Hippocampal–prefrontal input supports spatial encoding in working memory

Working memory: Looking back and looking forward

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Cellular basis of working memory

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

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Conjoint generalized and trajectory-specific coding of task structure by prefrontal neurons

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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

Gamma synchronization between the medial temporal lobe and medial frontal cortex for goal-directed visual attention in humans

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Hierarchical Replay of Multi-regional Sequential Spiking Associated with Working Memory

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

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The molecular diversity of plasticity mechanisms underlying memory: An evolutionary perspective

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Effects of indoor exposure to low level toluene on neural network alterations during working memory encoding

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A potential mechanism for first-person internal sensation of memory provides evidence for the relationship between learning and LTP induction

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Activation of D1-like dopamine receptors is involved in the impairment of spatial memory in the offspring of morphine-abstinent rats

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Epigenetic-Mediated N -Methyl-D-Aspartate Receptor Changes in the Brain of Isolated Reared Rats

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Sex and sex hormone differences in hippocampal neurogenesis and their relevance to Alzheimer’s disease

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Lateral Entorhinal Cortex Suppresses Drift in Cortical Memory Representations

Pilkiw, M., Jarovi, J., & Takehara‐Nishiuchi, K. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1439-21.2021 · Cited by 12

Detection of Microstructural Medial Prefrontal Cortex Changes Using Magnetic Resonance Imaging Texture Analysis in a Post-Traumatic Stress Disorder Rat Model

Zheng, S., Wang, H., Han, F., Chu, J., Zhang, F., Zhang, X., Shi, Y., & Zhang, L. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.805851 · Cited by 8

Comparison of Cognitive Functions Between Patients with Alzheimer Disease, Patients with Mild Cognitive Impairment, and Healthy People

Hedayatjoo, M., Doost, M. T., Vahabi, Z., Akbarfahimi, M., & Khosrowabadi, R. (2023) · Archives of Neuroscience · doi:10.5812/ans-131408 · 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

Neuronal dynamics of cerebellum and medial prefrontal cortex in adaptive motor timing

Ren, Z., Wang, X., Angelov, M., Zeeuw, C. I. D., & Gao, Z. (2025) · Nature Communications · doi:10.1038/s41467-025-55884-0 · Cited by 8

How can preclinical mouse models be used to gain insight into prefrontal cortex dysfunction in obsessive-compulsive disorder?

Manning, E. E., & Ahmari, S. E. (2018) · Brain and Neuroscience Advances · doi:10.1177/2398212818783896 · Cited by 8

Evaluation of Hemisphere Lateralization with Bilateral Local Field Potential Recording in Secondary Motor Cortex of Mice

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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

Deriving causal relationships in resting-state functional connectivity using SSFO-based optogenetic fMRI

Han, X., Cramer, S. R., & Zhang, N. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac9d66 · Cited by 7

Pausing and reorienting behaviors enhance the performance of a spatial working memory task

George, A. E., Stout, J. J., & Griffin, A. L. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114410 · Cited by 7

Functional network of contextual and temporal memory has increased amygdala centrality and connectivity with the retrosplenial cortex, thalamus, and hippocampus

Santos, T. B., Soares, J. C. K., Coelho, C. A. O., & Oliveira, M. G. M. (2023) · Scientific Reports · doi:10.1038/s41598-023-39946-1 · Cited by 8

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

Integrating Clinical and Genomic Analyses of Hippocampal-Prefrontal Circuit Disorder in Depression

Yuan, N., Tang, K., Da, X., Gan, H. T., He, L., Li, X., Ma, Q., & Chen, J. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2020.565749 · Cited by 7

Emergence of stable sensory and dynamic temporal representations in the hippocampus during working memoryPreprint

Taxidis, J., Pnevmatikakis, E. A., Mylavarapu, A. L., Arora, J. S., Samadian, K. D., Hoffberg, E. A., & Golshani, P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/474510 · Cited by 7

Task-dependent mixed selectivity in the subiculumPreprint

Ledergerber, D., Battistin, C., Blackstad, J. S., Gardner, R. J., Witter, M. P., Moser, M., Roudi, Y., & Moser, E. I. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.06.129221 · Cited by 7

Impaired theta and low-gamma directed information flow in the hippocampal-prefrontal circuit underlies working memory deficits in APP/PS1 mice

Ai, H., Zhang, S., Si, C., Liu, T., Zheng, X., Tian, X., & Bai, W. (2025) · Behavioral and Brain Functions · doi:10.1186/s12993-025-00285-y · Cited by 7

Astrocytic dopamine D1 receptor modulates glutamatergic transmission and synaptic plasticity in the prefrontal cortex through d-serine

Yin, Y., Hu, J., Wu, H., Yang, X., Qi, J., Huang, L., Luo, Z.-Y., Jin, S., Hu, N.-Y., Luo, Z.-C., et al. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.07.034 · Cited by 7

Wild canids and felids differ in their reliance on reused travel routeways

Fagan, W. F., Krishnan, A., Fleming, C. H., Ferreira, E., Chia, S., Swain, A., Abrahms, B. L., Bracis, C., Gurarie, E. D., Mueller, T., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2401042122 · Cited by 6

Spatiotemporal connectivity maps abnormal communication pathways in major depressive disorder underlying gamma oscillations

Chen, S., Liu, X., Huang, Z., Su, F., Zhang, W., Li, J., Liu, S., & Ming, D. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad204 · Cited by 6

Hypothalamic orexins as possible therapeutic agents in threat and spatial memory disorders

Mazur, F., & Całka, J. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1228056 · Cited by 6

Milk fat globule membrane promotes brain development in piglets by enhancing the connection of white matter fiber trace

Zhang, Y., Zhao, B., Man-Yau, S. I., Pan, Z., Gao, L., Li, Q., Tang, C., Wang, Y., Tang, X., Zhao, Z., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1248809 · Cited by 8

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

Genetic Depletion of BDNF Impairs Extinction Learning of a Spatial Appetitive Task in the Presence or Absence of the Acquisition Context

Méndez‐Couz, M., Krenzek, B., & Manahan‐Vaughan, D. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.658686 · Cited by 7

Elevated Gamma Connectivity in Nidopallium Caudolaterale of Pigeons during Spatial Path Adjustment

Li, M., Fan, J., Lin, L., Shang, Z., & Wan, H. (2022) · Animals · doi:10.3390/ani12081019 · Cited by 6

Temporal association activates projections from the perirhinal cortex and ventral CA1 to the prelimbic cortex and from the prelimbic cortex to the basolateral amygdala

Santos, T. B., Soares, J. C. K., Coelho, C. A. O., & Oliveira, M. G. M. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad375 · Cited by 8

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

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

Dendritic spine degeneration is associated with age-related decline in recognition and spatial memory in male mice

Monroy, E., Aguilar‐Hernández, L., de la Cruz‐López, F., Flores, G., & Morales‐Medina, J. C. (2025) · Brain Structure and Function · doi:10.1007/s00429-025-03002-7 · Cited by 5

Acetylcholine muscarinic M1 receptors in the rodent prefrontal cortex modulate cognitive abilities to establish social hierarchy

Chen, W., Chen, H., Li, Z., Huang, W., & Wu, J. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01785-z · Cited by 5

Selective vulnerability of the ventral hippocampus-prelimbic cortex axis parvalbumin interneuron network underlies learning deficits of fragile X mice

Bhandari, K., Kanodia, H., Donato, F., & Caroni, P. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114124 · Cited by 5

Explainable deep-learning framework: decoding brain states and prediction of individual performance in false-belief task at early childhood stage

Bhavna, K., Akhter, A., Banerjee, R., & Roy, D. (2024) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2024.1392661 · Cited by 5

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

Social subordination is associated with better cognitive performance and higher theta coherence of the mPFC-vHPC circuit in male rats

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GABAergic Signaling Underlying REM Sleep Deprivation‐Induced Spatial Working Memory Deficits

Varinthra, P., Shih, S., & Liu, I. Y. (2025) · Brain and Behavior · doi:10.1002/brb3.70607 · Cited by 6

The Role of Fatty Acid Binding Proteins in Neuropsychiatric Diseases: A Narrative Review

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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

An automated platform for Assessing Working Memory and prefrontal circuit function

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Execution of new trajectories toward a stable goal without a functional hippocampus

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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

A goal pointer for a cognitive map in the orbitofrontal cortex

Basu, R., & Ito, H. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102803 · Cited by 6

Effect of fine and gross motor training or motor imagery, delivered via novel or routine modes, on cognitive function

Brandwayn, N., Restrepo, D., Martínez, A. M. M., & Acevedo-Triana, C. A. (2019) · Applied Neuropsychology Adult · doi:10.1080/23279095.2019.1566133 · Cited by 5

CA1 Spike Timing is Impaired in the 129S Inbred Strain During Cognitive Tasks

Adeyelu, T. T., Shrestha, A., Adeniyi, P. A., Lee, C. C., & Ogundele, O. M. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.11.021 · Cited by 5

Brain and spinal cord trauma: what we know about the therapeutic potential of insulin growth factor 1 gene therapy

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CA2 Neuronal Activity Controls Hippocampal Oscillations and Social BehaviorPreprint

Alexander, G. M., Brown, L. Y., Farris, S., Lustberg, D. J., Pantazis, C. B., Gloss, B. R., Plummer, N. W., Riddick, N. V., Moy, S. S., Jensen, P., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/190504 · Cited by 5

Plasticity in prefrontal cortex induced by coordinated nucleus reuniens and hippocampal synaptic transmissionPreprint

Banks, P. J., Warburton, E. C., & Bashir, Z. I. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.11.197798 · Cited by 5

Highly task-specific and distributed neural connectivity in working memory revealed by single-trial decoding in mice and humansPreprint

Strahnen, D., Kapanaiah, S. K. T., Bygrave, A. M., Liss, B., Bannerman, D. M., Akam, T., Grewe, B. F., Johnson, E. L., & Kätzel, D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.20.440621 · Cited by 5

Executive dysfunction is associated with altered hippocampal-prefrontal functional connectivity in 3xTg Alzheimer’s model mice

Cunliffe, G., Tan, L. Y., Jung, S., Turner, J., & Gigg, J. (2025) · Communications Biology · doi:10.1038/s42003-025-08546-2 · Cited by 4

Orbitofrontal-sensory cortical interactions in learning and adaptive decision-making

Rao, R., Six, H., Cortese, A., & Banerjee, A. (2025) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2025.10.017 · Cited by 4

A large-scale optogenetic neurophysiology platform for improving accessibility in non-human primate behavioral experiments

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Hippocampal and Medial Prefrontal Cortical Maps Represent Episodes and Rules in a Common Task Space

Srinivasan, A., Srinivasan, A., Riceberg, J. S., Goodman, M. R., Guise, K. G., & Shapiro, M. L. (2022) · Cell Reports · doi:10.1016/j.celrep.2023.113296 · Cited by 5

The concentric model of human working memory: A validation study using complex span and updating tasks

Velichkovsky, B. B. (2017) · Psychology in Russia State of Art · doi:10.11621/pir.2017.0305 · Cited by 4

High-Throughput Automatic Training System for Spatial Working Memory in Free-Moving Mice

Zou, S., & Li, C. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00370-z · Cited by 4

Fermented Laminaria japonica improves working memory and antioxidant defense mechanism in healthy adults: a randomized, double-blind, and placebo-controlled clinical study

Kim, Y.-S., Reid, S. N. S., Ryu, J.-K., Lee, B.-J., & Jeon, B.-H. (2022) · Fisheries and aquatic sciences · doi:10.47853/fas.2022.e41 · Cited by 4

TAF15 downregulation contributes to the benefits of physical training on dendritic spines and working memory in aged mice

He, Y., Liu, B., Yang, F., Yang, Q., Xu, B., Liu, L., & Chen, Y. (2024) · Aging Cell · doi:10.1111/acel.14244 · Cited by 3

Chronic nicotine enhances object recognition memory via inducing long-term potentiation in the medial prefrontal cortex in mice

Izumi, S., Kawasaki, I., Waki, F., Nishikawa, K., Nishitani, N., Deyama, S., & Kaneda, K. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110435 · Cited by 4

An Overview of Machine Learning Applications in Mood Disorders

Topolski, N., Jeong, S. H., & Mwangi, B. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.017 · Cited by 4

Estimating Neural Background Input with Controlled and Fast Perturbations: A Bandwidth Comparison between Inhibitory Opsins and Neural Circuits

Eriksson, D. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00058 · Cited by 4

The Evolution of the Prefrontal Cortex in Early Primates and Anthropoids

Wise, S. P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820584-6.00028-3 · Cited by 4

Gamma band oscillations drives information flow in theta and delta band between hippocampus and medial pre-frontal cortexPreprint

Samuel, I. B. H. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/809962 · Cited by 3

Cognitive control of behavior and hippocampal information processing without medial prefrontal cortexPreprint

Park, E., Sparks, K. C. O., Grubbs, G., Taborga, D., Nicholas, K. R., Ahmed, A. S., Ruiz-Pérez, N., Kim, N., Segura-Carrillo, S., & Fenton, A. A. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.20.884262 · Cited by 4

Determinants of functional synaptic connectivity among amygdala-projecting prefrontal cortical neuronsPreprint

Printz, Y., Patil, P., Mahn, M., Benjamin, A., Litvin, A., Levy, R., Bringmann, M., & Yizhar, O. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.07.467611 · Cited by 4

Working and Reference Memory Tasks Trigger Opposed Long-Term Synaptic Changes in the Rat Dentate Gyrus

Missaire, M., Fraize, N., Comte, J., Truchet, B., Parmentier, R., Salin, P. A., & Malleret, G. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa405 · Cited by 6

Deep learning-based electroencephalic decoding of the phase-lagged transcranial alternating current stimulation

Kwon, J., & Min, B. (2025) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2025.1545726 · Cited by 3

Transdiagnostic homogeneity, and diagnostic-specific biomarkers among major depressive disorder, bipolar disorder and schizophrenia during 40 Hz auditory steady-state response: a normative modeling analysis

Chen, S., Guo, X., Liu, X., Liu, S., & Ming, D. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.120189 · Cited by 3

A shared hippocampal hub for anxiety and memory contrasts with depression-specific circuitry: A high-resolution 7T fMRI study

Du, C., Zhao, S., & Luo, Q. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.120493 · Cited by 3

Olfactory bulbectomy induces neurobiological alterations in the prefrontal cortex and hyperlocomotion in male rats

Bautista-Carro, M. A., Sánchez-Teoyotl, P., Juárez-Serrano, D., Iannitti, T., Díaz, A., Flores, G., & Morales‐Medina, J. C. (2026) · PLoS ONE · doi:10.1371/journal.pone.0339028 · Cited by 3

A neuromodulatory circuit-to-molecular pathway for reformatting aversive memories during recall

Tan, B. Z., Cuevas, J. N. S., Yoshida, R., Uematsu, A., Koivumaa, J., Ishizu, Y., Goda, Y., & Johansen, J. P. (2026) · Neuron · doi:10.1016/j.neuron.2026.01.006 · Cited by 4

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

Reduced Prefrontal-Thalamic Theta Flow During Working Memory Retrieval in APP/PS1 Mice

Zhang, S., Ai, H., Wang, J., Liu, T., Zheng, X., Tian, X., & Bai, W. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231078 · Cited by 3

Cognitive domains function complementation by NTNG gene paralogs

Prosselkov, P., Polygalov, D., Zhang, Q., McHugh, T. J., & Itohara, S. (2016) · Biomedical Genetics and Genomics · doi:10.1101/034645 · Cited by 3

Metamemory: Rats know the strength of their memory

Rutishauser, U. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.062 · Cited by 3

Inescapable footshocks induce molecular changes in the prefrontal cortex of rats in an amyloid-beta-42 model of Alzheimer’s disease

Faborode, O. S., Dallé, E., & Mabandla, M. V. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113679 · Cited by 4

Mood Disorders

(2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018 · Cited by 3

Impact of optogenetic pulse design on CA3 learning and replay: A neural model

Wilmerding, L. K., Yazdanbakhsh, A., & Hasselmo, M. E. (2022) · Cell Reports Methods · doi:10.1016/j.crmeth.2022.100208 · Cited by 4

[Phase amplitude coupling analysis of local field potentials in working memory of rats affected by transcranial magneto-acoustic-electrical stimulation].

Dang, J., Zhang, S., You, S., Du, W., & Xu, G. (2022) · PubMed Central · doi:10.7507/1001-5515.202108036 · Cited by 3

Novel shaking exercises for hippocampal and medial prefrontal cortex functioning maintain spatial working memory

Yao, R., Yamada, K., Kito, T., Aizu, N., Iwata, D., Izawa, S., Nishii, K., Sawada, H., & Chihara, T. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.112024 · Cited by 3

The olfactory working memory capacity paradigm: A more sensitive and robust method of assessing cognitive function in male 5XFAD mice

Jiang, L., Huang, G., Wang, H., Zhang, C., & Yu, X. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25265 · Cited by 3

The relationship of aerobic fitness with verbal and spatial working memory: An ERP study

Noh, K., Baumgartner, N. W., Onbaşı, S. İ., & Kao, S. (2024) · Progress in brain research · doi:10.1016/bs.pbr.2024.04.003 · Cited by 3

Altered Expression of Astrocytic ATP Channels and Ectonucleotidases in the Cerebral Cortex and Hippocampus of Chronic Social Defeat Stress-Susceptible BALB/c Mice

Nishioka, Y., Hayashi, K., Morito, K., Takayama, K., & Nagasawa, K. (2024) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b24-00236 · Cited by 4

Impact and Interrelationships of Striatal Proteins, EPHB2, OPRM1, and PER2 on Mild Cognitive Impairment

Campomayor, N. B., Kim, H. J., Lee, H. J., Sayson, L. V., Ortiz, D. M., Cho, E., Kim, D., Jeon, S. J., Kim, B.-N., Cheong, J. H., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04334-x · Cited by 3

Anatomo‐functional changes in neural substrates of cognitive memory in developmental amnesia: Insights from automated and manual Magnetic Resonance Imaging examinations

Chareyron, L. J., Chong, W. K., Banks, T., Burgess, N., Saunders, R. C., & Vargha‐Khadem, F. (2024) · Hippocampus · doi:10.1002/hipo.23638 · Cited by 6

THz Waves Improve Spatial Working Memory by Increasing the Activity of Glutamatergic Neurons in Mice

Song, L., He, Z., Dong, J., Wang, H., Zhang, J., Yao, B., Xu, X., Wang, H., Zhao, L., & Ruiyun, P. (2025) · Cells · doi:10.3390/cells14050370 · Cited by 3

Effects of endocannabinoid system, synthetic and nonsynthetic cannabinoid drugs on traumatic brain injury outcome: a narrative review

Amouzeshi, A., & Pourbagher-Shahri, A. (2019) · Journal of Surgery and Trauma · doi:10.32592/jsurgery.2019.7.1.101 · Cited by 3

Particle Filter on Episode for Learning Decision Making Rule

Ueda, R., Mizuta, K., Yamakawa, H., & Okada, H. (2017) · Advances in intelligent systems and computing · doi:10.1007/978-3-319-48036-7_54 · Cited by 3

A Group Analysis of Oscillatory Phase and Phase Synchronization in Cortical Networks

Wang, D., Sun, Y., Shi, H., & Wang, F. (2020) · IEEE Access · doi:10.1109/access.2020.2978161 · Cited by 3

The Impact of UCMAS Training Program on Potentiating Cognitive Capacity among 9-12 Year-Old Primary Schoolers in ShirazPreprint

Kamali, A., Shamsi, F., Zeraatpisheh, Z., Kamelmanesh, M.-M., & Nami, M. (2019) · arXiv (Cornell University) · doi:10.48550/arxiv.1904.07589 · Cited by 3

Awake hippocampal-prefrontal replay mediates spatial learning and decision makingPreprint

Shin, J. D., Tang, W., & Jadhav, S. P. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/632042 · Cited by 3

Striatum-projecting prefrontal cortex neurons support working memory maintenancePreprint

Chernysheva, M., Sych, Y., Fomins, A., Warren, J. L. A., Lewis, C., Capdevila, L. S., Boehringer, R., Amadei, E. A., Grewe, B. F., O’Connor, E. C., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.03.471159 · Cited by 3

Distinct contributions of hippocampal and prefrontal afferents to nucleus reuniens during spatial working memory

Emanuel, B. (2025) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/0fw0-gr23

Spatial information processing between hippocampus and prefrontal cortex: A hypothesis based on anatomy and physiology

Jung, M. W. (1998) · Korean Journal of Biological Sciences · doi:10.1080/12265071.1998.9647391

Prefrontal and hippocampal contributions to encoding and retrieval of spatial memory

Churchwell, J. C., Morris, A. M., Musso, N. D., & Kesner, R. P. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.12.008 · Cited by 132

Prefrontal-thalamo-hippocampal circuit contributions to spatial working memory

Hallock, H. L. (2024) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/91j6-wc29

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