Cited by 682Visual perception and processing mechanismsSpatial Neglect and Hemispheric DysfunctionMotor Control and Adaptation

The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.

Mapping of Contralateral Space in Retinotopic Coordinates by a Parietal Cortical Area in Humans

Sereno, M. I., Pitzalis, S., Martinez, A.·2001·Science

DOI 10.1126/science.1063695

Open this paper in CoChat — free account

Abstract

The internal organization of a higher level visual area in the human parietal cortex was mapped. Functional magnetic resonance images were acquired while the polar angle of a peripheral target for a delayed saccade was gradually changed. A region in the superior parietal cortex showed robust retinotopic mapping of the remembered target angle. The map reversed when the direction of rotation of the remembered targets was reversed and persisted unchanged when study participants detected rare target reappearances while maintaining fixation, or when the eccentricity of successive remembered targets was unpredictable. This region may correspond to the lateral intraparietal area in macaque monkeys.

Integrity signals

Registry

Crossref · 10.1126/science.1063695

Cites

42 of 42 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Cortical Surface-Based Analysis
Dale, A. M., Fischl, B., & Sereno, M. I. (1999) · NeuroImage · doi:10.1006/nimg.1998.0395 · Cited by 10,910
Self-citation
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
Cortical Surface-Based Analysis
Fischl, B., Sereno, M. I., & Dale, A. M. (1999) · NeuroImage · doi:10.1006/nimg.1998.0396 · Cited by 6,147
Self-citation
Preface: Cerebral Cortex Has Come of Age
Goldman, P. S., & RAKIC, P. T. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1-a · Cited by 3,537
Automatic 3D intersubject registration of MR volumetric data in standardized Talairach space
Collins, D. L., Neelin, P., Peters, T. M., & Evans, A. C. (1994) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199403000-00005 · Cited by 3,431
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-citation
Improved Localizadon of Cortical Activity by Combining EEG and MEG with MRI Cortical Surface Reconstruction: A Linear Approach
Dale, A. M., & Sereno, M. I. (1993) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1993.5.2.162 · Cited by 2,003
Self-citation
The neural mechanisms of top-down attentional control
Hopfinger, J. B., Buonocore, M. H., & Mangun, G. R. (2000) · Nature Neuroscience · doi:10.1038/72999 · Cited by 1,876
Voluntary orienting is dissociated from target detection in human posterior parietal cortex
Corbetta, M., Kincade, J. M., Ollinger, J. M., McAvoy, M. P., & Shulman, G. L. (2000) · Nature Neuroscience · doi:10.1038/73009 · Cited by 1,816
The parietal lobes
Critchley, M. (1966) · Medical Entomology and Zoology · Cited by 1,416

Flagged first, then by citations

Show all 42 references

Research works printed but not linked: 3

Kleist K., Ergeb. Neurol. Psychiatr. 1, 342 (1916).
Andersen R. A., Snyder L. H., Batista A. P., Buneo C. A., Cohen Y. E., Novartis Found. Symp. 218, 109 (1998).
]. Although the names “V3” and “V3A” were taken from macaque monkeys the functional and anatomical properties of the human areas differ from their macaque monkey namesakes. The strong response to motion and the heavy myelination of human V3A [see figure 5 in M. I. Sereno J. M. Allman in The Neural Basis of Visual Function A. Leventhal Ed. (Macmillan London 1991) pp. 160–172 and figure 8 in R. B. H. Tootell J. B. Taylor Cereb. Cortex 1995 5 39 (1995): labeled “possible/presumptive MT” in both instances] recall the direction selectivity and myelination of lower field–only macaque monkey V3 rather than macaque monkey V3A. Owl monkeys also have a dorsal heavily myelinated direction-selective area DM [

