The DOI matches its Crossref record; 101 of the 103 references it cites were found in a registry or an index.
SPACE AND ATTENTION IN PARIETAL CORTEX
Abstract
▪ Abstract The space around us is represented not once but many times in parietal cortex. These multiple representations encode locations and objects of interest in several egocentric reference frames. Stimulus representations are transformed from the coordinates of receptor surfaces, such as the retina or the cochlea, into the coordinates of effectors, such as the eye, head, or hand. The transformation is accomplished by dynamic updating of spatial representations in conjunction with voluntary movements. This direct sensory-to-motor coordinate transformation obviates the need for a single representation of space in environmental coordinates. In addition to representing object locations in motoric coordinates, parietal neurons exhibit strong modulation by attention. Both top-down and bottom-up mechanisms of attention contribute to the enhancement of visual responses. The saliance of a stimulus is the primary factor in determining the neural response to it. Although parietal neurons represent objects in motor coordinates, visual responses are independent of the intention to perform specific motor acts.
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“These neurons exhibited spatially selective persistent activity that predicted whether an eye movement was planned into the response field (RF) of the neuron on a memory guided saccade task(29–31).”
From Representation of Confidence Associated with a Decision by Neurons in the Parietal Cortex (2009) · cites this paper as [29]
In the citing paper
“LIP plays a multitude of cognitive and sensory-motor roles that could, in principle, change during training and account for the changes in LIP responses during motion viewing 20–22.”
From Neural correlates of perceptual learning in a sensory-motor, but not a sensory, cortical area (2008) · cites this paper as [20]
In the citing paper
“In addition, previous studies have shown that LIP responses are modulated by many factors, such as attention, expectation, time, motor intention, experienced value, reward, and the prior probability of making an eye movement12,13,39–42.”
From Microstimulation of macaque area LIP affects decision-making in a motion discrimination task (2006) · cites this paper as [12]
In the citing paper
“Although we refer to the core regions of these systems as if they were homogeneous elements (e.g., IPS or FEF), each contains multiple functional subcomponents (5-7, 18, 19).”
From Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems (2006) · cites this paper as [19]
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
Selective Attention Gates Visual Processing in the Extrastriate Cortex
Moran, J., & Desimone, R. (1985) · Science · doi:10.1126/science.4023713 · Cited by 2,433
Selective Attention Gates Visual Processing in the Extrastriate Cortex
Moran, J., & Desimone, R. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/2834.003.0024 · Cited by 2,164
Saccade target selection and object recognition: evidence for a common attentional mechanism.
Deubel, H., & Schneider, W. (1996) · Vision Research · doi:10.1016/0042-6989(95)00294-4 · Cited by 2,108
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
The updating of the representation of visual space in parietal cortex by intended eye movements
Duhamel, J.-R., Colby, C. L., & Goldberg, M. E. (1992) · Science · doi:10.1126/science.1553535 · Cited by 1,966
Self-citationAbrupt visual onsets and selective attention: evidence from visual search.
Yantis, S., & Jonides, J. (1984) · Journal of Experimental Psychology: Human Perception and Performance · doi:10.1037//0096-1523.10.5.601 · Cited by 1,759
Functional organization of inferior area 6 in the macaque monkey
Rizzolatti, G., Camarda, R., Fogassi, L., Gentilucci, M., Luppino, G., & Matelli, M. (1988) · Experimental Brain Research · doi:10.1007/bf00248742 · Cited by 1,550
Andersen, R. A., Snyder, L. H., Bradley, D. C., & Xing, J. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.303 · Cited by 1,486
Abrupt visual onsets and selective attention: voluntary versus automatic allocation.
Yantis, S., & Jonides, J. (1990) · Journal of Experimental Psychology: Human Perception and Performance · doi:10.1037/0096-1523.16.1.121 · Cited by 1,468
Research works printed but not linked: 5
- Bisiach E, Vallar G. 1988.Hemineglect in humans.InHandbook of Neuropsychology, ed. F Boller, J Grafman, pp. 195–222. Amsterdam: Elsevier
- Eskandar EN, 1997, Soc. Neurosci. Abstr., 23, 16
- Kusunoki M, Colby CL, Duhamel J-R, Goldberg ME. 1997.The role of the lateral intraparietal area in the control of visuospatial attention.InThe Association Cortex—Structure and Function, ed. H Sakata, J Fuster, A Mikami, pp. 191–206. Singapore: Harwood Academic
- Kusunoki M, 1993, Soc. Neurosci. Abstr., 19, 770
- 10.1101/SQB.1996.061.01.006 · DOI
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Parks, N. A., & Corballis, P. M. (2008) · Psychophysiology · doi:10.1111/j.1469-8986.2008.00669.x · Cited by 52
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Adam, J. J., Backes, W. H., Rijcken, J. M., Hofman, P. A. M., Kuipers, H., & Jolles, J. (2003) · Cognitive Brain Research · doi:10.1016/s0926-6410(02)00204-5 · Cited by 49
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Samuels, R. (2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.003.0007 · Cited by 48
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Berti, A., & Rizzolatti, G. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198508335.003.0008 · Cited by 43
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Peters, S., Handy, T. C., Lakhani, B., Boyd, L. A., & Garland, S. J. (2015) · Physical Therapy · doi:10.2522/ptj.20140492 · Cited by 45
Hickok, G. S. (2013) · Language Cognition and Neuroscience · doi:10.1080/01690965.2013.852907 · Cited by 44
Shushruth, S., Mazurek, M. E., & Shadlen, M. N. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0668-18.2018 · Cited by 45
Kaas, J. H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10030-6 · Cited by 48
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(2008) · Psychology Press eBooks · doi:10.4324/9780203809891-13 · Cited by 46
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Mandolesi, L., Addona, F., Foti, F., Menghini, D., Petrosini, L., & Vicari, S. (2009) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2009.01.004 · Cited by 46
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Manuela Piazza, A., Pinel, P., & Dehaene, S. (2006) · Cognitive Neuropsychology · doi:10.1080/02643290600780080 · Cited by 45
Cieslik, E. C., Zilles, K., Grefkes, C., & Eickhoff, S. B. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.089 · Cited by 43
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Morgan, H. M., Muthukumaraswamy, S. D., Hibbs, C. S., Shapiro, K. L., Bracewell, R. M., Singh, K. D., & Linden, D. E. J. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00246.2011 · Cited by 44
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Dravida, S., Noah, J. A., Zhang, X., & Joy Hirsch, C. (2020) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.00201 · Cited by 42
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Anderson, E. J., Husain, M., & Sumner, P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.10.046 · Cited by 49
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Prime, S. L., Vesia, M., & Crawford, J. D. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp148 · Cited by 47
Evaluation of selective attention under similarity transformations
Draper, B. A., & Lionelle, A. (2005) · Computer Vision and Image Understanding · doi:10.1016/j.cviu.2004.08.006 · Cited by 44
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Alexander, A. S., Tung, J. C., Chapman, G. W., Conner, A. M., Shelley, L. E., Hasselmo, M. E., & Nitz, D. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110504 · Cited by 42
Feurra, M., Bianco, G., Polizzotto, N. R., Innocenti, I., Rossi, A., & Rossi, S. (2011) · Frontiers in Neural Circuits · doi:10.3389/fncir.2011.00010 · Cited by 43
Zirnsak, M., Lappe, M., & Hamker, F. H. (2010) · Vision Research · doi:10.1016/j.visres.2010.02.002 · Cited by 44
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The neural circuits for arithmetic principles
Liu, J., Zhang, H., Chen, C., Chen, H., Cui, J., & Zhou, X. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.035 · Cited by 43
Gigliotta, O., Malkinson, T. S., Miglino, O., & Bartolomeo, P. (2017) · eNeuro · doi:10.1523/eneuro.0154-17.2017 · Cited by 43
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Watanabe, J., Sugiura, M., Miura, N., Watanabe, Y., Maeda, Y., Matsue, Y., & Kawashima, R. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.10.024 · Cited by 43
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Vincent, J. L., Kahn, I., Essen, D. C. V., & Buckner, R. L. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00546.2009 · Cited by 44
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Learning-dependent plasticity with and without training in the human brain
Zhang, J., & Kourtzi, Z. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002506107 · Cited by 42
Walter, E., & Dassonville, P. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.06.016 · Cited by 42
Prevosto, V., Graf, W. M., & Ugolini, G. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06885.x · Cited by 42
ALHO, J. S., Sato, M., Sams, M. E., Schwartz, J., Tiitinen, H., & Jääskeläinen, I. P. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.011 · Cited by 47
Hoshi, E. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00158 · Cited by 42
Ferreri, F., Vecchio, F., Guerra, A., Miraglia, F., Ponzo, D., Vollero, L., Iannello, G., Määttä, S., Mervaala, E., Rossini, P. M., et al. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.03.021 · Cited by 42
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Masse, N. Y., Hodnefield, J. M., & Freedman, D. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3903-16.2017 · Cited by 40
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Christopoulos, V. N., Bonaiuto, J. J., Kagan, I., & Andersen, R. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1068-15.2015 · Cited by 41
Dynamic, object-based remapping of visual features in trans-saccadic perception
Melcher, D. (2008) · Journal of Vision · doi:10.1167/8.14.2 · Cited by 41
Spatial relations and spatial locations are dissociated within prefrontal and parietal cortex
Ackerman, C. M., & Courtney, S. M. (2012) · Journal of Neurophysiology · doi:10.1152/jn.01024.2011 · Cited by 43
Intermanual Transfer of Prism Adaptation
Redding, G. M., & Wallace, B. (2008) · Journal of Motor Behavior · doi:10.3200/jmbr.40.3.246-264 · Cited by 41
Representation of numerosity in posterior parietal cortex
Roitman, J. D., Brannon, E. M., & Platt, M. L. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00025 · Cited by 42
Chapter 9 Finding a face in the crowd: parallel and serial neural mechanisms of visual selection
Bichot, N. P., & Desimone, R. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)55009-5 · Cited by 40
Metadata
- Authors
- Colby, C. L., & Goldberg, M. E.
- Affiliations
- University of Pittsburgh (US)
- Georgetown University (US)
- ORCID
- Goldberg, Michael E.
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 1999-03
- Volume
- 22
- Issue
- 1
- Pages
- 319-349
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2144200546
- Cited by
- 1,710
- References
- 103
- Citations by year
- 2026: 16 · 2025: 33 · 2024: 44 · 2023: 40 · 2022: 24 · 2021: 38 · 2020: 42 · 2019: 53 · 2018: 48 · 2017: 40 · 2016: 46 · 2015: 68 · 2014: 65 · 2013: 77 · 2012: 75
- FWCI
- 7.31
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Spatial Neglect and Hemispheric Dysfunction
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Keywords
- parietal cortex, spatial representation, attention, egocentric reference frame, top-down attention, bottom-up attention, salience, visual attention, object location, voluntary movement
- MeSH terms
- Animals, Attention, Brain Mapping, Eye Movements, Mouth, Parietal Lobe, Space Perception, Hand Strength
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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