Cited by 1,410

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Dissociation of Object and Spatial Processing Domains in Primate Prefrontal Cortex

Wilson, Fraser A. W., Scalaidhe, Séamas P. Ó., Goldman-Rakic, Patricia S.·1993·Science

Open this paper in CoChat — free account

Abstract

Areas and pathways subserving object and spatial vision are segregated in the visual system. Experiments show that the primate prefrontal cortex is similarly segregated into object and spatial domains. Neurons that code information related to stimulus identity are dissociable, both by function and region, from those that code information related to stimulus location. These findings indicate that the prefrontal cortex contains separate processing mechanisms for remembering "what" and "where" an object is.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1126/science.8316836

Cites

4 of 4 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

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
Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685
The functional logic of cortical connections
Zeki, S., & Shipp, S. (1988) · Nature · doi:10.1038/335311a0 · Cited by 1,067
A Neural Mechanism for Working and Recognition Memory in Inferior Temporal Cortex
Miller, E. K., Li, L., & Desimone, R. (1991) · Science · doi:10.1126/science.1962197 · Cited by 706

Show all 4 references

An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803
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
Working memory: Looking back and looking forward
Baddeley, A. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1201 · Cited by 5,200
Emotion, Decision Making and the Orbitofrontal Cortex
Bechara, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.295 · Cited by 3,589
From sensation to cognition
Mesulam, M. (1998) · Brain · doi:10.1093/brain/121.6.1013 · Cited by 3,072
Storage and Executive Processes in the Frontal Lobes
Smith, E. E., & Jonides, J. (1999) · Science · doi:10.1126/science.283.5408.1657 · Cited by 2,834
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
Self-citation
Neuronal Synchrony: A Versatile Code for the Definition of Relations?
Singer, W. (1999) · Neuron · doi:10.1016/s0896-6273(00)80821-1 · Cited by 2,581
The role of prefrontal cortex in working-memory capacity, executive attention, and general fluid intelligence: An individual-differences perspective
Kane, M. J., & Engle, R. W. (2002) · Psychonomic Bulletin & Review · doi:10.3758/bf03196323 · Cited by 2,229
Mechanisms of visual attention in the human cortex
Ungerleider, S. K. A. L. G. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.315 · Cited by 2,159
Basal ganglia and cerebellar loops: motor and cognitive circuits
Middleton, F. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00040-5 · Cited by 1,940
Neuroimaging studies of working memory:
Wager, T. D., & Smith, E. E. (2003) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.3.4.255 · Cited by 1,889
High-resolution EEG mapping of cortical activation related to working memory: effects of task difficulty, type of processing, and practice
Gevins, A. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.4.374 · Cited by 1,623
The Orbitofrontal Cortex and Reward
Rolls, E. T. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.284 · Cited by 1,595
Dissociation in prefrontal cortex of affective and attentional shifts
Dias, R., Robbins, T. W., & Roberts, A. C. (1996) · Nature · doi:10.1038/380069a0 · Cited by 1,527
Inferotemporal cortex and object vision
Tanaka, K. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.000545 · Cited by 1,402
Relative reward preference in primate orbitofrontal cortex
Tremblay, L., & Schultz, W. (1999) · Nature · doi:10.1038/19525 · Cited by 1,314
The functions of the orbitofrontal cortex
Rolls, E. T. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00277-x · Cited by 1,327
The prefrontal landscape: implications of functional architecture for understanding human mentation and the central executive
Goldman-Rakic, P. S. (1996) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1996.0129 · Cited by 1,072
Self-citation
Working memory dysfunction in schizophrenia
(1994) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/jnp.6.4.348 · Cited by 1,068
Neural mechanisms for visual memory and their role in attention
Desimone, R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13494 · Cited by 1,028
Working Memory: A View from Neuroimaging
Smith, E. E., & Jonides, J. (1997) · Cognitive Psychology · doi:10.1006/cogp.1997.0658 · Cited by 1,046
Cerebellar Projections to the Prefrontal Cortex of the Primate
Middleton, F. A., & Strick, P. L. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00700.2001 · Cited by 1,034
The Mind and Brain of Short-Term Memory
Jonides, J., Lewis, R. L., Nee, D. E., Lustig, C. A., Berman, M. G., & Moore, K. S. (2008) · Annual Review of Psychology · doi:10.1146/annurev.psych.59.103006.093615 · Cited by 957
Prefrontal and medial temporal lobe interactions in long-term memory
Simons, J. S., & Spiers, H. J. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1178 · Cited by 961
Neural correlates of a decision in the dorsolateral prefrontal cortex of the macaque
Kim, J.-N., & Shadlen, M. N. (1999) · Nature Neuroscience · doi:10.1038/5739 · Cited by 950
Reward processing in primate orbitofrontal cortex and basal ganglia
Schultz, W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.272 · Cited by 942
A cortical mechanism for triggering top-down facilitation in visual object recognition
Bar, M. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321662976 · Cited by 900
Electrophysiological studies of human face perception. I: Potentials generated in occipitotemporal cortex by face and non-face stimuli
Allison, T. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.415 · Cited by 882
Interactions between frontal cortex and basal ganglia in working memory: A computational model
FRANK, M. J., LOUGHRY, B., & O'REILLY, R. C. (2001) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.1.2.137 · Cited by 879
An adaptive coding model of neural function in prefrontal cortex
Duncan, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35097575 · Cited by 874
Attention: the mechanisms of consciousness.
Posner, M. I. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.16.7398 · Cited by 846
Neuronal correlates of parametric working memory in the prefrontal cortex
Romo, R., Brody, C. D., Hernández, A., & Lemus, L. (1999) · Nature · doi:10.1038/20939 · Cited by 822
Face and voice expression identification in patients with emotional and behavioural changes following ventral frontal lobe damage
Hornak, J., Rolls, E. T., & Wade, D. (1996) · Neuropsychologia · doi:10.1016/0028-3932(95)00106-9 · Cited by 735
Functional mapping of sequence learning in normal humans
Grafton, S. T., Hazeltine, E., & Ivry, R. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.4.497 · Cited by 720
Responses of Neurons in Inferior Temporal Cortex During Memory-Guided Visual Search
Chelazzi, L., Duncan, J., Miller, E. K., & Desimone, R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.6.2918 · Cited by 726
Human prefrontal cortex: processing and representational perspectives
Wood, J. N., & Grafman, J. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1033 · Cited by 721
Suppression of regional cerebral blood during emotional versus higher cognitive implications for interactions between emotion and cognition
Drevets, W. C., & Raichle, M. E. (1998) · Cognition & Emotion · doi:10.1080/026999398379646 · Cited by 702
Visual attention mediated by biased competition in extrastriate visual cortex
Desimone, R. (1998) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1998.0280 · Cited by 696
Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys
Carmichael, S. T., & Price, J. L. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903630409 · Cited by 678
Role of cortical N-methyl-D-aspartate receptors in auditory sensory memory and mismatch negativity generation: implications for schizophrenia.
Javitt, D. C., Steinschneider, M., Schroeder, C. E., & Arezzo, J. C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11962 · Cited by 662
Functional and Anatomical Aspects of Prefrontal Pathology in Schizophrenia
Goldman-Rakic, P. S., & Selemon, L. D. (1997) · Schizophrenia Bulletin · doi:10.1093/schbul/23.3.437 · Cited by 668
Self-citation
Effects of Neuromodulation in a Cortical Network Model of Object Working Memory Dominated by Recurrent Inhibition
Brunel, N., & Wang, X.-J. (2001) · Journal of Computational Neuroscience · doi:10.1023/a:1011204814320 · Cited by 620
Synchrony Unbound
Shadlen, M. N., & Movshon, J. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)80822-3 · Cited by 606
Remembering the past: two facets of episodic memory explored with positron emission tomography
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.11.1576 · Cited by 593
The neuropsychology of 3-D space.
Previc, F. H. (1998) · Psychological Bulletin · doi:10.1037/0033-2909.124.2.123 · Cited by 604
Activation of the prefrontal cortex in a nonspatial working memory task with functional MRI
Cohen, J. D., Forman, S. D., Braver, T. S., Casey, B. J., Servan‐Schreiber, D., & Noll, D. C. (1994) · Human Brain Mapping · doi:10.1002/hbm.460010407 · Cited by 576
Cortex and memory: emergence of a new paradigm
Fuster, J. M. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21280 · Cited by 559
Dopamine and Cognitive Control in Prefrontal Cortex
Ott, T., & Nieder, A. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.12.006 · Cited by 530
The development of nonverbal working memory and executive control processes in adolescents
Luciana, M., Conklin, H. M., Hooper, C. J., & Yarger, R. S. (2005) · Child Development · doi:10.1111/j.1467-8624.2005.00872.x · Cited by 567
Dissociable Forms of Inhibitory Control within Prefrontal Cortex with an Analog of the Wisconsin Card Sort Test: Restriction to Novel Situations and Independence from “On-Line” Processing
Dias, R., Robbins, T. W., & Roberts, A. C. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09285.1997 · Cited by 555
Integration of diverse information in working memory within the frontal lobe
Prabhakaran, V., Narayanan, K., Zhao, Z., & Gabrieli, J. D. E. (2000) · Nature Neuroscience · doi:10.1038/71156 · Cited by 539
The Temporal Correlation Hypothesis of Visual Feature Integration
Gray, C. M. (1999) · Neuron · doi:10.1016/s0896-6273(00)80820-x · Cited by 541
Physiological activation of a cortical network during performance of the Wisconsin Card Sorting Test: a positron emission tomography study
Berman, K. (1995) · Neuropsychologia · doi:10.1016/0028-3932(95)00035-2 · Cited by 534
Neural Correlates of Face and Object Recognition in Young Children with Autism Spectrum Disorder, Developmental Delay, and Typical Development
Dawson, G., Carver, L., Meltzoff, A. N., Panagiotides, H., McPartland, J., & Webb, S. J. (2002) · Child Development · doi:10.1111/1467-8624.00433 · Cited by 523
The What and Why of Binding
von der Malsburg, C. (1999) · Neuron · doi:10.1016/s0896-6273(00)80825-9 · Cited by 501
Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives
DAWSON, G., WEBB, S., SCHELLENBERG, G. D., DAGER, S., FRIEDMAN, S., AYLWARD, E., & RICHARDS, T. (2002) · Development and Psychopathology · doi:10.1017/s0954579402003103 · Cited by 467
Functional magnetic resonance imaging of human prefrontal cortex activation during a spatial working memory task.
McCarthy, G., Blamire, A. M., Puce, A., Nobre, A. C., Bloch, G., Hyder, F., Goldman-Rakic, P., & Shulman, R. G. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.18.8690 · Cited by 459
The Contribution of α2-Noradrenergic Mechanisms to Prefrontal Cortical Cognitive Function: Potential Significance for Attention-Deficit Hyperactivity Disorder
Arnsten, A. F. T. (1996) · Archives of General Psychiatry · doi:10.1001/archpsyc.1996.01830050084013 · Cited by 458
Cortex, Cognition and the Cell: New Insights into the Pyramidal Neuron and Prefrontal Function
Elston, G. N. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg093 · Cited by 440
Positron emission tomography and fluorodeoxyglucose studies of metabolic hyperfrontality and psychopathology in the psilocybin model of psychosis
Vollenweider, F. (1997) · Neuropsychopharmacology · doi:10.1016/s0893-133x(96)00246-1 · Cited by 444
Prospective coding for objects in primate prefrontal cortex
Rainer, G., Rao, S. C., & Miller, E. K. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05493.1999 · Cited by 432
“This has been found in previous studies (Fuster et al., 1982; Funahashi et al., 1989; di Pellegrino and Wise, 1991; Wilson et al., 1993; Miller et al., 1996; Rao et al., 1997; Asaad et al., 1998; Rainer et al., 1998a,b).”
Result
Electrophysiological studies of human face perception. III: Effects of top-down processing on face-specific potentials
Puce, A. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.445 · Cited by 422
FMRI studies of Stroop tasks reveal unique roles of anterior and posterior brain systems in attentional selection
Banich, M. T., Milham, M. P., Atchley, R., Cohen, N. J., Webb, A., Wszalek, T., Kramer, A. F., Liang, Z.-P., Wright, A., Shenker, J., et al. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137521 · Cited by 429
The role of prefrontal cortex in working memory: a mini review
Lara, A. H., & Wallis, J. D. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00173 · Cited by 402
Regional Dendritic and Spine Variation in Human Cerebral Cortex: a Quantitative Golgi Study
Jacobs, B. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.6.558 · Cited by 423
Cortical connections of the macaque anterior intraparietal (AIP) area
Borra, E., Belmalih, A., Calzavara, R., Gerbella, M., Murata, A., Rozzi, S., & Luppino, G. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm146 · Cited by 402
The role of the prefrontal cortex in dynamic filtering
Shimamura, A. P. (2000) · Psychobiology · doi:10.3758/bf03331979 · Cited by 394
An interactive framework for examining prefrontal cognitive processes
Roberts, R. J., & Pennington, B. F. (1996) · Developmental Neuropsychology · doi:10.1080/87565649609540642 · Cited by 392
Prefrontal modulation of visual processing in humans
Barceló, F., Suwazono, S., & Knight, R. T. (2000) · Nature Neuroscience · doi:10.1038/73975 · Cited by 374
A Comparison of Visual and Auditory Motion Processing in Human Cerebral Cortex
Lewis, J. W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.873 · Cited by 381
Metabolic hyperfrontality and psychopathology in the ketamine model of psychosis using positron emission tomography (PET) and [18F]fluorodeoxyglucose (FDG)
Vollenweider, F. X., Leenders, K. L., Scharfetter, C., Antonini, A., Maguire, P., Missimer, J., & Angst, J. (1997) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(96)00039-9 · Cited by 353
The role of the medial prefrontal cortex in cognition, ageing and dementia
Jobson, D. D., Hase, Y., Clarkson, A. N., & Kalaria, R. N. (2021) · Brain Communications · doi:10.1093/braincomms/fcab125 · Cited by 338
Functional connectivity during working memory maintenance
GAZZALEY, A., RISSMAN, J., & D'ESPOSITO, M. (2004) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.4.4.580 · Cited by 337
A role for inhibition in shaping the temporal flow of information in prefrontal cortex
Constantinidis, C., Williams, G. V., & Goldman-Rakic, P. S. (2002) · Nature Neuroscience · doi:10.1038/nn799 · Cited by 348
Self-citation
Fractionating Attentional Control Using Event-Related fMRI
Hampshire, A., & Owen, A. M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj116 · Cited by 329
Evidence for a dysfunctional prefrontal circuit in patients with an impulsive aggressive disorder
Best, M., Williams, J. M., & Coccaro, E. F. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.112604099 · Cited by 325
Working memory for complex figures: An fMRI comparison of letter and fractal n-back tasks
Ragland, J. D., Turetsky, B. I., Gur, R. C., Gunning-Dixon, F., Turner, T., Schroeder, L., Chan, R., & Gur, R. E. (2002) · Neuropsychology · doi:10.1037/0894-4105.16.3.370 · Cited by 327
Reward prediction in primate basal ganglia and frontal cortex
Schultz, W., Tremblay, L., & Hollerman, J. R. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00071-9 · Cited by 318
A comparative view of face perception.
Leopold, D. A., & Rhodes, G. (2010) · Journal of Comparative Psychology · doi:10.1037/a0019460 · Cited by 311
Intrinsic circuit organization of the major layers and sublayers of the dorsolateral prefrontal cortex in the rhesus monkey
Kritzer, M. F., & Goldman‐Rakic, P. S. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903590109 · Cited by 300
Self-citation
Pyramidal Cells of the Frontal Lobe: All the More Spinous to Think With
Elston, G. N. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-18-j0002.2000 · Cited by 289
Functional interactions between prefrontal and visual association cortex contribute to top-down modulation of visual processing
Gazzaley, A., Rissman, J., Cooney, J., Rutman, A., Seibert, T., Clapp, W., & D'Esposito, M. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm113 · Cited by 287
Phase-coupling of theta–gamma EEG rhythms during short-term memory processing
Schack, B., Vath, N., Petsche, H., Geissler, H.-G., & Möller, E. (2002) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(01)00199-4 · Cited by 281
Specialisation within the prefrontal cortex: the ventral prefrontal cortex and associative learning
Passingham, R. E., Toni, I., & Rushworth, M. F. S. (2000) · Experimental Brain Research · doi:10.1007/s002210000405 · Cited by 268
Treating Working Memory Deficits in Schizophrenia: A Review of the Neurobiology
Lett, T. A., Voineskos, A. N., Kennedy, J. L., Levine, B., & Daskalakis, Z. J. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.07.026 · Cited by 257
Role of Prefrontal Persistent Activity in Working Memory
Riley, M. R., & Constantinidis, C. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00181 · Cited by 251
Atypical form of Alzheimer's disease with prominent posterior cortical atrophy: A review of lesion distribution and circuit disconnection in cortical visual pathways
Hof, P. R., Vogt, B. A., Bouras, C., & Morrison, J. H. (1997) · Vision Research · doi:10.1016/s0042-6989(96)00240-4 · Cited by 246
The sensory nature of mnemonic representation in the primate prefrontal cortex
Constantinidis, C., Franowicz, M. N., & Goldman-Rakic, P. S. (2001) · Nature Neuroscience · doi:10.1038/85179 · Cited by 233
Self-citation
Prefrontal cortex and dynamic categorization tasks: representational organization and neuromodulatory control
O'Reilly, R. C. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.3.246 · Cited by 241
Damage to Association Fiber Tracts Impairs Recognition of the Facial Expression of Emotion
Philippi, C. L., Mehta, S., Grabowski, T., Adolphs, R., & Rudrauf, D. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0796-09.2009 · Cited by 238
Prefrontal activation evoked by infrequent target and novel stimuli in a visual target detection task: An event-related functional magnetic resonance imaging study
Kirino, E., Belger, A., Goldman-Rakic, P., & McCarthy, G. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06612.2000 · Cited by 226
Self-citation
The decade of the dendritic nmda spike
Antic, S. D., Zhou, W., Moore, A. R., Short, S. M., & Ikonomu, K. D. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22444 · Cited by 222
Resting-state BOLD networks versus task-associated functional MRI for distinguishing Alzheimer's disease risk groups
Fleisher, A. S., Sherzai, A., Taylor, C., Langbaum, J. B. S., Chen, K., & Buxton, R. B. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.021 · Cited by 217
Modulators in concert for cognition: Modulator interactions in the prefrontal cortex
Briand, L. A., Gritton, H., Howe, W. M., Young, D. A., & Sarter, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.06.007 · Cited by 216
Working memory, psychiatric symptoms, and academic performance at school
Aronen, E. T., Vuontela, V., Steenari, M.-R., Salmi, J., & Carlson, S. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.06.010 · Cited by 212
Attention and cognitive control as emergent properties of information representation in working memory
COURTNEY, S. M. (2004) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.4.4.501 · Cited by 198
Chapter 1 Top-down facilitation of visual object recognition: object-based and context-based contributions
Fenske, M. J., Aminoff, E., Gronau, N., & Bar, M. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)55001-0 · Cited by 190
The role of metaplasticity mechanisms in regulating memory destabilization and reconsolidation
Finnie, P. S. B., & Nader, K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.008 · Cited by 189
Virtual dissection and comparative connectivity of the superior longitudinal fasciculus in chimpanzees and humans
Hecht, E. E., Gutman, D. A., Bradley, B. A., Preuss, T. M., & Stout, D. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.12.039 · Cited by 175
“Chimpanzees showed strong connectivity with PMv, more moderate connectivity with IFG, and weak connectivity with PMd and DLPFC.”
Influential

Authors: Wilson, F. A. W., Scalaidhe, S. P. Ó., & Goldman-Rakic, P. S.
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 1993-06-25
Volume: 260
Issue: 5116
Pages: 1955-1958
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.8316836
OpenAlex: W2013755742
Cited by: 1,410
References: 4
FWCI: 36.26
Type: journal article
Language: en
Open access: closed

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

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.

Dissociation of Object and Spatial Processing Domains in Primate Prefrontal Cortex

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Metadata

Record

About these checks

Data sources