Coherent Theta Oscillations and Reorganization of Spike Timing in the Hippocampal- Prefrontal Network upon Learning

The Organization of Behavior

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

A neural substrate of prediction and reward

Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388

Distributed hierarchical processing in the primate cerebral cortex

Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783

The organization of behavior.

indicated, N. A. (1950) · Journal of Consulting Psychology · doi:10.1037/h0049612 · Cited by 6,984

Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory

McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256

The brainweb: phase synchronization and large-scale integration

Varela, F., Lachaux, J.-P., Rodriguez, E., & Martinerie, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35067550 · Cited by 4,761

Synaptic Modifications in Cultured Hippocampal Neurons: Dependence on Spike Timing, Synaptic Strength, and Postsynaptic Cell Type

Bi, G.-Q., & Poo, M.-M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10464.1998 · Cited by 4,744

A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.

Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284

Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs

Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832

Dynamic predictions: Oscillations and synchrony in top–down processing

Engel, A. K., Fries, P., & Singer, W. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094565 · Cited by 3,454

Separable neural mechanisms support intentional forgetting and thought substitution

Hubbard, R. J., & Sahakyan, L. (2021) · Cortex · doi:10.1016/j.cortex.2021.06.013 · Cited by 11

Scalable and accurate method for neuronal ensemble detection in spiking neural networks

Herzog, R. A., Morales, A., Mora, S., Araya, J., Escobar, M.-J., Palacios, A. G., & Cofré, R. (2021) · PLoS ONE · doi:10.1371/journal.pone.0251647 · Cited by 11

Optogenetic disruption of the prelimbic cortex alters long-term decision strategy but not valuation on a spatial delay discounting task

McLaughlin, A. E., & Redish, A. D. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107734 · Cited by 13

Dynamic Changes in Local Activity and Network Interactions among the Anterior Cingulate, Amygdala, and Cerebellum during Associative Learning

Halverson, H. E., Kim, J., & Freeman, J. H. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0731-23.2023 · Cited by 13

The characterization of hippocampal theta-driving neurons — a time-delayed mutual information approach

Li, S., Xu, J., Chen, G., Lin, L., Zhou, D., & Cai, D. (2017) · Scientific Reports · doi:10.1038/s41598-017-05527-2 · Cited by 13

Muscarinic Regulation of Spike Timing Dependent Synaptic Plasticity in the Hippocampus

Fuenzalida, M., Chiu, C. Q., & Chávez, A. E. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.08.015 · Cited by 11

Translation-Focused Approaches to GPCR Drug Discovery for Cognitive Impairments Associated with Schizophrenia

Hatzipantelis, C. J., Langiu, M., Vandekolk, T. H., Pierce, T. L., Nithianantharajah, J., Stewart, G. D., & Langmead, C. J. (2020) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.0c00117 · Cited by 13

Effect of ZNF804A gene polymorphism (rs1344706) on the plasticity of the functional coupling between the right dorsolateral prefrontal cortex and the contralateral hippocampal formation

Zhao, W., Chen, X., Zhang, Q.-M., Du, B., Deng, X., Ji, F., Xiang, Y., Wang, C., Dong, Q., Chen, C., et al. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102279 · Cited by 11

Flexible communication between cell assemblies and ‘reader’ neuronsPreprint

Pompili, M. N., Todorova, R., Boucly, C. J., Leroux, E. M., Wiener, S. I., & Zugaro, M. B. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.06.506754 · Cited by 11

Review on the role of hippocampus in autism spectrum disorder: recent insights into neuropathology, genetics, and emerging therapeutic strategies

Bhamidimarri, P. M., Alhosani, K., Cai, H., Al-Ali, H., Abukhaled, Y. M., Tawamie, H., Abdelaziz, S., Fawaz, M., Kashir, J., Sajjad, Y., et al. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107227 · Cited by 10

The medial prefrontal cortex during flexible decisions: Evidence for its role in distinct working memory processes

Kidder, K. S., Gillis, R., Miles, J. T., & Mizumori, S. J. Y. (2023) · Hippocampus · doi:10.1002/hipo.23594 · Cited by 13

Understanding the neurobiology of social behavior through exploring brain-wide dynamics of neural activity

Phalip, A., Netser, S., & Wagner, S. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105856 · Cited by 12

Environmental complexity modulates information processing and the balance between decision-making systems

Mugan, U., Hoffman, S. L., & Redish, A. D. (2024) · Neuron · doi:10.1016/j.neuron.2024.10.004 · Cited by 13

