Bidirectional prefrontal-hippocampal interactions support context-guided memory

AChE-stained horizontal sections of the rat brain in stereotaxic coordinates

Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501

The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes

Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · cited 1×

CircStat : A MATLAB Toolbox for Circular Statistics

Berens, P. (2009) · Journal of Statistical Software · doi:10.18637/jss.v031.i10 · Cited by 3,099

Mechanisms of Gamma Oscillations

Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796

The functional role of cross-frequency coupling

Canolty, R. T., & Knight, R. T. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.09.001 · Cited by 2,101

The MVGC multivariate Granger causality toolbox: A new approach to Granger-causal inference

Barnett, L., & Seth, A. K. (2013) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2013.10.018 · Cited by 1,038

Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat

Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 1,031

Prefrontal phase locking to hippocampal theta oscillations

Siapas, A. G., Lubenov, E. V., & Wilson, M. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.028 · Cited by 1,014

Theta-gamma coupling increases during the learning of item-context associations

Tort, A. B. L., Komorowski, R. W., Manns, J. R., Kopell, N. J., & Eichenbaum, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911331106 · Cited by 919

Coherent theta oscillations and reorganization of spike timing in the hippocampal- prefrontal network upon learning

Benchenane, K., Peyrache, A., Khamassi, M., Tierney, P. L., Gioanni, Y., Battaglia, F. P., & Wiener, S. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.013 · Cited by 872

The role of aberrant neural oscillations in the hippocampal-medial prefrontal cortex circuit in neurodevelopmental and neurological disorders

Shing, N., Walker, M. C., & Chang, P. (2022) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2022.107683 · Cited by 19

Disrupting the medial prefrontal cortex with designer receptors exclusively activated by designer drug alters hippocampal sharp‐wave ripples and their associated cognitive processes

Schmidt, B., & Redish, A. D. (2021) · Hippocampus · doi:10.1002/hipo.23367 · Cited by 20

Memory reactivation and suppression modulate integration of the semantic features of related memories in hippocampus

Morton, N. W., Zippi, E. L., & Preston, A. R. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad179 · Cited by 20

Probing the nature of episodic memory in rodents

Huston, J. P., & Chao, O. Y.-H. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104930 · Cited by 18

Fish oil omega-3 Fatty Acids Alleviate Postoperative delirium-like Behavior in aged mice by Attenuating Neuroinflammation and Oxidative Stress

Zhu, M., Li, M., Yang, S., Li, J., Gong, C., Yu, Q., Chen, C.-L., Zhang, Y., Lin, J., & Tu, F. (2023) · Neurochemical Research · doi:10.1007/s11064-023-04020-9 · Cited by 16

Do Brain Oscillations Orchestrate Memory?

Luo, W., & Guan, J. (2018) · Brain Science Advances · doi:10.26599/bsa.2018.9050008 · Cited by 22

The ventral hippocampus is required for behavioral flexibility but not for allocentric/egocentric learning

Torres‐Berrío, A., Vargas-López, V., & López-Canul, M. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.12.011 · Cited by 18

Detecting multivariate cross-correlation between brain regions

Rodu, J. S., Klein, N., Brincat, S. L., et al. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00869.2017 · Cited by 15

Polarity-specific high-definition transcranial direct current stimulation of the anterior and posterior default mode network improves remote memory retrieval

Huang, Y., Mohan, A., McLeod, S. L., Luckey, A. M., Hart, J., & Vanneste, S. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.06.007 · Cited by 15

Coordinated activity of a central pathway drives associative opioid analgesic tolerance

Hou, Y., Zou, G., Wang, X., Guo, H., Ma, X., Cheng, X., Xie, Z., Zuo, X., Xia, J., Mao, H., et al. (2023) · Science Advances · doi:10.1126/sciadv.abo5627 · Cited by 19

Effective connectivity during autobiographical memory search

Nawa, N. E., & Ando, H. (2020) · Brain and Behavior · doi:10.1002/brb3.1719 · Cited by 13

The direction and timing of theta and alpha traveling waves modulate human memory processingPreprint

Mohan, U. R., Zhang, H., & Jacobs, J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.07.479466 · Cited by 13

Dynamic prediction of goal location by coordinated representation of prefrontal-hippocampal theta sequences

Wang, Y., Wang, X., Wang, L., Li, Z., Meng, S., Zhu, N., An, X., Wang, L., Yang, J., Zheng, C., et al. (2024) · Current Biology · doi:10.1016/j.cub.2024.03.032 · Cited by 16

Cross state-dependency of learning between tramadol and MK-801 in the mouse dorsal hippocampus: involvement of nitric oxide (NO) signaling pathway

Jafari‐Sabet, M., Amiri, S., & Ataee, R. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4897-5 · Cited by 12

Ventral hippocampal cholecystokinin interneurons gate contextual reward memory

Nguyen, R., Sivakumaran, S., Lambe, E. K., & Kim, J. C. (2024) · iScience · doi:10.1016/j.isci.2024.108824 · Cited by 13

Grid codes underlie multiple cognitive maps in the human brain

Chen, D., Axmacher, N., & Wang, L. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102569 · Cited by 13

Hippocampal output suppresses orbitofrontal cortex schema cell formation

Zong, W., Zhou, J., Gardner, M., Zhang, Z., Costa, K. M., & Schoenbaum, G. M. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01928-z · Cited by 21

The dorsal and ventral hippocampus contribute differentially to spatial working memory and spatial coding in the prefrontal cortex

Babl, S. S., & Sigurdsson, T. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003140 · Cited by 13

The Anterior Prefrontal Cortex and the Hippocampus Are Negatively Correlated during False Memories

Jeye, B. M., Karanian, J. M., & Slotnick, S. D. (2017) · Brain Sciences · doi:10.3390/brainsci7010013 · Cited by 11

Coupled Dynamics of Stimulus-Evoked Gustatory Cortical and Basolateral Amygdalar Activity

Mahmood, A., Steindler, J. R., Germaine, H., Miller, P. C., & Katz, D. B. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1412-22.2022 · Cited by 12

Medial prefrontal cortex compresses concept representations through learning

Mack, M. L., Preston, A. R., & Love, B. C. (2017) · International Workshop on Pattern Recognition in NeuroImaging · doi:10.1109/prni.2017.7981500 · Cited by 10

Thalamic Functional Connectivity during Spatial Long-Term Memory and the Role of Sex

Spets, D. S., & Slotnick, S. D. (2020) · Brain Sciences · doi:10.3390/brainsci10120898 · Cited by 7

Phase-Synchronized Stimulus Presentation Augments Contingency Knowledge and Affective Evaluation in a Fear-Conditioning Task

Plog, E., Antov, M. I., Bierwirth, P., Keil, A., & Stockhorst, U. (2021) · eNeuro · doi:10.1523/eneuro.0538-20.2021 · Cited by 9

Hippocampal‐prefrontal theta phase synchrony in planning of multi‐step actions based on memory retrieval

Ishino, S., TAKAHASHI, S. Y., Ogawa, M., & Sakurai, Y. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13547 · Cited by 10

Dynamic laminar rerouting of inter-areal mnemonic signal by cognitive operations in primate temporal cortex

Takeda, M., Hirabayashi, T., Adachi, Y., & Miyashita, Y. (2018) · Nature Communications · doi:10.1038/s41467-018-07007-1 · Cited by 10

Large-scale coupling of prefrontal activity patterns as a mechanism for cognitive control in health and disease: evidence from rodent models

Negrón-Oyarzo, I., Dib, T., Chacana-Véliz, L., Quilodrán, N. L., & Urrutia-Piñones, J. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1286111 · Cited by 7

Neural computations underlying contextual processing in humans

Zheng, J., Skelin, I., & Lin, J. J. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111395 · Cited by 12

Generalization of cognitive maps across space and time

Sherrill, K. R., Molitor, R. J., Karagoz, A. B., Atyam, M., Mack, M. L., & Preston, A. R. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad092 · Cited by 14

Fine Spike Timing in Hippocampal–Prefrontal Ensembles Predicts Poor Encoding and Underlies Behavioral Performance in Healthy and Malformed Brains

Hernan, A. E., Mahoney, J. M., Curry, W., Mawe, S., & Scott, R. C. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa216 · Cited by 7

A procedure to increase the power of Granger-causal analysis through temporal smoothing

Spencer, E. R., Martinet, L., Eskandar, E. N., Chu, C. J., Kolaczyk, E. D., Cash, S. S., Eden, U. T., & Kramer, M. (2018) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2018.07.010 · Cited by 7

Solved problems and remaining challenges for Granger causality analysis in neuroscience: A response to Stokes and Purdon (2017)Preprint

Barnett, L., Barrett, A. B., & Seth, A. K. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1708.08001 · Cited by 7

Schemas, reinforcement learning, and the medial prefrontal cortexPreprint

Bein, O., & Niv, Y. (2023) · doi:10.31234/osf.io/spxq9 · Cited by 7

Electrophysiological insights into Alzheimer's disease: A review of human and animal studies

Calvin, K., McNeela, A. M., Osse, A. M. L., Bhasin, G., Ridenour, M., Kinney, J. W., & Hyman, J. M. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105987 · Cited by 8

Multiple memory systems for efficient temporal order memory

Jafarpour, A., Lin, J. J., Knight, R. T., & Buffalo, E. A. (2023) · Hippocampus · doi:10.1002/hipo.23550 · Cited by 7

Reply to Stokes and Purdon: A study of problems encountered in Granger causality analysis from a neuroscience perspectivePreprint

Barnett, L., Barrett, A. B., & Seth, A. K. (2017) · arXiv (Cornell University) · Cited by 7

Theta Activity Supports Landmark-Based Correction of Naturalistic Human Path Integration

Naveilhan, C., Zory, R., Gramann, K., & Ramanoël, S. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1005-25.2025 · Cited by 8

Goal Choices Modify Frontotemporal Memory Representations

Srinivasan, A., Riceberg, J. S., Goodman, M. R., Srinivasan, A., Guise, K. G., & Shapiro, M. L. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1939-22.2023 · Cited by 5

Schemas

Preston, A. R., Molitor, R. J., Pudhiyidath, A., & Schlichting, M. L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21074-2 · Cited by 6

Tarooneh extract relieves anxiety-like behaviors and cognitive deficits by inhibiting synaptic loss in the hippocampus and frontal cortex in rats subjected to chronic restraint stress

Hadipour, M., Refahi, S., Jangravi, Z., & Meftahi, G. H. (2023) · 3 Biotech · doi:10.1007/s13205-023-03577-0 · Cited by 5

Schema cell formation in orbitofrontal cortex is suppressed by hippocampal outputPreprint

Zong, W., Zhou, J., Gardner, M., Zhang, Z., Costa, K. M., & Schoenbaum, G. M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.03.539307 · Cited by 5

The role of prefrontal-hippocampal functional connectivity in schizophrenia-related cognitive dysfunction and the thalamic ventral midline involvement: in vivo and silico evidence

Černousova, A., & Patrono, E. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1653828 · Cited by 4

Performance Baseline of Phase Transfer Entropy Methods for Detecting Animal Brain Area Interactions

Zhu, J.-Y., Li, M., Zhang, Z., Liu, G., & Wan, H. (2023) · Entropy · doi:10.3390/e25070994 · Cited by 4

Effects of phase synchronization and frequency specificity in the encoding of conditioned fear–a web-based fear conditioning study

Plog, E., Antov, M. I., Bierwirth, P., & Stockhorst, U. (2023) · PLoS ONE · doi:10.1371/journal.pone.0281644 · Cited by 5

Cross state-dependent memory retrieval between cannabinoid CB1 and serotonergic 5-HT1A receptor agonists in the mouse dorsal hippocampus

Jafari‐Sabet, M., Amiri, S., Aghamiri, H., & Fatahi, N. (2022) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2022.107638 · Cited by 4

Coordinated hippocampal–entorhinal representations support human context-dependent spatial navigation

Lv, P., Chen, D., Zhang, C., Duan, W., Lu, P., Zhang, K., & Wang, L. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003398 · Cited by 5

Enhanced Hippocampus–Nidopallium Caudolaterale Interaction in Visual–Spatial Associative Learning of Pigeons

Zhu, J.-Y., Zhang, Z., Liu, G., & Wan, H. (2024) · Animals · doi:10.3390/ani14030456 · Cited by 3

Hippocampal‐Prelimbic Coupling During Context‐Dependent Extinction Retrieval in Rats

Mourão, F. A. G., Totty, M. S., Tuna, T., & Maren, S. (2025) · Hippocampus · doi:10.1002/hipo.70058 · Cited by 4

The Hippocampal-Cortical Networks Subserving Episodic Memory and Its Component Memory Systems for Object, Place and Temporal Order

Chao, O. Y.-H., Huston, J. P., & Silva, M. A. D. S. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00014-8 · Cited by 4

Memory-Based Prediction Deficits and Dorsolateral Prefrontal Dysfunction in Schizophrenia

Williams, A. B., Liu, X. L., Hsieh, F., Hurtado, M., Lesh, T. A., Niendam, T. A., Carter, C., Ranganath, C., & Ragland, J. D. (2022) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2022.05.006 · Cited by 3

Directionality of Medial Prefrontal Cortex and Hippocampal Interactions Is Task-Dependent

Negoita, S., Boone, C. E., & Anderson, W. S. (2016) · Neurosurgery · doi:10.1227/01.neu.0000508608.92059.64 · Cited by 3

Effects of dorsal hippocampus catecholamine depletion on paired-associates learning and place learning in rats

Roschlau, C., & Hauber, W. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.01.038 · Cited by 4

Simultaneous Reality Filtering and Encoding of Thoughts: The Substrate for Distinguishing between Memories of Real Events and Imaginations?

Thézé, R., Manuel, A. L., Nahum, L., Guggisberg, A. G., & Schnider, A. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00216 · Cited by 3

Piriform cortex provides a dominant gamma LFP oscillation in the anterior limbic systemPreprint

Carmichael, J. E., Yuen, M. M., & van der Meer, M. A. A. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/861021 · Cited by 4

Prefrontal top-down projections control context-dependent strategy selectionPreprint

Gschwend, O., Yang, T., van de Lisdonk, D., Zhang, X., Sharma, R., & Li, B. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.14.472559 · Cited by 2

Semantic Anchors Facilitate Task Encoding in Continual Learning

Habibi, M., Verbeke, P., Senoussi, M., & Braem, S. (2025) · Open Mind · doi:10.1162/opmi.a.28 · Cited by 3

Transcerebral information coordination in directional hippocampus-prefrontal cortex network during working memory based on bimodal neural electrical signals

Zhang, W., Guo, L., & Liu, D. (2022) · Cognitive Neurodynamics · doi:10.1007/s11571-022-09792-4 · Cited by 2

A fuzzy-oscillatory model of medial prefrontal cortex control function in spatial memory retrieval in human navigation function

Moghadam, M., Towhidkhah, F., & Gharibzadeh, S. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.972985 · Cited by 2

Temporal context-guided memory capabilities in rodents

Slater, B., Petkov, C. I., & Easton, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-95410-2 · Cited by 2

The molecular, cellular, and biological perspectives of memory

Mallakin, A. (2020) · Medicine and Clinical Science · doi:10.33425/2690-5191.1023 · Cited by 2

Novel Causal Relations between Neuronal Networks due to Synchronization

Wang, S., Chen, H., & Zhan, Y. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab219 · Cited by 2

A Fast and Efficient Ensemble Transfer Entropy and Applications in Neural Signals

Zhu, J.-Y., Chen, M., Lu, J., Zhao, K., Cui, E., Zhang, Z., & Wan, H. (2022) · Entropy · doi:10.3390/e24081118 · Cited by 3

Distributed dynamic coding for spatial working memory in hippocampal-prefrontal networksPreprint

Hernan, A. E., Mahoney, J. M., Curry, W. T., Mawe, S., & Scott, R. C. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/630673 · Cited by 2

Encoding and retrieval of associative recognition memory engage different sub-networks within a hippocampal-thalamo-cortical memory circuitPreprint

Barker, G., Tran, S., Gilroy, K. E., Bashir, Z. I., & Warburton, E. C. (2021) · Research Square · doi:10.21203/rs.3.rs-889826/v1 · Cited by 2

Retrosplenial cortex enables context-dependent goal-directed sensorimotor transformationPreprint

Bech, P., Dard, R. F., Lebert, J. M., Smith, L., Bisi, A., Renard, A., Crochet, S., & Petersen, C. C. H. (2025) · eLife · doi:10.7554/elife.109717.1 · Cited by 2

Distinct and Convergent Alterations of Entorhinal Cortical Circuits in Two Mouse Models for Alzheimer’s Disease and Related Disorders

Zhong, P., Cao, Q., & Yan, Z. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231413 · Cited by 1

Conflict Dynamics of Post-Retrieval Extinction: A Comparative Analysis of Unconditional and Conditional Reminders Using Skin Conductance Responses and EEG

Pan, D., Hoid, D., Wolf, O. T., Merz, C. J., & Li, X. (2024) · Brain Topography · doi:10.1007/s10548-024-01051-5 · Cited by 1

Theta-paced stimulation of the thalamic nucleus reuniens entrains mPFC-HPC oscillations and facilitates the acquisition of extinction memories

Tuna, T., Mourão, F. A. G., & Maren, S. (2025) · Brain stimulation · doi:10.1016/j.brs.2025.11.011 · Cited by 2

Episodic memory involves transient and sparse connectivity aligned to both internal and external events

Dede, A. J. O., Cross, Z. R., Gray, S. M., Kelly, J. P., Yin, Q., Vahidi, P., Asano, E., Schuele, S., Rosenow, J. M., Wu, J. Y., et al. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003481 · Cited by 3

Traveling-wave transcranial alternating current stimulation (twtACS) causally links neural timing to cognitive function

Lee, S., Park, J., Alekseichuk, I., Berger, T. A., Manea, A. M. G., Tran, H., Salazar, G. D., König, S. D., Herman, A. B., Darrow, D. P., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2527296123 · Cited by 1

Adaptive processing of predictions and prediction errors in hippocampal subregions

Bein, O., & Davachi, L. (2026) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2025.0239 · Cited by 4

Investigating the Roles of Parvalbumin and Cholecystokinin Interneurons of the Ventral Hippocampus and Medial Prefrontal Cortex in Schizophrenia-Related Behaviours

Nguyen, R. (2018) · TSpace (University of Toronto) · Cited by 1

Neural Computations Underpinning Anxiety in Health and Disease

Walters, C. J. (2021) · University of Minnesota Digital Conservancy (University of Minnesota) · Cited by 1

“Prefrontal cortical contributions to working memory loading, maintenance and recall are parsed by hippocampal-prefrontal oscillatory assembly dynamics”Preprint

Domanski, A. P. F., Kucewicz, M. T., Russo, E., Tricklebank, M. D., Robinson, E. S. J., Durstewitz, D., & Jones, M. W. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.20.473436 · Cited by 1

Molecular pathways responsible for NMDA receptor-mediated behavioural plasticity

Islam, R. (2016) · doi:10.26226/morressier.5785edc6d462b80296c9940a · Cited by 1

Ventral hippocampal CCK interneurons gate context-reward memoryPreprint

Nguyen, R., Sivakumaran, S., Lambe, E. K., & Kim, J. C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.27.538595 · Cited by 1

Sequential Development of Task Representation from Hippocampus to Prefrontal Cortex Supports Goal-Directed Spatial NavigationPreprint

Lim, H., Park, S., & Lee, I. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.05.680599 · Cited by 2

Retrosplenial cortex enables context-dependent goal-directed sensorimotor transformationPreprint

Bech, P., Dard, R. F., Lebert, J. M., Smith, L., Bisi, A., Renard, A., Crochet, S., & Petersen, C. C. H. (2025) · eLife · doi:10.7554/elife.109717 · Cited by 1

Molecular pathways responsible for NMDA receptor-mediated behavioural plasticity

Islam, R., Mielnik, C. A., Horsfall, W., Orser, B. A., & Ramsey, A. J. (2016) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(16)31169-5 · Cited by 1

Gamma oscillations during episodic memory processing reveal reversal of information flow between the hippocampus and prefrontal cortexPreprint

Seger, S. E., Rugg, M. D., & Lega, B. C. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/728469

Distinct contributions of the nucleus reuniens, prefrontal cortex, and hippocampus to spatial working memory

Maisson, D. J.-N. (2019) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/0m54-yx79

Harnessing 'time' to enhance memory: using closed-loop technology to facilitate oscillatory synchrony & support cognition

Garcia, A. (2019) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/xh10-qz47

Prefrontal cortical activity predicts the extra-place field spiking of hippocampal place cellsPreprint

Yu, J. Y., & Frank, L. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.23.395012

Neuroprotectin D1 Protects Against Postoperative Delirium-like Behaviors in Aged Mice by Regulating Neuroinflammation Induced by Surgical TraumaPreprint

Zhou, Y., Wang, J., Li, X., Li, K., Chen, L., Zhang, Z., & Peng, M. (2020) · doi:10.21203/rs.3.rs-28936/v1

Hippocampal-Prefrontal cortex network dynamics predict performance during retrieval in a context-guided object memory taskPreprint

Morici, J. F., Weisstaub, N., & Zold, C. L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.28.470274

Multiple memory systems for efficient temporal order memoryPreprint

Jafarpour, A., Lin, J. J., Knight, R. T., & Buffalo, E. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.10.495702

Anatomy of the hippocampus and the declarative memory system

Peng, X., Scaplen, K. M., Agster, K. L., & Burwell, R. D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00008-0

Declarative Memory Through the Lens of Single-Trial Peaks in High-Frequency PowerPreprint

Dede, A. J. O., Cross, Z. R., Gray, S. M., Kelly, J. P., Yin, Q., Vahidi, P., Asano, E., Schuele, S., Rosenow, J. M., Wu, J. Y., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.02.631123

