Memory engrams: Recalling the past and imagining the future

The Organization of Behavior

Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825

The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat

O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151

Millisecond-timescale, genetically targeted optical control of neural activity

Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015

The memory function of sleep

Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760

Reactivation of hippocampal ensemble memories during sleep

Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118

Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogene

Greenberg, M. E., & Ziff, E. B. (1984) · Nature · doi:10.1038/311433a0 · Cited by 2,992

Synaptic Plasticity and Memory: An Evaluation of the Hypothesis

Martin, S. J., Grimwood, P. D., & Morris, R. G. M. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.649 · Cited by 2,794

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

Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval

Nader, K., Schafe, G. E., & Le Doux, J. E. (2000) · Nature · doi:10.1038/35021052 · Cited by 2,706

Modality-Specific Retrograde Amnesia of Fear

Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483

Evolutionary learning in neural networks by heterosynaptic plasticity

Bi, Z., Fu, R., Chen, G., Yang, D., Zhou, Y., & Tian, L. (2025) · iScience · doi:10.1016/j.isci.2025.112340 · Cited by 2

Advancements in autism spectrum disorder research --from mechanisms to interventions

Qiu, Z. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103048 · Cited by 2

Do Adult Frogs Remember Their Lives as Tadpoles and Behave Accordingly? A Consideration of Memory and Personality in Anuran Amphibians

Lannoo, M. J., & Stiles, R. M. (2025) · Diversity · doi:10.3390/d17080506 · Cited by 2

Distributed and gradual microstructure changes are associated with the emergence of behavioural benefit from memory reactivation

Rakowska, M., Lazari, A., Cercignani, M., Bagrowska, P., Johansen‐Berg, H., & Lewis, P. A. (2025) · Imaging Neuroscience · doi:10.1162/imag.a.104 · Cited by 2

Forelimb Motor Learning and Memory Consolidation Drives Distinct Oligodendrocyte Plasticity to Regulate Task‐related Neuronal Activity

Wang, S., Xu, N., Wang, W., He, Y., Yang, Y., Zhang, L., Zou, Y., He, Y., Li, H., Gao, L., et al. (2025) · Advanced Science · doi:10.1002/advs.202505367 · Cited by 7

An Accidental Journey Into the Black Hole of the Hippocampus and How We Learned About What Makes a Context a Context

Fanselow, M. S. (2025) · Hippocampus · doi:10.1002/hipo.70042 · Cited by 2

Memory engram synapse 3D macromolecular architecture visualized by cryoCLEM-guided cryoET

Lovatt, C., O’Sullivan, T., Luis, C. O. S., Ryan, T. J., & Frank, R. A. W. (2025) · Structure · doi:10.1016/j.str.2025.10.014 · Cited by 3

Neuronal allocation and sparse coding of episodic memories in the human hippocampus

Tallman, C. W., Steinmetz, P. N., & Wixted, J. T. (2025) · Scientific Reports · doi:10.1038/s41598-025-21967-7 · Cited by 2

Polarized ATP synthase in synaptic mitochondria induced by learning and plasticity signals

Hu, Y., Wang, X., Liu, K., Xiong, S., Cai, B., Guan, J., Gu, M., & Xie, H. B. (2025) · Communications Biology · doi:10.1038/s42003-025-08963-3 · Cited by 4

Aversion Encoding and Behavioral State Modulation of Physiologically Defined Cell Types in the Lateral Habenula

Zouridis, I. S., Schmors, L., Lecca, S., Congiu, M., Mameli, M., Berens, P., Monteiro, F., Preston‐Ferrer, P., & Burgalossi, A. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70302 · Cited by 2

Distinct spatial distribution of potentiated dendritic spines in encoding- and recall-activated hippocampal neurons

Gobbo, F., Jacob, A., Pinto, B., Mainardi, M., Cancedda, L., & Cattaneo, A. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1751677 · Cited by 2

A Bionic Memory Replay Model Based on Hippocampal-Prefrontal Collaboration: Design, Mechanism, and Robot Navigation Verification

Lv, X., & Wang, D. (2026) · IEEE Transactions on Automation Science and Engineering · doi:10.1109/tase.2026.3657422 · Cited by 2

Persistently Increased Expression of PKMzeta and Unbiased Gene Expression Profiles Identify Hippocampal Molecular Traces of a Long‐Term Active Place Avoidance Memory and “Shadow” Proteins

