The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Specific Involvement of Human Parietal Systems and the Amygdala in the Perception of Biological Motion
Open accessAbstract
To explore the extent to which functional systems within the human posterior parietal cortex and the superior temporal sulcus are involved in the perception of action, we measured cerebral metabolic activity in human subjects by positron emission tomography during the perception of simulations of biological motion with point-light displays. The experimental design involved comparisons of activity during the perception of goal-directed hand action, whole body motion, object motion, and random motion. The results demonstrated that the perception of scripts of goal-directed hand action implicates the cortex in the intraparietal sulcus and the caudal part of the superior temporal sulcus, both in the left hemisphere. By contrast, the rostrocaudal part of the right superior temporal sulcus and adjacent temporal cortex, and limbic structures such as the amygdala, are involved in the perception of signs conveyed by expressive body movements.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Adolphs, R., Tranel, D., Damasio, H., & Damasio, A. (1994) · Nature · doi:10.1038/372669a0 · Cited by 2,360
Mountcastle, V. B., Lynch, J. C., Georgopoulos, A., Sakata, H., & Acuna, C. (1975) · Journal of Neurophysiology · doi:10.1152/jn.1975.38.4.871 · Cited by 2,061 · cited 4×
“Single-cell recording studies in monkeys have demonstrated that certain areas in the parietal cortex are involved in the reaching toward and manipulation of objects in space (Mountcastle et al., 1975; Taira et al., 1990; Sakata et al., 1992, 1995), as well as in the coding of the position of objects in relation to the…”
BackgroundInfluentialMaunsell, J., & van Essen, D. (1983) · The Journal of Neuroscience · doi:10.1523/jneurosci.03-12-02563.1983 · Cited by 1,602
Amygdalo‐cortical projections in the monkey ( Macaca fascicularis )
Amaral, D. G., & Price, J. L. (1984) · Journal of Comparative Neurology · doi:10.1002/cne.902300402 · Cited by 1,162
Boussaoud, D., Ungerleider, L. G., & Desimone, R. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902960311 · Cited by 634 · cited 2×
“These parietal areas receive input from the cortex of the caudal superior temporal sulcus (Seltzer and Pandya, 1978, 1984, 1991; Maunsell and Van Essen, 1983; Andersen et al., 1990; Boussaoud et al., 1990), where several areas involved in the perception of motion have been identified (Zeki, 1974; Van Essen et al.”
BackgroundUncus and Amygdala Lesions: Effects on Social Behavior in the Free-Ranging Rhesus Monkey
Dicks, D., Myers, R. E., & Kling, A. (1969) · Science · doi:10.1126/science.165.3888.69 · Cited by 132
Cited by
The distributed human neural system for face perception
Haxby, J. V., Hoffman, E. A., & Gobbini, M. I. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01482-0 · Cited by 4,891
Meeting of minds: the medial frontal cortex and social cognition
Amodio, D. M., & Frith, C. D. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1884 · Cited by 3,782
Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies
Cabeza, R., & Nyberg, L. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137585 · Cited by 3,598
Neurophysiological mechanisms underlying the understanding and imitation of action
Rizzolatti, G., Fogassi, L., & Gallese, V. (2001) · Nature Reviews Neuroscience · doi:10.1038/35090060 · Cited by 3,302
The amygdala: vigilance and emotion
Davis, M., & Whalen, P. J. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000812 · Cited by 2,882
Social perception from visual cues: Role of the STS region
Allison, T., Puce, A., & McCarthy, G. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01501-1 · Cited by 2,461
Development and neurophysiology of mentalizing
Frith, U., & Frith, C. D. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1218 · Cited by 2,306
Functional imaging of ‘theory of mind’
Gallagher, H. L., & Frith, C. D. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)00025-6 · Cited by 2,092
Social cognition and the brain: A meta-analysis
Van Overwalle, F. (2009) · Human Brain Mapping · doi:10.1002/hbm.20547 · Cited by 1,792
Cognitive neuroscience of human social behaviour
Adolphs, R. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1056 · Cited by 1,657
Gaze cueing of attention: visual attention, social cognition, and individual differences
Frischen, A., Bayliss, A. P., & Tipper, S. P. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.4.694 · Cited by 1,473
The neurobiology of social cognition
Adolphs, R. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00202-6 · Cited by 1,432
Gallagher, H. L., Happé, F., Brunswick, N., Fletcher, P. C., Frith, U., & Frith, C. D. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00053-6 · Cited by 1,394
Castelli, F. (2002) · Brain · doi:10.1093/brain/awf189 · Cited by 1,377
Mapping brain maturation and cognitive development during adolescence
