Similarity breeds proximity: pattern similarity within and across contexts is related to later mnemonic judgments of temporal proximity
Open accessAbstract
Experiences unfold over time, but little is known about the mechanisms that support the formation of coherent episodic memories for temporally extended events. Recent work in animals has provided evidence for signals in hippocampus that could link events across temporal gaps; however, it is unknown whether and how such signals might be related to later memory for temporal information in humans. We measured patterns of fMRI BOLD activity as people encoded items that were separated in time and manipulated the presence of shared or distinct context across items. We found that hippocampal pattern similarity in the BOLD response across trials predicted later temporal memory decisions when context changed. By contrast, pattern similarity in lateral occipital cortex was related to memory only when context remained stable. These data provide evidence in humans that representational stability in hippocampus across time may be a mechanism for temporal memory organization.
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
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Abrupt changes in stimulus features and/or task goals produce separation in memory.
“In particular, inducing abrupt changes in stimulus features and/or task goals creates separation in memory [19,23–25].”
From Does mental context drift or shift? (2017) · cites this paper as [19]
The amount of change in neural activity patterns across events is associated with memory for temporal order and temporal distance.
“Furthermore, the degree to which neural activity patterns change across events has been associated with memory for temporal order and distance [16–19].”
From Does mental context drift or shift? (2017) · cites this paper as [19]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The fusiform face area: a module in human extrastriate cortex specialized for face perception
Kanwisher, N., McDermott, J., & Chun, M. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04302.1997 · Cited by 7,738 · see citing works
Modeling the Shape of the Scene: A Holistic Representation of the Spatial Envelope
Oliva, A., & Torralba, A. B. (2001) · International Journal of Computer Vision · doi:10.1023/a:1011139631724 · Cited by 6,321 · see citing works
(1983) · Medical Entomology and Zoology · Cited by 6,051 · see citing works
A cortical representation of the local visual environment
Epstein, R. A., & Kanwisher, N. (1998) · Nature · doi:10.1038/33402 · Cited by 2,960 · see citing works
Martı́nez, A. M. (1998) · CTIT technical reports series · Cited by 2,791 · see citing works
A Bayesian model of shape and appearance for subcortical brain segmentation
Patenaude, B., Smith, S. M., Kennedy, D. N., & Jenkinson, M. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.046 · Cited by 2,287 · see citing works
Repetition and the brain: neural models of stimulus-specific effects
Grill-Spector, K., Henson, R., & Martin, A. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.11.006 · Cited by 2,256 · see citing works
Information-based functional brain mapping
Kriegeskorte, N., Goebel, R., & Bandettini, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600244103 · Cited by 2,113 · see citing works
Martı́nez, A. M. (1998) · Medical Entomology and Zoology · Cited by 1,982 · see citing works
Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex.
Malach, R., Reppas, J. B., Benson, R. R., Kwong, K. K., Jiang, H., Kennedy, W. A., Ledden, P. J., Brady, T. J., Rosen, B. R., & Tootell, R. B. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.18.8135 · Cited by 1,761 · see citing works
Memory, amnesia, and the hippocampal system
(1994) · Choice Reviews Online · doi:10.5860/choice.31-5148 · Cited by 1,533 · see citing works
The lateral occipital complex and its role in object recognition
Kalanit Grill-spector, A., Kourtzi, Z., & Kanwisher, N. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00073-6 · Cited by 1,410 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Self-citationClassical conditioning and brain systems: the role of awareness
Clark, R. E., & Squire, L. R. (1998) · Science · doi:10.1126/science.280.5360.77 · Cited by 1,138 · see citing works
Multiple routes to memory: distinct medial temporal lobe processes build item and source memories
Davachi, L., Mitchell, J. P., & Wagner, A. D. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337195100 · Cited by 899 · see citing works
Self-citationCritical role of the hippocampus in memory for sequences of events
Fortin, N. J., Agster, K. L., & Eichenbaum, H. B. (2002) · Nature Neuroscience · doi:10.1038/nn834 · Cited by 881 · see citing works
Conjunctive representations in learning and memory: Principles of cortical and hippocampal function.
O'Reilly, R. C., & Rudy, J. W. (2001) · Psychological Review · doi:10.1037//0033-295x.108.2.311 · Cited by 865 · see citing works
Hippocampal representation in place learning
Eichenbaum, H., Stewart, C., & Morris, R. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-11-03531.1990 · Cited by 798 · see citing works
Deconvolving BOLD activation in event-related designs for multivoxel pattern classification analyses
Mumford, J. A., Turner, B. O., Ashby, F. G., & Poldrack, R. A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.076 · Cited by 729 · see citing works
A context maintenance and retrieval model of organizational processes in free recall
Polyn, S. M., Norman, K. A., & Kahana, M. J. (2009) · Psychological Review · doi:10.1037/a0014420 · Cited by 726 · see citing works
Solomon, P. R., Schaaf, E. R. V., Thompson, R. F., & Weisz, D. J. (1986) · Behavioral Neuroscience · doi:10.1037//0735-7044.100.5.729 · Cited by 724 · see citing works
Solomon, P. R., Vander Schaaf, E. R., Thompson, R. F., & Weisz, D. J. (1986) · Behavioral Neuroscience · doi:10.1037/0735-7044.100.5.729 · Cited by 724 · see citing works
Prospective and retrospective duration judgments: A meta-analytic review
Block, R. A., & Zakay, D. (1997) · Psychonomic Bulletin & Review · doi:10.3758/bf03209393 · Cited by 713 · see citing works
A Neural Mechanism for Working and Recognition Memory in Inferior Temporal Cortex
Miller, E. K., Li, L., & Desimone, R. (1991) · Science · doi:10.1126/science.1962197 · Cited by 706 · see citing works
Category-Specific Cortical Activity Precedes Retrieval During Memory Search
Polyn, S. M., Natu, V. S., Cohen, J. D., & Norman, K. A. (2005) · Science · doi:10.1126/science.1117645 · Cited by 690 · see citing works
Dissociable correlates of recollection and familiarity within the medial temporal lobes
Ranganath, C., Yonelinas, A. P., Cohen, M. X., Dy, C. J., Tom, S. M., & D’Esposito, M. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2003.07.006 · Cited by 689 · see citing works
Stern, C. E., Corkin, S., González, R. G., Guimarães, A. R., Baker, J. R., Jennings, P. J., Carr, C. A., Sugiura, R., Vedantham, V., & Rosen, B. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8660 · Cited by 640 · see citing works
Memory for the time of past events.
Friedman, W. J. (1993) · Psychological Bulletin · doi:10.1037/0033-2909.113.1.44 · Cited by 639 · see citing works
Associative retrieval processes in free recall
Kahana, M. J. (1996) · Memory & Cognition · doi:10.3758/bf03197276 · Cited by 605 · see citing works
Statistical theory of spontaneous recovery and regression
Estes, W. K. (1955) · Psychological Review · doi:10.1037/h0048509 · Cited by 511 · see citing works
The Long and the Short of It: Relational Memory Impairments in Amnesia, Even at Short Lags
Hannula, D. E., Tranel, D., & Cohen, N. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5222-05.2006 · Cited by 436 · see citing works
Shaping of Object Representations in the Human Medial Temporal Lobe Based on Temporal Regularities
Schapiro, A. C., Kustner, L. V., & Turk-Browne, N. B. (2012) · Current Biology · doi:10.1016/j.cub.2012.06.056 · Cited by 430 · see citing works
Working Memory for Conjunctions Relies on the Medial Temporal Lobe
Olson, I. R., Page, K., Moore, K., Chatterjee, A., & Verfaellie, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1923-05.2006 · Cited by 426 · see citing works
Gradual changes in hippocampal activity support remembering the order of events
Manns, J. R., Howard, M. W., & Eichenbaum, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.017 · Cited by 397 · see citing works
Event boundaries in perception affect memory encoding and updating
Swallow, K. M., Zacks, J. M., & Abrams, R. A. (2009) · Journal of Experimental Psychology: General · doi:10.1037/a0015631 · Cited by 382 · see citing works
Neuronal code for extended time in the hippocampus
Mankin, E. A., Sparks, F. T., Slayyeh, B., Sutherland, R. J., Leutgeb, S., & Leutgeb, J. K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214107109 · Cited by 371 · see citing works
Greater Neural Pattern Similarity Across Repetitions Is Associated with Better Memory
Xue, G., Dong, Q., Chen, C., Lu, Z., Mumford, J. A., & Poldrack, R. A. (2010) · Science · doi:10.1126/science.1193125 · Cited by 369 · see citing works
Implicit Perceptual Anticipation Triggered by Statistical Learning
Turk‐Browne, N. B., Scholl, B. J., Johnson, M. K., & Chun, M. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0858-10.2010 · Cited by 360 · see citing works
Medial temporal lobe activation during encoding and retrieval of novel face‐name pairs
Kirwan, C. B., & Stark, C. E. L. (2004) · Hippocampus · doi:10.1002/hipo.20014 · Cited by 325 · see citing works
An Unexpected Sequence of Events: Mismatch Detection in the Human Hippocampus
Kumaran, D., & Maguire, E. A. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040424 · Cited by 324 · see citing works
Distinct hippocampal time cell sequences represent odor memories in immobilized rats
MacDonald, C. J., Carrow, S., Place, R., & Eichenbaum, H. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1537-13.2013 · Cited by 312 · see citing works
The role of the hippocampus in memory for the temporal order of a sequence of odors.
Kesner, R. P., Gilbert, P. E., & Barua, L. A. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.2.286 · Cited by 309 · see citing works
Neural Similarity Between Encoding and Retrieval is Related to Memory Via Hippocampal Interactions
Ritchey, M., Wing, E. A., LaBar, K. S., & Cabeza, R. E. L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs258 · Cited by 303 · see citing works
What constitutes an episode in episodic memory?
Ezzyat, Y., & Davachi, L. (2011) · Psychological Science · doi:10.1177/0956797610393742 · Cited by 298 · see citing works
Self-citationThe influence of context boundaries on memory for the sequential order of events
DuBrow, S., & Davachi, L. (2013) · Journal of Experimental Psychology: General · doi:10.1037/a0034024 · Cited by 289 · see citing works
Self-citationMind the Gap: Binding Experiences across Space and Time in the Human Hippocampus
Staresina, B. P., & Davachi, L. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.024 · Cited by 273 · see citing works
Self-citationRecollection, familiarity, and cortical reinstatement: a multivoxel pattern analysis
Johnson, J. D., McDuff, S. G. R., Rugg, M. D., & Norman, K. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.011 · Cited by 262 · see citing works
The role of the hippocampus in memory for the temporal order of a sequence of odors.
Kesner, R. P., Gilbert, P. E., & Barua, L. A. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.2.286 · Cited by 261 · see citing works
Integrating what and when across the primate medial temporal lobe
Naya, Y., & Suzuki, W. A. (2011) · Science · doi:10.1126/science.1206773 · Cited by 257 · see citing works
Eichenbaum, H. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.12.007 · Cited by 242 · see citing works
Linking Implicit and Explicit Memory: Common Encoding Factors and Shared Representations
Turk‐Browne, N. B., Yi, D.-J., & Chun, M. M. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.030 · Cited by 238 · see citing works
Oscillatory patterns in temporal lobe reveal context reinstatement during memory search
Manning, J. R., Polyn, S. M., Baltuch, G. H., Litt, B., & Kahana, M. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015174108 · Cited by 234 · see citing works
The Hippocampus and Disambiguation of Overlapping Sequences
Agster, K. L., Fortin, N. J., & Eichenbaum, H. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05760.2002 · Cited by 231 · see citing works
Episodic reinstatement in the medial temporal lobe
Staresina, B. P., Henson, R. N. A., Kriegeskorte, N., & Alink, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4156-12.2012 · Cited by 228 · see citing works
Global Similarity and Pattern Separation in the Human Medial Temporal Lobe Predict Subsequent Memory
LaRocque, K. F., Smith, M. E., Carr, V. A., Witthoft, N., Kalanit Grill-spector, A., & Wagner, A. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4293-12.2013 · Cited by 222 · see citing works
Staresina, B. P., & Davachi, L. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20104 · Cited by 222 · see citing works
Self-citationOnly some spatial patterns of fMRI response are read out in task performance
Williams, M., Dang, S., & Kanwisher, N. (2007) · Nature Neuroscience · doi:10.1038/nn1900 · Cited by 213 · see citing works
A Specific Role of the Human Hippocampus in Recall of Temporal Sequences
Lehn, H., Steffenach, H.-A., van Strien, N. M., Veltman, D. J., Witter, M. P., & Haberg, A. K. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5370-08.2009 · Cited by 177 · see citing works
Evidence for Neural Effects of Repetition that Directly Correlate with Behavioral Priming
Maccotta, L., & Buckner, R. L. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042568451 · Cited by 143 · see citing works
Ekstrom, A. D., & Bookheimer, S. Y. (2007) · Learning & Memory · doi:10.1101/lm.575107 · Cited by 139 · see citing works
Medial Temporal Lobe Contributions to Episodic Sequence Encoding
Tubridy, S. M., & Davachi, L. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq092 · Cited by 137 · see citing works
Self-citationThe Short and Long of It: Neural Correlates of Temporal-order Memory for Autobiographical Events
Jacques, P. L. S., Rubin, D. C., LaBar, K. S., & Cabeza, R. E. L. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20091 · Cited by 129 · see citing works
Kuhl, B. A., Rissman, J., & Wagner, A. D. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.09.002 · Cited by 112 · see citing works
A neural substrate in the human hippocampus for linking successive events
Paz, R., Gelbard-Sagiv, H., Mukamel, R., Harel, M., Malach, R., & Fried, I. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910834107 · Cited by 101 · see citing works
Ward, E. J., Chun, M. M., & Kuhl, B. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4889-12.2013 · Cited by 100 · see citing works
Predicting judged similarity of natural categories from their neural representations
Weber, M. J., Thompson‐Schill, S. L., Osherson, D. N., Haxby, J. V., & Parsons, L. M. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.12.029 · Cited by 93 · see citing works
Xue, G., Dong, Q., Chen, C., Lu, Z., Mumford, J. A., & Poldrack, R. A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs143 · Cited by 91 · see citing works
McDuff, S. G. R., Tsibris, H. C., & Norman, K. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3587-08.2009 · Cited by 83 · see citing works
Critical Role of the Hippocampus in Memory for Elapsed Time
Jacobs, N. S., Allen, T. A., Nguyen, N., & Fortin, N. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1733-13.2013 · Cited by 83 · see citing works
Two Kinds of fMRI Repetition Suppression? Evidence for Dissociable Neural Mechanisms
Epstein, R. A., Parker, W. E., & Feiler, A. M. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90376.2008 · Cited by 78 · see citing works
Dudukovic, N. M., & Wagner, A. D. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.02.025 · Cited by 78 · see citing works
Scene Representations in Parahippocampal Cortex Depend on Temporal Context
Turk‐Browne, N. B., Simon, M. G., & Sederberg, P. B. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0942-12.2012 · Cited by 75 · see citing works
Qin, S., Piekema, C., Petersson, K. M., Han, B., Luo, J., & Fernández, G. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.020 · Cited by 66 · see citing works
Category-Specific Neural Oscillations Predict Recall Organization During Memory Search
Morton, N. W., Kahana, M. J., Rosenberg, E. A., Baltuch, G. H., Litt, B., Sharan, A. D., Sperling, M. R., & Polyn, S. M. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs229 · Cited by 47 · see citing works
Hales, J. B., & Brewer, J. B. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.07.025 · Cited by 40 · see citing works
The Effect of Attention on Repetition Suppression and Multivoxel Pattern Similarity
Moore, K. S., Yi, D.-J., & Chun, M. M. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00387 · Cited by 23 · see citing works
Xiong (1999) · doi:10.1002/(sici)1097-0193(1999)8:2/3
Flagged first, then by citations
Cited by
Sorted by citations
The cognitive map in humans: spatial navigation and beyond
Epstein, R. A., Patai, E. Z., Julian, J. B., & Spiers, H. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4656 · Cited by 921 · see citing works
Time cells in the hippocampus: a new dimension for mapping memories
Eichenbaum, H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3827 · Cited by 843 · see citing works
Navigating cognition: Spatial codes for human thinking
Bellmund, J. L. S., Gärdenfors, P., Moser, E. I., & Doeller, C. F. (2018) · Science · doi:10.1126/science.aat6766 · Cited by 643 · see citing works
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 · see citing works
Integrating time from experience in the lateral entorhinal cortex
Tsao, A., Sugar, J., Lu, L., Wang, C., Knierim, J. J., Moser, M.-B., & Moser, E. I. (2018) · Nature · doi:10.1038/s41586-018-0459-6 · Cited by 490 · see citing works
A map of abstract relational knowledge in the human hippocampal-entorhinal cortex
Garvert, M. M., Dolan, R. J., & Behrens, T. E. (2017) · eLife · doi:10.7554/elife.17086 · Cited by 379 · see citing works
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 · see citing works
Self-citationHow the hippocampus preserves order: the role of prediction and context
Davachi, L., & DuBrow, S. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.12.004 · Cited by 328 · see citing works
Self-citationHippocampal CA2 activity patterns change over time to a larger extent than between spatial contexts
Mankin, E. A., Diehl, G. W., Sparks, F. T., Leutgeb, S., & Leutgeb, J. K. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.001 · Cited by 279 · see citing works
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 · see citing works
Self-citationMemory: organization and control.
Eichenbaum, H. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044131 · Cited by 257 · see citing works
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 · see citing works
Self-citationA distributed representation of internal time
Howard, M. W., Shankar, K. H., Aue, W. R., & Criss, A. H. (2015) · Psychological Review · doi:10.1037/a0037840 · Cited by 133 · see citing works
The role of the hippocampus in memory and mental construction
Sheldon, S., & Levine, B. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13006 · Cited by 155 · see citing works
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 · see citing works
Does mental context drift or shift?
DuBrow, S., Rouhani, N., Niv, Y., & Norman, K. A. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.08.003 · Cited by 118 · see citing works
Neurophysiology of Remembering
Buzsáki, G., McKenzie, S., & Davachi, L. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-021721-110002 · Cited by 84 · see citing works
Self-citationFrom remembering to reconstruction: The transformative neural representation of episodic memory.
Xue, G. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102351 · Cited by 49 · see citing works
The human brain uses spatial schemas to represent segmented environments
Peer, M., & Epstein, R. A. (2021) · Current Biology · doi:10.1016/j.cub.2021.08.012 · Cited by 38 · see citing works
- Authors
- Ezzyat, Y., & Davachi, L.
- Affiliations
- New York University (US)
- Corresponding author
- Davachi, Lila
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2014-03
- Volume
- 81
- Issue
- 5
- Pages
- 1179-1189
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC3983791
- OpenAlex
- W2097347024
- Cited by
- 321
- References
- 80
- Citations by year
- 2026: 22 · 2025: 28 · 2024: 38 · 2023: 35 · 2022: 29 · 2021: 23 · 2020: 24 · 2019: 19 · 2018: 26 · 2017: 30 · 2016: 19 · 2015: 18 · 2014: 9 · 2013: 1
- FWCI
- 14.13
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- 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
- temporal memory, hippocampus, pattern similarity, episodic memory, representational stability, lateral occipital cortex, BOLD signal, time gap, memory organization
- MeSH terms
- Adolescent, Adult, Female, Hippocampus, Humans, Judgment, Magnetic Resonance Imaging, Male, Pattern Recognition, Visual, Photic Stimulation, Time Perception, Visual Cortex, Young Adult, Memory, Episodic
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
