The pulvinar and visual salience

Orienting of Attention

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Analysis of visual behavior

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Effects of parietal injury on covert orienting of attention

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The primate mediodorsal (MD) nucleus and its projection to the frontal lobe

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The Neurobiology of Saccadic Eye Movements

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The ascending projections of the superior colliculus in the rhesus monkey (Macaca mulatta)

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Ascending pathways from the monkey superior colliculus: An autoradiographic analysis

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Contributions of the pulvinar to visual spatial attention

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Pulvinar nuclei of the behaving rhesus monkey: visual responses and their modulation

Petersen, S. E., Robinson, D. L., & Keys, W. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.54.4.867 · Cited by 378 · see citing works

The neural basis of visual function

Leventhal, A. G. (1991) · CRC Press eBooks · Cited by 365 · see citing works

Positron emission tomographic measurements of pulvinar activity during an attention task

LaBerge, D., & Buchsbaum, M. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00613.1990 · Cited by 353 · see citing works

The thalamic relations of the caudal inferior parietal lobule and the lateral prefrontal cortex in monkeys: Divergent cortical projections from cell clusters in the medial pulvinar nucleus

Asanuma, C., Andersen, R. A., & Cowan, W. M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902410309 · Cited by 294 · see citing works

Subcortical projections of area MT in the macaque

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Attentional Control of Visual Perception: Cortical and Subcortical Mechanisms

Desimone, R., Wessinger, M., Thomas, L., & Schneider, W. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.090 · Cited by 235 · see citing works

Areal and laminar distribution of some pulvinar cortical efferents in rhesus monkey

Trojanowski, J. Q., & Jacobson, S. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901690307 · Cited by 213 · see citing works

Retinotopic organization of macaque pulvinar.

Bender, D. B. (1981) · Journal of Neurophysiology · doi:10.1152/jn.1981.46.3.672 · Cited by 205 · see citing works

Use of an extraretinal signal by monkey superior colliculus neurons to distinguish real from self-induced stimulus movement

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A retrograde cell degeneration study of the cortical projection field of the pulvinar in the monkey

Chow, K. L. (1950) · The Journal of Comparative Neurology · doi:10.1002/cne.900930302 · Cited by 161 · see citing works

Visual activation of neurons in the primate pulvinar depends on cortex but not colliculus

Bender, D. B. (1983) · Brain Research · doi:10.1016/0006-8993(83)90188-9 · Cited by 146 · see citing works

Influences of lesions of parietal cortex on visual spatial attention in humans

Petersen, S. E., Robinson, D. L., & Currie, J. N. (1989) · Experimental Brain Research · doi:10.1007/bf00247887 · Cited by 140 · see citing works

Receptive-field properties of neurons in the macaque inferior pulvinar.

Bender, D. B. (1982) · Journal of Neurophysiology · doi:10.1152/jn.1982.48.1.1 · Cited by 139 · see citing works

Thalamic projections of the superior colliculus in the rhesus monkey, Macaca mulatta. A light and electron microscopic study

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The development and recovery of motor function in spinal cats

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BRAIN AND HUMAN BEHAVIOR

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Visual and somatosensory receptive fields of neurons in the squirrel monkey pulvinar

Mathers, L. H., & Rapisardi, S. C. (1973) · Brain Research · doi:10.1016/0006-8993(73)90171-6 · Cited by 105 · see citing works

A representation of the visual field in the inferior nucleus of the pulvinar in the owl monkey (Aotus Trivirgatus)

Allman, J. M., Kaas, J. H., Lane, R. H., & Miezin, F. M. (1972) · Brain Research · doi:10.1016/0006-8993(72)90135-7 · Cited by 93 · see citing works

LACK OF BEHAVIORAL EFFECTS FOLLOWING DESTRUCTION OF SOME THALAMIC ASSOCIATION NUCLEI IN MONKEY

Chow, K. L. (1954) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1954.02320420090008 · Cited by 84 · see citing works

Visual receptive fields of units in the pulvinar of cebus monkey

Gattass, R., Oswaldo‐Cruz, Ė., & Sousa, A. P. B. (1979) · Brain Research · doi:10.1016/0006-8993(79)91070-9 · Cited by 83 · see citing works

A review of cat and monkey studies implicating the pulvinar in visual function

Chalupa, L. M. (1977) · Behavioral Biology · doi:10.1016/s0091-6773(77)90721-0 · Cited by 78 · see citing works

Visual responses of single neurons in the caudal lateral pulvinar of the macaque monkey

Benevento, L., & Miller, J. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-11-01268.1981 · Cited by 74 · see citing works

Saccade-related and visual activities in the pulvinar nuclei of the behaving rhesus monkey

Robinson, D. L., Petersen, S. E., & Keys, W. (1986) · Experimental Brain Research · doi:10.1007/bf00236042 · Cited by 65 · see citing works

Pulvinar-latero posterior afferents to cortical area 7 in monkeys demonstrated by horseradish peroxidase tracing technique

Baleydier, C., & Maugui�re, F. (1977) · Experimental Brain Research · doi:10.1007/bf00239039 · Cited by 65 · see citing works

Sensorimotor unit activity related to intention in the Pulvinar of behaving Cebus Apella monkeys

Acu�a, C., González, F., & Dominguez, R. (1983) · Experimental Brain Research · doi:10.1007/bf00238034 · Cited by 59 · see citing works

Selectivity for relative motion in the monkey superior colliculus

Davidson, R. M., & Bender, D. B. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.5.1115 · Cited by 55 · see citing works

Orbital position and eye movement influences on visual responses in the pulvinar nuclei of the behaving macaque

Robinson, D. L., McClurkin, J. W., & Kertzman, C. (1990) · Experimental Brain Research · doi:10.1007/bf00231243 · Cited by 52 · see citing works

Visual responses of pulvinar and collicular neurons during eye movements of awake, trained macaques

Robinson, D. L., McClurkin, J. W., Kertzman, C., & Petersen, S. E. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.2.485 · Cited by 50 · see citing works

Brainstem mechanisms underlying visually guided responses in the rhesus monkey.

Thompson, R., & Myers, R. E. (1971) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0030562 · Cited by 49 · see citing works

Single unit response types in the pulvinar of the cebus monkey to multisensory stimulation

Gattass, R., Sousa, A. P. B., & Oswaldo‐Cruz, Ė. (1978) · Brain Research · doi:10.1016/0006-8993(78)90007-0 · Cited by 49 · see citing works

Cells of origin of several efferent pathways from the superior colliculus inGalago senegalensis

Raczkowski, D., & DIAMOND, I. T. (1978) · Brain Research · doi:10.1016/0006-8993(78)90979-4 · Cited by 48 · see citing works

Lateral-posterior and pulvinar reaching cells?comparison with parietal area 5a: a study in behaving Macaca nemestrina monkeys

Acu�a, C., Cudeiro, J., González, F., et al. (1990) · Experimental Brain Research · doi:10.1007/bf00230847 · Cited by 43 · see citing works

Auditory- and movement-related neural activity interact in the pulvinar of the behaving rhesus monkey

Yirmiya, R., & Hocherman, S. (1987) · Brain Research · doi:10.1016/0006-8993(87)91051-1 · Cited by 37 · see citing works

Responses of pulvinar neurons to real and self-induced stimulus movement

Robinson, D. L., & Petersen, S. E. (1985) · Brain Research · doi:10.1016/0006-8993(85)90176-3 · Cited by 36 · see citing works

Human pulvinar units, spontaneous activity and sensory-motor influences

Martín-Rodríguez, J. G., Buño, W., & García-Austt, E. (1982) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(82)90202-4 · Cited by 26 · see citing works

Pulvinar neuron responses to spontaneous and trained eye movements and to light flashes in squirrel monkeys

Perryman, K. M., Lindsley, D. F., Lindsley, D. F., et al. (1980) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(80)90361-2 · Cited by 23 · see citing works

Monkey pulvinar units related to motor activity and sensory response

Magariños-Ascone, C. M., Buño, W., & García-Austt, E. (1988) · Brain Research · doi:10.1016/0006-8993(88)91070-0 · Cited by 22 · see citing works

Neural Mechanisms of Selective Visual Attention

Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388 · see citing works

Computational modelling of visual attention

Itti, L., & Koch, C. (2001) · Nature Reviews Neuroscience · doi:10.1038/35058500 · Cited by 4,733 · see citing works

Salience processing and insular cortical function and dysfunction

Uddin, L. Q. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3857 · Cited by 2,083 · see citing works

A neuromodulatory role for the human amygdala in processing emotional facial expressions

Morris, J. (1998) · Brain · doi:10.1093/brain/121.1.47 · Cited by 1,291 · see citing works

