Hippocampal–prefrontal input supports spatial encoding in working memory

Working memory: Looking back and looking forward

Baddeley, A. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1201 · Cited by 5,200

Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?

Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358

Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex

Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685

Cellular basis of working memory

Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663

A mesoscale connectome of the mouse brain

Oh, S. W., Harris, J. A., Ng, L., Winslow, B., Cain, N., Mihalas, S., Wang, Q., Lau, C., Kuan, L., Henry, A. M., et al. (2014) · Nature · doi:10.1038/nature13186 · Cited by 2,612

Models of Working Memory: Mechanisms of Active Maintenance and Executive Control

Miyake, A., & Shah, P. (1999) · Cited by 2,404

Principles of Neurodynamics: Perceptrons and the Theory of Brain Mechanisms

White, B. W., & Rosenblatt, F. (1963) · The American Journal of Psychology · doi:10.2307/1419730 · Cited by 1,818

PRINCIPLES OF NEURODYNAMICS. PERCEPTRONS AND THE THEORY OF BRAIN MECHANISMS

ROSENBLATT, F. (1961) · doi:10.21236/ad0256582 · Cited by 1,691

The importance of mixed selectivity in complex cognitive tasks

Rigotti, M., Barak, O., Warden, M. R., Wang, X.-J., Daw, N. D., Miller, E. K., & Fusi, S. (2013) · Nature · doi:10.1038/nature12160 · Cited by 1,639

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

Hoover, W. B., & Vertes, R. P. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0150-4 · Cited by 1,365

Awake Hippocampal-Prefrontal Replay Mediates Spatial Learning and Decision MakingPreprint

Shin, J. D., Tang, W., & Jadhav, S. P. (2019) · SSRN Electronic Journal · doi:10.2139/ssrn.3385138 · Cited by 4

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

Park, E. H., 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. (2024) · eLife · doi:10.7554/elife.104475 · Cited by 4

Supramammillary Theta Oscillations in Water Maze Learning

Young, C. K., Ruan, M., & McNaughton, N. (2024) · Hippocampus · doi:10.1002/hipo.23646 · Cited by 2

Nonspecific ensemble reactivation in mouse dentate gyrus disrupts spatial working memory

Wilmerding, L. K., Kondratyev, I., Shi, W. B., Ramirez, S., & Hasselmo, M. E. (2025) · iScience · doi:10.1016/j.isci.2025.113566 · Cited by 2

From stress to Alzheimer’s: A circuit-based framework for prefrontal cognitive dysfunction

Yi, J. H. (2025) · Neuroscience Letters · doi:10.1016/j.neulet.2025.138424 · Cited by 3

Molecular hydrogen-mediated SIRT1 activation alleviates sepsis-associated encephalopathy by promoting mitophagy

Liu, J., Meng, S., Wang, Z., Fan, Y., Pei, S., Cui, J., Liu, J., Song, Y., Huang, X., Li, X., et al. (2025) · European journal of medical research · doi:10.1186/s40001-025-03600-5 · Cited by 2

Stimulation of Ca 2+ channel Ca V 1.2 activity by dopamine signaling augments spatial working memory

Man, K. N. M., Rougé, S. L. S., Berumen, R. A., Jacobi, A. A., Weiner, J. C., Naderi, S. Y., Ireton, K. E., Estrada‐Tobar, Z. M., Zeng, Z., Martinez, J. M., et al. (2025) · Science Signaling · doi:10.1126/scisignal.adp7760 · Cited by 3

Fornix subdivisions and spatial learning: a diffusion MRI study

Hodgetts, C. J., Postans, M., Williams, A. N., Graham, K. S., & Lawrence, A. D. (2025) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2025.109350 · Cited by 2

The pairwise phase consistency in cortical network and its relationship with neuronal activation

Wang, D., & Sun, Y. (2017) · BIO Web of Conferences · doi:10.1051/bioconf/20170802006 · Cited by 2