Han, J., Grau-Perales, A. B., Harris, R. M., Lesburguères, E., Kao, H., Pal, A., Alarcón, J. M., Sacktor, T. C., Martiniani, S., Hofmann, H. A., et al. (2026) · Advanced Science · doi:10.1002/advs.202521254 · Cited by 4

Towards Circuit Mechanisms of the Creative Process

Seiler, J. P.-H., Eppler, J.-B., Dan, O., Elpelt, J., Kaschube, M., & Rumpel, S. (2026) · Creativity Research Journal · doi:10.1080/10400419.2026.2646676 · Cited by 5

Possessions and the extended and incorporated self

Lima, V., & Belk, R. W. (2026) · Journal of the Academy of Marketing Science · doi:10.1007/s11747-026-01142-8 · Cited by 4

Dynamic compression of whole-brain neural trajectories during human motor learning

Mohseni, H., Rezaei, A., Esfeh, M. A., Areshenkoff, C. N., Gale, D. J., Nashed, J. Y., Oby, E. R., Chen, J., Wammes, J. D., Cook, D. J., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2601546123 · Cited by 2

A new paradigm for investigating temporal order memory shows higher order associations are present in recent but not in remote retrieval

Shridhar, S., Singh, V., Bhatt, R., Kundu, S., & Balaji, J. (2022) · Experimental Brain Research · doi:10.1007/s00221-021-06282-7 · Cited by 1

Hippocampal cellular functional organization for fear memory: Effects of sleep

Cho, J., & Pavlides, C. (2022) · Hippocampus · doi:10.1002/hipo.23477 · Cited by 2

ARC/Arg3.1 expression in the lateral geniculate body of monocular form deprivation amblyopic kittens

Fan, H., Wang, Y., Zou, Y., Song, W., Xie, J., Tang, X., & Chen, S. (2023) · BMC Ophthalmology · doi:10.1186/s12886-022-02757-5 · Cited by 2

α7 nicotinic acetylcholine receptors in the medial prefrontal cortex control rewarding but not aversive memory expression in a dopamine-sensitive manner

Pastor, V. E., Dalto, J. F., & Medina, J. H. (2023) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2023.173594 · Cited by 2

$C^{2}N^{2}$: Complex-Valued Contourlet Neural Network

Liu, M., Jiao, L., Liu, X., Li, L., Liu, F., Yang, S., Guo, Y., & Chen, P. (2024) · IEEE Journal of Selected Topics in Applied Earth Observations and Remote Sensing · doi:10.1109/jstars.2024.3358846 · Cited by 2

The effects of the detection stimulus duration on the persistence of the attentional boost effect

Meng, Y., Huang, F., Lin, H., Zheng, S., & Xin, Z. (2024) · Current Psychology · doi:10.1007/s12144-024-06100-7 · Cited by 2

Memory Storage in Distributed Engram Cell Ensembles

Zhang, Y., & Roy, D. S. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-62983-9_3 · Cited by 1

Neural waves and computation in a neural net model II: Data-like structures and the dynamics of episodic memory

Selesnick, S. A. (2024) · Journal of Computational Neuroscience · doi:10.1007/s10827-024-00876-0 · Cited by 2

Comparative analysis of the excitatory and inhibitory hippocampal neurons activity during associative context memory retrieval

Toropova, K. A., Ivashkina, O. I., Vorobyeva, N. S., & Anokhin, K. V. (2024) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467724020034 · Cited by 2

STDP-based Associative Memory Model on Spiking Neural Networks

Jiang, W., Wang, L., Qin, L., & Yan, R. (2024) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn60899.2024.10650836 · Cited by 2

Temporal asymmetries in inferring unobserved past and future events

Xu, X., Zhu, Z., Zheng, X., & Manning, J. R. (2024) · Nature Communications · doi:10.1038/s41467-024-52627-5 · Cited by 2

AUTS2 expression within mammalian lineage: A predictor of neural networks involved in autism spectrum disorders

Lepagnol-Bestel, A.-M., Loe-Mie, Y., Bensaid, M., & Simonneau, M. (2024) · Genes & Diseases · doi:10.1016/j.gendis.2024.101440 · Cited by 2

Role of the Thalamic Reticular Nucleus in Social Memory

Liu, X., Zhu, J., Zheng, J., & Xu, H. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01331-x · Cited by 2

Adaptive Memory-Augmented Unfolding Network for Compressed Sensing

Feng, M., Ning, D., & Yang, S. (2024) · Sensors · doi:10.3390/s24248085 · Cited by 2

