Cited by 361Visual perception and processing mechanismsMemory and Neural MechanismsFace Recognition and Perception

The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.

Viewpoint-Specific Scene Representations in Human Parahippocampal Cortex

Open access

Epstein, Russell, Graham, Kim S., Downing, Paul E.·2003·Neuron

Open this paper in CoChat — free account Open PDF

Abstract

The "parahippocampal place area" (PPA) responds more strongly in functional magnetic resonance imaging (fMRI) to scenes than to faces, objects, or other visual stimuli. We used an event-related fMRI adaptation paradigm to test whether the PPA represents scenes in a viewpoint-specific or viewpoint-invariant manner. The PPA responded just as strongly to viewpoint changes that preserved intrinsic scene geometry as it did to complete scene changes, but less strongly to object changes within the scene. In contrast, lateral occipital cortex responded more strongly to object changes than to spatial changes. These results demonstrate that scene processing in the PPA is viewpoint specific and suggest that the PPA represents the relationship between the observer and the surfaces that define local space.

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

Crossref · 10.1016/s0896-6273(03)00117-x

Cites

83 of 83 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
The fusiform face area: a module in human extrastriate cortex specialized for face perception
Kanwisher, N., McDermott, J., & Chun, M. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04302.1997 · Cited by 7,738
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
Distributed and overlapping representations of faces and objects in ventral temporal cortex
Haxby, J. V., Gobbini, M. I., Furey, M. L., Ishai, A., Schouten, J. L., & Pietrini, P. (2001) · Science · doi:10.1126/science.1063736 · Cited by 3,940
A cortical representation of the local visual environment
Epstein, R. A., & Kanwisher, N. (1998) · Nature · doi:10.1038/33402 · Cited by 3,083
Self-citation
A cortical area selective for visual processing of the human body
Downing, P. E., Jiang, Y., Shuman, M., & Kanwisher, N. (2001) · Science · doi:10.1126/science.1063414 · Cited by 2,043
Self-citation
Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex.
Malach, R., Reppas, J. B., Benson, R. R., Kwong, K. K., Jiang, H., Kennedy, W. A., Ledden, P. J., Brady, T. J., Rosen, B. R., & Tootell, R. B. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.18.8135 · Cited by 1,761
Building Memories: Remembering and Forgetting of Verbal Experiences as Predicted by Brain Activity
Wagner, A. D., Schacter, D. L., Rotte, M., Koutstaal, W., Maril, A., Dale, A. M., Rosen, B. R., & Buckner, R. L. (1998) · Science · doi:10.1126/science.281.5380.1188 · Cited by 1,644
Increased Activity in Human Visual Cortex during Directed Attention in the Absence of Visual Stimulation
Kastner, S., Pinsk, M. A., De Weerd, P., Desimone, R., & Ungerleider, L. G. (1999) · Neuron · doi:10.1016/s0896-6273(00)80734-5 · Cited by 1,622
The lateral occipital complex and its role in object recognition
Kalanit Grill-spector, A., Kourtzi, Z., & Kanwisher, N. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00073-6 · Cited by 1,492

