The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.
Anterior Hippocampus and Goal-Directed Spatial Decision Making
Open accessAbstract
Planning spatial paths through our environment is an important part of everyday life and is supported by a neural system including the hippocampus and prefrontal cortex. Here we investigated the precise functional roles of the components of this system in humans by using fMRI as participants performed a simple goal-directed route-planning task. Participants had to choose the shorter of two routes to a goal in a visual scene that might contain a barrier blocking the most direct route, requiring a detour, or might be obscured by a curtain, requiring memory for the scene. The participant's start position was varied to parametrically manipulate their proximity to the goal and the difference in length of the two routes. Activity in medial prefrontal cortex, precuneus, and left posterior parietal cortex was associated with detour planning, regardless of difficulty, whereas activity in parahippocampal gyrus was associated with remembering the spatial layout of the visual scene. Activity in bilateral anterior hippocampal formation showed a strong increase the closer the start position was to the goal, together with medial prefrontal, medial and posterior parietal cortices. Our results are consistent with computational models in which goal proximity is used to guide subsequent navigation and with the association of anterior hippocampal areas with nonspatial functions such as arousal and reward expectancy. They illustrate how spatial and nonspatial functions combine within the anterior hippocampus, and how these functions interact with parahippocampal, parietal, and prefrontal areas in decision making and mnemonic function.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“In recently learned environments, the hippocampus has been shown to encode the distance to the goal (Spiers and Maguire 2007b; Viard et al. 2011; Sherrill et al. 2013; Howard et al. 2014; Chrastil et al. 2015; Balaguer et al. 2016; Spiers et al. 2017)”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Viard et al. 2011
In the citing paper
“Consistent with this argument, prior fMRI studies using recently encountered environments containing less perceptual detail found that the hippocampal activity increased with proximity to the goal (Viard et al. 2011; Sherrill et al. 2013).”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Viard et al. 2011
In the citing paper
“The correlation of hippocampal activity to distance to goal during travel periods in navigation routes in the recently learned environment agrees with prior fMRI reports of similar coding (Viard et al. 2011; Sherrill et al. 2013; Howard et al. 2014; Balaguer et al. 2016) and supports models which argue the hippocampus computes information about the future path to goal for navigational guidance (Er”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Viard et al. 2011
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Reinforcement Learning: An Introduction
Sutton, R. S., & Barto, A. (2005) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.2004.842673 · Cited by 25,268
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
The precuneus: a review of its functional anatomy and behavioural correlates
Cavanna, A. E., & Trimble, M. R. (2006) · Brain · doi:10.1093/brain/awl004 · Cited by 5,128
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358
A cortical representation of the local visual environment
Epstein, R. A., & Kanwisher, N. (1998) · Nature · doi:10.1038/33402 · Cited by 3,096
Common regions of the human frontal lobe recruited by diverse cognitive demands
Duncan, J., & Owen, A. M. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01633-7 · Cited by 2,498
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401
Self-citationBarto, A. (1998) · IFAC Proceedings Volumes · doi:10.1016/s1474-6670(17)38315-5 · Cited by 2,172
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
Research works printed but not linked: 1
- Dayan P (1991) in Advances in neural information processing systems 3, Navigating through temporal difference, eds Lippman RP Moody JE Touretzky DS (Morgan Kaufmann, San Mateo, CA), pp 464–470.