Paus, T. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.12.008 · Cited by 1,348
Semantic memory and the brain: structure and processes
Martin, A., & Chao, L. L. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00196-3 · Cited by 1,339
Human neural systems for face recognition and social communication
Haxby, J. V., Hoffman, E. A., & Gobbini, M. I. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01330-0 · Cited by 1,287
Cortical pathways to the mammalian amygdala
McDonald, A. J. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00003-3 · Cited by 1,303
Social intelligence in the normal and autistic brain: An fMRI study
Baron‐Cohen, S., Ring, H. A., Wheelwright, S., Bullmore, E. T., Brammer, M. J., Simmons, A., & Williams, S. C. R. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00621.x · Cited by 1,320
Baron-Cohen, S., Ring, H. A., Bullmore, E. T., Wheelwright, S., Ashwin, C., & Williams, S. C. R. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(00)00011-7 · Cited by 1,130
Automatic and intentional brain responses during evaluation of trustworthiness of faces
Winston, J. S., Strange, B. A., O'Doherty, J., & Dolan, R. J. (2002) · Nature Neuroscience · doi:10.1038/nn816 · Cited by 993
Pitkänen, A., Savander, V., & LeDoux, J. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01125-9 · Cited by 980
Neural mechanisms for the recognition of biological movements
Giese, M. A., & Poggio, T. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1057 · Cited by 955
Brain activity during observation of actions. Influence of action content and subject's strategy
Decety, J. (1997) · Brain · doi:10.1093/brain/120.10.1763 · Cited by 942
Understanding the recognition of facial identity and facial expression
Calder, A. J., & Young, A. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1724 · Cited by 948
The enactive mind, or from actions to cognition: lessons from autism
Klin, A., Jones, W., Schultz, R., & Volkmar, F. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1202 · Cited by 890
(2016) · doi:10.3389/fpsyg · Cited by 801
Towards the neurobiology of emotional body language
de Gelder, B. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1872 · Cited by 786
Electrophysiology and brain imaging of biological motion
Puce, A., & Perrett, D. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1221 · Cited by 693
Oberman, L. M., & Ramachandran, V. S. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.2.310 · Cited by 630
Mind Blindness and the Brain in Autism
Frith, U. (2001) · Neuron · doi:10.1016/s0896-6273(01)00552-9 · Cited by 637
Human brain activity time-locked to perceptual event boundaries
Zacks, J. M., Braver, T. S., Sheridan, M. A., Donaldson, D. I., Snyder, A. Z., Ollinger, J. M., Buckner, R. L., & Raichle, M. E. (2001) · Nature Neuroscience · doi:10.1038/88486 · Cited by 572
Postuma, R. B., & Dagher, A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj088 · Cited by 579
de Gelder, B., Snyder, J., Greve, D., Gerard, G., & Hadjikhani, N. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407042101 · Cited by 511
Theory of Mind: A Neural Prediction Problem
Koster-Hale, J., & Saxe, R. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.020 · Cited by 513
Functional organization of social perception and cognition in the superior temporal sulcus
Deen, B., Koldewyn, K., Kanwisher, N., & Saxe, R. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv111 · Cited by 443
The role of the fusiform face area in social cognition: implications for the pathobiology of autism
Schultz, R. T., Grelotti, D. J., Klin, A., Kleinman, J., Van der Gaag, C., Marois, R., & Skudlarski, P. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1208 · Cited by 469
Consensus Paper: The Role of the Cerebellum in Perceptual Processes
Baumann, O., Borra, R. J., Bower, J. M., Cullen, K. E., Habas, C., Ivry, R. B., Leggio, M., Mattingley, J. B., Molinari, M., Moulton, E. A., et al. (2015) · The Cerebellum · doi:10.1007/s12311-014-0627-7 · Cited by 462
Pelphrey, K. A., Morris, J. P., & McCarthy, G. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042947900 · Cited by 454
The phi complex as a neuromarker of human social coordination
Tognoli, E., Lagarde, J., DeGuzman, G. C., & Kelso, J. A. S. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611453104 · Cited by 437
Two Takes on the Social Brain: A Comparison of Theory of Mind Tasks
Gobbini, M. I., Koralek, A. C., Bryan, R. E., Montgomery, K. J., & Haxby, J. V. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.11.1803 · Cited by 436
Puce, A. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.445 · Cited by 422
Peelen, M. V., Wiggett, A. J., & Downing, P. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.02.004 · Cited by 402
Depersonalization: neurobiological perspectives.
Sierra, M., & Berrios, G. E. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00015-8 · Cited by 394
Emotion and cognition and the amygdala: From “what is it?” to “what's to be done?”