Show all 82 references

Sorted by citations

Items 101–200 of 361

fMR-adaptation reveals a distributed representation of inanimate objects and places in human visual cortex
Ewbank, M., Schluppeck, D., & Andrews, T. J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.036 · Cited by 80
Two Kinds of fMRI Repetition Suppression? Evidence for Dissociable Neural Mechanisms
Epstein, R. A., Parker, W. E., & Feiler, A. M. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90376.2008 · Cited by 78
Self-citation
Allocentric memory impaired and egocentric memory intact as assessed by virtual reality in recent-onset schizophrenia
Weniger, G., & Irle, E. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.01.011 · Cited by 78
Sensorimotor Cognition and Natural Language Syntax
Knott, A. (2012) · The MIT Press eBooks · doi:10.7551/mitpress/8938.001.0001 · Cited by 76
Path integration and lesions within the head direction cell circuit: Comparison between the roles of the anterodorsal thalamus and dorsal tegmental nucleus.
Frohardt, R. J., Bassett, J. P., & Taube, J. S. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.1.135 · Cited by 76
The Timing of Perceptual Decisions for Ambiguous Face Stimuli in the Human Ventral Visual Cortex
McKeeff, T. J., & Tong, F. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk015 · Cited by 76
Full Scenes produce more activation than Close-up Scenes and Scene-Diagnostic Objects in parahippocampal and retrosplenial cortex: An fMRI study
Henderson, J. M., Larson, C. L., & Zhu, D. C. (2007) · Brain and Cognition · doi:10.1016/j.bandc.2007.05.001 · Cited by 75
Human Spatial Memory and Navigation
McNamara, T. P., Sluzenski, J., & Rump, B. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00176-5 · Cited by 79
Dissociating Task Performance from fMRI Repetition Attenuation in Ventral Visual Cortex
Xu, Y., Turk‐Browne, N. B., & Chun, M. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5527-06.2007 · Cited by 72
Functional analysis of the periphery effect in human building related areas
Levy, I., Hasson, U., Harel, M., & Malach, R. (2004) · Human Brain Mapping · doi:10.1002/hbm.20010 · Cited by 71
Hemispheric Asymmetry of Visual Scene Processing in the Human Brain: Evidence from Repetition Priming and Intrinsic Activity
Stevens, W. D., Kahn, I., Wig, G. S., & Schacter, D. L. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr273 · Cited by 70
Posterior cerebral artery infarcts and semantic category dissociations: a study of 28 patients
Capitani, E., Laiacona, M., Pagani, R., Capasso, R., Zampetti, P., & Miceli, G. (2009) · Brain · doi:10.1093/brain/awp013 · Cited by 69
Where Vision Meets Memory: Prefrontal–Posterior Networks for Visual Object Constancy during Categorization and Recognition
Schendan, H. E., & Stern, C. E. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm197 · Cited by 70
Repetition Suppression versus Enhancement--It's Quantity That Matters
Müller, N., Strumpf, H., Scholz, M., Baier, B., & Melloni, L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs009 · Cited by 67
Spatial frequency processing in scene-selective cortical regions
Kauffmann, L., Ramanoël, S., Guyader, N., Chauvin, A., & Peyrin, C. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.058 · Cited by 76
On user involvement in production of images used in visual authentication
Renaud, K. (2009) · Journal of Visual Languages and Computing · doi:10.1016/j.jvlc.2008.04.001 · Cited by 79
Face-Identity Change Activation Outside the Face System: “Release from Adaptation” May Not Always Indicate Neuronal Selectivity
Mur, M., Ruff, D. A., Bodurka, J., Bandettini, P. A., & Kriegeskorte, N. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp272 · Cited by 67
Neural responses to visual scenes reveals inconsistencies between fMRI adaptation and multivoxel pattern analysis
Epstein, R. A., & Vass, L. K. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.09.042 · Cited by 65
Self-citation
Simulated self-motion in a visual gravity field: Sensitivity to vertical and horizontal heading in the human brain
Indovina, I., Maffei, V., Pauwels, K., Macaluso, E., Orban, G. A., & Lacquaniti, F. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.01.005 · Cited by 69
Object Representations for Multiple Visual Categories Overlap in Lateral Occipital and Medial Fusiform Cortex
Pourtois, G., Schwartz, S., Spiridon, M., Martuzzi, R., & Vuilleumier, P. O. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn210 · Cited by 66
Stimulus Similarity-Contingent Neural Adaptation Can Be Time and Cortical Area Dependent
Verhoef, B.-E., Kayaert, G., Frankó, E., Vangeneugden, J., & Vogels, R. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3333-08.2008 · Cited by 65
Functional Organization of the Parahippocampal Cortex: Dissociable Roles for Context Representations and the Perception of Visual Scenes
Baumann, O., & Mattingley, J. B. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3368-15.2016 · Cited by 65
Neural Representations Integrate the Current Field of View with the Remembered 360° Panorama in Scene-Selective Cortex
Robertson, C. E., Hermann, K. L., Mynick, A., Kravitz, D. J., & Kanwisher, N. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.002 · Cited by 64
When is the perirhinal cortex necessary for the performance of spatial memory tasks?
Aggleton, J. P., Kyd, R. J., & Bilkey, D. K. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.08.007 · Cited by 64
Neural substrates of processing path and manner information of a moving event
