CA1 and CA3 differentially support spontaneous retrieval of episodic contexts within human hippocampal subfields
Open accessPublished version of a preprint
Abstract
The hippocampus plays a critical role in spatial and episodic memory. Mechanistic models predict that hippocampal subfields have computational specializations that differentially support memory. However, there is little empirical evidence suggesting differences between the subfields, particularly in humans. To clarify how hippocampal subfields support human spatial and episodic memory, we developed a virtual reality paradigm where participants passively navigated through houses (spatial contexts) across a series of videos (episodic contexts). We then used multivariate analyses of high-resolution fMRI data to identify neural representations of contextual information during recollection. Multi-voxel pattern similarity analyses revealed that CA1 represented objects that shared an episodic context as more similar than those from different episodic contexts. CA23DG showed the opposite pattern, differentiating between objects encountered in the same episodic context. The complementary characteristics of these subfields explain how we can parse our experiences into cohesive episodes while retaining the specific details that support vivid recollection.
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?
Recent human imaging studies show distinct but complementary characteristics of CA1 and CA3 in episodic memory.
“Recent human imaging studies shed light on the distinct but complementary characteristics of CA1 and CA3 in episodic memory (Copara et al., 2014; Dimsdale-Zucker et al., 2018).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Dimsdale-Zucker et al., 2018
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
Fitting Linear Mixed-Effects Models Using <b>lme4</b>
Bates, D., Mächler, M., Bolker, B., & Walker, S. (2015) · Journal of Statistical Software · doi:10.18637/jss.v067.i01 · Cited by 86,835 · see citing works
Random effects structure for confirmatory hypothesis testing: Keep it maximal
Barr, D. J., Levy, R., Scheepers, C., & Tily, H. J. (2013) · Journal of Memory and Language · doi:10.1016/j.jml.2012.11.001 · Cited by 10,328 · see citing works
Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.018 · Cited by 7,429 · see citing works
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 · see citing works
Self-citationRepresentational similarity analysis-connecting the branches of systems neuroscience
Kriegeskorte, N. (2008) · Frontiers in Systems Neuroscience · doi:10.3389/neuro.06.004.2008 · Cited by 3,355 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
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 · see citing works
Self-citationThe human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401 · see citing works
Evaluating significance in linear mixed-effects models in R
Luke, S. G. (2016) · Behavior Research Methods · doi:10.3758/s13428-016-0809-y · Cited by 1,812 · see citing works
Meta-analysis of experiments with matched groups or repeated measures designs
Dunlap, W. P., Cortina, J. M., Vaslow, J. B., & Burke, M. J. (1996) · Psychological Methods · doi:10.1037/1082-989x.1.2.170 · Cited by 1,693 · see citing works
Pattern separation in the hippocampus
Yassa, M. A., & Stark, C. E. L. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.06.006 · Cited by 1,544 · see citing works
Internally Generated Cell Assembly Sequences in the Rat Hippocampus
Pastalkova, E., Itskov, V., Amarasingham, A., & Buzsáki, G. (2008) · Science · doi:10.1126/science.1159775 · Cited by 1,301 · 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
Imaging recollection and familiarity in the medial temporal lobe: a three-component model
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.08.001 · Cited by 1,154 · see citing works
Self-citationItem, 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
Précis of Elements of episodic memory
Tulving, E. (1984) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0004440x · Cited by 809 · 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
How does nature program neuron types?
Borst, A. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.016.2008 · Cited by 705 · see citing works
Linear models and linear mixed effects models in R with linguistic applicationsPreprint
Winter, B. (2013) · arXiv.org · doi:10.48550/arxiv.1308.5499 · Cited by 658 · see citing works
Can We Reconcile the Declarative Memory and Spatial Navigation Views on Hippocampal Function?