Pessoa, L. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.06.038 · Cited by 403
Autism, the superior temporal sulcus and social perception
Zilbovicius, M., Meresse, I., Chabane, N., Brunelle, F., Samson, Y., & Boddaert, N. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.06.004 · Cited by 392
Pelphrey, K. A., Morris, J. P., Michelich, C. R., Allison, T., & McCarthy, G. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi064 · Cited by 369
Integrating automatic and controlled processes into neurocognitive models of social cognition
Satpute, A. B., & Lieberman, M. D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.01.005 · Cited by 347
Brain activity evoked by inverted and imagined biological motion
Grossman, E. D., & Blake, R. (2001) · Vision Research · doi:10.1016/s0042-6989(00)00317-5 · Cited by 333
Brain activity evoked by the perception of human walking: controlling for meaningful coherent motion
Pelphrey, K. A., Mitchell, T. V., McKeown, M. J., Goldstein, J., Allison, T., & McCarthy, G. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06819.2003 · Cited by 314
Seeing fearful body expressions activates the fusiform cortex and amygdala
Hadjikhani, N., & de Gelder, B. (2003) · Current Biology · doi:10.1016/j.cub.2003.11.049 · Cited by 298
Brain regions involved in human movement perception: A quantitative voxel‐based meta‐analysis
Grosbras, M., Beaton, S., & Eickhoff, S. B. (2012) · Human Brain Mapping · doi:10.1002/hbm.21222 · Cited by 284
Cortical Regions for Judgments of Emotions and Personality Traits from Point-light Walkers
Heberlein, A. S., Adolphs, R., Tranel, D., & Damasio, H. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929041920423 · Cited by 257
Underconnectivity between voice-selective cortex and reward circuitry in children with autism
Abrams, D. A., Lynch, C. J., Cheng, K. M., Phillips, J., Supekar, K., Ryali, S., Uddin, L. Q., & Menon, V. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302982110 · Cited by 250
Automatic Attention Cueing Through Eye Movement in 2-Year-Old Children With Autism
Chawarska, K., Klin, A., & Volkmar, F. (2003) · Child Development · doi:10.1111/1467-8624.00595 · Cited by 244
Human brain regions involved in recognizing environmental sounds
Lewis, J. W., Wightman, F. L., Brefczynski, J. A., Phinney, R. E., Binder, J. R., & DeYoe, E. A. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh061 · Cited by 230
Similarities and differences in perceiving threat from dynamic faces and bodies. An fMRI study
Kret, M. E., Pichon, S., Grèzes, J., & de Gelder, B. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.012 · Cited by 204
ALE meta-analysis on facial judgments of trustworthiness and attractiveness
Bzdok, D., Langner, R., Caspers, S., Kurth, F., Habel, U., Zilles, K., Laird, A., & Eickhoff, S. B. (2011) · Brain Structure and Function · doi:10.1007/s00429-010-0287-4 · Cited by 183
Attention, biological motion, and action recognition.
Thompson, J., & Parasuraman, R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.044 · Cited by 155
Fishburn, F. A., Murty, V. P., Hlutkowsky, C. O., MacGillivray, C. E., Bemis, L. M., Murphy, M. E., Huppert, T. J., & Perlman, S. B. (2018) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsy060 · Cited by 144
Left inferior parietal dominance in gesture imitation: an fMRI study
Mühlau, M., Hermsdörfer, J., Goldenberg, G., Wohlschläger, A. M., Castrop, F., Stahl, R., Röttinger, M., Erhard, P., Haslinger, B., Ceballos-Baumann, A. O., et al. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.10.004 · Cited by 141
The role of MT+/V5 during biological motion perception in Asperger syndrome: An fMRI study
Herrington, J. D., Baron-Cohen, S., Wheelwright, S. J., Singh, K. D., Bullmore, E. T., Brammer, M., & Williams, S. C. R. (2007) · Research in Autism Spectrum Disorders · doi:10.1016/j.rasd.2006.07.002 · Cited by 138
Mier, D., Lis, S., Neuthe, K., Sauer, C., Esslinger, C., Gallhofer, B., & Kirsch, P. (2010) · Psychophysiology · doi:10.1111/j.1469-8986.2010.01031.x · Cited by 126
Charting the typical and atypical development of the social brain
Pelphrey, K. A., & Carter, E. J. (2008) · Development and Psychopathology · doi:10.1017/s0954579408000515 · Cited by 126
Deen, B., & McCarthy, G. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.01.028 · Cited by 101
Heberlein, A. S., & Saxe, R. R. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.064 · Cited by 93
Engell, A. D., & McCarthy, G. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.02.025 · Cited by 77
“The intersection of the anterior occipital and inferior temporal sulci has been shown to have a category-selective response to biological motion (Bonda et al., 1996; Grezes et al., 2007; Peelen et al., 2006; Pichon et al., 2008; but see Grossman and Blake, 2002) and”
BackgroundMethodInfluentialOxytocin, sexually dimorphic features of the social brain, and autism
Yamasue, H., Kuwabara, H., Kawakubo, Y., & Kasai, K. (2009) · Psychiatry and Clinical Neurosciences · doi:10.1111/j.1440-1819.2009.01944.x · Cited by 78
Social-Network Complexity in Humans Is Associated With the Neural Response to Social Information
Dziura, S. L., & Thompson, J. C. (2014) · Psychological Science · doi:10.1177/0956797614549209 · Cited by 40
Cohen, M. X., David, N., Vogeley, K., & Elger, C. E. (2009) · Psychophysiology · doi:10.1111/j.1469-8986.2008.00724.x · Cited by 31
Metadata
- Authors
- Bonda, E., Petrides, M., Ostry, D., & Evans, A.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1996-06-01
- Volume
- 16
- Issue
- 11
- Pages
- 3737-3744
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W1499043868
- Cited by
- 737
- References
- 6
- FWCI
- 24.66
- Type
- journal article
- Language
- en
- Open access
- hybrid
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
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.