Wu, D. H., Morganti, A., & Chatterjee, A. K. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.09.016 · Cited by 64
It's all about timing: An electrophysiological examination of feedback-based learning with immediate and delayed feedback
Arbel, Y., Hong, L., Baker, T. E., & Holroyd, C. B. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.03.003 · Cited by 69
Visuospatial working memory and changes of the point of view in 3D space
Schmidt, D., Krause, B. J., Weiss, P. H., Fink, G. R., Shah, N. J., Amorim, M., Müller, H., & Berthoz, A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.050 · Cited by 63
Brain Images, Babies, and Bathwater: Critiquing Critiques of Functional Neuroimaging
Farah, M. J. (2014) · The Hastings Center Report · doi:10.1002/hast.295 · Cited by 68
Perceived egocentric distance sensitivity and invariance across scene-selective cortex
Persichetti, A. S., & Dilks, D. D. (2016) · Cortex · doi:10.1016/j.cortex.2016.02.006 · Cited by 64
Repetition Priming Influences Distinct Brain Systems: Evidence From Task-Evoked Data and Resting-State Correlations
Wig, G. S., Buckner, R. L., & Schacter, D. L. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91213.2008 · Cited by 62
The Emergence of Perceived Position in the Visual System
Fischer, J., Spotswood, N., & Whitney, D. C. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21417 · Cited by 63
Selectivity for low-level features of objects in the human ventral stream
Andrews, T. J., Clarke, A., Pell, P. J., & Hartley, T. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.046 · Cited by 62
Object recognition in Williams syndrome: uneven ventral stream activation
O’Hearn, K. M., Roth, J. K., Courtney, S. M., Luna, B., Street, W. N., Terwillinger, R., & Landau, B. (2010) · Developmental Science · doi:10.1111/j.1467-7687.2010.01002.x · Cited by 59
Evidence for the incorporation of temporal duration information in human hippocampal long-term memory sequence representations
Thavabalasingam, S., O’Neil, E. B., Tay, J., Nestor, A., & Lee, A. C. H. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1819993116 · Cited by 62
Neuroarchitecture: How the Perception of Our Surroundings Impacts the Brain
Abbas, S., Okdeh, N., Roufayel, R., Kovacic, H., Sabatier, J., Fajloun, Z., & Khattar, Z. A. (2024) · Biology · doi:10.3390/biology13040220 · Cited by 71
Neural representation of object location and route direction: An event-related fMRI study
Janzen, G., & Weststeijn, C. G. (2007) · Brain Research · doi:10.1016/j.brainres.2007.05.074 · Cited by 62
Modulation of Face Processing by Emotional Expression and Gaze Direction during Intracranial Recordings in Right Fusiform Cortex
Pourtois, G., Spinelli, L., Seeck, M., & Vuilleumier, P. O. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21404 · Cited by 62
Preserved function of the fusiform face area in schizophrenia as revealed by fMRI
Yoon, J. H., D’Esposito, M., & Carter, C. S. (2006) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2006.06.002 · Cited by 58
The human parahippocampal cortex subserves egocentric spatial learning during navigation in a virtual maze
Weniger, G., Siemerkus, J., Schmidt‐Samoa, C., Mehlitz, M., Baudewig, J., Dechent, P., & Irle, E. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.08.003 · Cited by 56
Event-Related Nociceptive Arousal Enhances Memory Consolidation for Neutral Scenes
Schwarze, U., Bingel, U., & Sommer, T. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4497-11.2012 · Cited by 63
Reduced visual processing capacity in sleep deprived persons
Kong, D., Soon, C. S., & Chee, M. W. L. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.12.057 · Cited by 55
Visual Agnosia and Posterior Cerebral Artery Infarcts: An Anatomical-Clinical Study
Martinaud, O., Pouliquen, D., Gérardin, E., Loubeyre, M., Hirsbein, D., Hannequin, D., & Cohen, L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030433 · Cited by 56
Human hippocampal processing of environmental novelty during spatial navigation
Kaplan, R., Horner, A. J., Bandettini, P. A., Doeller, C. F., & Burgess, N. (2014) · Hippocampus · doi:10.1002/hipo.22264 · Cited by 56
Distinct representations of spatial and categorical relationships across human scene-selective cortex
Persichetti, A. S., & Dilks, D. D. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903057116 · Cited by 57
Posterior parahippocampal gyrus lesions in the human impair egocentric learning in a virtual environment
Weniger, G., & Irle, E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05108.x · Cited by 54
Differential Connectivity Within the Parahippocampal Place Area
Baldassano, C. A., Beck, D. M., & Fei-Fei, L. (2013) · Journal of Vision · doi:10.1167/13.9.1096 · Cited by 53
Functional Magnetic Resonance Adaptation in Visual Neuroscience
Weigelt, S., Muckli, L. F., & Kohler, A. (2008) · Reviews in the Neurosciences · doi:10.1515/revneuro.2008.19.4-5.363 · Cited by 53
Temporal Components in the Parahippocampal Place Area Revealed by Human Intracerebral Recordings
Bastin, J., Vidal, J. R., Bouvier, S., Perrone‐Bertolotti, M., Benis, D., Kahane, P., Olivier David, A., Lachaux, J.-P., & Epstein, R. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4646-12.2013 · Cited by 58
Self-citation
Abnormal fMRI Adaptation to Unfamiliar Faces in a Case of Developmental Prosopamnesia
Williams, M., Berberovic, N., & Mattingley, J. B. (2007) · Current Biology · doi:10.1016/j.cub.2007.06.042 · Cited by 52
The Cortical Underpinnings of Context-based Memory Distortion
