The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Impaired attentional selection following lesions to human pulvinar: Evidence for homology between human and monkey
Open accessAbstract
We examined the contributions of the human pulvinar to goal directed selection of visual targets in 3 patients with chronic, unilateral lesions involving topographic maps in the ventral pulvinar. Observers completed 2 psychophysical tasks in which they discriminated the orientation of a lateralized target grating in the presence of vertically-aligned distracters. In experiment 1, where distracter contrast was varied while target contrast remained constant, the patients' contralesional contrast thresholds for discriminating the orientation of grating stimuli were elevated only when the task required selection of a visual target in the face of competition from a salient distracter. Attentional selectivity was restored in the patients in experiment 2 where target contrast was varied while distracter contrast remained constant. These observations provide the first evidence that the human pulvinar plays a necessary role in modulating physical saliency in attentional selection, and supports a homology in global pulvinar structure between humans and monkey.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Damage to the pulvinar in humans can result in visual hemi-neglect [44,45], deficits in feature binding [46] or focal attention [47].”
From Cerebral hierarchies: predictive processing, precision and the pulvinar (2015) · cites this paper as [47]
Citations
Cites
Brainard, D. H. (1997) · Spatial Vision · doi:10.1163/156856897x00357 · Cited by 20,012
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
The VideoToolbox software for visual psychophysics: transforming numbers into movies
Pelli, D. G. (1997) · Spatial Vision · doi:10.1163/156856897x00366 · Cited by 11,110
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
Function of the thalamic reticular complex: the searchlight hypothesis
Crick, F. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.14.4586 · Cited by 1,651
Neural mechanisms of spatial selective attention in areas V1, V2, and V4 of macaque visual cortex
Luck, S. J., Chelazzi, L., Hillyard, S. A., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.1.24 · Cited by 1,615
Corbetta, M., Miezin, F. M., Dobmeyer, S., Shulman, G. L., & Petersen, S. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02383.1991 · Cited by 1,590
VISUAL ATTENTION: Control, Representation, and Time Course
Egeth, H. E., & Yantis, S. (1997) · Annual Review of Psychology · doi:10.1146/annurev.psych.48.1.269 · Cited by 1,328
Competitive Mechanisms Subserve Attention in Macaque Areas V2 and V4
Reynolds, J. H., Chelazzi, L., & Desimone, R. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-05-01736.1999 · Cited by 1,236
Mechanisms of Directed Attention in the Human Extrastriate Cortex as Revealed by Functional MRI
Kästner, S., Weerd, P. D., Desimone, R., & Ungerleider, L. G. (1998) · Science · doi:10.1126/science.282.5386.108 · Cited by 976
Cited by
Sorted by citations
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
Emotional perception: Meta-analyses of face and natural scene processing
Sabatinelli, D., Fortune, E. E., Li, Q., Siddiqui, A. P., Krafft, C. E., Oliver, W. T., Beck, S., & Jeffries, J. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.011 · Cited by 715
Thalamic functions in distributed cognitive control
Halassa, M. M., & Kästner, S. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0020-1 · Cited by 540
Cognitive and Perceptual Functions of the Visual Thalamus
Saalmann, Y. B., & Kästner, S. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.027 · Cited by 461
Mechanisms of top-down attention
Baluch, F., & Itti, L. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.02.003 · Cited by 437
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
Pulvinar-Cortex Interactions in Vision and Attention
Zhou, H., Schafer, R. J., & Desimone, R. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.034 · Cited by 384
Saalmann, Y. B. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00083 · Cited by 343
The impact of the human thalamus on brain-wide information processing
Shine, J. M., Lewis, L. D., Garrett, D. D., & Hwang, K. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00701-0 · Cited by 335
Induction of Empathy by the Smell of Anxiety
Prehn‐Kristensen, A., Wiesner, C. D., Bergmann, T. O., Wolff, S., Jansen, O., Mehdorn, H. M., Ferstl, R., & Pause, B. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005987 · Cited by 264
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
Pulvinar Inactivation Disrupts Selection of Movement Plans
Wilke, M., Turchi, J. N., Smith, K., Mishkin, M., & Leopold, D. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0953-10.2010 · Cited by 191
Fiebelkorn, I. C., Pinsk, M. A., & Kästner, S. (2019) · Nature Communications · doi:10.1038/s41467-018-08151-4 · Cited by 179
Different functions in the cingulate cortex, a meta-analytic connectivity modeling study
Torta, D. M. E., & Cauda, F. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.066 · Cited by 173
Schrier, J. E., Harper, J. S., Hankinson, G. J., Hulsebos, L., Povar, M. L., Mathiesen, E., & Schrier, A. M. (2009) · Cited by 166
Pulvinar: Associative role in cortical function and clinical correlations
Benarroch, E. E. (2015) · Neurology · doi:10.1212/wnl.0000000000001276 · Cited by 160
Engagement of Pulvino-cortical Feedforward and Feedback Pathways in Cognitive Computations
Jaramillo, J., Mejías, J. F., & Wang, X. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.023 · Cited by 166
The activation of interactive attentional networks
Xuan, B., Mackie, M., Spagna, A., Wu, T., Tian, Y., Hof, P. R., & Fan, J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.01.017 · Cited by 157
Gain control in the visual thalamus during perception and cognition
Saalmann, Y. B., & Kastner, S. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.05.007 · Cited by 156
Higher-Order Thalamic Circuits Channel Parallel Streams of Visual Information in Mice
Bennett, C., Gale, S. D., Garrett, M., Newton, M. L., Callaway, E. M., Murphy, G. J., & Olsen, S. R. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.010 · Cited by 166
Pulvinar Projections to the Striatum and Amygdala in the Tree Shrew
Day‐Brown, J. D., Wei, H., Chomsung, R. D., Petry, H. M., & Bickford, M. E. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00143 · Cited by 133
Attention gates visual coding in the human pulvinar
Fischer, J., & Whitney, D. (2012) · Nature Communications · doi:10.1038/ncomms2054 · Cited by 127
Thalamic Control of Human Attention Driven by Memory and Learning
Bourbon‐Teles, J., Bentley, P., Koshino, S., Shah, K., Dutta, A., Malhotra, P., Egner, T., Husain, M., & Soto, D. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.024 · Cited by 135
Finding thalamic BOLD correlates to posterior alpha EEG
Liu, Z., de Zwart, J. A., Yao, B., van Gelderen, P., Kuo, L.-W., & Duyn, J. H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.025 · Cited by 104
Organizing principles of pulvino-cortical functional coupling in humans
Arcaro, M. J., Pinsk, M. A., Chen, J., & Kästner, S. (2018) · Nature Communications · doi:10.1038/s41467-018-07725-6 · Cited by 98
Learning to read alters cortico-subcortical cross-talk in the visual system of illiterates
Skeide, M. A., Kumar, U., Mishra, R. K., Tripathi, V. N., Guleria, A., Singh, J. P., Eisner, F., & Huettig, F. (2017) · Science Advances · doi:10.1126/sciadv.1602612 · Cited by 92
A multisensory perspective onto primate pulvinar functions
Froesel, M., Cappe, C., & Hamed, S. B. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.043 · Cited by 90
Melcher, D., & Manuela Piazza, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0029296 · Cited by 90
Cortical Sensory Responses Are Enhanced by the Higher-Order Thalamus
Mease, R. A., Metz, M., & Groh, A. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.12.026 · Cited by 90
Shaw, P., Sharp, W. S., Sudre, G. P., Wharton, A., GREENSTEIN, D. K., Raznahan, A., Evans, A. C., Chakravarty, M. M., Lerch, J. P., & Rapoport, J. L. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.3 · Cited by 89
Neuronal responses to face-like stimuli in the monkey pulvinar
Nguyen, M. N., Hori, E., Matsumoto, J., Tran, A. H., Ono, T., & Nishijo, H. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12020 · Cited by 87
Subcortical connections of area V4 in the macaque
Gattass, R., Galkin, T. W., Desimone, R., & Ungerleider, L. G. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23513 · Cited by 87
The pulvinar as a hub of visual processing and cortical integration
Cortes, N., Ladret, H., Farishta, R. A., & Casanova, C. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.11.008 · Cited by 87
Superior colliculus modulates cortical coding of somatosensory information
Gharaei, S., Honnuraiah, S., Arabzadeh, E., & Stuart, G. J. (2020) · Nature Communications · doi:10.1038/s41467-020-15443-1 · Cited by 78
Chipika, R. H., Finegan, E., Shing, S. L. H., McKenna, M. C., Christidi, F., Chang, K. M., Doherty, M. A., Hengeveld, J. C., Vajda, A., Pender, N. P., et al. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102300 · Cited by 77
Biesbroek, J. M., Verhagen, M. G., der Stigchel, S. V., & Biessels, G. J. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.13563 · Cited by 78
Hu, F., Kamigaki, T., Zhang, Z., Zhang, S., Dan, U., & Dan, Y. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.019 · Cited by 73
Disentangling the influences of multiple thalamic nuclei on prefrontal cortex and cognitive control
Phillips, J. M., Kambi, N. A., Redinbaugh, M. J., Mohanta, S., & Saalmann, Y. B. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.06.042 · Cited by 75
Troiani, V., & Schultz, R. T. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00241 · Cited by 74
Neuropsychological evidence of multi-domain network hubs in the human thalamus
Hwang, K., Shine, J. M., Bruss, J., Tranel, D., & Boes, A. D. (2021) · eLife · doi:10.7554/elife.69480 · Cited by 71
Liang, M., Mouraux, A., & Iannetti, G. D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr363 · Cited by 71
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
Dominguez‐Vargas, A., Schneider, L., Wilke, M., & Kagan, I. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1984-16.2016 · Cited by 60
Pulvino-cortical interaction: An integrative role in the control of attention
Bourgeois, A., Guedj, C., Carrera, E., & Vuilleumier, P. O. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.005 · Cited by 55
Chu, C. W., Wu, J. C., Yew, D. T.-W., Zhang, L., Shi, L., Yeung, D. K. W., Wang, D., Tong, R. K., Chan, Y., Lao, L., et al. (2012) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm.2012.18.3.305 · Cited by 55
Unseen fearful faces promote amygdala guidance of attention
Troiani, V., Price, E. T., & Schultz, R. T. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss116 · Cited by 58
Relevance of subcortical visual pathways disruption to visual symptoms in dementia with Lewy bodies
Pizzi, S. D., Maruotti, V., Taylor, J., Franciotti, R., Caulo, M., Tartaro, A., Thomas, A., ONOFRJ, M. C., & Bonanni, L. (2014) · Cortex · doi:10.1016/j.cortex.2014.07.003 · Cited by 51
Spatial Attention Deficits Are Causally Linked to an Area in Macaque Temporal Cortex
Bogadhi, A. R., Bollimunta, A., Leopold, D. A., & Krauzlis, R. J. (2019) · Current Biology · doi:10.1016/j.cub.2019.01.028 · Cited by 50
Gouws, A. D., Alvarez, I., Watson, D. M., Uesaki, M., Rogers, J., & Morland, A. B. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0164-14.2014 · Cited by 55
Network Localization of Executive Function Deficits in Patients with Focal Thalamic Lesions
Hwang, K., Bruss, J., Tranel, D., & Boes, A. D. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01628 · Cited by 54
Dynamic pulvino-cortical interactions in the primate attention network
Kästner, S., Fiebelkorn, I. C., & Eradath, M. K. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.08.002 · Cited by 49
Nair, A., Jalal, R., Liu, J., Tsang, T., McDonald, N. M., Jackson, L., Ponting, C., Jeste, S., Bookheimer, S. Y., & Dapretto, M. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab078 · Cited by 53
Li, K., Zhang, H., Yang, Y., Zhu, J., Wang, B., Shi, Y., Li, X., Zhang, M., Lv, L., & Zhang, H. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.111982 · Cited by 46
Contribution of the central thalamus to the generation of volitional saccades
Tanaka, M., & Kunimatsu, J. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07699.x · Cited by 47
Effects of arousal and movement on secondary somatosensory and visual thalamus
Petty, G. H., Kinnischtzke, A. K., Hong, Y. K., & Bruno, R. M. (2021) · eLife · doi:10.7554/elife.67611 · Cited by 45
A Normalization Framework for Emotional Attention
Zhang, X., JAPEE, S. A., Safiullah, Z. N., Mlynaryk, N., & Ungerleider, L. G. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002578 · Cited by 46
Conserved patterns of functional organization between cortex and thalamus in mice
Miller-Hansen, A. J., & Sherman, S. M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2201481119 · Cited by 43
Thalamocortical contributions to cognitive task activity
Sorenson, E., Shine, J. M., Cole, M. W., & Hwang, K. (2022) · eLife · doi:10.7554/elife.81282 · Cited by 46
Cho, K. I. K., Kwak, Y. B., Hwang, W. J., Lee, J., Kim, M., Lee, T. Y., & Kwon, J. S. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.05.019 · Cited by 44
Deep Predictive Learning in Neocortex and Pulvinar
O’Reilly, R. C., Russin, J., Zolfaghar, M., & Rohrlich, J. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01708 · Cited by 49
Extensive Connectivity Between the Medial Pulvinar and the Cortex Revealed in the Marmoset Monkey
Homman‐Ludiye, J., Mundiñano, I.-C., Kwan, W. C., & Bourne, J. A. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz203 · Cited by 42
Mai, J. K., & Forutan, F. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10019-7 · Cited by 45
Di, T., He, Z., Lin, Y., Liu, C., & Tao, Q. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117686 · Cited by 46
A causal role for the pulvinar in coordinating task‐independent cortico–cortical interactions
Eradath, M. K., Pinsk, M. A., & Kästner, S. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25193 · Cited by 45
Rotshtein, P., Soto, D., Grecucci, A., Geng, J. J., & Humphreys, G. W. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.12.002 · Cited by 40
Self-citationThe Thalamus as a Blackboard for Perception and Planning
Worden, R., Bennett, M. S., & Neacsu, V. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.633872 · Cited by 46
Pulvinar Lesions Disrupt Fear-Related Implicit Visual Processing in Hemianopic Patients
Bertini, C., Pietrelli, M., Braghittoni, D., & Làdavas, E. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02329 · Cited by 38
Leow, Y. N., Zhou, B., Sullivan, H. A., Barlowe, A. R., Wickersham, I. R., & Sur, M. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25317 · Cited by 38
Hakamata, Y., Sato, E., Komi, S., Moriguchi, Y., Izawa, S., Murayama, N., Hanakawa, T., Inoue, Y., & Tagaya, H. (2016) · Scientific Reports · doi:10.1038/srep34777 · Cited by 37
Corticothalamic pathways from layer 5: emerging roles in computation and pathology
Mease, R. A., & Gonzalez, A. J. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.730211 · Cited by 36
Pulvinar Modulates Contrast Responses in the Visual Cortex as a Function of Cortical Hierarchy
de Souza, B. O. F., Cortes, N., & Casanova, C. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz149 · Cited by 33
Reach and grasp deficits following damage to the dorsal pulvinar
Wilke, M., Schneider, L., Dominguez‐Vargas, A., Schmidt‐Samoa, C., Miloserdov, K., Nazzal, A. M., Dechent, P., Cabral‐Calderín, Y., Scherberger, H., Kagan, I., et al. (2017) · Cortex · doi:10.1016/j.cortex.2017.10.011 · Cited by 32
Wintermann, G.-B., Donix, M., Joraschky, P., Gerber, J., & Petrowski, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074655 · Cited by 31
Spatially Distributed Encoding of Covert Attentional Shifts in Human Thalamus
Hulme, O. J., Whiteley, L., & Shipp, S. D. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00303.2010 · Cited by 32
Neuronal modulation in the mouse superior colliculus during covert visual selective attention
Wang, L., Herman, J. P., & Krauzlis, R. J. (2022) · Scientific Reports · doi:10.1038/s41598-022-06410-5 · Cited by 30
Neural correlates of and processes underlying generalized and differential return of fear
Scharfenort, R., & Lonsdorf, T. B. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv142 · Cited by 30
Thalamic-Medial Temporal Lobe Connectivity Underpins Familiarity Memory
Kafkas, A., Mayes, A. R., & Montaldi, D. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhz345 · Cited by 30
Increased error-related thalamic activity during early compared to late cocaine abstinence
Li, C. R., Luo, X., Sinha, R., Rounsaville, B. J., Carroll, K. M., Malison, R. T., Ding, Y., Zhang, S., & Ide, J. S. (2010) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2010.01.008 · Cited by 31
A review of lateralization of spatial functioning in nonhuman primates
Oleksiak, A., Postma, A., van der Ham, I. J. M., Klink, P. C., & Wezel, R. J. A. V. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.11.002 · Cited by 31
Multisensory integration in neurons of the medial pulvinar of macaque monkey
Vittek, A., Juan, C., Nowak, L. G., Girard, P., & Cappe, C. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac337 · Cited by 28
Cortico‐thalamocortical interactions for learning, memory and decision‐making
Perry, B. A. L., Méndez, J. C., & Mitchell, A. S. (2022) · The Journal of Physiology · doi:10.1113/jp282626 · Cited by 27
Mantovani, A., Neri, F., D’Urso, G., Mencarelli, L., Tatti, E., Momi, D., Menardi, A., Sprugnoli, G., Santarnecchi, E., & Rossi, S. (2020) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2020.10.030 · Cited by 28
Spatio-temporal indications of sub-cortical involvement in leftward bias of spatial attention
Okon‐Singer, H., Podlipsky, I., Siman-Tov, T., Simon, E. B., Zhdanov, A. V., Neufeld, M. Y., & Hendler, T. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.078 · Cited by 24
Dissociable spatial and non-spatial attentional deficits after circumscribed thalamic stroke
Kraft, A., Irlbacher, K., Finke, K., Kaufmann, C., Kehrer, S., Liebermann, D., Bundesen, C., & Brandt, S. A. (2014) · Cortex · doi:10.1016/j.cortex.2014.12.005 · Cited by 24
Human thalamic and amygdala modulation in emotional scene perception
Frank, D. W., & Sabatinelli, D. (2014) · Brain Research · doi:10.1016/j.brainres.2014.08.061 · Cited by 24
Cocaine dependence and thalamic functional connectivity: a multivariate pattern analysis
Zhang, S., Hu, S., Sinha, R., Potenza, M. N., Malison, R. T., & Li, C. R. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.08.006 · Cited by 24
Attentional modulation of secondary somatosensory and visual thalamus of micePreprint
Petty, G. H., & Bruno, R. M. (2024) · eLife · doi:10.7554/elife.97188.3 · Cited by 24
Transthalamic Pathways for Cortical Function
Sherman, S. M., & Usrey, W. M. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0909-24.2024 · Cited by 26
Oculomotor integration in patients with a pulvinar lesion
der Stigchel, S. V., Arend, I. C., van Koningsbruggen, M. G., & Rafal, R. D. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.07.035 · Cited by 22
Self-citationAttention and Thalamocortical Interactions
Kästner, S., & Usrey, W. M. (2023) · Oxford University Press eBooks · doi:10.1093/med/9780197676158.003.0045 · Cited by 21
Tadayonnejad, R., Ajilore, O., Mickey, B. J., Crane, N. A., Hsu, D. T., Kumar, A., Zubieta, J., & Langenecker, S. A. (2016) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2016.04.013 · Cited by 21
The Neural Selection and Integration of Actions and Objects: An fMRI Study
Yoon, E. Y., Humphreys, G. W., Kumar, S., & Rotshtein, P. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00256 · Cited by 20
Self-citationModulation of pulvinar connectivity with cortical areas in the control of selective visual attention
Guedj, C., & Vuilleumier, P. O. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119832 · Cited by 18
Moon, W., Kim, H.-J., Roh, H. G., Choi, J. W., & Han, S. (2012) · Korean Journal of Radiology · doi:10.3348/kjr.2012.13.6.674 · Cited by 17
Yu, C., Sellers, K. K., Radtke‐Schuller, S., Lu, J., Xing, L., Ghukasyan, V., Li, Y., Shih, Y. I., Murrow, R. W., & Frӧhlich, F. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13116 · Cited by 16
Unexpected Sounds Nonselectively Inhibit Active Visual Stimulus Representations
Soh, C., & Wessel, J. R. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa315 · Cited by 20
Kwak, Y. B., Cho, K. I. K., Hwang, W. J., Kim, A., Ha, M., Park, H., Lee, J., Lee, T. Y., Kim, M., & Kwon, J. S. (2021) · Scientific Reports · doi:10.1038/s41598-021-99170-7 · Cited by 16
Hagan, M. A., Rosa, M. G. P., & Lui, L. L. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22426 · Cited by 18
Task-demands and audio-visual stimulus configurations modulate neural activity in the human thalamus
Bonath, B., Tyll, S., Budinger, E., Krauel, K., Hopf, J., & Noesselt, T. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.018 · Cited by 15
Exploring Thalamocortical Interactions
Sherman, S. M., & Usrey, W. M. (2021) · Oxford University Press eBooks · doi:10.1093/med/9780197503874.001.0001 · Cited by 14
Metadata
- Authors
- Snow, J. C., Allen, H. A., Rafal, R. D., & Humphreys, G. W.
- Affiliations
- Western University (CA)
- University of Birmingham (GB)
- Bangor University (GB)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2009-03-10
- Volume
- 106
- Issue
- 10
- Pages
- 4054-4059
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2656203
- OpenAlex
- W2090263161
- Cited by
- 188
- References
- 48
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 10 · 2023: 14 · 2022: 9 · 2021: 30 · 2020: 13 · 2019: 10 · 2018: 8 · 2017: 9 · 2016: 11 · 2015: 8 · 2014: 11 · 2013: 7 · 2012: 17
- FWCI
- 5.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Funders
- Wellcome Trust
- Biotechnology and Biological Sciences Research Council
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Spatial Neglect and Hemispheric Dysfunction
- Physical Sciences › Computer Science › Computer Vision and Pattern Recognition › Visual Attention and Saliency Detection
- Keywords
- pulvinar, selective attention, visual attention, topographic map, orientation discrimination, contrast threshold
- MeSH terms
- Adult, Aged, Animals, Haplorhini, Attention, Female, Humans, Male, Middle Aged, Orientation, Photic Stimulation, Visual Fields, Pulvinar
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