Critical role of the hippocampus in memory for sequences of events

Episodic memory, amnesia, and the hippocampal–anterior thalamic axis

Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879

Brain Maps: Structure of the Rat Brain

Swanson, L. W. (1992) · Medical Entomology and Zoology · Cited by 1,878

Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory

Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746

Brain maps: structure of the rat brain

Guillery, R. W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90187-q · Cited by 1,669

Recognition memory: What are the roles of the perirhinal cortex and hippocampus?

Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,624

Episodic-like memory during cache recovery by scrub jays

Clayton, N. S., & Dickinson, A. (1998) · Nature · doi:10.1038/26216 · Cited by 1,464

Computational analysis of the role of the hippocampus in memory

Treves, A., & Rolls, E. T. (1994) · Hippocampus · doi:10.1002/hipo.450040319 · Cited by 1,272

Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus

Mishkin, M. (1978) · Nature · doi:10.1038/273297a0 · Cited by 1,196

Two functional components of the hippocampal memory system

Eichenbaum, H., Otto, T., & Cohen, N. J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035391 · Cited by 1,114

The Hippocampus, Memory, and Place Cells

Eichenbaum, H., Dudchenko, P., Wood, E., Shapiro, M., & Tanila, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)80773-4 · Cited by 1,064

The firing rate of hippocampal CA1 place cells is modulated with a circadian period

Munn, R. G. K., & Bilkey, D. K. (2011) · Hippocampus · doi:10.1002/hipo.20969 · Cited by 28

Is episodic-like memory like episodic memory?

Davies, J. R., & Clayton, N. S. (2024) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2023.0397 · Cited by 27

Human Brain Functional Network Organization Is Disrupted After Whole-Brain Radiation Therapy

Mitchell, T. J., Seitzman, B. A., Ballard, N., Petersen, S. E., Shimony, J. S., & Leuthardt, E. C. (2020) · Brain Connectivity · doi:10.1089/brain.2019.0713 · Cited by 28

Mixing memory and desire: How memory reactivation supports deliberative decision‐making

Wang, S., Feng, S. F., & Bornstein, A. M. (2021) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1581 · Cited by 28

Astrocyte-mediated metaplasticity in the hippocampus: Help or hindrance?

Jones, O. D. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.035 · Cited by 30

Hippocampal contributions to serial‐order memory

Long, N. M., & Kahana, M. J. (2018) · Hippocampus · doi:10.1002/hipo.23025 · Cited by 29

Age-related differences in the topological efficiency of the brain structural connectome in amnestic mild cognitive impairment

Zhao, T., Sheng, C., Bi, Q., Niu, W., Shu, N., & Han, Y. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.08.005 · Cited by 27

In a Temporally Segmented Experience Hippocampal Neurons Represent Temporally Drifting Context But Not Discrete Segments

Bladon, J. H., Sheehan, D. J., Freitas, C. S. D., & Howard, M. W. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1420-18.2019 · Cited by 27

In the temporal organization of episodic memory, the hippocampus supports the experience of elapsed time

Sabariego, M., Tabrizi, N. S., Marshall, G. J., McLagan, A. N., Jawad, S., & Hales, J. B. (2020) · Hippocampus · doi:10.1002/hipo.23261 · Cited by 26

Steroids, Learning and Memory

Dohanich, G. P., Korol, D. L., & Shors, T. J. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00015-2 · Cited by 25

Dissociating the past from the present in the activity of place cells

de Hoz, L., & Wood, E. R. (2006) · Hippocampus · doi:10.1002/hipo.20207 · Cited by 26

Lesions of the dorsal subiculum and the dorsal hippocampus impaired pattern separation in a task using distinct and overlapping visual stimuli

Potvin, O., Doré, F. Y., & Goulet, S. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.10.003 · Cited by 26

Behavioral analysis of olfactory coding and computation in rodents

Mainen, Z. F. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.06.003 · Cited by 29

SAHA improves depressive symptoms, cognitive impairment and oxidative stress: rise of a new antidepressant class

Ershadi, A. S. B., Amini-Khoei, H., Hosseini, M.-J., & Dehpour, A. R. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03263-8 · Cited by 25

Sequential order spatial memory in male rats: Characteristics and impact of medial prefrontal cortex and hippocampus disruption

Lee, S. L. T., Timmerman, B. M., Pflomm, R., Roy, N., Kumar, M., & Markus, E. J. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107739 · Cited by 26

A Situation-Aware Fear Learning (SAFEL) model for robots

Rizzi, C., Johnson, C. G., Fabris, F., & Vargas, P. A. (2016) · Neurocomputing · doi:10.1016/j.neucom.2016.09.035 · Cited by 26

Temporal-Sequential Learning With a Brain-Inspired Spiking Neural Network and Its Application to Musical Memory

Liang, Q. Y., Zeng, Y., & Xu, B. (2020) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2020.00051 · Cited by 27

Microinjection of Reelin into the mPFC prevents MK-801-induced recognition memory impairment in mice

Sawahata, M., Asano, H., Nagai, T., Ito, N., Kohno, T., Nabeshima, T., Hattori, M., & Yamada, K. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105832 · Cited by 24

MRI biomarkers and neuropsychological assessments of hippocampal and parahippocampal regions affected by ALS : A systematic review

Mohammadi, S., Ghaderi, S., & Fatehi, F. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14578 · Cited by 25

Neural modeling of sequential inferences and learning over episodic memory

Subagdja, B., & Tan, A. (2015) · Neurocomputing · doi:10.1016/j.neucom.2015.02.038 · Cited by 26

Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders

Hunsaker, M. R. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.12.001 · Cited by 26

The neural basis of nonvisual object recognition memory in the rat.

Albasser, M. M., Olarte‐Sánchez, C. M., Amin, E., Horne, M. R., Newton, M. J., Warburton, E. C., & Aggleton, J. P. (2012) · Behavioral Neuroscience · doi:10.1037/a0031216 · Cited by 25

Fractionating spatial memory with glutamate receptor subunit-knockout mice

Bannerman, D. M. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371323 · Cited by 25

Heterarchic reinstatement of long-term memory: A concept on hippocampal amnesia in rodent memory research

Lee, J. Q., Zelinski, E. L., McDonald, R. J., & Sutherland, R. J. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.034 · Cited by 26

Forefront Users’ Experience Evaluation by Employing Together Virtual Reality and Electroencephalography: A Case Study on Cognitive Effects of Scents

Mancini, M., Cherubino, P., Cartocci, G., Martinez-Levy, A. C., Borghini, G., Guastamacchia, E., Flumeri, G. D., Rossi, D., Modica, E., Menicocci, S., et al. (2021) · Brain Sciences · doi:10.3390/brainsci11020256 · Cited by 27

Significant life events and the shape of memories to come: A hypothesis

Shors, T. J. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.09.004 · Cited by 25

The frequency of hippocampal theta rhythm is modulated on a circadian period and is entrained by food availability

Munn, R. G. K., Tyree, S. M., McNaughton, N., & Bilkey, D. K. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00061 · Cited by 24

The role of hippocampal theta oscillations in working memory impairment in multiple sclerosis

Costers, L., Schependom, J. V., Laton, J., Baijot, J., Sjøgård, M., Wens, V., Tiège, X. D., Goldman, S., D’haeseleer, M., D'hooghe, M. B., et al. (2020) · Human Brain Mapping · doi:10.1002/hbm.25299 · Cited by 23

Distinct Neural Representations of Content and Ordinal Structure in Auditory Sequence Memory

Fan, Y., Han, Q., Guo, S., & Luo, H. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0320-21.2021 · Cited by 22

Working memory for temporal order is impaired after selective neonatal hippocampal lesions in adult rhesus macaques

Heuer, E., & Bachevalier, J. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.10.043 · Cited by 25

Localization and Intrinsic Function

Rathkopf, C. A. (2013) · Philosophy of Science · doi:10.1086/668878 · Cited by 26

Sex differences in adult cognitive deficits after adolescent nicotine exposure in rats

Pickens, L. R. G., Rowan, J. D., Bevins, R. A., & Fountain, S. B. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2013.05.001 · Cited by 25

Evaluation of Metric, Topological, and Temporal Ordering Memory Tasks after Lateral Fluid Percussion Injury

Gurkoff, G. G., Gahan, J. D., Ghiasvand, R., Hunsaker, M. R., Van, K. C., Feng, J., Shahlaie, K., Berman, R. F., Lyeth, B. G., & Folkerts, M. M. (2012) · Journal of Neurotrauma · doi:10.1089/neu.2012.2463 · Cited by 24

Hippocampal and neocortical interactions during context discrimination: Electrophysiological evidence from the rat

Mizumori, S. J. Y., Smith, D. M., & Puryear, C. B. (2007) · Hippocampus · doi:10.1002/hipo.20317 · Cited by 29

Memory systems

Eichenbaum, H. (2010) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.49 · Cited by 31

Prior sexual experience increases hippocampal cell proliferation and decreases risk assessment behavior in response to acute predator odor stress in the male rat

Spritzer, M. D., Weinberg, A., Viau, V., & Galea, L. A. M. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.01.003 · Cited by 27

Lateral septum modulates cortical state to tune responsivity to threat stimuli

Hashimoto, M., Brito, S. I., Venner, A., Pasqualini, A. L., Yang, T. L., Allen, D. F., Stankowicz, S. J., Fuller, P. M., & Anthony, T. E. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111521 · Cited by 23

Dynamic coding of dorsal hippocampal neurons between tasks that differ in structure and memory demand

Hallock, H. L., & Griffin, A. L. (2012) · Hippocampus · doi:10.1002/hipo.22079 · Cited by 23

Genetic overexpression of glutathione peroxidase-1 attenuates microcystin-leucine-arginine-induced memory impairment in mice

Shin, E., Hwang, Y., Pham, D. T., Lee, J., Lee, Y. J., Pyo, D., Lei, X. G., Jeong, J. H., & Kim, H. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2018.06.006 · Cited by 24

Time, memory, and the legacy of Howard Eichenbaum

Ranganath, C. (2018) · Hippocampus · doi:10.1002/hipo.23007 · Cited by 27

Rodent models of serial reaction time tasks and their implementation in neurobiological research

Schwarting, R. K. W. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.07.004 · Cited by 23

Olfactory Memory

Eichenbaum, H., & Robitsek, R. J. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04012.x · Cited by 24

Electroacupuncture Improves Synaptic Function in SAMP8 Mice Probably via Inhibition of the AMPK/eEF2K/eEF2 Signaling Pathway

Dong, W., Yang, W.-D., Li, F., Guo, W.-Q., Qian, C., Wang, F., Li, C., Lin, L., & Lin, R. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/8260815 · Cited by 24

GluR-A-dependent synaptic plasticity is required for the temporal encoding of nonspatial information.

Reisel, D., Bannerman, D. M., Deacon, R. M. J., Sprengel, R., Seeburg, P. H., & Rawlins, J. N. P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.5.1298 · Cited by 23

Mapping parahippocampal systems for recognition and recency memory in the absence of the rat hippocampus

Kinnavane, L., Amin, E., Horne, M., & Aggleton, J. P. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12740 · Cited by 21

Thinking about order: a review of common processing of magnitude and learned orders in animals

Gazes, R. P., Templer, V. L., & Lazareva, O. F. (2022) · Animal Cognition · doi:10.1007/s10071-022-01713-6 · Cited by 22

Plastic processes in the dentate gyrus: a computational perspective

Derrick, B. E. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63024-6 · Cited by 22

Involvement of nitric oxide in insulin induced memory improvement

Choopani, S., Moosavi, M., & Naghdi, N. (2008) · Peptides · doi:10.1016/j.peptides.2008.01.005 · Cited by 23

Stress induced a shift from dorsal hippocampus to prefrontal cortex dependent memory retrieval: role of regional corticosterone

Dominguez, G., Faucher, P., Henkous, N., Krazem, A., Pierard, C., & Béracochéa, D. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00166 · Cited by 22

On the evolution of the human self: A data-driven review and reconsideration

Skowronski, J. J., & Sedikides, C. (2017) · Self and Identity · doi:10.1080/15298868.2017.1350601 · Cited by 23

Sequential behavior in the rat: A new model using food-reinforced instrumental behavior

Domenger, D., & Schwarting, R. K. W. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.12.002 · Cited by 22

Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans

Marzia De Lucia, E., Constantinescu, I., Virginie Sterpenich, A., Pourtois, G., Seeck, M., & Schwartz, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028630 · Cited by 22

Cognitive ‘Omics’: Pattern-Based Validation of Potential Drug Targets

Gyertyán, I. (2016) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2016.10.010 · Cited by 20

Noncommutative Biology: Sequential Regulation of Complex Networks

Letsou, W., & Cai, L. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005089 · Cited by 21

Dissociation of item and source memory in rhesus monkeys

Basile, B. M., & Hampton, R. R. (2017) · Cognition · doi:10.1016/j.cognition.2017.06.009 · Cited by 20

Early transcriptome changes in response to chemical long-term potentiation induced via activation of synaptic NMDA receptors in mouse hippocampal neurons

Bliim, N., Leshchyns'ka, I., Keable, R., Chen, B. J., Curry-Hyde, A., Gray, L., Sytnyk, V., & Janitz, M. (2019) · Genomics · doi:10.1016/j.ygeno.2018.11.019 · Cited by 17

A role for GABA in the modulation of striatal and hippocampal systems under stress

Dolfen, N., Veldman, M. P., Gann, M. A., von Leupoldt, A., Puts, N. A. J., Edden, R. A. E., Mikkelsen, M. E., Swinnen, S. P., Schwabe, L., Albouy, G., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02535-x · Cited by 20

The CAN‐In network: A biologically inspired model for self‐sustained theta oscillations and memory maintenance in the hippocampus

Giovannini, F., Knauer, B., Yoshida, M., & Buhry, L. (2017) · Hippocampus · doi:10.1002/hipo.22704 · Cited by 23

Goal‐directed interaction of stimulus and task demand in the parahippocampal region

Lee, S., Jin, S., Park, S., Park, E., Lee, C., Lee, H., Lim, H., Yoo, S., Ahn, J. R., Shin, J., et al. (2021) · Hippocampus · doi:10.1002/hipo.23295 · Cited by 21

Role of inhibitory autophosphorylation of calcium/calmodulin-dependent kinase II (αCAMKII) in persistent (>24h) hippocampal LTP and in LTD facilitated by novel object-place learning and recognition in mice

Goh, J. J., & Manahan‐Vaughan, D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.01.022 · Cited by 20

Mnemonic contributions of hippocampal place cells

Mizumori, S. J. Y., Smith, D. M., & Puryear, C. B. (2007) · Elsevier eBooks · doi:10.1016/b978-012372540-0/50006-6 · Cited by 22

Memory for sequences of events impaired in typical agingPreprint

Allen, T. A., Morris, A. M., Stark, S. M., Fortin, N. J., & Stark, C. E. L. (2015) · Learning & Memory · doi:10.1101/lm.036301.114 · Cited by 21

Hippocampal-entorhinal cognitive maps and cortical motor system represent action plans and their outcomes

Barnaveli, I., Viganò, S., Reznik, D., Haggard, P., & Doeller, C. F. (2025) · Nature Communications · doi:10.1038/s41467-025-59153-y · Cited by 22

Locus coeruleus activation “resets” hippocampal event representations and separates adjacent memories

Clewett, D., Huang, R., & Davachi, L. (2025) · Neuron · doi:10.1016/j.neuron.2025.05.013 · Cited by 30

Megamap: flexible representation of a large space embedded with nonspatial information by a hippocampal attractor network

Hedrick, K. R., & Zhang, K. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00856.2015 · Cited by 19

Scopolamine Impairs Spatial Information Recorded With “Miniscope” Calcium Imaging in Hippocampal Place Cells

Sun, D., Unnithan, R. R., & French, C. R. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.640350 · Cited by 22

Nonspatial sequence coding varies along the CA1 transverse axis

Ng, C.-W., Elias, G. A., Asem, J. S. A., Allen, T. A., & Fortin, N. J. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.10.015 · Cited by 19

Virtual Reality Visualization Model (VRVM) of the Tricarboxylic Acid (TCA) Cycle of Carbohydrate Metabolism for Medical Biochemistry Education

Kim, S. H., Heo, R., Chung, Y., ‍Kim, J. M., Kwon, M. P., Seo, S., Park, G. H., & Kim, M.-K. (2019) · Journal of Science Education and Technology · doi:10.1007/s10956-019-09790-y · Cited by 22

Contrasting networks for recognition memory and recency memory revealed by immediate-early gene imaging in the rat

Olarte-Sánchez, C. M., Kinnavane, L., Amin, E., & Aggleton, J. P. (2014) · Behavioral Neuroscience · doi:10.1037/a0037055 · Cited by 18

Developing an animal model of human amnesia: The role of the hippocampus

Kesner, R. P., & Goodrich‐Hunsaker, N. J. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.10.027 · Cited by 18

Different patterns of age-related central olfactory decline in men and women as quantified by olfactory fMRI

Martinez, B., Karunanayaka, P., Wang, J., Tobia, M. J., Vasavada, M. M., Eslinger, P. J., & Yang, Q. X. (2017) · Oncotarget · doi:10.18632/oncotarget.16977 · Cited by 17

Sequential inference as a mode of cognition and its correlates in fronto-parietal and hippocampal brain regions

FitzGerald, T. H. B., Hämmerer, D., Friston, K. J., Li, S., & Dolan, R. J. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005418 · Cited by 20

Hippocampal contributions to memory for time: evidence from neuropsychological studies

Palombo, D. J., & Verfaellie, M. H. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.07.015 · Cited by 18

Environmental Enrichment Expedites Acquisition and Improves Flexibility on a Temporal Sequencing Task in Mice

Rountree-Harrison, D., Burton, T. J., Leamey, C. A., & Sawatari, A. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00051 · Cited by 19

Hippocampal state transitions at the boundaries between trial epochs

Bulkin, D. A., Sinclair, D. G., Law, L. M., & Smith, D. M. (2019) · Hippocampus · doi:10.1002/hipo.23180 · Cited by 19

Longitudinal Development of Memory for Temporal Order in Early to Middle Childhood

Canada, K. L., Pathman, T., & Riggins, T. (2020) · The Journal of Genetic Psychology · doi:10.1080/00221325.2020.1741504 · Cited by 18

A preclinical cognitive test battery to parallel the National Institute of Health Toolbox in humans: bridging the translational gap

Snigdha, S., Milgram, N. W., Willis, S. L., Albert, M. S., Weıntraub, S., Fortin, N. J., & Cotman, C. W. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.01.018 · Cited by 21

Memory asymmetry of forward and backward associations in recognition tasks.

Yang, J., Zhao, P., Zhu, Z., Mecklinger, A., Fang, Z., & Li, H. (2012) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/a0028875 · Cited by 18

The hippocampus, medial prefrontal cortex, and selective memory retrieval: Evidence from a rodent model of the retrieval‐induced forgetting effect

Wu, J. Q., Peters, G. J., Rittner, P., Cleland, T. A., & Smith, D. M. (2014) · Hippocampus · doi:10.1002/hipo.22291 · Cited by 18

Eye Movements Provide an Index of Veridical Memory for Temporal Order

Pathman, T., & Ghetti, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125648 · Cited by 18

Effects of rat medial prefrontal cortex lesions on olfactory serial reversal and delayed alternation tasks

Kinoshita, S., Yokoyama, C., Masaki, D., Yamashita, T., Tsuchida, H., Nakatomi, Y., & Fukui, K. (2007) · Neuroscience Research · doi:10.1016/j.neures.2007.10.012 · Cited by 19

Conditional Motor Learning in the Nonspatial Domain: Effects of Errorless Learning and the Contribution of the Fornix to One-Trial Learning.

Brasted, P. J., Bussey, T. J., Murray, E. A., & Wise, S. P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.3.662 · Cited by 18

Fornix Transection Impairs Learning of Randomly Changing Object Discriminations

Wilson, C. R. E., Charles, D. P., Buckley, M. J., & Gaffan, D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3536-07.2007 · Cited by 19

The effects of aging on memory for sequentially presented objects in rats.

Hauser, E., Tolentino, J. C., Pirogovsky, E., Weston, E., & Gilbert, P. E. (2009) · Behavioral Neuroscience · doi:10.1037/a0017681 · Cited by 17

Representations of stimulus features in the ventral hippocampus

Biane, J. S., Ladow, M. A., Fan, A., Choi, H. S., Zhou, L. Z., Hassan, S., Apodaca-Montano, D. L., Kwon, A. O., Bratsch-Prince, J. X., & Kheirbek, M. A. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.007 · Cited by 19

Functional Interactions of Prefrontal Cortex and the Hippocampus in Learning and Memory

Shapiro, M. L., Riceberg, J. S., Seip-Cammack, K., & Guise, K. G. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_19 · Cited by 19

Lesions in the anterior thalamic nuclei of rats do not disrupt acquisition of stimulus sequence learning

Aggleton, J. P., Amin, E., Jenkins, T. A., Pearce, J. M., & Ward-Robinson, J. (2010) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470218.2010.495407 · Cited by 17

Theta and gamma hippocampal–neocortical oscillations during the episodic-like memory test: Impairment in epileptogenic rats

Malkov, A., Shevkova, L., Latyshkova, A., & Kitchigina, V. F. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114110 · Cited by 18

The Human Medial Temporal Lobe Is Necessary for Remembering Durations within a Sequence of Events but Not Durations of Individual Events

Palombo, D. J., Reid, A. G., Thavabalasingam, S., Hunsberger, R., Lee, A. C. H., & Verfaellie, M. H. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01489 · Cited by 17

Distortion of time interval reproduction in an epileptic patient with a focal lesion in the right anterior insular/inferior frontal cortices

Monfort, V., Pfeuty, M., Klein, M., Collé, S., Brissart, H., Jonas, J., & Maillard, L. G. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.09.004 · Cited by 17

Time and treason to the trisynaptic teachings: Theoretical comment on Kesner et al. (2005).

Manns, J. R., & Eichenbaum, H. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.1140 · Cited by 17

Topological Schemas of Memory Spaces

Babichev, A., & Dabaghian, Y. A. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00027 · Cited by 15

Region-specific metabolic characterization of the type 1 diabetic brain in mice with and without cognitive impairment

Xu, P., Ning, J., Jiang, Q., Li, C., Yan, J., Zhao, L., Gao, H., & Zheng, H. X. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104941 · Cited by 16

Transgenerational effects of adolescent nicotine exposure in rats: Evidence for cognitive deficits in adult female offspring

Renaud, S. M., & Fountain, S. B. (2016) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2016.06.002 · Cited by 16

The serotonin system in the hippocampus CA3 involves in effects of CSDS on social recognition in adult female mandarin voles (Microtus mandarinus)

Wang, L., He, Z., Zhu, Z., Yuan, W., Cai, W., Li, L., Zhang, J., Hou, W., Yang, Y., Zhang, X., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109704 · Cited by 16

Cue-triggered activity replay in human early visual cortex

Lu, J., Luo, L., Wang, Q., Fang, F., & Chen, N. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1726-5 · Cited by 17

The Influence of Markov Decision Process Structure on the Possible Strategic Use of Working Memory and Episodic Memory

Zilli, E. A., & Hasselmo, M. E. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002756 · Cited by 16

Improvement of Learning and Memory in Senescence-Accelerated Mice by S-Allylcysteine in Mature Garlic Extract

Hashimoto, M., Nakai, T., Masutani, T., Unno, K., & Akao, Y. (2020) · Nutrients · doi:10.3390/nu12061834 · Cited by 15

Cell-Type-Specific Optogenetic Techniques Reveal Neural Circuits Crucial for Episodic Memories

Yamamoto, N., Marks, W. D., & 北村, 貴. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-8763-4_28 · Cited by 14

Contextual prediction errors reorganize naturalistic episodic memories in time

Yazin, F., Das, M., Banerjee, A., & Roy, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-90990-1 · Cited by 19

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

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

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

Hippocampal ensembles represent sequential relationships among discrete nonspatial eventsPreprint

Shahbaba, B., Li, L., Agostinelli, F., Saraf, M., Elias, G. A., Baldi, P., & Fortin, N. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/840199 · Cited by 5

Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events

Shahbaba, B., Li, L., Agostinelli, F., Saraf, M., Cooper, K. W., Haghverdian, D., Elias, G. A., Baldi, P., & Fortin, N. J. (2022) · Nature Communications · doi:10.1038/s41467-022-28057-6 · Cited by 53