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‘What’ Is Happening in the Dorsal Visual Pathway
Abstract
The cortical visual system is almost universally thought to be segregated into two anatomically and functionally distinct pathways: a ventral occipitotemporal pathway that subserves object perception, and a dorsal occipitoparietal pathway that subserves object localization and visually guided action. Accumulating evidence from both human and non-human primate studies, however, challenges this binary distinction and suggests that regions in the dorsal pathway contain object representations that are independent of those in ventral cortex and that play a functional role in object perception. We review here the evidence implicating dorsal object representations, and we propose an account of the anatomical organization, functional contributions, and origins of these representations in the service of perception.
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Citations
Cites
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
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
Friston, K. J., Harrison, L., & Penny, W. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00202-7 · Cited by 4,583
Ungerleider, L. G. (1982) · Medical Entomology and Zoology · Cited by 4,531
Ingle, D., Goodale, M. A., & Mansfield, R. J. W. (1982) · The MIT Press eBooks · Cited by 4,118
Unbiased average age-appropriate atlases for pediatric studies
Fonov, V., Evans, A. C., Botteron, K., Almli, C. R., McKinstry, R. C., & Collins, D. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.033 · Cited by 2,290
Mechanisms of visual attention in the human cortex
Ungerleider, S. K. A. L. G. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.315 · Cited by 2,159
A neurological dissociation between perceiving objects and grasping them
Goodale, M. A., Milner, A. D., Jakobson, L. S., & Carey, D. P. (1991) · Nature · doi:10.1038/349154a0 · Cited by 1,510
A 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
Representation of Manipulable Man-Made Objects in the Dorsal Stream
Chao, L. L., & Martin, A. (2000) · NeuroImage · doi:10.1006/nimg.2000.0635 · Cited by 1,250
Grill-Spector, K., & Malach, R. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144220 · Cited by 1,184
Grill-Spector, K., Kushnir, T., Edelman, S., Avidan, G., Itzchak, Y., & Malach, R. (1999) · Neuron · doi:10.1016/s0896-6273(00)80832-6 · Cited by 1,166
Size-contrast illusions deceive the eye but not the hand
Aglioti, S., DeSouza, J. F. X., & Goodale, M. A. (1995) · Current Biology · doi:10.1016/s0960-9822(95)00133-3 · Cited by 1,087
Puce, A., Allison, T., Asgari, M., Gore, J. C., & McCarthy, G. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05205.1996 · Cited by 987 · cited 1×
“For example, greater face sensitivity is usually observed in the right hemisphere, while the left ventral pathway exhibits greater sensitivity to written words [122,123], although this lateralization is graded rather than absolute.”
Murata, A., Gallese, V., Luppino, G., Kaseda, M., & Sakata, H. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2580 · Cited by 841
The functional architecture of the ventral temporal cortex and its role in categorization
Grill-Spector, K., & Weiner, K. S. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3747 · Cited by 837
Neuroimaging of cognitive functions in human parietal cortex
Culham, J. C., & Kanwisher, N. G. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00191-4 · Cited by 821
Grefkes, C., & Fink, G. R. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00426.x · Cited by 759
Neural Mechanisms of Visual Guidance of Hand Action in the Parietal Cortex of the Monkey
Sakata, H., Taira, M., Murata, A., & Mine, S. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.5.429 · Cited by 696
Cortical Regions Involved in Perceiving Object Shape
Kourtzi, Z., & Kanwisher, N. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03310.2000 · Cited by 673
Visually guided grasping produces fMRI activation in dorsal but not ventral stream brain areas
Culham, J. C., Danckert, S. L., Souza, J. F. X. D., Gati, J. S., Menon, R. S., & Goodale, M. A. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1591-5 · Cited by 637
Extrastriate body area in human occipital cortex responds to the performance of motor actions
Astafiev, S. V., Stanley, C. M., Shulman, G. L., & Corbetta, M. (2004) · Nature Neuroscience · doi:10.1038/nn1241 · Cited by 629
Neural correlates of reach errors
Diedrichsen, J., Hashambhoy, Y., Rane, T., & Shadmehr, R. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1874-05.2005 · Cited by 622
Ventral occipital lesions impair object recognition but not object‐directed grasping: an fMRI study
James, T. W., Culham, J., Humphrey, G. K., Milner, A. D., & Goodale, M. A. (2003) · Brain · doi:10.1093/brain/awg248 · Cited by 577
Husain, M., & Nachev, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.10.011 · Cited by 514
Macaque monkey retrosplenial cortex: III. Cortical efferents
Kobayashi, Y., & Amaral, D. G. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21346 · Cited by 487
Farah, M. J. (1990) · Cited by 482
Cortical responses to invisible objects in the human dorsal and ventral pathways
Fang, F., & He, S. (2005) · Nature Neuroscience · doi:10.1038/nn1537 · Cited by 477
Two hierarchically organized neural systems for object information in human visual cortex
Konen, C. S., & Kastner, S. (2008) · Nature Neuroscience · doi:10.1038/nn2036 · Cited by 475
The role of parietal cortex in visuomotor control: What have we learned from neuroimaging?
Culham, J. C., Cavina-Pratesi, C., & Singhal, A. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.11.003 · Cited by 461
Cortical Networks Related to Human Use of Tools
Lewis, J. W. (2006) · The Neuroscientist · doi:10.1177/1073858406288327 · Cited by 451
Shape selectivity in primate lateral intraparietal cortex
Sereno, A. B., & Maunsell, J. H. R. (1998) · Nature · doi:10.1038/26752 · Cited by 436
Systems in development: Motor skill acquisition facilitates three-dimensional object completion.
Soska, K. C., Adolph, K. E., & Johnson, S. P. (2010) · Developmental Psychology · doi:10.1037/a0014618 · Cited by 430
Fogassi, L. (2001) · Brain · doi:10.1093/brain/124.3.571 · Cited by 429
Cortical connections of the macaque anterior intraparietal (AIP) area
Borra, E., Belmalih, A., Calzavara, R., Gerbella, M., Murata, A., Rozzi, S., & Luppino, G. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm146 · Cited by 402 · cited 1×
“One obvious interpretation of the dorsal object-selectivity is that it might simply be a consequence of the anatomical and functional coupling between dorsal and ventral regions [19,42,50], perhaps via the vertical occipital fasciculus which connects the pathways posteriorly [51,52] or via the efferent projections tha…”
Rust, N. C., & DiCarlo, J. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0179-10.2010 · Cited by 387
Deficit of hand preshaping after muscimol injection in monkey parietal cortex
Gallese, V., Murata, A., Kaseda, M., Niki, N., & Sakata, H. (1994) · NeuroReport · doi:10.1097/00001756-199407000-00029 · Cited by 378
Macaque monkey retrosplenial cortex: II. Cortical afferents
Kobayashi, Y., & Amaral, D. G. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10883 · Cited by 378
Spatial thought, mental rotation and the right cerebral hemisphere
Ratcliff, G. (1979) · Neuropsychologia · doi:10.1016/0028-3932(79)90021-6 · Cited by 360
Objects automatically potentiate action: an fMRI study of implicit processing
Grèzes, J., Tucker, M., Armony, J., Ellis, R., & Passingham, R. E. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02695.x · Cited by 359
Decoding the content of visual short-term memory under distraction in occipital and parietal areas
Bettencourt, K. C., & Xu, Y. (2016) · Nature Neuroscience · doi:10.1038/nn.4174 · Cited by 338
Explicit information for category-orthogonal object properties increases along the ventral stream
Hong, H., Yamins, D. L. K., Majaj, N. J., & DiCarlo, J. J. (2016) · Nature Neuroscience · doi:10.1038/nn.4247 · Cited by 337
Extracting 3D from Motion: Differences in Human and Monkey Intraparietal Cortex
Vanduffel, W., Fize, D., Peuskens, H., Denys, K., Sunaert, S., Todd, J. T., & Orban, G. A. (2002) · Science · doi:10.1126/science.1073574 · Cited by 334
Visual motion serves but is not under the purview of the dorsal pathway
Gilaie-Dotan, S. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.07.018 · Cited by 325
The lateral occipitotemporal cortex in action
Lingnau, A., & Downing, P. E. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.03.006 · Cited by 324
Cavina-Pratesi, C., Monaco, S., Fattori, P., Galletti, C., McAdam, T. D., Quinlan, D. J., Goodale, M. A., & Culham, J. C. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2023-10.2010 · Cited by 324
Distributed circuits, not circumscribed centers, mediate visual recognition
Behrmann, M., & Plaut, D. C. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.03.007 · Cited by 289
Self-citationSelectivity for 3D Shape That Reveals Distinct Areas Within Macaque Inferior Temporal Cortex
Janssen, P., Vogels, R., & Orban, G. A. (2000) · Science · doi:10.1126/science.288.5473.2054 · Cited by 272
Dynamic coding of behaviourally relevant stimuli in parietal cortex
Toth, L. J., & Assad, J. A. (2002) · Nature · doi:10.1038/415165a · Cited by 269
Rohlfing, T., Kroenke, C. D., Sullivan, E. V., Dubach, M. F., Bowden, D. M., Grant, K. A., & Pfefferbaum, A. (2012) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2012.00027 · Cited by 262
Decoding Action Intentions from Preparatory Brain Activity in Human Parieto-Frontal Networks
Gallivan, J. P., McLean, D. A., Valyear, K. F., Pettypiece, C. E., & Culham, J. C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0080-11.2011 · Cited by 261
Dissociations and Associations between Shape and Category Representations in the Two Visual Pathways
Bracci, S., & Op de Beeck, H. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2314-15.2016 · Cited by 261
The vertical occipital fasciculus: A century of controversy resolved by in vivo measurements
Yeatman, J. D., Weiner, K. S., Pestilli, F., Rokem, A., Mezer, A., & Wandell, B. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418503111 · Cited by 258
Neural coding within human brain areas involved in actions
Gallivan, J. P., & Culham, J. C. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.03.012 · Cited by 248
Weiner, K. S., & Grill-Spector, K. (2013) · Psychological Research · doi:10.1007/s00426-011-0392-x · Cited by 244
Dissociation between Ventral and Dorsal fMRI Activation during Object and Action Recognition
Shmuelof, L., & Zohary, E. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.034 · Cited by 227
Visual control of action but not perception requires analytical processing of object shape
Ganel, T., & Goodale, M. A. (2003) · Nature · doi:10.1038/nature02156 · Cited by 222
Representation of the Perceived 3-D Object Shape in the Human Lateral Occipital Complex
Kourtzi, Z. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.9.911 · Cited by 219
The Processing of Three-Dimensional Shape from Disparity in the Human Brain
Georgieva, S., Peeters, R., Kolster, H., Todd, J. T., & Orban, G. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4753-08.2009 · Cited by 211
BOLD Activity during Mental Rotation and Viewpoint-Dependent Object Recognition
Gauthier, I., Hayward, W. G., Tarr, M. J., Anderson, A. W., Skudlarski, P., & Gore, J. C. (2002) · Neuron · doi:10.1016/s0896-6273(02)00622-0 · Cited by 196
A Major Human White Matter Pathway Between Dorsal and Ventral Visual Cortex
Takemura, H., Rokem, A., Winawer, J., Yeatman, J. D., Wandell, B. A., & Pestilli, F. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv064 · Cited by 173
Libertus, K., & Needham, A. (2011) · Developmental Science · doi:10.1111/j.1467-7687.2011.01084.x · Cited by 171
Trade-Off between Object Selectivity and Tolerance in Monkey Inferotemporal Cortex
Zoccolan, D., Kouh, M., Poggio, T., & DiCarlo, J. J. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1897-07.2007 · Cited by 169
Bringing the real world into the fMRI scanner: Repetition effects for pictures versus real objects
Snow, J. C., Pettypiece, C. E., McAdam, T. D., McLean, A. D., Stroman, P. W., Goodale, M. A., & Culham, J. C. (2011) · Scientific Reports · doi:10.1038/srep00130 · Cited by 160
On the usefulness of ‘what’ and ‘where’ pathways in vision
de Haan, E. H. F., & Cowey, A. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.08.005 · Cited by 159
The Anatomy of Object Recognition—Visual Form Agnosia Caused by Medial Occipitotemporal Stroke
Karnath, H., Rüter, J., Mandler, A., & Himmelbach, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5192-08.2009 · Cited by 157
Integration of Perspective and Disparity Cues in Surface-Orientation–Selective Neurons of Area CIP
Tsutsui, K., Jiang, M., Yara, K., Sakata, H., & Taira, M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.6.2856 · Cited by 148
The Extraction of 3D Shape in the Visual System of Human and Nonhuman Primates
Orban, G. A. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113819 · Cited by 136
Human Brain Activity Related to the Perception of Spatial Features of Objects
Faillenot, I., Decety, J., & Jeannerod, M. (1999) · NeuroImage · doi:10.1006/nimg.1999.0449 · Cited by 131
Srivastava, S., Orban, G. A., Mazière, P. D., & Janssen, P. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6016-08.2009 · Cited by 130
Konen, C. S., Mruczek, R. E. B., Montoya, J. L., & Kästner, S. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00657.2012 · Cited by 129
Spatial and Effector Processing in the Human Parietofrontal Network for Reaches and Saccades
Beurze, S. M., de Lange, F. P., Toni, I., & Medendorp, W. P. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91194.2008 · Cited by 127
Some Temporal and Parietal Cortical Connections Converge in CA1 of the Primate Hippocampus
Rockland, K. S., & Hoesen, G. W. V. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.3.232 · Cited by 125
Parietal regions processing visual 3D shape extracted from disparity
Durand, J., Peeters, R. R., Norman, J. F., Todd, J. T., & Orban, G. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.03.023 · Cited by 125
Real-world objects are more memorable than photographs of objects
Snow, J. C., Skiba, R. M., Coleman, T. L., & Berryhill, M. E. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00837 · Cited by 124
Disentangling Representations of Object and Grasp Properties in the Human Brain
Fabbri, S., Stubbs, K. D., Cusack, R., & Culham, J. C. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0313-16.2016 · Cited by 118
The Extraction of 3D Shape from Texture and Shading in the Human Brain
Georgieva, S., Todd, J. T., Peeters, R. R., & Orban, G. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn002 · Cited by 115
Behaviorally Relevant Abstract Object Identity Representation in the Human Parietal Cortex
Jeong, S. K., & Xu, Y. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1016-15.2016 · Cited by 115
Dorsal–ventral integration in object recognition
Farivar, R. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.05.006 · Cited by 114
Coding of Shape and Position in Macaque Lateral Intraparietal Area
Janssen, P., Srivastava, S., Ombelet, S., & Orban, G. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0499-08.2008 · Cited by 114
Ding, S., Hoesen, G. W. V., & Rockland, K. S. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001002)425:4<510::aid-cne4>3.0.co;2-r · Cited by 108
Distinctive Neural Mechanisms Supporting Visual Object Individuation and Identification
Xu, Y. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21024 · Cited by 101
Posterior Parietal Cortex Drives Inferotemporal Activations During Three-Dimensional Object Vision
Dromme, I. C. V., Premereur, E., Verhoef, B.-E., Vanduffel, W., & Janssen, P. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002445 · Cited by 97
Neuroimaging of amblyopia and binocular vision: a review
Joly, O., & Frankó, E. (2014) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2014.00062 · Cited by 91
Ventral and Dorsal Visual Stream Contributions to the Perception of Object Shape and Object Location
Zachariou, V., Klatzky, R. L., & Behrmann, M. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00475 · Cited by 90
Self-citationDistinct Encoding of Spatial and Nonspatial Visual Information in Parietal Cortex
Freedman, D. J., & Assad, J. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2878-08.2009 · Cited by 89
Reference Frames for Reach Planning in Human Parietofrontal Cortex
Beurze, S. M., Toni, I., Pisella, L., & Medendorp, W. P. (2010) · Journal of Neurophysiology · doi:10.1152/jn.01044.2009 · Cited by 85
The representation of tool and non-tool object information in the human intraparietal sulcus
Mruczek, R. E. B., von Loga, I. S., & Kästner, S. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00658.2012 · Cited by 84
fMRI Repetition Suppression for Familiar But Not Arbitrary Actions with Tools
Valyear, K. F., Gallivan, J. P., McLean, D. A., & Culham, J. C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5270-11.2012 · Cited by 82
The posterior arcuate fasciculus and the vertical occipital fasciculus
Weiner, K. S., Yeatman, J. D., & Wandell, B. A. (2016) · Cortex · doi:10.1016/j.cortex.2016.03.012 · Cited by 81
Toward an understanding of the neural processing for 3D shape perception
Sakata, H., Tsutsui, K., & Taira, M. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.11.003 · Cited by 74
Freud, E., Ganel, T., Shelef, I., Hammer, M. D., Avidan, G., & Behrmann, M. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv229 · Cited by 73
Self-citationActivity patterns in the category‐selective occipitotemporal cortex predict upcoming motor actions
Gallivan, J. P., Chapman, C. S., McLean, D. A., Flanagan, J. R., & Culham, J. C. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12215 · Cited by 73
Verhoef, B.-E., Vogels, R., & Janssen, P. (2010) · Current Biology · doi:10.1016/j.cub.2010.03.058 · Cited by 71
Chainay, H., & Humphreys, G. W. (2001) · Cognitive Neuropsychology · doi:10.1080/02643290125964 · Cited by 71
Monaco, S., Chen, Y., Medendorp, W. P., Crawford, J. D., Fiehler, K., & Henriques, D. Y. P. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht006 · Cited by 71
Nishimura, M., Scherf, K. S., Zachariou, V., Tarr, M. J., & Behrmann, M. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00720 · Cited by 69
Self-citationSynchronization between the end stages of the dorsal and the ventral visual stream
Verhoef, B.-E., Vogels, R., & Janssen, P. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00924.2010 · Cited by 61
Sim, E.-J., Helbig, H. B., Graf, M., & Kiefer, M. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu087 · Cited by 61
Holmes, S. A., & Heath, M. D. (2013) · Brain and Cognition · doi:10.1016/j.bandc.2013.02.005 · Cited by 60
Temporal Frequency Tuning Reveals Interactions between the Dorsal and Ventral Visual Streams
Kristensen, S., Garcea, F. E., Mahon, B. Z., & Almeida, J. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00969 · Cited by 59
Do we understand high-level vision?
Cox, D. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.016 · Cited by 58
Spatial Mechanisms within the Dorsal Visual Pathway Contribute to the Configural Processing of Faces
Zachariou, V., Nikas, C. V., Safiullah, Z. N., Gotts, S. J., & Ungerleider, L. G. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw224 · Cited by 58
Response of MSTd Neurons to Simulated 3D Orientation of Rotating Planes
杉原, 弘., Murakami, I., Shenoy, K. V., Andersen, R. A., & Komatsu, H. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00900.2000 · Cited by 55
Dorsal and ventral stream activation and object recognition performance in school-age children
Dekker, T. M., Mareschal, D., Sereno, M. I., & Johnson, M. H. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.005 · Cited by 54
Visual Object Representation: Interpreting Neurophysiological Data within a Computational Framework
Plaut, D. C., & Farah, M. J. (1990) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1990.2.4.320 · Cited by 53
Self-citationShape representations in the primate dorsal visual stream
Theys, T., Romero, M. C., Loon, J. V., & Janssen, P. (2015) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2015.00043 · Cited by 48
Parietal Mapping of Visuomotor Transformations during Human Tool Grasping
Stark, A., & Zohary, E. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm260 · Cited by 48
Resilience to the contralateral visual field bias as a window into object representations
Garcea, F. E., Kristensen, S., Almeida, J., & Mahon, B. Z. (2016) · Cortex · doi:10.1016/j.cortex.2016.04.006 · Cited by 41
Cortical Connections of the Caudal Portion of Posterior Parietal Cortex in Prosimian Galagos
Stepniewska, I., Cerkevich, C. M., & Kaas, J. H. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv132 · Cited by 38
Face preference in infancy and its relation to motor activity
Libertus, K., & Needham, A. W. (2014) · International Journal of Behavioral Development · doi:10.1177/0165025414535122 · Cited by 37
The Extraction of Depth Structure from Shading and Texture in the Macaque Brain
Nelissen, K., Joly, O., Durand, J., Todd, J. T., Vanduffel, W., & Orban, G. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008306 · Cited by 36
Chen, J., Sperandio, I., & Goodale, M. A. (2014) · Psychological Science · doi:10.1177/0956797614556776 · Cited by 33
3D Shape Perception in Posterior Cortical Atrophy: A Visual Neuroscience Perspective
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Self-citationChoice-related Activity in the Anterior Intraparietal Area during 3-D Structure Categorization
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Cited by
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Deep Predictive Learning: A Comprehensive Model of Three Visual Streams
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Metadata
- Authors
- Freud, E., Plaut, D. C., & Behrmann, M.
- Venue
- Trends in Cognitive Sciences
- Publisher
- Elsevier BV
- Published
- 2016-10
- Volume
- 20
- Issue
- 10
- Pages
- 773-784
- ISSN
- 1364-6613 (ISSN-L)
- OpenAlex
- W2508691184
- Cited by
- 286
- References
- 121
- FWCI
- 2.82
- Type
- journal article
- Language
- en
- Open access
- closed
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 ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.