Phase-synchronized brain connectivity during emotion regulation: attachment as a moderator

Domic‐Siede, M., Guzmán‐González, M., Ortiz, R., Hernández, S., & Carvallo, C. (2025) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsaf069 · Cited by 11

Using synchronized brain rhythms to bias memory-guided decisions

Stout, J. J., George, A. E., Kim, S., Hallock, H. L., & Griffin, A. L. (2023) · eLife · doi:10.7554/elife.92033 · Cited by 16

A novel versatile hybrid infusion-multielectrode recording (HIME) system for acute drug delivery and multisite acquisition of neuronal activity in freely moving mice

Senkov, O., Mironov, A. A., & Dityatev, A. E. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00425 · Cited by 10

Dopamine Receptors Influence Internally Generated Oscillations during Rule Processing in Primate Prefrontal Cortex

Ott, T., Westendorff, S., & Nieder, A. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01248 · Cited by 10

The maximum points-based supervised learning rule for spiking neural networks

Xie, X., Liu, G., Cai, Q., Qu, H., & Zhang, M. (2018) · Soft Computing · doi:10.1007/s00500-018-3576-0 · Cited by 10

A general spectral decomposition of causal influences applied to integrated information

Cohen, D., Sasai, S., Tsuchiya, N., & Oizumi, M. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108443 · Cited by 12

Alterations of Neuronal Dynamics as a Mechanism for Cognitive Impairment in Epilepsy

Lenck‐Santini, P., & Sakkaki, S. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_193 · Cited by 12

Enhanced synaptic properties of the prefrontal cortex and hippocampus after learning a spatial working memory task in adult male mice

Stavroulaki, V., Ioakeimidis, V., Konstantoudaki, X., & Sidiropoulou, K. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24833 · Cited by 10

The Overnight Retention of Novel Metaphors Associates With Slow Oscillation–Spindle Coupling but Not With Respiratory Phase at Encoding

Halonen, R., Kuula, L., Antila, M., & Pesonen, A. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.712774 · Cited by 14

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

Inferred Model of the Prefrontal Cortex Activity Unveils Cell Assemblies and Memory ReplayPreprint

Tavoni, G., Ferrari, U., Battaglia, F. P., Cocco, S., & Monasson, R. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/028316 · Cited by 10

The generalized spatial representation in the prefrontal cortex is inherited from the hippocampusPreprint

Nardin, M., Kaefer, K., & Csicsvari, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.30.462269 · Cited by 9

Flexible decision-making is related to strategy learning, vicarious trial and error, and medial prefrontal rhythms during spatial set-shiftingPreprint

Miles, J. T., Mullins, G. L., & Mizumori, S. J. Y. (2024) · Learning & Memory · doi:10.1101/lm.053911.123 · Cited by 11

Hippocampal representations of alternative possibilities are flexibly generated to meet cognitive demandsPreprint

Comrie, A. E., Monroe, E. J., Kahn, A. E., Denovellis, E. L., Joshi, A., Guidera, J. A., Krausz, T. A., Berke, J. D., Daw, N. D., & Frank, L. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.23.613567 · Cited by 10

Allergen Induces Depression-like Behavior in Association with Altered Prefrontal-hippocampal Circuit in Male Rats

Dehdar, K., Salimi, M., Tabasi, F., Dehghan, S., Sumiyoshi, A., Garousi, M., Jamaati, H., Javan, M., & Raoufy, M. R. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.05.034 · Cited by 9

Hippocampal-prefrontal high-gamma flow during performance of a spatial working memory

Bai, W., Liu, Y., Liu, A., Xu, X., Zheng, X., Tian, X., & Liu, T. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.110887 · Cited by 9

Ventral Tegmental Area Dopamine Neural Activity Switches Simultaneously with Rule Representations in the Medial Prefrontal Cortex and Hippocampus

Ding, M., Tomsick, P. L., Young, R. A., & Jadhav, S. P. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1670-24.2025 · Cited by 14

Theta and Alpha Oscillatory Activity During Working Memory Maintenance in Long-Term Cannabis Users: The Importance of the Polydrug Use Context

Binkowska, A. A., Jakubowska, N., Krystecka, K., Galant, N., Piotrowska‐Cyplik, A., & Brzezicka, A. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.740277 · Cited by 11

Accounting for multiscale processing in adaptive real-world decision-making via the hippocampus

