Integrating time from experience in the lateral entorhinal cortex

LIBLINEAR: A Library for Large Linear Classification

Fan, R.-E., Chang, K., Hsieh, C., Xiang-rui, W., & Lin, C. (2008) · doi:10.5555/1390681.1442794 · Cited by 6,684

On the Surprising Behavior of Distance Metrics in High Dimensional Space

Aggarwal, C. C., Hinneburg, A., & Keim, D. A. (2001) · Lecture notes in computer science · doi:10.1007/3-540-44503-x_27 · Cited by 2,179

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

Episodic-like memory during cache recovery by scrub jays

Clayton, N. S., & Dickinson, A. (1998) · Nature · doi:10.1038/26216 · Cited by 1,464

Internally Generated Cell Assembly Sequences in the Rat Hippocampus

Pastalkova, E., Itskov, V., Amarasingham, A., & Buzsáki, G. (2008) · Science · doi:10.1126/science.1159775 · Cited by 1,301

Deconstructing episodic memory with construction

Hassabis, D., & Maguire, E. A. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.001 · Cited by 1,229

Hippocampal ‘time cells’ bridge the gap in memory for discontiguous events

MacDonald, C. J., Lepage, K. Q., Eden, U. T., & Eichenbaum, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.012 · Cited by 1,193

A Distributed Representation of Temporal Context

Howard, M. W., & Kahana, M. J. (2002) · Journal of Mathematical Psychology · doi:10.1006/jmps.2001.1388 · Cited by 1,174

Long-term dynamics of CA1 hippocampal place codes

Ziv, Y., Burns, L. D., Cocker, E. D., Hamel, E. O., Ghosh, K. K., Kitch, L. J., Gamal, A. E., & Schnitzer, M. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3329 · Cited by 1,155

Hippocampal Neurons Encode Information about Different Types of Memory Episodes Occurring in the Same Location

Wood, E. R., Dudchenko, P. A., Robitsek, R. J., & Eichenbaum, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)00071-4 · Cited by 992

Inactivation of the Medial Entorhinal Cortex Selectively Disrupts Learning of Interval Timing

Heys, J. G., Wu, Z.-H., Mascaro, A. L. A., & Dombeck, D. A. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108163 · Cited by 36

Neural circuits and symbolic processing

Do, Q. H., & Hasselmo, M. E. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107552 · Cited by 38

Entorhinal cortex–hippocampal circuit connectivity in health and disease

Hernández‐Frausto, M., & Vivar, C. (2024) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2024.1448791 · Cited by 41

Neural circuits for goal-directed navigation across species

Basu, J., & Nagel, K. I. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.09.005 · Cited by 35

Content-based Dissociation of Hippocampal Involvement in Prediction

Kok, P., Rait, L. I., & Turk‐Browne, N. B. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01509 · Cited by 34

Links between autobiographical memory richness and temporal discounting in older adults

Lempert, K. M., MacNear, K. A., Wolk, D. A., & Kable, J. W. (2020) · Scientific Reports · doi:10.1038/s41598-020-63373-1 · Cited by 35

Time as the fourth dimension in the hippocampus

Banquet, J. P., Gaussier, P., Cuperlier, N., Hok, V., Save, É., Poucet, B., Quoy, M., & Wiener, S. I. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101920 · Cited by 33

Focusing on what matters: Modulation of the human hippocampus by relational attention

Córdova, N. I., Turk‐Browne, N. B., & Aly, M. (2019) · Hippocampus · doi:10.1002/hipo.23082 · Cited by 34

The learning of prospective and retrospective cognitive maps within neural circuits

Namboodiri, V. M. K., & Stuber, G. D. (2021) · Neuron · doi:10.1016/j.neuron.2021.09.034 · Cited by 32

Mental navigation in the primate entorhinal cortex

Neupane, S., Fiete, I., & Jazayeri, M. (2024) · Nature · doi:10.1038/s41586-024-07557-z · Cited by 36

Anterior cingulate cortex provides the neural substrates for feedback-driven iteration of decision and value representation

Chen, W., Liang, J., Wu, Q., & Han, Y. (2024) · Nature Communications · doi:10.1038/s41467-024-50388-9 · Cited by 32

Event structure sculpts neural population dynamics in the lateral entorhinal cortex

Kanter, B. R., Lykken, C. M., Polti, I., Moser, M., & Moser, E. I. (2025) · Science · doi:10.1126/science.adr0927 · Cited by 30

Grid coding, spatial representation, and navigation: Should we assume an isomorphism?

Ekstrom, A. D., Harootonian, S. K., & Huffman, D. J. (2019) · Hippocampus · doi:10.1002/hipo.23175 · Cited by 32

The thermodynamics of cognition: A mathematical treatment

Déli, É., Peters, J. F., & Kisvárday, Z. F. (2021) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2021.01.008 · Cited by 32

Local projections of layer Vb-to-Va are more prominent in lateral than in medial entorhinal cortex

Ohara, S., Blankvoort, S., Nair, R. R., Nigro, M. J., Nilssen, E. S., Kentros, C. G., & Witter, M. P. (2021) · eLife · doi:10.7554/elife.67262 · Cited by 31

Signatures of life course socioeconomic conditions in brain anatomy

Loued‐Khenissi, L., Trofimova, O., Vollenweider, P., Marques-Vidal, P. M., Preisig, M., Lutti, A., Kliegel, M., Sandi, C., Kherif, F., Stringhini, S., et al. (2022) · Human Brain Mapping · doi:10.1002/hbm.25807 · Cited by 30

Altered alpha and theta oscillations correlate with sequential working memory in Parkinson’s disease

Ye, Z., Heldmann, M., Herrmann, L., Brüggemann, N., & Münte, T. F. (2022) · Brain Communications · doi:10.1093/braincomms/fcac096 · Cited by 29

Distal tuft dendrites predict properties of new hippocampal place fields

O’Hare, J. K., Wang, J., Shala, M. D., Polleux, F., & Losonczy, A. (2024) · Neuron · doi:10.1016/j.neuron.2025.03.029 · Cited by 28

Acquisition of temporal order requires an intact CA3 commissural/associational (C/A) feedback system in mice

Cox, B. M., Cox, C. D., Gunn, B. G., Le, A. A., Inshishian, V. C., Gall, C. M., & LYNCH, G. S. (2019) · Communications Biology · doi:10.1038/s42003-019-0494-3 · Cited by 30

Distinct Patterns of Hippocampal and Neocortical Evolution in Primates

Vanier, D. R., Sherwood, C. C., & Smaers, J. B. (2019) · Brain Behavior and Evolution · doi:10.1159/000500625 · Cited by 29

Object and object‐memory representations across the proximodistal axis of CA1

Vandrey, B., Duncan, S., & Ainge, J. A. (2021) · Hippocampus · doi:10.1002/hipo.23331 · Cited by 28

The fasciola cinereum subregion of the hippocampus is important for the acquisition of visual contextual memory

Park, S., Lim, H., Lee, E., Yoo, S.-W., Jung, H.-S., Lee, E., Sun, W., & Lee, I. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102217 · Cited by 29

Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales

Zou, F., Guo, W., Allen, E., Wu, Y., Charest, I., Naselaris, T., Kay, K., Kuhl, B. A., Hutchinson, J. B., & DuBrow, S. (2023) · Nature Communications · doi:10.1038/s41467-023-40100-8 · Cited by 29

Time, space, memory and brain–body rhythms

Buzsáki, G. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00987-2 · Cited by 32

In a Temporally Segmented Experience Hippocampal Neurons Represent Temporally Drifting Context But Not Discrete Segments

Bladon, J. H., Sheehan, D. J., Freitas, C. S. D., & Howard, M. W. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1420-18.2019 · Cited by 27

Neural encoding of time in the animal brain

Tallot, L., & Doyère, V. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.12.033 · Cited by 34

Sequence chunking through neural encoding of ordinal positions

Ding, N. (2025) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2025.01.014 · Cited by 29

Keeping time and rhythm by internal simulation of sensory stimuli and behavioral actions

de Lafuente, V., Jazayeri, M., Merchant, H., García‐Garibay, O., Cadena-Valencia, J., & Malagón, A. M. (2024) · Science Advances · doi:10.1126/sciadv.adh8185 · Cited by 26

OCT parameters of the optic nerve head and the retina as surrogate markers of brain volume in a normal population, a pilot study

Mejia-Vergara, A. J., Karanjia, R., & Sadun, A. A. (2020) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2020.117213 · Cited by 27

Multiplexing working memory and time in the trajectories of neural networks

Zhou, S., Seay, M. J., Taxidis, J., Golshani, P., & Buonomano, D. V. (2023) · Nature Human Behaviour · doi:10.1038/s41562-023-01592-y · Cited by 26

Sharpening the blades of the dentate gyrus: how adult‐born neurons differentially modulate diverse aspects of hippocampal learning and memory

Berdugo‐Vega, G., Dhingra, S., & Calegari, F. (2023) · The EMBO Journal · doi:10.15252/embj.2023113524 · Cited by 29

Integration and competition between space and time in the hippocampus

Chen, S., Cheng, N., Chen, X., & Wang, C. (2024) · Neuron · doi:10.1016/j.neuron.2024.08.007 · Cited by 25

A unified neurocomputational model of prospective and retrospective timing.

de Jong, J., Voelker, A. R., Stewart, T. C., Akyürek, E. G., Eliasmith, C., & van Rijn, H. (2025) · Psychological Review · doi:10.1037/rev0000519 · Cited by 26

Hippocampal Contribution to Ordinal Psychological Time in the Human Brain

Gauthier, B., Prabhu, P., Karunakar, A. K., & van Wassenhove, V. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01586 · Cited by 28

Distinct cortical systems reinstate the content and context of episodic memories

Kragel, J. E., Ezzyat, Y., Lega, B. C., Sperling, M. R., Worrell, G. A., Gross, R. E., Jobst, B. C., Sheth, S. A., Zaghloul, K. A., Stein, J. M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24393-1 · Cited by 29

Hippocampal-Medial Prefrontal Event Segmentation and Integration Contribute to Episodic Memory Formation

Liu, W., Shi, Y., Cousins, J. N., Kohn, N., & Fernández, G. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab258 · Cited by 28

A novel parallel merge neural network with streams of spiking neural network and artificial neural network

Yang, J., & Zhao, J. (2023) · Information Sciences · doi:10.1016/j.ins.2023.119034 · Cited by 25

A neural code for time and space in the human brain

Schonhaut, D. R., Aghajan, Z. M., Kahana, M. J., & Fried, I. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113238 · Cited by 25

Neuronal ensembles in memory processes

Carrillo‐Reid, L. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.04.004 · Cited by 28

Fan cells in lateral entorhinal cortex directly influence medial entorhinal cortex through synaptic connections in layer 1

Vandrey, B., Armstrong, J., Brown, C. M., Garden, D. L. F., & Nolan, M. F. (2022) · eLife · doi:10.7554/elife.83008 · Cited by 28

The spatiotemporal organization of episodic memory and its disruption in a neurodevelopmental disorder

Mastrogiuseppe, M., Bertelsen, N., Bedeschi, M. F., & Lee, S. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-53823-w · Cited by 29

Minute-encoding neurons in hippocampal-striatal circuits

Shikano, Y., Ikegaya, Y., & Sasaki, T. (2021) · Current Biology · doi:10.1016/j.cub.2021.01.032 · Cited by 24

Concept and location neurons in the human brain provide the ‘what’ and ‘where’ in memory formation

Mackay, S., Reber, T. P., Bausch, M., Boström, J. P., Elger, C. E., & Mormann, F. (2024) · Nature Communications · doi:10.1038/s41467-024-52295-5 · Cited by 27

A whole-brain single-cell atlas of circadian neural activity in mice

Yamashita, K., Kinoshita, F. L., Yoshida, S., Matsumoto, K., Mitani, T. T., Fujishima, H., Minami, Y., Morii, E., Yamada, R. G., Okada, S., et al. (2025) · Science · doi:10.1126/science.aea3381 · Cited by 24

Laminar Organization of the Entorhinal Cortex in Macaque Monkeys Based on Cell-Type-Specific Markers and Connectivity

Ohara, S., Yoshino, R., Kimura, K., Kawamura, T., Tanabe, S., Zheng, A., Nakamura, S., Inoue, K., Takada, M., Tsutsui, K., et al. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.790116 · Cited by 23

Lateral entorhinal cortex lesions impair odor‐context associative memory in male rats

Persson, B. M., Ambrozova, V., Duncan, S., Wood, E. R., O’Connor, A. R., & Ainge, J. A. (2022) · Journal of Neuroscience Research · doi:10.1002/jnr.25027 · Cited by 27

Single voxel autocorrelation uncovers gradients of temporal dynamics in the hippocampus and entorhinal cortex during rest and navigation

Bouffard, N. R., Golestani, A., Brunec, I. K., Bellana, B., Park, J. Y., Barense, M. D., & Moscovitch, M. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac480 · Cited by 23

Persistent firing in LEC III neurons is differentially modulated by learning and aging

Lin, C., Sherathiya, V. N., Oh, M. M., & Disterhoft, J. F. (2020) · eLife · doi:10.7554/elife.56816 · Cited by 23

Modality-Specific Impairment of Hippocampal CA1 Neurons of Alzheimer’s Disease Model Mice

Takamura, R., Mizuta, K., Sekine, Y., Islam, T., Saito, T., Sato, M., Ohkura, M., Nakai, J., Ohshima, T., Saido, T. C., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0208-21.2021 · Cited by 24

Neural temporal context reinstatement of event structure during memory recall.

Lohnas, L. J., Healey, M. K., & Davachi, L. (2023) · Journal of Experimental Psychology General · doi:10.1037/xge0001354 · Cited by 25

Distinct Neural Representations of Content and Ordinal Structure in Auditory Sequence Memory

Fan, Y., Han, Q., Guo, S., & Luo, H. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0320-21.2021 · Cited by 22

Involvement of a lateral entorhinal cortex engram in episodic-like memory recall

Tozzi, F., Guglielmo, S., Paraciani, C., van den Oever, M. C., Mainardi, M., Cattaneo, A., & Origlia, N. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114795 · Cited by 24

Episodic memory: Mental time travel or a quantum “memory wave” function?

Manning, J. R. (2021) · Psychological Review · doi:10.1037/rev0000283 · Cited by 24

Evaluation of brain structure abnormalities in children with autism spectrum disorder (ASD) using structural magnetic resonance imaging

Khadem-Reza, Z. K., & Zare, H. (2022) · The Egyptian Journal of Neurology Psychiatry and Neurosurgery · doi:10.1186/s41983-022-00576-5 · Cited by 21

Obesity and muscle may have synergic effect more than independent effects on brain volume in community-based elderly

Lee, H., Seo, H. S., Kim, R. E. Y., Lee, S. K., Lee, Y. H., & Shin, C. (2020) · European Radiology · doi:10.1007/s00330-020-07407-2 · Cited by 21

Dissociable neural indices for time and space estimates during virtual distance reproduction

Robinson, E. M., & Wiener, M. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117607 · Cited by 22

Prefrontal and Medial Temporal Lobe Cortical Contributions to Visual Short-Term Memory

Wu, Z., & Buckley, M. J. (2022) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01937 · Cited by 17

Distinct spatial maps and multiple object codes in the lateral entorhinal cortex

Huang, X., Schlesiger, M. I., Barriuso-Ortega, I., Leibold, C., MacLaren, D. A. A., Bieber, N., & Monyer, H. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.020 · Cited by 20

Optogenetic reduction of theta oscillations induces remapping of time cells without memory impairment

Yong, H. C., Chang, H., & Brandon, M. P. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.118192 · Cited by 18

Structural connectivity-based segmentation of the human entorhinal cortex

Syversen, I. F., Witter, M. P., Kobro‐Flatmoen, A., Goa, P. E., Schröder, T. N., & Doeller, C. F. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118723 · Cited by 22

Developmental decrease of entorhinal-hippocampal communication in immune-challenged DISC1 knockdown mice

Xu, X., Song, L., Kringel, R., & Hanganu‐Opatz, I. L. (2021) · Nature Communications · doi:10.1038/s41467-021-27114-w · Cited by 20

Stimulation of an entorhinal-hippocampal extinction circuit facilitates fear extinction in a post-traumatic stress disorder model

Lin, Z.-J., Gu, X., Gong, W., Wang, M., Wu, Y., Wang, Q., Wu, X., Zhao, X.-Y., Zhu, M. X., Wang, L., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci181095 · Cited by 19

Memory-directed acupuncture as a neuromodulatory treatment for PTSD: Theory, clinical model and case studies

Assouline, A., Mendelsohn, A., & Reshef, A. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01876-3 · Cited by 20

Medial entorhinal cortex mediates learning of context-dependent interval timing behavior

Bigus, E. R., Lee, H., Bowler, J. C., Shi, J., & Heys, J. G. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01683-7 · Cited by 20

An immune molecule segregates memories in time

Terceros, A. A., & Rajasethupathy, P. (2022) · Nature · doi:10.1038/d41586-022-01166-4 · Cited by 18

A time-causal and time-recursive scale-covariant scale-space representation of temporal signals and past time

Lindeberg, T. (2023) · Biological Cybernetics · doi:10.1007/s00422-022-00953-6 · Cited by 17

Hippocampal orchestration of associative and sequential memory networks for episodic retrieval

Kim, J. S., & Lee, S. A. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112989 · Cited by 19

Competitive integration of time and reward explains value-sensitive foraging decisions and frontal cortex ramping dynamics

Bukwich, M., Campbell, M. G., Zoltowski, D. M., Kingsbury, L., Tomov, M. S., Stern, J., Kim, H. R., Drugowitsch, J., Linderman, S. W., & Uchida, N. (2025) · Neuron · doi:10.1016/j.neuron.2025.07.008 · Cited by 20

Prefrontal Neural Ensembles Develop Selective Code for Stimulus Associations within Minutes of Novel Experiences

Takehara‐Nishiuchi, K., Morrissey, M. D., & Pilkiw, M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1503-20.2020 · Cited by 20

The Human Medial Temporal Lobe Is Necessary for Remembering Durations within a Sequence of Events but Not Durations of Individual Events

Palombo, D. J., Reid, A. G., Thavabalasingam, S., Hunsberger, R., Lee, A. C. H., & Verfaellie, M. H. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01489 · Cited by 17

Contextual prediction errors reorganize naturalistic episodic memories in time

Yazin, F., Das, M., Banerjee, A., & Roy, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-90990-1 · Cited by 19

Superficial‐layer versus deep‐layer lateral entorhinal cortex: Coding of allocentric space, egocentric space, speed, boundaries, and corners

Wang, C., Lee, H., Rao, G., Yoganarasimha, D., Savelli, F., & Knierim, J. J. (2023) · Hippocampus · doi:10.1002/hipo.23528 · Cited by 18

Neural population clocks: Encoding time in dynamic patterns of neural activity.

Zhou, S., & Buonomano, D. V. (2022) · Behavioral Neuroscience · doi:10.1037/bne0000515 · Cited by 18

Episodic boundary cells in human medial temporal lobe during the free recall task

Yoo, H. B., Umbach, G. S., & Lega, B. C. (2022) · Hippocampus · doi:10.1002/hipo.23421 · Cited by 18

Probing the nature of episodic memory in rodents

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

Loss of functional heterogeneity along the CA3 transverse axis in aging

Lee, H., Wang, Z., Tillekeratne, A., Lukish, N., Puliyadi, V., Zeger, S. L., Gallagher, M., & Knierim, J. J. (2022) · Current Biology · doi:10.1016/j.cub.2022.04.077 · Cited by 15

Brain-wide genome-wide colocalization study for integrating genetics, transcriptomics and brain morphometry in Alzheimer's disease

Bao, J., Wen, J., Wen, Z., Yang, S., Cui, Y., Yang, Z., Erus, G., Saykin, A. J., Long, Q., Davatzikos, C. A., et al. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120346 · Cited by 15

Long-term, multi-event surprise correlates with enhanced autobiographical memory

Antony, J. W., Dam, J. V., Massey, J., Barnett, A. J., & Bennion, K. A. (2023) · Nature Human Behaviour · doi:10.1038/s41562-023-01631-8 · Cited by 15

Genetic and neural bases of the neuroticism general factor

Kim, Y., Saunders, G., Giannelis, A., Willoughby, E. A., DeYoung, C. G., & Lee, J. J. (2023) · Biological Psychology · doi:10.1016/j.biopsycho.2023.108692 · Cited by 15

Cognitive computation using neural representations of time and space in the Laplace domainPreprint

Howard, M. W., & Hasselmo, M. E. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2003.11668 · Cited by 19

Quantitative and histologically validated measures of the entorhinal subfields in ex vivo MRI

Oltmer, J., Slepneva, N., Rodríguez, J. L., Greve, D. N., Williams, E. M., Wang, R., Champion, S. N., Lang‐Orsini, M., Nestor, K., Fernandez-Ros, N., et al. (2022) · Brain Communications · doi:10.1093/braincomms/fcac074 · Cited by 14

Ramping cells in the rodent medial prefrontal cortex encode time to past and future events via real Laplace transform

Cao, R., Bright, I. M., & Howard, M. W. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2404169121 · Cited by 14

Neural population dynamics and temporal context cells in macaque medial parietal cortex support temporal order memory

Zuo, S., Wang, C., Wang, L., Jin, Z., Zhou, X., 苏宁, Liu, J., McHugh, T. J., Kusunoki, M., & Kwok, S. C. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003759 · Cited by 14

Time Reproduction Deficits at Young Adult Follow-Up in Childhood ADHD: The Role of Persistence of Disorder and Executive Functioning

Barkley, R. A., & Fischer, M. (2018) · Developmental Neuropsychology · doi:10.1080/87565641.2018.1541992 · Cited by 14

The anatomy and function of the postrhinal cortex.

Estela-Pro, V. J., & Burwell, R. D. (2021) · Behavioral Neuroscience · doi:10.1037/bne0000500 · Cited by 16

Untethered firing fields and intermittent silences: Why grid‐cell discharge is so variable

Nagele, J., Herz, A. V. M., & Stemmler, M. (2020) · Hippocampus · doi:10.1002/hipo.23191 · Cited by 14

“A compressed representation of spatial distance in the rodent hippocampus’’

Sheehan, D. J., Charczynski, S., Fordyce, B. A., Hasselmo, M. E., & Howard, M. W. (2021) · doi:10.1101/2021.02.15.431306 · Cited by 13

Rat hippocampal CA1 region represents learning-related action and reward events with shorter latency than the lateral entorhinal cortex

Soma, S., Ohara, S., Nonomura, S., Suematsu, N., Yoshida, J., Pastalkova, E., Sakai, Y., Tsutsui, K., & Isomura, Y. (2023) · Communications Biology · doi:10.1038/s42003-023-04958-0 · Cited by 13

Tell me why: the missing w in episodic memory’s what, where, and when

Morales-Calva, F., & Leal, S. L. (2024) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-024-01234-4 · Cited by 16

Evidence Accumulation in a Laplace Domain Decision Space

Howard, M. W., Luzardo, A., & Tiganj, Z. (2018) · Computational Brain & Behavior · doi:10.1007/s42113-018-0016-2 · Cited by 13

Discounting future reward in an uncertain world.

Story, G. W., Kurth-Nelson, Z. L., Moutoussis, M., Iigaya, K., Will, G., Hauser, T. U., Blain, B., Vlaev, I., & Dolan, R. J. (2023) · Decision · doi:10.1037/dec0000219 · Cited by 17

Improving sensory representations using episodic memory

Görler, R., Wiskott, L., & Cheng, S. (2019) · Hippocampus · doi:10.1002/hipo.23186 · Cited by 13

Brain Macro-Structural Alterations in Aging Rats: A Longitudinal Lifetime Approach

Gull, S., Gaser, C., Herrmann, K., Urbach, A., Boehme, M., Afzal, S., Reichenbach, J. R., Witte, O. W., & Schmidt, S. (2023) · Cells · doi:10.3390/cells12030432 · Cited by 12

How Do You Build a Cognitive Map? The Development of Circuits and Computations for the Representation of Space in the Brain

Donato, F., Schwartzlose, A. X., & Mendes, R. A. V. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-090922-010618 · Cited by 14

Randomized controlled trials of non-pharmacological interventions for healthy seniors: Effects on cognitive decline, brain plasticity and activities of daily living—A 23-year scoping review

James, C. E., Müller, D., Müller, C. A. H., van de Looij, Y., ALTENMÜLLER, E. O., Kliegel, M., Ville, D. V. D., & Marié, D. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e26674 · Cited by 15

Context and space coding in mossy cell population activity

Huang, L.-W., Torelli, F., Chen, H.-L., & Bartos, M. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114386 · Cited by 12

Building and Breaking the Chain: A Model of Reward Prediction Error Integration and Segmentation of Memory

Rouhani, N., Clewett, D., & Antony, J. W. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02215 · Cited by 12

The influence of emotion on temporal context models

Lohnas, L. J., & Howard, M. W. (2024) · Cognition & Emotion · doi:10.1080/02699931.2024.2371075 · Cited by 14

Scene construction processes in the anterior hippocampus during temporal episodic memory retrieval

Hwang, M. J., & Lee, S. A. (2024) · Hippocampus · doi:10.1002/hipo.23624 · Cited by 12

Ramping dynamics in the frontal cortex unfold over multiple timescales during motor planning

Affan, R. O., Bright, I. M., Pemberton, L. N., Cruzado, N. A., Scott, B. B., & Howard, M. W. (2025) · Journal of Neurophysiology · doi:10.1152/jn.00234.2024 · Cited by 12

It’s about time

Whalley, K. (2018) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0066-4

Structuring time in the hippocampal-entorhinal system

Doeller, C. F. (2019)

Episodic time in the brain: A new world order

Buhusi, C. V. (2019) · Learning & Behavior · doi:10.3758/s13420-019-00379-4 · Cited by 8

Episodic memory: Neuronal codes for what, where, and when

Sugar, J., & Moser, M. (2019) · Hippocampus · doi:10.1002/hipo.23132 · Cited by 216

Human hippocampal and entorhinal neurons encode the temporal structure of experience

Tacikowski, P., Kalender, G., Ciliberti, D., & Fried, I. (2024) · Nature · doi:10.1038/s41586-024-07973-1 · Cited by 89