Structure learning and the posterior parietal cortex
Abstract
We propose a theory of structure learning in the primate brain. We argue that the parietal cortex is critical for learning about relations among the objects and categories that populate a visual scene. We suggest that current deep learning models exhibit poor global scene understanding because they fail to perform the relational inferences that occur in the primate dorsal stream. We review studies of neural coding in primate posterior parietal cortex (PPC), drawing the conclusion that neurons in this brain area represent potentially high-dimensional inputs on a low-dimensional manifold that encodes the relative position of objects or features in physical space, and relations among entities in abstract conceptual space. We argue that this low-dimensional code supports generalisation of relational information, even in nonspatial domains. Finally, we propose that structure learning is grounded in the actions that primates take when they reach for objects or fixate them with their eyes. We sketch a model of how this might occur in neural circuits.
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?
A posterior region, such as AG, may bind the contents and the structure of experience at a higher level of abstraction than does the HPC and is probably an important area for relating spatial gists to spatial schema.
“A posterior region, such as AG, may bind the contents and the structure of experience at a higher level of abstraction than does the HPC 161 and, thus, is probably an important area for relating spatial gists to spatial schema (summarised in Fig. 1).”
From From cognitive maps to spatial schemas (2023) · cites this paper as [161]
Cites
ImageNet classification with deep convolutional neural networks
Krizhevsky, A., Sutskever, I., & Hinton, G. E. (2017) · Communications of the ACM · doi:10.1145/3065386 · Cited by 112,155 · see citing works
LeCun, Y., Bengio, Y., & Hinton, G. (2015) · Nature · doi:10.1038/nature14539 · Cited by 84,126 · see citing works
ImageNet Large Scale Visual Recognition Challenge
Russakovsky, O., Deng, J., Su, H., Krause, J., Satheesh, S., Ma, S., Huang, Z., Karpathy, A., Khosla, A., Bernstein, M., et al. (2015) · International Journal of Computer Vision · doi:10.1007/s11263-015-0816-y · Cited by 39,380 · see citing works
The Ecological Approach to Visual Perception
Bornstein, M. H., & Gibson, J. J. (1980) · The Journal of Aesthetics and Art Criticism · doi:10.2307/429816 · Cited by 22,935 · see citing works
Separate visual pathways for perception and action
Goodale, M. A., & Milner, A. D. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90344-8 · Cited by 6,519 · 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
Neural Information Processing Systems
(2018) · The MIT Press eBooks · doi:10.7551/mitpress/11474.003.0014 · Cited by 3,775 · see citing works
The Neural Basis of Decision Making
Gold, J. I., & Shadlen, M. N. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113038 · Cited by 3,764 · see citing works
Deep neural networks are easily fooled: High confidence predictions for unrecognizable images
Nguyen, A., Yosinski, J., & Clune, J. (2015) · 2015 IEEE Conference on Computer Vision and Pattern Recognition (CVPR) · doi:10.1109/cvpr.2015.7298640 · Cited by 3,258 · see citing works
Deep Neural Networks are Easily Fooled: High Confidence Predictions for Unrecognizable Images
Nguyen, A., Yosinski, J., & Clune, J. (2014) · arXiv · doi:10.48550/arxiv.1412.1897 · Cited by 3,258 · see citing works
Kronenfeld, D. B. (1978) · Language · doi:10.2307/412850 · Cited by 3,094 · see citing works
Scripts, Plans, Goals, and Understanding: An Inquiry into Human Knowledge Structures
Hunt, E. B., Schank, R. C., & Abelson, R. P. (1979) · The American Journal of Psychology · doi:10.2307/1421499 · Cited by 2,967 · see citing works
Human-level concept learning through probabilistic program induction
Lake, B. M., Salakhutdinov, R., & Tenenbaum, J. B. (2015) · Science · doi:10.1126/science.aab3050 · Cited by 2,817 · see citing works
Murphy, G. L. (2002) · The MIT Press eBooks · doi:10.7551/mitpress/1602.001.0001 · Cited by 2,797 · see citing works
The mental representation of parity and number magnitude.
Dehaene, S., Bossini, S., & Giraux, P. (1993) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.122.3.371 · Cited by 2,635 · see citing works
Building machines that learn and think like people
Lake, B. M., Ullman, T. D., Tenenbaum, J. B., & Gershman, S. J. (2017) · Behavioral and Brain Sciences · doi:10.1017/s0140525x16001837 · Cited by 2,550 · see citing works
A theory of magnitude: common cortical metrics of time, space and quantity
Walsh, V. (2003) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2003.09.002 · Cited by 2,044 · see citing works
Performance-optimized hierarchical models predict neural responses in higher visual cortex
Yamins, D. L. K., Hong, H., Cadieu, C. F., Solomon, E. A., Seibert, D., & DiCarlo, J. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1403112111 · Cited by 1,924 · see citing works
Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey
Shadlen, M. N., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1916 · Cited by 1,755 · see citing works
Neural correlates of decision variables in parietal cortex
Platt, M. L., & Glimcher, P. W. (1999) · Nature · doi:10.1038/22268 · Cited by 1,721 · see citing works
Understanding Neural Networks Through Deep VisualizationPreprint
Yosinski, J., Clune, J., Nguyen, A. M., Fuchs, T. J., & Lipson, H. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1506.06579 · Cited by 1,687 · see citing works
Using goal-driven deep learning models to understand sensory cortex
Yamins, D. L. K., & DiCarlo, J. J. (2016) · Nature Neuroscience · doi:10.1038/nn.4244 · Cited by 1,621 · see citing works
Neuroscience-Inspired Artificial Intelligence
Hassabis, D., Kumaran, D., Summerfield, C., & Botvinick, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.011 · Cited by 1,557 · 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
A simple neural network module for relational reasoning
Santoro, A., Raposo, D., Barrett, D. G. T., Malinowski, M., Pascanu, R., Battaglia, P., & Lillicrap, T. (2017) · arXiv · doi:10.48550/arxiv.1706.01427 · Cited by 1,281 · see citing works
Interactions between number and space in parietal cortex
Hubbard, E. M., Manuela Piazza, A., Pinel, P., & Dehaene, S. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1684 · Cited by 1,263 · see citing works
Deep supervised, but not unsupervised, models may explain IT cortical representation
Khaligh-Razavi, S.-M., & Kriegeskorte, N. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003915 · Cited by 1,204 · see citing works
Geometric determinants of the place fields of hippocampal neurons
O'Keefe, J., & Burgess, N. (1996) · Nature · doi:10.1038/381425a0 · Cited by 1,166 · see citing works
The imagery debate: Analogue media versus tacit knowledge.
