The DOI matches its Crossref record; 48 of the 49 references it cites were found in a registry or an index.
The Hippocampus and Entorhinal Cortex Encode the Path and Euclidean Distances to Goals during Navigation
Open accessAbstract
BACKGROUND: Despite decades of research on spatial memory, we know surprisingly little about how the brain guides navigation to goals. While some models argue that vectors are represented for navigational guidance, other models postulate that the future path is computed. Although the hippocampal formation has been implicated in processing spatial goal information, it remains unclear whether this region processes path- or vector-related information. RESULTS: We report neuroimaging data collected from subjects navigating London's Soho district; these data reveal that both the path distance and the Euclidean distance to the goal are encoded by the medial temporal lobe during navigation. While activity in the posterior hippocampus was sensitive to the distance along the path, activity in the entorhinal cortex was correlated with the Euclidean distance component of a vector to the goal. During travel periods, posterior hippocampal activity increased as the path to the goal became longer, but at decision points, activity in this region increased as the path to the goal became closer and more direct. Importantly, sensitivity to the distance was abolished in these brain areas when travel was guided by external cues. CONCLUSIONS: The results indicate that the hippocampal formation contains representations of both the Euclidean distance and the path distance to goals during navigation. These findings argue that the hippocampal formation houses a flexible guidance system that changes how it represents distance to the goal depending on the fluctuating demands of navigation.
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
Figures






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
“The hippocampus mask was a combination of right mid and posterior sections (a priori based on the results of Howard et al. 2014).”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Howard et al. 2014
In the citing paper
“such distance tracking is not automatic and requires goal-directed navigation.”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Howard et al. 2014
In the citing paper
“However, while Howard et al. (2014) found a positive correlation between posterior right hippocampal activity and distance, we observed a negative correlation in the recently learned environments.”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Howard et al. 2014
In the citing paper
“The observation that this was specific to navigation routes and not present in control routes is consistent with prior evidence (Howard et al. 2014) that such distance tracking is not automatic and requires goal-directed navigation.”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Howard et al. 2014
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 Howard et al. 2014
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
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
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
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809
Andersen, R. A., Snyder, L. H., Bradley, D. C., & Xing, J. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.303 · Cited by 1,486
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377
Knowing Where and Getting There: A Human Navigation Network
Maguire, E. A., Burgess, N., Donnett, J. G., Frackowiak, R. S. J., Frith, C. D., & O'Keefe, J. (1998) · Science · doi:10.1126/science.280.5365.921 · Cited by 1,303
Hippocampal place-cell sequences depict future paths to remembered goals
Pfeiffer, B. E., & Foster, D. J. (2013) · Nature · doi:10.1038/nature12112 · Cited by 1,216
Long-axis specialization of the human hippocampus
Poppenk, J., Evensmoen, H. R., Moscovitch, M., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.03.005 · Cited by 1,100
Neural ensembles in CA3 transiently encode paths forward of the animal at a decision point
Johnson, A., & Redish, A. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3761-07.2007 · Cited by 1,003
Cited by
Sorted by citations
Items 201–295 of 295
Neural Representation Precision of Distance Predicts Children's Arithmetic Performance
Zhao, H., Wang, Q., Xu, J., Yao, Y., Lyu, J., Yang, J., & Qin, S. (2025) · Human Brain Mapping · doi:10.1002/hbm.70184 · Cited by 3
Rank labels scaffold social cognitive maps in the hippocampal-entorhinal system
