Cited by 284Action Observation and SynchronizationFace Recognition and PerceptionVisual perception and processing mechanisms

The DOI matches its Crossref record; 155 of the 155 references it cites were found in a registry or an index.

Brain regions involved in human movement perception: A quantitative voxel‐based meta‐analysis

Open access

Grosbras, Marie‐Hélène, Beaton, Susan, Eickhoff, Simon B.·2012·Human Brain Mapping

DOI 10.1002/hbm.21222PMC PMC6869986

Open this paper in CoChat — free account Open PDF

Abstract

Face, hands, and body movements are powerful signals essential for social interactions. In the last 2 decades, a large number of brain imaging studies have explored the neural correlates of the perception of these signals. Formal synthesis is crucially needed, however, to extract the key circuits involved in human motion perception across the variety of paradigms and stimuli that have been used. Here, we used the activation likelihood estimation (ALE) meta‐analysis approach with random effect analysis. We performed meta‐analyses on three classes of biological motion: movement of the whole body, hands, and face. Additional analyses of studies of static faces or body stimuli and sub‐analyses grouping experiments as a function of their control stimuli or task employed allowed us to identify main effects of movements and forms perception, as well as effects of task demand. In addition to specific features, all conditions showed convergence in occipito‐temporal and fronto‐parietal regions, but with different peak location and extent. The conjunction of the three ALE maps revealed convergence in all categories in a region of the right posterior superior temporal sulcus as well as in a bilateral region at the junction between middle temporal and lateral occipital gyri. Activation in these regions was not a function of attentional demand and was significant also when controlling for non‐specific motion perception. This quantitative synthesis points towards a special role for posterior superior temporal sulcus for integrating human movement percept, and supports a specific representation for body parts in middle temporal, fusiform, precentral, and parietal areas. Hum Brain Mapp, 2012. © 2011 Wiley Periodicals, Inc.

Integrity signals

Registry

Crossref · 10.1002/hbm.21222

Cites

155 of 155 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

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 MIRROR-NEURON SYSTEM
Rizzolatti, G., & Craighero, L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144230 · Cited by 7,433
Action recognition in the premotor cortex
Gallese, V., Fadiga, L., Fogassi, L., & Rizzolatti, G. (1996) · Brain · doi:10.1093/brain/119.2.593 · Cited by 4,968
The mirror neuron system
Cattaneo, L., & Rizzolatti, G. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.41 · Cited by 3,137
Stereotaxic Display of Brain Lesions
Rorden, C., & Brett, M. (2000) · Behavioural Neurology · doi:10.1155/2000/421719 · Cited by 2,573
Action observation activates premotor and parietal areas in a somatotopic manner: an fMRI study
Buccino, G., Binkofski, F., Fink, G. R., Fadiga, L., Fogassi, L., Gallese, V., Seitz, R. J., Zilles, K., Rizzolatti, G., & Freund, H. ‐. (2001) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2001.01385.x · Cited by 2,488
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
Action Observation and Acquired Motor Skills: An fMRI Study with Expert Dancers
Calvo‐Merino, B., Glaser, D. E., Grèzes, J., Passingham, R. E., & Haggard, P. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhi007 · Cited by 2,095
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
Neural mechanisms of empathy in humans: a relay from neural systems for imitation to limbic areas
Carr, L., Iacoboni, M., Dubeau, M.-C., Mazziotta, J. C., & Lenzi, G. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0935845100 · Cited by 1,978

Flagged first, then by citations

Show all 155 references

Sorted by citations

The neural network of motor imagery: An ALE meta-analysis
Hétu, S., Grégoire, M., Saimpont, A., Coll, M., Eugène, F., Michon, P., & Jackson, P. L. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.03.017 · Cited by 900
Mirror neurons: from origin to function
Cook, R., Bird, G., Catmur, C., Press, C., & Heyes, C. (2014) · Behavioral and Brain Sciences · doi:10.1017/s0140525x13000903 · Cited by 647
Toward a hierarchical model of social cognition: A neuroimaging meta-analysis and integrative review of empathy and theory of mind.
Schurz, M., Raduà, J., Tholen, M. G., Maliske, L., Margulies, D. S., Mars, R. B., Sallet, J., & Kanske, P. (2020) · Psychological Bulletin · doi:10.1037/bul0000303 · Cited by 702
Cortical Mechanisms Underlying the Organization of Goal-Directed Actions and Mirror Neuron-Based Action Understanding
Rizzolatti, G., Cattaneo, L., Fabbri‐Destro, M., & Rozzi, S. (2014) · Physiological Reviews · doi:10.1152/physrev.00009.2013 · Cited by 523
The mirror mechanism: a basic principle of brain function
Rizzolatti, G., & Sinigaglia, C. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.135 · Cited by 521
The human vestibular cortex revealed by coordinate-based activation likelihood estimation meta-analysis
Lopez, C., Blanke, O., & Mast, F. W. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.028 · Cited by 453
Consensus Paper: Cerebellum and Social Cognition
Overwalle, F. V., Manto, M. U., Cattaneo, Z., Clausi, S., Ferrari, C., Gabrieli, J. D. E., Guell, X., Heleven, E., Lupo, M., Ma, Q., et al. (2020) · The Cerebellum · doi:10.1007/s12311-020-01155-1 · Cited by 465
Concept representation reflects multimodal abstraction: A framework for embodied semantics
Fernandino, L., Binder, J. R., Desai, R. H., Pendl, S. L., Humphries, C. J., Gross, W. L., Conant, L. L., & Seidenberg, M. S. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv020 · Cited by 305
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 336
Multiple roles of motor imagery during action observation
Vogt, S., Rienzo, F. D., Collet, C., Collins, A. F., & Guillot, A. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00807 · Cited by 319
Autism Spectrum Disorders and Schizophrenia: Meta-Analysis of the Neural Correlates of Social Cognition
Sugranyes, G., Kyriakopoulos, M., Corrigall, R. J., Taylor, E., & Frangou, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025322 · Cited by 289
Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition
Schilbach, L., Bzdok, D., Timmermans, B., Fox, P. T., Laird, A. R., Vogeley, K. T., & Eickhoff, S. B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030920 · Cited by 234
Self-citation
Potential for social involvement modulates activity within the mirror and the mentalizing systems
Begliomini, C., Cavallo, A., Manera, V., Becchio, C., Stramare, R., Miotto, D., & Castiello, U. (2017) · Scientific Reports · doi:10.1038/s41598-017-14476-9 · Cited by 231
Two neural pathways of face processing: A critical evaluation of current models
Bernstein‐Eliav, M., & Yovel, G. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.06.010 · Cited by 219
Action Concepts in the Brain: An Activation Likelihood Estimation Meta-analysis
Watson, C. E., Cardillo, E. R., Ianni, G. R., & Chatterjee, A. K. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00401 · Cited by 178
The impact of aesthetic evaluation and physical ability on dance perception
Cross, E. S. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00102 · Cited by 171
Neuroanatomical substrates of action perception and understanding: an anatomic likelihood estimation meta-analysis of lesion-symptom mapping studies in brain injured patients
Urgesi, C., Candidi, M., & Avenanti, A. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00344 · Cited by 157
Predicting personality from network-based resting-state functional connectivity
Nostro, A. D., Müller, V. I., Varikuti, D. P., Pläschke, R. N., Hoffstaedter, F., Langner, R., Patil, K. R., & Eickhoff, S. B. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1651-z · Cited by 151
Self-citation
The macaque lateral grasping network: A neural substrate for generating purposeful hand actions
Borra, E., Gerbella, M., Rozzi, S., & Luppino, G. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.017 · Cited by 149
A meta-analysis of neuroimaging studies on pain empathy: investigating the role of visual information and observers’ perspective