Pylyshyn, Z. W. (1981) · Psychological Review · doi:10.1037/0033-295x.88.1.16 · Cited by 1,099 · see citing works
Kriegeskorte, N. (2015) · Annual Review of Vision Science · doi:10.1146/annurev-vision-082114-035447 · Cited by 1,093 · see citing works
What Is a Cognitive Map? Organizing Knowledge for Flexible Behavior
Behrens, T. E. J., Muller, T. H., Whittington, J. C. R., Mark, S., Baram, A. B., Stachenfeld, K. L., & Kurth-Nelson, Z. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.002 · Cited by 1,055 · see citing works
Decision-based adversarial attacks: Reliable attacks against black-box machine learning models
Brendel, W., Rauber, J., & Bethge, M. (2017) · arXiv · doi:10.48550/arxiv.1712.04248 · Cited by 1,018 · 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
Organizing conceptual knowledge in humans with a gridlike code
Constantinescu, A. O., O’Reilly, J. X., & Behrens, T. E. J. (2016) · Science · doi:10.1126/science.aaf0941 · Cited by 937 · see citing works
Deep Learning: A Critical Appraisal
Marcus, G. (2018) · arXiv · doi:10.48550/arxiv.1801.00631 · Cited by 853 · see citing works
Structure-mapping: A theoretical framework for analogy
GENTNER, D. (1983) · Cognitive Science · doi:10.1016/s0364-0213(83)80009-3 · Cited by 816 · see citing works
Intention, Action Planning, and Decision Making in Parietal-Frontal Circuits
Andersen, R. A., & Cui, H. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.028 · Cited by 707 · see citing works
The Code for Facial Identity in the Primate Brain
Chang, L., & Tsao, D. Y. (2017) · Cell · doi:10.1016/j.cell.2017.05.011 · Cited by 644 · see citing works
Navigating cognition: Spatial codes for human thinking
Bellmund, J. L. S., Gärdenfors, P., Moser, E. I., & Doeller, C. F. (2018) · Science · doi:10.1126/science.aat6766 · Cited by 643 · see citing works
The hippocampus and memory for orderly stimulus relations
Dusek, J. A., & Eichenbaum, H. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.13.7109 · Cited by 610 · see citing works
A century of Gestalt psychology in visual perception: II. Conceptual and theoretical foundations.
Wagemans, J. P., Feldman, J., Gepshtein, S., Kimchi, R., Pomerantz, J. R., van der Helm, P. A., & van Leeuwen, C. (2012) · Psychological Bulletin · doi:10.1037/a0029334 · Cited by 555 · see citing works
Clower, D. M., West, R. A., Lynch, J. C., & Strick, P. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06283.2001 · Cited by 549 · see citing works
Experience-dependent representation of visual categories in parietal cortex
Freedman, D. J., & Assad, J. A. (2006) · Nature · doi:10.1038/nature05078 · Cited by 542 · see citing works
Parietal Contributions to Visual Feature Binding: Evidence from a Patient with Bilateral Lesions
Friedman‐Hill, S. R., Robertson, L. C., & Treisman, A. (1995) · Science · doi:10.1126/science.7638604 · Cited by 538 · see citing works
Nieder, A., & Miller, E. K. (2003) · Neuron · doi:10.1016/s0896-6273(02)01144-3 · Cited by 514 · see citing works
Generalisation in humans and deep neural networksPreprint
Geirhos, R., Temme, C. R. M., Rauber, J., Schütt, H. H., Bethge, M., & Wichmann, F. A. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1808.08750 · Cited by 498 · see citing works
A map of visual space in the primate entorhinal cortex
Killian, N. J., Jutras, M. J., & Buffalo, E. A. (2012) · Nature · doi:10.1038/nature11587 · Cited by 471 · see citing works
Nieder, A. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.40 · Cited by 389 · see citing works
The Neurobiology of the Prefrontal Cortex: Anatomy, Evolution, and the Origin of Insight
Passingham, R. E., & Wise, S. P. (2012) · doi:10.1093/acprof:osobl/9780199552917.001.0001 · Cited by 379 · see citing works
Object-vector coding in the medial entorhinal cortex
Høydal, Ø. A., Skytøen, E. R., Andersson, S. O., Moser, M.-B., & Moser, E. I. (2019) · Nature · doi:10.1038/s41586-019-1077-7 · Cited by 366 · see citing works
A theory of the discovery and predication of relational concepts.
Doumas, L. A. A., Hummel, J. E., & Sandhofer, C. M. (2008) · Psychological Review · doi:10.1037/0033-295x.115.1.1 · Cited by 354 · see citing works
Numerical representation for action in the parietal cortex of the monkey
Sawamura, H., Shima, K., & Tanji, J. (2002) · Nature · doi:10.1038/415918a · Cited by 323 · see citing works
Sparse but not ‘Grandmother-cell’ coding in the medial temporal lobe
Quiroga, R. Q., Kreiman, G., Christof Koch, A., & Fried, I. (2008) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.12.003 · Cited by 291 · see citing works
Inferotemporal neurons represent low-dimensional configurations of parameterized shapes
de Beeck, H. O., Wagemans, J. P., & Vogels, R. (2001) · Nature Neuroscience · doi:10.1038/nn767 · Cited by 287 · see citing works
Dissociated functional significance of decision-related activity in the primate dorsal stream
Katz, L. N., Yates, J. L., Pillow, J. W., & Huk, A. C. (2016) · Nature · doi:10.1038/nature18617 · Cited by 277 · see citing works
MONet: Unsupervised Scene Decomposition and Representation
Burgess, C. P., Matthey, L., Watters, N., Kabra, R., Higgins, I., Botvinick, M., & Lerchner, A. (2019) · arXiv · doi:10.48550/arxiv.1901.11390 · Cited by 270 · see citing works
Monotonic Coding of Numerosity in Macaque Lateral Intraparietal Area
Roitman, J. D., Brannon, E. M., & Platt, M. L. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050208 · Cited by 256 · see citing works
A cognitive map for object memory in the hippocampusPreprint
Manns, J. R., & Eichenbaum, H. (2009) · Learning & Memory · doi:10.1101/lm.1484509 · Cited by 240 · see citing works
Space, Time and Number in the Brain: Searching for the Foundations of Mathematical Thought
Dehaene, S., & Brannon, E. M. (2011) · CERN Document Server (European Organization for Nuclear Research) · Cited by 236 · see citing works
Measuring abstract reasoning in neural networksPreprint
Barrett, D. G. T., Hill, F., Santoro, A., Morcos, A. S., & Lillicrap, T. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1807.04225 · Cited by 233 · see citing works
View‐responsive neurons in the primate hippocampal complex
Rolls, E. T., & O’Mara, S. M. (1995) · Hippocampus · doi:10.1002/hipo.450050504 · Cited by 229 · see citing works
Virtual Dyscalculia Induced by Parietal-Lobe TMS Impairs Automatic Magnitude Processing
Kadosh, R. C., Kadosh, K. C., Schuhmann, T., Kaas, A. L., Goebel, R., Henik, A., & Sack, A. T. (2007) · Current Biology · doi:10.1016/j.cub.2007.02.056 · Cited by 227 · see citing works
Structure-Mapping in Metaphor Comprehension
Wolff, P., & Gentner, D. (2011) · Cognitive Science · doi:10.1111/j.1551-6709.2011.01194.x · Cited by 226 · see citing works
A neural mechanism for sensing and reproducing a time interval
Jazayeri, M., & Shadlen, M. N. (2015) · Current Biology · doi:10.1016/j.cub.2015.08.038 · Cited by 210 · see citing works
Grid-like Neural Representations Support Olfactory Navigation of a Two-Dimensional Odor Space
Bao, X., Gjorgieva, E., Shanahan, L. K., Howard, J. D., Kahnt, T., & Gottfried, J. A. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.034 · Cited by 207 · see citing works
Causal Inference in the Multisensory Brain
Cao, Y., Summerfield, C., Park, H., Giordano, B. L., & Kayser, C. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.043 · Cited by 201 · see citing works
Self-citationA common cortical metric for spatial, temporal, and social distance
Parkinson, C., Liu, S., & Wheatley, T. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2159-13.2014 · Cited by 198 · see citing works
White, B. J., Berg, D. J., Kan, J. Y., Marino, R. A., Itti, L., & Munoz, D. P. (2017) · Nature Communications · doi:10.1038/ncomms14263 · Cited by 191 · see citing works
Supramodal numerosity selectivity of neurons in primate prefrontal and posterior parietal cortices
Nieder, A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1204580109 · Cited by 190 · see citing works
Bennur, S., & Gold, J. I. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4417-10.2011 · Cited by 188 · see citing works
The Emergence and Representation of Knowledge about Social and Nonsocial Hierarchies
Kumaran, D., Melo, H., & Düzel, E. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.035 · Cited by 187 · see citing works
Hexadirectional coding of visual space in human entorhinal cortex
Nau, M., Navarro Schröder, T., Bellmund, J. L. S., & Doeller, C. F. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0050-8 · Cited by 182 · see citing works
Dordek, Y., Soudry, D., Meir, R., & Derdikman, D. (2016) · eLife · doi:10.7554/elife.10094 · Cited by 175 · see citing works
Neuronal correlates of a visual “sense of number” in primate parietal and prefrontal cortices
Viswanathan, P., & Nieder, A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308141110 · Cited by 168 · see citing works
One-dimensional dynamics of attention and decision making in LIP
Ganguli, S., Bisley, J. W., Roitman, J. D., Shadlen, M. N., Goldberg, M. E., & Miller, K. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.038 · Cited by 152 · see citing works
Freedman, D. J., & Ibos, G. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.044 · Cited by 151 · see citing works
Comparing machines and humans on a visual categorization test
Fleuret, F., Li, T., Dubout, C., Wampler, E. K., Yantis, S., & Geman, D. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109168108 · Cited by 142 · see citing works
Superior colliculus encodes visual saliency before the primary visual cortex
White, B. J., Kan, J. Y. Y., Levy, R., Itti, L., & Munoz, D. P. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701003114 · Cited by 139 · see citing works
Posterior parietal cortex plays a causal role in perceptual and categorical decisions
Zhou, Y., & Freedman, D. J. (2019) · Science · doi:10.1126/science.aaw8347 · Cited by 139 · see citing works
Neuronal Mechanisms of Visual Categorization: An Abstract View on Decision Making
Freedman, D. J., & Assad, J. A. (2016) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033919 · Cited by 138 · see citing works
Toward an integration of deep learning and neuroscience
Marblestone, A. H., Wayne, G., & Kording, K. P. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00094 · Cited by 119 · see citing works
Origins and Development of Generalized Magnitude Representation
Lourenco, S. F., & Longo, M. R. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-385948-8.00015-3 · Cited by 110 · see citing works
Nasr, K., Viswanathan, P., & Nieder, A. (2019) · Science Advances · doi:10.1126/sciadv.aav7903 · Cited by 110 · see citing works
Toward the neural implementation of structure learning
Tervo, D. G. R., Tenenbaum, J. B., & Gershman, S. J. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.01.014 · Cited by 106 · see citing works
Chafee, M. V., Averbeck, B. B., & Crowe, D. A. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm017 · Cited by 101 · see citing works
Generalized associative representations in parietal cortex
Fitzgerald, J. K., Freedman, D. J., & Assad, J. A. (2011) · Nature Neuroscience · doi:10.1038/nn.2878 · Cited by 87 · see citing works
Rutishauser, U., Aflalo, T., Rosario, E. R., Pouratian, N., & Andersen, R. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.029 · Cited by 85 · see citing works
Neural structure mapping in human probabilistic reward learning
Luyckx, F., Nili, H., Spitzer, B., & Summerfield, C. (2019) · eLife · doi:10.7554/elife.42816 · Cited by 84 · see citing works
Self-citationSCAN: Learning Hierarchical Compositional Visual ConceptsPreprint
Higgins, I., Sonnerat, N., Matthey, L., Pal, A., Burgess, C., Bošnjak, M., Shanahan, M., Botvinick, M., Hassabis, D., & Lerchner, A. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1707.03389 · Cited by 79 · see citing works
Behavior and ecology ofmacaca fascicularis in Mauritius: A preliminary study
Sussman, R. W., & Tattersall, I. (1981) · Primates · doi:10.1007/bf02382610 · Cited by 76 · see citing works
Constructional Apraxia in Patients With Discrete Missile Wounds of the Brain
Black, F. W., & Strub, R. L. (1976) · Cortex · doi:10.1016/s0010-9452(76)80002-0 · Cited by 74 · see citing works
Biased Associative Representations in Parietal Cortex
Fitzgerald, J. K., Freedman, D. J., Fanini, A., Bennur, S., Gold, J. I., & Assad, J. A. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.014 · Cited by 62 · see citing works
Psychlab: A Psychology Laboratory for Deep Reinforcement Learning AgentsPreprint
Leibo, J. Z., d’Autume, C. D. M., Zoran, D., Amos, D., Beattie, C., Anderson, K., Castañeda, A. G., Sanchez, M., Green, S., Gruslys, A., et al. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1801.08116 · Cited by 55 · see citing works
The enigma of Bálint's syndrome: neural substrates and cognitive deficits
Chechlacz, M., & Humphreys, G. W. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00123 · Cited by 47 · see citing works
Processing number and length in the parietal cortex: Sharing resources, not a common code
Borghesani, V., de Hevia, M. D., Viarouge, A., Pinheiro‐Chagas, P., Eger, E., & Manuela Piazza, A. (2018) · Cortex · doi:10.1016/j.cortex.2018.07.017 · Cited by 42 · see citing works
Pure Global Acalculia Following a Left Subangular Lesion
Martory, M.-D., Mayer, E., Pegna, A. J., Annoni, J., Landis, T., & Khateb, A. (2003) · Neurocase · doi:10.1076/neur.9.4.319.15549 · Cited by 33 · see citing works
Teichmann, L., Grootswagers, T., Carlson, T. A., & Rich, A. N. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01257 · Cited by 32 · see citing works
Automatic system for analysis of locomotor activity in rodents—A reproducibility study
Aragão, R. D. S., Rodrigues, M. A. B., Barros, K. M. F. T., Silva, S. R. F., Toscano, A. E., de Souza, R. E., & Manhães‐de‐Castro, R. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.12.016 · Cited by 28 · see citing works
Visual pathways from the perspective of cost functions and multi-task deep neural networks
Scholte, H. S., Losch, M., Ramakrishnan, K., de Haan, E. H. F., & Bohté, S. M. (2017) · Cortex · doi:10.1016/j.cortex.2017.09.019 · Cited by 26 · see citing works
Chafee, M. V. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.025 · Cited by 12 · see citing works
Cognitive Deficit of Deep Learning in Numerosity
Wu, X., Zhang, X., & Shu, X. (2019) · Proceedings of the AAAI Conference on Artificial Intelligence · doi:10.1609/aaai.v33i01.33011303 · Cited by 11 · see citing works
CA1 pyramidal cells organize an episode by segmented and ordered eventsPreprint
Sun, C., Yang, W., Martin, J., & Tonegawa, S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/565689 · Cited by 4 · see citing works
Cognitive Deficit of Deep Learning in NumerosityPreprint
Wu, X., Zhang, X., & Shu, X. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1802.05160 · Cited by 3 · see citing works
Biased neural representation of feature-based attention in the human brainPreprint
Gong, M., & Liu, T. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/688226 · Cited by 2 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Knowledge Across Reference Frames: Cognitive Maps and Image Spaces
Bottini, R., & Doeller, C. F. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.05.008 · Cited by 152 · 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
George, D., Rikhye, R. V., Gothoskar, N., Guntupalli, J. S., Dedieu, A., & Lázaro-Gredilla, M. (2021) · Nature Communications · doi:10.1038/s41467-021-22559-5 · Cited by 109 · see citing works
Abstract task representations for inference and control
Vaidya, A. R., & Badre, D. (2022) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2022.03.009 · Cited by 78 · see citing works
Cross, L., Cockburn, J., Yue, Y., & O’Doherty, J. P. (2020) · Neuron · doi:10.1016/j.neuron.2020.11.021 · Cited by 73 · see citing works
Neural state space alignment for magnitude generalization in humans and recurrent networks
Sheahan, H., Luyckx, F., Nelli, S., Teupe, C., & Summerfield, C. (2021) · Neuron · doi:10.1016/j.neuron.2021.02.004 · Cited by 67 · see citing works
Self-citationNeural knowledge assembly in humans and neural networks
Nelli, S., Braun, L., Dumbalska, T., Saxe, A., & Summerfield, C. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.014 · Cited by 57 · see citing works
Self-citationGoal-oriented representations in the human hippocampus during planning and navigation
Crivelli-Decker, J. E., Clarke, A., Park, S. A., Huffman, D. J., Boorman, E. D., & Ranganath, C. (2023) · Nature Communications · doi:10.1038/s41467-023-35967-6 · Cited by 40 · see citing works
Mnemonic construction and representation of temporal structure in the hippocampal formation
Bellmund, J. L. S., Deuker, L., Montijn, N. D., & Doeller, C. F. (2022) · Nature Communications · doi:10.1038/s41467-022-30984-3 · Cited by 50 · see citing works
Cognitive maps and novel inferences: a flexibility hierarchy
Boorman, E. D., Sweigart, S. C., & Park, S. A. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2021.02.017 · Cited by 36 · see citing works
The precuneus as a central node in declarative memory retrieval
Flanagin, V. L., Klinkowski, S., Brodt, S., Graetsch, M., Roselli, C., Glasauer, S., & Gais, S. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac476 · Cited by 35 · see citing works
Rowland, J. M., van der Plas, T. L., Loidolt, M., Lees, R. M., Keeling, J., Dehning, J., Akam, T., Priesemann, V., & Packer, A. M. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01413-5 · Cited by 33 · see citing works
Brain-imaging evidence for compression of binary sound sequences in human memory
Planton, S., Roumi, F. A., Wang, L., & Dehaene, S. (2023) · eLife · doi:10.7554/elife.84376 · Cited by 30 · see citing works
Deep learning models to study sentence comprehension in the human brain
Arana, S., Lerousseau, J. P., & Peter Hagoort, A. (2023) · Language Cognition and Neuroscience · doi:10.1080/23273798.2023.2198245 · Cited by 28 · see citing works
The Structure of Systematicity in the Brain
O’Reilly, R. C., Charan Ranganath, A., & Russin, J. (2022) · Current Directions in Psychological Science · doi:10.1177/09637214211049233 · Cited by 27 · see citing works
Spontaneous eye movements reflect the representational geometries of conceptual spaces
Viganò, S., Bayramova, R., Doeller, C. F., & Bottini, R. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2403858121 · Cited by 24 · see citing works
Distinct Neural Representations of Content and Ordinal Structure in Auditory Sequence Memory
Fan, Y., Han, Q., Guo, S., & Luo, H. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0320-21.2021 · Cited by 22 · see citing works
Geary, D., Scofield, J. E., Hoard, M. K., & Nugent, L. (2020) · Developmental Science · doi:10.1111/desc.13063 · Cited by 19 · see citing works
Summerfield, C. (2022) · doi:10.1093/oso/9780192843883.001.0001 · Cited by 23 · see citing works
Self-citationNeural correlates of transitive inference: An SDM meta-analysis on 32 fMRI studies
Zhang, X., Qiu, Y., Li, J., Jia, C., Liao, J., Chen, K., Qiu, L., Yuan, Z., & Huang, R. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119354 · Cited by 21 · see citing works
The relational bottleneck as an inductive bias for efficient abstraction
Webb, T. W., Frankland, S., Altabaa, A., Segert, S., Krishnamurthy, K., Campbell, D. I., Russin, J., Giallanza, T., O’Reilly, R. C., Lafferty, J., et al. (2024) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2024.04.001 · Cited by 21 · see citing works
Integrating when and what information in the left parietal lobe allows language rule generalization
Orpella, J., Ripollés, P., Ruzzoli, M., Amengual, J. L., Callejas, A., Martinez‐Alvarez, A., Soto‐Faraco, S., & de Diego‐Balaguer, R. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000895 · Cited by 21 · see citing works
The Evolved Mind and Modern Education
Geary, D. C. (2024) · Cambridge University Press eBooks · doi:10.1017/9781009454858 · Cited by 18 · see citing works
Moving beyond domain-specific versus domain-general options in cognitive neuroscience
Asano, R., Boeckx, C. A., & Fujita, K. (2022) · Cortex · doi:10.1016/j.cortex.2022.05.004 · Cited by 18 · see citing works
A mathematical theory of relational generalization in transitive inference
Lippl, S., Kay, K., Jensen, G., Ferrera, V. P., & Abbott, L. F. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2314511121 · Cited by 14 · see citing works
Karami, A., Castaldi, E., Eger, E., & Manuela Piazza, A. (2025) · Communications Biology · doi:10.1038/s42003-025-08395-z · Cited by 16 · see citing works
Emergent neural dynamics and geometry for generalization in a transitive inference task
Kay, K., Biderman, N., Khajeh, R., Beirán, M., Cueva, C. J., Shohamy, D., Jensen, G., Wei, X.-X., Ferrera, V. P., & Abbott, L. F. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011954 · Cited by 14 · see citing works
The growth and form of knowledge networks by kinesthetic curiosity
Zhou, D., Lydon‐Staley, D. M., Zurn, P., & Bassett, D. S. (2020) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2020.09.007 · Cited by 18 · see citing works
The interplay between spatial and non-spatial grouping cues over approximate number perception
Adriano, A., & Ciccione, L. (2024) · Attention Perception & Psychophysics · doi:10.3758/s13414-024-02908-4 · Cited by 11 · see citing works
A double dissociation between semantic and spatial cognition in visual to default network pathwaysPreprint
Alam, T. R. G., Krieger‐Redwood, K., Varga, D., Gao, Z., Horner, A. J., Hartley, T., de Schotten, M. T., Sliwinska, M. W., Pitcher, D., Margulies, D. S., et al. (2024) · eLife · doi:10.7554/elife.94902.3 · Cited by 17 · see citing works
Adaptive cognitive maps for curved surfaces in the 3D world
kim, M.-S., & Doeller, C. F. (2022) · Cognition · doi:10.1016/j.cognition.2022.105126 · Cited by 11 · see citing works
Reactivating ordinal position information from auditory sequence memory in human brains
Fan, Y., & Luo, H. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac471 · Cited by 8 · see citing works
Disentangling Abstraction from Statistical Pattern Matching in Human and Machine Learning
Kumar, S., Dasgupta, I., Daw, N. D., Cohen, J. D., & Griffiths, T. L. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011316 · Cited by 11 · see citing works
Neurocomputational mechanisms underlying fear-biased adaptation learning in changing environments
Wang, Z., Nan, T., Goerlich, K. S., Li, Y., Aleman, A., Luo, Y., & Xu, P. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3001724 · Cited by 13 · see citing works
Identifying content-invariant neural signatures of perceptual vividness
Barnett, B., Andersen, L. M., Fleming, S. M., & Dijkstra, N. (2024) · PNAS Nexus · doi:10.1093/pnasnexus/pgae061 · Cited by 9 · see citing works
Inferior parietal cortex represents relational structures for explicit transitive inference
Xu, B., Wu, J., Xiao, H., Münte, T. F., & Ye, Z. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae137 · Cited by 9 · see citing works
The neural representation of absolute direction during mental navigation in conceptual spaces
Viganò, S., Rubino, V., Buiatti, M., & Manuela Piazza, A. (2021) · Communications Biology · doi:10.1038/s42003-021-02806-7 · Cited by 9 · see citing works
Context-independent scaling of neural responses to task difficulty in the multiple-demand network
Wen, T., & Egner, T. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac479 · Cited by 7 · see citing works
Learning cognitive maps as structured graphs for vicarious evaluationPreprint
Rikhye, R. V., Gothoskar, N., Guntupalli, J. S., Dedieu, A., Lázaro-Gredilla, M., & George, D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/864421 · Cited by 8 · see citing works
Hochmann, J., & Papeo, L. (2021) · doi:10.31234/osf.io/hm49p · Cited by 8 · see citing works
Rowland, J. M., van der Plas, T. L., Loidolt, M., Lees, R. M., Keeling, J., Dehning, J., Akam, T. E., Priesemann, V., & Packer, A. M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.28.474343 · Cited by 8 · see citing works
Space as a scaffold for rotational generalisation of abstract concepts
Lerousseau, J. P., & Summerfield, C. (2024) · eLife · doi:10.7554/elife.93636 · Cited by 5 · see citing works
Self-citationBellmund, J. L. S., Deuker, L., Montijn, N. D., & Doeller, C. F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.23.440002 · Cited by 7 · see citing works
Neural knowledge assembly in humans and deep networksPreprint
Nelli, S., Braun, L., Dumbalska, T., Saxe, A., & Summerfield, C. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.21.465374 · Cited by 7 · see citing works
Self-citationSex, mathematics, and the brain: An evolutionary perspective
Geary, D. C. (2021) · Developmental Review · doi:10.1016/j.dr.2021.101010 · Cited by 7 · see citing works
Gonering, B., & Corina, D. P. (2023) · Frontiers in Language Sciences · doi:10.3389/flang.2023.1176233 · Cited by 7 · see citing works
Electrophysiological hallmarks for event relations and event roles in working memory
Yu, X., Li, J., Zhu, H., Tian, X., & Lau, E. F. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1282869 · Cited by 6 · see citing works
Osei, P. C., & Bjorklund, D. F. (2024) · Developmental Review · doi:10.1016/j.dr.2024.101118 · Cited by 6 · see citing works
Cartography and Neural Networks: A Scientometric Analysis Based on CiteSpace
Cheng, S., Zhang, J., Wang, G., Zhou, Z., Du, J., Wang, L., Li, N., & Wang, J. (2024) · ISPRS International Journal of Geo-Information · doi:10.3390/ijgi13060178 · Cited by 6 · see citing works
Zero-shot counting with a dual-stream neural network model
Thompson, J. A. F., Sheahan, H., Dumbalska, T., Sandbrink, J. D., Manuela Piazza, A., & Summerfield, C. (2024) · Neuron · doi:10.1016/j.neuron.2024.10.008 · Cited by 6 · see citing works
Self-citationEvolution of neural activity in circuits bridging sensory and abstract knowledge
Mastrogiuseppe, F., Hiratani, N., & Latham, P. E. (2023) · eLife · doi:10.7554/elife.79908 · Cited by 7 · see citing works
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 · see citing works
The growth and form of knowledge networks by kinesthetic curiosityPreprint
Zhou, D., Lydon‐Staley, D. M., Zurn, P., & Bassett, D. S. (2020) · doi:10.31234/osf.io/z6pcg · Cited by 6 · see citing works
Luber, B. M., Beynel, L., Spellman, T., Gura, H., Ploesser, M., Termini, K., & Lisanby, S. H. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.883337 · Cited by 4 · see citing works
Human intelligence relates to neural measures of cognitive map formation
Tenderra, R. M., & Theves, S. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116033 · Cited by 5 · see citing works
Language Experience in Cognitive Maps and Image Spaces
Bottini, R., & Doeller, C. F. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.08.003 · Cited by 4 · see citing works
Do grid codes afford generalization and flexible decision-making?Preprint
Yu, L. Q., Park, S. A., Sweigart, S. C., Boorman, E. D., & Nassar, M. R. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2106.16219 · Cited by 5 · see citing works
Dual transcranial electromagnetic stimulation of the precuneus boosts human long-term memory
Borghi, I., Mencarelli, L., Maiella, M., Casula, E. P., Ferraresi, M., Candeo, F., Savastano, E., Assogna, M., Bonnı̀, S., & Koch, G. (2025) · eLife · doi:10.7554/elife.104220.4 · Cited by 3 · see citing works
Reward history alters priority map based on spatial relationship, but not absolute location
Tan, Q., Jia, O., Anderson, B. A., Jia, K., & Gong, M. (2025) · Psychonomic Bulletin & Review · doi:10.3758/s13423-025-02682-w · Cited by 5 · see citing works
Distinct roles of hippocampus and neocortex in symbolic compositional generalization
Liang, Z., Glitz, L., Nau, M., Hefner, M. B., Lan, D. C. L., Klein-Flügge, M. C., & Summerfield, C. (2026) · Neuron · doi:10.1016/j.neuron.2026.05.024 · Cited by 2 · see citing works
Self-citationIntelligence correlates with the temporal variability of brain networks
Shi, M., Li, Y., Sun, J., Li, X., Han, Y., Liu, Z., & Qiu, J. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.08.001 · Cited by 2 · see citing works
Jia, O., Tan, Q., Zhang, S., Jia, K., & Gong, M. (2025) · npj Science of Learning · doi:10.1038/s41539-025-00342-1 · Cited by 2 · see citing works
Mondal, S. S., Frankland, S., Webb, T. W., & Cohen, J. D. (2024) · eLife · doi:10.7554/elife.89911.3 · Cited by 2 · see citing works
Summerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0006 · Cited by 1 · see citing works
Self-citationNeural representation of time across complementary reference frames
Xu, Y., Sartorato, N., Dutriaux, L., & Bottini, R. (2026) · eLife · doi:10.7554/elife.107273.4 · Cited by 1 · see citing works
The recipe for intelligence in natural and artificial systems
Summerfield, C., & Stachenfeld, K. (2026) · Neuron · doi:10.1016/j.neuron.2026.08.013 · Cited by 1 · see citing works
Self-citationComplementary Brain Signals for Categorical Decisions
Muhle-Karbe, P. S., & Flesch, T. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0785-20.2020 · Cited by 1 · see citing works
Xu, S., & Ren, W. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad449 · Cited by 1 · see citing works
Category Learning as a Cognitive Foundation of Language Evolution
Zhang, E. Q., Shi, E. R., & Pleyer, M. (2025) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.70007 · Cited by 1 · see citing works
Extrapolatable Relational Reasoning With Comparators in Low-Dimensional ManifoldsPreprint
Wang, D., Jamnik, M., & Lió, P. (2020) · arXiv (Cornell University) · doi:10.17863/cam.57939 · Cited by 1 · see citing works
Learning Canonical TransformationsPreprint
Dulberg, Z., & Cohen, J. D. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2011.08822 · Cited by 1 · see citing works
Evolution of neural activity in circuits bridging sensory and abstract knowledgePreprint
Mastrogiuseppe, F., Hiratani, N., & Latham, P. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.29.478317 · Cited by 1 · see citing works
Space as a Scaffold for Rotational Generalisation of Abstract ConceptsPreprint
Lerousseau, J. P., & Summerfield, C. (2024) · eLife · doi:10.7554/elife.93636.1 · Cited by 1 · see citing works
Self-citationBorghi, I., Mencarelli, L., Maiella, M., Casula, E. P., Ferraresi, M., Candeo, F., Savastano, E., Assogna, M., Bonnı̀, S., & Koch, G. (2025) · eLife · doi:10.7554/elife.104220.1 · Cited by 1 · see citing works
Yang, Y., & Maass, W. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.17.642834 · Cited by 1 · see citing works
Shi, D., Shu, L., & Yu, Q. (2025) · doi:10.1101/2025.11.26.690703 · Cited by 1 · see citing works
Spike-based symbolic computations on bit strings and numbersPreprint
Kraišniković, C., Maass, W., & Legenstein, R. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.14.452347
Summerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0008
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0003
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0007
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0002
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0004
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.002.0003
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.002.0004
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.002.0006
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0005
Self-citationSummerfield, C. (2022) · Oxford University Press eBooks · doi:10.1093/oso/9780192843883.003.0001
Self-citationSpace as a Scaffold for Rotational Generalisation of Abstract ConceptsPreprint
Lerousseau, J. P., & Summerfield, C. (2023) · doi:10.31234/osf.io/zt6e4
Self-citationBridging stimulus generalization and representation learning via rational dimensionality reductionPreprint
Neugebauer, L., & Büchel, C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.09.549352
Mondal, S. S., Frankland, S., Webb, T. W., & Cohen, J. D. (2023) · eLife · doi:10.7554/elife.89911 · Cited by 2 · see citing works
Adriano, A., Ciccione, L., & Zhan, M. (2023) · doi:10.31234/osf.io/e2x8c
Synchronous Brain Activities in Mathematical Task Processing
Tobler, S., Poikonen, H., Gashaj, V., Trninić, D., Formaz, C., & Kapur, M. (2023) · Proceedings. · doi:10.22318/icls2023.172722
Space as a Scaffold for Rotational Generalisation of Abstract ConceptsPreprint
Lerousseau, J. P., & Summerfield, C. (2024) · eLife · doi:10.7554/elife.93636.2
Self-citationMondal, S. S., Frankland, S., Webb, T. W., & Cohen, J. D. (2024) · eLife · doi:10.7554/elife.89911.2
Space as a scaffold for rotational generalisation of abstract concepts
Lerousseau, J. P., & Summerfield, C. (2024) · eLife · doi:10.7554/elife.93636.3
Self-citationVisual to default network pathways: A double dissociation between semantic and spatial cognitionPreprint
Alam, T. R. G., Krieger‐Redwood, K., Varga, D., Gao, Z., Horner, A. J., Hartley, T., de Schotten, M. T., Sliwinska, M. W., Pitcher, D., Margulies, D. S., et al. (2024) · eLife · doi:10.7554/elife.94902.1
Reward history modulates attention based on spatial relationshipPreprint
Tan, Q., Jia, O., Anderson, B. A., Jia, K., & Gong, M. (2024) · doi:10.31234/osf.io/e62a7
Visual to default network pathways: A double dissociation between semantic and spatial cognitionPreprint
Alam, T. R. G., Krieger‐Redwood, K., Varga, D., Gao, Z., Horner, A. J., Hartley, T., de Schotten, M. T., Sliwinska, M. W., Pitcher, D., Margulies, D. S., et al. (2024) · eLife · doi:10.7554/elife.94902.2
Split-second insights from the brain’s dual-stream visual system
Paik, S. (2024) · Neuron · doi:10.1016/j.neuron.2024.11.014
Dual transcranial electromagnetic stimulation of the precuneus boosts human long-term memoryPreprint
Borghi, I., Mencarelli, L., Maiella, M., Casula, E. P., Ferraresi, M., Candeo, F., Savastano, E., Assogna, M., Bonnı̀, S., & Koch, G. (2025) · eLife · doi:10.7554/elife.104220
- Authors
- Summerfield, C., Luyckx, F., & Sheahan, H.
- Affiliations
- University of Oxford (GB)
- Corresponding author
- Summerfield, Christopher
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2020-01
- Volume
- 184
- Pages
- 101717
- ISSN
- 0301-0082 (ISSN-L)
- OpenAlex
- W2981514504
- Cited by
- 118
- References
- 103
- Citations by year
- 2026: 12 · 2025: 19 · 2024: 23 · 2023: 15 · 2022: 25 · 2021: 12 · 2020: 10 · 2019: 2
- FWCI
- 7.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Progress in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Horizon 2020
- European Research Council
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- structure learning, posterior parietal cortex, relational inference, dorsal stream, scene understanding, neural coding, conceptual space, action-based learning, deep learning limitations
- MeSH terms
- Deep Learning, Animals, Gestalt Theory, Humans, Learning, Models, Biological, Parietal Lobe, Primates, Space Perception, Visual Perception, Mathematical Concepts
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