Retrosplenial cortex maps the conjunction of internal and external spaces

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat

O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151 · see citing works

Microstructure of a spatial map in the entorhinal cortex

Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068 · see citing works

<b>CircStat</b> : A <i>MATLAB</i> Toolbox for Circular Statistics

Berens, P. (2009) · Journal of Statistical Software · doi:10.18637/jss.v031.i10 · Cited by 3,099 · see citing works

The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells

Muller, R., & Kubie, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-07-01951.1987 · Cited by 1,581 · 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

Encoding of Spatial Location by Posterior Parietal Neurons

Andersen, R., Essick, G. K., & Siegel, R. M. (1985) · Science · doi:10.1126/science.4048942 · Cited by 1,413 · see citing works

Remembering the past and imagining the future: A neural model of spatial memory and imagery.

Byrne, P., Becker, S., & Burgess, N. (2007) · Psychological Review · doi:10.1037/0033-295x.114.2.340 · Cited by 1,011 · see citing works

Head-direction cells recorded from the postsubiculum in freely moving rats. II. Effects of environmental manipulations

Taube, J. S., Muller, R., & Ranck, J. B. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00436.1990 · Cited by 887 · see citing works

The Cortex of the Rat

Zilles, K. (1985) · Springer eBooks · doi:10.1007/978-3-642-70573-1 · Cited by 756 · see citing works

Head-direction cells in the rat posterior cortex: I. anatomical distribution and behavioral modulation

Chen, L. L., Lin, L.-H., Green, E. J., Barnes, C. A., & McNaughton, B. L. (1994) · Experimental Brain Research · doi:10.1007/bf00243212 · Cited by 543 · see citing works

Cortical connections between rat cingulate cortex and visual, motor, and postsubicular cortices

Vogt, B. A., & Miller, M. W. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902160207 · Cited by 528 · see citing works

Retrosplenial amnesia

VALENSTEIN, E., BOWERS, D., VERFAELLIE, M., HEILMAN, K. M., DAY, A., & WATSON, R. T. (1987) · Brain · doi:10.1093/brain/110.6.1631 · Cited by 487 · see citing works

A category-free neural population supports evolving demands during decision-making

Raposo, D. C., Kaufman, M. T., & Churchland, A. K. (2014) · Nature Neuroscience · doi:10.1038/nn.3865 · Cited by 474 · see citing works

Reference frames for representing visual and tactile locations in parietal cortex

Avillac, M., Denève, S., Olivier, E., Pouget, A., & Duhamel, J.-R. (2005) · Nature Neuroscience · doi:10.1038/nn1480 · Cited by 464 · see citing works

Spatial Transformations in the Parietal Cortex Using Basis Functions

Pouget, A., & B, T. J. S. A. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.2.222 · Cited by 426 · see citing works

Connections of the retrosplenial granular a cortex in the rat

van Groen, T., & Wyss, J. M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903000412 · Cited by 419 · see citing works

Multisensory Control of Hippocampal Spatiotemporal Selectivity

Ravassard, P., Kees, A. L., Willers, B., Ho, D. G., Aharoni, D. B., Cushman, J. D., Aghajan, Z. M., & Mehta, M. R. (2013) · Science · doi:10.1126/science.1232655 · Cited by 388 · see citing works

Head direction, place, and movement correlates for cells in the rat retrosplenial cortex.

Cho, J., & Sharp, P. E. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.1.3 · Cited by 385 · see citing works

Head position signals used by parietal neurons to encode locations of visual stimuli

Brotchie, P., Andersen, R. A., Snyder, L. H., & Goodman, S. J. (1995) · Nature · doi:10.1038/375232a0 · Cited by 382 · see citing works

Connections between the retrosplenial cortex and the hippocampal formation in the rat: A review

Wyss, J. M., & van Groen, T. (1992) · Hippocampus · doi:10.1002/hipo.450020102 · Cited by 379 · see citing works

Thoughts, behaviour, and brain dynamics during navigation in the real world

Spiers, H. J., & Maguire, E. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.037 · Cited by 371 · see citing works

Fragmentation of grid cell maps in a multicompartment environment

Derdikman, D., Whitlock, J. R., Tsao, A., Fyhn, M., Hafting, T., Moser, M.-B., & Moser, E. I. (2009) · Nature Neuroscience · doi:10.1038/nn.2396 · Cited by 330 · see citing works

Connections of the retrosplenial granular b cortex in the rat

van Groen, T., & Wyss, J. M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10757 · Cited by 302 · see citing works

Dissociable Retrosplenial and Hippocampal Contributions to Successful Formation of Survey Representations

Wolbers, T., & Büchel, C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4705-04.2005 · Cited by 301 · see citing works

