The Distributed Nature of Working Memory
Open accessAbstract
Studies in humans and non-human primates have provided evidence for storage of working memory contents in multiple regions ranging from sensory to parietal and prefrontal cortex. We discuss potential explanations for these distributed representations: (i) features in sensory regions versus prefrontal cortex differ in the level of abstractness and generalizability; and (ii) features in prefrontal cortex reflect representations that are transformed for guidance of upcoming behavioral actions. We propose that the propensity to produce persistent activity is a general feature of cortical networks. Future studies may have to shift focus from asking where working memory can be observed in the brain to how a range of specialized brain areas together transform sensory information into a delayed behavioral response.
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
Cites
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.
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?
Short-term memory consistently involves the prefrontal cortex and angular gyrus.
“the known cerebral correlates of short-term memory, which consistently involve the PFC and AG [49, 50]”
From Brain functional connectivity upon awakening from sleep predicts interindividual differences in dream recall frequency (2020) · cites this paper as [49]
The 'Storage of Working Memory Contents' section reports working-memory-related activity in the PFC and parietal cortex. It does not identify the angular gyrus specifically, and its account of distributed activity does not establish that both regions are consistently involved. (LLM, conf=0.86)
Experimental — accuracy not yet measuredWorking memory effects on neuronal firing rates occur in many cortical areas, from primary sensory cortices coding elementary sensory features to frontal cortex coding abstract aspects, object categories, motor intentions, and task instructions.
“The effects of working memory on neuronal firing rates occur in many cortical areas (Christophel et al., 2017), ranging from primary sensory cortices that code for the memories of elementary sensory features”
From Conscious Processing and the Global Neuronal Workspace Hypothesis (2020) · cites this paper as Christophel et al., 2017
The widespread presence of working-memory effects is important for the large diversity of contents that can enter working memory.
“Its widespread presence is important for the large diversity of contents that can enter into working memory (Christophel et al., 2017).”
From Conscious Processing and the Global Neuronal Workspace Hypothesis (2020) · cites this paper as Christophel et al., 2017
The delayed response enhancement in V1 during figure-ground perception is thought to be caused by feedback from higher visual areas to V1.
“This delayed response enhancement is thought to be caused by feedback from higher visual areas to V1 (Christophel et al., 2017; Klink et al., 2017; Lamme and Roelfsema, 2000).”
From Conscious Processing and the Global Neuronal Workspace Hypothesis (2020) · cites this paper as Christophel et al., 2017
The Different Levels of Abstraction section discusses a possible bias signal from prefrontal cortex to early visual cortex during working memory, not delayed V1 response enhancement during figure–ground perception. Searches for figure–ground perception and feedback from higher visual areas to V1 found no passage in our copy addressing that claim. (LLM, conf=0.75)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The magical number seven, plus or minus two: Some limits on our capacity for processing information.
Miller, G. A. (1994) · Psychological Review · doi:10.1037/0033-295x.101.2.343 · Cited by 17,469 · see citing works
Levels of processing: A framework for memory research
Craik, F. I. M., & Lockhart, R. S. (1972) · Journal of Verbal Learning and Verbal Behavior · doi:10.1016/s0022-5371(72)80001-x · Cited by 9,566 · see citing works
On computable numbers, with an application to the entscheidungsproblem
Turing, A. M. (1937) · Proceedings of the London Mathematical Society · doi:10.1112/plms/s2-42.1.230 · Cited by 8,283 · see citing works
The magical number 4 in short-term memory: A reconsideration of mental storage capacity
Cowan, N. (2001) · Behavioral and Brain Sciences · doi:10.1017/s0140525x01003922 · Cited by 6,779 · see citing works
The Organization of Behavior; A Neuropsychological Theory.
Attneave, F., B., M., & Hebb, D. O. (1950) · The American Journal of Psychology · doi:10.2307/1418888 · Cited by 5,146 · see citing works
Working Memory: Theories, Models, and Controversies
Baddeley, A. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100422 · Cited by 4,271 · see citing works
The Organization of Behavior: A Neuropsychological Theory
(1950) · JAMA · doi:10.1001/jama.1950.02910470083028 · Cited by 4,271 · see citing works
The capacity of visual working memory for features and conjunctions
Luck, S. J., & Vogel, E. K. (1997) · Nature · doi:10.1038/36846 · Cited by 4,053 · see citing works
Distributed and overlapping representations of faces and objects in ventral temporal cortex
Haxby, J. V., Gobbini, M. I., Furey, M. L., Ishai, A., Schouten, J. L., & Pietrini, P. (2001) · Science · doi:10.1126/science.1063736 · Cited by 3,940 · see citing works
Hierarchical models of object recognition in cortex
Riesenhuber, M., & Poggio, T. (1999) · Nature Neuroscience · doi:10.1038/14819 · Cited by 3,309 · see citing works
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 · see citing works
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663 · see citing works
The distinct modes of vision offered by feedforward and recurrent processing
Lamme, V. A. F., & Roelfsema, P. R. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01657-x · Cited by 2,338 · see citing works
Self-citationInformation-based functional brain mapping
Kriegeskorte, N., Goebel, R., & Bandettini, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600244103 · Cited by 2,113 · see citing works
Neuron Activity Related to Short-Term Memory
Fuster, J. M., & Alexander, G. E. (1971) · Science · doi:10.1126/science.173.3997.652 · Cited by 2,085 · see citing works
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 · see citing works
Decoding the visual and subjective contents of the human brain