Neuroimaging Studies of Effects of Psychotherapy in Depression

Bauer, I. E., & Meyer, T. D. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.021 · Cited by 2

Sustained Hippocampal Neural Plasticity Questions the Reproducibility of an Amyloid-β-Induced Alzheimer’s Disease Model

Paulo, S. L., Ribeiro‐Rodrigues, L., Rodrigues, R. S., Mateus, J. M., Fonseca‐Gomes, J., Soares, R., Diógenes, M. J., Solá, S., Sebastião, A. M., Ribeiro, F. F., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201567 · Cited by 2

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

Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry

Park, A. J. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1091082 · Cited by 3

Neurodevelopment effects of early life bisphenol-A exposure on visual memory: Insights into recovery dynamics

Zhang, W., Zhang, L., Liang, W., Wang, H., & Hu, F. (2023) · Toxicology · doi:10.1016/j.tox.2023.153718 · Cited by 2

Acute optogenetic induction of the prodromal endophenotype of CA1 hyperactivity causes schizophrenia-related deficits in cognition and salience attribution

Kapanaiah, S. K. T., Grimm, C., & Kätzel, D. (2024) · Schizophrenia · doi:10.1038/s41537-024-00513-w · Cited by 2

Gene Deficiency of δ Subunit-Containing GABAA Receptor in mPFC Lead Learning and Memory Impairment in Mice

Cong, L., Zhang, T., Zhang, T., Liu, Y., Li, Y., Pang, X., Zhao, L., Wu, T., Ding, S., Liu, Y., et al. (2025) · Neurochemical Research · doi:10.1007/s11064-024-04320-8 · Cited by 2

An ace in the hole? Opportunities and limits of using mice to understand schizophrenia neurobiology

Villarin, J. M., & Kellendonk, C. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03060-7 · Cited by 2

Employing Optogenetics in Memory Research

Regev, L., & Goshen, I. (2017) · Neuromethods · doi:10.1007/978-1-4939-7417-7_12 · Cited by 1

The Adenosine Receptor: A Homeostatic Neuromodulator for Fine-Tuning Control of Cognition

Chen, J. (2018) · Springer eBooks · doi:10.1007/978-3-319-90808-3_15 · Cited by 2

Electrophysiological Biomarkers for Mood Disorders

Ramakrishnan, N., Murphy, N., Selvaraj, S., & Cho, R. Y. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.015 · Cited by 2

The antioxidative effect of esculin on lead acetate-induced neurotoxicity in the hippocampus and cortex of C57BL/6 mice

Sumathi, T., Murugan, A., Rajavel, S., & IPerumal, S. S. (2023) · International Journal of Pharmaceutical Sciences and Drug Research · doi:10.25004/ijpsdr.2023.150401 · Cited by 2

The “psychiatric” neuron: the psychic neuron of the cerebral cortex, revisited

Flynn, L. T., Bouras, N. N., Migovich, V. M., Clarin, J. D., & Gao, W. (2024) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2024.1356674 · Cited by 3

Modeling Oscillatory Phase and Phase Synchronization With Neuronal Excitation and Input Strength in Cortical Network

Wang, D., Sun, Y., Wang, F., & Li, J. (2018) · IEEE Access · doi:10.1109/access.2018.2845301 · Cited by 2

Maladaptive learning and the amygdala—prefrontal circuit

Likhtik, E., & Paz, R. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813983-7.00021-5 · Cited by 2

Microglia inhibition rescues developmental hypofrontality in a mouse model of mental illnessPreprint

Chini, M., Lindemann, C., Pöpplau, J. A., Xu, X., Ahlbeck, J., Bitzenhofer, S. H., Mulert, C., & Hanganu‐Opatz, I. L. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/254656 · Cited by 2

Beta2 oscillations in the hippocampal-cortical novelty detection circuitPreprint

França, A. S. C., Borgesius, N. Z., Souza, B. C., & Cohen, M. X. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.15.151969 · Cited by 2