Liu, J., Zhou, Y., Wang, H., Yang, L., & Li, H. (2025) · NeuroImage · doi:10.1016/j.neuroimage.2025.121366 · Cited by 3
Zhao, H., Zhao, B., He, J., & Liu, M. (2025) · Nature Communications · doi:10.1038/s41467-025-64986-8 · Cited by 3
McNamara, T. P., & Qi, Y. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00022-5 · Cited by 3
Temporal dynamics of object location processing in allocentric reference frame
Török, Á., Kóbor, A., Persa, G., Galambos, P., Bárányi, P., Csépe, V., & Honbolygó, F. (2017) · Psychophysiology · doi:10.1111/psyp.12886 · Cited by 3
Neurophenomenal structuralism and the role of computational context
Päßler, M., & Doerig, A. (2025) · Philosophy and the Mind Sciences · doi:10.33735/phimisci.2025.11824 · Cited by 3
Neuroscience: Teleporting Mind into Body and Space
Javadi, A., & Spiers, H. J. (2015) · Current Biology · doi:10.1016/j.cub.2015.04.010 · Cited by 3
Self-citationTask-related connectivity of decision points during spatial navigation in a schematic map
Qi, Q., Weng, Y., Zheng, S., Wang, S., Liu, S., Huang, Q., & Huang, R. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02466-1 · Cited by 5
Author response: Neural Trajectories of Conceptually Related Events
Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2024) · eLife · doi:10.7554/elife.96895.1.sa3 · Cited by 3
Human Hippocampal Theta Oscillations Organise Distance to Goal CodingPreprint
Huang, Z., Bisby, J. A., Burgess, N., & Bush, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.12.628182 · Cited by 3
Map-like representations of emotion knowledge in hippocampal-prefrontal systems
Ma, Y., & Kragel, P. A. (2026) · Nature Communications · doi:10.1038/s41467-025-68240-z · Cited by 4
Human hippocampal theta–gamma coupling coordinates sequential planning during navigation
Huang, Z., Bisby, J. A., Burgess, N., & Bush, D. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2513547123 · Cited by 2
Robinson, J. C., LaChance, P. A., Malmberg, S., Fang, J., Sankaranarayanan, S., Stern, C. E., & Hasselmo, M. E. (2026) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2025.0251 · Cited by 2
The vicarious nature of hippocampal theta sequences
Damphousse, C. C., Gagliardi, C. M., Peterson, J. G., Feng, C., Schmidt, B., Mugan, U., & Redish, A. D. (2026) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2025.0242 · Cited by 2
Kadieva, D., Gallo, F., Ulanov, M., Шестакова, А. Н., Moiseeva, V., Khodorovskaya, A. М., & Agranovich, O. Е. (2023) · Genes and Cells · doi:10.23868/gc568311 · Cited by 2
Integration of Euclidean and path distances in hippocampal maps
Ottink, L., de Haas, N., & Doeller, C. F. (2025) · Scientific Reports · doi:10.1038/s41598-025-90504-3 · Cited by 4
Hippocampus Parcellation via Discriminative Embedded Clustering of fMRI Functional Connectivity
Peng, L., Hou, C., Su, J., Shen, H., Wang, L., Hu, D., & Zeng, L. (2023) · Brain Sciences · doi:10.3390/brainsci13050757 · Cited by 2
Javadi, A., Patai, E. Z., Margois, A., Tan, H. M., Kumaran, D., Marko Nardini, A., Penny, W. D., Düzel, E., Dayan, P., & Spiers, H. J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/301697 · Cited by 2
Self-citationTracking the emergence of location-based spatial representations in human scene-selective cortexPreprint
Berens, S. C., Joensen, B. H., & Horner, A. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/547976 · Cited by 2
Human Navigation in a Multilevel Travelling Salesperson ProblemPreprint
Mavros, P., van Eggermond, M. A. B., & Hölscher, C. (2022) · doi:10.31234/osf.io/4sv5w · Cited by 2
Human path integration and the neural underpinnings
Chrastil, E. R. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00016-4 · Cited by 2
Ottink, L., van den Berg, L., Peters, I., van der Geest, T., Haak, K. V., Doeller, C. F., & Wezel, R. J. A. V. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.20.563338 · Cited by 2
The cognitive map and its intrinsic mechanisms
Wenyan, W. U., & Wang, L. (2023) · Advances in Psychological Science · doi:10.3724/sp.j.1042.2023.01856 · Cited by 1
Sivanesan, S., Howell, M. D., Kaushik, V., Rajadas, J., Pari, S. S., & Goyal, P. (2024) · Current Alzheimer Research · doi:10.2174/0115672050324909240823104209 · Cited by 1
Akan, O., Chandreswaran, V., Bierbrauer, A., Soldan, H. D., Axmacher, N., Wolf, O. T., & Merz, C. J. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003661 · Cited by 2
How Does Aging Impact the Structure and Function of Parallel Navigation Circuits across Mammals?
