Anatomical substrates for direct interactions between hippocampus, medial prefrontal cortex, and the thalamic nucleus reuniens

The Rat Brain in Stereotaxic Coordinates

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

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Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?

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Theta oscillations in the hippocampus

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Reactivation of hippocampal ensemble memories during sleep

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The development and application of optogenetics

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Reverse replay of behavioural sequences in hippocampal place cells during the awake state

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Selective suppression of hippocampal ripples impairs spatial memory

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Differential projections of the infralimbic and prelimbic cortex in the rat

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Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat

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Thalamo-cortical coupling during encoding and consolidation is linked to durable memory formation

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Modes of cognition: Evidence from metastable brain dynamics

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A prefrontal-thalamic circuit encodes social information for social recognition

Chen, Z., Han, Y., Ma, Z., Wang, X., Xu, S., Tang, Y. Y., Vyssotski, A. L., Si, B., & Zhan, Y. (2024) · Nature Communications · doi:10.1038/s41467-024-45376-y · Cited by 35

Prefrontal cortex modulates firing pattern in the nucleus reuniens of the midline thalamus via distinct corticothalamic pathways

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NREM sleep spindles are associated with dream recall

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Calretinin and calbindin architecture of the midline thalamus associated with prefrontal–hippocampal circuitry

Viena, T. D., Rasch, G. E., da Silva, D. M., & Allen, T. A. (2020) · Hippocampus · doi:10.1002/hipo.23271 · Cited by 35

Nucleus reuniens of the thalamus controls fear memory reconsolidation

Troyner, F., & Bertoglio, L. J. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107343 · Cited by 28

Task-specific oscillatory synchronization of prefrontal cortex, nucleus reuniens, and hippocampus during working memory

Malsen, J. G. D. M., Röhrdanz, N., Buschhoff, A.-S., Schiffelholz, T., Sigurdsson, T., & Wulff, P. (2023) · iScience · doi:10.1016/j.isci.2023.107532 · Cited by 32

Repetition reveals ups and downs of hippocampal, thalamic, and neocortical engagement during mnemonic decisions

Reagh, Z. M., Murray, E. A., & Yassa, M. A. (2016) · Hippocampus · doi:10.1002/hipo.22681 · Cited by 29

Functional Connectivity between Hippocampus and Lateral Septum is Affected in Very Young Alzheimer’s Transgenic Mouse Model

Mondragón‐Rodríguez, S., Gu, N., Fasano, C., Peña‐Ortega, F., & Williams, S. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.12.042 · Cited by 29

Expanding the canon: An inclusive neurobiology of thalamic and subthalamic fear circuits

Venkataraman, A., & Dias, B. G. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109380 · Cited by 26

Sleep’s contribution to memory formation

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Theta oscillations as a substrate for medial prefrontal-hippocampal assembly interactions

Nardin, M., Kaefer, K., Stella, F., & Csicsvari, J. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113015 · Cited by 27

The activity of thalamic nucleus reuniens is critical for memory retrieval, but not essential for the early phase of “off-line” consolidationPreprint

Mei, H., Logothetis, N. K., & Eschenko, O. (2018) · Learning & Memory · doi:10.1101/lm.047134.117 · Cited by 28

A Gradient of Hippocampal Inputs to the Medial Mesocortex

Ferreira‐Fernandes, E., Pinto-Correia, B., Quintino, C., & Remondes, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.011 · Cited by 23

Pathways for Memory, Cognition and Emotional Context: Hippocampal, Subgenual Area 25, and Amygdalar Axons Show Unique Interactions in the Primate Thalamic Reuniens Nucleus

Joyce, M. K. P., Marshall, L. G., Banik, S. L., Wang, J., Xiao, D., Bunce, J. G., & Barbas, H. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1724-21.2021 · Cited by 26

Differential role of the anterior and intralaminar/lateral thalamic nuclei in systems consolidation and reconsolidation

Lopez, J., Gamache, K., Milo, C., & Nader, K. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1475-2 · Cited by 24

Input Convergence, Synaptic Plasticity and Functional Coupling Across Hippocampal-Prefrontal-Thalamic Circuits

Bueno-Júnior, L. S., & Leite, J. P. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00040 · Cited by 24

Cortico-Hippocampal Circuits for Memory Consolidation: The Role of the Prefrontal Cortex

Genzel, L., & Battaglia, F. P. (2017) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-319-45066-7_16 · Cited by 22

Searching basic units in memory traces: associative memory cells

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Thalamic nucleus reuniens regulates fear memory destabilization upon retrieval

Troyner, F., & Bertoglio, L. J. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107313 · Cited by 21

To sleep or not to sleep – Effects on memory in normal aging and disease

Kroeger, D., & Vetrivelan, R. (2023) · Aging Brain · doi:10.1016/j.nbas.2023.100068 · Cited by 28

In vitro characterization of cell‐level neurophysiological diversity in the rostral nucleus reuniens of adult mice

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Detection of time-, frequency- and direction-resolved communication within brain networks

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Duration of night sleep and cognitive performance of community older adults

Alves, É. D. S., Pavarini, S. C. I., Luchesi, B. M., Ottaviani, A. C., Cardoso, J. D. F. Z., & Inouye, K. (2021) · Revista Latino-Americana de Enfermagem · doi:10.1590/1518-8345.4269.3439 · Cited by 23

Post-learning paradoxical sleep deprivation impairs reorganization of limbic and cortical networks associated with consolidation of remote contextual fear memory in mice

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A Temporal Activity of CA1 Neurons Underlying Short-Term Memory for Social Recognition Altered in PTEN Mouse Models of Autism Spectrum Disorder

Chai, A., Chen, X.-F., Xu, X.-S., Zhang, N., Li, M., Li, J., Zhang, L., Zhang, D., Zhang, X., Mao, R., et al. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.699315 · Cited by 24

Dual medial prefrontal cortex and hippocampus projecting neurons in the paraventricular nucleus of the thalamus

Viena, T. D., Rasch, G. E., & Allen, T. A. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02478-x · Cited by 24

Pathway-specific GABAergic inhibition contributes to the gain of resilience against anorexia-like behavior of adolescent female mice

Aoki, C. J., & Santiago, A. N. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.990354 · Cited by 20

Executive functioning-specific behavioral impairments in a rat model of human third trimester binge drinking implicate prefrontal-thalamo-hippocampal circuitry in Fetal Alcohol Spectrum Disorders

Gursky, Z. H., Savage, L. M., & Klintsova, A. Y. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113208 · Cited by 25

Stimulating forebrain communications: Slow sinusoidal electric fields over frontal cortices dynamically modulate hippocampal activity and cortico-hippocampal interplay during slow-wave states

Greenberg, A., Whitten, T. A., & Dickson, C. T. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.02.070 · Cited by 21

Single-day Postnatal Alcohol Exposure Induces Apoptotic Cell Death and Causes long-term Neuron Loss in Rodent Thalamic Nucleus Reuniens

Gursky, Z. H., Spillman, E. C., & Klintsova, A. Y. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.03.046 · Cited by 29

Role of the reuniens and rhomboid thalamic nuclei in anxiety‐like avoidance behavior in the rat

Linley, S. B., Athanason, A. C., Rojas, A. K. P., & Vertes, R. P. (2021) · Hippocampus · doi:10.1002/hipo.23302 · Cited by 20

Separate cortical and hippocampal cell populations target the rat nucleus reuniens and mammillary bodies

Mathiasen, M. L., Amin, E., Nelson, A. J. D., Dillingham, C. M., O’Mara, S. M., & Aggleton, J. P. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14341 · Cited by 19

Centrifugal projections to the main olfactory bulb revealed by transsynaptic retrograde tracing in mice

Schneider, N. Y., Chaudy, S., Epstein, A. L., Viollet, C., Bénani, A., Pénicaud, L., Grosmaître, X., Datiche, F., & Gascuel, J. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24846 · Cited by 19

Medial prefrontal and ventral hippocampal contributions to incidental context learning and memory in adolescent rats

Heroux, N. A., Horgan, C. J., Pinizzotto, C. C., Rosen, J. B., & Stanton, M. E. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107091 · Cited by 18

Long-term potentiation of the nucleus reuniens and entorhinal cortex to CA1 distal dendritic synapses in mice

Vu, T., Gugustea, R., & Leung, L.-W. S. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02095-6 · Cited by 18

Dual projecting cells linking thalamic and cortical communication routes between the medial prefrontal cortex and hippocampus

Schlecht, M., Jayachandran, M., Rasch, G. E., & Allen, T. A. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2022.107586 · Cited by 19

The ventral midline thalamus coordinates prefrontal–hippocampal neural synchrony during vicarious trial and error

Stout, J. J., Hallock, H. L., George, A. E., Adiraju, S. S., & Griffin, A. L. (2022) · Scientific Reports · doi:10.1038/s41598-022-14707-8 · Cited by 21

The roles of rat medial prefrontal and orbitofrontal cortices in relapse to cocaine-seeking: A comparison across methods for identifying neurocircuits

Mesa, J. R., Wesson, D. W., Schwendt, M., & Knackstedt, L. A. (2022) · Addiction Neuroscience · doi:10.1016/j.addicn.2022.100031 · Cited by 17

Midline Thalamic Damage Associated with Alcohol-Use Disorders: Disruption of Distinct Thalamocortical Pathways and Function

Savage, L. M., Nunes, P. T., Gursky, Z. H., Milbocker, K. A., & Klintsova, A. Y. (2020) · Neuropsychology Review · doi:10.1007/s11065-020-09450-8 · Cited by 22

Representation of prefrontal axonal efferents in the thalamic nucleus reuniens in a rodent model of fetal alcohol exposure during third trimester

Smith, E. A., Gursky, Z. H., & Klintsova, A. Y. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.993601 · Cited by 16

Identifying the midline thalamus in humans in vivo

Reeders, P. C., Núñez, M. V. R., Vertes, R. P., Mattfeld, A. T., & Allen, T. A. (2023) · Brain Structure and Function · doi:10.1007/s00429-022-02607-6 · Cited by 16

Taming the oscillatory zoo in the hippocampus and neo-cortex: a review of the commentary of Lockmann and Tort on Roy et al.

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Parsing neural circuits of fear learning and extinction across basic and clinical neuroscience: Towards better translation

Namkung, H., Thomas, K. L., Hall, J., & Sawa, A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.12.025 · Cited by 17

Projections from the five divisions of the orbital cortex to the thalamus in the rat

Vertes, R. P., Hoover, W. B., Witter, M. P., Yanik, M. F., Rojas, A. K. P., & Linley, S. B. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25419 · Cited by 15

Prefrontal-Hippocampal Pathways Through the Nucleus Reuniens Are Functionally Biased by Brain State

Hauer, B. E., Pagliardini, S., & Dickson, C. T. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.804872 · Cited by 16

Thalamic spindles and Up states coordinate cortical and hippocampal co-ripples in humans

Dickey, C. W., Verzhbinsky, I. A., Kajfez, S., Rosen, B. Q., Gonzalez, C. E., Chauvel, P., Cash, S. S., Pati, S. B. B., & Halgren, E. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002855 · Cited by 15

Neuronal Oscillations and Reactivation Subserving Memory Consolidation

Bergmann, T. O., & Staresina, B. P. (2017) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-319-45066-7_12 · Cited by 14

Magnocellular and parvocellular contributions to brain network dysfunction during learning and memory: Implications for schizophrenia

Kody, E., & Diwadkar, V. A. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.10.055 · Cited by 16

Carboxypeptidase E conditional knockout mice exhibit learning and memory deficits and neurodegeneration

Fan, F.-C., Du, Y., Zheng, W., Loh, Y. P., & Cheng, Y. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02429-y · Cited by 15

An ultra-short-acting benzodiazepine in thalamic nucleus reuniens undermines fear extinction via intermediation of hippocamposeptal circuits

Cheung, H., Yu, T.-Z., Yi, X., Wu, Y., Wang, Q., Gu, X., Xu, M., Cai, M., Wen, W., Li, X.-N., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06417-w · Cited by 13

Convergent direct and indirect cortical streams shape avoidance decisions in mice via the midline thalamus

Ma, J., O’Malley, J. J., Kreiker, M., Leng, Y., Khan, I., Kindel, M., & Penzo, M. A. (2024) · Nature Communications · doi:10.1038/s41467-024-50941-6 · Cited by 15

Behavioral profiling reveals an enhancement of dentate gyrus paired pulse inhibition in a rat model of PTSD

Albrecht, A., Ben-Yishay, E., & Richter‐Levin, G. (2021) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2021.103601 · Cited by 12

Longitudinal tracing of neurochemical metabolic disorders in working memory neural circuit and optogenetics modulation in rats with vascular cognitive impairment

Lin, H., Jin, T., Chen, L., Dai, Y., Jia, W., He, X., Yang, M., Li, J., Liang, S., Wu, J., et al. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.02.013 · Cited by 12

Characterization and manipulation of Corticothalamic neurons in associative cortices using Syt6‐Cre transgenic mice

Vaasjo, L. O., Han, X., Thurmon, A. N., Tiemroth, A. S., Berndt, H., Korn, M., Figueroa, A., Reyes, R., Feliciano‐Ramos, P. A., & Galazo, M. J. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25256 · Cited by 13

Regional differences in BDNF expression and behavior as a function of sex and enrichment type: oxytocin matters

Faraji, J., Lotfi, H., Moharrerie, A., Jafari, S. Y., Soltanpour, N., Tamannaiee, R., Marjani, K., Roudaki, S., Naseri, F., Moeeini, R., et al. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab395 · Cited by 12

Binge alcohol alters exercise-driven neuroplasticity

Barton, E. A., Lu, Y., Megjhani, M., Maynard, M. E., Kulkarni, P. M., Roysam, B., & Leasure, J. L. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.041 · Cited by 12

Dorsal prefrontal and premotor cortex of the ferret as defined by distinctive patterns of thalamo-cortical projections

Radtke‐Schuller, S., Town, S. M., Yin, P., Elgueda, D., Schuller, G., Bizley, J. K., Shamma, S., & Fritz, J. B. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02086-7 · Cited by 13

Sleep and memory consolidation in aging: A neuroimaging perspective

Hamel, A., Mary, A., & Rauchs, G. (2023) · Revue Neurologique · doi:10.1016/j.neurol.2023.08.003 · Cited by 12

Respiration organizes gamma synchrony in the prefronto-thalamic network

Basha, D., Chauvette, S., Sheroziya, M., & Timofeev, I. (2023) · Scientific Reports · doi:10.1038/s41598-023-35516-7 · Cited by 14

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

Functional Reuniens and Rhomboid Nuclei Are Required for Proper Acquisition and Expression of Cued and Contextual Fear in Trace Fear Conditioning

Wu, Y., & Chang, C. (2021) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyab094 · Cited by 10

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

Requiring collaboration: Hippocampal-prefrontal networks needed in spatial working memory and ageing. A multivariate analysis approach

Zancada-Menéndez, C., Álvarez-Suárez, P., Sampedro‐Piquero, P., Cuesta, M., & Begega, A. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.02.008 · Cited by 11

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

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

Multisensory integration and white matter pathology: Contributions to cognitive dysfunction

Hebert, J. R., & Filley, C. M. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.1051538 · Cited by 11

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

PV-dependent reorganization of prelimbic cortex sub-engrams during systems consolidation

Golbabaei, A., Josselyn, S. A., & Frankland, P. W. (2025) · Neuron · doi:10.1016/j.neuron.2025.09.033 · Cited by 11

Coupling between the prelimbic cortex, nucleus reuniens, and hippocampus during NREM sleep remains stable under cognitive and homeostatic demands

Bozic, I., Rusterholz, T., Mikutta, C. A., Rio‐Bermudez, C. D., Nissen, C., & Adamantidis, A. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15853 · Cited by 10

Systems Consolidation, Transformation, and Reorganization

Moscovitch, M., & Gilboa, A. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.43 · Cited by 14

Assigning Function to Adult-Born Neurons: A Theoretical Framework for Characterizing Neural Manipulation of Learning

Hersman, S., Barrera, V. R., & Fanselow, M. S. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00182 · Cited by 9

Investigating cognition in midlife

Novotný, J., Gonzalez-Rivas, J. P., Medina‐Inojosa, J. R., López-Jiménez, F. A., Geda, Y. E., & Stokin, G. B. (2021) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12234 · Cited by 9

Enhanced Medial Prefrontal Cortex and Hippocampal Activity Improves Memory Generalization in APP/PS1 Mice: A Multimodal Animal MRI Study

Liu, W., Li, J., Li, L., Zhang, Y., Yang, M., Liang, S., Li, L., Dai, Y., Chen, L., Jia, W., et al. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.848967 · Cited by 9

Dorsal–Caudal and Ventral Hippocampi Target Different Cell Populations in the Medial Frontal Cortex in Rodents

Alemán-Andrade, P., Witter, M. P., Tsutsui, K., & Ohara, S. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0217-25.2025 · Cited by 9

Changes in Representation of Thalamic Projection Neurons within Prefrontal-Thalamic-Hippocampal Circuitry in a Rat Model of Third Trimester Binge Drinking

Gursky, Z. H., & Klintsova, A. Y. (2021) · Brain Sciences · doi:10.3390/brainsci11030323 · Cited by 11

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

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

Projections from thalamic nucleus reuniens to medial septum enable extinction of remote fear memory

Tomaszewski, K. F., Gajewska‐Woźniak, O., Ziółkowska, M., Łukasiewicz, K., Cały, A., Sotoudeh, N., Puchalska, M., Salamian, A., & Radwańska, K. (2026) · Acta Neurobiologiae Experimentalis · doi:10.55782/zd27ss41 · Cited by 7

A Direct Comparison of Afferents to the Rat Anterior Thalamic Nuclei and Nucleus Reuniens: Overlapping But Different

Mathiasen, M. L., Nelson, A. J. D., Amin, E., O’Mara, S. M., & Aggleton, J. P. (2021) · eNeuro · doi:10.1523/eneuro.0103-20.2021 · Cited by 11

Dorsal Hippocampal Activation Suppresses Neuropathic Pain Behaviors: Chronic pain as extinction-resistant pain-related memory tracesPreprint

Xuhong, W., Ren, W., Centeno, M. V., Procissi, D., Xu, T., Jabakhanji, R., Martina, M., Radulović, J., Surmeier, D. J., Liu, X. G., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/292094 · Cited by 8

Inhibition of the ventral midline thalamus does not alter encoding, short-term holding or retrieval of spatial information in rats performing a water-escape working memory task

Boch, L., Morvan, T., Neige, T., Kobakhidze, N., Panzer, É., Cosquer, B., de Vasconcelos, A. P., Stéphan, A., & Cassel, J. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113979 · Cited by 7

Stratum Lacunosum-moleculare Interneurons of the Hippocampus Coordinate Memory Encoding and RetrievalPreprint

Guo, J. Q., Oliveros, H. C., Oh, S. J., Liang, B., Li, Y., Kavalali, E. T., Lin, D., & Xu, W. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.21203/rs.3.rs-310894/v1 · Cited by 8

Reuniens transiently synchronizes memory networks at beta frequenciesPreprint

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Nucleus

(2016)

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