Sorted by citations

Items 301–400 of 681

Decoding Trans-Saccadic Memory
Edwards, G., VanRullen, R., & Cavanagh, P. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0854-17.2017 · Cited by 40
Visual processing, learning and feedback in the primate eye movement system
Trommershäuser, J., Glimcher, P. W., & Gegenfurtner, K. R. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.07.004 · Cited by 43
Endoscopic eye tracking system for fMRI
Kanowski, M., Rieger, J. W., Noesselt, T., Tempelmann, C., & Hinrichs, H. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.08.001 · Cited by 44
The Attentional Field Revealed by Single-Voxel Modeling of fMRI Time Courses
Puckett, A. M., & DeYoe, E. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3754-14.2015 · Cited by 48
Two forms of touch perception in the human brain
Spitoni, G. F., Galati, G., Antonucci, G., Haggard, P., & Pizzamiglio, L. (2010) · Experimental Brain Research · doi:10.1007/s00221-010-2446-5 · Cited by 44
Human intraparietal sulcus (IPS) and competition between exogenous and endogenous saccade plans
Anderson, E. J., Husain, M., & Sumner, P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.10.046 · Cited by 49
Exploring cross-linguistic vocabulary effects on brain structures using voxel-based morphometry
Green, D. W., Crinion, J., & Price, C. J. (2007) · Bilingualism Language and Cognition · doi:10.1017/s1366728907002933 · Cited by 46
Spatio-Temporal Brain Mapping of Motion-Onset VEPs Combined with fMRI and Retinotopic Maps
Pitzalis, S., Strappini, F., Gasperis, M. D., Bultrini, A., & Russo, F. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035771 · Cited by 43
Self-citation
Attention allocation before antisaccades
Klapetek, A., Jonikaitis, D., & Deubel, H. (2016) · Journal of Vision · doi:10.1167/16.1.11 · Cited by 43
Salience maps in parietal cortex: Imaging and computational modeling
Roggeman, C., Fias, W., & Verguts, T. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.060 · Cited by 41
Can IPS reach visual awareness without V1? Evidence from TMS in healthy subjects and hemianopic patients
Mazzi, C., Mancini, F., & Savazzi, S. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.09.026 · Cited by 42
Distinct representations for shifts of spatial attention and changes of reward contingencies in the human brain
Tosoni, A., Shulman, G. L., Pope, A. L. W., McAvoy, M. P., & Corbetta, M. (2012) · Cortex · doi:10.1016/j.cortex.2012.03.022 · Cited by 42
The impact of top-down spatial attention on laterality and hemispheric asymmetry in the human parietal cortex
Jeong, S. K., & Yaoda Xu, A. (2016) · Journal of Vision · doi:10.1167/16.10.2 · Cited by 42
Mnemonic Encoding and Cortical Organization in Parietal and Prefrontal Cortices
Masse, N. Y., Hodnefield, J. M., & Freedman, D. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3903-16.2017 · Cited by 40
Suppression of brain activity related to a car-following task with an auditory task: An fMRI study
Uchiyama, Y., Toyoda, H., Sakai, H., Shin, D., Ebe, K., & Sadato, N. (2011) · Transportation Research Part F Traffic Psychology and Behaviour · doi:10.1016/j.trf.2011.11.002 · Cited by 42
Integration of Multiple Motion Vectors Over Space: An fMRI Study of Transparent Motion Perception
Muckli, L. F. (2002) · NeuroImage · doi:10.1006/nimg.2002.1085 · Cited by 42
The Microstructure of Attentional Control in the Dorsal Attention Network
Rajan, A., Meyyappan, S., Liu, Y., Samuel, I. B. H., Nandi, B., Mangun, G. R., & Ding, M. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01710 · 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
Self-citation
Mapping subcomponents of numerical cognition in relation to functional and anatomical landmarks of human parietal cortex
Castaldi, E., Vignaud, A., & Eger, E. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117210 · Cited by 43
Structural connectivity of visuotopic intraparietal sulcus
Bray, S., Arnold, A. E. G. F., Iaria, G., & MacQUEEN, G. M. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.080 · Cited by 42
Delayed match to object or place: An event-related fMRI study of short-term stimulus maintenance and the role of stimulus pre-exposure
Schön, K., Tinaz, S., Somers, D. C., & Stern, C. E. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.023 · Cited by 39
TMS Over the Intraparietal Sulcus Induces Perceptual Fading
Kanai, R., Muggleton, N. G., & Walsh, V. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90885.2008 · Cited by 42
Hemispheric Asymmetry in Memory-Guided Pointing During Single-Pulse Transcranial Magnetic Stimulation of Human Parietal Cortex
Vesia, M., Monteon, J. A., Sergio, L. E., & Crawford, J. D. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00411.2006 · Cited by 41
Dissociable Roles of Dorsolateral Prefrontal Cortex and Frontal Eye Fields During Saccadic Eye Movements
Cameron, I. G. M., Riddle, J., & D’Esposito, M. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00613 · Cited by 45
A putative human homologue of the macaque area PEc
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
Self-citation
Attention maps in the brain
Somers, D. C., & Sheremata, S. (2013) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1230 · Cited by 41
Delta-Band Oscillations in Motor Regions Predict Hand Selection for Reaching
Hamel-Thibault, A., Thénault, F., Whittingstall, K., & Bernier, P. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw392 · Cited by 40
Predicting eye movement patterns from fMRI responses to natural scenes
O’Connell, T. P., & Chun, M. M. (2018) · Nature Communications · doi:10.1038/s41467-018-07471-9 · Cited by 39
Functional clusters in the human parietal cortex as revealed by an observer-independent meta-analysis of functional activation studies
Nickel, J., & Seitz, R. J. (2005) · Anatomy and Embryology · doi:10.1007/s00429-005-0037-1 · Cited by 39
Visuospatial perspective taking in a dynamic environment: Perceiving moving objects from a first-person-perspective induces a disposition to act
Kockler, H., Scheef, L., Tepest, R., David, N., Bewernick, B. H., Newen, A., Schild, H. H., May, M., & Vogeley, K. (2010) · Consciousness and Cognition · doi:10.1016/j.concog.2010.03.003 · Cited by 37
Visual Short-Term Memory Activity in Parietal Lobe Reflects Cognitive Processes beyond Attentional Selection
Sheremata, S., Somers, D. C., & Shomstein, S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1716-17.2017 · Cited by 37
Interhemispheric transfer of phosphenes generated by occipital versus parietal transcranial magnetic stimulation
Marzi, C. A., Mancini, F., & Savazzi, S. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1496-4 · Cited by 37
The Evolution of the Parietal Lobes in the Genus Homo
Bruner, E., Amano, H., Pereira‐Pedro, A. S., & Ogihara, N. (2017) · Springer eBooks · doi:10.1007/978-4-431-56582-6_15 · Cited by 36
Frontal-to-Parietal Top-Down Causal Streams along the Dorsal Attention Network Exclusively Mediate Voluntary Orienting of Attention
Ozaki, T. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020079 · Cited by 41
Cortical Connections of the Caudal Portion of Posterior Parietal Cortex in Prosimian Galagos
Stepniewska, I., Cerkevich, C. M., & Kaas, J. H. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv132 · Cited by 37
Altered processing of corollary discharge in thalamic lesion patients
Bellebaum, C., Hoffmann, K., Koch, B., Schwarz, M., & Daum, I. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05114.x · Cited by 35
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-citation
Visual Field Map Organization in Human Visual Cortex
Alyssa, A., & Barto, B. (2012) · InTech eBooks · doi:10.5772/51914 · Cited by 36
Cytoarchitectonic mapping of attentional selection and reorienting in parietal cortex
Gillebert, C. R., Mantini, D., Peeters, R. R., Dupont, P. J., & Vandenberghe, R. R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.11.026 · Cited by 39
Memory Accumulation Mechanisms in Human Cortex Are Independent of Motor Intentions
Sestieri, C., Tosoni, A., Mignogna, V., McAvoy, M. P., Shulman, G. L., Corbetta, M., & Romani, G. L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3911-13.2014 · Cited by 33
Egomotion‐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
Self-citation
Functional dissociation of saccade and hand reaching control with bilateral lesions of the medial wall of the intraparietal sulcus: Implications for optic ataxia
Trillenberg, P., Sprenger, A., Petersen, D., Kömpf, D., Heide, W., & Helmchen, C. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.038 · Cited by 35
Areas activated during naturalistic reading comprehension overlap topological visual, auditory, and somatotomotor maps
Sood, M. R., & Sereno, M. I. (2016) · Human Brain Mapping · doi:10.1002/hbm.23208 · Cited by 34
Self-citation
Spatial re-orienting of visual attention along the horizontal or the vertical axis
Macaluso, E., & Patria, F. (2007) · Experimental Brain Research · doi:10.1007/s00221-006-0841-8 · Cited by 34
Horizontal space misrepresentation in unilateral brain damage
Doricchi, F., Galati, G., DeLuca, L., Nico, D., & D’Olimpio, F. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00010-6 · Cited by 34
Long-term stress and trait anxiety affect brain network balance in dynamic cognitive computations
Liu, L., Wu, J., Geng, H., Liu, C., Luo, Y., Luo, J., & Qin, S. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab393 · Cited by 40
Understanding location- and feature-based processing along the human intraparietal sulcus
Bettencourt, K. C., & Yaoda Xu, A. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00404.2016 · Cited by 33
Common capacity-limited neural mechanisms of selective attention and spatial working memory encoding
Fusser, F., Linden, D., Rahm, B., Hampel, H., Haenschel, C., & Mayer, J. S. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07794.x · Cited by 38
Numerical and Spatial Intuitions: A Role for Posterior Parietal Cortex?
Hubbard, E. M., Manuela Piazza, A., Pinel, P., & Dehaene, S. (2009) · The MIT Press eBooks · doi:10.7551/mitpress/9780262012935.003.0201 · Cited by 38
Differences between Spatial and Visual Mental Representations
Sima, J. F., Schultheis, H., & Barkowsky, T. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00240 · Cited by 32
Thalamo-cortical coupling during encoding and consolidation is linked to durable memory formation
Wagner, I. C., van Buuren, M., & Fernández, G. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.04.055 · Cited by 34
Decision and action planning signals in human posterior parietal cortex during delayed perceptual choices
Tosoni, A., Corbetta, M., Calluso, C., Committeri, G., Pezzulo, G., Romani, G. L., & Galati, G. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12511 · Cited by 33
The Noninvasive Dissection of the Human Visual Cortex: Using fMRI and TMS to Study the Organization of the Visual Brain
McKeefry, D. J., Gouws, A. D., Burton, M. P., & Morland, A. B. (2009) · The Neuroscientist · doi:10.1177/1073858409334424 · Cited by 32
Retinotopic organization of extrastriate cortex in the owl monkey—dorsal and lateral areas
Sereno, M. I., MCDONALD, C. T., & Allman, J. M. (2015) · Visual Neuroscience · doi:10.1017/s0952523815000206 · Cited by 32
Self-citation
Spatiotopic updating across saccades revealed by spatially-specific fMRI adaptation
Fairhall, S. L., Schwarzbach, J. V., Lingnau, A., van Koningsbruggen, M. G., & Melcher, D. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.071 · Cited by 31
Mental imagery can generate and regulate acquired differential fear conditioned reactivity
Greening, S. G., Lee, T., Burleigh, L. M., Grégoire, L., Robinson, T., Jiang, X., Mather, M., & Kaplan, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-05019-y · Cited by 35
(Con)text-specific effects of visual dysfunction on reading in posterior cortical atrophy
Yong, K. X. X., Shakespeare, T. J., Cash, D. M., Henley, S. M. D., Warren, J. D., & Crutch, S. J. (2014) · Cortex · doi:10.1016/j.cortex.2014.03.010 · Cited by 31
Time course of cross-hemispheric spatial updating in the human parietal cortex
Bellebaum, C., & Daum, I. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.01.001 · Cited by 32
Cortical Temporal Dynamics of Visually Guided Behavior
Hinkley, L. B. N., Nagarajan, S. S., Dalal, S. S., Guggisberg, A. G., & Disbrow, E. A. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq102 · Cited by 29
Neural Substrates Underlying the Passive Observation and Active Control of Translational Egomotion
Huang, R., Chen, C., & Sereno, M. I. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2647-14.2015 · Cited by 30
Self-citation
Interaction between gaze and visual and proprioceptive position judgements
Fiehler, K., Rösler, F., & Henriques, D. Y. P. (2010) · Experimental Brain Research · doi:10.1007/s00221-010-2251-1 · Cited by 29
Individual variation in the location of the parietal eye fields: a TMS study
Ryan, S., Bonilha, L., & Jackson, S. R. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0379-9 · Cited by 30
An investigation of positive and inverted hemodynamic response functions across multiple visual areas
Puckett, A. M., Mathis, J. R., & DeYoe, E. A. (2014) · Human Brain Mapping · doi:10.1002/hbm.22569 · Cited by 29
Cortical Functional Anatomy of Voluntary Saccades in Parkinson Disease
Rieger, J. W., Kim, A., Árgyelán, M., Farber, M., Glazman, S., Liebeskind, M., Meyer, T., & Bodis-Wollner, I. G. (2008) · Clinical EEG and Neuroscience · doi:10.1177/155005940803900404 · Cited by 29
Possible Role of Dendritic Compartmentalization in the Spatial Working Memory Circuit
Morita, K. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0059-08.2008 · Cited by 31
Attending to Moving Objects
Holcombe, A. O. (2023) · Cambridge University Press eBooks · doi:10.1017/9781009003414 · Cited by 31
TMS Over the Right Precuneus Reduces the Bilateral Field Advantage in Visual Short Term Memory Capacity
Kraft, A., Dyrholm, M., Kehrer, S., Kaufmann, C., Brüning, J., Kathmann, N., Bundesen, C., Irlbacher, K., & Brandt, S. A. (2014) · Brain stimulation · doi:10.1016/j.brs.2014.11.004 · Cited by 28
The retention of simultaneous tones in auditory short-term memory: A magnetoencephalography study
Nolden, S., Grimault, S., Guimond, S., Lefebvre, C., Bermudez, P., & Jolicœur, P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.002 · Cited by 28
ERP correlates of anticipatory attention: spatial and non-spatial specificity and relation to subsequent selective attention
Dale, C. L., Simpson, G. V., Foxe, J. J., Luks, T. L., & Worden, M. S. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1338-4 · Cited by 28
Optic ataxia as a model to investigate the role of the posterior parietal cortex in visually guided action: evidence from studies of patient M.H.
Cavina‐Pratesi, C., Connolly, J. D., & Milner, A. D. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00336 · Cited by 37
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
Global versus local: double dissociation between MT+ and V3A in motion processing revealed using continuous theta burst transcranial magnetic stimulation
Cai, P., Chen, N., Zhou, T., Thompson, B. S., & Fang, F. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-4084-9 · Cited by 29
Non-retinotopic feature integration decreases response-locked brain activity as revealed by electrical neuroimaging
Plomp, G., Mercier, M. R., Otto, T. U., Blanke, O., & Herzog, M. H. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.031 · Cited by 28
Synchronous retinotopic frontal–temporal activity during long-term memory for spatial location
Slotnick, S. D. (2010) · Brain Research · doi:10.1016/j.brainres.2010.03.051 · Cited by 26
Functional magnetic resonance imaging of sensorimotor transformations in saccades and antisaccades
Herweg, N. A., Weber, B., Kasparbauer, A., Meyhöfer, I., Steffens, M., Smyrnis, N., & Ettinger, U. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.08.033 · Cited by 29
Predicting the retinotopic organization of human visual cortex from anatomy using geometric deep learning
Ribeiro, F. L., Bollmann, S., & Puckett, A. M. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118624 · Cited by 27
