Cited by 1,318Spatial Neglect and Hemispheric DysfunctionVisual Attention and Saliency DetectionNeural and Behavioral Psychology Studies

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Spatial Neglect and Attention Networks

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Corbetta, Maurizio, Shulman, Gordon L.·2011·Annual Review of Neuroscience

DOI 10.1146/annurev-neuro-061010-113731PMC PMC3790661

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Abstract

Unilateral spatial neglect is a common neurological syndrome following predominantly right hemisphere injuries and is characterized by both spatial and non-spatial deficits. Core spatial deficits involve mechanisms for saliency coding, spatial attention, and short-term memory and occur in conjunction with nonspatial deficits that involve reorienting, target detection, and arousal/vigilance. We argue that neglect is better explained by the dysfunction of distributed cortical networks for the control of attention than by structural damage of specific brain regions. Ventral lesions in right parietal, temporal, and frontal cortex that cause neglect directly impair nonspatial functions partly mediated by a ventral frontoparietal attention network. Structural damage in ventral cortex also induces physiological abnormalities of task-evoked activity and functional connectivity in a dorsal frontoparietal network that controls spatial attention. The anatomy and right hemisphere dominance of neglect follow from the anatomy and laterality of the ventral regions that interact with the dorsal attention network.

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Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881
Self-citation
The attention system of the human brain
Posner, M. I., & Petersen, S. E. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.000325 · Cited by 8,070
An integrative theory of locus coeruleus-norepinephrine function: adaptive gain and optimal performance
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472
The reorienting system of the human brain: from environment to theory of mind
Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889
Self-citation
Shifts in Selective Visual Attention: Towards the Underlying Neural Circuitry
Koch, C., & Ullman, S. (1987) · Springer eBooks · doi:10.1007/978-94-009-3833-5_5 · Cited by 3,762
Inhibition and the right inferior frontal cortex
Aron, A. R., Robbins, T. W., & Poldrack, R. A. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.02.010 · Cited by 3,197
New cognitive neurosciences
Gazzaniga, M. S., & Bizzi, E. (2000) · Cited by 2,547
A cortical network for directed attention and unilateral neglect
Mesulam, M. ‐. (1981) · Annals of Neurology · doi:10.1002/ana.410100402 · Cited by 2,498 · cited 2×
“Perhaps the most widely accepted, standard theory of neglect postulates that the right hemisphere controls shifts of attention to both sides of space. while the left hemisphere only controls attention to the right side (Mesulam 1981).”
Effects of parietal injury on covert orienting of attention
Posner, M., Walker, J., Friedrich, F., & Rafal, R. (1984) · The Journal of Neuroscience · doi:10.1523/jneurosci.04-07-01863.1984 · Cited by 2,191
Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems
Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604187103 · Cited by 2,101
Self-citation

Show all 161 references

Research works printed but not linked: 5

10.1037//0096-3445.128.4.450 · DOI
Heilman KM, 1987, The Handbook of Physiology. Section 1: The Nervous System. Volume V. Higher Functions of the Brain Part 2, 461
Koch C, 1985, Hum. Neurobiol., 4, 219
O'Keefe J., 2006, The Hippocampus Book, 475
Thimm M, 2008, Restor. Neurol. Neurosci., 26, 481

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Authors: Corbetta, M., & Shulman, G. L.
Affiliations: Washington University in St. Louis (US)
ORCID: Corbetta, Maurizio
Shulman, Gordon L.
Venue: Annual Review of Neuroscience
Publisher: Annual Reviews
Published: 2011-07-21
Volume: 34
Issue: 1
Pages: 569-599
ISSN: 0147-006X (ISSN-L)
1545-4126
DOI: 10.1146/annurev-neuro-061010-113731
PMC: PMC3790661
OpenAlex: W2141447814
Cited by: 1,318
References: 161
Citations by year: 2026: 74 · 2025: 88 · 2024: 95 · 2023: 75 · 2022: 99 · 2021: 101 · 2020: 83 · 2019: 117 · 2018: 83 · 2017: 88 · 2016: 95 · 2015: 93 · 2014: 75 · 2013: 86 · 2012: 52
FWCI: 6.00
Type: journal article
Language: en
Open access: green
europepmc.org
Locations: Annual Review of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Padua Research Archive (University of Padova) (submittedVersion, other-oa)
Funders: University of Pennsylvania
Johns Hopkins University
University of Oregon
University College London
Université de Genève
Medical Research Council
National Institute of Mental Health (R01 MH 71920-06, R01MH071920)
National Institute of Child Health and Human Development
Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD061117)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Spatial Neglect and Hemispheric Dysfunction
Physical Sciences › Computer Science › Computer Vision and Pattern Recognition › Visual Attention and Saliency Detection
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords: hemispatial neglect, right hemisphere dominance, attentional networks, dorsal attention network, spatial attention, short-term memory, sustained attention, functional connectivity, right parietal cortex, right temporal cortex, right frontal cortex
MeSH terms: Animals, Attention, Humans, Functional Laterality, Neural Pathways, Perceptual Disorders

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