Eichenbaum, H., & Cohen, N. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.032 · Cited by 609 · see citing works
Yushkevich, P. A., Pluta, J. B., Wang, H., Xie, L., Ding, S., Gertje, E. C., Mancuso, L., Kliot, D., Das, S. R., & Wolk, D. A. (2014) · Human Brain Mapping · doi:10.1002/hbm.22627 · Cited by 587 · see citing works
Hippocampal “Time Cells”: Time versus Path Integration
Kraus, B. J., Robinson, R. J., White, J. A., Eichenbaum, H., & Hasselmo, M. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.015 · Cited by 526 · 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
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
Schlichting, M. L., Mumford, J. A., & Preston, A. R. (2015) · Nature Communications · doi:10.1038/ncomms9151 · Cited by 381 · see citing works
Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375 · see citing works
McKenzie, S., Frank, A. J., Kinsky, N. R., Porter, B., Rivière, P. D., & Eichenbaum, H. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.019 · Cited by 373 · 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
Ensemble Dynamics of Hippocampal Regions CA3 and CA1
Guzowski, J. F., Knierim, J. J., & Moser, E. I. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.003 · Cited by 354 · see citing works
O'Reilly, R. C., & Norman, K. A. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)02005-3 · Cited by 351 · see citing works
A computational theory of hippocampal function, and tests of the theory: New developments
Kesner, R. P., & Rolls, E. T. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.009 · Cited by 347 · see citing works
Yushkevich, P. A., Amaral, R. S. C., Augustinack, J. C., Bender, A. R., Bernstein, J. D., Boccardi, M., Bocchetta, M., Burggren, A. C., Carr, V. A., Chakravarty, M. M., et al. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.004 · Cited by 342 · see citing works
Self-citationHippocampal mechanisms for the context-dependent retrieval of episodes
Hasselmo, M. E., & Eichenbaum, H. (2005) · Neural Networks · doi:10.1016/j.neunet.2005.08.007 · Cited by 298 · see citing works
Recollection and the Reinstatement of Encoding-Related Cortical Activity
Johnson, J. D., & Rugg, M. D. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl156 · Cited by 261 · see citing works
A Double Dissociation between Hippocampal Subfields
Lee, I., Rao, G., & Knierim, J. J. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.010 · Cited by 236 · see citing works
Pattern separation, pattern completion, and new neuronal codes within a continuous CA3 map
Leutgeb, S., & Leutgeb, J. K. (2007) · Learning & Memory · doi:10.1101/lm.703907 · Cited by 234 · see citing works
Nearly automatic segmentation of hippocampal subfields in in vivo focal T2-weighted MRI
Yushkevich, P. A., Wang, H., Pluta, J. B., Das, S. R., Craige, C. P., Avants, B., Weiner, M. W., & Mueller, S. G. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.040 · Cited by 231 · 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
Activity dynamics and behavioral correlates of CA3 and CA1 hippocampal pyramidal neurons
Mizuseki, K., Royer, S., Diba, K., & Buzsáki, G. (2012) · Hippocampus · doi:10.1002/hipo.22002 · Cited by 216 · see citing works
Confounds in multivariate pattern analysis: Theory and rule representation case study
Todd, M. T., Nystrom, L. E., & Cohen, J. D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.039 · Cited by 199 · see citing works
Ji, J.-Z., & Maren, S. (2008) · Learning & memory (Cold Spring Harbor, N.Y.) · doi:10.1101/lm.794808 · Cited by 195 · see citing works
Attention promotes episodic encoding by stabilizing hippocampal representations
Aly, M., & Turk-Browne, N. (2016) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1518931113 · Cited by 194 · see citing works
Time cells in hippocampal area CA3
Salz, D. M., Tiganj, Z., Khasnabish, S., Kohley, A., Sheehan, D., Howard, M. W., & Eichenbaum, H. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0087-16.2016 · Cited by 183 · see citing works
Gordon, A. M., Rissman, J., Kiani, R., & Wagner, A. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht194 · Cited by 173 · see citing works
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 163 · see citing works
Favila, S. E., Chanales, A. J. H., & Kuhl, B. A. (2016) · Nature Communications · doi:10.1038/ncomms11066 · Cited by 162 · see citing works
Role of CA3 and CA1 subregions of the dorsal hippocampus on temporal processing of objects