Barnes, C. A., Srivathsa, S., Hill, P. F., Srokova, S., & Ekstrom, A. D. (2026) · Springer eBooks · doi:10.1007/978-3-032-20563-6_13 · Cited by 1
Cognitive maps as a medium for thought
Yousif, S. R., & Epstein, R. A. (2026) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2026.07.010 · Cited by 2
Dissociation of categorical and coordinate spatial relations on dynamic network organization states
Hao, X., Chen, Z., Huang, T., Song, Y., Kong, X., & Liu, J. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.972375 · Cited by 1
Representation of the inferred relationships in a map‐like space
Li, J., Liang, Q., Liao, J., Zheng, S., Chen, K., & Huang, R. (2023) · Human Brain Mapping · doi:10.1002/hbm.26309 · Cited by 1
Being a body, having a body: Looking down and looking out in architecture and neuroscience
Zisch, F., & Gage, S. A. (2024) · ARENA Journal of Architectural Research · doi:10.55588/ajar.404 · Cited by 1
Altered dendritic morphology of MEC II pyramidal and stellate cells in Rett syndrome mice
Krishnan, M., Mydeen, A. B., Nakhal, M. M., Ibrahim, M. F., Jayaraj, R. L., Ljubisavljević, M., Hamad, M. I. K., & Ismail, F. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1580435 · Cited by 1
Han, D., Qin, T., Yang, T., Liao, H., Hei, Q., Yu, F., Si, B., & Dong, W. (2025) · Geo-spatial Information Science · doi:10.1080/10095020.2025.2541878 · Cited by 2
Big neuroimaging data-informed mind-brain association studies: Methodology and applications
Zuo, X., & Yang, Z. (2015) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/n972014-00806 · Cited by 1
Brunec, I. K., Ozubko, J. D., Ander, T., Moscovitch, M., & Barense, M. D. (2018) · OSF Preprints (OSF Preprints) · doi:10.31219/osf.io/g6dp3 · Cited by 2
Clements, M. (2020) · University of Hertfordshire Research Archive (University of Hertfordshire) · doi:10.18745/th.22616 · Cited by 1
Hippocampal Place-like Signal in Latent SpacePreprint
Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.15.499827 · Cited by 1
Hu, G., Li, N., Dai, M., Liu, Q., Shi, X., & Gu, Y. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4169250 · Cited by 1
Pink, D., Ilkel, E., Chandreswaran, V., Moser, D., Getzmann, S., Gajewski, P. D., Axmacher, N., & Zhang, H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.11.556925 · Cited by 2
Navigation in real-world environments
Kessler, F., Frankenstein, J., & Rothkopf, C. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00091-7 · Cited by 1
Neural Trajectories of Conceptually Related EventsPreprint
Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2024) · eLife · doi:10.7554/elife.96895 · Cited by 1
A multiplexed striatal architecture for generalized spatial goal progressPreprint
Takakuwa, N., Golipour, Z., & Ito, H. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.08.716650 · Cited by 1
Geoinformation zur Navigationsunterstützung
Winter, S. (2019) · Springer Reference Naturwissenschaften · doi:10.1007/978-3-662-47096-1_65
Neural plasticity in decision making and memory formation
Garvert, M. M. (2016) · UCL Discovery (University College London)
Sage, R. (2017) · SensePublishers eBooks · doi:10.1007/978-94-6351-185-8_2
Sage, R. (2017) · SensePublishers eBooks · doi:10.1007/978-94-6351-185-8_1
Jordan, J. T., Tong, Y., & Pytte, C. L. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/437491
The Human Hippocampus Contributes to Egocentric Coding of Distance to a Local LandmarkPreprint
Chen, X., Vieweg, P., & Wolbers, T. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/465997
Spatial Navigation in Rats and Humans: A Neuropsychological Perspective
Stuart, I. (2019) · Brain Impairment · doi:10.1017/brimp.2019.5
Neurogenesis is Altered Between and Across Brain Regions After Neurodegeneration and Injury
Perez, A. (2019) · CUNY Academic Works (City University of New York)
Interhemispheric Communication and Lateralization in the Mouse Hippocampus
Jordan, J. T. (2019) · CUNY Academic Works (City University of New York)
Murray, E. A., Wise, S. P., Baldwin, M. K. L., & Graham, K. S. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780198828051.003.0004
The role of the default mode network in contextual control