Mehrotra, D., & Dubé, L. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1200842 · Cited by 9

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

Modafinil augments oscillatory power in middle frequencies during rule selection

Minzenberg, M., Gomes, G. C., Yoon, J. H., Watrous, A. J., Geng, J. J., Firl, A. J., & Carter, C. S. (2014) · Psychophysiology · doi:10.1111/psyp.12201 · Cited by 10

Rapid learning in visual cortical networks

Wang, Y., & Dragoi, V. (2015) · eLife · doi:10.7554/elife.08417 · Cited by 8

Phase offset between slow oscillatory cortical inputs influences competition in a model of the basal ganglia

Fountas, Z., & Shanahan, M. (2014) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2014.6889687 · Cited by 9

Reward-related dynamical coupling between basolateral amygdala and nucleus accumbens

Hsu, C.-C., Madsen, T. E., O’Gorman, E., Gourley, S. L., & Rainnie, D. G. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02099-2 · Cited by 9

Theta Oscillations Gate the Transmission of Reliable Sequences in the Medial Entorhinal Cortex

Neru, A., & Assisi, C. G. (2021) · eNeuro · doi:10.1523/eneuro.0059-20.2021 · Cited by 10

Inference of brain pathway activities for Alzheimer's disease classification

Lee, J., Kim, Y., Jeong, Y., Na, D. L., Kim, J., Lee, K. H., & Lee, D. (2015) · BMC Medical Informatics and Decision Making · doi:10.1186/1472-6947-15-s1-s1 · Cited by 8

Rapid memory stabilization by transient theta coherence in the human medial temporal lobe

Thézé, R., Guggisberg, A. G., Nahum, L., & Schnider, A. (2015) · Hippocampus · doi:10.1002/hipo.22534 · Cited by 9

Reduced ERPs and theta oscillations underlie working memory deficits in Toxoplasma gondii infected seniors

Gajewski, P. D., Falkenstein, M., Hengstler, J. G., & Golka, K. (2016) · Biological Psychology · doi:10.1016/j.biopsycho.2016.08.002 · Cited by 9

Choice Behaviors and Prefrontal–Hippocampal Coupling Are Disrupted in a Rat Model of Fetal Alcohol Spectrum Disorders

Rosenblum, H. L., Kim, S., Stout, J. J., Klintsova, A. Y., & Griffin, A. L. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1241-24.2025 · Cited by 9

Differential roles of nucleus reuniens and perirhinal cortex in Pavlovian trace fear conditioning in rats

Jhuang, Y.-C., & Chang, C. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac287 · Cited by 8

Increased coherence among striatal regions in the theta range during attentive wakefulness

Lepski, G. A., Arévalo, A. L., Valle, A. C., Ballester, G., & Gharabaghi, A. (2012) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2012007500104 · Cited by 8

State-dependent entrainment of cerebellar nuclear neurons to the local field potential during voluntary movements

Baumel, Y., & Cohen, D. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00551.2020 · Cited by 8

Reinstatement of Cortical Outcome Representations during Higher-Order Learning

Luettgau, L., Porcu, E., Tempelmann, C., & Jocham, G. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab196 · Cited by 8

Discriminating Sleep From Freezing With Cortical Spindle Oscillations

Pompili, M. N., & Todorova, R. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.783768 · Cited by 7

Nucleus Reuniens: Circuitry, Function, and Dysfunction

Vertes, R. P., Linley, S. B., & Viena, T. D. (2022) · Neuromethods · doi:10.1007/978-1-0716-2631-3_4 · Cited by 8

Pattern dynamics and stochasticity of the brain rhythms

Hoffman, C., Cheng, J., Ji, D., & Dabaghian, Y. A. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2218245120 · Cited by 8

Pattern segmentation with activity dependent natural frequency shift and sub-threshold resonance

Shtrahman, E. A., & Żochowski, M. (2015) · Scientific Reports · doi:10.1038/srep08851 · Cited by 8

A Wireless EEG Recording Method for Rat Use inside the Water Maze

Pinnell, R., Almajidy, R. K., Kirch, R. D., Cassel, J., & Hofmann, U. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147730 · Cited by 8

A Dynamic Bayesian Model for Characterizing Cross-Neuronal Interactions During Decision-Making

Zhou, B., Moorman, D. E., Behseta, S., Ombao, H., & Shahbaba, B. (2015) · Journal of the American Statistical Association · doi:10.1080/01621459.2015.1116988 · Cited by 8

Running wheel training does not change neurogenesis levels or alter working memory tasks in adult rats

Acevedo-Triana, C. A., Rojas, M. J., & Cárdenas, F. P. (2017) · PeerJ · doi:10.7717/peerj.2976 · Cited by 9

Distinct Neurophysiological Mechanisms Support the Online Formation of Individual and Across-Episode Memory Representations

Sans-Dublanc, A., Herrero, E. M., Marco‐Pallarés, J., & Fuentemilla, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw231 · Cited by 7

Individualized frequency and montage tACS to engage theta-gamma coupling and enhance working memory in mild cognitive impairment

Mirjalili, M., Palamarchuk, I. S., Brooks, H., Zomorrodi, R., Melichercik, A., Wang, W., Nestor, S. M., Blumberger, D. M., Datta, A., Bowie, C. R., et al. (2025) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2025.1565881 · Cited by 8

Integration of rate and phase codes by hippocampal cell-assemblies supports flexible encoding of spatiotemporal context

Russo, E., Becker, N., Domanski, A. P. F., Howe, T., Freud, K., Durstewitz, D., & Jones, M. W. (2024) · Nature Communications · doi:10.1038/s41467-024-52988-x · Cited by 7

Integration of Action, Joint Action and Learning in Robot Cognitive Architectures

Khamassi, M., Girard, B., Clodic, A., Devin, S., Renaudo, E., Pacherie, É., Alami, R., & Chatila, R. (2016) · Intellectica Revue de l Association pour la Recherche Cognitive · doi:10.3406/intel.2016.1794 · Cited by 10

Environmental enrichment increases prefrontal EEG power and synchrony with the hippocampus in rats with anterior thalamus lesions

Ulrich, K., Spriggs, M. J., Abraham, W. C., Dalrymple‐Alford, J. C., & McNaughton, N. (2018) · Hippocampus · doi:10.1002/hipo.23022 · Cited by 7

Phase‐amplitude coupling profiles differ in frontal and auditory cortices of bats

García‐Rosales, F., López‐Jury, L., González‐Palomares, E., Cabral‐Calderín, Y., Kössl, M., & Hechavarría, J. C. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14986 · Cited by 8

Effects of antipsychotic drugs and potassium channel modulators on spectral properties of local field potentials in mouse hippocampus and pre-frontal cortex

Sun, D., Kermani, M., Hudson, M. R., He, X., Unnithan, R. R., & French, C. R. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108572 · Cited by 8

Model-Based and Model-Free Replay Mechanisms for Reinforcement Learning in Neurorobotics

Massi, E., Barthélemy, J.-G., Mailly, J., Dromnelle, R., Canitrot, J., Poniatowski, E., Girard, B., & Khamassi, M. (2022) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2022.864380 · Cited by 7

Effects of theta burst stimulation on the coherence of local field potential during working memory task in rats

Wang, T., Guo, M., Wang, N., Zhai, H., Wang, Z., & Xu, G. (2023) · Brain Research · doi:10.1016/j.brainres.2023.148408 · Cited by 7

Rhythmic oscillations in the midbrain dopaminergic nuclei in mice

Oberto, V. J., Matsumoto, J., Pompili, M. N., Todorova, R., Papaleo, F., Nishijo, H., Venance, L., Vandecasteele, M., & Wiener, S. I. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1131313 · Cited by 8

Modafinil Effects on Middle-Frequency Oscillatory Power During Rule Selection in Schizophrenia

Minzenberg, M., Yoon, J. H., Cheng, Y., & Carter, C. S. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.155 · Cited by 7

The atypical dopamine receptor agonist SKF 83959 enhances hippocampal and prefrontal cortical neuronal network activity in a rat model of cognitive dysfunction

Perreault, M. L., Fan, T., Banasikowski, T. J., Grace, A. A., & George, S. R. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13635 · Cited by 6

Inferring oscillatory modulation in neural spike trains

Arai, K., & Kass, R. E. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005596 · Cited by 7

Neonatal Monosodium Glutamate Administration Disrupts Place Learning and Alters Hippocampal–Prefrontal Learning-Related Theta Activity in the Adult Rat

López‐Vázquez, M. A., Gama-García, C. E., Estrada-Reyes, Y., Gaytán-Tocavén, L., Cervantes-Alfaro, J. M., & Olvera‐Cortés, M. E. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.07.007 · Cited by 7

Oscillation-Driven Memory Encoding, Maintenance, and Recall in an Entorhinal–Hippocampal Circuit Model

Kurikawa, T., Mizuseki, K., & Fukai, T. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa343 · Cited by 9

Encoding of rat working memory by power of multi-channel local field potentials via sparse non-negative matrix factorization

Liu, X., Liu, T., Bai, W., Hu, Y., Li, S., & Tian, X. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1333-z · Cited by 7

Dynamical modulation of theta-gamma coupling during REM sleepPreprint

Bandarabadi, M., Boyce, R., Herrera, C. G., Bassetti, C. L., Williams, S., Schindler, K. A., & Adamantidis, A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/169656 · Cited by 7

The Prefrontal Cortex and Human MemoryPreprint

Diamond, N. B., & Levine, B. (2018) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/u9hgx · Cited by 8

Low-intensity transcranial ultrasound stimulation improves memory behavior in an ADHD rat model by modulating cortical functional network connectivity

Wang, M., Xie, Z., Wang, T., Dong, S., Ma, Z., Zhang, X., Li, X., & Yuan, Y. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120841 · Cited by 6

Synchronous Theta Networks Characterize Successful Memory Retrieval

Rao, A. M., DeHaan, R. D., & Kahana, M. J. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1332-24.2025 · Cited by 6

Disruption of hippocampal-prefrontal neural dynamics and risky decision-making in a mouse model of Alzheimer’s disease

Kim, E. J., Park, S., Schuessler, B. P., Boo, H., Cho, J., & Kim, J. J. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116081 · Cited by 10

Critical Periods and Beyond: Dynamic Functions of Perineuronal Nets in Cognition, Development, and Disease

Sakata, J. T., Alonge, K. M., Diethorn, E. J., Krishnan, K., Milman, N., Ramsaran, A. I., Wan, X., & Sorg, B. A. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1367-25.2025 · Cited by 8

Hippocampal theta sweeps indicate goal direction during navigation

Yu, C., Ji, Z., Ormond, J., O'Keefe, J. M., & Burgess, N. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02365-2 · Cited by 17

Phase locking of hippocampal CA3 neurons to distal CA1 theta oscillations selectively predicts memory performance

Ku, S.-P., Atucha, E., Alavi, N., Mulla-Osman, H., Kayumova, R., Yoshida, M., Csicsvari, J., & Sauvage, M. M. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114276 · Cited by 6

Sleep’s Role in Schema Learning and Creative Insights

Durrant, S. J., & Johnson, J. M. (2021) · Current Sleep Medicine Reports · doi:10.1007/s40675-021-00202-5 · Cited by 7

The Rehabilitation Potential of Neurostimulation for Mild Traumatic Brain Injury in Animal and Human Studies

McNerney, M. W., Gurkoff, G. G., Beard, C., & Berryhill, M. E. (2023) · Brain Sciences · doi:10.3390/brainsci13101402 · Cited by 7

Border cells without theta rhythmicity in the medial prefrontal cortex

Long, X., Deng, B., Shen, R., Yang, L. S., Chen, L., Ran, Q., Du, X., & Zhang, S. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2321614121 · Cited by 5

Polyrhythms of the Brain

Battaglia, F. P., & McNaughton, B. L. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.019 · Cited by 6

Predictive nature of prefrontal theta oscillation on the performance of trace conditioned eyeblink responses in guinea pigs

Chen, H., Wang, Y.-J., Li, Y., Hu, C., Ke, X.-F., Fan, Z.-L., Sui, J.-F., & Hu, B. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.02.020 · Cited by 6

Prediction of Successful Memory Encoding Based on Lateral Temporal Cortical Gamma Power

Jun, S., Kim, J. S., & Chung, C. K. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.517316 · Cited by 6

Canonical correlation between LFP network and spike network during working memory task in rat

Hu, Y., Zhang, X., Bai, W., Liu, T., & Tian, X. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.042 · Cited by 6

NMDARs in prefrontal cortex – Regulation of synaptic transmission and plasticity

Banks, P. J., & Bashir, Z. I. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108614 · Cited by 7

Control of Functional Connectivity in Cerebral Cortex by Basal Ganglia Mediated SynchronizationPreprint

Pouzzner, D. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1708.00779 · Cited by 6

Unsupervised clustering of temporal patterns in high-dimensional neuronal ensembles using a novel dissimilarity measurePreprint

Großberger, L., Battaglia, F. P., & Vinck, M. A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/252791 · Cited by 7

Theta Stimulation Enhances Early Consolidation of Semantic Memory

Shtoots, L., Barzilay, R., Gigi, T., Kostovetsky, V., Pollock, A., & Levy, D. A. (2025) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02322 · Cited by 5

Human iPSC‐Derived Mononuclear Phagocytes Improve Cognition and Neural Health across Multiple Mouse Models of Aging and Alzheimer's Disease

Moser, V. A., Dimas‐Harms, L. J., Lipman, R. M., Inzalaco, J., Bell, S., Alcantara, M., Valenzuela, E., Lawless, G. M., Kreimer, S. D., Parker, S. J., et al. (2025) · Advanced Science · doi:10.1002/advs.202417848 · Cited by 5

Dominance hierarchy regulates social behavior during spatial movement

Lara-Vásquez, A., Espinosa, N., Morales, C., Moran, C., Billeke, P. B., Gallagher, J., Strohl, J. J., Huerta, P. T., & Fuentealba, P. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1237748 · Cited by 7

The role of ventral hippocampal-medial prefrontal glutamatergic pathway on the non-affected side in post-stroke cognitive impairment

Zhao, Y., Peng, Y., Pan, Y., Lv, Y., Zhou, H., Wu, J., Gong, J., & Wang, X. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149168 · Cited by 5

Electrophysiological Signatures in Global Cerebral Ischemia: Neuroprotection Via Chemogenetic Inhibition of CA1 Pyramidal Neurons in Rats

Liu, P., Xu, J., Chen, Y. L., Xu, Q., Zhang, W., Hu, B., Li, A., & Zhu, Q. (2024) · Journal of the American Heart Association · doi:10.1161/jaha.124.036146 · Cited by 6

Theanine boosts frontal theta and hippocampal beta and gamma oscillations for familiarity in object recognition

Watanabe, K., Takeda, K., Nagahiro, T., Iijima, S., Ikegaya, Y., & Matsumoto, N. (2025) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2025.08.002 · Cited by 5

Neuronal dynamics supporting formation and recombination of cross-modal olfactory-tactile association in the rat hippocampal formation

Boisselier, L., Gervasoni, D., Garcia, S., Ferry, B., & Gervais, R. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00666.2017 · Cited by 5

Oscillations as a window into neuronal mechanisms underlying dorsal anterior cingulate cortex function

Voloh, B., Knoebl, R., Hayden, B. Y., & Zimmermann, J. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.11.003 · Cited by 5

Rat anterior cingulate neurons responsive to rule or strategy changes are modulated by the hippocampal theta rhythm and sharp‐wave ripples

Khamassi, M., Peyrache, A., Benchenane, K., Hopkins, D. A., Lebas, N., Douchamps, V., Jacques Droulez, A., Battaglia, F. P., & Wiener, S. I. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16496 · Cited by 5

Sleep, Synaptic Plasticity, and Memory

Golbert, D. C. F., Souza, A. C., Filho, D. A., & Ribeiro, S. T. G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21118-8 · Cited by 5

Goal-Directed Sequences in the Hippocampus

Schmidt, B., Wikenheiser, A. M., & Redish, A. D. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812098-9.00006-1 · Cited by 5

Coding Dynamics of the Striatal Networks During Learning

Villet, M., Reynaud-Bouret, P., Poitreau, J., Baldi, J., Jaffard, S., James, A., Muzy, A., Kartsaki, E., Scarella, G., Sargolini, F., et al. (2024) · eNeuro · doi:10.1523/eneuro.0436-23.2024 · Cited by 5

Neuron Article 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. (2013)

Coherence of Theta Rhythm between Hippocampus and Medial Prefrontal Cortex Modulates Prefrontal Network Activity During Learning in Rats

Wiener, S. I. (2009) · Frontiers in Systems Neuroscience · doi:10.3389/conf.neuro.01.2009.04.132 · Cited by 3

Theta synchronizes the activity of medial prefrontal neurons during learningPreprint

Paz, R., Bauer, E. P., & Paré, D. (2008) · Learning & Memory · doi:10.1101/lm.932408 · Cited by 118

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

Dynamic θ Frequency Coordination within and between the Prefrontal Cortex-Hippocampus Circuit during Learning of a Spatial Avoidance Task

Dickson, C. R., Holmes, G. L., & Barry, J. M. (2022) · eNeuro · doi:10.1523/eneuro.0414-21.2022 · Cited by 7