Kamitani, Y., & Tong, F. (2005) · Nature Neuroscience · doi:10.1038/nn1444 · Cited by 1,829 · see citing works
Decoding mental states from brain activity in humans
Haynes, J., & Rees, G. E. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1931 · Cited by 1,804 · see citing works
Self-citationThe Cognitive Neuroscience of Working Memory
D'Esposito, M., & Postle, B. R. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015031 · Cited by 1,653 · see citing works
Attention and memory: an integrated framework
(1995) · Choice Reviews Online · doi:10.5860/choice.33-2415 · Cited by 1,652 · see citing works
The importance of mixed selectivity in complex cognitive tasks
Rigotti, M., Barak, O., Warden, M. R., Wang, X.-J., Daw, N. D., Miller, E. K., & Fusi, S. (2013) · Nature · doi:10.1038/nature12160 · Cited by 1,639 · see citing works
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 · see citing works
Andersen, R. A., Snyder, L. H., Bradley, D. C., & Xing, J. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.303 · Cited by 1,486 · see citing works
Control of Cognitive Processes: Attention and Performance XVIII
Monsell, S., & Driver, J. (2000) · UCL Discovery (University College London) · Cited by 1,451 · see citing works
Neural Mechanisms of Visual Working Memory in Prefrontal Cortex of the Macaque
Miller, E. K., Erickson, C. A., & Desimone, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05154.1996 · Cited by 1,441 · see citing works
Top-down modulation: bridging selective attention and working memory
Gazzaley, A., & Nobre, A. C. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.11.014 · Cited by 1,404 · see citing works
Decoding reveals the contents of visual working memory in early visual areas
Harrison, S. A., & Tong, F. (2009) · Nature · doi:10.1038/nature07832 · Cited by 1,347 · see citing works
Alvarez, G. A., & Cavanagh, P. (2004) · Psychological Science · doi:10.1111/j.0963-7214.2004.01502006.x · Cited by 1,330 · see citing works
Synaptic theory of working memory
Mongillo, G., Barak, O., & Tsodyks, M. (2008) · Science · doi:10.1126/science.1150769 · Cited by 1,253 · see citing works
Visual field maps in human cortex.
Wandell, B. A., Dumoulin, S. O., & Brewer, A. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.012 · Cited by 1,231 · see citing works
Overlapping mechanisms of attention and spatial working memory
Awh, E., & Jonides, J. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01593-x · Cited by 1,229 · see citing works
Population receptive field estimates in human visual cortex
Dumoulin, S. O., & Wandell, B. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.034 · Cited by 1,181 · see citing works
Working memory as an emergent property of the mind and brain
Postle, B. R. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.06.005 · Cited by 1,151 · see citing works
Changing concepts of working memory
Ma, W. J., Masud Husain, B., & Bays, P. M. (2014) · Nature Neuroscience · doi:10.1038/nn.3655 · Cited by 1,128 · see citing works
Categorical Representation of Visual Stimuli in the Primate Prefrontal Cortex
Freedman, D. J., Riesenhuber, M., Poggio, T., & Miller, E. K. (2001) · Science · doi:10.1126/science.291.5502.312 · Cited by 1,123 · see citing works
Waugh, N. C., & Norman, D. A. (1965) · Psychological Review · doi:10.1037/h0021797 · Cited by 1,120 · see citing works
A neural basis for visual search in inferior temporal cortex
Chelazzi, L., Miller, E. K., Duncan, J., & Desimone, R. (1993) · Nature · doi:10.1038/363345a0 · Cited by 1,114 · see citing works
Visual working memory capacity: from psychophysics and neurobiology to individual differences
Luck, S. J., & Vogel, E. K. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.06.006 · Cited by 1,088 · see citing works
The representation of visual salience in monkey parietal cortex
Gottlieb, J. P., Kusunoki, M., & Goldberg, M. E. (1998) · Nature · doi:10.1038/35135 · Cited by 1,078 · see citing works
O’Reilly, R. C., & Frank, M. J. (2005) · Neural Computation · doi:10.1162/089976606775093909 · Cited by 1,066 · see citing works
Synaptic reverberation underlying mnemonic persistent activity
Wang, X.-J. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01868-3 · Cited by 1,059 · see citing works
A relationship between behavioral choice and the visual responses of neurons in macaque MT
Britten, K. H., Newsome, W. T., Shadlen, M. N., Celebrini, S., & Movshon, J. A. (1996) · Visual Neuroscience · doi:10.1017/s095252380000715x · Cited by 1,049 · see citing works
A change of the leading player in flow Visualization technique
Mizuno, A., & Ohta, Y. (2006) · Journal of Visualization · doi:10.1007/bf03181556 · Cited by 1,042 · see citing works
A hierarchy of intrinsic timescales across primate cortex
Murray, J. D., Bernacchia, A., Freedman, D. J., Romo, R., Wallis, J. D., Cai, X., Padoa-Schioppa, C., Pasternak, T., Seo, H., Lee, D., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3862 · Cited by 990 · see citing works
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 · see citing works
The precision of visual working memory is set by allocation of a shared resource
Bays, P. M., Catalão, R., & Masud Husain, B. (2009) · Journal of Vision · doi:10.1167/9.10.7 · Cited by 943 · see citing works
Simon, H. A. (1974) · Science · doi:10.1126/science.183.4124.482 · Cited by 925 · see citing works
Object and Spatial Visual Working Memory Activate Separate Neural Systems in Human Cortex
Courtney, S. M., Ungerleider, L. G., Keil, K., & Haxby, J. V. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.1.39 · Cited by 891 · see citing works
Neuronal correlate of pictorial short-term memory in the primate temporal cortexYasushi Miyashita
Miyashita, Y., & Chang, H. S. (1988) · Nature · doi:10.1038/331068a0 · Cited by 880 · see citing works
Integration of What and Where in the Primate Prefrontal Cortex
Rao, S. C., Rainer, G., & Miller, E. K. (1997) · Science · doi:10.1126/science.276.5313.821 · Cited by 877 · see citing works
‘Activity-silent’ working memory in prefrontal cortex: a dynamic coding framework
Stokes, M. G. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.05.004 · Cited by 850 · see citing works
Gamma and Beta Bursts Underlie Working Memory
Lundqvist, M., Rose, J., Herman, P., Brincat, S. L., Buschman, T. J., & Miller, E. K. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.028 · Cited by 846 · see citing works
Coding of visual space by premotor neurons.