Evolution of diverse (and advanced) cognitive abilities through adaptive fine-tuning of learning and chunking mechanisms

Lotem, A., & Halpern, J. Y. (2025) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2024.0117 · Cited by 3

DNA Methylation in Long-Term Memory

Chen, X., Peng, Y., & Liu, X. S. (2025) · Physiology · doi:10.1152/physiol.00032.2024 · Cited by 2

Striatal arbitration between choice strategies guides few-shot adaptation

Yang, M. A., Jung, M. W., & Lee, S. W. (2025) · Nature Communications · doi:10.1038/s41467-025-57049-5 · Cited by 2

MicroRNAs modulate CaMKIIα/SIRT1 signaling pathway as a biomarker of cognitive ability in adolescents

Lee, L., Su, M., Bao, L., Lee, P., Tutwiler, M. S., Yeh, T., & Chang, C. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.100970 · Cited by 2

Non-synaptic plasticity enables memory-dependent local learning

Romain, F., Baronig, M., Unger, F., & Legenstein, R. A. (2025) · PLoS ONE · doi:10.1371/journal.pone.0313331 · Cited by 3

Evidence for indirect strengthening through reactivation of contextually bound memories

Berón, J. C., Bavassi, L., Pedreira, M. E., & Fernández, R. S. (2025) · Communications Psychology · doi:10.1038/s44271-025-00250-5 · Cited by 3

Burst firing represents learned composite stimuli in primary sensory cortices

Jia, H., Wang, M., Pakan, J. M. P., Li, S. C., & Chen, X. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103039 · Cited by 3

Awake reactivation of cortical memory traces predicts subsequent memory retrieval

Duan, W., Lu, P., Xu, Z., Wang, J., Lu, Y., Wang, M., Paller, K. A., Axmacher, N., & Wang, L. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102778 · Cited by 2

Reorganization of Social Representations in the Insular Cortex During Conspecific Familiarization and Discrimination

Sato, M., Overton, E. T. N., Fujima, S., & Takumi, T. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70190 · Cited by 3

Dynamic mapping of network-level LTP in the hippocampus via high-resolution bioelectrical sensing

Khanzada, S., Hu, X., Emery, B. A., Średniawa, W., Wojcik, D. K., Kempermann, G., & Amin, H. (2025) · APL Bioengineering · doi:10.1063/5.0258985 · Cited by 3

Manipulating Engram Histone Acetylation Alters Memory Consolidation

Watt, L., Glauser, L., Coda, D. M., & Gräff, J. (2025) · Hippocampus · doi:10.1002/hipo.70041 · Cited by 2

Conditions for replay of neuronal assemblies

Cano, G., & Kempter, R. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013844 · Cited by 2

Psychiatric View of Generalization and Nonspecific Memory After Traumatic Stress

Lin, C.-C., & Liu, Y. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.07.022 · Cited by 2

Learning and memory: Scaling new areas

Radulescu, C. I., & Barnes, S. J. (2021) · Current Biology · doi:10.1016/j.cub.2021.04.023 · Cited by 2

The universal brain code a genetic mechanism for memory

Rosenberg, R. N. (2021) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2021.118073 · Cited by 2

Fear memory modulation by incentive down and up-shifts

Mugnaini, M., Alfei, J. M., Bueno, A. M., Monti, R. I. F., & Urcelay, G. P. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113766 · Cited by 2

Modeling Unsupervised Empirical Adaptation by DPGMM and DPGMM-RNN Hybrid Model to Extract Perceptual Features for Low-Resource ASR

Wu, B., Sakti, S., Zhang, J., & Nakamura, S. (2022) · IEEE/ACM Transactions on Audio Speech and Language Processing · doi:10.1109/taslp.2022.3150220 · Cited by 2

Can Forgetting Be Due to Changes in Engram Cell Plasticity?