Smith, V. (2019) · Apollo (University of Cambridge) · doi:10.17863/cam.49069
Zhang, B., Wang, F., Zhang, Q., & Naya, Y. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.22.215517
Javadi, A., Patai, E. Z., Marin-Garcia, E., Margois, A., Tan, H. M., Kumaran, D., Marko Nardini, A., Penny, W. D., Düzel, E., Dayan, P., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/362319
Self-citationWang, S.-F., Carr, V. A., Favila, S. E., Bailenson, J. N., Brown, T. I., Jiang, J., & Wagner, A. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.18.389346
Hippocampal Contributions to Structuring and Segmenting Experience
Brunec, I. K. (2019) · TSpace (University of Toronto)
Wild Animals as the Model Subjects to Study the Hippocampal Formation, Spatial Navigation and Memory
Pleskacheva, M. G. (2021) · Advances in intelligent systems and computing · doi:10.1007/978-3-030-71637-0_57
A Scale-Dependent Neural System for Human Spatial NavigationPreprint
Dong, W., Wang, S., Liu, Y., Wan, X., Liu, J., Hu, S., Pei, T., & Meng, L. (2021) · Research Square · doi:10.21203/rs.3.rs-284228/v1
Geoinformation zur Navigationsunterstützung
Winter, S. (2015) · Springer eBooks · doi:10.1007/978-3-662-46900-2_65-1
The non-Euclidean properties of human spatial representation
Du, Y. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00070-x
State-Dependent Online Reactivations for Different Learning Strategies in ForagingPreprint
Son, S., Wang, M. Z., Hayden, B. Y., & Yoo, S. B. M. (2024) · SSRN Electronic Journal · doi:10.1101/2024.03.25.586512 · Cited by 1
Effects of brain lesions on human spatial navigation
Li, A., Lei, X., & Rosenbaum, R. S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00153-4
Reviewer #1 (Public Review): Neural Trajectories of Conceptually Related Events
Schafer, M., Kamilar-Britt, P., Sahani, V., et al. (2024) · eLife · doi:10.7554/elife.96895.1.sa1
Reviewer #2 (Public Review): Neural Trajectories of Conceptually Related Events
Schafer, M., Kamilar-Britt, P., Sahani, V., et al. (2024) · eLife · doi:10.7554/elife.96895.1.sa0
eLife Assessment: Neural Trajectories of Conceptually Related Events
Diedrichsen, J. (2024) · eLife · doi:10.7554/elife.96895.1.sa2
Neural Trajectories of Conceptually Related EventsPreprint
Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2024) · eLife · doi:10.7554/elife.96895.1
Becker, S. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.17 · Cited by 1
Computational Models of Hippocampal Cognitive Function
Bush, D., & Burgess, N. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0016
Cerrotti, F., Salvador, A., Hamroun, S., Lebreton, M. P., & Palminteri, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.15.648746
Hippocampal Plasticity and Navigational Skills in Blindness
Bleau, M., Chebat, D., Schneider, F., & Ptito, M. (2025) · IntechOpen eBooks · doi:10.5772/intechopen.1011497
Glennerster, A. (2025) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2025.109233
Kannan, A. L., Patnaik, A., Theurer, A., Demuth, L., Körte, M., Landsberger, N., & Zagrebelsky, M. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115457
Cai, Y., Wang, J., Qiu, Y., & Huang, R. (2025) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.a.101
Qiu, Y., Zheng, S., Li, H., Lin, S. T., & Huang, R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.20.683540
Graph properties drive navigational selection between equidistant routes
Chi, L., Starrett, M. J., Rao, Y., & Chrastil, E. R. (2025) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2025.109310
Age-related spatial discrimination: Investigating hippocampal structural foundations
Wu, J., Zhang, J., & Li, H. (2025) · Brain and Cognition · doi:10.1016/j.bandc.2025.106380
Qiu, Y., Zheng, S., Li, H., Lin, S. T., & Huang, R. (2025) · eLife · doi:10.7554/elife.107265
Qiu, Y., Zheng, S., Li, H., Lin, S. T., & Huang, R. (2025) · eLife · doi:10.7554/elife.107265.1
Investigating the Effects of Complexity and Landmarks on Cognitive Maps Using Virtual RealityPreprint
Rushton, J. D., & Mattingley, J. B. (2025) · SSRN Electronic Journal · doi:10.21203/rs.3.rs-8350357/v1
Spatial updating in amnesia using an eye movement analogue of a path integration task
Khosla, A., Rosenbaum, R. S., Moscovitch, M., & Ryan, J. D. (2025) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2025.109354
Construction of individual-specific social cognitive maps in the human brain
Gao, T., Deng, Y., & Han, S. (2026) · Cell Reports · doi:10.1016/j.celrep.2025.116890
Neural Trajectories of Conceptually Related EventsPreprint
Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2026) · eLife · doi:10.7554/elife.96895.2
Spatial Navigation in Humans and Rodents
Ólafsdóttir, H. F., Bičanski, A., Creem-Regehr, S. H., Dilks, D. D., Donato, F., Epstein, R. A., Farran, E. K., Jacobs, J., Kunz, L., Wills, T. J., et al. (2026) · Springer eBooks · doi:10.1007/978-3-032-20563-6_9
Planning and Imagination in the Navigational Domain
Jadhav, S. P. (2026) · Springer eBooks · doi:10.1007/978-3-032-20563-6_10
Hippocampo-cortical interaction underlying episodic memory
Bochereau, A. (2020) · theses.fr (ABES) · doi:10.70675/8f206effz0c76z40d0z91e6z15ccb174c9f1
Prefrontal brain-to-brain synchrony during human group hunting: Evidence from fNIRS hyperscanningPreprint
Yavuz, E., Xu, C., Liu, W., Slinn, C., Mitchell, A., Ali, J., Bloom, N., Khatun, N., Kirk, P. A., Zisch, F., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.05.716331
Self-citationYovel, Y. (2026) · Current Biology · doi:10.1016/j.cub.2026.03.052
Feld, G. B., Velasco, P. F., Gahnstrom, C. J., Gerchen, M. F., Mian, Q., Bernard, M., Garvert, M. M., Dick, F., & Spiers, H. J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.24.740285
Self-citationReliability of Spatial Cues Modifies Entorhinal-Hippocampal Functional Connectivity
Merhav, M. (2026) · Lecture notes in computer science · doi:10.1007/978-3-032-36716-7_10
Acute Hypoxia Disrupts Multiple Processes Supporting Spatial NavigationPreprint
McKeown, D. J., Bahnson-Wright, H. M., Caldwell, T., Marks, M., Marshall, G. R., Newton, H., Stenholm, D., Young, M., Angus, D. J., & Schinazi, V. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.24.753962
Successor representation supports structural learning of syllable sequencesPreprint
Liu, J., Wang, Y., Feng, J., Zhao, H., He, Q., Yang, X., & Liang, B. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.03.756368
Ferreira, J. M. A., & Tukaiev, S. (2026) · Advances in Molecular Imaging · doi:10.4236/ami.2026.154004
Mısır, E., Aydın, Ö., Koçak, O. M., Öztürk-Işık, E., Çíçek, M., Üstün, S., Kırkıcı, B., Eren, E. E., & Pekacar, S. (2026) · Biological Psychology · doi:10.1016/j.biopsycho.2026.109421
Metadata
- Authors
- Howard, L. R., Javadi, A. H., Yu, Y., Mill, R. D., Morrison, L. C., Knight, R., Loftus, M. M., Staskute, L., & Spiers, H. J.
- Affiliations
- German Center for Neurodegenerative Diseases (DE)
- University College London (GB)
- University of St Andrews (GB)
- University of Hertfordshire (GB)
- Corresponding author
- Spiers, Hugo J.
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2014-06
- Volume
- 24
- Issue
- 12
- Pages
- 1331-1340
- ISSN
- 0960-9822 (ISSN-L)
- PMC
- PMC4062938
- OpenAlex
- W2098497273
- Cited by
- 298
- References
- 49
- Citations by year
- 2026: 18 · 2025: 29 · 2024: 30 · 2023: 29 · 2022: 24 · 2021: 22 · 2020: 24 · 2019: 27 · 2018: 31 · 2017: 28 · 2016: 18 · 2015: 14 · 2014: 3
- FWCI
- 11.72
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Current Biology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Kent Academic Repository (University of Kent) (acceptedVersion)
- University of Hertfordshire Research Archive (University of Hertfordshire) (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- DZNE Pub (submittedVersion)
- University of Hertfordshire Research Archive (University of Hertfordshire) (submittedVersion, cc-by)
- Funders
- James S. McDonnell Foundation
- Wellcome Trust (094850/Z/10/Z, 094850)
- Biotechnology and Biological Sciences 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
- hippocampus, entorhinal cortex, path distance, Euclidean distance, spatial navigation, goal-directed navigation, vector representation, medial temporal lobe, external cues, spatial memory
- MeSH terms
- Adult, Cues, Hippocampus, Humans, London, Male, Orientation, Temporal Lobe, Entorhinal Cortex, Young Adult, Spatial Navigation
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