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
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.
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
“A human homologous of monkey’s LIP has been identified by using retinotopic mapping and has been implicated 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).”
From Neuroanatomical correlates of peripersonal space: bridging the gap between perception, action, emotion and social cognition (2024) · cites this paper as Sereno et al. 2001
Citations
Cites
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-citationDistributed 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-citationPreface: 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-citationDale, A. M., & Sereno, M. I. (1993) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1993.5.2.162 · Cited by 2,003
Self-citationThe 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
Critchley, M. (1966) · Medical Entomology and Zoology · Cited by 1,416
Flagged first, then by citations
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 [
Cited by
Sorted by citations
Items 501–600 of 681
Shape effects on reflexive spatial attention are driven by the dorsal stream
Red, S. D., Patel, S. S., & Sereno, A. B. (2012) · Vision Research · doi:10.1016/j.visres.2011.12.007 · Cited by 8
Gong, M., & Liu, T. (2019) · Cognitive Neuroscience · doi:10.1080/17588928.2019.1601074 · Cited by 8
Aberrant visual population receptive fields in human albinism
Duwell, E. J., Woertz, E. N., Mathis, J. R., Carroll, J., & DeYoe, E. A. (2021) · Journal of Vision · doi:10.1167/jov.21.5.19 · Cited by 8
Causal manipulation of gaze-following in the macaque temporal cortex
Chong, I. D., Ramezanpour, H., & Thier, P. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102466 · Cited by 7
Subregions of human parietal cortex selectively encoding object orientation
Aso, T., Hanakawa, T., Matsuo, K., Toma, K., Shibasaki, H., Fukuyama, H., & Nakai, T. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.01.051 · Cited by 8
Losing our Brainless Minds: How Neuroimaging Informs Cognition
Jack, A. I., Sylvester, C. M., & Corbetta, M. (2006) · Cortex · doi:10.1016/s0010-9452(08)70373-3 · Cited by 8
Retinotopy and attention to the face and house images in the human visual cortex
Wang, B., Yan, T., Ohno, S., Kanazawa, S., & Wu, J. (2016) · Experimental Brain Research · doi:10.1007/s00221-016-4562-3 · Cited by 8
Guidotti, R., Tosoni, A., & Sestieri, C. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02124-4 · Cited by 8
Hand Use and the Evolution of Posterior Parietal Cortex in Primates
Hinkley, L. B. N., Padberg, J., Krubitzer, L. A., & Disbrow, E. A. (2007) · Elsevier eBooks · doi:10.1016/b0-12-370878-8/00040-9 · Cited by 8
Computational Neuroimaging : Color Signals in the Visual Pathways
Wandell, B. A., Dumoulin, S. O., & Brewer, A. A. (2006) · 神経眼科 = Neuro-ophthalmology Japan · Cited by 8
Sulpizio, V., Teghil, A., Pitzalis, S., & Boccia, M. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02790-8 · Cited by 7
Self-citationLeft-right compatibility in the processing of trading verbs
Vicario, C. M., & Rumiati, R. I. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00016 · Cited by 7
Intermodal attention modulates visual processing in dorsal and ventral streams
Cate, A. D., Herron, T. J., Kang, X., Yund, E. W., & Woods, D. L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.026 · Cited by 7
Gaze-Dependent Topography in Human Posterior Parietal Cortex
Connolly, J. D., Vuong, Q. C., & Thiele, A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht344 · Cited by 7
What counts in estimation? The nature of the preverbal system
Karolis, V. R., & Butterworth, B. L. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.04.025 · Cited by 7
The maintenance and updating of representations of no longer visible objects and their parts
McCarthy, J. D., Erlikhman, G., & Caplovitz, G. P. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2017.07.010 · Cited by 7
Nee, D. E., & D'Esposito, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00050-6 · Cited by 6
Patterns of Activity in the Human Frontal and Parietal Cortex Differentiate Large and Small Saccades
Grosbras, M. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00034 · Cited by 7
Quantifying spatial uncertainty of visual area boundaries in neuroimaging data
Kirson, D., Huk, A. C., & Cormack, L. K. (2008) · Journal of Vision · doi:10.1167/8.10.10 · Cited by 7
The “Diagonal Effect”: a Systematic Error in Oblique Antisaccades
Koehn, J. D., Roy, E., & Barton, J. J. S. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90268.2008 · Cited by 7
Underestimation of contralateral space in neglect: a deficit in the “where” task
Pitzalis, S., Russo, F. D., Figliozzi, F., & Spinelli, D. (2004) · Experimental Brain Research · doi:10.1007/s00221-004-1954-6 · Cited by 6
Self-citationKalberlah, C., Chen, Y., Heinzle, J., & Haynes, J. (2011) · International Journal of Imaging Systems and Technology · doi:10.1002/ima.20278 · Cited by 6
Diffeomorphic Smoothing for Retinotopic Mapping
Tu, Y., Tal, D., Lu, Z., & Wang, Y. (2020) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi45749.2020.9098316 · Cited by 6
Bencivenga, F., Tullo, M. G., Maltempo, T., von Gal, A., Serra, C., Pitzalis, S., & Galati, G. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac223 · Cited by 7
Self-citationYamamoto, H., Ban, H., Fukunaga, M., Tanaka, C., Umeda, M., & Ejima, Y. (2008) · Institutional Repositories DataBase (IRDB) · Cited by 6
Domijan, D. (2011) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-011-0054-x · Cited by 6
Probing the architecture of visual number sense with parietal tRNS
Karolis, V. R., Grinyaev, M., Epure, A., Tsoy, V., Rietz, E. D., Banissy, M. J., Cappelletti, M., & Kovas, Y. V. (2018) · Cortex · doi:10.1016/j.cortex.2018.08.030 · Cited by 6
Developmental Plasticity: FMRI Investigations into Human Visual Cortex
Brewer, A. A., & Barton, B. (2014) · InTech eBooks · doi:10.5772/58277 · Cited by 6
Marigold, D. S. (2006) · UWSpace (University of Waterloo) · Cited by 6
Comparing brain connections in different species using diffusion weighted imaging
Rushworth, M. F. S., Boorman, E., & Mars, R. B. (2009) · Diffusion MRI · doi:10.1016/b978-0-12-374709-9.00020-1 · Cited by 5
Arsenovic, A., Ischebeck, A. K., & Zaretskaya, N. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0723-22.2022 · Cited by 6
Visual loss alters multisensory face maps in humans
Pasqualotto, A., Furlan, M., Proulx, M. J., & Sereno, M. I. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1713-2 · Cited by 5
Self-citationEgomotion-related visual areas respond to goal-directed movements
Bellagamba, M., Sulpizio, V., Fattori, P., Galati, G., Galletti, C., Maltempo, T., & Pitzalis, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02523-9 · Cited by 5
Self-citationDeYoe, E. A., Ulmer, J. L., Mueller, W. M., Hacein‐Bey, L., Szeder, V., Maciejewski, M. J., Medler, K. A., Reitsma, D., & Mathis, J. R. (2011) · Springer eBooks · doi:10.1007/978-1-4419-0345-7_26 · Cited by 6
Viewed actions are mapped in retinotopic coordinates in the human visual pathways
Porat, Y., Pertzov, Y., & Zohary, E. (2011) · Journal of Vision · doi:10.1167/11.12.17 · Cited by 5
Asscheman, S. J., Thakkar, K. N., & Neggers, S. F. W. (2015) · Journal of Experimental Neuroscience · doi:10.4137/jen.s32736 · Cited by 5
Spatial Organization of Magnitude in the Representation of Number and Emotion
Holmes, K. J., & Lourenco, S. F. (2009) · eScholarship (California Digital Library) · Cited by 5
Auditory‐visual integration modulates location‐specific repetition suppression of auditory responses
Shrem, T., Murray, M. M., & Deouell, L. Y. (2017) · Psychophysiology · doi:10.1111/psyp.12955 · Cited by 5
Vandenberghe, R. R., & Gillebert, C. R. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00040-3 · Cited by 6
Visual Processing in the Primate Brain
Baker, C. I. (2012) · Wiley eBooks · doi:10.1002/9781118133880.hop203004 · Cited by 6
Saccades influence functional modularity in the human cortical vision network
Tomou, G., Baltaretu, B. R., Ghaderi, A., & Crawford, J. D. (2025) · Scientific Reports · doi:10.1038/s41598-025-95568-9 · Cited by 6
Neuroimaging evidence for the direct role of auditory scene analysis in object perception
Gurariy, G., Randall, R., & Greenberg, A. S. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac501 · Cited by 4
I know where you'll look: an fMRI study of oculomotor intention and a change of motor plan
Kleiser, R., Konen, C. S., Seitz, R. J., & Bremmer, F. (2009) · Behavioral and Brain Functions · doi:10.1186/1744-9081-5-27 · Cited by 4
Differential parietal activations for spatial remapping and saccadic control in a visual memory task
Pierce, J. E., Saj̈, A., & Vuilleumier, P. O. (2019) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2019.05.010 · Cited by 4
Bells, S., Isabella, S. L., Brien, D. C., Coe, B. C., Munoz, D. P., Mabbott, D., & Cheyne, D. (2020) · Human Brain Mapping · doi:10.1002/hbm.24922 · Cited by 6
Navigating in a Three-Dimensional World
Jeffery, K. J. (2011) · The MIT Press eBooks · doi:10.7551/mitpress/9780262016636.003.0003 · Cited by 6
Dissociations within Association Cortex
Culham, J. C. (2002) · Neuron · doi:10.1016/s0896-6273(02)00584-6 · Cited by 4
Vohryzek, J., Cabral, J., Timmermann, C., Atasoy, S., Roseman, L., Nutt, D. J., Carhart-Harris, R. L., Deco, G., & Kringelbach, M. L. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.20.554019 · Cited by 4
Luzio, P. D., Tarasi, L., Avenanti, A., Silvanto, J., Sel, A., & Romei, V. (2026) · Communications Biology · doi:10.1038/s42003-026-10770-3 · Cited by 4
Using fMRI to examine nonlinear mixed selectivity tuning to task and category in the human brain
Taylor, J., & Xu, Y. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00354 · Cited by 4
Spatial Constraints in Multisensory Attention
Macaluso, E. (2011) · Frontiers in neuroscience · doi:10.1201/9781439812174-32 · Cited by 3
Functional Imaging of the Human Visual System
Orban, G. A., & Ferri, S. (2016) · Neuromethods · doi:10.1007/978-1-4939-5611-1_18 · Cited by 3
Choy, E. E. H., & Cheung, H. (2017) · Cognitive Processing · doi:10.1007/s10339-017-0817-6 · Cited by 3
Aberrant Visual Population Receptive Fields in Human AlbinismPreprint
Duwell, E. J., Woertz, E. N., Mathis, J., Carroll, J., & DeYoe, E. A. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/572289 · Cited by 3
Ribeiro, F. L., Bollmann, S., & Puckett, A. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.11.934471 · Cited by 4
Liu, L.-Y., Wu, J.-H., Geng, H.-Y., Liu, C., Luo, Y.-J., Luo, J., & Qin, S. (2021) · bioRxiv · doi:10.1101/2021.05.07.442883 · Cited by 1
A neural substrate for Bayesian integration in human parietal cortexPreprint
Singletary, N. M., Gottlieb, J. P., & Horga, G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.30.466508 · Cited by 3
Neural Correlates of High-Level Visual Saliency ModelsPreprint
Kroner, A., Senden, M., & Goebel, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.29.551075 · Cited by 3
Chandra, S., Khona, M., Konkle, T., & Fiete, I. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.07.574543 · Cited by 5
Cortical field maps across human sensory cortex
Brewer, A. A., & Barton, B. (2023) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2023.1232005 · Cited by 4
Linking cortical surface area to computational properties in human visual perception
Murray, S. O., Kolodny, T., & Webb, S. J. (2024) · iScience · doi:10.1016/j.isci.2024.110490 · Cited by 2
EEG Inner Speech Classification Using Machine Learning Cascade Model
Ekizyan, A. K., Shaposhnikov, P. D., Kostulin, D. V., Shevchenko, I. G., & Shaposhnikov, D. G. (2025) · Studies in computational intelligence · doi:10.1007/978-3-031-80463-2_27 · Cited by 2
Normal Alert Consciousness: A Central Executive Model of Hippocampal Function
Burman, D. D. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.111569 · Cited by 3
Schultheis, H., & Barkowsky, T. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x13000551 · Cited by 2
Functional MRI of the Visual System
Dumoulin, S. O. (2015) · Biological magnetic resonance · doi:10.1007/978-1-4899-7591-1_15 · Cited by 4
Comparing Connections in the Brains of Humans and Other Primates Using Diffusion-Weighted Imaging
Rushworth, M. F. S., Sallet, J., Boorman, E. D., & Mars, R. B. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-396460-1.00024-x · Cited by 2
Cloverleaf Clusters: A Common Macrostructural Organization across Human Visual and Auditory Cortex
Brewer, A. A., & Barton, B. (2018) · InTech eBooks · doi:10.5772/intechopen.77964 · Cited by 2
The spatial properties of adaptation-induced distance compression
Jovanović, L., McGraw, P. V., Roach, N. W., & Johnston, A. (2022) · Journal of Vision · doi:10.1167/jov.22.11.7 · Cited by 2
Brain mapping of attention and neglect after stroke
Carter, A. R., Shulman, G. L., & Corbetta, M. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511777547.014 · Cited by 2
Smith, A. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01860-x · Cited by 2
Die multimodale Untersuchung kognitiver Prozesse der Mentalen Rotation
Paschke, K. (2012) · doi:10.53846/goediss-1147 · Cited by 2
Transforming bottom-up topographic representations with top-down signals in the brain
Tinsley, C. J. (2007) · Biosystems · doi:10.1016/j.biosystems.2007.05.006 · Cited by 2
Understanding economical outcomes with the mental number linePreprint
Vicario, C. M. (2011) · Nature Precedings · doi:10.1038/npre.2011.5775.1 · Cited by 2
Spatial Remapping Mechanisms and their impairments in patients with right parietal lesions
Bucher, L. (2008) · doi:10.5282/edoc.9647 · Cited by 2
A fronto-temporo-parietal network disambiguates potential objects of joint attentionPreprint
Kraemer, P. M., Görner, M., Ramezanpour, H., Dicke, P. W., & Thier, P. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/542555 · Cited by 2
Biased neural representation of feature-based attention in the human brainPreprint
Gong, M., & Liu, T. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/688226 · Cited by 2
Bayesian Semiparametric Longitudinal Drift-Diffusion Mixed Models for Tone Learning in Adults
Paulon, G., Llanos, F., Chandrasekaran, B., & Sarkar, A. (2021) · Figshare · doi:10.6084/m9.figshare.12931153 · Cited by 2
Ren, J., Konrad, B. N., Zhu, Y., Li, F., Czisch, M., Dresler, M., & Wagner, I. C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.24.639840 · Cited by 3
Errors in visuospatial working memory across space and time
Jiang, L., & Leung, H. (2021) · Scientific Reports · doi:10.1038/s41598-021-93858-6 · Cited by 1
Funahashi, S. (2022) · Brain science · doi:10.1007/978-981-19-7268-3_5 · Cited by 1
Bakhit, M. S., Hiruta, R., Iwatate, K., & Fujii, M. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae376 · Cited by 1
Functional Imaging of the Human Visual System
Orban, G. A., & Ürgen, B. A. (2025) · Neuromethods · doi:10.1007/978-1-0716-4438-6_19 · Cited by 2
Dual-format attentional template during preparation in human visual cortexPreprint
Chen, Y. K., Liu, T., Jia, K., Theeuwes, J., & Gong, M. (2024) · eLife · doi:10.7554/elife.103425.4 · Cited by 4
Janko, D., Agostino, C. S., Willmes, K., & Knops, A. (2026) · ZDM · doi:10.1007/s11858-026-01777-5 · Cited by 1
Asada, T., Takayama, Y., Oita, J., & Fukuyama, H. (2013) · Neurocase · doi:10.1080/13554794.2012.741254 · Cited by 1
Retinotopy and selective visual attention in humans and computers
Salah, A. A., & Saygın, A. P. (2008) · Signal Processing and Communications Applications Conference (SIU) · doi:10.1109/siu.2008.4632746 · Cited by 1
Bertel, S., Sima, J. F., & Lindner, M. (2009) · National Conference on Artificial Intelligence · Cited by 1
DeYoe, E. A., Ulmer, J. L., Mueller, W. M., Hacein‐Bey, L., Szeder, V., Maciejewski, M. J., Medler, K. A., Reitsma, D., & Mathis, J. R. (2023) · Springer eBooks · doi:10.1007/978-3-031-10909-6_29 · Cited by 1
The development of visual cognition: The emergence of spatial congruency bias
Gao, M., Starks, M. D., Golomb, J. D., & Sloutsky, V. M. (2024) · Developmental Science · doi:10.1111/desc.13482 · Cited by 1
Trevarrow, M. P., Munoz, M. J., Rivera, Y. M., Arora, R., Drane, Q. H., Pal, G. D., Metman, L. V., Goelz, L. C., Corcos, D. M., & David, F. J. (2024) · Physiological Reports · doi:10.14814/phy2.16150 · Cited by 1
Kinesthetic information facilitates saccades towards proprioceptive-tactile targets
Voudouris, D., Goettker, A., Mueller, S., & Fiehler, K. (2016) · Vision Research · doi:10.1016/j.visres.2016.03.008 · Cited by 1
rfDemons: Resting fMRI-Based Cortical Surface Registration Using the BrainSync Transform
Joshi, A. A., Li, J., Chong, M., Akrami, H., & Leahy, R. M. (2018) · Lecture notes in computer science · doi:10.1007/978-3-030-00931-1_23 · Cited by 1
Visual-Motor Integration in the Primate Brain
Hagan, M. A., Wong, Y. T., & Pesaran, B. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.24265-x · Cited by 2
Functional Imaging of the Human Visual System
Orban, G. A., & Kourtzi, Z. (2009) · Neuromethods · doi:10.1007/978-1-60327-919-2_17 · Cited by 1
Reynell, C. (2013) · UCL Discovery (University College London) · Cited by 1
Coding of distributed, topographic and non-specific representations within the brain
Tinsley, C. J. (2008) · Biosystems · doi:10.1016/j.biosystems.2008.02.001 · Cited by 1
Correlated With Saccadic Reaction Time fMRI Activation in the Human Frontal Eye Field Is
Goodale, M. A., Goltz, H. C., Munoz, D. P., Astle, D. E., Nixon, E., Jackson, S. R., Jackson, G. M., Jerde, T. A., Merriam, E. P., Riggall, A. C., et al. (2007) · Cited by 1
Attending to moving objectsPreprint
Holcombe, A. O. (2022) · doi:10.31234/osf.io/c75x4 · Cited by 1
Representation of illusory shapes within the topographic areas of the posterior parietal cortexPreprint
Arsenovic, A., Ischebeck, A. K., & Zaretskaya, N. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.12.488016 · Cited by 1
Vericel, M., Baraduc, P., Duhamel, J., & Wirth, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.06.565451 · Cited by 1
Metadata
- 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.
- Venue
- Science
- Published
- 2001-11-09
- Volume
- 294
- Issue
- 5545
- Pages
- 1350-1354
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- 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