Distinct spatial frequency sensitivities for processing faces and emotional expressions

Vuilleumier, P., Armony, J. L., Driver, J., & Dolan, R. J. (2003) · Nature Neuroscience · doi:10.1038/nn1057 · Cited by 1,117 · see citing works

The pulvinar regulates information transmission between cortical areas based on attention demands

Saalmann, Y. B., Pinsk, M. A., Wang, L., Li, X., & Kastner, S. (2012) · Science · doi:10.1126/science.1223082 · Cited by 1,016 · see citing works

Subcortical face processing

Johnson, M. H. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1766 · Cited by 969 · see citing works

Eye guidance in natural vision: reinterpreting salience

Tatler, B. W., Hayhoe, M. M., Land, M. F., & Ballard, D. H. (2011) · Journal of Vision · doi:10.1167/11.5.5 · Cited by 775 · see citing works

The reinterpretation of dreams: An evolutionary hypothesis of the function of dreaming

Revonsuo, A. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00004015 · Cited by 676 · see citing works

Differential extrageniculostriate and amygdala responses to presentation of emotional faces in a cortically blind field

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The neuropsychology of 3-D space.

Previc, F. H. (1998) · Psychological Bulletin · doi:10.1037/0033-2909.124.2.123 · Cited by 604 · see citing works

Cerebral hierarchies: predictive processing, precision and the pulvinar

Kanai, R., Komura, Y., Shipp, S., & Friston, K. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0169 · Cited by 432 · see citing works

Mechanisms of top-down attention

Baluch, F., & Itti, L. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.02.003 · Cited by 437 · see citing works

The graphical brain: Belief propagation and active inference

Friston, K. J., Parr, T., & de Vries, B. (2017) · Network Neuroscience · doi:10.1162/netn_a_00018 · Cited by 415 · see citing works

The functional logic of cortico-pulvinar connections

Shipp, S. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1213 · Cited by 411 · see citing works

The brain circuitry of attention

Shipp, S. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.03.004 · Cited by 402 · see citing works

Identification of common neural circuit disruptions in emotional processing across psychiatric disorders

McTeague, L. M., Rosenberg, B. M., Lopez, J. W., Carreon, D. M., Huemer, J., Jiang, Y., Chick, C. F., Eickhoff, S. B., & Etkin, A. (2020) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2019.18111271 · Cited by 388 · see citing works

The organization of two new cortical interneuronal circuits

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Vision and cognition in Alzheimer’s disease

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Attention deficits without cortical neuronal deficits

Zénon, A., & Krauzlis, R. J. (2012) · Nature · doi:10.1038/nature11497 · Cited by 234 · see citing works

Gating and control of primary visual cortex by pulvinar

Purushothaman, G., Marion, R., Li, K., & Casagrande, V. A. (2012) · Nature Neuroscience · doi:10.1038/nn.3106 · Cited by 236 · see citing works

Functional Imaging of the Human Lateral Geniculate Nucleus and Pulvinar

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Pain and analgesia: the value of salience circuits

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Comparative Perspectives on Oxytocin and Vasopressin Receptor Research in Rodents and Primates: Translational Implications

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Impaired attentional selection following lesions to human pulvinar: Evidence for homology between human and monkey

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Neuroanatomical distribution of oxytocin and vasopressin 1a receptors in the socially monogamous coppery titi monkey (Callicebus cupreus)

Freeman, S. M., Walum, H., Inoue, K., Smith, A. L., Goodman, M. M., Bales, K. L., & Young, L. J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.055 · Cited by 153 · see citing works

Neurobiological correlates of cognitions in fear and anxiety: A cognitive-neurobiological information processing model

Hofmann, S. G., Ellard, K. K., & Siegle, G. J. (2012) · Cognition and Emotion · doi:10.1080/02699931.2011.579414 · Cited by 132 · see citing works

Thalamic pathways for active vision

Wurtz, R. H., McAlonan, K., Cavanaugh, J., & Berman, R. A. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.02.004 · Cited by 127 · see citing works

Attention gates visual coding in the human pulvinar

Fischer, J., & Whitney, D. (2012) · Nature Communications · doi:10.1038/ncomms2054 · Cited by 127 · see citing works

The medial pulvinar: function, origin and association with neurodevelopmental disorders

Homman‐Ludiye, J., & Bourne, J. A. (2019) · Journal of Anatomy · doi:10.1111/joa.12932 · Cited by 117 · see citing works

Visual Salience Affects Performance in a Working Memory Task

Fine, M. S., & Minnery, B. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5503-08.2009 · Cited by 115 · see citing works

Thalamic shape and connectivity abnormalities in children with attention- deficit/hyperactivity disorder

Xia, S., Li, X., Kimball, A. E., Kelly, M. S., Lesser, I., & Branch, C. (2012) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2012.04.011 · Cited by 92 · see citing works

Canonical Organization of Layer 1 Neuron-Led Cortical Inhibitory and Disinhibitory Interneuronal Circuits

Lee, A. J., Wang, G., Jiang, X., Johnson, S. M., Hoang, E. T., Lanté, F., Stornetta, R. L., Beenhakker, M. P., Shen, Y., & Julius Zhu, J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu020 · Cited by 94 · see citing works

Single neurons with both form/color differential responses and saccade-related responses in the nonretinotopic pulvinar of the behaving macaque monkey

Benevento, L. A., & Port, J. D. (1995) · Visual Neuroscience · doi:10.1017/s0952523800008439 · Cited by 86 · see citing works

Relative Effectiveness of Emotion Induction Procedures and the Role of Personal Relevance in a Clinical Sample: A Comparison of Film, Images, and Music

Ellard, K. K., Farchione, T. J., & Barlow, D. H. (2012) · Journal of Psychopathology and Behavioral Assessment · doi:10.1007/s10862-011-9271-4 · Cited by 66 · see citing works

Scaling of neuron number and volume of the pulvinar complex in new world primates: Comparisons with humans, other primates, and mammals

Chalfin, B. P., Cheung, D. T., Muniz, J. A. P. C., de Lima Silveira, L. C., & Finlay, B. L. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21406 · Cited by 61 · see citing works

The role of the pulvinar in distractor processing and visual search

Strumpf, H., Mangun, G. R., Boehler, C. N., Stoppel, C., Schoenfeld, M. A., Heinze, H., & Hopf, J. (2013) · Human Brain Mapping · doi:10.1002/hbm.21496 · Cited by 56 · see citing works

The effects of methylphenidate on resting-state striatal, thalamic and global functional connectivity in healthy adults

Farr, O. M., Zhang, S., Hu, S., Matuskey, D., Abdelghany, O., Malison, R. T., & Li, C.-S. R. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714000674 · Cited by 57 · see citing works

Distracted by danger: Temporal and spatial dynamics of visual selection in the presence of threat

Mulckhuyse, M., & Dalmaijer, E. S. (2016) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-015-0391-2 · Cited by 38 · see citing works

Neuronal responses to a delayed-response delayed-reward go/nogo task in the monkey posterior insular cortex

Asahi, T., Uwano, T., Eifuku, S., Tamura, R., Endo, S., Ono, T., & Nishijo, H. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.008 · Cited by 19 · see citing works

The contributions of anatomical studies to knowledge of perceptual processing

Guillery, R. W. (2008) · Anatomy (International Journal of Experimental and Clinical Anatomy) · doi:10.2399/ana.08.009 · Cited by 1 · see citing works

Identity salience: understanding when identity affects consumption

Kettle, K. L. (2019) · Edward Elgar Publishing eBooks · doi:10.4337/9781788117739.00010 · Cited by 14 · see citing works

On understanding idiomatic language: The salience hypothesis assessed by ERPs

Laurent, J., Denhières, G., Passerieux, C., Iakimova, G., & Hardy-Baylé, M. C. (2006) · Brain Research · doi:10.1016/j.brainres.2005.10.076 · Cited by 95 · see citing works

Translating Case Salience into Measurable Explanatory Variables

Jaegere, J. D. (2019) · Intersentia eBooks · doi:10.1017/9781780688619.009

The View from the Driver's Seat: What Good Is Salience?

McCarley, J. S., Steelman, K. S., & Horrey, W. J. (2013) · Applied Cognitive Psychology · doi:10.1002/acp.2955 · Cited by 15 · see citing works

Contextual and Temporal Constraints for Attentional Capture: Commentary on Theeuwes’ 2023 Review “The Attentional Capture Debate: When Can We Avoid Salient Distractors and when Not?”

Noonan, M. P., & Störmer, V. S. (2023) · Journal of Cognition · doi:10.5334/joc.274 · Cited by 1 · see citing works