Schacter, D. L., Aminoff, E., & Bar, M. (2008) · Digital Access to Scholarship at Harvard (DASH) (Harvard University) · Cited by 52
Visual passwords
Renaud, K., & Angeli, A. D. (2009) · Communications of the ACM · doi:10.1145/1610252.1610287 · Cited by 51
Multiple Forms of Learning Yield Temporally Distinct Electrophysiological Repetition Effects
Race, E., Badre, D., & Wagner, A. D. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp233 · Cited by 50
Scene-selective coding by single neurons in the human parahippocampal cortex
Mormann, F., Kornblith, S., Cerf, M., Ison, M. J., Kraskov, A., Tran, M., Knieling, S., Quiroga, R. Q., Koch, C., & Fried, I. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608159113 · Cited by 54
Top–down biases win against focal attention in the fusiform face area
Reddy, L., Moradi, F., & Christof Koch, A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.006 · Cited by 50
A Neural Basis for Developmental Topographic Disorientation
Kim, J. G., Aminoff, E., Kästner, S., & Behrmann, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0640-15.2015 · Cited by 50
Neural representation of scene boundaries
Ferrara, K., & Park, S. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.05.012 · Cited by 48
fMRI-adaptation evidence of overlapping neural representations for objects related in function or manipulation
Yee, E., Drucker, P. D. D. M., & Thompson‐Schill, S. L. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.036 · Cited by 51
Good Exemplars of Natural Scene Categories Elicit Clearer Patterns than Bad Exemplars but Not Greater BOLD Activity
Torralbo, A., Walther, D. B., Chai, B., Caddigan, E., Fei-Fei, L., & Beck, D. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058594 · Cited by 53
Animal detection and identification in natural scenes: Image statistics and emotional valence
Naber, M., Hilger, M., & Einhäuser, W. (2012) · Journal of Vision · doi:10.1167/12.1.25 · Cited by 49
Cortical activation to indoor versus outdoor scenes: an fMRI study
Henderson, J. M., Larson, C. L., & Zhu, D. C. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0766-2 · Cited by 49
Neural Representation of Navigational Relevance Is Rapidly Induced and Long Lasting
Janzen, G., Wagensveld, B., & van Turennout, M. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl008 · Cited by 53
Toward a conceptualization of retrohippocampal contributions to learning and memory
Bucci, D. J., & Robinson, S. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.05.007 · Cited by 48
Contrasting roles of neural firing rate and local field potentials in human memory
Ekstrom, A. D., Viskontas, I. V., Kahana, M. J., Jacobs, J., Upchurch, K., Bookheimer, S. Y., & Fried, I. (2007) · Hippocampus · doi:10.1002/hipo.20300 · Cited by 49
A neural wayfinding mechanism adjusts for ambiguous landmark information
Janzen, G., & Jansen, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.083 · Cited by 49
Common Neural Representations for Visually Guided Reorientation and Spatial Imagery
Vass, L. K., & Epstein, R. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv343 · Cited by 45
Self-citation
Do object-category selective regions in the ventral visual stream represent perceived distance information?
Amit, E., Mehoudar, E., Yaacov Trope, B., & Yovel, G. (2012) · Brain and Cognition · doi:10.1016/j.bandc.2012.06.006 · Cited by 46
When a Thought Equals a Look: Refreshing Enhances Perceptual Memory
Yi, D.-J., Turk‐Browne, N. B., Chun, M. M., & Johnson, M. K. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20094 · Cited by 45
Developmental continuity and change in responses to social and nonsocial categories in human extrastriate visual cortex
Pelphrey, K. A. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.025.2009 · Cited by 43
Behavioral and Neural Representations of Spatial Directions across Words, Schemas, and Images
Weisberg, S. M., Marchette, S. A., & Chatterjee, A. K. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3250-17.2018 · Cited by 42
Large-scale dissociations between views of objects, scenes, and reachable-scale environments in visual cortex
Josephs, E., & Konkle, T. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912333117 · Cited by 45
The human hippocampus beyond the cognitive map: evidence from a densely amnesic patient
Lavenex, P. B., Colombo, F., Lambert, F. R., & Lavenex, P. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00711 · Cited by 48
Evidencing a place for the hippocampus within the core scene processing network
Hodgetts, C. J., Shine, J. P., Lawrence, A. D., Downing, P. E., & Graham, K. S. (2016) · Human Brain Mapping · doi:10.1002/hbm.23275 · Cited by 48
Self-citation
Neural Systems for Visual Scene Recognition
Epstein, R. A. (2014) · The MIT Press eBooks · doi:10.7551/mitpress/9780262027854.003.0006 · Cited by 43
Self-citation
Spatial encoding and underlying circuitry in scene-selective cortex
Nasr, S., Devaney, K. J., & Tootell, R. B. H. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.030 · Cited by 44
Disentangling Spatial Perception and Spatial Memory in the Hippocampus: A Univariate and Multivariate Pattern Analysis fMRI Study
Lee, A. C. H., Brodersen, K. H., & Rudebeck, S. R. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00301 · Cited by 41
Coarse-to-fine Categorization of Visual Scenes in Scene-selective Cortex
Musel, B., Kauffmann, L., Ramanoël, S., Giavarini, C., Guyader, N., Chauvin, A., & Peyrin, C. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00643 · Cited by 46
The AudioMaze : An EEG and motion capture study of human spatial navigation in sparse augmented reality
Miyakoshi, M., Gehrke, L., Gramann, K., Makeig, S., & Iversen, J. R. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15131 · Cited by 41
Neural structures and mechanisms involved in scene recognition: A review and interpretation
Sewards, T. V. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.11.018 · Cited by 40
The dorsal prefrontal and dorsal anterior cingulate cortices exert complementary network signatures during encoding and retrieval in associative memory
Woodcock, E. A., White, R. T., & Diwadkar, V. A. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.050 · Cited by 39
Beyond scene gist: Objects guide search more than scene background.
Koehler, K., & Eckstein, M. P. (2017) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/xhp0000363 · Cited by 38
Multiscale Integration of Contextual Information During a Naturalistic Task
Keidel, J. L., Oedekoven, C., Tut, A. C., & Bird, C. M. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx218 · Cited by 33
Spatially Specific fMRI Repetition Effects in Human Visual Cortex
Murray, S. O., Olman, C. A., & Kersten, D. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01236.2005 · Cited by 37
Single neurons in the human medial temporal lobe flexibly shift representations across spatial and memory tasks
Donoghue, T., Cao, R., Han, C. Z., Holman, C. M., Brandmeir, N. J., Wang, S., & Jacobs, J. (2023) · Hippocampus · doi:10.1002/hipo.23539 · Cited by 35
Neural representation of geometry and surface properties in object and scene perception
Lowe, M. X., Rajsic, J., Gallivan, J. P., Ferber, S., & Cant, J. S. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.06.043 · Cited by 36
Neural correlates of strategic memory retrieval: Differentiating between spatial‐associative and temporal‐associative strategies
de Rover, M., Petersson, K. M., van der Werf, S. P., Cools, A. R., Berger, H. J. C., & Fernández, G. (2007) · Human Brain Mapping · doi:10.1002/hbm.20445 · Cited by 36
Feature diagnosticity and task context shape activity in human scene-selective cortex
Lowe, M. X., Gallivan, J. P., Ferber, S., & Cant, J. S. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.089 · Cited by 34
Why are places so special? Uncovering how our brain reacts to meaningful places
Gatersleben, B., Wyles, K., Myers, A., & Opitz, B. (2020) · Landscape and Urban Planning · doi:10.1016/j.landurbplan.2020.103758 · Cited by 15
Different mental representations for place recognition and goal localization
Valiquette, C. M., & McNamara, T. P. (2007) · Psychonomic Bulletin & Review · doi:10.3758/bf03196820 · Cited by 34
Perceptual dissociations among views of objects, scenes, and reachable spaces.
Josephs, E., & Konkle, T. (2019) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/xhp0000626 · Cited by 32
Place-related neuronal activity in the monkey parahippocampal gyrus and hippocampal formation during virtual navigation
Furuya, Y., Matsumoto, J., Hori, E., Boas, C. V., Tran, A. H., Shimada, Y., Ono, T., & Nishijo, H. (2013) · Hippocampus · doi:10.1002/hipo.22209 · Cited by 35
The Parahippocampal Cortex Mediates Contextual Associative Memory: Evidence from an fMRI Study
Li, M., Lu, S., & Zhong, N. (2016) · BioMed Research International · doi:10.1155/2016/9860604 · Cited by 32
The topographical N170: Electrophysiological evidence of a neural mechanism for human spatial navigation
Baker, T. E., & Holroyd, C. B. (2013) · Biological Psychology · doi:10.1016/j.biopsycho.2013.05.004 · Cited by 32
Suppression weakens unwanted memories via a sustained reduction of neural reactivation
Meyer, A.-K., & Benoit, R. G. (2022) · eLife · doi:10.7554/elife.71309 · Cited by 27
Fixed versus dynamic orientations in environmental learning from ground-level and aerial perspectives
Shelton, A. L., & Pippitt, H. A. (2006) · Psychological Research · doi:10.1007/s00426-006-0088-9 · Cited by 30
Whether Visual-related Structural and Functional Changes Occur in Brain of Patients with Acute Incomplete Cervical Cord Injury: A Multimodal Based MRI Study
Chen, Q., Zheng, W., Chen, X., Li, X., Wang, L., Qin, W., Li, K., & Chen, N. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.10.014 · Cited by 30
Age-Related Differences in Spatial Frequency Processing during Scene Categorization
Ramanoël, S., Kauffmann, L., Cousin, É., Michel Dojat, D., & Peyrin, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134554 · Cited by 37
Formation of Category Representations in Superior Temporal Sulcus
van der Linden, M., van Turennout, M., & Indefrey, P. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21270 · Cited by 29
Relating Visual Production and Recognition of Objects in Human Visual Cortex
Fan, J. E., Wammes, J. D., Gunn, J. B., Yamins, D. L. K., Norman, K. A., & Turk‐Browne, N. B. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1843-19.2019 · Cited by 29
Hippocampal Complex Contribution to Retention and Retrieval of Recent and Remote Episodic and Semantic Memories: Evidence from Behavioral and Neuroimaging Studies of Healthy and Brain-Damaged People
Moscovitch, M., Westmacott, R., Gilboa, A., Addis, D. R., Rosenbaum, R. S., Viskontas, I. V., Priselac, S., Svoboda, E., Ziegler, M., Black, S. E., et al. (2006) · Springer eBooks · doi:10.1007/4-431-27431-6_14 · Cited by 29
Impaired egocentric memory and reduced somatosensory cortex size in temporal lobe epilepsy with hippocampal sclerosis
Weniger, G., Ruhleder, M., Lange, C., & Irle, E. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.043 · Cited by 30

Authors: Epstein, R., Graham, K. S., & Downing, P. E.
Affiliations: MRC Cognition and Brain Sciences Unit (GB)
Bangor University (GB)
Corresponding author: Epstein, Russell
ORCID: Epstein, Russell
Graham, Kim S.
Downing, Paul E.
Venue: Neuron
Publisher: Elsevier BV
Published: 2003-03
Volume: 37
Issue: 5
Pages: 865-876
ISSN: 0896-6273 (ISSN-L)
DOI: 10.1016/s0896-6273(03)00117-x
OpenAlex: W2125607983
Cited by: 360
References: 82
Citations by year: 2026: 3 · 2025: 8 · 2024: 12 · 2023: 5 · 2022: 5 · 2021: 10 · 2020: 11 · 2019: 30 · 2018: 12 · 2017: 14 · 2016: 14 · 2015: 16 · 2014: 17 · 2013: 18 · 2012: 21
FWCI: 10.09
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/open-access/userlicense/1.0/ (vor, 3791 d)
Locations: Neuron (publishedVersion)
PubMed (publishedVersion)
Funders: Medical 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 › Face Recognition and Perception
Keywords: parahippocampal place area, scene processing, viewpoint invariance, lateral occipital cortex, object recognition, spatial representation
MeSH terms: Adult, Analysis of Variance, Evoked Potentials, Female, Humans, Magnetic Resonance Imaging, Male, Photic Stimulation, Visual Cortex, Parahippocampal Gyrus

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

Viewpoint-Specific Scene Representations in Human Parahippocampal Cortex

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks