Major Dissociation Between Medial and Lateral Entorhinal Input to Dorsal Hippocampus

The Medial Temporal Lobe and Recognition Memory

Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580 · see citing works

Path integration and the neural basis of the 'cognitive map'

McNaughton, B. L., Battaglia, F. P., Jensen, O., Moser, E. I., & Moser, M.-B. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1932 · Cited by 2,024 · see citing works

Place Cells, Grid Cells, and the Brain's Spatial Representation System

Moser, E. I., Kropff, E., & Moser, M.-B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.061307.090723 · Cited by 1,934 · see citing works

Coordinated memory replay in the visual cortex and hippocampus during sleep

Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669 · see citing works

Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus

Leutgeb, J. K., Leutgeb, S., Moser, M.-B., & Moser, E. I. (2007) · Science · doi:10.1126/science.1135801 · Cited by 1,601 · see citing works

Conjunctive Representation of Position, Direction, and Velocity in Entorhinal Cortex

Sargolini, F., Fyhn, M., Hafting, T., McNaughton, B. L., Witter, M. P., Moser, M.-B., & Moser, E. I. (2006) · Science · doi:10.1126/science.1125572 · Cited by 1,485 · see citing works

The hippocampal CA2 region is essential for social memory

Hitti, F. L., & Siegelbaum, S. A. (2014) · Nature · doi:10.1038/nature13028 · Cited by 976 · see citing works

Mapping of a non-spatial dimension by the hippocampal-entorhinal circuit

Aronov, D., Nevers, R., & Tank, D. W. (2017) · Nature · doi:10.1038/nature21692 · Cited by 773 · see citing works

Early-onset behavioral and synaptic deficits in a mouse model of Alzheimer's disease

Jacobsen, J. S., Wu, C.-C., Redwine, J. M., Comery, T. A., Arias, R., Bowlby, M., Martone, R., Morrison, J. H., Pangalos, M. N., Reinhart, P. H., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600948103 · Cited by 701 · see citing works

Theta oscillations provide temporal windows for local circuit computation in the entorhinal-hippocampal loop

Mizuseki, K., Sirota, A., Pastalkova, E., & Buzsáki, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.037 · Cited by 718 · see citing works

Spatial representation in the hippocampal formation: a history

Moser, E. I., Moser, M.-B., & McNaughton, B. L. (2017) · Nature Neuroscience · doi:10.1038/nn.4653 · Cited by 560 · see citing works

Direct recordings of grid-like neuronal activity in human spatial navigation

Jacobs, J., Weidemann, C. T., Miller, J. F., Solway, A., Burke, J. F., Wei, X.-X., Suthana, N., Sperling, M. R., Sharan, A. D., Fried, I., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3466 · Cited by 564 · see citing works

Dendritic Inhibition in the Hippocampus Supports Fear Learning

Lovett-Barron, M., Kaifosh, P., Kheirbek, M. A., Danielson, N., Zaremba, J. D., Reardon, T. R., Turi, G. F., Hen, R., Zemelman, B. V., & Losonczy, A. (2014) · Science · doi:10.1126/science.1247485 · Cited by 509 · see citing works

Integrating time from experience in the lateral entorhinal cortex

Tsao, A., Sugar, J., Lu, L., Wang, C., Knierim, J. J., Moser, M.-B., & Moser, E. I. (2018) · Nature · doi:10.1038/s41586-018-0459-6 · Cited by 490 · see citing works

Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks

Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465 · see citing works

Functional correlates of the lateral and medial entorhinal cortex: objects, path integration and local-global reference frames

Knierim, J. J., Neunuebel, J. P., & Deshmukh, S. S. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0369 · Cited by 425 · see citing works

Network Analysis of Corticocortical Connections Reveals Ventral and Dorsal Processing Streams in Mouse Visual Cortex

Wang, Q., Sporns, O., & Burkhalter, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6063-11.2012 · Cited by 410 · see citing works

Influence of boundary removal on the spatial representations of the medial entorhinal cortex

Savelli, F., Yoganarasimha, D., & Knierim, J. J. (2008) · Hippocampus · doi:10.1002/hipo.20511 · Cited by 363 · see citing works

A unified framework for the functional organization of the medial temporal lobes and the phenomenology of episodic memory

Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375 · see citing works

The hippocampus and related neocortical structures in memory transformation

Sekeres, M. J., Winocur, G., & Moscovitch, M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.05.006 · Cited by 370 · see citing works

Towards a functional organization of episodic memory in the medial temporal lobe

Eichenbaum, H., Sauvage, M., Fortin, N., Komorowski, R., & Lipton, P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.07.006 · Cited by 354 · see citing works

Hippocampal CA2 activity patterns change over time to a larger extent than between spatial contexts

Mankin, E. A., Diehl, G. W., Sparks, F. T., Leutgeb, S., & Leutgeb, J. K. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.001 · Cited by 279 · see citing works

Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition

Basu, J., Zaremba, J. D., Cheung, S. K., Hitti, F. L., Zemelman, B. V., Losonczy, A., & Siegelbaum, S. A. (2016) · Science · doi:10.1126/science.aaa5694 · Cited by 274 · see citing works

Traces of experience in the lateral entorhinal cortex

Tsao, A., Moser, M.-B., & Moser, E. I. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.036 · Cited by 290 · see citing works

Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1

Danielson, N. B., Zaremba, J. D., Kaifosh, P., Bowler, J., Ladow, M., & Losonczy, A. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.020 · Cited by 288 · see citing works

Egocentric coding of external items in the lateral entorhinal cortex

Wang, C., Chen, X., Lee, H., Deshmukh, S. S., Yoganarasimha, D., Savelli, F., & Knierim, J. J. (2018) · Science · doi:10.1126/science.aau4940 · Cited by 276 · see citing works

Heterogeneity within classical cell types is the rule: lessons from hippocampal pyramidal neurons

Cembrowski, M. S., & Spruston, N. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0125-5 · Cited by 258 · see citing works

A neural-level model of spatial memory and imagery

Bicanski, A., & Burgess, N. (2018) · eLife · doi:10.7554/elife.33752 · Cited by 230 · see citing works

Hypothalamic and other connections with dorsal CA2 area of the mouse hippocampus

Cui, Z., Gerfen, C. R., & Young, W. S. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23263 · Cited by 214 · see citing works

Selective Vulnerability of Neurons in Layer II of the Entorhinal Cortex during Aging and Alzheimer's Disease

Stranahan, A. M., & Mattson, M. P. (2010) · Neural Plasticity · doi:10.1155/2010/108190 · Cited by 198 · see citing works

Medial entorhinal cortex lesions only partially disrupt hippocampal place cells and hippocampus-dependent place memory

Hales, J. B., Schlesiger, M. I., Leutgeb, J. K., Squire, L. R., Leutgeb, S., & Clark, R. E. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.009 · Cited by 204 · see citing works

Distinct roles of medial and lateral entorhinal cortex in spatial cognition

Van Cauter, T., Camon, J., Alvernhe, A., Elduayen, C., Sargolini, F., & Save, E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs033 · Cited by 196 · see citing works

Place cells are more strongly tied to landmarks in deep than in superficial CA1

Geiller, T., Fattahi, M., Choi, J.-S., & Royer, S. (2017) · Nature Communications · doi:10.1038/ncomms14531 · Cited by 163 · see citing works

A role for synaptic inputs at distal dendrites: instructive signals for hippocampal long-term plasticity

Dudman, J. T., Tsay, D., & Siegelbaum, S. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.020 · Cited by 192 · see citing works

The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties

Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works

Framing Spatial Cognition: Neural Representations of Proximal and Distal Frames of Reference and Their Roles in Navigation

Knierim, J. J., & Hamilton, D. A. (2011) · Physiological Reviews · doi:10.1152/physrev.00021.2010 · Cited by 148 · see citing works

Conflicts between local and global spatial frameworks dissociate neural representations of the lateral and medial entorhinal cortex

Neunuebel, J. P., Yoganarasimha, D., Rao, G., & Knierim, J. J. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0946-13.2013 · Cited by 126 · see citing works

Subcircuits of Deep and Superficial CA1 Place Cells Support Efficient Spatial Coding across Heterogeneous Environments

Sharif, F., Tayebi, B., Buzsáki, G., Royer, S., & Fernandez-Ruiz, A. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.034 · Cited by 111 · see citing works

Hippocampal Remapping and Its Entorhinal Origin

Latuske, P., Kornienko, O., Kohler, L., & Allen, K. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00253 · Cited by 102 · see citing works

Adult hippocampal neurogenesis and its role in cognition.

Oomen, C. A., Bekinschtein, P., Kent, B. A., Saksida, L. M., & Bussey, T. J. (2014) · WIREs Cognitive Science · doi:10.1002/wcs.1304 · Cited by 93 · see citing works

The medial and lateral entorhinal cortex both contribute to contextual and item recognition memory: A test of the binding ofitems and context model

Hunsaker, M. R., Chen, V., Tran, G. T., & Kesner, R. P. (2013) · Hippocampus · doi:10.1002/hipo.22097 · Cited by 88 · see citing works

Prefrontal feature representations drive memory recall

Yadav, N., Noble, C., Niemeyer, J. E., Terceros, A., Victor, J., Liston, C., & Rajasethupathy, P. (2022) · Nature · doi:10.1038/s41586-022-04936-2 · Cited by 61 · see citing works

Grid scale drives the scale and long-term stability of place maps

Mallory, C. S., Hardcastle, K., Bant, J. S., & Giocomo, L. M. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0055-3 · Cited by 46 · see citing works

Dopamine and norepinephrine receptors participate in methylphenidate enhancement of in vivo hippocampal synaptic plasticity

Jenson, D., Yang, K., Acevedo-Rodriguez, A., Levine, A., Broussard, J. I., Tang, J., & Dani, J. A. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.029 · Cited by 52 · see citing works

Behavior‐driven<i>arc</i>expression is reduced in all ventral hippocampal subfields compared to CA1, CA3, and dentate gyrus in rat dorsal hippocampus

Chawla, M. K., Sutherland, V. L., Olson, K., McNaughton, B. L., & Barnes, C. A. (2018) · Hippocampus · doi:10.1002/hipo.22820 · Cited by 49 · see citing works

The memory for time and space differentially engages the proximal and distal parts of the hippocampal subfields CA1 and CA3

Beer, Z., Vavra, P., Atucha, E., Rentzing, K., Heinze, H.-J., & Sauvage, M. M. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2006100 · Cited by 44 · see citing works

Diminution of context association memory structure in subjects with subjective cognitive decline

Fan, L., Lai, Y., Chen, T., Hsu, Y., Chen, P., Huang, K., Cheng, T., Tseng, W. I., Hua, M., Chen, Y., et al. (2018) · Human Brain Mapping · doi:10.1002/hbm.24022 · Cited by 40 · see citing works

Processing of spatial and non-spatial information in rats with lesions of the medial and lateral entorhinal cortex: environmental complexity matters

Rodo, C., Sargolini, F., & Save, E. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.12.009 · Cited by 42 · see citing works

Novel encoding and updating of positional, or directional, spatial cues are processed by distinct hippocampal subfields: evidence for parallel information processing and the "what" stream

Hoang, T., Aliane, V., & Manahan‐Vaughan, D. (2018) · Hippocampus · doi:10.1002/hipo.22833 · Cited by 37 · see citing works

Addictive Nicotine Alters Local Circuit Inhibition during the Induction of<i>In Vivo</i>Hippocampal Synaptic Potentiation

Zhang, T. A., Tang, J., Pidoplichko, V. I., & Dani, J. A. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0458-10.2010 · Cited by 33 · see citing works

Spatial information is preferentially processed by the distal part of CA3: implication for memory retrieval

Flasbeck, V., Atucha, E., Nakamura, N. H., Yoshida, M., & Sauvage, M. M. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.07.023 · Cited by 19 · see citing works

Linking neuronal structure to function in rodent hippocampus: a methodological prospective

Preston-Ferrer, P., & Burgalossi, A. (2018) · Cell and Tissue Research · doi:10.1007/s00441-017-2732-7 · Cited by 11 · see citing works