memory in aspects of large-scale brain networks
Jeong, W., Chung, C. K., & Kim, J. S. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00454 · Cited by 130
A Locus Coeruleus- Dorsal CA1 Dopaminergic Circuit Modulates Memory Linking
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) · Neuron · doi:10.1016/j.neuron.2022.08.001 · Cited by 122
Associative Prediction of Visual Shape in the Hippocampus
Kok, P., & Turk‐Browne, N. B. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0163-18.2018 · Cited by 121
An Alternative to Mapping a Word onto a Concept in Language Acquisition: Pragmatic Frames
Rohlfing, K. J., Wrede, B., Vollmer, A.-L., & Oudeyer, P.-Y. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.00470 · Cited by 113
The ebb and flow of experience determines the temporal structure of memory
Clewett, D., & Davachi, L. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.08.013 · Cited by 121
Self-citationThe neural bases for timing of durations
Tsao, A., Yousefzadeh, S. A., Meck, W. H., Moser, M., & Moser, E. I. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00623-3 · Cited by 114
The hippocampus and the regulation of human food intake.
Stevenson, R. J., & Francis, H. (2017) · Psychological Bulletin · doi:10.1037/bul0000109 · Cited by 114
Reward prediction errors create event boundaries in memory
Rouhani, N., Norman, K. A., Niv, Y., & Bornstein, A. M. (2020) · Cognition · doi:10.1016/j.cognition.2020.104269 · Cited by 112
Madore, K. P., Szpunar, K. K., Addis, D. R., & Schacter, D. L. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1612278113 · Cited by 104
Aqrabawi, A. J., & Kim, J. C. (2018) · Nature Communications · doi:10.1038/s41467-018-05131-6 · Cited by 106
A Time and Place for Everything: Developmental Differences in the Building Blocks of Episodic Memory
Lee, J. K., Wendelken, C., Bunge, S. A., & Ghetti, S. (2015) · Child Development · doi:10.1111/cdev.12447 · Cited by 99
Bonner, M. F., & Epstein, R. A. (2021) · Nature Communications · doi:10.1038/s41467-021-24368-2 · Cited by 96
Statistical prediction of the future impairs episodic encoding of the present
Sherman, B. E., & Turk‐Browne, N. B. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2013291117 · Cited by 96
Neurophysiology of Remembering
Buzsáki, G., McKenzie, S., & Davachi, L. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-021721-110002 · Cited by 84
Self-citationStatistical Learning Signals in Macaque Inferior Temporal Cortex
Kaposvari, P., Kumar, S., & Vogels, R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhw374 · Cited by 91
Keeping order in the brain: The supramarginal gyrus and serial order in short-term memory
Guidali, G., Pisoni, A., Bolognini, N., & Papagno, C. (2019) · Cortex · doi:10.1016/j.cortex.2019.04.009 · Cited by 86
Mapping sequence structure in the human lateral entorhinal cortex
Bellmund, J. L. S., Deuker, L., & Doeller, C. F. (2019) · eLife · doi:10.7554/elife.45333 · Cited by 98
Event boundaries shape temporal organization of memory by resetting temporal context
Pu, Y., Kong, X., Charan Ranganath, A., & Melloni, L. (2022) · Nature Communications · doi:10.1038/s41467-022-28216-9 · Cited by 84
Long, N. M., Lee, H., & Kuhl, B. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1850-16.2016 · Cited by 74
Speed of time-compressed forward replay flexibly changes in human episodic memory
Michelmann, S., Staresina, B. P., Bowman, H., & Hanslmayr, S. (2018) · Nature Human Behaviour · doi:10.1038/s41562-018-0491-4 · Cited by 88
Brain mechanisms underlying the subjective experience of remembering
Simons, J. S., Ritchey, M., & Fernyhough, C. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-030221-025439 · Cited by 70
Lee, J. K., Fandakova, Y., Johnson, E. G., Cohen, N. J., Bunge, S. A., & Ghetti, S. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.100741 · Cited by 70
Successful memory formation is driven by contextual encoding in the core memory network
Long, N. M., & Kahana, M. J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.06.073 · Cited by 69
Prior expectations induce pre-stimulus sensory templatesPreprint
Kok, P., Mostert, P., & de Lange, F. P. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/119073 · Cited by 69
Wang, L., Kuperberg, G. R., & Jensen, O. B. (2018) · eLife · doi:10.7554/elife.39061 · Cited by 66
Expectation-driven novelty effects in episodic memory
Frank, D., & Kafkas, A. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107466 · Cited by 78
Event segmentation protects emotional memories from competing experiences encoded close in time
Dunsmoor, J. E., Kroes, M. C. W., Moscatelli, C. M., Evans, M. D., Davachi, L., & Phelps, E. A. (2018) · Nature Human Behaviour · doi:10.1038/s41562-018-0317-4 · Cited by 77
Self-citationMechanisms of Memory Consolidation and Transformation
Sekeres, M. J., Moscovitch, M., & Winocur, G. (2017) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-319-45066-7_2 · Cited by 75
Coding of serial order in verbal, visual and spatial working memory.
Ginsburg, V., Archambeau, K., van Dijck, J., Chetail, F., & Gevers, W. (2017) · Journal of Experimental Psychology General · doi:10.1037/xge0000278 · Cited by 65
Cognitive components underpinning the development of model-based learning
Potter, T. C. S., Bryce, N. V., & Hartley, C. A. (2016) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.10.005 · Cited by 69
Michelmann, S., Price, A. R., Aubrey, B., Strauss, C. K., Doyle, W., Friedman, D. J., Dugan, P. C., Devinsky, O., Devore, S., Flinker, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25376-y · Cited by 63
Fonken, Y. M., Kam, J. W. Y., & Knight, R. T. (2019) · Psychophysiology · doi:10.1111/psyp.13400 · Cited by 68
Bomyea, J. A., Johnson, A., & Lang, A. J. (2016) · Psychopathology Review · doi:10.5127/pr.037214 · Cited by 70
The tie that binds: temporal coding and adaptive emotion
Wang, J., Tambini, A., & Lapate, R. C. (2022) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2022.09.005 · Cited by 60
Law, L. L. F., Mok, V., & Yau, M. K.-S. (2019) · Alzheimer s Research & Therapy · doi:10.1186/s13195-019-0548-2 · Cited by 57
Olfaction, navigation, and the origin of isocortex
Aboitiz, F., & Montiel, J. F. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00402 · Cited by 54
Learning Naturalistic Temporal Structure in the Posterior Medial Network
Aly, M., Chen, J., Turk‐Browne, N. B., & Hasson, U. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01308 · Cited by 55
Zheng, L., Gao, Z., McAvan, A. S., Isham, E. A., & Ekstrom, A. D. (2021) · Nature Communications · doi:10.1038/s41467-021-26560-w · Cited by 54
Temporal Anticipation Based on Memory
Cravo, A. M., Rohenkohl, G., Santos, K. M., & Nobre, A. C. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01172 · Cited by 55
Eichenbaum, H., Amaral, D. G., Buffalo, E. A., Buzsáki, G., Cohen, N. J., Davachi, L., Frank, L. M., Heckers, S., Morris, R., Moser, E. I., et al. (2016) · Hippocampus · doi:10.1002/hipo.22616 · Cited by 55
Self-citationAitken, F., & Kok, P. (2022) · Nature Communications · doi:10.1038/s41467-022-31040-w · Cited by 59
Nucleus reuniens transiently synchronizes memory networks at beta frequencies
Jayachandran, M., Viena, T. D., Garcia, A., Veliz, A. V., Leyva, S., Roldan, V., Vertes, R. P., & Allen, T. A. (2023) · Nature Communications · doi:10.1038/s41467-023-40044-z · Cited by 70
Recasens, M., Groß, J., & Uhlhaas, P. J. (2018) · Scientific Reports · doi:10.1038/s41598-018-32385-3 · Cited by 51
Schemas, reinforcement learning and the medial prefrontal cortex
Bein, O., & Niv, Y. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00893-z · Cited by 77
Liu, C., Ye, Z., Chen, C., Axmacher, N., & Xue, G. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab304 · Cited by 51
Doré, B., Rodrik, O., Boccagno, C. E., Hubbard, A. D., Weber, J., Stanley, B., Oquendo, M. A., Miller, J. M., Sublette, M. E., Mann, J. J., et al. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.01.002 · Cited by 48
Multiple routes to enhanced memory for emotionally relevant events
Rouhani, N., Niv, Y., Frank, M. J., & Schwabe, L. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.06.006 · Cited by 52
Treating a novel plasticity defect rescues episodic memory in Fragile X model mice
Wang, W., Cox, B. M., Jia, Y., Le, A. A., Cox, C. D., Jung, K., Hou, B., Piomelli, D., Gall, C. M., & LYNCH, G. S. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.221 · Cited by 45
A matter of time: how does emotion influence temporal aspects of remembering?
Petrucci, A. S., & Palombo, D. J. (2021) · Cognition & Emotion · doi:10.1080/02699931.2021.1976733 · Cited by 49
Collective events and individual affect shape autobiographical memory
Rouhani, N., Stanley, D. A., COVID-Dynamic Team, Adolphs, R., Rouhani, N., Stanley, D., Adolphs, R., Maoz, U., Paul, L. K., & Rusch, T. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2221919120 · Cited by 54
Turns during navigation act as boundaries that enhance spatial memory and expand time estimation
Brunec, I. K., Ozubko, J. D., Ander, T., Guo, R., Moscovitch, M., & Barense, M. D. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107437 · Cited by 43
Dave, S., VanHaerents, S. A., & Voss, J. L. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0595-20.2020 · Cited by 42
The Anatomy and Physiology of Eyeblink Classical Conditioning
Takehara‐Nishiuchi, K. (2016) · Current topics in behavioral neurosciences · doi:10.1007/7854_2016_455 · Cited by 41
Multiple interactive memory representations underlie the induction of false memory
Zhu, B., Chen, C., Shao, X., Liu, W., Ye, Z., Zhuang, L., Li, Z., Loftus, E. F., & Xue, G. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1817925116 · Cited by 55
Hippocampal CA1 Subregion as a Context Decoder
Barrientos, S. A., & Tiznado, V. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1107-16.2016 · Cited by 40
Reconstructing relational information
Horecka, K. M., Dulas, M. R., Schwarb, H. D., Lucas, H. D., Duff, M. C., & Cohen, N. J. (2017) · Hippocampus · doi:10.1002/hipo.22819 · Cited by 36
Sequential predictive learning is a unifying theory for hippocampal representation and replayPreprint
Levenstein, D., Efremov, A., Eyono, R. H., Peyrache, A., & Richards, B. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.28.591528 · Cited by 42
Time Regained: How the Human Brain Constructs Memory for Time
Cohn‐Sheehy, B. I., & Ranganath, C. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.08.005 · Cited by 42
Individual susceptibility to TMS affirms the precuneal role in meta-memory upon recollection
Ye, Q., Zou, F., Dayan, M., Lau, H. C., Hu, Y., & Kwok, S. C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01909-6 · Cited by 36
Hippocampal hierarchical networks for space, time, and memory
Collin, S. H. P., Milivojevic, B., & Doeller, C. F. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.06.007 · Cited by 40
Decoding hierarchical control of sequential behavior in oscillatory EEG activity
Kikumoto, A., & Mayr, U. (2018) · eLife · doi:10.7554/elife.38550 · Cited by 36
Sleep, cognition and cortisol in addison’s disease: a mechanistic relationship
Henry, M., Thomas, K. G. F., & Ross, I. L. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.694046 · Cited by 34
Tempesta, D., Socci, V., Coppo, M., Ioio, G. D., Nepa, V., Gennaro, L. D., & Ferrara, M. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.03.007 · Cited by 34
Lee, A. C. H., Thavabalasingam, S., Alushaj, D., Çavdaroğlu, B., & Ito, R. (2019) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2019.107300 · Cited by 38
Content-based Dissociation of Hippocampal Involvement in Prediction
Kok, P., Rait, L. I., & Turk‐Browne, N. B. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01509 · Cited by 34
The hippocampus, prefrontal cortex, and perirhinal cortex are critical to incidental order memory
Allen, L. M., Lesyshyn, R. A., O’Dell, S. J., Allen, T. A., & Fortin, N. J. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112215 · Cited by 32
Reward prediction errors create event boundaries in memoryPreprint
Rouhani, N., Norman, K. A., Niv, Y., & Bornstein, A. M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/725440 · Cited by 32
Bein, O., Trzewik, M., & Maril, A. (2019) · Journal of Memory and Language · doi:10.1016/j.jml.2019.03.006 · Cited by 28
The Medial Temporal Lobe Is Critical for Spatial Relational Perception
Ruiz, N. A., Meager, M. R., Agarwal, S., & Aly, M. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01583 · Cited by 30
Focusing on what matters: Modulation of the human hippocampus by relational attention
Córdova, N. I., Turk‐Browne, N. B., & Aly, M. (2019) · Hippocampus · doi:10.1002/hipo.23082 · Cited by 34
Metadata
- Authors
- Davachi, L., & DuBrow, S.
- Affiliations
- New York University (US)
- Venue
- Trends in Cognitive Sciences
- Publisher
- Elsevier BV
- Published
- 2015-02
- Volume
- 19
- Issue
- 2
- Pages
- 92-99
- ISSN
- 1364-6613 (ISSN-L)
- 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
- 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