The retrosplenial contribution to human navigation: a review of lesion and neuroimaging findings
Abstract
The clinical and neuroimaging literatures are surveyed in order to collate for the first time the available data on retrosplenial involvement in human navigation. Several notable features emerge from consideration of the case reports of relatively pure topographical disorientation in the presence of a retrosplenial lesion. The majority of cases follow damage to the right retrosplenial cortex, with Brodmann's area 30 apparently compromised in most cases. All patients displayed impaired learning of new routes, and defective navigation in familiar environments complaining they could not use preserved landmark recognition to aid orientation. The deficit generally resolved within eight weeks of onset. The majority of functional neuroimaging studies involving navigation or orientation in large-scale space also activate the retrosplenial cortex, usually bilaterally, with good concordance in the locations of the voxel of peak activation across studies, again with Brodmann's area 30 featuring prominently. While there is strong evidence for right medial temporal lobe involvement in navigation, it now seems that the inputs the hippocampus and related structures receive from and convey to right retrosplenial cortex have a similar spatial preference, while the left medial temporal and left retrosplenial cortices seem primarily concerned with more general aspects of episodic memory.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Unilateral retrosplenial damage can cause topographic disorientation.
“Meanwhile, unilateral retrosplenial damage, which presumably involves the cingulum, can cause topographic disorientation (Maguire, 2001; Takahashi et al., 1997)”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as Maguire, 2001
Cited by
Sorted by citations
Investigations into resting-state connectivity using independent component analysis
Beckmann, C. F., DeLuca, M., Devlin, J. T., & Smith, S. M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1634 · Cited by 3,398 · see citing works
Bar, M. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1476 · Cited by 1,613 · see citing works
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377 · see citing works
What does the retrosplenial cortex do?
Vann, S. D., Aggleton, J. P., & Maguire, E. A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2733 · Cited by 1,409 · see citing works
Self-citationA new neural framework for visuospatial processing
Kravitz, D. J., Saleem, K. S., Baker, C. I., & Mishkin, M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3008 · Cited by 1,325 · see citing works
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 · see citing works
Self-citationRemembering 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
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
Beckmann, M., Johansen-Berg, H., & Rushworth, M. F. S. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3328-08.2009 · Cited by 789 · see citing works
Functional neuroimaging of autobiographical memory
Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736 · see citing works
The cingulum bundle: Anatomy, function, and dysfunction
Bubb, E. J., Metzler-Baddeley, C., & Aggleton, J. P. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.05.008 · Cited by 740 · see citing works
“Meanwhile, unilateral retrosplenial damage, which presumably involves the cingulum, can cause topographic disorientation (Maguire, 2001; Takahashi et al., 1997), emphasising a specific role in landmark navigation (Auger et al., 2012).”
The construction system of the brain
Hassabis, D., & Maguire, E. A. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0296 · Cited by 483 · see citing works
Self-citationCytology and functionally correlated circuits of human posterior cingulate areas
Vogt, B. A., Vogt, L., & Laureys, S. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.07.048 · Cited by 484 · 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
Self-citationNavigation around London by a taxi driver with bilateral hippocampal lesions
Maguire, E. A., Nannery, R., & Spiers, H. J. (2006) · Brain · doi:10.1093/brain/awl286 · Cited by 335 · see citing works
Self-citationAnchoring the neural compass: coding of local spatial reference frames in human medial parietal lobe
Marchette, S. A., Vass, L. K., Ryan, J., & Epstein, R. A. (2014) · Nature Neuroscience · doi:10.1038/nn.3834 · Cited by 287 · see citing works
van Reekum, C. M., Johnstone, T., Urry, H. L., Thurow, M. E., Schaefer, H. S., Alexander, A. L., & Davidson, R. J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.052 · Cited by 271 · see citing works
Maguire, E. A. (2001) · Brain · doi:10.1093/brain/124.6.1156 · Cited by 266 · see citing works
Self-citationOffline Persistence of Memory-Related Cerebral Activity during Active Wakefulness
Peigneux, P., Orban, P., Balteau, E., Degueldre, C., Luxen, A., Laureys, S., & Maquet, P. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040100 · Cited by 263 · see citing works
Rosenbaum, R. S., Ziegler, M., Winocur, G., Grady, C. L., & Moscovitch, M. (2004) · Hippocampus · doi:10.1002/hipo.10218 · Cited by 258 · see citing works
Kondo, H., Saleem, K. S., & Price, J. L. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20796 · Cited by 236 · see citing works
Hippocampal—diencephalic—cingulate networks for memory and emotion: an anatomical guide
Bubb, E. J., Kinnavane, L., & Aggleton, J. P. (2017) · Brain and Neuroscience Advances · doi:10.1177/2398212817723443 · Cited by 234 · see citing works
Retrosplenial cortex codes for permanent landmarks
Auger, S. D., Mullally, S. L., & Maguire, E. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043620 · Cited by 205 · see citing works
Self-citationRende, B., Ramsberger, G., & Miyake, A. (2002) · Neuropsychology · doi:10.1037//0894-4105.16.3.309 · Cited by 203 · see citing works
The Neural Basis of Personal Goal Processing When Envisioning Future Events
D'Argembeau, A., Stawarczyk, D., Majerus, S., Collette, F., Van der Linden, M., Feyers, D., Maquet, P., & Salmon, E. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21314 · Cited by 194 · see citing works
Ekstrom, A. D., Huffman, D. J., & Starrett, M. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00531.2017 · Cited by 186 · see citing works
Fenske, M. J., Aminoff, E., Gronau, N., & Bar, M. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)55001-0 · Cited by 190 · see citing works
Gramann, K., Onton, J., Riccobon, D., Mueller, H. J., Bardins, S., & Makeig, S. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21369 · Cited by 172 · see citing works
Sugiura, M., Shah, N. J., Zilles, K., & Fink, G. R. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929053124956 · Cited by 167 · see citing works
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
Visual Scene Processing in Familiar and Unfamiliar Environments
Epstein, R. A., Higgins, J. S., Jablonski, K., & Feiler, A. M. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00003.2007 · Cited by 153 · see citing works
Neural foundations of emerging route knowledge in complex spatial environments
Wolbers, T., Weiller, C., & Büchel, C. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.06.013 · Cited by 146 · see citing works
Beyond the Edges of a View: Boundary Extension in Human Scene-Selective Visual Cortex
Park, S., Intraub, H., Yi, D.-J., Widders, D., & Chun, M. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.006 · Cited by 144 · see citing works
Imagining Being Somewhere Else: Neural Basis of Changing Perspective in Space
Lambrey, S., Doeller, C., Berthoz, A., & Burgess, N. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr101 · Cited by 130 · see citing works
Abstract Representations of Location and Facing Direction in the Human Brain
Vass, L. K., & Epstein, R. A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3873-12.2013 · Cited by 131 · see citing works
Nonconscious formation and reactivation of semantic associations by way of the medial temporal lobe
Henke, K., Mondadori, C. R. A., Treyer, V., Nitsch, R. M., Buck, A., & Hock, C. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(03)00035-6 · Cited by 128 · see citing works
fMRI evidence for multisensory recruitment associated with rapid eye movements during sleep.
Hong, C. C., Harris, J. C., Pearlson, G. D., Kim, J., Calhoun, V. D., Fallon, J. H., Golay, X., Gillen, J. S., Simmonds, D. J., van Zijl, P. C. M., et al. (2009) · Human Brain Mapping · doi:10.1002/hbm.20635 · Cited by 124 · see citing works
Being a self: considerations from functional imaging
Gusnard, D. A. (2005) · Consciousness and Cognition · doi:10.1016/j.concog.2005.04.004 · Cited by 116 · see citing works
The neuroscience of remote spatial memory: A tale of two cities
Spiers, H. J., & Maguire, E. A. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.056 · Cited by 117 · see citing works
Self-citationCiaramelli, E., Rosenbaum, R. S., Solcz, S., Levine, B., & Moscovitch, M. (2010) · Journal of Experimental Psychology: Learning, Memory, and Cognition · doi:10.1037/a0019181 · Cited by 112 · see citing works
Pagnoni, G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4135-11.2012 · Cited by 107 · see citing works
Computational mechanisms underlying cortical responses to the affordance properties of visual scenes
Bonner, M. F., & Epstein, R. A. (2018) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1006111 · Cited by 94 · see citing works
Hirshhorn, M., Grady, C., Rosenbaum, R. S., Winocur, G., & Moscovitch, M. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.08.008 · Cited by 85 · see citing works
Navigation-associated medial parietal neurons in monkeys
Sato, N., Sakata, H., Tanaka, Y. L., & Taira, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604277103 · Cited by 82 · see citing works
Daulatzai, M. A. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1404-6 · Cited by 63 · see citing works
Rosenbaum, R. S., Winocur, G., Grady, C. L., Ziegler, M., & Moscovitch, M. (2007) · Hippocampus · doi:10.1002/hipo.20354 · Cited by 58 · see citing works
Coulombe, M.-A., Lawrence, K. S., Moulin, D. E., Morley-Forster, P., Shokouhi, M., Nielson, W. R., & Davis, K. D. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00047 · Cited by 53 · see citing works
Activation of the hippocampal complex during tactile maze solving in congenitally blind subjects
Gagnon, L., Schneider, F. C., Siebner, H. R., Paulson, O. B., Kupers, R., & Ptito, M. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.03.022 · Cited by 45 · see citing works
Herdman, K. A., Calarco, N., Moscovitch, M., Hirshhorn, M., & Rosenbaum, R. S. (2015) · Cortex · doi:10.1016/j.cortex.2015.06.008 · Cited by 46 · see citing works
Shibata, H., & Yukie, M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02868.x · Cited by 39 · see citing works
Lin, H.-C., Pan, H.-C., Lin, S.-H., Lo, Y.-C., Shen, E. T.-H., Liao, L.-D., Liao, P.-H., Chien, Y.-W., Liao, K.-D., Jaw, F.-S., et al. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00087 · Cited by 29 · see citing works
Buckwalter, J. A., Schumann, C. M., & Van Hoesen, G. W. (2008) · Experimental Brain Research · doi:10.1007/s00221-007-1203-x · Cited by 26 · see citing works
Cortico-spinal modularity in the parieto-frontal system: A new perspective on action control
Bufacchi, R. J., Battaglia-Mayer, A., Iannetti, G. D., & Caminiti, R. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102537 · Cited by 22 · see citing works
Sato, N. (2021) · Scientific Reports · doi:10.1038/s41598-021-81943-9 · Cited by 16 · see citing works
- Authors
- Maguire, E.
- Affiliations
- UCL Queen Square Institute of Neurology (GB)
- Corresponding author
- Maguire, Eleanor
- ORCID
- Maguire, Eleanor
- Venue
- Scandinavian Journal of Psychology
- Publisher
- Wiley
- Published
- 2001-07
- Volume
- 42
- Issue
- 3
- Pages
- 225-238
- ISSN
- 0036-5564 (ISSN-L)
- 1467-9450
- OpenAlex
- W2084404187
- Cited by
- 584
- References
- 0
- Citations by year
- 2026: 11 · 2025: 19 · 2024: 25 · 2023: 21 · 2022: 26 · 2021: 28 · 2020: 22 · 2019: 21 · 2018: 34 · 2017: 28 · 2016: 27 · 2015: 30 · 2014: 27 · 2013: 27 · 2012: 21
- FWCI
- 46.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Scandinavian Journal of Psychology (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
- Keywords
- retrosplenial cortex, human navigation, spatial orientation, topographical disorientation, route learning, landmark detection, hippocampus, medial temporal lobe, episodic memory, hemispheric lateralization, lesion studies, functional neuroimaging
- MeSH terms
- Animals, Gyrus Cinguli, Homing Behavior, Humans, Magnetic Resonance Imaging, Models, Neurological, Orientation, Space Perception, Tomography, Emission-Computed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review