Hoge, J., & Kesner, R. P. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.04.013 · Cited by 156 · see citing works
Attention Stabilizes Representations in the Human Hippocampus
Aly, M., & Turk‐Browne, N. B. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv041 · Cited by 149 · see citing works
Nonspatial 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 149 · see citing works
Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval
Ritchey, M., Montchal, M. E., Yonelinas, A. P., & Ranganath, C. (2015) · eLife · doi:10.7554/elife.05025 · Cited by 148 · see citing works
Self-citationDistinct roles for dorsal CA3 and CA1 in memory for sequential nonspatial events
Farovik, A., Dupont, L. M., & Eichenbaum, H. (2010) · Learning & Memory · doi:10.1101/lm.1616209 · Cited by 140 · see citing works
Hunsaker, M. R., Fieldsted, P. M., Rosenberg, J. S., & Kesner, R. P. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.643 · Cited by 127 · see citing works
Local generation of multineuronal spike sequences in the hippocampal CA1 region
Stark, E., Roux, L., Eichler, R., & Buzsáki, G. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508785112 · Cited by 115 · see citing works
Application of Cortical Unfolding Techniques to Functional MRI of the Human Hippocampal Region
Zeineh, M., Engel, S. A., & Bookheimer, S. Y. (2000) · NeuroImage · doi:10.1006/nimg.2000.0561 · Cited by 106 · see citing works
Advances in high-resolution imaging and computational unfolding of the human hippocampus
Ekstrom, A. D., Bazih, A., Suthana, N., Al-Hakim, R. A., Ogura, K., Zeineh, M., Burggren, A. C., & Bookheimer, S. Y. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.03.017 · Cited by 101 · see citing works
Self-citationEvaluating the temporal context of episodic memory: The role of CA3 and CA1
Hunsaker, M. R. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.11.015 · Cited by 101 · see citing works
Neural Differentiation of Incorrectly Predicted Memories
Kim, G., Norman, K. A., & Turk‐Browne, N. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3272-16.2017 · Cited by 97 · see citing works
Lee, I., Jerman, T. S., & Kesner, R. P. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.06.002 · Cited by 95 · see citing works
Kyle, C. T., Stokes, J. D., Lieberman, J. S., Hassan, A. S., & Ekstrom, A. D. (2015) · eLife · doi:10.7554/elife.10499 · Cited by 92 · see citing works
Self-citationGusev, P. A., Cui, C., Alkon, D. L., & Gubin, A. N. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0832-05.2005 · Cited by 90 · see citing works
Frankó, E., Insausti, A. M., Artacho-Pérula, E., Insausti, R., & Chavoix, C. (2014) · Human Brain Mapping · doi:10.1002/hbm.22170 · Cited by 85 · see citing works
Stokes, J. D., Kyle, C. T., & Ekstrom, A. D. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00736 · Cited by 75 · see citing works
Self-citationSharp, P. E., Blair, H. T., & Brown, M. A., Sr. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:6 · Cited by 64 · see citing works
Prediction strength modulates responses in human area CA1 to sequence violations
Chen, J., Cook, P. A., & Wagner, A. D. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00149.2015 · Cited by 64 · see citing works
The role of the dorsal CA1 and ventral CA1 in memory for the temporal order of a sequence of odors
Kesner, R. P., Hunsaker, M. R., & Ziegler, W. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.08.010 · Cited by 63 · see citing works
Roth, E. D., Yu, X., Rao, G., & Knierim, J. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036035 · Cited by 58 · see citing works
Roles of human hippocampal subfields in retrieval of spatial and temporal context
Kyle, C. T., Smuda, D. N., Hassan, A. S., & Ekstrom, A. D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.034 · Cited by 51 · see citing works
Self-citationBrown, T. I., Hasselmo, M. E., & Stern, C. E. (2014) · Hippocampus · doi:10.1002/hipo.22273 · Cited by 48 · see citing works
Temporal context processing within hippocampal subfields
Wang, F., & Diana, R. A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.048 · Cited by 18 · see citing works
Overlap among spatial memories triggers repulsion of hippocampal representationsPreprint
Chanales, A. J. H., Oza, A., Favila, S. E., & Kuhl, B. A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/099226 · Cited by 13 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [60]Bates, D. lme4: Mixed-effects Modeling with R (Springer, Madison, WI, 2010).
Cited by
Sorted by citations
Roddy, D. W., Farrell, C., Doolin, K., Roman, E., Tozzi, L., Frodl, T., O’Keane, V., & O’Hanlon, E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.08.021 · Cited by 287 · see citing works
Space, time, and episodic memory: The hippocampus is all over the cognitive map
Ekstrom, A. D., & Ranganath, C. (2017) · Hippocampus · doi:10.1002/hipo.22750 · Cited by 250 · see citing works
Self-citationInhibitory stabilization and cortical computation
Sadeh, S., & Clopath, C. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00390-z · Cited by 183 · see citing works
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works
Nonmonotonic Plasticity: How Memory Retrieval Drives Learning
Ritvo, V. J. H., Turk‐Browne, N. B., & Norman, K. A. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.06.007 · Cited by 146 · see citing works
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 120 · see citing works
Multimodal Parcellations and Extensive Behavioral Profiling Tackling the Hippocampus Gradient
Plachti, A., Eickhoff, S. B., Hoffstaedter, F., Patil, K. R., Laird, A. R., Fox, P. T., Amunts, K., & Genon, S. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy336 · Cited by 110 · see citing works
Episodic recognition memory and the hippocampus in Parkinson's disease: A review
Das, T., Hwang, J. J., & Poston, K. L. (2018) · Cortex · doi:10.1016/j.cortex.2018.11.021 · Cited by 112 · see citing works
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 111 · see citing works
Mnemonic prediction errors bias hippocampal states
Bein, O., Duncan, K. D., & Davachi, L. (2020) · Nature Communications · doi:10.1038/s41467-020-17287-1 · Cited by 103 · see citing works
Representational Similarity Analyses
Dimsdale-Zucker, H. R., & Charan Ranganath, A. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00027-6 · Cited by 93 · see citing works
Self-citationEnhancing the Ecological Validity of fMRI Memory Research Using Virtual Reality
Reggente, N., Essoe, J. K.-Y., Aghajan, Z. M., Tavakoli, A. V., Mcguire, J. F., Suthana, N., & Rissman, J. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00408 · Cited by 91 · see citing works
Molitor, R. J., Sherrill, K. R., Morton, N. W., Miller, A. A., & Preston, A. R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-20.2020 · Cited by 89 · see citing works
Yao, Z., Fu, Y., Wu, J., Zhang, W., Yu, Y., Zhang, Z., Wu, X., Wang, Y., & Hu, B. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-018-0003-1 · Cited by 87 · see citing works
Dalton, M. A., D’Souza, A., Lv, J., & Calamante, F. (2022) · eLife · doi:10.7554/elife.76143 · Cited by 83 · see citing works
The Primacy of Spatial Context in the Neural Representation of Events
Robin, J., Buchsbaum, B. R., & Moscovitch, M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1638-17.2018 · Cited by 84 · see citing works
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 78 · see citing works
Prolonged Cannabidiol Treatment Effects on Hippocampal Subfield Volumes in Current Cannabis Users
Beale, C., Broyd, S. J., Chye, Y., Suo, C., Schira, M. M., Galettis, P., Martin, J. H., Yücel, M., & Solowij, N. (2018) · Cannabis and Cannabinoid Research · doi:10.1089/can.2017.0047 · Cited by 76 · see citing works
Differentiable Processing of Objects, Associations, and Scenes within the Hippocampus
Dalton, M. A., Zeidman, P., McCormick, C., & Maguire, E. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0263-18.2018 · Cited by 69 · see citing works
Virtual reality video game improves high-fidelity memory in older adults
Wais, P. E., Arioli, M., Anguera‐Singla, R., & Gazzaley, A. H. (2021) · Scientific Reports · doi:10.1038/s41598-021-82109-3 · Cited by 67 · see citing works
Mızrak, E., Bouffard, N. R., Libby, L. A., Boorman, E. D., & Ranganath, C. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110065 · Cited by 69 · see citing works
Abrupt hippocampal remapping signals resolution of memory interference
Guo, W., Favila, S. E., Kim, G., Molitor, R. J., & Kuhl, B. A. (2021) · Nature Communications · doi:10.1038/s41467-021-25126-0 · Cited by 64 · see citing works
Moscovitch, M., & Gilboa, A. (2021) · doi:10.31234/osf.io/yxbrs · Cited by 62 · see citing works
Extra-hippocampal contributions to pattern separation