Cited by
Sorted by citations
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738
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
Viewpoints: how the hippocampus contributes to memory, navigation and cognition
Lisman, J., Buzsáki, G., Eichenbaum, H., Nadel, L., Ranganath, C., & Redish, A. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4661 · Cited by 851
Anterior hippocampus: the anatomy of perception, imagination and episodic memory
Zeidman, P., & Maguire, E. A. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.24 · Cited by 542
Hippocampal theta sequences reflect current goals
Wikenheiser, A. M., & Redish, A. D. (2015) · Nature Neuroscience · doi:10.1038/nn.3909 · Cited by 367
Aggleton, J. P. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.09.005 · Cited by 339
Howard, L. R., Javadi, A. H., Yu, Y., Mill, R. D., Morrison, L. C., Knight, R., Loftus, M. M., Staskute, L., & Spiers, H. J. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.001 · Cited by 298
Boccia, M., Nemmi, F., & Guariglia, C. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9247-8 · Cited by 222
Coding of navigational affordances in the human visual system
Bonner, M., & Epstein, R. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618228114 · Cited by 209
Grid-like processing of imagined navigation
Horner, A. J., Bisby, J. A., Zotow, E., Bush, D., & Burgess, N. (2016) · Current Biology · doi:10.1016/j.cub.2016.01.042 · Cited by 173
Self-citationHippocampus 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
Neural Mechanisms of Hierarchical Planning in a Virtual Subway Network
Balaguer, J., Spiers, H., Hassabis, D., & Summerfield, C. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.037 · Cited by 163
The role of the hippocampus in memory and mental construction
Sheldon, S., & Levine, B. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13006 · Cited by 155
Origins of landmark encoding in the brain
Yoder, R. M., Clark, B. J., & Taube, J. S. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.08.004 · Cited by 159
Hippocampal Contributions to Model-Based Planning and Spatial Memory
Vikbladh, O. M., Meager, M. R., King, J. A., Blackmon, K., Devinsky, O., Shohamy, D., Burgess, N., & Daw, N. D. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.014 · Cited by 159
Self-citationSpatial goal coding in the hippocampal formation
Nyberg, N., Duvelle, É., Barry, C., & Spiers, H. J. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.012 · Cited by 141
Brainstem Pain-Control Circuitry Connectivity in Chronic Neuropathic Pain
Mills, E. P., Pietro, F. D., Alshelh, Z., Peck, C. C., Murray, G. M., Vickers, E. R., & Henderson, L. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1647-17.2017 · Cited by 141
Goal-oriented searching mediated by ventral hippocampus early in trial-and-error learning
Ruediger, S., Spirig, D., Donato, F., & Caroni, P. (2012) · Nature Neuroscience · doi:10.1038/nn.3224 · Cited by 135
The Versatile Wayfinder: Prefrontal Contributions to Spatial Navigation
Patai, E. Z., & Spiers, H. J. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.02.010 · Cited by 141
Chrastil, E. R., Sherrill, K. R., Hasselmo, M. E., & Stern, C. E. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1209-15.2015 · Cited by 128
Neural evidence supports a novel framework for spatial navigation
Chrastil, E. R. (2013) · Psychonomic Bulletin & Review · doi:10.3758/s13423-012-0351-6 · Cited by 126
Medina, A. M., Seasholtz, A. F., Sharma, V., Burke, S., Bunney, W. E., Myers, R., Schatzberg, A. F., Akil, H., & Watson, S. J. (2012) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2012.11.002 · Cited by 125
Bilateral Vestibular Hypofunction: Challenges in Establishing the Diagnosis in Adults
van de Berg, R., van Tilburg, M. J., & Kingma, H. (2015) · ORL · doi:10.1159/000433549 · Cited by 117
Neural systems supporting navigation
Spiers, H. J., & Barry, C. (2014) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2014.08.005 · Cited by 125
Serino, S., Pedroli, E., Tuena, C., Leo, G. D., Stramba‐Badiale, M., Goulene, K., Mariotti, N. G., & Riva, G. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00240 · Cited by 119
The influence of action on episodic memory: A virtual reality study
Plancher, G., Barra, J., Orriols, É., & Piolino, P. (2012) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470218.2012.722657 · Cited by 116
Phase-tuned neuronal firing encodes human contextual representations for navigational goals
Watrous, A. J., Miller, J. F., Qasim, S. E., Fried, I., & Jacobs, J. (2018) · eLife · doi:10.7554/elife.32554 · Cited by 110
Patai, E. Z., Javadi, A.-H., Ozubko, J. D., O’Callaghan, A., Ji, S., Robin, J., Grady, C., Winocur, G., Rosenbaum, R. S., Moscovitch, M., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz044 · Cited by 102
Effects of Enactment in Episodic Memory: A Pilot Virtual Reality Study with Young and Elderly Adults
Jebara, N., Orriols, É., Zaoui, M., Berthoz, A., & Piolino, P. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00338 · Cited by 107
Solving the detour problem in navigation: a model of prefrontal and hippocampal interactions
Spiers, H. J., & Gilbert, S. J. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00125 · Cited by 94
Mapping sequence structure in the human lateral entorhinal cortex
Bellmund, J. L. S., Deuker, L., & Doeller, C. F. (2019) · eLife · doi:10.7554/elife.45333 · Cited by 98
Self-citationBornstein, A. M., & Daw, N. D. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003387 · Cited by 96
Sensory Substitution and the Neural Correlates of Navigation in Blindness
Chebat, D., Harrar, V., Kupers, R. C., Maidenbaum, S., Amedi, A., & Ptito, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-54446-5_6 · Cited by 90
Persson, J., Herlitz, A., Engman, J., Morell, A., Sjölie, D., Wikström, J., & Söderlund, H. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.050 · Cited by 82
Compensation Following Bilateral Vestibular Damage
McCall, A. A., & Yates, B. J. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00088 · Cited by 80
The Neural Representation of Prospective Choice during Spatial Planning and Decisions
Kaplan, R., King, J. A., Koster, R., Penny, W. D., Burgess, N., & Friston, K. J. (2017) · PLoS Biology · doi:10.1371/journal.pbio.1002588 · Cited by 81
Self-citationChrastil, E. R., Sherrill, K. R., Aselcioglu, I., Hasselmo, M. E., & Stern, C. E. (2017) · eNeuro · doi:10.1523/eneuro.0346-16.2017 · Cited by 74
Viard, A., Desgranges, B., Eustache, F., & Piolino, P. (2012) · Brain and Cognition · doi:10.1016/j.bandc.2012.05.004 · Cited by 71
Self-citationBeaujoin, J., Palomero‐Gallagher, N., Boumezbeur, F., Axer, M., Bernard, J., Poupon, F., Schmitz, D., Mangin, J., & Poupon, C. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1617-1 · Cited by 72
Goal-directed actions transiently depend on dorsal hippocampus
Bradfield, L. A., Leung, B. K., Boldt, S., Liang, S., & Balleine, B. W. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0693-8 · Cited by 65
Increase in hippocampal theta oscillations during spatial decision making
Belchior, H., Lopes‐dos‐Santos, V., Tort, A. B. L., & Ribeiro, S. T. G. (2014) · Hippocampus · doi:10.1002/hipo.22260 · Cited by 66
Hippocampal neuronal activity is aligned with action plans
Zutshi, I., Apostolelli, A., Yang, W., Zheng, Z. S., Dohi, T., Balzani, E., Williams, A. H., Savin, C., & Buzsáki, G. (2025) · Nature · doi:10.1038/s41586-024-08397-7 · Cited by 63
Time Is Not Space: Core Computations and Domain-Specific Networks for Mental Travels
Gauthier, B., & van Wassenhove, V. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1400-16.2016 · Cited by 63
Meilinger, T., Strickrodt, M., & Bülthoff, H. (2016) · Cognition · doi:10.1016/j.cognition.2016.06.003 · Cited by 60
Distributed cognitive maps reflecting real distances between places and views in the human brain
Sulpizio, V., Committeri, G., & Galati, G. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00716 · Cited by 51
Functional connectivity of hippocampal subregions in PTSD: relations with symptoms
Malivoire, B. L., Girard, T. A., Patel, R., & Monson, C. M. (2018) · BMC Psychiatry · doi:10.1186/s12888-018-1716-9 · Cited by 52
Brown, T. I., Hasselmo, M. E., & Stern, C. E. (2014) · Hippocampus · doi:10.1002/hipo.22273 · Cited by 51
Which way and how far? Tracking of translation and rotation information for human path integration
Chrastil, E. R., Sherrill, K. R., Hasselmo, M. E., & Stern, C. E. (2016) · Human Brain Mapping · doi:10.1002/hbm.23265 · Cited by 50
Anxiety-related activity of ventral hippocampal interneurons
Forro, T., Volitaki, E., Malagon‐Vina, H., Klausberger, T., Nevian, T., & Ciocchi, S. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102368 · Cited by 51
Autobiographical memory in semantic dementia: New insights from two patients using fMRI
Viard, A., Desgranges, B., Matuszewski, V., Lebreton, K., Belliard, S., Sayette, V. D. L., Eustache, F., & Piolino, P. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.08.007 · Cited by 41
Self-citationPoucet, B., & Hok, V. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.06.003 · Cited by 43
Wagner, G., Gussew, A., Köhler, S., de la Cruz, F., Smesny, S., Reichenbach, J. R., & Bär, K. (2016) · Cortex · doi:10.1016/j.cortex.2016.03.022 · Cited by 40
Hippocampal CA1 activity correlated with the distance to the goal and navigation performance
Spiers, H. J., Ólafsdóttir, H. F., & Lever, C. (2017) · Hippocampus · doi:10.1002/hipo.22813 · Cited by 42
Contracted time and expanded space: the impact of circumnavigation on judgements of space and time
Brunec, I. K., Javadi, A.-H., Zisch, F. E. L., & Spiers, H. J. (2017) · Cognition · doi:10.1016/j.cognition.2017.06.004 · Cited by 37
Ploran, E. J., Tang, C. C., Mackay, M. C., SMALL, M. P., Anderson, E., Storbeck, J., Bascetta, B., Kang, S., Aranow, C. B., Sartori, C., et al. (2019) · Lupus Science & Medicine · doi:10.1136/lupus-2019-000327 · Cited by 35
Spatial Attention, Motor Intention, and Bayesian Cue Predictability in the Human Brain
Kuhns, A. B., Dombert, P. L., Mengotti, P., Fink, G. R., & Vossel, S. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3255-16.2017 · Cited by 34
The hippocampo-cortical loop: Spatio-temporal learning and goal-oriented planning in navigation
Hirel, J., Gaussier, P., Quoy, M., Banquet, J. P., Save, É., & Poucet, B. (2013) · Neural Networks · doi:10.1016/j.neunet.2013.01.023 · Cited by 40
Baumann, O., & Mattingley, J. B. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00073 · Cited by 33
The ventral hippocampus is involved in multi‐goal obstacle‐rich spatial navigation
Contreras, M., Pelc, T., Llofriu, M., Weitzenfeld, A., & Fellous, J. (2018) · Hippocampus · doi:10.1002/hipo.22993 · Cited by 37
A map of spatial navigation for neuroscience
Parra-Barrero, E., Vijayabaskaran, S., Seabrook, E., Wiskott, L., & Cheng, S. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105200 · Cited by 39
Dissociable Representations of Environmental Size and Complexity in the Human Hippocampus
Baumann, O., & Mattingley, J. B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0350-13.2013 · Cited by 31
Javadi, A., Patai, E. Z., Marin-Garcia, E., Margolis, A., Tan, H. M., Kumaran, D., Marko Nardini, A., Penny, W. D., Düzel, E., Dayan, P., et al. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01414 · Cited by 33
Chaposhloo, M., Nicholson, A. A., Becker, S., McKinnon, M. C., Lanius, R. A., Shaw, S. B., & Initiative, A. D. N. (2023) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103417 · Cited by 27
Functional correlates of likelihood and prior representations in a virtual distance task
Wiener, M., Michaelis, K., & Thompson, J. C. (2016) · Human Brain Mapping · doi:10.1002/hbm.23232 · Cited by 26
The Key of the Maze: The role of mental imagery and cognitive flexibility in navigational planning
Bocchi, A., Carrieri, M., Lancia, S., Quaresima, V., & Piccardi, L. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.05.009 · Cited by 29
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
Scale-Free Navigational Planning by Neuronal Traveling Waves
Alijani, A. K., Urbanczik, R., & Senn, W. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127269 · Cited by 25
Ferretti, F., Adornetti, I., Cosentino, E., & Marini, A. (2012) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2012.11.001 · Cited by 25
Bär, K., Herbsleb, M., Schumann, A., de la Cruz, F., Gabriel, H. W., & Wagner, G. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00145 · Cited by 27
Christiansen, K., Metzler‐Baddeley, C., Parker, G. D., Muhlert, N., Jones, D. K., Aggleton, J. P., & Vann, S. D. (2016) · Brain and Behavior · doi:10.1002/brb3.604 · Cited by 24
Parietal and medial temporal lobe interactions in working memory goal-directed behavior
Lee, B., Kim, J. S., & Chung, C. K. (2022) · Cortex · doi:10.1016/j.cortex.2022.02.005 · Cited by 22
Multi-scale goal distance representations in human hippocampus during virtual spatial navigation
Liu, J., Chen, D., Xiao, X., Zhang, H., Zhou, W., Liang, S., Kunz, L., Schulze‐Bonhage, A., Axmacher, N., & Wang, L. (2023) · Current Biology · doi:10.1016/j.cub.2023.04.033 · Cited by 23
Reynolds-Lallement, N. C., Zhong, J. Y., Clendinen, C., Moffat, S. D., & Magnusson, K. R. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116069 · Cited by 23
Dombrovski, A. Y., Luna, B., & Hallquist, M. N. (2020) · Nature Communications · doi:10.1038/s41467-020-18864-0 · Cited by 20
Chen, Q., Zhao, Q., Jin, J., Sun, Y., Chen, W., Lu, J., Lv, P., Liu, J., Li, X., Wang, J., et al. (2021) · Cortex · doi:10.1016/j.cortex.2020.12.022 · Cited by 21
Carrieri, M., Lancia, S., Bocchi, A., Ferrari, M., Piccardi, L., & Quaresima, V. (2017) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9734-7 · Cited by 16
Rigid reduced successor representation as a potential mechanism for addiction
Shimomura, K., Kato, A., & Morita, K. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15227 · Cited by 15
Distinct encoding of risk and value in economic choice between multiple risky options
Wright, N. D., Symmonds, M., & Dolan, R. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.023 · Cited by 15
Human spatial representation: what we cannot learn from the studies of rodent navigation
Zhao, M. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00781.2017 · Cited by 18
Dissociable Influences of Skewness and Valence on Economic Choice and Neural Activity
Wright, N. D., Symmonds, M., Morris, L. S., & Dolan, R. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083454 · Cited by 13
Remote memory and temporal lobe epilepsy
McAndrews, M. P. (2012) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199580286.003.0013 · Cited by 11
Liang, Q., Liao, J., Li, J., Zheng, S., Jiang, X., & Huang, R. (2022) · Human Brain Mapping · doi:10.1002/hbm.26069 · Cited by 10
Spatial Cognition: Goal-Vector Cells in the Bat Hippocampus
de Cothi, W., & Spiers, H. J. (2017) · Current Biology · doi:10.1016/j.cub.2017.01.061 · Cited by 11
In vivo structural connectivity of the reward system along the hippocampal long axis
Elliott, B. L., Mohyee, R. A., Ballard, I. C., Olson, I. R., Ellman, L. M., & Murty, V. P. (2024) · Hippocampus · doi:10.1002/hipo.23608 · Cited by 9
Situationally appropriate behavior: translating situations into appetitive behavior modes
Behrendt, R. (2013) · Reviews in the Neurosciences · doi:10.1515/revneuro-2013-0037 · Cited by 9
Accounting for multiscale processing in adaptive real-world decision-making via the hippocampus
Mehrotra, D., & Dubé, L. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1200842 · Cited by 9
Norman (2017) · doi:10.1016/j.pscychresns.2017.07.007 · Cited by 9
Extending neural systems for navigation to hunting behavior
Goodroe, S. C., & Spiers, H. J. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102545 · Cited by 9
Negative BOLD Response in the Hippocampus during Short-term Spatial Memory Retrieval
Nilsson, J., Ferrier, I. N., Coventry, K. R., Bester, A., & Finkelmeyer, A. E. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00396 · Cited by 10
Human Navigation Without and With Vision - the Role of Visual Experience and Visual RegionsPreprint
Maidenbaum, S., Chebat, D., & Amedi, A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/480558 · Cited by 9
HUANG, Y., Jiang, C., Hongzhi, L. I. U., & Li, S. (2023) · Acta Psychologica Sinica · doi:10.3724/sp.j.1041.2023.00994 · Cited by 8
Sulpizio, V., Teghil, A., Pitzalis, S., & Boccia, M. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02790-8 · Cited by 7
Tuena, C., Riva, G., Murru, I., Campana, L., Goulene, K., Pedroli, E., & Stramba‐Badiale, M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.992498 · Cited by 8
Create your own path: social cerebellum in sequence-based self-guided navigation
Li, M., Haihambo, N. P., Bylemans, T., Ma, Q., Heleven, E., Baeken, C., Baetens, K., Deroost, N., & Overwalle, F. V. (2024) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsae015 · Cited by 7
Outcome contingency selectively affects the neural coding of outcomes but not of tasks
Wisniewski, D., Forstmann, B. U., & Braß, M. (2019) · Scientific Reports · doi:10.1038/s41598-019-55887-0 · Cited by 7
Jeffery, K. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21077-8 · Cited by 9
Ziegler, M. G., Liu, Z.-X., Arsenault, J., Dang, C., Grady, C., Rosenbaum, R. S., & Moscovitch, M. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad272 · Cited by 6
Gurguryan, L., Fenerci, C., Ngo, N., & Sheldon, S. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02170 · Cited by 8
Hasantash, M., Li, Y., Torres-Herraez, A., Kellendonk, C., & Anacker, C. (2025) · Science Advances · doi:10.1126/sciadv.adx7514 · Cited by 7
Jamal, A., Walker, T. L., Nguyen, A., Berman, R. F., Kempermann, G., & Waldau, B. (2015) · Cell Transplantation · doi:10.3727/096368915x687011 · Cited by 5
Metadata
- Authors
- Viard, A., Doeller, C. F., Hartley, T., Bird, C. M., & Burgess, N.
- Affiliations
- University College London (GB)
- Radboud University Nijmegen (NL)
- UCL Queen Square Institute of Neurology (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-03-23
- Volume
- 31
- Issue
- 12
- Pages
- 4613-4621
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6622909
- OpenAlex
- W2132041417
- Cited by
- 144
- References
- 83
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 4 · 2023: 12 · 2022: 11 · 2021: 5 · 2020: 8 · 2019: 8 · 2018: 12 · 2017: 20 · 2016: 11 · 2015: 7 · 2014: 10 · 2013: 12 · 2012: 7
- FWCI
- 5.36
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Figshare (submittedVersion, cc-by)
- Sussex Research Online (University of Sussex) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion, other-oa)
- Funders
- Wellcome Trust
- University College London
- European Commission
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- anterior hippocampus, goal-directed navigation, spatial decision-making, route planning, parahippocampal gyrus, medial prefrontal cortex, posterior parietal cortex, precuneus, goal proximity, spatial memory, reward expectancy, arousal
- MeSH terms
- Adult, Arousal, Behavior, Decision Making, Female, Goals, Hippocampus, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Memory, Oxygen, Parietal Lobe, Reaction Time, Reward, Space Perception, Visual Perception, Prefrontal Cortex, Young Adult
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