Gisquet-Verrier, P. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.945985 · Cited by 2

Organ Systems

Smith, F. (2022) · Springer eBooks · doi:10.1007/978-3-031-13388-6_8 · Cited by 2

3′UTR of mRNA Encoding CPEB Protein Orb2 Plays an Essential Role in Intracellular Transport in Neurons

Kozlov, E., Deev, R. V., Tokmacheva, E. V., Tvorogova, A. V., Kachaev, Z. M., Gilmutdinov, R. A., Zhukova, M. V., Savvateeva-Popova, E. V., Schedl, P. D., & Shidlovskii, Y. V. (2023) · Cells · doi:10.3390/cells12131717 · Cited by 2

Human-like general language processingPreprint

Feng, Q., & Jiang, G. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2005.09175 · Cited by 2

Social Reactivation of Fear Engrams Enhances Memory RecallPreprint

Finkelstein, A. B., Leblanc, H., Cole, R. H., Gallerani, T., Vieira, A., Zaki, Y., & Ramirez, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.07.425728 · Cited by 2

Autophagy in DG engrams mediates Rac1-dependent forgetting via TLR2/4 signals in microgliaPreprint

Wang, Z., Chen, R., Lin, Q., Jiang, Y., Le, Q., Liu, X., Ma, L., & Wang, F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.26.457763 · Cited by 2

Evolutionary learning in the brain by heterosynaptic plasticityPreprint

Bi, Z., Chen, G., Yang, D., Zhou, Y., & Tian, L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.14.472260 · Cited by 3

Editorial: From Whole-Cell to Single Synapse Engrams - Breaking the Code for Memory Formation, Storage and Recall

Cattaneo, A., & Mainardi, M. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.845516 · Cited by 2

Control of contextual memory through interneuronal α5-GABA A receptorsPreprint

Zhu, M., Abdulzahir, A., Perkins, M. G., Chu, C. C., Krause, B. M., Casey, C., Lennertz, R. C., Ruhl, D. A., Hentschke, H., Nagarajan, R., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.03.482912 · Cited by 2

Grand Unified Theory of Mind and Brain - Part II: Neural Holographic Tomography (NHT) and Holographic Ring Attractor Lattice (HAL)Preprint

Arisaka, K. (2022) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/vu2kz · Cited by 2

A prefrontal to lateral entorhinal pathway disrupts memoryPreprint

Hisey, E. E., & Soderling, S. H. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.21.480888 · Cited by 1

Drift of neural ensembles driven by slow fluctuations of intrinsic excitabilityPreprint

Delamare, G., Zaki, Y., Cai, D. J., & Claudia Clopath, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.16.532958 · Cited by 2

Spatial and single-cell transcriptomics reveal neuron-astrocyte interplay in long-term memoryPreprint

Sun, W., Liu, Z., Jiang, X., Chen, M. B., Dong, H., Liu, J. Z., Südhof, T. C., & Quake, S. R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.20.533566 · Cited by 2

Patterns of host plant use do not explain mushroom body expansion in Heliconiini butterfliesPreprint

Young, F. J., Monllor, M., McMillan, W. O., & Montgomery, S. H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.06.535866 · Cited by 2

Emerging many-to-one weighted mapping in hippocampus-amygdala network underlies memory formationPreprint

Liu, J., Hall, A. F., & Wang, D. V. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.06.556568 · Cited by 2

Neuromorphic Computing Applications in Robotics

Zins, N. (2023) · Digital Commons - Michigan Tech (Michigan Technological University) · doi:10.37099/mtu.dc.etdr/1608 · Cited by 2

Presence of a remote fear memory engram in the central amygdala.Preprint

Hammack, R. J., Fischer, V. E., Andrade, M. A., & Toney, G. M. (2023) · PubMed Central · doi:10.1101/lm.053833.123 · Cited by 2

Ventral hippocampus neurons encode meal-related memoryPreprint

Décarie-Spain, L., Gu, C., Lauer, L. T., Subramanian, K. S., Chehimi, S. N., Kao, A. E., Deng, I., Bashaw, A. G., Klug, M. E., Galbokke, A. H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.10.561731 · Cited by 2

Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutonsPreprint

Kim, O., Okamoto, Y., Brose, N., Shigemoto, R., & Jónás, P. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.04.569907 · Cited by 2

2P-NucTag: on-demand phototagging for molecular analysis of functionally identified cortical neuronsPreprint

Shi, J., Nutkovich, B., Kushinsky, D., Rao, B. Y., Herrlinger, S. A., Tsivourakis, E., Mihaila, T. S., Paredes, M. E. C., Malina, K. C.-K., O’Toole, C. K., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.21.586118 · Cited by 2

An orbitocortical-thalamic circuit suppresses binge alcohol-drinkingPreprint

Giménez‐Gómez, P., Le, T., Zinter, M., M'angale, P. G., Durán‐Laforet, V., Freels, T. G., Pavchinskiy, R. G., Molas, S., Schafer, D. P., Tapper, A. R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.03.601895 · Cited by 2

Dynamic gamma modulation of hippocampal place cells predominates development of theta sequencesPreprint

Wang, N., Wang, Y., Guo, M., Wang, L., Wang, X., Zhu, N., Yang, J., Wang, L., Zheng, C., & Ming, D. (2024) · eLife · doi:10.7554/elife.97334 · Cited by 2

The human hippocampus is involved in implicit motor learningPreprint

Griffa, G., Deleglise, Á., Solano, A., Jacobacci, F., Pino, G. D., & Della‐Maggiore, V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.30.610548 · Cited by 2

Cellular and circuit features distinguish dentate gyrus semilunar granule cells and granule cells activated during contextual memory formationPreprint

Dovek, L., Marrero, K., Zagha, E., & Santhakumar, V. (2024) · eLife · doi:10.7554/elife.101428.1 · Cited by 2

Early changes in the properties of CA3 engram cells explored with a novel viral tool in mice

Cupolillo, D., Grosjean, N., Marneffe, C., Viotti, J., Reynaud, C., Deforges, S., Carta, M., & Mulle, C. (2025) · eLife · doi:10.7554/elife.105452 · Cited by 3

Lysine crotonylation acts as an epigenetic switch for glutamate neurotransmission and spatial memory

Mukherjee, U., Basu, B., Suryavanshi, P. S., Beyer, S. E., Ghodsi, S., Robillard, N., Vanrobaeys, Y. S., Taylor, E. B., Glykys, J., Abel, T. G., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1101/2025.02.19.639114 · Cited by 1

Combinative protein expression of immediate early genes c-Fos, Arc, and Npas4 along aversive- and reward-related neural networksPreprint

Arai, M., Osanai, H., Snell, C. C., 北村, 貴., & Ogawa, S. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.21.649441 · Cited by 2

Understanding the hippocampus as an apex of the cortical hierarchy and self-supervised predictive learning engine

DeKraker, J., Eichert, N., Hong, S.-J., Evans, A. C., & Bernhardt, B. C. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106890 · Cited by 1

Role of the hippocampus in systems consolidation of remote fear memory

Park, H., & Kaang, B.-K. (2026) · Experimental & Molecular Medicine · doi:10.1038/s12276-026-01680-9 · Cited by 1

Decision Support System in a Memristor-Based Mobile CIM Architecture Applied on Big Data Computation and Storage

Li, W., & Deng, Z. (2021) · Scientific Programming · doi:10.1155/2021/9041150 · Cited by 1

COLOR PERCEPTION AND ITS CODING IN SIMIAN NEOCORTEX

Aseyev, N. (2023) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467723010045 · Cited by 1

Introduction to the topical collection ‘locating representations in the brain: interdisciplinary perspectives’

Robins, S., & Brigard, F. D. (2024) · Synthese · doi:10.1007/s11229-024-04565-4 · Cited by 1

Effect of flavonol from chamomile (Matricaria recutita) flavonoids on memory disorders and determination of oxidative stress in Alzheimers rats

Seyed, R. P. (2024) · African Journal of Pharmacy and Pharmacology · doi:10.5897/ajpp2024.5386 · Cited by 1

Plasticity of intrinsic excitability as a mechanism for memory storage

Mozzachiodi, R., & Byrne, J. H. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00041-9 · Cited by 1

Reconstructing Childhood via Reimagined Memories: Life Writing in Children’s Literature

Silva, E.-L. (2024) · Literature · doi:10.3390/literature4040016 · Cited by 1

Autonomous and ubiquitous in-node learning algorithms of active directed graphs and its storage behavior

Wei, H., Li, F., & Miao, W. (2024) · PLOS complex systems. · doi:10.1371/journal.pcsy.0000019 · Cited by 2

Metaplasticity and memory in multilevel recurrent feed-forward networks

Zanardi, G., Bettotti, P., Morand, J., Pavesi, L., & Tubiana, L. (2024) · Physical review. E · doi:10.1103/physreve.110.054304 · Cited by 1

Transcriptional and epigenetic regulation of memory storage

Abel, T. G., Basu, B., & Chatterjee, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00076-6 · Cited by 1

Advances in fear memory erasure and its neural mechanisms

Guo, W., Wang, X., Zhou, Z., Li, Y., Hou, Y., Wang, K., Wei, R., Ma, X., & Zhang, H. (2025) · Frontiers in Neurology · doi:10.3389/fneur.2024.1481450 · Cited by 1

GluA1-containing AMPA receptors are necessary for sparse memory engram formation

Willems, T. S., Xiong, H., Kessels, H. W. H. G., & Lesuis, S. L. (2025) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2025.108031 · Cited by 2

Memories of a cold place trigger bodily responses to warm up

Toh, P., & Rajbhandari, A. K. (2025) · Nature · doi:10.1038/d41586-025-01132-w · Cited by 1

Dynamic memory enqrams: Unveiling the celular mechanisms of memory encoding, consolidation, generalizaton, and updating in the brain

Teng, S.-W., Chen, X.-L., & Chen, Z.-Y. (2025) · Brain medicine : · doi:10.61373/bm025i.0044 · Cited by 1

The Astrocyte: A New Component of The Engram Regulates Memory Recall

Li, R., Luo, Z., Ding, Z., Deng, X., & Gao, L. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01409-0 · Cited by 1

Second-order threat conditioning in the amygdala-posterior piriform cortex network

Sepahvand, T., Qin, T., Hasan, Z., Power, K. D., Carew, S. J., Nazari, N., Janes, A. M., Salman, A., Xia, Y., Benoukraf, T., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08287-2 · Cited by 1

Neuronal ensembles formed rapidly in the prelimbic cortex mediate initial and maintained cocaine-seeking behavior in male and female rats

Sortman, B. W., Rakela, S., Cerci, B., Paprotna, S., Harrow, J., Hao, S., van den Oever, M. C., & Warren, B. L. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110684 · Cited by 1

Unsilenced inhibitory cortical ensemble gates remote memory retrieval

Wang, S., Sheng, T., Su, F., He, Y., Cao, R., Wang, Q., Fang, W., Zhang, C., & Lu, W. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116360 · Cited by 1

Memory traces and the (anti)causalism debate

Camillo, J. C. (2025) · Philosophical Psychology · doi:10.1080/09515089.2025.2571449 · Cited by 1

Unlocking the epigenetic secrets of memory

Mauger, O., & Binder, E. B. (2025) · Nature Genetics · doi:10.1038/s41588-025-02369-x · Cited by 1

Distinct Patterns of Evoked Firing in Engram and Non‐Engram Neurons in the Dentate Gyrus of Hippocampal Slices

Shu, W., & Jackson, M. B. (2025) · Hippocampus · doi:10.1002/hipo.70049 · Cited by 1

Improvements to dark experience replay and reservoir sampling for better balance between consolidation and plasticity

Kobayashi, T. (2026) · Frontiers in Artificial Intelligence · doi:10.3389/frai.2026.1649239 · Cited by 3

Local Neuronal Ensembles That Coreactivate across Regions during Sleep Are Preferentially Stabilized

Miyawaki, H., & Mizuseki, K. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1125-25.2025 · Cited by 1

Sleep transcends limited knowledge to support logical reward-related decisions in a novel task in male mice

Fayed, M. R., Ghandour, K., Choucry, A., Abdou, K., & Inokuchi, K. (2025) · Molecular Brain · doi:10.1186/s13041-025-01267-x · Cited by 1

Progressive remote memory decline coincides with parvalbumin interneuron hyperexcitability and enhanced inhibition of cortical engram cells in a mouse model of Alzheimer’s disease

van Adrichem, J. J., van der Loo, R. J., Defendi, R. A., Smit, A. B., van den Oever, M. C., & van Kesteren, R. E. (2025) · eLife · doi:10.7554/elife.106866.3 · Cited by 2

Heroes of the Engram

Josselyn, S. A., Köhler, S., & Frankland, P. W. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0056-17.2017 · Cited by 134

What is memory? The present state of the engram

Poo, M.-M., Pignatelli, M., Ryan, T. J., Tonegawa, S., Bonhoeffer, T., Martin, K. C., Rudenko, A., Tsai, L., Tsien, R. W., Fishell, G., et al. (2016) · BMC Biology · doi:10.1186/s12915-016-0261-6 · Cited by 409

Engram cell connectivity: an evolving substrate for information storage

Ryan, T. J., Luis, C. O. S., Pezzoli, M., & Sen, S. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.01.006 · Cited by 41

Engram neurons: Encoding, consolidation, retrieval, and forgetting of memory

Guskjolen, A. J., & Cembrowski, M. S. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02137-5 · Cited by 161

Memory Engram Cells Have Come of Age

Tonegawa, S., Liu, X., Ramirez, S., & Redondo, R. L. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.002 · Cited by 661