Amer, T., & Davachi, L. (2023) · eLife · doi:10.7554/elife.82250 · Cited by 71 · see citing works
Surface-based hippocampal subfield segmentation
DeKraker, J., Köhler, S., & KHAN, A. R. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.06.005 · Cited by 59 · see citing works
3D Hippocampal Place Field Dynamics in Free-Flying Echolocating Bats
Wohlgemuth, M. J., Yu, C., & Moss, C. F. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00270 · Cited by 55 · see citing works
Sequence Memory in the Hippocampal–Entorhinal Region
Bellmund, J. L. S., Polti, I., & Doeller, C. F. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01592 · Cited by 55 · see citing works
Adaptive Repulsion of Long-Term Memory Representations Is Triggered by Event Similarity
Chanales, A. J. H., Tremblay-McGaw, A. G., Drascher, M. L., & Kuhl, B. A. (2021) · Psychological Science · doi:10.1177/0956797620972490 · Cited by 53 · see citing works
Exploring the Facets of Emotional Episodic Memory: Remembering “What,” “When,” and “Which”
Palombo, D. J., Te, A. A., Checknita, K. J., & Madan, C. R. (2021) · Psychological Science · doi:10.1177/0956797621991548 · Cited by 52 · see citing works
Morikawa, M., Tanaka, Y., Cho, H., Yoshihara, M., & Hirokawa, N. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.05.089 · Cited by 49 · see citing works
Parker, T. D., Slattery, C. F., Yong, K. X. X., Nicholas, J. M., Paterson, R. W., Foulkes, A., Malone, I. B., Thomas, D. L., Cash, D. M., Crutch, S. J., et al. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.101632 · Cited by 51 · see citing works
Increasing stimulus similarity drives nonmonotonic representational change in hippocampus
Wammes, J. D., Norman, K. A., & Turk-Browne, N. B. (2022) · eLife · doi:10.7554/elife.68344 · Cited by 50 · see citing works
Sex Differences in Cognition Across Aging
Lee, B. H., Richard, J. E., de leon, R. G., Yagi, S., & Galea, L. A. M. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_309 · Cited by 51 · see citing works
Liu, C., Ye, Z., Chen, C., Axmacher, N., & Xue, G. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab304 · Cited by 51 · see citing works
Hippocampal Shape Maturation in Childhood and Adolescence
Lynch, K. M., Shi, Y., Toga, A. W., Clark, K. A., & Pediatric Imaging, N. A. G. S. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy244 · Cited by 49 · see citing works
From 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
Martin, C. B., Hong, B., Newsome, R. N., Savel, K., Meade, M. E., Xia, A., Honey, C. J., & Barense, M. D. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2214285119 · Cited by 47 · see citing works
Identifying the cognitive processes underpinning hippocampal-dependent tasks.
Clark, I. A., Hotchin, V., Monk, A. M., Pizzamiglio, G., Liefgreen, A., & Maguire, E. A. (2019) · Journal of Experimental Psychology General · doi:10.1037/xge0000582 · Cited by 41 · see citing works
Goal-oriented representations in the human hippocampus during planning and navigation
Crivelli-Decker, J. E., Clarke, A., Park, S. A., Huffman, D. J., Boorman, E. D., & Ranganath, C. (2023) · Nature Communications · doi:10.1038/s41467-023-35967-6 · Cited by 40 · see citing works
Dimensions and mechanisms of memory organization
de Sousa, A. F., Chowdhury, A., & Silva, A. J. (2021) · Neuron · doi:10.1016/j.neuron.2021.06.014 · Cited by 46 · see citing works
The Hippocampus Generalizes across Memories that Share Item and Context Information
Libby, L. A., Reagh, Z. M., Bouffard, N. R., Ragland, J. D., & Ranganath, C. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01345 · Cited by 42 · see citing works
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 42 · see citing works
Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
Vanrobaeys, Y. S., Mukherjee, U., Langmack, L., Beyer, S. E., Bahl, E., Lin, L., Michaelson, J. J., Abel, T. G., & Chatterjee, S. (2023) · Nature Communications · doi:10.1038/s41467-023-41715-7 · Cited by 39 · see citing works
Alves, J. M., LUO, S. H., Chow, T., Herting, M. M., Xiang, A. H., & Page, K. A. (2020) · Brain and Behavior · doi:10.1002/brb3.1522 · Cited by 42 · see citing works
Hippocampal ripples signal contextually mediated episodic recall
Sakon, J. J., & Kahana, M. J. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2201657119 · Cited by 40 · see citing works
Multiple Memory Subsystems: Reconsidering Memory in the Mind and Brain
Sherman, B. E., Turk‐Browne, N. B., & Goldfarb, E. V. (2023) · Perspectives on Psychological Science · doi:10.1177/17456916231179146 · Cited by 42 · see citing works
Koch, S. B. J., van Ast, V. A., Kaldewaij, R., Hashemi, M. M., Zhang, W., Klumpers, F., & Karin Roelofs, A. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-00947-7 · Cited by 38 · see citing works
Molecular evidences on anti‐inflammatory, anticancer, and memory‐boosting effects of frankincense
Khajehdehi, M., Khalaj‐Kondori, M., & Baradaran, B. (2022) · Phytotherapy Research · doi:10.1002/ptr.7399 · Cited by 37 · see citing works
Lum, P. T., Sekar, M., Seow, L.-J., Shaikh, M. F., Arulsamy, A., Retinasamy, T., Gan, S. H., Gnanaraj, C., Esa, N. M., Ramachawolran, G., et al. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1189957 · Cited by 36 · see citing works
Neural substrates of human fear generalization: A 7T-fMRI investigation
Huggins, A. A., Tomas, C. W., Parisi, E. A., Bennett, K. P., Miskovic, V., & Larson, C. L. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118308 · Cited by 28 · see citing works
Distinct Patterns of Hippocampal and Neocortical Evolution in Primates
Vanier, D. R., Sherwood, C. C., & Smaers, J. B. (2019) · Brain Behavior and Evolution · doi:10.1159/000500625 · Cited by 28 · see citing works
Skouras, S., Torner, J., Andersson, P. U., Koush, Y., Falcón, C., Minguillón, C., Fauria, K., Alpiste, F., Blenow, K., Zetterberg, H., et al. (2020) · Brain · doi:10.1093/brain/awaa011 · Cited by 27 · see citing works
Adaptive Memory Distortions Are Predicted by Feature Representations in Parietal Cortex
Zhao, Y., Chanales, A. J. H., & Kuhl, B. A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2875-20.2021 · Cited by 27 · see citing works
Structure–Function Dissociations of Human Hippocampal Subfield Stiffness and Memory Performance
Delgorio, P. L., Hiscox, L. V., Daugherty, A. M., Sanjana, F., McIlvain, G., Pohlig, R. T., McGarry, M., Martens, C. R., Schwarb, H. D., & Johnson, C. L. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0592-22.2022 · Cited by 27 · see citing works
Hippocampal contributions to serial‐order memory
Long, N. M., & Kahana, M. J. (2018) · Hippocampus · doi:10.1002/hipo.23025 · Cited by 27 · see citing works
Zou, F., Guo, W., Allen, E., Wu, Y., Charest, I., Naselaris, T., Kay, K., Kuhl, B. A., Hutchinson, J. B., & DuBrow, S. (2023) · Nature Communications · doi:10.1038/s41467-023-40100-8 · Cited by 27 · see citing works
Bein, O., & Davachi, L. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0627-23.2023 · Cited by 24 · see citing works
Update on temporal lobe‐dependent information processing, in health and disease
Chauvière, L. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14594 · Cited by 25 · see citing works
Content-specific vulnerability of recent episodic memories in Alzheimer's disease
Grande, X., Berron, D., Maaß, A., Bainbridge, W. A., & Düzel, E. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2021.107976 · Cited by 22 · see citing works
Hippocampal circuits underlie improvements in self‐reported anxiety following mindfulness training
Sevinc, G., Greenberg, J., Hölzel, B. K., Gard, T., Calahan, T., Brunsch, V., Hashmi, J. A., Vangel, M. G., Orr, S. P., Milad, M. R., et al. (2020) · Brain and Behavior · doi:10.1002/brb3.1766 · Cited by 23 · see citing works
Visualization of Information Retrieval in Smart Library Based on Virtual Reality Technology
Fang, S. (2020) · Complexity · doi:10.1155/2020/6646673 · Cited by 23 · see citing works
RetractedTime, memory, and the legacy of Howard Eichenbaum
Ranganath, C. (2018) · Hippocampus · doi:10.1002/hipo.23007 · Cited by 26 · see citing works
Higher post-encoding cortisol benefits the selective consolidation of emotional aspects of memory
Cunningham, T. J., Mattingly, S. M., Tlatenchi, A., Wirth, M. M., Alger, S. E., Kensinger, E. A., & Payne, J. D. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107411 · Cited by 22 · see citing works
Brain health is independently impaired by E-vaping and high-fat diet
Chen, H., Wang, B., Li, G., Steele, J. R., Stayte, S., Vissel, B., Chan, Y. L., Yi, C., Saad, S., Machaalani, R., et al. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.11.028 · Cited by 23 · see citing works
Xu, H.-B., Liu, Y., Wang, L., Zeng, X., Xu, Y., & Wang, Z. (2023) · NeuroImage: Clinical · doi:10.1016/j.nicl.2023.103370 · Cited by 23 · see citing works
Volumetric Analysis of Amygdala and Hippocampal Subfields for Infants with Autism
Li, G., Chen, M., Li, G., Wu, D., Lian, C., Sun, Q., Rushmore, J., & Wang, L. (2022) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-022-05535-w · Cited by 20 · see citing works
Reggente, N. (2023) · Current topics in behavioral neurosciences · doi:10.1007/7854_2023_425 · Cited by 11 · see citing works
Cui, Y., Zhang, Z., Zhang, B., Zhao, L., Hou, C., Zeng, Q., Nie, J., Yu, J., Zhao, Y., Gao, T., et al. (2018) · Toxicology Letters · doi:10.1016/j.toxlet.2018.08.020 · Cited by 19 · see citing works
Liu, G., Liu, C., Qiu, A., & Initiative, T. A. D. N. (2021) · Human Brain Mapping · doi:10.1002/hbm.25414 · Cited by 18 · see citing works
Cao, J., Tang, Y., Chen, S., Yu, S., Wan, K., Yin, W., Zhen, W., Zhao, W., Zhou, X., Zhu, X., et al. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231114 · Cited by 16 · see citing works
Zhang, K., Chen, L., Li, Y., Paez, A. G., Miao, X., Cao, D., Gu, C., Pekar, J. J., van Zijl, P. C. M., Hua, J., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1488-22.2023 · Cited by 16 · see citing works
Hippocampal subfield alterations in schizophrenia: A selective review of structural MRI studies
Hu, N., Luo, C., Zhang, W., Yang, X., Xiao, Y., Sweeney, J. A., Lui, S., & Gong, Q. (2020) · Biomarkers in Neuropsychiatry · doi:10.1016/j.bionps.2020.100026 · Cited by 16 · see citing works
Matos, P., & Albuquerque, P. B. (2021) · Cognitive Processing · doi:10.1007/s10339-021-01016-7 · Cited by 16 · see citing works
Tompary, A., & Davachi, L. (2024) · eLife · doi:10.7554/elife.84359 · Cited by 14 · see citing works
Near-Death High-Frequency Hyper-Synchronization in the Rat Hippocampus
Zhang, Y., Li, Z., Zhang, J., Zhao, Z., Zhang, H., Vreugdenhil, M., & Lu, C. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00800 · Cited by 15 · see citing works
Association of Hippocampal Subfield Volumes with Amyloid-Beta Deposition in Alzheimer’s Disease
Baek, M. S., Lee, N., Kim, J. W., & Hong, J. Y. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11061526 · Cited by 14 · see citing works
He, M., Li, Y., Zhou, L., Li, Y., Lei, T., Yan, W., Song, J., & Chen, L. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.823535 · Cited by 13 · see citing works
Representations of Complex Contexts: A Role for Hippocampus
Dimsdale-Zucker, H. R., Montchal, M. E., Reagh, Z. M., Wang, S.-F., Libby, L. A., & Charan Ranganath, A. (2022) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01919 · Cited by 14 · see citing works
Self-citationZheng, L. J., Lin, L., Schoepf, U. J., Varga‐Szemes, Á., Savage, R. H., Zhang, H., Wang, Y. F., Zhang, X. Y., Luo, S. J., Liu, Y., et al. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02292-2 · Cited by 13 · see citing works
Subcortical brain volume variations in autistic individuals across the lifespan
Christensen, D., Shin, Y. S., Wang, J., Cuomo, C. R., Dentry, T., Gemmell, H. M., Pulver, S. L., Orlando, A., McKinney, W. S., Stevens, C. J., et al. (2025) · Molecular Autism · doi:10.1186/s13229-025-00673-1 · Cited by 12 · see citing works
A neural network model of differentiation and integration of competing memories
Ritvo, V. J. H., Nguyen, A., Turk‐Browne, N. B., & Norman, K. A. (2024) · eLife · doi:10.7554/elife.88608.3 · Cited by 12 · see citing works
Samara, A., Raji, C. A., Li, Z. A., & Hershey, T. G. (2021) · American Journal of Neuroradiology · doi:10.3174/ajnr.a7244 · Cited by 14 · see citing works
Chi, C.-H., Yang, F., & Chang, Y. (2022) · Brain and Cognition · doi:10.1016/j.bandc.2022.105877 · Cited by 12 · see citing works
Challenges in Understanding the Role of Reactivation in Modifying Hippocampal Representations
Tarder-Stoll, H., Gasser, C., Yu, W., & Dimsdale-Zucker, H. R. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0334-21.2021 · Cited by 11 · see citing works
Self-citationDynamics of Brain Structure and its Genetic Architecture over the Lifespan
Brouwer, R. M., Klein, M., Grasby, K. L., Schnack, H. G., Jahanshad, N., Teeuw, J., Thomopoulos, S. I., Sprooten, E., Franz, C. E., Gogtay, N., et al. (2020) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.5658141 · Cited by 9 · see citing works
Elucidating behavioral and functional connectivity markers of aberrant threat discrimination in PTSD
Keefe, J. R., Suarez-Jimenez, B., Zhu, X., Lazarov, A., Durosky, A., Such, S., Marohasy, C., Lissek, S., & Neria, Y. (2022) · Depression and Anxiety · doi:10.1002/da.23295 · Cited by 10 · see citing works
Chen, H., Zhou, W., & Yang, J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.3181-18.2019 · Cited by 12 · see citing works
Reduction in hippocampal volumes subsequent to heavy cannabis use: a 3-year longitudinal study
Wang, Y., Zuo, C., Wang, W., Xu, Q., & Lei, H. C. (2020) · Psychiatry Research · doi:10.1016/j.psychres.2020.113588 · Cited by 13 · see citing works
Wang, K., Li, X., Wang, X., Hommel, B., Xia, X., Qiu, J., Fu, Y., & Zhou, Z. (2023) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2023.07.012 · Cited by 10 · see citing works
Dimsdale-Zucker, H. R., Maciejewska, K., Kim, K., Yonelinas, A. P., & Ranganath, C. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2022.108287 · Cited by 10 · see citing works
Self-citationStress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
Grob, A.-M., Milivojevic, B., Alink, A., Doeller, C. F., & Schwabe, L. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119804 · Cited by 12 · see citing works
Kwon, D., Kim, J., Yoo, S. B. M., & Shim, W. M. (2025) · Nature Communications · doi:10.1038/s41467-025-55833-x · Cited by 10 · see citing works
Mishra, A., Tostaeva, G., Nentwich, M., Espinal, E., Markowitz, N., Winfield, J., Freund, E., Gherman, S., Leszczyński, M., Schroeder, C. E., et al. (2025) · Science Advances · doi:10.1126/sciadv.adv0986 · Cited by 12 · see citing works
The Neural Correlates of Analogy Component Processes
Parsons, J., & Davies, J. (2022) · Cognitive Science · doi:10.1111/cogs.13116 · Cited by 9 · see citing works
Chen, R., Cai, G., Xu, S., Sun, Q., Luo, J., Wang, Y., Li, M., Lin, H., & Liu, J. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.905035 · Cited by 9 · see citing works
Systems Consolidation, Transformation, and Reorganization
Moscovitch, M., & Gilboa, A. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.43 · Cited by 9 · see citing works
Ranganath, C. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.6 · Cited by 10 · see citing works
Hsieh, C. C., Lo, Y., Li, S., Lin, T., Chang, C., Chen, T., Yang, S., Lee, Y., & Chen, Y. (2020) · Brain Pathology · doi:10.1111/bpa.12870 · Cited by 9 · see citing works
Cremona, S., Zago, L., Mellet, E., Petit, L., Laurent, A., Pepe, A., Tsuchida, A., Beguedou, N., Joliot, M., Tzourio, C., et al. (2021) · Human Brain Mapping · doi:10.1002/hbm.25614 · Cited by 6 · see citing works
Affective Episodic Memory System for Virtual Creatures: The First Step of Emotion‐Oriented Memory
Martin, L., Rosales, J.-H., Jaime, K., & Ramos, F. (2021) · Computational Intelligence and Neuroscience · doi:10.1155/2021/7954140 · Cited by 7 · see citing works
- Authors
- Dimsdale-Zucker, H. R., Ritchey, M., Ekstrom, A. D., Yonelinas, A. P., & Ranganath, C.
- Affiliations
- University of California, Davis (US)
- Boston College (US)
- Corresponding author
- Dimsdale-Zucker, Halle R.
- Venue
- Nature Communications
- Published
- 2018-01-18
- Volume
- 9
- Issue
- 1
- Pages
- 294-294
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC5773497
- OpenAlex
- W2953335281
- Cited by
- 205
- References
- 70
- Citations by year
- 2026: 20 · 2025: 23 · 2024: 34 · 2023: 24 · 2022: 22 · 2021: 27 · 2020: 19 · 2019: 14 · 2018: 21 · 2017: 1
- FWCI
- 12.06
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation (1650042)
- University of California, Davis
- National Institute of Mental Health (K99MH103401, R00MH103401)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
- Keywords
- hippocampal subfields, CA1, CA3, episodic memory, spatial memory, recollection, contextual memory, virtual reality navigation, multivariate pattern analysis, human hippocampus
- MeSH terms
- Brain Mapping, Female, Humans, Magnetic Resonance Imaging, Male, Mental Recall, Space Perception, Young Adult, CA1 Region, Hippocampal, CA3 Region, Hippocampal, 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