Control of Parallel Hippocampal Output Pathways by Amygdalar Long-Range InhibitionPreprint

AlSubaie, R., Wee, R. W. S., Ritoux, A., Mishchanchuk, K., Passlack, J., Regester, D., & MacAskill, A. F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.08.434367 · Cited by 2

Using synchronized brain rhythms to bias memory-guided decisionsPreprint

Stout, J. J., George, A. E., Kim, S., Hallock, H. L., & Griffin, A. L. (2024) · eLife · doi:10.7554/elife.92033.2 · Cited by 1

SIV infection induces alterations in gene expression and loss of interneurons in Rhesus Macaque frontal cortex during early systemic infection

Crist, R. C., Chehimi, S. N., Divakaran, S. S., Montague, M. J., Tremblay, S., Snyder‐Mackler, N., Bohlen, M. O., Chiou, K. L., Zintel, T. M., Brent, L. J. N., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03261-2 · Cited by 2

Mechanism insight into selenium-rich tea mediates the neuroprotective effect on the treatment of Alzheimer’s disease

He, Z., Li, X., Cao, Y., Wang, Z., Liu, Y., Ye, Y., Luo, C., Qiao, Y., Du, X., Ni, J., et al. (2025) · Food Science and Human Wellness · doi:10.26599/fshw.2025.9250635 · Cited by 1

Projections from prefrontal cortex to dorsal hippocampus mediate lipopolysaccharide induced recognition memory deficits in mice

Zhao, X.-Y., Han, J. Y., Cheng, X.-Y., Gan, Z.-H., Wang, S.-J., Song, Y., Hao, J., Sun, N., Tong, K., & Gao, C. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110716 · Cited by 1

Social hierarchy modulates cognitive flexibility through basal forebrain-prefrontal cholinergic projections

Wu, J., Luo, Z.-C., Xiong, N., Gan, C., & Chen, W. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.124052 · Cited by 1

Cannabinoid type 1 receptors in the mice prefrontal cortex regulate object location memory acquisition via GABAergic neurons

Tokutake, T., Yokose, J., Yano, Y., Shigetsura, Y., Muramatsu, S., & Nitta, A. (2025) · Behavioral and Brain Functions · doi:10.1186/s12993-025-00306-w · Cited by 1

Prefrontal Default Mode Network Interactions with Posterior Hippocampus during Exploration

Papale, A. E., Brown, V. M., Ianni, A. M., Hallquist, M. N., Luna, B., & Dombrovski, A. Y. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0399-25.2025 · Cited by 2

Cognitive stimulation exerts long-lasting protective effects on the hippocampal vasculature and memory function in a rat model of vascular cognitive impairment

Chapman, A. C., Thaqi, A., Kalish, R. L., Deng, B., DeMarco, G. M., Shehryar, A., Baumoel, E. J., Bergson, P., & Papavangjeli, S. (2025) · npj Aging · doi:10.1038/s41514-025-00304-2 · Cited by 1

Developmental Selective GSK3α Inhibition Rescues Working Memory Deficits in a Mouse Model of Schizophrenia Predisposition

Passecker, J., Aloimonos, C. M., Dagunts, A., Wagner, F. F., Kupferschmidt, D. A., Gogos, J. A., & Gordon, J. A. (2025) · Complex Psychiatry · doi:10.1159/000547800 · Cited by 1

Developmental embedding of parvalbumin-positive interneurons drives local and crosshemispheric prefrontal gamma synchrony

Offermanns, A., Pöpplau, J. A., & Hanganu‐Opatz, I. L. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102866 · Cited by 2

Cognitive training shapes brain plasticity and schematic representations

Chen, W., & Hao, Y. (2025) · Behavioral and Brain Functions · doi:10.1186/s12993-025-00300-2 · Cited by 3

Discrete Circuits of the Ventral Hippocampus in Threat‐Based Learning and Memory

Dong, T. N., & Clem, R. L. (2026) · Hippocampus · doi:10.1002/hipo.70059 · Cited by 1

Altered thalamo–prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition

Hupalo, S., Kupferschmidt, D. A., Ikegami, A., Railing, M., Myroshnychenko, M., Loewinger, G., Pereira, F., Gogos, J. A., & Gordon, J. A. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02532-w · Cited by 1

Cerebellar iTBS ameliorates post-stroke cognitive impairment via the dentate nucleus-ventromedial thalamus pathway

Pan, Y., Huai, Y., Lv, Y., Liang, Y., Li, Q., Zou, Y., Zhong, Z., Gong, J., & Wang, X. (2026) · Brain Research · doi:10.1016/j.brainres.2026.150190 · Cited by 1

Default mode network connectivity is associated with executive and language performance in mild cognitive impairment

Nasiri, H., Mohammadtaheri, B., KHOSRAVI, F., Ghadiminia, N., Saberian, P., Mohammadian, M., Shakeri, S., Hendudari, F., Rood, Y. K. S., Hassanpoor, A., et al. (2026) · Neuroscience Letters · doi:10.1016/j.neulet.2026.138545 · Cited by 1

Facilitating Thought Progression: A Neurocognitive Framework Linking Thought Dynamics and Mood Disorders

Bar, M., & Baror, S. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.04.018 · Cited by 1

Prefrontal spine loss in neuropsychiatric disorders: circuit consequences for cognition

Bitzenhofer, S. H., & Günther, A. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1730869 · Cited by 1

Essential role of VGLUT2-negative claustro-prefrontal projections in working memory

Tan, J. Y., Chong, H. R., Ho, M. Z. H., Ouyang, X., Ramesh, P., Graf, M., Augustine, G. J., & Kamigaki, T. (2026) · Current Biology · doi:10.1016/j.cub.2026.04.067 · Cited by 1

Divergent transcriptomic pathways underlie sex-biased cognitive rescue by developmental GSK3B inhibition in a mouse model of 22q11.2 deletion syndrome

Passecker, J., Chang, C., Dagunts, A., Aloimonos, C. M., Leitner, L., Petryk, A., Wagner, F. F., Myroshnychenko, M., Kupferschmidt, D. A., Gogos, J. A., et al. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-04108-0 · Cited by 1

Adolescent exposure to the psychedelic 25C-NBOMe in rats induces lasting competitive avoidance through disrupted hippocampal–prefrontal synchrony

Yu, Z.-P., Zhang, Z.-Y., Li, Q., Hu, Y., Zhang, T., Zhang, X., Wang, Z.-C., Zhou, W.-H., & Shen, H. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02369-y · Cited by 1

Mapping prefrontal afferents along development

Günther, A., Stelzer, M., Franzelin, A., Marquardt, A., Oertner, T. G., Hanganu‐Opatz, I. L., & Pöpplau, J. A. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1861524 · Cited by 1

Thalamofrontal synaptic weakening underlies short-term memory deficits from adolescent NMDAR hypofunction

Yu, J., Choi, I. S., Kim, G. H., Bahn, S.-K., Kim, J., Bae, S., Lee, T., Choi, J. H., Kwon, J. S., Kim, M., et al. (2026) · Science Advances · doi:10.1126/sciadv.aee2152 · Cited by 1

Many heads are better than one: A multiscale neural information feature fusion framework for spatial route selections decoding from multichannel neural recordings of pigeons

Li, M., Cheng, S., Fan, J., Shang, Z., & Wan, H. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.03.007 · Cited by 2

Tertiary damage: Hippocampal and brain changes after spinal cord injury

Jure, I., & Labombarda, F. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822427-4.00023-x · Cited by 1

Limited evidence of a shared genetic relationship between C-reactive protein levels and cognitive function in older UK adults of European ancestry

Packer, A. E., Corbett, A., Arathimos, R., Ballard, C. G., Aarsland, D., Hampshire, A., Dima, D., Creese, B., Malanchini, M., & Powell, T. R. (2023) · Frontiers in Dementia · doi:10.3389/frdem.2023.1093223 · Cited by 1

Navigation Through the Complex World: The Neurophysiology of Decision-Making Processes

Mugan, U., Amemiya, S., Regier, P. S., & Redish, A. D. (2024) · Springer eBooks · doi:10.1007/978-3-031-55889-4_6 · Cited by 2

PD-1 deficiency disrupts in vivo neural activity in mouse Hippocampus and cortex

Hu, M., Lv, C., Zhu, J., Zhang, H., Wang, X., You, L., Xie, J., Liu, W., Wei, X., Chen, K., et al. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107002 · Cited by 2

Regulation of working memory switches from striatal dopamine D2-receptor to D1-receptor neurons under high cognitive load

Chen, X., Li, F. Y., Zhao, X., Chen, L., Xue, J., Yao, Z., Gan, Z., Lian, X., Liu, Z., Tong, L., et al. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003289 · Cited by 1

Brainwide hemodynamics predict EEG neural rhythms across sleep and wakefulness in humans

Jacob, L. P. L., Bailes, S. M., Williams, S. D., Stringer, C., & Lewis, L. D. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013497 · Cited by 3

Acute ethanol enhances septohippocampal coordination but disrupts intrinsic hippocampal theta dynamics during foraging

Darden, C. B., Marks, M. D., & Kesner, A. J. (2025) · Alcohol · doi:10.1016/j.alcohol.2025.11.001 · Cited by 1

Brain Imaging and the Mechanisms of Antidepressant Action

Godlewska, B. R., Selvaraj, S., & Cowen, P. J. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.020 · Cited by 1

Effects of Lithium on Brain Structure in Bipolar Disorder

Kaur, J., Kafantaris, V., & Szeszko, P. R. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.018 · Cited by 1

Functional Connectome in Bipolar Disorder

Cha, J., & Anand, A. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.008 · Cited by 1

Deriving mechanistic insights from machine learning and its possible implications in non-invasive brain stimulation research

Shukla, S., & Thirugnanasambandam, N. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.06.013 · Cited by 1

Evaluating the Therapeutic Effect of an Hsp90 Inhibitor in Mouse Models of Alzheimer’s Disease

Wang, B. (2016) · doi:10.21007/etd.cghs.2016.0412 · Cited by 1

MOLECULAR CORRELATE OF MOUSE EXECUTIVE FUNCTION. TOP-DOWN AND BOTTOM-UP COMPLEMENTATIONS BY PRESYNAPTIC VERTEBRATE BRAIN-SPECIFIC Ntng GENE PARALOGSPreprint

Prosselkov, P., Zhang, Q., Goto, H., Polygalov, D., McHugh, T. J., & Itohara, S. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/139444 · Cited by 1

Cerebellar Purkinje cell simple spike activity in awake mice represents phase differences between oscillations in medial prefrontal cortex and hippocampusPreprint

McAfee, S. S., Liu, Y., Sillitoe, R. V., & Heck, D. H. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/173849 · Cited by 1

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

Oscillation-driven memory encoding, maintenance and recall in an entorhinal-hippocampal circuit modelPreprint

Kurikawa, T., Mizuseki, K., & Fukai, T. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/804062 · Cited by 1

Behaviorally emergent hippocampal place maps remain stable during memory recallPreprint

Zemla, R., Moore, J. J., & Basu, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.08.451449 · 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

Simultaneous transcranial electrical and magnetic stimulation boost gamma oscillations in the dorsolateral prefrontal cortexPreprint

Maiella, M., Casula, E. P., Borghi, I., Assogna, M., D’Acunto, A., Pezzopane, V., Mencarelli, L., Pellicciari, M. C., & Koch, G. (2022) · Research Square · doi:10.21203/rs.3.rs-1550621/v1 · Cited by 1

A persistent prefrontal reference frame across time and task rulesPreprint

Muysers, H., Chen, H.-L., Sauer, J., & Bartos, M. (2022) · Research Square · doi:10.21203/rs.3.rs-1803838/v1 · Cited by 1

Oligodendrocyte dynamics dictate individual performance outcomes of working memory training in micePreprint

Shimizu, T., Nayar, S. G., Swire, M., Jiang, Y., Grist, M., Kaller, M. S., Sampaio‐Baptista, C., Bannerman, D. M., Johansen‐Berg, H., Ogasawara, K., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.17.524381 · Cited by 1

Using synchronized brain rhythms to bias memory-guided decisionsPreprint

Stout, J. J., George, A. E., Kim, S., Hallock, H. L., & Griffin, A. L. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.02.535279 · 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

Systematic characterization of a non-transgenic A β 1–42 amyloidosis model: synaptic plasticity and memory deficits in female and male micePreprint

Jiménez‐Herrera, R., Contreras, A., Iborra‐Lázaro, G., Jeremic, D., Djebari, S., Navarro‐López, J. D., & Jiménez‐Díaz, L. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.09.539973 · Cited by 1

Using synchronized brain rhythms to bias memory-guided decisionsPreprint

Stout, J. J., George, A. E., Kim, S., Hallock, H. L., & Griffin, A. L. (2023) · eLife · doi:10.7554/elife.92033.1 · Cited by 1

Population analyses reveal heterogenous encoding in the medial prefrontal cortex during naturalistic foragingPreprint

Jeong, J. H., & Choi, J.-S. (2024) · eLife · doi:10.7554/elife.93994 · Cited by 1

Distinct contributions of the dorsal and ventral hippocampus to spatial working memory and spatial coding in the prefrontal cortexPreprint

Babl, S. S., & Sigurdsson, T. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.16.607133 · Cited by 1

Prefrontal representations of retrospective spatial working memory in a rodent radial maze taskPreprint

Taliaferro, J. P., Posani, L., Greenwald, J. E., Lim, S. C., McGowan, J. C., Pekarskaya, E. A., Lacefield, C., Fusi, S., & Kellendonk, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.10.617655 · Cited by 1

Population analyses reveal heterogenous encoding in the medial prefrontal cortex during naturalistic foragingPreprint

Jeong, J. H., & Choi, J.-S. (2025) · eLife · doi:10.7554/elife.93994.2 · Cited by 1

Intrinsic cellular persistent firing sustains hippocampal spatial representations during working memory

Sabermarouf, B., Reboreda, A., Theissen, F., Kaushik, R., Sauvage, M. M., Dityatev, A. E., & Yoshida, M. (2026) · Science Advances · doi:10.1101/2025.06.27.661493 · Cited by 1

Impaired Spatiotemporal Encoding of Social Behavior and Anxiety in the Prefrontal Cortex of Mice Lacking ASD-Risk Gene Shank3Preprint

Walker, H., Kwak, D., Devaraju, P., Curd, B. C., Chikuni, A. M., & Frost, N. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.15.664892 · Cited by 1

Activity-induced weakening of hippocampal input to prefrontal VIP interneurons reshapes inhibitory microcircuit function: implications for spatial working memory task acquisitionPreprint

Silverstein, S. E., Clarity, T. T., Deshpande, M. S., Vaughan, E., Novik, S., Yarur, H. E., Zhang, S., Tsai, V. S., Ye, R., Mikofsky, R. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.21.665987 · 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

Hippocampus-reuniens beta coupling supports goal-directed spatial navigationPreprint

Baumann, T., Mei, H., & Eschenko, O. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.20.726518 · Cited by 2

Task learning reveals neural signatures of internal models in rodent prefrontal cortexPreprint

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