Graziano, M. S. A., Yap, G. S., & Gross, C. G. (1994) · Science · doi:10.1126/science.7973661 · Cited by 841 · see citing works
Stimulus-Specific Delay Activity in Human Primary Visual Cortex
Serences, J. T., Ester, E. F., Vogel, E. K., & Awh, E. (2009) · Psychological Science · doi:10.1111/j.1467-9280.2009.02276.x · Cited by 833 · see citing works
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 · see citing works
FOSTER, J. M. (1996) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-199606000-00014 · Cited by 761 · see citing works
Hierarchical process memory: memory as an integral component of information processing
Hasson, U., Chen, J., & Honey, C. J. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.04.006 · Cited by 749 · see citing works
Activity of neurons in anterior inferior temporal cortex during a short- term memory task
Miller, E. K., Li, L., & Desimone, R. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-04-01460.1993 · Cited by 732 · see citing works
The Retinotopy of Visual Spatial Attention
Tootell, R. B. H., Hadjikhani, N. K., Hall, E., Marrett, S., Vanduffel, W., Vaughan, J. T., & Dale, A. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80659-5 · Cited by 714 · see citing works
Dynamic Coding for Cognitive Control in Prefrontal Cortex
Stokes, M. G., Kusunoki, M., Sigala, N., Nili, H., Gaffan, D., & Duncan, J. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.039 · Cited by 711 · see citing works
Representation of the Quantity of Visual Items in the Primate Prefrontal Cortex
Nieder, A., Freedman, D. J., & Miller, E. K. (2002) · Science · doi:10.1126/science.1072493 · Cited by 703 · see citing works
Different states in visual working memory: when it guides attention and when it does not
Olivers, C. N. L., Peters, J. C., Houtkamp, R., & Roelfsema, P. R. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.05.004 · Cited by 679 · see citing works
Self-citationWorking memory in primate sensory systems
Pasternak, T., & Greenlee, M. W. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1603 · Cited by 678 · see citing works
Neurocognitive Architecture of Working Memory
Eriksson, J., Vogel, E. K., Lansner, A., Bergström, F., & Nyberg, L. H. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.020 · Cited by 655 · see citing works
Parallel Neuronal Mechanisms for Short-Term Memory
Miller, E. K., & Desimone, R. (1994) · Science · doi:10.1126/science.8290960 · Cited by 630 · see citing works
Dopamine-Mediated Stabilization of Delay-Period Activity in a Network Model of Prefrontal Cortex
Durstewitz, D., Seamans, J. K., & B, T. J. S. A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.3.1733 · Cited by 617 · see citing works
Brain imaging of the central executive component of working memory
Collette, F., & Van der Linden, M. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00063-x · Cited by 617 · see citing works
Neural Activity in the Primate Prefrontal Cortex during Associative Learning
Asaad, W. F., Rainer, G., & Miller, E. K. (1998) · Neuron · doi:10.1016/s0896-6273(00)80658-3 · Cited by 593 · see citing works
Decoding and Reconstructing Color from Responses in Human Visual Cortex
Brouwer, G. J., & Heeger, D. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3577-09.2009 · Cited by 586 · see citing works
Selective representation of relevant information by neurons in the primate prefrontal cortex
Rainer, G., Asaad, W. F., & Miller, E. K. (1998) · Nature · doi:10.1038/31235 · Cited by 585 · see citing works
Localization of function within the dorsolateral prefrontal cortex of the rhesus monkey
Goldman, P. S., & Rosvold, H. E. (1970) · Experimental Neurology · doi:10.1016/0014-4886(70)90222-0 · Cited by 581 · see citing works
THE SELECTIVE IMPAIRMENT OF AUDITORY VERBAL SHORT-TERM MEMORY
Warrington, E. K., & Shallice, T. (1969) · Brain · doi:10.1093/brain/92.4.885 · Cited by 561 · see citing works
Attention and memory: An integrated framework
Otten, L. J. (1996) · Biological Psychology · doi:10.1016/s0301-0511(96)05264-7 · Cited by 550 · see citing works
A Comparison of Primate Prefrontal and Inferior Temporal Cortices during Visual Categorization
Freedman, D. J., Riesenhuber, M., Poggio, T., & Miller, E. K. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05235.2003 · Cited by 538 · see citing works
Shared representations for working memory and mental imagery in early visual cortex
Albers, A. M., Kok, P., Toni, I., Dijkerman, H. C., & de Lange, F. P. (2013) · Current Biology · doi:10.1016/j.cub.2013.05.065 · Cited by 528 · see citing works
Fuster, J. M. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01128-4 · Cited by 516 · see citing works
Neural Evidence for a Distinction between Short-term Memory and the Focus of Attention
Lewis‐Peacock, J. A., Drysdale, A. T., Oberauer, K., & Postle, B. R. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00140 · Cited by 507 · see citing works
Robust neuronal dynamics in premotor cortex during motor planning
Li, N., Daie, K., Svoboda, K., & Druckmann, S. (2016) · Nature · doi:10.1038/nature17643 · Cited by 492 · cited 1× · see citing works
“, redundant) side when one side was optogenetically silenced [152].”
BackgroundPetrides, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00359.1995 · Cited by 464 · see citing works
Neuronal firing in the inferotemporal cortex of the monkey in a visual memory task
Fuster, J. M., & Jervey, J. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-03-00361.1982 · Cited by 463 · see citing works
The role of parietal cortex in visuomotor control: What have we learned from neuroimaging?
Culham, J. C., Cavina‐Pratesi, C., & Singhal, A. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.11.003 · Cited by 457 · see citing works
Hazy, T. E., Frank, M. J., & O’Reilly, R. C. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2055 · Cited by 450 · see citing works
Inferotemporal Neurons Distinguish and Retain Behaviorally Relevant Features of Visual Stimuli
Fuster, J. M., & Jervey, J. P. (1981) · Science · doi:10.1126/science.7233192 · Cited by 436 · see citing works
Revisiting the role of persistent neural activity during working memory
Sreenivasan, K. K., Curtis, C. E., & D’Esposito, M. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.12.001 · Cited by 433 · see citing works
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 · cited 2× · see citing works
“, [137]) and tasks that involve any form of explicit mental transformation [192,193] or explicitly learned association [132] are excluded.”
BackgroundEster, E. F., Sprague, T. C., & Serences, J. T. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.013 · Cited by 403 · see citing works
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 · see citing works
Nieder, A. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.40 · Cited by 389 · see citing works
The Hebbian paradigm reintegrated: local reverberations as internal representations
Amit, D. J. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00040164 · Cited by 388 · see citing works
Riggall, A. C., & Postle, B. R. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.1892-12.2012 · Cited by 385 · see citing works
Banishing the homunculus: Making working memory work
Hazy, T. E., Frank, M. J., & O’Reilly, R. C. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.067 · Cited by 385 · see citing works
Object and Place Memory in the Macaque Entorhinal Cortex
SUZUKI, W. A., Miller, E. K., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.1062 · Cited by 383 · see citing works
The functional neuroanatomy of working memory: Contributions of human brain lesion studies
Müller, N., & Knight, R. T. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.09.018 · Cited by 382 · see citing works
Charan Ranganath, A., Cohen, M. X., Dam, C., & D’Esposito, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5053-03.2004 · Cited by 382 · see citing works
The dependence of span and delayed-response performance on prefrontal cortex.
D’Esposito, M., & Postle, B. R. (1999) · Neuropsychologia · doi:10.1016/s0028-3932(99)00021-4 · Cited by 350 · see citing works
Separate Signals for Target Selection and Movement Specification in the Superior Colliculus
Horwitz, G. D., & Newsome, W. T. (1999) · Science · doi:10.1126/science.284.5417.1158 · Cited by 346 · see citing works
Neural substrates of cognitive capacity limitations
Buschman, T. J., Siegel, M., Roy, J. E., & Miller, E. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1104666108 · Cited by 343 · see citing works
Decoding the content of visual short-term memory under distraction in occipital and parietal areas
Bettencourt, K. C., & Yaoda Xu, A. (2015) · Nature Neuroscience · doi:10.1038/nn.4174 · Cited by 343 · see citing works
Flexible cognitive resources: competitive content maps for attention and memory
Franconeri, S., Alvarez, G. A., & Cavanagh, P. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.01.010 · Cited by 336 · see citing works
Multisensory Space Representations in the Macaque Ventral Intraparietal Area
Schlack, A., Sterbing-D'Angelo, S. J., Hartung, K., Hoffmann, K.-P., & Bremmer, F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0455-05.2005 · Cited by 318 · see citing works
Paulsen, J. S. (1996) · American Journal of Psychiatry · doi:10.1176/ajp.153.11.1496 · Cited by 312 · see citing works
Responses of Neurons in Macaque Area V4 During Memory-guided Visual Search
Chelazzi, L., Miller, E. K., Duncan, J., & Desimone, R. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.8.761 · Cited by 312 · see citing works
Cue-Invariant Shape Selectivity of Macaque Inferior Temporal Neurons
Sáry, G., Vogels, R., & Orban, G. A. (1993) · Science · doi:10.1126/science.8493538 · Cited by 311 · see citing works
A Neural Correlate of Working Memory in the Monkey Primary Visual Cortex
Supèr, H., Spekreijse, H., & Lamme, V. A. F. (2001) · Science · doi:10.1126/science.1060496 · Cited by 305 · see citing works
Decoding the Contents of Visual Short-Term Memory from Human Visual and Parietal Cortex
Christophel, T. B., Hebart, M. N., & Haynes, J.-D. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0184-12.2012 · Cited by 295 · see citing works
Self-citationBae, G., Olkkonen, M., Allred, S., & Flombaum, J. (2015) · Journal of Experimental Psychology General · doi:10.1037/xge0000076 · Cited by 286 · see citing works
A source for feature-based attention in the prefrontal cortex
Bichot, N. P., Heard, M. T., DeGennaro, E. M., & Desimone, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.001 · Cited by 283 · see citing works
Working models of working memory
Barak, O., & Tsodyks, M. V. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.008 · Cited by 281 · see citing works
Decoding Attended Information in Short-term Memory: An EEG Study
LaRocque, J. J., Lewis‐Peacock, J. A., Drysdale, A. T., Oberauer, K., & Postle, B. R. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00305 · Cited by 280 · see citing works
Decoding a Perceptual Decision Process across Cortex
Hernández, A., Nácher, V., Luna, R., Zainos, A., Lemus, L., Álvarez, M., Vázquez, Y., Camarillo, L., & Romo, R. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.031 · Cited by 269 · see citing works
Attention modulates spatial priority maps in the human occipital, parietal and frontal cortices
Sprague, T. C., & Serences, J. T. (2013) · Nature Neuroscience · doi:10.1038/nn.3574 · Cited by 266 · see citing works
Prefrontal contributions to visual selective attention
Squire, R. F., Noudoost, B., Schafer, R. J., & Moore, T. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150439 · Cited by 260 · see citing works
Orientation Decoding Depends on Maps, Not Columns
Freeman, J., Brouwer, G. J., Heeger, D. J., & Merriam, E. P. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5160-10.2011 · Cited by 256 · see citing works
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 · see citing works
Neuronal activity in posterior parietal area 7a during the delay periods of a spatial memory task
Constantinidis, C., & Steinmetz, M. A. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.2.1352 · Cited by 248 · see citing works
Zaksas, D., & Pasternak, T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3420-06.2006 · Cited by 247 · see citing works
Goal-dependent dissociation of visual and prefrontal cortices during working memory
Lee, S., Kravitz, D. J., & Baker, C. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3452 · Cited by 247 · see citing works
Primate spinal interneurons show pre-movement instructed delay activity
Prut, Y., & Fetz, E. E. (1999) · Nature · doi:10.1038/44145 · Cited by 242 · see citing works
INTERFERENCE FACTORS IN DELAYED RESPONSE IN MONKEYS AFTER REMOVAL OF FRONTAL LOBES
Malmo, R. B. (1942) · Journal of Neurophysiology · doi:10.1152/jn.1942.5.4.295 · Cited by 240 · see citing works
Sharp emergence of feature-selective sustained activity along the dorsal visual pathway
Mendoza-Halliday, D., Torres, S., & Martínez-Trujillo, J. (2014) · Nature Neuroscience · doi:10.1038/nn.3785 · Cited by 239 · see citing works
Visual categorization and the primate prefrontal cortex: neurophysiology and behavior.
Freedman, D. J., Riesenhuber, M., Poggio, T., & Miller, E. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.929 · Cited by 238 · see citing works
Object-Centered Direction Selectivity in the Macaque Supplementary Eye Field
Olson, C. R., & Gettner, S. N. (1995) · Science · doi:10.1126/science.7638625 · Cited by 238 · see citing works
Spatial maps in frontal and prefrontal cortex
Hagler, D. J., & Sereno, M. I. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.058 · Cited by 235 · see citing works
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 · see citing works
Feature-Based Attention in the Frontal Eye Field and Area V4 during Visual Search
Zhou, H., & Desimone, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.032 · Cited by 227 · see citing works
A Brain System for Auditory Working Memory
Kumar, S., Joseph, S., Gander, P. E., Barascud, N., Halpern, A. R., & Griffiths, T. D. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4341-14.2016 · Cited by 227 · see citing works
Neural mechanisms of information storage in visual short-term memory
Serences, J. T. (2016) · Vision Research · doi:10.1016/j.visres.2016.09.010 · Cited by 227 · see citing works
EFFECTS OF SMALL FRONTAL LESIONS ON DELAYED ALTERNATION IN MONKEYS
Mishkin, M. (1957) · Journal of Neurophysiology · doi:10.1152/jn.1957.20.6.615 · Cited by 226 · see citing works
Prioritized Maps of Space in Human Frontoparietal Cortex
Jerde, T. A., Merriam, E. P., Riggall, A. C., Hedges, J. H., & Curtis, C. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3810-12.2012 · Cited by 208 · see citing works
A neural measure of precision in visual working memory
Ester, E. F., Anderson, D. E., Serences, J. T., & Awh, E. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00357 · Cited by 207 · see citing works
Reconstructions of Information in Visual Spatial Working Memory Degrade with Memory Load
Sprague, T. C., Ester, E. F., & Serences, J. T. (2014) · Current Biology · doi:10.1016/j.cub.2014.07.066 · Cited by 202 · see citing works
Visual and spatial working memory: From boxes to networks
Zimmer, H. D. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.05.016 · Cited by 200 · see citing works
Supramodal numerosity selectivity of neurons in primate prefrontal and posterior parietal cortices
Nieder, A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1204580109 · Cited by 190 · see citing works
Decay of Visual Information from a Single Letter
Posner, M. I., & Keele, S. W. (1967) · Science · doi:10.1126/science.158.3797.137 · Cited by 190 · see citing works
Visual Similarity Effects in Immediate Verbal Serial Recall
Logie, R. H., Sala, S. D., Wynn, V., & Baddeley, A. (2000) · The Quarterly Journal of Experimental Psychology Section A · doi:10.1080/713755916 · Cited by 189 · see citing works
A neural basis for real-world visual search in human occipitotemporal cortex
Peelen, M. V., & Kästner, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1101042108 · Cited by 186 · see citing works
Mnemonic neuronal activity in somatosensory cortex.
Zhou, Y. D., & Fuster, J. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.19.10533 · Cited by 182 · see citing works
Conversion of sensory signals into perceptual decisions
Romo, R., & de Lafuente, V. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.03.007 · Cited by 181 · see citing works
Attraction of Position Preference by Spatial Attention throughout Human Visual Cortex
Klein, B. P., Harvey, B. M., & Dumoulin, S. O. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.047 · Cited by 175 · see citing works
Coding the Locations of Objects in the Dark
Graziano, M. S. A., Hu, X. T., & Gross, C. G. (1997) · Science · doi:10.1126/science.277.5323.239 · Cited by 169 · see citing works
Neural correlates of categories and concepts
Miller, E. K., Nieder, A., Freedman, D. J., & Wallis, J. D. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00037-0 · Cited by 164 · see citing works
Visuokinetic activities of primate prefrontal neurons during delayed-response performance.
Kubota, K., Iwamoto, T., & Suzuki, H. (1974) · Journal of Neurophysiology · doi:10.1152/jn.1974.37.6.1197 · Cited by 162 · see citing works
RECENT DEVELOPMENTS IN SHORT‐TERM MEMORY
Murdock, B. B. (1967) · British Journal of Psychology · doi:10.1111/j.2044-8295.1967.tb01099.x · Cited by 158 · see citing works
Gallivan, J. P., McLean, D. A., Smith, F. W., & Culham, J. C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1058-11.2011 · Cited by 157 · see citing works
Selective neuronal discharge in monkey putamen reflects intended direction of planned limb movements
Alexander, G. E. (1987) · Experimental Brain Research · doi:10.1007/bf00247293 · Cited by 155 · see citing works
Lévy, R., & Goldman, P. S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05149.1999 · Cited by 154 · see citing works
The human Turing machine: a neural framework for mental programs
Zylberberg, A., Dehaene, S., Roelfsema, P. R., & Sigman, M. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.05.007 · Cited by 151 · see citing works
Self-citationActivity of Neurons in Cortical Area MT During a Memory for Motion Task
Bisley, J. W., Zaksas, D., Droll, J. A., & Pasternak, T. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00870.2003 · Cited by 141 · see citing works
Distributed and Dynamic Storage of Working Memory Stimulus Information in Extrastriate Cortex
Sreenivasan, K. K., Vytlacil, J. J., & D’Esposito, M. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00556 · Cited by 140 · see citing works
Selection and Maintenance of Spatial Information by Frontal Eye Field Neurons
Armstrong, K. M., Chang, M. H., & Moore, T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4465-09.2009 · Cited by 139 · see citing works
Executive control processes underlying multi-item working memory
Lara, A. H., & Wallis, J. D. (2014) · Nature Neuroscience · doi:10.1038/nn.3702 · Cited by 137 · see citing works
Thalamic mediodorsal nucleus and working memory
Watanabe, Y., & Funahashi, S. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.05.003 · Cited by 135 · see citing works
Jacob, S. N., & Nieder, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.009 · Cited by 131 · see citing works
Stimulus Selectivity in Dorsal and Ventral Prefrontal Cortex after Training in Working Memory Tasks
Meyer, T., Qi, X.-L., Stanford, T. R., & Constantinidis, C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6798-10.2011 · Cited by 129 · see citing works
Oscillatory Correlates of Vibrotactile Frequency Processing in Human Working Memory
Spitzer, B., Wacker, E., & Blankenburg, F. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6041-09.2010 · Cited by 122 · see citing works
Self-citationStimulus-dependent EEG activity reflects internal updating of tactile working memory in humans
Spitzer, B., & Blankenburg, F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1104189108 · Cited by 115 · see citing works
Self-citationSingle unit activity in the auditory cortex of a monkey performing a short term memory task
Gottlieb, Y., Vaadia, E., & Abeles, M. (1989) · Experimental Brain Research · doi:10.1007/bf00248287 · Cited by 110 · see citing works
A Neural Parametric Code for Storing Information of More than One Sensory Modality in Working Memory
Vergara, J. R. A., Rivera, N., Rossi-Pool, R., & Romo, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.11.026 · Cited by 109 · see citing works
Short-Term Memory Trace in Rapidly Adapting Synapses of Inferior Temporal Cortex
Sugase-Miyamoto, Y., Liu, Z., Wiener, M. C., Optican, L. M., & Richmond, B. J. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000073 · Cited by 98 · see citing works
Spatial specificity of working memory representations in the early visual cortex
Pratte, M. S., & Tong, F. (2014) · Journal of Vision · doi:10.1167/14.3.22 · Cited by 94 · see citing works
Parietal and early visual cortices encode working memory content across mental transformations
Christophel, T. B., Cichy, R. M., Hebart, M. N., & Haynes, J. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.11.018 · Cited by 93 · see citing works
Self-citationNeural Dynamics in Inferior Temporal Cortex during a Visual Working Memory Task
Woloszyn, L., & Sheinberg, D. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5785-08.2009 · Cited by 91 · see citing works
Qi, X.-L. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00012 · Cited by 90 · see citing works
Supramodal Parametric Working Memory Processing in Humans
Spitzer, B., & Blankenburg, F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5280-11.2012 · Cited by 87 · see citing works
Self-citationDecoding Successive Computational Stages of Saliency Processing
Bogler, C., Bode, S., & Haynes, J. (2011) · Current Biology · doi:10.1016/j.cub.2011.08.039 · Cited by 87 · see citing works
Self-citationThe Verbal-Loop Hypothesis: Conventional Figures
Glanzer, M., & Clark, W. H. (1964) · The American Journal of Psychology · doi:10.2307/1420773 · Cited by 84 · see citing works
Visual, Somatosensory, and Bimodal Activities in the Macaque Parietal Area PEc
Breveglieri, R., Galletti, C., Monaco, S., & Fattori, P. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm127 · Cited by 83 · see citing works
Stimulus-specific suppression preserves information in auditory short-term memory
Linke, A. C., Vicente-Grabovetsky, A., & Cusack, R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102118108 · Cited by 82 · see citing works
Neural Anatomy of Primary Visual Cortex Limits Visual Working Memory
Bergmann, J., Genç, E., Kohler, A., Singer, W., & Pearson, J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu168 · Cited by 72 · see citing works
Working Memory and Decision Processes in Visual Area V4
Hayden, B. Y., & Gallant, J. L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00018 · Cited by 69 · see citing works
Working Memory Coding of Analog Stimulus Properties in the Human Prefrontal Cortex
Spitzer, B., Gloel, M., Schmidt, T. T., & Blankenburg, F. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht084 · Cited by 65 · see citing works
Self-citationDecoding complex flow-field patterns in visual working memory
Christophel, T. B., & Haynes, J. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.01.025 · Cited by 64 · see citing works
Self-citationShort-term memory after frontal-lobe injury in man.
Ghent, L., Mishkin, M. M., & Teuber, H. (1962) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0047520 · Cited by 63 · see citing works
Multi-Voxel Decoding and the Topography of Maintained Information During Visual Working Memory
Lee, S., & Baker, C. I. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2016.00002 · Cited by 63 · see citing works
How Attention Can Create Synaptic Tags for the Learning of Working Memories in Sequential Tasks
Rombouts, J. O., Bohté, S. M., & Roelfsema, P. R. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004060 · Cited by 60 · see citing works
Self-citationThe effect of white noise upon the recall of vocalized lists.
Murray, D. J. (1965) · Canadian Journal of Psychology/Revue Canadienne de Psychologie · doi:10.1037/h0082913 · Cited by 59 · see citing works
Holding Multiple Items in Short Term Memory: A Neural Mechanism
Rolls, E. T., Dempere‐Marco, L., & Deco, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061078 · Cited by 53 · see citing works
Spitzer, B., Fleck, S., & Blankenburg, F. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4580-13.2014 · Cited by 50 · see citing works
Self-citationExploring the role of gaze behavior and object detection in scene understanding
Yun, K., Peng, Y., Samaras, D., Zelinsky, G. J., & Berg, T. L. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00917 · Cited by 50 · see citing works
Working Memory in the Service of Executive Control Functions
Mansouri, F. A., Rosa, M. G. P., & Atapour, N. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00166 · Cited by 44 · see citing works
Short-term recognition memory for complex free-form figures
Cermak, G. W. (1971) · Psychonomic Science · doi:10.3758/bf03329095 · Cited by 39 · see citing works
Prefrontal cortex and sensory cortices during working memory: quantity and quality
Ku, Y., Bodner, M., & Zhou, Y. (2015) · Neuroscience Bulletin · doi:10.1007/s12264-014-1503-7 · Cited by 39 · see citing works
The Contribution of Human Superior Intraparietal Sulcus to Visual Short-Term Memory and Perception
Yaoda Xu, A., & Jeong, S. K. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801371-7.00004-1 · Cited by 33 · see citing works
Effects of coding strategy on perceptual memory.
Haber, R. N. (1964) · Journal of Experimental Psychology · doi:10.1037/h0040403 · Cited by 30 · see citing works
Unilateral Prefrontal Lesions Impair Memory-Guided Comparisons of Contralateral Visual Motion
Pasternak, T., Lui, L. L., & Spinelli, P. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5265-14.2015 · Cited by 28 · see citing works
Multimodal representation of limb endpoint position in the posterior parietal cortex
Shi, Y., Apker, G. A., & Buneo, C. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00223.2012 · Cited by 25 · see citing works
Neural representation of object-specific attentional priority
Liu, T. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.01.034 · Cited by 22 · see citing works
Working memory resources are shared across sensory modalities
Salmela, V. R., Moisala, M., & Alho, K. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-014-0714-3 · Cited by 21 · see citing works
Bancroft, T. D., Hockley, W. E., & Servos, P. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-013-0604-0 · Cited by 13 · see citing works
Wimmer, K., Spinelli, P., & Pasternak, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0843-16.2016 · Cited by 13 · see citing works
The Effects of Acoustic and Semantic Similarity on Concept Identification
Coltheart, V. (1972) · Quarterly Journal of Experimental Psychology · doi:10.1080/14640747208400268 · Cited by 11 · see citing works
Working Memory Representations of Visual Motion along the Primate Dorsal Visual Pathway
Mendoza-Halliday, D., Torres, S., & Martínez-Trujillo, J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801371-7.00013-2 · Cited by 5 · see citing works
What are the Roles of Sensory and Parietal Activity in Visual Short-Term Memory?
Emrich, S. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801371-7.00006-5 · Cited by 4 · see citing works
Decoding invariant representations in visual working memory
Christophel, T. B., Endisch, C., & Haynes, J. (2013) · Journal of Vision · doi:10.1167/13.9.927 · Cited by 2 · see citing works
Self-citationAlpha-band and raw EEG reflect distinct maintenance mechanisms during working memory
Fahrenfort, J. J., van Leeuwen, J., Foster, J. J., et al. (2016) · Journal of Vision · doi:10.1167/16.12.711 · Cited by 2 · see citing works
Flagged first, then by citations
Research works printed but not linked: 3
- [1]1. Baddeley, A.D. (1986) Working Memory, Clarendon Press
- [49]49. van Kerkoerle, T. et al. The influence of attention and working memory on neuronal activity in the different layers of primary visual cortex. Nat. Commun. (in press).
- [178]178. Norris, J.R. (1997) Markov Chains, Cambridge University Press 179.
Cited by
Sorted by citations
Conscious Processing and the Global Neuronal Workspace Hypothesis
Mashour, G. A., Roelfsema, P., Changeux, J.-P., & Dehaene, S. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.026 · Cited by 1,164 · see citing works
“The effects of working memory on neuronal firing rates occur in many cortical areas (Christophel et al., 2017), ranging from primary sensory cortices that code for the memories of elementary sensory features (MendozaHalliday et al.”
BackgroundSelf-citationMiller, E. K., Lundqvist, M., & Bastos, A. M. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.023 · Cited by 797 · see citing works
The Border Between Seeing and Thinking
Block, N. (2023) · doi:10.1093/oso/9780197622223.001.0001 · Cited by 367 · see citing works
Persistent Single-Neuron Activity during Working Memory in the Human Medial Temporal Lobe
Kornblith, S., Quian Quiroga, R., Koch, C., Fried, I., & Mormann, F. (2017) · Current Biology · doi:10.1016/j.cub.2017.02.013 · Cited by 133 · see citing works
Dynamic causal brain circuits during working memory and their functional controllability
Cai, W., Ryali, S., Pasumarthy, R., Talasila, V., & Menon, V. (2021) · Nature Communications · doi:10.1038/s41467-021-23509-x · Cited by 105 · see citing works
Redefining Visual Working Memory: A Cognitive-Strategy, Brain-Region Approach
Pearson, J., & Keogh, R. (2019) · Current Directions in Psychological Science · doi:10.1177/0963721419835210 · Cited by 90 · see citing works
Tasks and their role in visual neuroscience
Kay, K., Bonnen, K., Denison, R. N., Arcaro, M. J., & Barack, D. L. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.022 · Cited by 61 · see citing works
Linking cortical circuit models to human cognition with laminar fMRI
Yang, J., Huber, L., Yu, Y., & Bandettini, P. A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.07.005 · Cited by 52 · see citing works
From remembering to reconstruction: The transformative neural representation of episodic memory.
Xue, G. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102351 · Cited by 49 · see citing works
Vallat, R., Nicolas, A., & Ruby, P. (2020) · Sleep · doi:10.1093/sleep/zsaa116 · Cited by 31 · see citing works
Wanke, N., & Schwabe, L. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhz298 · Cited by 28 · see citing works
Jia, K., Li, Y., Gong, M., Huang, H., Wang, Y., & Li, S. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.2780-20.2021 · Cited by 25 · see citing works
Functional alterations of the prefrontal circuit underlying cognitive aging in mice
Chong, H. R., Ranjbar-Slamloo, Y., Ho, M. Z. H., Ouyang, X., & Kamigaki, T. (2023) · Nature Communications · doi:10.1038/s41467-023-43142-0 · Cited by 19 · see citing works
The Cooperative Neuron: Cellular Foundations of Mental Life
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.001.0001 · Cited by 13 · see citing works
Jiang, Y., Guo, Z., Zhou, X., Jiang, N., & He, J. (2025) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-025-01594-z · Cited by 7 · see citing works
Ao, M., Ren, S., Yu, Y., Huang, H., Miao, X., Ao, Y., & Wang, W. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1151799 · Cited by 4 · see citing works
Nested Learning: The Illusion of Deep Learning Architectures
Behrouz, A., Razaviyayn, M., Zhong, P., & Mirrokni, V. (2025) · arXiv · doi:10.48550/arxiv.2512.24695 · Cited by 1 · see citing works
- Authors
- Christophel, T. B., Klink, P. C., Spitzer, B., Roelfsema, P. R., & Haynes, J.-D.
- Affiliations
- Bernstein Center for Computational Neuroscience Berlin (DE)
- Netherlands Institute for Neuroscience (NL)
- University of Oxford (GB)
- Humboldt-Universität zu Berlin (DE)
- Corresponding author
- Christophel, Thomas B.
- ORCID
- Venue
- Trends in Cognitive Sciences
- Publisher
- Elsevier BV
- Published
- 2017-02
- Volume
- 21
- Issue
- 2
- Pages
- 111-124
- ISSN
- 1364-6613 (ISSN-L)
- OpenAlex
- W2568841898
- Cited by
- 882
- References
- 195
- Citations by year
- 2026: 95 · 2025: 105 · 2024: 114 · 2023: 147 · 2022: 91 · 2021: 97 · 2020: 74 · 2019: 82 · 2018: 46 · 2017: 29
- FWCI
- 7.07
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Trends in Cognitive Sciences (publishedVersion)
- PubMed (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (submittedVersion)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (submittedVersion)
- VU Research Portal (submittedVersion, other-oa)
- Funders
- Deutsche Forschungsgemeinschaft (JA945/3-1, EXC257, KFO-247, SP 1510/2-1, SFB940)
- Bundesministerium für Bildung und Forschung (SFB 940, 01GQ1001C)
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (451-13-023, ALW grant 823-02-010, 823-02-010)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Abilities and Testing
- Keywords
- working memory, distributed representations, prefrontal cortex, parietal cortex, sensory cortex, persistent activity, cortical networks, memory storage, generalization
- MeSH terms
- Animals, Brain, Brain Mapping, Humans, Memory, Short-Term, Prefrontal Cortex
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