Critical Influence of Prefrontal Cortex-hippocampus Interactions on False Memories

Liu, H. (2025) · Highlights in Science Engineering and Technology · doi:10.54097/peafjq74

Schemas

Preston, A. R., Molitor, R. J., Pudhiyidath, A., & Schlichting, M. L. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00094-8

Retrosplenial cortex enables context-dependent goal-directed sensorimotor transformation

Bech, P., Dard, R. F., Lebert, J. M., Smith, L., Bisi, A., Renard, A., Crochet, S., & Petersen, C. C. H. (2026) · eLife · doi:10.1101/2025.10.31.685738

Selective enhancement of fronto-temporal mechanisms for adaptive memoryPreprint

Slater, B., Griffiths, T. D., Caffaratti, H., Sallet, J., Degenaar, P. A., Kaiser, M., Easton, A., Kikuchi, Y., & Petkov, C. I. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.19.695543

The Hippocampal-Prefrontal-Striatal network during successive learning and set-shifting

Oberto, V. J. (2017) · theses.fr (ABES) · doi:10.70675/d64848adzf26az4072zb8e2z0dc40420582c

Oscillatory dynamics of the hippocampo-cortical dialogue underlying memory formation and consolidation

Abdallah, N. H.-B. (2020) · theses.fr (ABES) · doi:10.70675/f33c8cd2z87e6z4346zbfcez57d516772a52

Excessive inhibition in the medial prefrontal cortex contributes to cognitive susceptibility in aging

Keramidis, I., Desrosiers, P., Verreault, A.-A., Sansonetti, R., Hazrati, R., Godin, A. G., & Koninck, Y. D. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107385

Making Decisions in Context in Post-9/11 Veterans with Comorbid Chronic Blast Mild Traumatic Brain Injury and Posttraumatic Stress Disorder

Newsome, M. R., de Souza, N. L., Avci, G., Zeno, D., Su, M., Helmer, D. A., Podell, K., Durand-Sanchez, A. V., Figner, B., Hollowell, L. L., et al. (2026) · Military Medicine · doi:10.1093/milmed/usag120

Retrosplenial cortex enables context-dependent goal-directed sensorimotor transformationPreprint

Bech, P., Dard, R. F., Lebert, J. M., Smith, L., Bisi, A., Renard, A., Crochet, S., & Petersen, C. C. H. (2026) · eLife · doi:10.7554/elife.109717.2

Hippocampal engrams configure prefrontal context representations to guide flexible decisionsPreprint

Julian, J. B., Kaminsky, J. C., Tank, D. W., & Brody, C. D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.06.732916

Hippocampal–Cortical Circuits and Memory

Liu, C., Harvey, R. E., & Fernández‐Ruiz, A. (2026) · The Neuroscientist · doi:10.1177/10738584261469147

Distinct Working Memory for Near and Far in a T-Maze Delayed Alternation Task: Evidence for Dual-Process Dynamics in Hippocampal-Prefrontal CoordinationPreprint

Takita, M., & Ichitani, Y. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.06.743185

Frequency-Specific Neural Dynamics and Decoding of Hierarchical Auditory Sequences Revealed by Magnetoencephalography

Zhao, X., Yao, Q., & Jiang, Y. (2026) · Neuroscience Bulletin · doi:10.1007/s12264-026-01709-z

Spatial and color working memory in patients with lateral prefrontal cortex lesions

Baldo, J. V., & Shimamura, A. P. (2000) · Psychobiology · doi:10.3758/bf03331975 · Cited by 28

Control of interference during working memory updating.

Szmalec, A., Verbruggen, F., Vandierendonck, A., & Kemps, E. (2011) · Journal of Experimental Psychology: Human Perception and Performance · doi:10.1037/a0020365 · Cited by 133

Balancing Flexibility and Interference in Working Memory

Buschman, T. J. (2021) · Annual Review of Vision Science · doi:10.1146/annurev-vision-100419-104831 · Cited by 51

Allocentric Spatial Memory Performance in a Virtual Reality-Based Task is Conditioned by Visuospatial Working Memory Capacity

Castillo, J., Castro, J. J. F., Baliyan, S., Ortells-Pareja, J. J., Ortells, J. J., & Cimadevilla, J. M. (2020) · Brain Sciences · doi:10.3390/brainsci10080552 · Cited by 24

Visual Working Memory Capacity and Proactive Interference

Hartshorne, J. K. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002716 · Cited by 93