Jauniaux, J., Khatibi, A., Rainville, P., & Jackson, P. L. (2019) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsz055 · Cited by 154
Neural correlates of the happy life: The amplitude of spontaneous low frequency fluctuations predicts subjective well-being
Kong, F., Hu, S., Wang, X., Song, Y., & Liu, J. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.11.033 · Cited by 139
Biological motion perception in autism spectrum disorder: a meta-analysis
Todorova, G. K., Hatton, R. E. M., & Pollick, F. E. (2019) · Molecular Autism · doi:10.1186/s13229-019-0299-8 · Cited by 138
Anomalous Perception of Biological Motion in Autism: A Conceptual Review and Meta-Analysis
Federici, A., Parma, V., Vicovaro, M., Radassao, L., Casartelli, L., & Ronconi, L. (2020) · Scientific Reports · doi:10.1038/s41598-020-61252-3 · Cited by 128
Distinct Neural Mechanisms for Body Form and Body Motion Discriminations
Vangeneugden, J., Peelen, M. V., Tadin, D., & Battelli, L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4032-13.2014 · Cited by 112
Global processing in amblyopia: a review
Hamm, L. M., Black, J. M., Dai, S. H., & Thompson, B. S. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00583 · Cited by 116
Effects of TMS over Premotor and Superior Temporal Cortices on Biological Motion Perception
van Kemenade, B. M., Muggleton, N. G., Walsh, V., & Saygın, A. P. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00194 · Cited by 109
Boosting and Decreasing Action Prediction Abilities Through Excitatory and Inhibitory tDCS of Inferior Frontal Cortex
Avenanti, A., Paracampo, R., Annella, L., Tidoni, E., & Aglioti, S. M. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx041 · Cited by 108
Hearing feelings: A quantitative meta-analysis on the neuroimaging literature of emotional prosody perception
Witteman, J., van Heuven, V. J., & Schiller, N. O. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.026 · Cited by 105
Functionally distinct language and Theory of Mind networks are synchronized at rest and during language comprehension
Paunov, A. M., Blank, I., & Fedorenko, E. G. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00619.2018 · Cited by 101
Dance as a subject for empirical aesthetics.
Christensen, J. F., & Calvo‐Merino, B. (2013) · Psychology of Aesthetics Creativity and the Arts · doi:10.1037/a0031827 · Cited by 112
Biological motion task performance predicts superior temporal sulcus activity.
Herrington, J., Nymberg, C., & Schultz, R. (2011) · Brain and Cognition · doi:10.1016/j.bandc.2011.09.001 · Cited by 98
Embodiment in the aging mind
Kuehn, E., Perez-Lopez, M. B., Diersch, N., Doehler, J., Wolbers, T., & Riemer, M. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.11.016 · Cited by 102
Differential mirror neuron system (MNS) activation during action observation with and without social-emotional components in autism: a meta-analysis of neuroimaging studies
Chan, M. M. Y., & Han, Y. M. Y. (2020) · Molecular Autism · doi:10.1186/s13229-020-00374-x · Cited by 96
Structural and effective brain connectivity underlying biological motion detection
Sokolov, A. A., Zeidman, P., Erb, M., Ryvlin, P., Friston, K. J., & Pavlova, M. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812859115 · Cited by 94
The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity
Genon, S., Li, H., Fan, L., Müller, V. I., Cieslik, E. C., Hoffstaedter, F., Reid, A., Langner, R., Grefkes, C., Fox, P. T., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw065 · Cited by 92
Self-citation
Neural networks related to dysfunctional face processing in autism spectrum disorder
Nickl‐Jockschat, T., Rottschy, C., Thommes, J., Schneider, F. W., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0791-z · Cited by 85
Self-citation
Sensorimotor Network Crucial for Inferring Amusement from Smiles
Paracampo, R., Tidoni, E., Borgomaneri, S., di Pellegrino, G., & Avenanti, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw294 · Cited by 85
The neural correlates of ‘vitality form’ recognition: an fMRI study
Cesare, G. D., Dio, C. D., Rochat, M. J., Sinigaglia, C., Bruschweiler‐Stern, N., Stern, D. N., & Rizzolatti, G. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst068 · Cited by 85
A computational neuroethology perspective on body and expression perception
de Gelder, B., & Solanas, M. P. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.05.010 · Cited by 78
Neuroanatomical correlates of biological motion detection
Gilaie‐Dotan, S., Kanai, R., Bahrami, B., Rees, G. E., & Saygın, A. P. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.11.027 · Cited by 78
The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization
Genon, S., Reid, A., Li, H., Fan, L., Müller, V. I., Cieslik, E. C., Hoffstaedter, F., Langner, R., Grefkes, C., Laird, A. R., et al. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.034 · Cited by 77
Self-citation
Attention and awareness each influence amygdala activity for dynamic bodily expressions—a short review
de Gelder, B., Hortensius, R., & Tamietto, M. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00054 · Cited by 70
Naturalistic stimuli reveal a dominant role for agentic action in visual representation
Haxby, J. V., Gobbini, M. I., & Nastase, S. A. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116561 · Cited by 70
Sex and gender affect the social brain: Beyond simplicity
Pavlova, M. A. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23871 · Cited by 70
The functional organization of the left STS: a large scale meta-analysis of PET and fMRI studies of healthy adults
Liebenthal, E., Desai, R. H., Humphries, C., Sabri, M., & Desai, A. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00289 · Cited by 68
A functional dissociation of face-, body- and scene-selective brain areas based on their response to moving and static stimuli
Pitcher, D., Ianni, G. R., & Ungerleider, L. G. (2019) · Scientific Reports · doi:10.1038/s41598-019-44663-9 · Cited by 63
Stimulating the brain to study social interactions and empathy
Hétu, S., Taschereau‐Dumouchel, V., & Jackson, P. L. (2012) · Brain stimulation · doi:10.1016/j.brs.2012.03.005 · Cited by 70
The Functional Neuroanatomy of Lexical Tone Perception: An Activation Likelihood Estimation Meta-Analysis
Liang, B., & Du, Y. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00495 · Cited by 64
Differential activation of brain areas in children with developmental coordination disorder during tasks of manual dexterity: An ALE meta‐analysis
Fuelscher, I., Caeyenberghs, K., Enticott, P., Williams, J., Lum, J., & Hyde, C. (2018) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.01.002 · Cited by 59
What the Human Brain Likes About Facial Motion
Schultz, J., Brockhaus, M., Bülthoff, H., & Pilz, K. S. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs106 · Cited by 63
Bilateral parietal activations for complex visual-spatial functions: Evidence from a visual-spatial construction task
Seydell-Greenwald, A., Ferrara, K., Chambers, C. E., Newport, E., & Landau, B. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.10.005 · Cited by 58
Social and emotional learning in the cerebellum
Overwalle, F. V. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00871-5 · Cited by 70
Cortical and subcortical responses to biological motion
Chang, D. H. F., Ban, H., Ikegaya, Y., Fujita, I., & Troje, N. F. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.03.013 · Cited by 57
Functional anatomy of the macaque temporo-parieto-frontal connectivity.
Borra, E., & Luppino, G. (2017) · Cortex; a journal devoted to the study of the nervous system and behavior · doi:10.1016/j.cortex.2016.12.007 · Cited by 53
Visual, sensorimotor and cognitive routes to understanding others' enjoyment: An individual differences rTMS approach to empathic accuracy
Paracampo, R., Pirruccio, M., Costa, M., Borgomaneri, S., & Avenanti, A. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.01.043 · Cited by 59
Primary somatosensory cortex necessary for the perception of weight from other people's action: A continuous theta-burst TMS experiment
Valchev, N. S., Tidoni, E., Hamilton, A. F. D. C., Gazzola, V., & Avenanti, A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.075 · Cited by 63
MEG-based neurofeedback for hand rehabilitation
Foldes, S. T., Weber, D. J., & Collinger, J. L. (2015) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-015-0076-7 · Cited by 57
How Does the “Default Mode” Network Contribute to Semantic Cognition?
Fernandino, L., & Binder, J. R. (2024) · Brain and Language · doi:10.1016/j.bandl.2024.105405 · Cited by 70
Uni- and Multisensory Brain Areas are Synchronised across Spectators When Watching Unedited Dance Recordings
Jola, C., McAleer, P., Grosbras, M., Love, S., Morison, G., & Pollick, F. E. (2013) · i-Perception · doi:10.1068/i0536 · Cited by 56
Self-citation
The neural basis of perceiving person interactions
Susanne Quadflieg, A., Gentile, F., & Rossion, B. (2015) · Cortex · doi:10.1016/j.cortex.2014.12.020 · Cited by 56
“Hearing faces and seeing voices”: Amodal coding of person identity in the human brain
Hasan, B. A. S., Valdés-Sosa, M. J., Groß, J., & Belin, P. (2016) · Scientific Reports · doi:10.1038/srep37494 · Cited by 55
Social Cognition in a Research Domain Criteria Perspective: A Bridge Between Schizophrenia and Autism Spectra Disorders
Barlati, S., Minelli, A., Ceraso, A., Nibbio, G., Silva, R. C., Deste, G., Turrina, C., & Vita, A. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00806 · Cited by 54
Distinct Regions of Right Temporal Cortex Are Associated with Biological and Human–Agent Motion: Functional Magnetic Resonance Imaging and Neuropsychological Evidence
Han, Z., Bi, Y., Chen, J., Chen, Q., Yong He, A., & Caramazza, A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5868-12.2013 · Cited by 52
Computation-Based Feature Representation of Body Expressions in the Human Brain
Solanas, M. P., Vaessen, M. J., & de Gelder, B. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa196 · Cited by 52
Integrating faces and bodies: Psychological and neural perspectives on whole person perception
Hu, Y., Baragchizadeh, A., & O’Toole, A. J. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.02.021 · Cited by 55
Moving Toward versus Away from Another: How Body Motion Direction Changes the Representation of Bodies and Actions in the Visual Cortex
Bellot, E., Abassi, E., & Papeo, L. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa382 · Cited by 48
The organization of the posterior parietal cortex devoted to upper limb actions: An fMRI study
Ferri, S., Rizzolatti, G., & Orban, G. A. (2015) · Human Brain Mapping · doi:10.1002/hbm.22882 · Cited by 51
Network Interactions Explain Sensitivity to Dynamic Faces in the Superior Temporal Sulcus
Nicholas Furl, A., Henson, R. N., Friston, K. J., & Calder, A. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu083 · Cited by 50
Ventral aspect of the visual form pathway is not critical for the perception of biological motion
Gilaie‐Dotan, S., Saygın, A. P., Lorenzi, L. J., Rees, G. E., & Behrmann, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414974112 · Cited by 49
Differences in fMRI intersubject correlation while viewing unedited and edited videos of dance performance
Herbeć, A., Kauppi, J., Jola, C., Tohka, J., & Pollick, F. E. (2015) · Cortex · doi:10.1016/j.cortex.2015.06.026 · Cited by 53
Biological motion processing in schizophrenia – Systematic review and meta-analysis
Okruszek, Ł., & Pilecka, I. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.03.013 · Cited by 49
Modulation of Brain Activity during Action Observation: Influence of Perspective, Transitivity and Meaningfulness
Hétu, S., Mercier, C., Eugène, F., Michon, P., & Jackson, P. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024728 · Cited by 49
Constructing Visual Perception of Body Movement with the Motor Cortex
Orgs, G., Dovern, A., Hagura, N., Haggard, P., Fink, G. R., & Weiss, P. H. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv262 · Cited by 48
Real-Time Avatar-Based Feedback to Enhance the Symmetry of Spatiotemporal Parameters After Stroke: Instantaneous Effects of Different Avatar Views
Liu, L. Y., Sangani, S. G., Patterson, K. K., Fung, J., & Lamontagne, A. (2020) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2020.2979830 · Cited by 45
Motor Imagery Decoding Enhancement Based on Hybrid EEG-fNIRS Signals
Xu, T., Zhou, Z., Yang, Y., Li, Y., Li, J., Bezerianos, A., & Wang, H. (2023) · IEEE Access · doi:10.1109/access.2023.3289709 · Cited by 45
Large-scale temporo–parieto–frontal networks for motor and cognitive motor functions in the primate brain
Borra, E., & Luppino, G. (2018) · Cortex · doi:10.1016/j.cortex.2018.09.024 · Cited by 49
Developmental trajectory of interpersonal motor alignment: Positive social effects and link to social cognition
Rauchbauer, B., & Grosbras, M. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.07.032 · Cited by 47
Self-citation
Dance and emotion in posterior parietal cortex: A low-frequency rTMS study
Grosbras, M., Tan, H., & Pollick, F. E. (2012) · Brain stimulation · doi:10.1016/j.brs.2012.03.013 · Cited by 44
Self-citation
Mirroring the Social Aspects of Speech and Actions: The Role of the Insula
Cesare, G. D., Marchi, M., Errante, A., Fasano, F., & Rizzolatti, G. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx051 · Cited by 43
More Than the Face: Representations of Bodies in the Inferior Temporal Cortex
Vogels, R. (2022) · Annual Review of Vision Science · doi:10.1146/annurev-vision-100720-113429 · Cited by 43
Stereoscopic depth increases intersubject correlations of brain networks
Gaebler, M., Bießmann, F., Lamke, J.-P., Müller, K., Walter, H., & Hetzer, S. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.008 · Cited by 42
Concepts in the Brain: The View From Cross-linguistic Diversity
Kemmerer, D. (2019) · doi:10.1093/oso/9780190682620.001.0001 · Cited by 42
Virtual lesion of right posterior superior temporal sulcus modulates conscious visual perception of fearful expressions in faces and bodies
Candidi, M., Stienen, B. M. C., Aglioti, S. M., & de Gelder, B. (2015) · Cortex · doi:10.1016/j.cortex.2015.01.012 · Cited by 39
The theory-of-mind network in support of action verb comprehension: Evidence from an fMRI study
Lin, N., Bi, Y., Zhao, Y., Luo, C., & Li, X. (2014) · Brain and Language · doi:10.1016/j.bandl.2014.11.004 · Cited by 41
Holding Biological Motion in Working Memory: An fMRI Study
Lu, X., Huang, J., Yi, Y., Shen, M., Weng, X., & Gao, Z. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00251 · Cited by 39
A shared neural code for the physics of actions and object events
Akbıyık, S., Caramazza, A., & Wurm, M. F. (2023) · Nature Communications · doi:10.1038/s41467-023-39062-8 · Cited by 47
Arousal Decrease inSleeping Beauty: Audiences' Neurophysiological Correlates to Watching a Narrative Dance Performance of two-and-a-half hours
Jola, C., Pollick, F. E., & Grosbras, M. (2011) · Dance Research · doi:10.3366/drs.2011.0025 · Cited by 39
Self-citation
The Semantics of Syntax: The Grounding of Transitive and Intransitive Constructions
van Dam, W. O., & Desai, R. H. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00926 · Cited by 42
A human homologue of monkey F5c
Ferri, S., Peeters, R. R., Nelissen, K., Vanduffel, W., Rizzolatti, G., & Orban, G. A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.033 · Cited by 39
Emotion modulation of the body-selective areas in the developing brain
Ross, P. D., de Gelder, B., Crabbe, F., & Grosbras, M. (2019) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.100660 · Cited by 36
Self-citation
Body-selective areas in the visual cortex are less active in children than in adults
Ross, P. D., de Gelder, B., Crabbe, F., & Grosbras, M. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00941 · Cited by 35
Self-citation
Frontocingular Dysfunction in Bulimia Nervosa when Confronted with Disease‐specific Stimuli
Joos, A. A. B., Saum, B., Zeeck, A., Perlov, E., Glauche, V., Hartmann, A., Freyer, T., Sandholz, A., Unterbrink, T., van Elst, L. T., et al. (2011) · European Eating Disorders Review · doi:10.1002/erv.1150 · Cited by 35
Effects of Emotional Contexts on Cerebello-Thalamo-Cortical Activity during Action Observation
Mazzola, V., Vuilleumier, P., Latorre, V., Petito, A., Gallese, V., Popolizio, T., Arciero, G., & Bondolfi, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075912 · Cited by 34
The cross-domain functional organization of posterior lateral temporal cortex: insights from ALE meta-analyses of 7 cognitive domains spanning 12,000 participants
Hodgson, V. J., Ralph, M. A. L., & Jackson, R. L. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac394 · Cited by 32
Insula Connections With the Parieto-Frontal Circuit for Generating Arm Actions in Humans and Macaque Monkeys
Cesare, G. D., Pinardi, C., Carapelli, C., Caruana, F., Marchi, M., Gerbella, M., & Rizzolatti, G. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy095 · Cited by 34
Violence as a source of pleasure or displeasure is associated with specific functional connectivity with the nucleus accumbens
Porges, E. C., & Decety, J. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00447 · Cited by 34
Increasing the Efficacy of Emotional Appeal Ads on Online Video-Watching Platforms: The Effects of Goals and Emotional Approach Tendency on Ad-Skipping Behavior
Jeon, Y. A., Ryoo, Y., & Yoon, H. J. (2022) · Journal of Advertising · doi:10.1080/00913367.2022.2073299 · Cited by 33
Removing Hand Form Information Specifically Impairs Emotion Recognition for Fearful and Angry Body Stimuli
Ross, P. D., & Flack, T. R. (2019) · Perception · doi:10.1177/0301006619893229 · Cited by 33
Dysconnectivity of the inferior frontal gyrus: Implications for an impaired self-other distinction in patients with schizophrenia
Backasch, B., Sommer, J. B., Klöhn-Saghatolislam, F., Müller, M. J., Kircher, T. T. J., & Leube, D. (2014) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2014.05.007 · Cited by 33
Social cerebellum in goal-directed navigation
Li, M., Ma, Q., Baetens, K., Pu, M., Deroost, N., Baeken, C., Heleven, E., & Overwalle, F. V. (2021) · Social Neuroscience · doi:10.1080/17470919.2021.1970017 · Cited by 36

Authors: Grosbras, M., Beaton, S., & Eickhoff, S. B.
Affiliations: University of Glasgow (GB)
Forschungszentrum Jülich (DE)
ORCID: Grosbras, Marie‐Hélène
Eickhoff, Simon B.
Venue: Human Brain Mapping
Publisher: Wiley
Published: 2011-03-09
Volume: 33
Issue: 2
Pages: 431-454
ISSN: 1065-9471 (ISSN-L)
1097-0193
DOI: 10.1002/hbm.21222
PMC: PMC6869986
OpenAlex: W1995284850
Cited by: 284
References: 155
Citations by year: 2026: 6 · 2025: 16 · 2024: 15 · 2023: 21 · 2022: 23 · 2021: 8 · 2020: 23 · 2019: 27 · 2018: 23 · 2017: 22 · 2016: 17 · 2015: 22 · 2014: 20 · 2013: 18 · 2012: 16
FWCI: 2.46
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Human Brain Mapping (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
JuSER (Forschungszentrum Jülich) (submittedVersion)
RWTH Publications (RWTH Aachen) (submittedVersion)
Funders: Deutsche Forschungsgemeinschaft (IRTG1328)
National Institutes of Health (R01-MH074457-01A1, MH074457)
Medical Research Council
Economic and Social Research Council (ES/E020933/1, RES-060-25-0010)
National Institute of Mental Health (R01MH074457)
Topics: Social Sciences › Psychology › Social Psychology › Action Observation and Synchronization
Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Keywords: human motion perception, biological motion, posterior superior temporal sulcus, middle temporal gyrus, fusiform gyrus, occipitotemporal cortex, frontoparietal cortex, representation of the body, social cognition, activation likelihood estimation
MeSH terms: Brain, Brain Mapping, Face, Hand, Humans, Motion Perception, Task Performance and Analysis

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

Brain regions involved in human movement perception: A quantitative voxel‐based meta‐analysis

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks