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Mapping multisensory parietal face and body areas in humans
Open accessAbstract
Detection and avoidance of impending obstacles is crucial to preventing head and body injuries in daily life. To safely avoid obstacles, locations of objects approaching the body surface are usually detected via the visual system and then used by the motor system to guide defensive movements. Mediating between visual input and motor output, the posterior parietal cortex plays an important role in integrating multisensory information in peripersonal space. We used functional MRI to map parietal areas that see and feel multisensory stimuli near or on the face and body. Tactile experiments using full-body air-puff stimulation suits revealed somatotopic areas of the face and multiple body parts forming a higher-level homunculus in the superior posterior parietal cortex. Visual experiments using wide-field looming stimuli revealed retinotopic maps that overlap with the parietal face and body areas in the postcentral sulcus at the most anterior border of the dorsal visual pathway. Starting at the parietal face area and moving medially and posteriorly into the lower-body areas, the median of visual polar-angle representations in these somatotopic areas gradually shifts from near the horizontal meridian into the lower visual field. These results suggest the parietal face and body areas fuse multisensory information in peripersonal space to guard an individual from head to toe.
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“Using surface-based fMRI, researchers have described a detailed map of the human face that integrates visual and tactile inputs (Sereno and Huang 2006; Huang et al. 2012).”
From Neuroanatomical correlates of peripersonal space: bridging the gap between perception, action, emotion and social cognition (2024) · cites this paper as Huang et al. 2012
Citations
Cites
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
Hall, E. T. (1973) · Leonardo · doi:10.2307/1572461 · Cited by 4,883
Borders of Multiple Visual Areas in Humans Revealed by Functional Magnetic Resonance Imaging
Sereno, M. I., Dale, A. M., Reppas, J. B., Kwong, K. K., Belliveau, J. W., Brady, T. J., Rosen, B. R., & Tootell, R. B. H. (1995) · Science · doi:10.1126/science.7754376 · Cited by 2,663
Self-citationPenfield, W. G. (1950) · Digital Commons - RU (Rockefeller University) · Cited by 1,387
That's my hand! Activity in premotor cortex reflects feeling of ownership of a limb
Ehrsson, H. H., Spence, C., & Passingham, R. E. (2004) · Science · doi:10.1126/science.1097011 · Cited by 1,348
Complex Movements Evoked by Microstimulation of Precentral Cortex
Graziano, M. S. A., Taylor, C. S. R., & Moore, T. (2002) · Neuron · doi:10.1016/s0896-6273(02)00698-0 · Cited by 921
Coding of visual space by premotor neurons.
Graziano, M. S. A., Yap, G. S., & Gross, C. G. (1994) · Science · doi:10.1126/science.7973661 · Cited by 841
Mishkin, M., & Ungerleider, L. G. (1982) · Behavioural Brain Research · doi:10.1016/0166-4328(82)90081-x · Cited by 810
Polymodal Motion Processing in Posterior Parietal and Premotor Cortex
Bremmer, F., Schlack, A., Shah, N. J., Zafiris, O., Kubischik, M., Hoffmann, K.-P., Zilles, K., & Fink, G. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00198-2 · Cited by 803
Ventral intraparietal area of the macaque: congruent visual and somatic response properties
Duhamel, J.-R., Colby, C. L., & Goldberg, M. E. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.126 · Cited by 789
Research works printed but not linked: 1
- T Heed, B Röder in The Neural Bases of Multisensory Processes, eds MM Murray, MT Wallace (CRC Press, Boca Raton, FL), pp. 557–580 (2011). · DOI
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Sorted by citations
Behavioral, Neural, and Computational Principles of Bodily Self-Consciousness
Blanke, O., Slater, M., & Serino, A. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.029 · Cited by 698
Serino, A. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.01.016 · Cited by 304
Holmes, N., Leggett, J., Boto, E., Roberts, G., Hill, R. M., Tierney, T. M., Shah, V., Barnes, G. R., Brookes, M. J., & Bowtell, R. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.07.028 · Cited by 250
Grivaz, P., Blanke, O., & Serino, A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.052 · Cited by 203
Multisensory maps in parietal cortex
Sereno, M. I., & Huang, R. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.08.014 · Cited by 204
Self-citationBrain (re)organisation following amputation: Implications for phantom limb pain
Makin, T. R., & Flor, H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116943 · Cited by 230
The vestibular system: a spatial reference for bodily self-consciousness.
Pfeiffer, C., Serino, A., & Blanke, O. (2014) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2014.00031 · Cited by 165
Salomon, R., Noel, J.-P., Łukowska, M., Faivre, N., Metzinger, T., Serino, A., & Blanke, O. (2017) · Cognition · doi:10.1016/j.cognition.2017.05.028 · Cited by 142
Maselli, A., & Slater, M. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00693 · Cited by 141
Full body action remapping of peripersonal space: The case of walking
Noel, J.-P., Grivaz, P., Marmaroli, P., Lissek, H., Blanke, O., & Serino, A. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.08.030 · Cited by 130
Development differentially sculpts receptive fields across early and high-level human visual cortex
Gomez, J., Natu, V. S., Jeska, B., Barnett, M., & Kalanit Grill-spector, A. (2018) · Nature Communications · doi:10.1038/s41467-018-03166-3 · Cited by 130
Brozzoli, C., Ehrsson, H. H., & Farnè, A. (2014) · The Neuroscientist · doi:10.1177/1073858413511153 · Cited by 125
Sheth, B. R., & Young, R. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00037 · Cited by 136
The human cortical areas V6 and V6A
Pitzalis, S., Fattori, P., & Galletti, C. (2015) · Visual Neuroscience · doi:10.1017/s0952523815000048 · Cited by 117
Kaas, J. H., & Stepniewska, I. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23838 · Cited by 110
Fujimoto, K., Polimeni, J. R., van der Kouwe, A. J. W., Reuter, M., Kober, T., Benner, T., Fischl, B. R., & Wald, L. L. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.12.012 · Cited by 108
Approaching threat modulates visuotactile interactions in peripersonal space
de Haan, A. M., Smit, M., der Stigchel, S. V., & Dijkerman, H. C. (2016) · Experimental Brain Research · doi:10.1007/s00221-016-4571-2 · Cited by 114
State estimation in posterior parietal cortex: Distinct poles of environmental and bodily states
Medendorp, W. P., & Heed, T. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.101691 · Cited by 89
Carey, D., Caprini, F., Allen, M., Lutti, A., Weiskopf, N., Rees, G. E., Callaghan, M. F., & Dick, F. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.066 · Cited by 85
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Passarelli, L., Gamberini, M., & Fattori, P. (2021) · Journal of Integrative Neuroscience · doi:10.31083/j.jin.2021.01.334 · Cited by 91
Kästner, S., Chen, Q., Jeong, S. K., & Mruczek, R. E. B. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.01.034 · Cited by 88
Akselrod, M., Martuzzi, R., Serino, A., van der Zwaag, W., Gassert, R., & Blanke, O. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.06.021 · Cited by 78
Bernasconi, F., Noel, J.-P., Park, H. D., Faivre, N., Seeck, M., Spinelli, L., Schaller, K., Blanke, O., & Serino, A. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy156 · Cited by 77
Structural connectivity and functional properties of the macaque superior parietal lobule
Gamberini, M., Passarelli, L., Fattori, P., & Galletti, C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01976-9 · Cited by 81
Apps, M. A. J., Tajadura‐Jiménez, A., Sereno, M. I., Blanke, O., & Manos Tsakiris, A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht199 · Cited by 79
Self-citationCoello, Y., & Cartaud, A. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.636124 · Cited by 78
Gentile, G., Björnsdotter, M., Petkova, V. I., Abdulkarim, Z., & Ehrsson, H. H. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.008 · Cited by 73
The sense of body ownership relaxes temporal constraints for multisensory integration
Maselli, A., Kilteni, K., López‐Moliner, J., & Slater, M. (2016) · Scientific Reports · doi:10.1038/srep30628 · Cited by 70
Aura and Head pain: relationship and gaps in the translational models
Bolay, H., Vurallı, D., & Goadsby, P. J. (2019) · The Journal of Headache and Pain · doi:10.1186/s10194-019-1042-8 · Cited by 64
Carey, D., Krishnan, S., Callaghan, M. F., Sereno, M. I., & Dick, F. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhw393 · Cited by 63
Self-citationDistortion of mental body representations
Longo, M. R. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.11.005 · Cited by 72
A common neural substrate for processing scenes and egomotion-compatible visual motion
Sulpizio, V., Galati, G., Fattori, P., Galletti, C., & Pitzalis, S. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02112-8 · Cited by 59
Neural bases of self‐ and object‐motion in a naturalistic vision
Pitzalis, S., Serra, C., Sulpizio, V., Committeri, G., de Pasquale, F., Fattori, P., Galletti, C., Sepe, R., & Galati, G. (2019) · Human Brain Mapping · doi:10.1002/hbm.24862 · Cited by 54
Causal Inference of Body Ownership in the Posterior Parietal Cortex
Chancel, M., Iriye, H., & Ehrsson, H. H. (2022) · The Journal of Neuroscience · doi:10.1523/jneurosci.0656-22.2022 · Cited by 55
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Huang, R., & Sereno, M. I. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00007-3 · Cited by 59
Self-citationThe organization of the posterior parietal cortex devoted to upper limb actions: An fMRI study
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Ross, P. D., & Atkinson, A. P. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.00309 · Cited by 51
Chan, A. W.-Y., & Baker, C. I. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3621-14.2015 · Cited by 49
Sensory properties of the caudal aspect of the macaque’s superior parietal lobule
Gamberini, M., Bò, G. D., Breveglieri, R., Briganti, S., Passarelli, L., Fattori, P., & Galletti, C. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1593-x · Cited by 48
Zlatkina, V., Amiez, C., & Petrides, M. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13049 · Cited by 45
Tal, Z., Geva, R., & Amedi, A. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx024 · Cited by 44
Functional organization of the caudal part of the human superior parietal lobule
Sulpizio, V., Fattori, P., Pitzalis, S., & Galletti, C. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105357 · Cited by 43
Whole brain mapping of visual and tactile convergence in the macaque monkey
Guipponi, O., Cléry, J., Odouard, S., Wardak, C., & Ben Hamed, S. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.05.022 · Cited by 40
de Borst, A. W., Sanchez-Vives, M. V., Slater, M., & de Gelder, B. (2020) · eNeuro · doi:10.1523/eneuro.0263-19.2019 · Cited by 46
Iachini, T., Ruggiero, G., Ruotolo, F., & Vinciguerra, M. (2014) · Acta Psychologica · doi:10.1016/j.actpsy.2014.09.001 · Cited by 40
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Pitzalis, S., Serra, C., Sulpizio, V., Marco, S. D., Fattori, P., Galati, G., & Galletti, C. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116092 · Cited by 39
Depth: the Forgotten Dimension in Multisensory Research
der Stoep, N. V., Serino, A., Farnè, A., Luca, M. D., & Spence, C. J. (2016) · Multisensory Research · doi:10.1163/22134808-00002525 · Cited by 41
Topological Maps and Brain Computations From Low to High
Sereno, M. I., Sood, M. R., & Huang, R. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.787737 · Cited by 32
Self-citationEgomotion‐related visual areas respond to active leg movements
Serra, C., Galletti, C., Marco, S. D., Fattori, P., Galati, G., Sulpizio, V., & Pitzalis, S. (2019) · Human Brain Mapping · doi:10.1002/hbm.24589 · Cited by 33
Reconstructing neural representations of tactile space
Tamè, L., Tucciarelli, R., Sadibolova, R., Sereno, M. I., & Longo, M. R. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117730 · Cited by 39
Self-citationSood, M. R., & Sereno, M. I. (2016) · Human Brain Mapping · doi:10.1002/hbm.23208 · Cited by 34
Self-citationThe ‘creatures’ of the human cortical somatosensory system
Saadon‐Grosman, N., Loewenstein, Y., & Arzy, S. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa003 · Cited by 38
A conceptual framework on body representations and their relevance for mental disorders
Möllmann, A., Heinrichs, N., & Herwig, A. (2024) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1231640 · Cited by 37
Neural encoding of actual and imagined touch within human posterior parietal cortex
Chivukula, S., Zhang, C. Y., Aflalo, T., Jafari, M., Pejsa, K., Pouratian, N., & Andersen, R. A. (2021) · eLife · doi:10.7554/elife.61646 · Cited by 31
Somatotopic finger mapping using MEG: Toward an optimal stimulation paradigm
Jamali, S., & Roß, B. (2013) · Clinical Neurophysiology · doi:10.1016/j.clinph.2013.01.027 · Cited by 33
Spitoni, G. F., Giorgio, P., Cimmino, R. L., Galati, G., Priori, A., Michal Lavidor, B., Jacobson, L., & Pizzamiglio, L. (2013) · Experimental Brain Research · doi:10.1007/s00221-013-3538-9 · Cited by 33
Personal space increases during the COVID-19 pandemic in response to real and virtual humans
Holt, D. J., Zapetis, S. L., Babadi, B., Zimmerman, J., & Tootell, R. B. H. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.952998 · Cited by 29
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Self-citationBoth developmental and adult vision shape body representations
Nava, E., Steiger, T. K., & Röder, B. (2014) · Scientific Reports · doi:10.1038/srep06622 · Cited by 29
Ngo, G. N., Haak, K. V., Beckmann, C. F., & Menon, R. S. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118031 · Cited by 28
Where and how our brain represents the temporal structure of observed action
Thomas, R. M., Sanctis, T. D., Gazzola, V., & Keysers, C. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.08.056 · Cited by 27
Dynamic spatial coding in parietal cortex mediates tactile-motor transformation
Klautke, J., Foster, C., Medendorp, W. P., & Heed, T. (2023) · Nature Communications · doi:10.1038/s41467-023-39959-4 · Cited by 27
Discontinuity of cortical gradients reflects sensory impairment
Saadon‐Grosman, N., Tal, Z., Itshayek, E., Amedi, A., & Arzy, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506214112 · Cited by 27
Krishnan, S., Leech, R., Mercure, E., Lloyd‐Fox, S., & Dick, F. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu120 · Cited by 28
A Whole-Body Sensory-Motor Gradient is Revealed in the Medial Wall of the Parietal Lobe
Zeharia, N., Hofstetter, S., Flash, T., & Amedi, A. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0727-18.2019 · Cited by 25
Marco, S. D., Fattori, P., Galati, G., Galletti, C., Lappe, M., Maltempo, T., Serra, C., Sulpizio, V., & Pitzalis, S. (2021) · Cortex · doi:10.1016/j.cortex.2020.12.021 · Cited by 25
Tal, Z., Geva, R., & Amedi, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.058 · Cited by 25
Basile, G. A., Tatti, E., Bertino, S., Milardi, D., Genovese, G., Bruno, A., Muscatello, M. R. A., Ciurleo, R., Cerasa, A., Quartarone, A., et al. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02781-9 · Cited by 24
“Using surface-based fMRI, researchers have described a detailed map of the human face that integrates visual and tactile inputs (Sereno and Huang 2006; Huang et al. 2012).”
BackgroundMapping the complex topological organization of the human parietal face area
Huang, R.-S., Chen, C.-F., & Sereno, M. I. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.09.004 · Cited by 23
Self-citationde Borst, A. W., & de Gelder, B. (2022) · Brain Sciences · doi:10.3390/brainsci12030391 · Cited by 21
Validation of periodic fMRI signals in response to wearable tactile stimulation
Chen, C., Kreutz-Delgado, K., Sereno, M. I., & Huang, R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.024 · Cited by 21
Self-citationThe macaque ventral intraparietal area has expanded into three homologue human parietal areas
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Drudik, K., Zlatkina, V., & Petrides, M. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac132 · Cited by 19
Somers, D. C., Michalka, S., Tobyne, S. M., & Noyce, A. L. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2021.05.002 · Cited by 20
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Tamè, L., & Longo, M. R. (2023) · Nature Reviews Psychology · doi:10.1038/s44159-023-00197-6 · Cited by 21
Encoding schemes in somatosensation: From micro- to meta-topography
Kuehn, E., & Pleger, B. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117255 · Cited by 17
Marco, S. D., Sulpizio, V., Bellagamba, M., Fattori, P., Galati, G., Galletti, C., Lappe, M., Maltempo, T., & Pitzalis, S. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118581 · Cited by 17
Spatiotemporal integration of looming visual and tactile stimuli near the face
Huang, R., Chen, C., & Sereno, M. I. (2018) · Human Brain Mapping · doi:10.1002/hbm.23995 · Cited by 17
Self-citationMaltempo, T., Pitzalis, S., Bellagamba, M., Marco, S. D., Fattori, P., Galati, G., Galletti, C., & Sulpizio, V. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02254-3 · Cited by 19
Tactile representation of the head and shoulders assessed by fMRI in the nonhuman primate
Wardak, C., Guipponi, O., Pinède, S., & Hamed, S. B. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00633.2015 · Cited by 14
Jia, S., Wang, L., Wang, H., Lv, X., Wu, J., Yan, T., Li, C., & Hu, B. (2020) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.27144 · Cited by 13
Sulpizio, V., Strappini, F., Fattori, P., Galati, G., Galletti, C., Pecchinenda, A., & Pitzalis, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02549-z · Cited by 12
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Lei, V. L. C., Leong, T. I., Leong, C. T., Liu, L., Choi, C. U., Sereno, M. I., Li, D., & Huang, R. (2024) · Human Brain Mapping · doi:10.1002/hbm.26617 · Cited by 11
Self-citationUnraveling the spatiotemporal brain dynamics during a simulated reach-to-eat task
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Gopinath, K., Krishnamurthy, V., Lacey, S., & Sathian, K. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0522 · Cited by 10
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Senna, I., Cardinali, L., Farnè, A., & Brozzoli, C. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.01681 · Cited by 11
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Kuroda, N., & Teramoto, W. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06269-4 · Cited by 9
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Coello, Y., & Iachini, T. (2021) · Oxford University Press eBooks · doi:10.1093/oso/9780198851738.003.0015 · Cited by 7
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Froesel, M., Hamed, S. B., & Cléry, J. C. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99193-3.00009-x · Cited by 6
Huang, C., Lin, C., Lin, Y., Tsai, H.-Y., & Tseng, M. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab301 · Cited by 6
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Drewing, K. (2016) · Springer eBooks · doi:10.1007/978-3-642-53898-8_4 · Cited by 6
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Self-citationEgomotion-related visual areas respond to goal-directed movements
Bellagamba, M., Sulpizio, V., Fattori, P., Galati, G., Galletti, C., Maltempo, T., & Pitzalis, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02523-9 · Cited by 5
Metadata
- Authors
- Huang, R.-S., Chen, C.-F., Tran, A. T., Holstein, K. L., & Sereno, M. I.
- Affiliations
- Institute for Neural Computation,
- Department of Electrical and Computer Engineering, and
- University of California San Diego (US)
- University of London (GB)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-10-15
- Volume
- 109
- Issue
- 44
- Pages
- 18114-18119
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3497759
- OpenAlex
- W2062140410
- Cited by
- 131
- References
- 57
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 8 · 2023: 7 · 2022: 7 · 2021: 19 · 2020: 11 · 2019: 10 · 2018: 8 · 2017: 12 · 2016: 10 · 2015: 13 · 2014: 6 · 2013: 6
- FWCI
- 10.71
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- BIROn (Birkbeck, University of London) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- National Institute of Mental Health (R01MH081990)
- Topics
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- posterior parietal cortex, peripersonal space, multisensory integration, somatotopic mapping, retinotopic mapping, looming stimuli, air-puff stimulation, postcentral sulcus, defensive movements, obstacle avoidance, homunculus
- MeSH terms
- Brain, Face, Humans, Magnetic Resonance Imaging, Touch, Vision, Ocular
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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