Connections of the retrosplenial dysgranular cortex in the rat

van Groen, T., & Wyss, J. M. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903150207 · Cited by 299 · see citing works

Neurons of area 7 activated by both visual stimuli and oculomotor behavior

Andersen, R. A., Essick, G. K., & Siegel, R. M. (1987) · Experimental Brain Research · doi:10.1007/bf00248552 · Cited by 298 · see citing works

Rat posterior parietal cortex: topography of corticocortical and thalamic connections

Reep, R. L., Chandler, H. C., King, V. R., & Corwin, J. V. (1994) · Experimental Brain Research · doi:10.1007/bf00227280 · Cited by 245 · see citing works

Encoding and storage of spatial information in the retrosplenial cortex

Czajkowski, R., Jayaprakash, B., Wiltgen, B. J., Rogerson, T., Karlsson, M. G., Barth, A. L., Trachtenberg, J. T., & Silva, A. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313222111 · Cited by 229 · see citing works

Cortical Representation of Motion during Unrestrained Spatial Navigation in the Rat

McNaughton, B. L., Mizumori, S. J. Y., Barnes, C. A., Leonard, B. W., Marquis, M., & Green, E. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.1.27 · Cited by 224 · see citing works

Tracking Route Progression in the Posterior Parietal Cortex

Nitz, D. A. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.037 · Cited by 209 · see citing works

Head-direction cells in the rat posterior cortex

Chen, L. L., Lin, L.-H., Barnes, C. A., & McNaughton, B. L. (1994) · Experimental Brain Research · doi:10.1007/bf00243213 · Cited by 209 · see citing works

Interaction of Egocentric and World-Centered Reference Frames in the Rat Posterior Parietal Cortex

Wilber, A. A., Clark, B. J., Forster, T. C., Tatsuno, M., & McNaughton, B. L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0511-14.2014 · Cited by 200 · see citing works

Temporary Inactivation of the Retrosplenial Cortex Causes a Transient Reorganization of Spatial Coding in the Hippocampus

Cooper, B. G., & Mizumori, S. J. Y. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-11-03986.2001 · Cited by 196 · see citing works

Hippocampus and retrosplenial cortex combine path integration signals for successful navigation

Sherrill, K. R., Erdem, U. M., Ross, R. S., Brown, T. I., Hasselmo, M. E., & Stern, C. E. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1825-13.2013 · Cited by 167 · see citing works

Retrosplenial cortex inactivation selectively impairs navigation in darkness

Cooper, B. G., & Mizumori, S. J. Y. (1999) · Neuroreport · doi:10.1097/00001756-199902250-00033 · Cited by 161 · see citing works

Functional Split between Parietal and Entorhinal Cortices in the Rat

Whitlock, J. R., Pfuhl, G., Dagslott, N. C., Moser, M., & Moser, E. I. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.028 · Cited by 158 · see citing works

Finding your way in the dark: The retrosplenial cortex contributes to spatial memory and navigation without visual cues.

Cooper, B. G., Manka, T. F., & Mizumori, S. J. Y. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.5.1012 · Cited by 131 · see citing works

Selective role of lingual/parahippocampal gyrus and retrosplenial complex in spatial memory across viewpoint changes relative to the environmental reference frame

Sulpizio, V., Committeri, G., Lambrey, S., Berthoz, A., & Galati, G. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.12.031 · Cited by 118 · see citing works

Spaces within spaces: rat parietal cortex neurons register position across three reference frames

Nitz, D. A. (2012) · Nature Neuroscience · doi:10.1038/nn.3213 · Cited by 95 · see citing works

Directional Disorientation Following Left Retrosplenial Hemorrhage: a Case Report with FMRI Studies

Ino, T., Doi, T., Hirose, S., Kimura, T., Ito, J., & Fukuyama, H. (2007) · Cortex · doi:10.1016/s0010-9452(08)70479-9 · Cited by 95 · see citing works

Selective dysgranular retrosplenial cortex lesions in rats disrupt allocentric performance of the radial-arm maze task.

Vann, S. D., & Aggleton, J. P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.6.1682 · Cited by 94 · see citing works

Complimentary roles of the hippocampus and retrosplenial cortex in behavioral context discrimination

Smith, D. M., Barredo, J., & Mizumori, S. J. Y. (2011) · Hippocampus · doi:10.1002/hipo.20958 · Cited by 93 · see citing works

Assessing the mechanism of response in the retrosplenial cortex of good and poor navigators

Auger, S. D., & Maguire, E. A. (2013) · Cortex · doi:10.1016/j.cortex.2013.08.002 · Cited by 91 · see citing works

Parietal cortex, navigation, and the construction of arbitrary reference frames for spatial information

Nitz, D. A. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.08.007 · Cited by 82 · see citing works

Involvement of the retrosplenial cortex in processing multiple conditioned stimuli.

Keene, C. S., & Bucci, D. J. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.651 · Cited by 62 · see citing works

Damage to the retrosplenial cortex produces specific impairments in spatial working memory

Keene, C. S., & Bucci, D. J. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.10.009 · Cited by 56 · see citing works

Superficially Projecting Principal Neurons in Layer V of Medial Entorhinal Cortex in the Rat Receive Excitatory Retrosplenial Input

Czajkowski, R., Sugar, J., Zhang, S., Couey, J. J., Ye, J., & Witter, M. P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2646-13.2013 · Cited by 54 · see citing works

The rat retrosplenial cortex is required when visual cues are used flexibly to determine location

Hindley, E. L., Nelson, A. J. D., Aggleton, J. P., & Vann, S. D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.01.028 · Cited by 53 · see citing works

The retrosplenial cortex is necessary for path integration in the dark

Elduayen, C., & Save, É. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.009 · Cited by 48 · see citing works

Memory impairment and spatial disorientation following a left retrosplenial lesion

Maeshima, S., Ozaki, F., Masuo, O., Yamaga, H., Okita, R., & Moriwaki, H. (2001) · Journal of Clinical Neuroscience · doi:10.1054/jocn.2000.0801 · Cited by 37 · see citing works

Path shape impacts the extent of CA1 pattern recurrence both within and across environments

Nitz, D. A. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00573.2010 · Cited by 35 · see citing works

Medial Entorhinal Grid Cells and Head Direction Cells Rotate with a T-Maze More Often During Less Recently Experienced Rotations

Gupta, K., Beer, N. J., Keller, L. A., & Hasselmo, M. E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht020 · Cited by 17 · see citing works

Repeating Firing Fields of CA1 Neurons Shift Forward in Response to Increasing Angular Velocity

Cowen, S. L., & Nitz, D. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1199-13.2014 · Cited by 13 · see citing works

The cognitive map in humans: spatial navigation and beyond

Epstein, R. A., Patai, E. Z., Julian, J. B., & Spiers, H. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4656 · Cited by 921 · see citing works

Spatial navigation deficits — overlooked cognitive marker for preclinical Alzheimer disease?

Coughlan, G., Laczó, J., Hort, J., Minihane, A.-M., & Hornberger, M. (2018) · Nature Reviews Neurology · doi:10.1038/s41582-018-0031-x · Cited by 500 · see citing works

Experience-dependent spatial expectations in mouse visual cortex

Fiser, A., Mahringer, D., Oyibo, H. K., Petersen, A. V., Leinweber, M., & Keller, G. B. (2016) · Nature Neuroscience · doi:10.1038/nn.4385 · Cited by 332 · see citing works

Scene Perception in the Human Brain

Epstein, R. A., & Baker, C. I. (2019) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091718-014809 · Cited by 350 · see citing works

Structuring knowledge with cognitive maps and cognitive graphs

Peer, M., Brunec, I. K., Newcombe, N. S., & Epstein, R. A. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.10.004 · Cited by 283 · see citing works

Retrosplenial cortex and its role in spatial cognition

Mitchell, A. S., Czajkowski, R., Zhang, N., Jeffery, K. J., & Nelson, A. J. D. (2018) · Brain and Neuroscience Advances · doi:10.1177/2398212818757098 · Cited by 266 · see citing works

An independent, landmark-dominated head-direction signal in dysgranular retrosplenial cortex

Jacob, P.-Y., Casali, G., Spieser, L., Page, H., Overington, D., & Jeffery, K. (2017) · Nature Neuroscience · doi:10.1038/nn.4465 · Cited by 227 · see citing works

The representation of space in the brain

Grieves, R. M., & Jeffery, K. J. (2016) · Behavioural Processes · doi:10.1016/j.beproc.2016.12.012 · Cited by 230 · 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

Sparse orthogonal population representation of spatial context in the retrosplenial cortex

Mao, D., Kandler, S., McNaughton, B. L., & Bonin, V. (2017) · Nature Communications · doi:10.1038/s41467-017-00180-9 · Cited by 212 · see citing works

Egocentric boundary vector tuning of the retrosplenial cortex

Alexander, A. S., Carstensen, L. C., Hinman, J. R., Raudies, F., Chapman, G. W., & Hasselmo, M. E. (2020) · Science Advances · doi:10.1126/sciadv.aaz2322 · Cited by 197 · see citing works

Causal Influence of Visual Cues on Hippocampal Directional Selectivity

Acharya, L., Aghajan, Z. M., Vuong, C., Moore, J. J., & Mehta, M. R. (2016) · Cell · doi:10.1016/j.cell.2015.12.015 · Cited by 196 · see citing works

Dissociable Structural and Functional Hippocampal Outputs via Distinct Subiculum Cell Classes

Cembrowski, M. S., Phillips, M. G., DiLisio, S. F., Shields, B. C., Winnubst, J., Chandrashekar, J. V., Bas, E., & Spruston, N. (2018) · Cell · doi:10.1016/j.cell.2018.03.031 · Cited by 195 · see citing works

Principles governing the integration of landmark and self-motion cues in entorhinal cortical codes for navigation

Campbell, M. G., Ocko, S. A., Mallory, C. S., Low, I. I. C., Ganguli, S., & Giocomo, L. M. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0189-y · Cited by 187 · see citing works

Neuronal vector coding in spatial cognition

Bicanski, A., & Burgess, N. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0336-9 · Cited by 172 · see citing works

Spatial representations in the primate hippocampus, and their functions in memory and navigation

Rolls, E. T., & Wirth, S. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.09.004 · Cited by 160 · see citing works

The Human Retrosplenial Cortex and Thalamus Code Head Direction in a Global Reference Frame

Shine, J. P., Valdés-Herrera, J. P., Hegarty, M., & Wolbers, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1268-15.2016 · Cited by 155 · see citing works

Optogenetic reactivation of memory ensembles in the retrosplenial cortex induces systems consolidation

de Sousa, A. F., Cowansage, K. K., Zutshi, I., Cardozo, L. M., Yoo, E. J., Leutgeb, S., & Mayford, M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1818432116 · Cited by 138 · see citing works

Rethinking retrosplenial cortex: Perspectives and predictions

Alexander, A. S., Place, R., Starrett, M. J., Chrastil, E. R., & Nitz, D. A. (2022) · Neuron · doi:10.1016/j.neuron.2022.11.006 · Cited by 157 · see citing works

Area-Specificity and Plasticity of History-Dependent Value Coding During Learning

Hattori, R., Danskin, B. P., Babic, Z., Mlynaryk, N., & Komiyama, T. (2019) · Cell · doi:10.1016/j.cell.2019.04.027 · Cited by 151 · see citing works

Why Does Space Feel the Way it Does? Towards a Principled Account of Spatial Experience

Haun, A., & Tononi, G. (2019) · Entropy · doi:10.3390/e21121160 · Cited by 143 · see citing works

Egocentric and allocentric representations of space in the rodent brain

Wang, C., Chen, X., & Knierim, J. J. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.11.005 · Cited by 141 · see citing works

Spatially Periodic Activation Patterns of Retrosplenial Cortex Encode Route Sub-spaces and Distance Traveled

Alexander, A. S., & Nitz, D. A. (2017) · Current Biology · doi:10.1016/j.cub.2017.04.036 · Cited by 141 · see citing works

Cholinergic modulation of spatial learning, memory and navigation

Solari, N., & Hangya, B. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14089 · Cited by 139 · see citing works

Boundaries Shape Cognitive Representations of Spaces and Events

Brunec, I. K., Moscovitch, M., & Barense, M. D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.03.013 · Cited by 141 · see citing works

A novel somatosensory spatial navigation system outside the hippocampal formation

Long, X., & Zhang, S. (2021) · Cell Research · doi:10.1038/s41422-020-00448-8 · Cited by 136 · see citing works

Locomotion-dependent remapping of distributed cortical networks

Clancy, K. B., Oršolić, I., & Mrsic‐Flogel, T. D. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0357-8 · Cited by 137 · see citing works

Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway

Nitzan, N., McKenzie, S., Beed, P. S., English, D. F., Oldani, S., Tukker, J. J., Buzsáki, G., & Schmitz, D. (2020) · Nature Communications · doi:10.1038/s41467-020-15787-8 · Cited by 129 · see citing works

A sense of space in postrhinal cortex

LaChance, P. A., Todd, T. P., & Taube, J. S. (2019) · Science · doi:10.1126/science.aax4192 · Cited by 129 · see citing works

A Circuit for Integration of Head- and Visual-Motion Signals in Layer 6 of Mouse Primary Visual Cortex

Vélez‐Fort, M., Bracey, E. F., Keshavarzi, S., Rousseau, C. V., Cossell, L., Lenzi, S. C., Strom, M., & Margrie, T. W. (2018) · Neuron · doi:10.1016/j.neuron.2018.02.023 · Cited by 125 · see citing works

Hippocampus-dependent emergence of spatial sequence coding in retrosplenial cortex

Mao, D., Neumann, A. R., Sun, J., Bonin, V., Mohajerani, M. H., & McNaughton, B. L. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1803224115 · Cited by 123 · see citing works

Transformation of a Spatial Map across the Hippocampal-Lateral Septal Circuit

Tingley, D., & Buzsáki, G. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.028 · Cited by 120 · see citing works

The Neurocognitive Basis of Spatial Reorientation

Julian, J. B., Keinath, A. T., Marchette, S. A., & Epstein, R. A. (2018) · Current Biology · doi:10.1016/j.cub.2018.04.057 · Cited by 117 · see citing works

Retrosplenial Cortical Neurons Encode Navigational Cues, Trajectories and Reward Locations During Goal Directed Navigation

Vedder, L. C., Miller, A. M. P., Harrison, M. B., & Smith, D. M. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw192 · Cited by 116 · see citing works

From cognitive maps to spatial schemas

Farzanfar, D., Spiers, H. J., Moscovitch, M., & Rosenbaum, R. S. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-022-00655-9 · Cited by 115 · see citing works

Neuronal representation of environmental boundaries in egocentric coordinates

Hinman, J. R., Chapman, G. W., & Hasselmo, M. E. (2019) · Nature Communications · doi:10.1038/s41467-019-10722-y · Cited by 112 · see citing works

Representation of visual landmarks in retrosplenial cortex

Fischer, L. F., Soto-Albors, R. M., Buck, F., & Harnett, M. T. (2020) · eLife · doi:10.7554/elife.51458 · Cited by 104 · see citing works

Retrosplenial cortex and its role in cue-specific learning and memory

Todd, T. P., Fournier, D. I., & Bucci, D. J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.04.016 · Cited by 105 · see citing works

CA1-projecting subiculum neurons facilitate object–place learning

Sun, Y., Jin, S., Lin, X., Chen, L., Qiao, X., Jiang, L., Zhou, P., Johnston, K. G., Golshani, P., Nie, Q. H., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0496-y · Cited by 111 · see citing works

A cortico-collicular circuit for orienting to shelter during escape

Campagner, D., do Vale, R. D., Tan, Y. L., Ιορδανίδου, Π., Arocas, O. P., Claudi, F., Stempel, A. V., Keshavarzi, S., Petersen, R. S., Margrie, T. W., et al. (2022) · Nature · doi:10.1038/s41586-022-05553-9 · Cited by 111 · see citing works

Neural correlates of sparse coding and dimensionality reduction

Beyeler, M., Rounds, E. L., Carlson, K. D., Dutt, N., & Krichmar, J. L. (2019) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1006908 · Cited by 104 · see citing works

The Spatial Structure of Neural Encoding in Mouse Posterior Cortex during Navigation

Minderer, M., Brown, K. D., & Harvey, C. D. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.029 · Cited by 101 · see citing works

Active dendritic integration and mixed neocortical network representations during an adaptive sensing behavior

Ranganathan, G. N., Apostolides, P. F., Harnett, M. T., Xu, N.-L., Druckmann, S., & Magee, J. C. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0254-6 · Cited by 115 · see citing works

Subiculum neurons map the current axis of travel

Olson, J. M., Tongprasearth, K., & Nitz, D. A. (2016) · Nature Neuroscience · doi:10.1038/nn.4464 · Cited by 96 · see citing works

The retrosplenial-parietal network and reference frame coordination for spatial navigation.

Clark, B. J., Simmons, C. M., Berkowitz, L. E., & Wilber, A. A. (2018) · Behavioral Neuroscience · doi:10.1037/bne0000260 · Cited by 95 · see citing works

Origin and role of path integration in the cognitive representations of the hippocampus: computational insights into open questions

Savelli, F., & Knierim, J. J. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.188912 · Cited by 93 · see citing works

Multisensory coding of angular head velocity in the retrosplenial cortex

Keshavarzi, S., Bracey, E. F., Faville, R., Campagner, D., Tyson, A. L., Lenzi, S. C., Branco, T., & Margrie, T. W. (2021) · Neuron · doi:10.1016/j.neuron.2021.10.031 · Cited by 88 · see citing works

Retrosplenial Cortical Representations of Space and Future Goal Locations Develop with Learning

Miller, A. M. P., Mau, W., & Smith, D. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.05.034 · Cited by 84 · see citing works

Distance-tuned neurons drive specialized path integration calculations in medial entorhinal cortex

Campbell, M. G., Attinger, A., Ocko, S. A., Ganguli, S., & Giocomo, L. M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109669 · Cited by 77 · see citing works

A New Projection From the Deep Cerebellar Nuclei to the Hippocampus via the Ventrolateral and Laterodorsal Thalamus in Mice

Bohne, P., Schwarz, M. K., Herlitze, S., & Mark, M. D. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00051 · Cited by 85 · see citing works

Hippocampal spatial view cells for memory and navigation, and their underlying connectivity in humans

Rolls, E. T. (2022) · Hippocampus · doi:10.1002/hipo.23467 · Cited by 82 · see citing works

The human posterior parietal cortex: effective connectome, and its relation to function

Rolls, E. T., Deco, G., Huang, C., & Feng, J. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac266 · Cited by 82 · see citing works

How the Brain’s Navigation System Shapes Our Visual Experience

Nau, M., Julian, J. B., & Doeller, C. F. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.06.008 · Cited by 79 · see citing works

Somatic and Dendritic Encoding of Spatial Variables in Retrosplenial Cortex Differs during 2D Navigation

Voigts, J., & Harnett, M. T. (2019) · Neuron · doi:10.1016/j.neuron.2019.10.016 · Cited by 79 · see citing works

Entorhinal-retrosplenial circuits for allocentric-egocentric transformation of boundary coding

G., V. W. J. B., Babl, S. S., & Ito, H. (2020) · eLife · doi:10.7554/elife.59816 · Cited by 77 · see citing works

Environmental Anchoring of Head Direction in a Computational Model of Retrosplenial Cortex

Bičanski, A., & Burgess, N. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0516-16.2016 · Cited by 73 · see citing works

Unfolding the cognitive map: The role of hippocampal and extra-hippocampal substrates based on a systems analysis of spatial processing

Hunsaker, M. R., & Kesner, R. P. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.11.012 · Cited by 68 · see citing works

Influence of claustrum on cortex varies by area, layer, and cell type

McBride, E. G., Gandhi, S. R., Kuyat, J. R., Ollerenshaw, D. R., Arkhipov, A. S., Christof Koch, A., & Olsen, S. R. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.026 · Cited by 69 · see citing works

Processing of different spatial scales in the human brain

Peer, M., Ron, Y., Monsa, R., & Arzy, S. (2019) · eLife · doi:10.7554/elife.47492 · Cited by 63 · see citing works

Gated transformations from egocentric to allocentric reference frames involving retrosplenial cortex, entorhinal cortex, and hippocampus

Alexander, A. S., Robinson, J. C., Stern, C. E., & Hasselmo, M. E. (2023) · Hippocampus · doi:10.1002/hipo.23513 · Cited by 66 · see citing works

The gut–brain axis underlying hepatic encephalopathy in liver cirrhosis

He, X., Hu, M., Xu, Y., Xia, F., Tan, Y., Wang, Y., Xiang, H., Wu, H., Ji, T., Xu, Q., et al. (2025) · Nature Medicine · doi:10.1038/s41591-024-03405-9 · Cited by 66 · see citing works

Parahippocampal and retrosplenial connections of rat posterior parietal cortex

Olsen, G. M., Ohara, S., Iijima, T., & Witter, M. P. (2016) · Hippocampus · doi:10.1002/hipo.22701 · Cited by 66 · see citing works

Three brain states in the hippocampus and cortex

Kay, K., & Frank, L. M. (2018) · Hippocampus · doi:10.1002/hipo.22956 · Cited by 63 · see citing works

Vision and Locomotion Combine to Drive Path Integration Sequences in Mouse Retrosplenial Cortex

Mao, D., Molina, L. A., Bonin, V., & McNaughton, B. L. (2020) · Current Biology · doi:10.1016/j.cub.2020.02.070 · Cited by 65 · see citing works

The Visual Cortex in Context

Froudarakis, E., Fahey, P. G., Reimer, J., Smirnakis, S. M., Tehovnik, E. J., & Tolias, A. S. (2019) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091517-034407 · Cited by 63 · see citing works

Hippocampal Ripple Coordinates Retrosplenial Inhibitory Neurons during Slow-Wave Sleep

Opalka, A. N., Huang, W., Liu, J., Liang, H.-L., & Wang, D. V. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.038 · Cited by 55 · see citing works

Stable Encoding of Visual Cues in the Mouse Retrosplenial Cortex

Powell, A. L., Connelly, W. M., Vasalauskaite, A., Nelson, A. J. D., Vann, S. D., Aggleton, J. P., Sengpiel, F., & Ranson, A. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa030 · Cited by 63 · see citing works

Electrophysiological Evidence That the Retrosplenial Cortex Displays a Strong and Specific Activation Phased with Hippocampal Theta during Paradoxical (REM) Sleep

Koike, B. D. V., Farias, K. S., Billwiller, F., Filho, D. A., Libourel, P., Tiran‐Cappello, A., Parmentier, R., Blanco, W., Ribeiro, S. T. G., Luppi, P., et al. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0026-17.2017 · Cited by 59 · see citing works

Architecture and organization of mouse posterior parietal cortex relative to extrastriate areas

Hovde, K., Gianatti, M., Witter, M. P., & Whitlock, J. R. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14280 · Cited by 59 · see citing works

Virtual Enactment Effect on Memory in Young and Aged Populations: A Systematic Review

Tuena, C., Serino, S., Dutriaux, L., Riva, G., & Piolino, P. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8050620 · Cited by 58 · see citing works

Heterogeneity of executive function revealed by a functional random forest approach across ADHD and ASD

Cordova, M., Shada, K., Demeter, D. V., Doyle, O., Miranda-Dominguez, O., Perrone, A., Schifsky, E., Graham, A., Fombonne, E., Langhorst, B., et al. (2020) · NeuroImage: Clinical · doi:10.1016/j.nicl.2020.102245 · Cited by 54 · see citing works

Disentangling the Role of the MEC and LEC in the Processing of Spatial and Non-Spatial Information: Contribution of Lesion Studies

Save, É., & Sargolini, F. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00081 · Cited by 53 · see citing works

Multivoxel Pattern Analysis Reveals 3D Place Information in the Human Hippocampus

kim, M.-S., Jeffery, K. J., & Maguire, E. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2703-16.2017 · Cited by 53 · see citing works

The separate and combined properties of the granular (area 29) and dysgranular (area 30) retrosplenial cortex

Aggleton, J. P., Yanakieva, S., Sengpiel, F., & Nelson, A. J. D. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107516 · Cited by 55 · see citing works

A distributed and efficient population code of mixed selectivity neurons for flexible navigation decisions

Kira, S., Safaai, H., Morcos, A. S., Panzeri, S., & Harvey, C. D. (2023) · Nature Communications · doi:10.1038/s41467-023-37804-2 · Cited by 48 · see citing works

Schematic representations of local environmental space guide goal-directed navigation

Marchette, S. A., Ryan, J., & Epstein, R. A. (2017) · Cognition · doi:10.1016/j.cognition.2016.10.005 · Cited by 50 · see citing works

Differential dendritic integration of long-range inputs in association cortex via subcellular changes in synaptic AMPA-to-NMDA receptor ratio

Lafourcade, M., van der Goes, M.-S. H., Vardalaki, D., Brown, N. J., Voigts, J., Yun, D. H., Kim, M. E., Ku, T., & Harnett, M. T. (2022) · Neuron · doi:10.1016/j.neuron.2022.01.025 · Cited by 50 · see citing works

Spatial coordinate transforms linking the allocentric hippocampal and egocentric parietal primate brain systems for memory, action in space, and navigation

Rolls, E. T. (2019) · Hippocampus · doi:10.1002/hipo.23171 · Cited by 52 · see citing works

Neurophysiological signatures of temporal coordination between retrosplenial cortex and the hippocampal formation.

Alexander, A. S., Rangel, L. M., Tingley, D., & Nitz, D. A. (2018) · Behavioral Neuroscience · doi:10.1037/bne0000254 · Cited by 52 · see citing works

The Neuroscience of Spatial Navigation and the Relationship to Artificial Intelligence

Bermudez-Contreras, E. J., Clark, B. J., & Wilber, A. A. (2020) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2020.00063 · Cited by 50 · see citing works

A Computational Model for Spatial Navigation Based on Reference Frames in the Hippocampus, Retrosplenial Cortex, and Posterior Parietal Cortex

Oess, T., Krichmar, J. L., & Röhrbein, F. (2017) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2017.00004 · Cited by 50 · see citing works

Shared and specialized coding across posterior cortical areas for dynamic navigation decisions

Tseng, S.-Y., Chettih, S. N., Arlt, C., Barroso-Luque, R., & Harvey, C. D. (2022) · Neuron · doi:10.1016/j.neuron.2022.05.012 · Cited by 45 · see citing works

Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex

Alexander, A. S., Robinson, J. C., Dannenberg, H., Kinsky, N. R., Levy, S. J., Mau, W., Chapman, G. W., Sullivan, D. W., & Hasselmo, M. E. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820972871 · Cited by 43 · see citing works

Hippocampus, Retrosplenial and Parahippocampal Cortices Encode Multicompartment 3D Space in a Hierarchical Manner

Kim, M., & Maguire, E. A. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy054 · Cited by 45 · see citing works

Secondary Motor Cortex Transforms Spatial Information into Planned Action during Navigation

Olson, J. M., Li, J. K., Montgomery, S. E., & Nitz, D. A. (2020) · Current Biology · doi:10.1016/j.cub.2020.03.016 · Cited by 44 · see citing works

Hyperexcitable Neurons Enable Precise and Persistent Information Encoding in the Superficial Retrosplenial Cortex

Brennan, E. K. W., Sudhakar, S., Jedrasiak‐Cape, I., John, T. T., & Ahmed, O. J. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.093 · Cited by 43 · see citing works

Adaptive integration of self-motion and goals in posterior parietal cortex

Alexander, A. S., Tung, J. C., Chapman, G. W., Conner, A. M., Shelley, L. E., Hasselmo, M. E., & Nitz, D. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110504 · Cited by 43 · see citing works

Coregistration of heading to visual cues in retrosplenial cortex

Sit, K. K., & Goard, M. J. (2023) · Nature Communications · doi:10.1038/s41467-023-37704-5 · Cited by 42 · see citing works

Noncanonical projections to the hippocampal CA3 regulate spatial learning and memory by modulating the feedforward hippocampal trisynaptic pathway

Lin, X., Amalraj, M., Blanton, C., Avila, B., Holmes, T. C., Nitz, D. A., & Xu, X. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001127 · Cited by 48 · see citing works

Neural mechanisms of navigation involving interactions of cortical and subcortical structures

Hinman, J. R., Dannenberg, H., Alexander, A. S., & Hasselmo, M. E. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00498.2017 · Cited by 42 · see citing works

A Liaison Brought to Light: Cerebellum-Hippocampus, Partners for Spatial Cognition

Rondi‐Reig, L., Paradis, A., & Fallahnezhad, M. (2022) · The Cerebellum · doi:10.1007/s12311-022-01422-3 · Cited by 39 · see citing works

The limbic memory circuit and the neural basis of contextual memory

Smith, D. M., Yang, Y., Subramanian, D. L., Miller, A. M. P., Bulkin, D. A., & Law, L. M. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107557 · Cited by 38 · see citing works

Encoding of 3D head direction information in the human brain

kim, M.-S., & Maguire, E. A. (2018) · Hippocampus · doi:10.1002/hipo.23060 · Cited by 38 · see citing works

Mapping vestibular and visual contributions to angular head velocity tuning in the cortex

Hennestad, E., Witoelar, A., Chambers, A. R., & Vervaeke, K. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110134 · Cited by 36 · see citing works

Representation of human spatial navigation responding to input spatial information and output navigational strategies: An ALE meta-analysis

Qiu, Y., Wu, Y., Liu, R., Wang, J., Huang, H., & Huang, R. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.012 · Cited by 34 · see citing works

Retrosplenial cortex in spatial memory: focus on immediate early genes mapping

Balcerek, E., Włodkowska, U., & Czajkowski, R. (2021) · Molecular Brain · doi:10.1186/s13041-021-00880-w · Cited by 36 · see citing works

Postnatal development of retrosplenial projections to the parahippocampal region of the rat

Sugar, J., & Witter, M. P. (2016) · eLife · doi:10.7554/elife.13925 · Cited by 36 · see citing works

Time to put the mammillothalamic pathway into context

Dillingham, C. M., Milczarek, M. M., Perry, J. C., & Vann, S. D. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.031 · Cited by 37 · see citing works

A distributed circuit for associating environmental context with motor choice in retrosplenial cortex

Franco, L. M., & Goard, M. J. (2021) · Science Advances · doi:10.1126/sciadv.abf9815 · Cited by 36 · see citing works

Secondary motor cortex: Broadcasting and biasing animal's decisions through long-range circuits

Yang, J.-H., & Kwan, A. C. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.11.008 · Cited by 35 · see citing works

Integrative functions of the retrosplenial cortex in rats: anatomy, connectomics, and cellular electrophysiology

Mineeva, O. A., Bezryadnov, D. V., Чехов, С. А., Svarnik, О. E., & Anokhin, K. V. (2019) · Annals of Clinical and Experimental Neurology · doi:10.25692/acen.2019.1.6 · Cited by 2 · see citing works

Extraction and encoding of spatial relationships in the retrosplenial cortex

Alexander, A. S. (2017) · eScholarship (California Digital Library)

The retrosplenial-parietal network and reference frame coordination for spatial navigationPreprint

Clark, B. J., Simmons, C. M., Berkowitz, L., & Wilber, A. A. (2018) · doi:10.31234/osf.io/9nb53 · Cited by 7 · see citing works

Introduction to the special issue on the cognitive functions of the retrosplenial cortex.

Bucci, D. J., & Stern, C. E. (2018) · Behavioral Neuroscience · doi:10.1037/bne0000279

Conjunctive processing of spatial border and locomotion in retrosplenial cortex during spatial navigation

Sun, H., Cai, R., Li, R., Li, M., Gao, L., & Li, X. (2024) · The Journal of Physiology · doi:10.1113/jp286434 · Cited by 5 · see citing works