The Temporal Evolution of Electromagnetic Markers Sensitive to the Capacity Limits of Visual Short-Term Memory
Mitchell, D. J., & Cusack, R. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00018 · Cited by 26
The Place Code of Saccade Metrics in the Lateral Bank of the Intraparietal Sulcus
Savaki, H. E., Gregoriou, G. G., Bakola, S., Raos, V., & Moschovakis, A. K. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2268-09.2010 · Cited by 25
Retinotopic maps and hemodynamic delays in the human visual cortex measured using arterial spin labeling
Çavuşoğlu, M., Bartels, A., Yesilyurt, B., & Uludaǧ, K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.056 · Cited by 28
Eye position modulates retinotopic responses in early visual areas: a bias for the straight-ahead direction
Strappini, F., Pitzalis, S., Snyder, A. Z., McAvoy, M. P., Sereno, M. I., Corbetta, M., & Shulman, G. L. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0808-7 · Cited by 27
Self-citation
Categorical evidence, confidence, and urgency during probabilistic categorization
Braunlich, K., & Seger, C. A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.011 · Cited by 24
Differential contributions to the interception of occluded ballistic trajectories by the temporoparietal junction, area hMT/V5+, and the intraparietal cortex
Monache, S. D., Lacquaniti, F., & Bosco, G. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00068.2017 · Cited by 23
Neuroanatomical correlates of peripersonal space: bridging the gap between perception, action, emotion and social cognition
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
“A human homologous of monkey’s LIP has been identified by using retinotopic mapping and has been impli - cated in gaze-centered updating of visual space (Sereno et al. 2001; Medendorp et al. 2003), as well as in response to looming visuo-tactile stimuli (Huang et al. 2018).”
Representation of Eye Position in the Human Parietal Cortex
Williams, A. L., & Smith, A. T. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00713.2009 · Cited by 22
View-Independent Working Memory Representations of Artificial Shapes in Prefrontal and Posterior Regions of the Human Brain
Christophel, T. B., Allefeld, C., Endisch, C., & Haynes, J. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx119 · Cited by 25
Biased Neural Representation of Feature-Based Attention in the Human Frontoparietal Network
Gong, M., & Liu, T. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0690-20.2020 · Cited by 26
Variation in functional connectivity along anterior-to-posterior intraparietal sulcus, and relationship with age across late childhood and adolescence
Vinette, S. A., & Bray, S. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.04.004 · Cited by 26
A hemodynamic correlate of lateralized visual short-term memories
Cutini, S., Scarpa, F., Scatturin, P., Jolicœur, P., Pluchino, P., Zorzi, M., & Dell’Acqua, R. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.12.009 · Cited by 22
Mapping 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-citation
Neural Determinants of Task Performance during Feature-Based Attention in Human Cortex
Jigo, M., Gong, M., & Liu, T. (2018) · eNeuro · doi:10.1523/eneuro.0375-17.2018 · Cited by 23
The Saccadic Re-Centering Bias is Associated with Activity Changes in the Human Superior Colliculus
Krebs, R. M., Schoenfeld, M. A., Boehler, C. N., Song, A. W., & Woldorff, M. G. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00193 · Cited by 23
Visual Mental Imagery
Ganis, G. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5879-1_2 · Cited by 22
Saccades to a Remembered Location Elicit Spatially Specific Activation in Human Retinotopic Visual Cortex
Geng, J. J., Ruff, C. C., & Driver, J. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21025 · Cited by 23
Dynamic representations of visual space for perception and action
Medendorp, W. P., de Brouwer, A. J., & Smeets, J. B. J. (2016) · Cortex · doi:10.1016/j.cortex.2016.11.013 · Cited by 22
Separating memoranda in depth increases visual working memory performance
Chunharas, C., Rademaker, R. L., Sprague, T. C., Brady, T. F., & Serences, J. T. (2019) · Journal of Vision · doi:10.1167/19.1.4 · Cited by 22
Spatiotemporal characteristics of perceptual decision making in the human brain
Philiastides, M. G., & Heekeren, H. R. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.00008-x · Cited by 24
Neural Resources Associated with Perceptual Judgment across Sensory Modalities
Yang, J., Szeverenyi, N. M., & Ts’o, D. Y. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm029 · Cited by 23
Gradients of functional organization in posterior parietal cortex revealed by visual attention, visual short-term memory, and intrinsic functional connectivity
Lefco, R. W., Brissenden, J. A., Noyce, A. L., Tobyne, S. M., & Somers, D. C. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117029 · Cited by 21
On the Emergence of Primary Visual Perception
Pollen, D. A. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq285 · Cited by 22
Adaptive smoothing based on Gaussian processes regression increases the sensitivity and specificity of fMRI data
Strappini, F., Gilboa, E., Pitzalis, S., Kay, K., McAvoy, M. P., Nehorai, A., & Snyder, A. Z. (2016) · Human Brain Mapping · doi:10.1002/hbm.23464 · Cited by 21
Self-citation

Authors: Sereno, M. I., Pitzalis, S., & Martinez, A.
Affiliations: University of California San Diego (US)
Department of Cognitive Science,
Department of Radiology, University of California, San Diego, La Jolla, CA 92093-0515, USA.
Corresponding author: Sereno, M. I.
Pitzalis, S.
ORCID: Sereno, M. I.
Pitzalis, S.
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 2001-11-09
Volume: 294
Issue: 5545
Pages: 1350-1354
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.1063695
OpenAlex: W1967533781
Cited by: 682
References: 42
Citations by year: 2026: 9 · 2025: 9 · 2024: 20 · 2023: 14 · 2022: 14 · 2021: 19 · 2020: 14 · 2019: 22 · 2018: 20 · 2017: 22 · 2016: 27 · 2015: 24 · 2014: 34 · 2013: 34 · 2012: 40
FWCI: 8.57
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Funders: National Institute of Mental Health (MH-25594)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD 22614, R01HD022614)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Spatial Neglect and Hemispheric Dysfunction
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Keywords: retinotopic mapping, parietal cortex, superior parietal cortex, lateral intraparietal area, visual working memory, eccentricity, functional mapping
MeSH terms: Brain Mapping, Fixation, Ocular, Humans, Magnetic Resonance Imaging, Memory, Parietal Lobe, Saccades, Visual Cortex, Visual Pathways, Visual Perception, Echo-Planar Imaging

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

Mapping of Contralateral Space in Retinotopic Coordinates by a Parietal Cortical Area in Humans

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks