Cited by 13Neural dynamics and brain functionNeuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

The DOI matches its Crossref record, with a small difference in title or year; 426 of the 428 references it cites were found in a registry or an index.

The Cooperative Neuron: Cellular Foundations of Mental Life

Phillips, William A.·2023

DOI 10.1093/oso/9780198876984.001.0001

Open this paper in CoChat — free account

Abstract

The Cooperative Neuron roots our understanding of mental life, as consciously experienced and as studied by psychologists, in recent discoveries in cellular neurophysiology, which show that many neurons in the mammalian neocortex have capabilities that transcend those assumed by twentieth-century psychology and systems neuroscience. These neurons receive information from many other parts of the brain and amplify their information transmission when appropriate in that context. Amplification is defined and quantified using recent advances in information theory by which the contributions of different inputs to information transmission can be distinguished. This context-sensitive cooperative style of Big Data processing produces widespread coherence from operations that are localized within each of a multitude of local neuronal processors. This book shows how this provides cellular foundations for contextual disambiguation in perception, selective attention, working memory and imagery, emotional prioritization, cognitive control, and learning, which has profound implications for neurobiology, psychology, neurology, psychiatry, and philosophy. The book is written for a wide audience, and it explains the neuroscience to the psychologists, the psychology to the neuroscientists, and both fields to philosophers, to students of the behavioural and brain sciences, and to all intrigued by the enduring mystery of how brains can be minds. Finally, it identifies many issues inviting explora…

Integrity signals

Registry

Crossref · 10.1093/oso/9780198876984.001.0001

Cites

426 of 426 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Items 201–400 of 426

Increased Threshold for Spike-Timing-Dependent Plasticity Is Caused by Unreliable Calcium Signaling in Mice Lacking Fragile X Gene Fmr1
Meredith, R. M., Holmgren, C. D., Weidum, M., Burnashev, N., & Mansvelder, H. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.028 · Cited by 190
Inherited cortical HCN1 channel loss amplifies dendritic calcium electrogenesis and burst firing in a rat absence epilepsy model
Kole, M. H. P., Bräuer, A. U., & Stuart, G. J. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.122028 · Cited by 189
The ascending arousal system shapes neural dynamics to mediate awareness of cognitive states
Munn, B., Müller, E. J., Wainstein, G., & Shine, J. M. (2021) · Nature Communications · doi:10.1038/s41467-021-26268-x · Cited by 188
A blanket of inhibition: functional inferences from dense inhibitory connectivity
Karnani, M. M., Agetsuma, M., & Yuste, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.015 · Cited by 188
Cerebral cortex : principles of operation
Rolls, E. T. (2016) · doi:10.82444/warw.33712699 · Cited by 187
Brain-Wide Maps of Synaptic Input to Cortical Interneurons
Wall, N. R., Parra, M. D. L., Sorokin, J. M., Taniguchi, H., Huang, Z. J., & Callaway, E. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3967-15.2016 · Cited by 186
Functional clustering of dendritic activity during decision-making
Kerlin, A., Mohar, B., Flickinger, D., MacLennan, B. J., Dean, M. B., Davis, C., Spruston, N., & Svoboda, K. (2019) · eLife · doi:10.7554/elife.46966 · Cited by 186
Layer- and Cell Type-Specific Modulation of Excitatory Neuronal Activity in the Neocortex
Radnikow, G., & Feldmeyer, D. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00001 · Cited by 185
Sparse bursts optimize information transmission in a multiplexed neural code
Naud, R., & Sprekeler, H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1720995115 · Cited by 185
Different glutamate receptors convey feedforward and recurrent processing in macaque V1
Self, M. W., Kooijmans, R. N., Supèr, H., Lamme, V. A., & Roelfsema, P. R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119527109 · Cited by 184
Locus Coeruleus Norepinephrine in Learned Behavior: Anatomical Modularity and Spatiotemporal Integration in Targets
Breton‐Provencher, V., Drummond, G. T., & Sur, M. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.638007 · Cited by 182
N-Methyl-D-Aspartate Receptor Antagonist Effects on Prefrontal Cortical Connectivity Better Model Early Than Chronic Schizophrenia
Anticevic, A., Corlett, P. R., Cole, M. W., Savic, A., Gancsos, M., Tang, Y., Repovs, G., Murray, J. D., Driesen, N. R., Morgan, P. T., et al. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.07.022 · Cited by 181
The Diversity of Cortical Inhibitory Synapses
Kubota, Y., Karube, F., Nomura, M., & Kawaguchi, Y. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00027 · Cited by 180
Differential Role of Prefrontal and Parietal Cortices in Controlling Level of Consciousness
Pal, D., Dean, J. G., Liu, T., Li, D., Watson, C. J., Hudetz, A. G., & Mashour, G. A. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.025 · Cited by 177
A Disinhibitory Circuit for Contextual Modulation in Primary Visual Cortex
Keller, A. J., Dipoppa, M., Roth, M., Caudill, M. S., Ingrosso, A., Miller, K. D., & Scanziani, M. (2020) · Neuron · doi:10.1016/j.neuron.2020.11.013 · Cited by 177
Does moderate drinking harm the fetal brain? Insights from animal models
Valenzuela, C. F., Morton, R. A., Diaz, M. R., & Topper, L. A. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.01.006 · Cited by 172
Explaining and inducing savant skills: privileged access to lower level, less-processed information
Snyder, A. W. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0290 · Cited by 166
THEORY FOR THE DEVELOPMENT OF NEURON SELECTIVITY: ORIENTATION SPECIFICITY AND BINOCULAR INTERACTION IN VISUAL CORTEX
Bienenstock, E., Cooper, L. N., & Munro, P. (1995) · World Scientific series in 20th century physics · doi:10.1142/9789812795885_0006 · Cited by 165
Coupling the State and Contents of Consciousness
Aru, J., Suzuki, M., Rutiku, R., Larkum, M. E., & Bachmann, T. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00043 · Cited by 164
Developmental mechanisms channeling cortical evolution
Finlay, B. L., & Uchiyama, R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.11.004 · Cited by 163
Perirhinal input to neocortical layer 1 controls learning
Doron, G., Shin, J. N., Takahashi, N., Drüke, M., Bocklisch, C., Skenderi, S., de Mont, L., Toumazou, M., Ledderose, J., Brecht, M., et al. (2020) · Science · doi:10.1126/science.aaz3136 · Cited by 160
Information Decomposition of Target Effects from Multi-Source Interactions: Perspectives on Previous, Current and Future Work
Lizier, J. T., Bertschinger, N., Jost, J., & Wibral, M. (2018) · Entropy · doi:10.3390/e20040307 · Cited by 159
Human Cortical Pyramidal Neurons: From Spines to Spikes via Models
Eyal, G., Verhoog, M. B., Testa-Silva, G., Deitcher, Y., Benavides‐Piccione, R., DeFelipe, J., de Kock, C. P. J., Mansvelder, H. D., & Segev, I. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00181 · Cited by 158
Potassium Channels Control the Interaction between Active Dendritic Integration Compartments in Layer 5 Cortical Pyramidal Neurons
Harnett, M. T., Xu, N.-L., Magee, J. C., & Williams, S. R. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.005 · Cited by 157
Learning with three factors: modulating Hebbian plasticity with errors
Kuśmierz, Ł., Isomura, T., & Toyoizumi, T. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.08.020 · Cited by 155
Partial information decomposition as a unified approach to the specification of neural goal functions
Wibral, M., Priesemann, V., Kay, J., Lizier, J. T., & Phillips, W. A. (2015) · Brain and Cognition · doi:10.1016/j.bandc.2015.09.004 · Cited by 154
Self-citation
A Feedback Model of Visual Attention
Spratling, M., & Johnson, M. H. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/089892904322984526 · Cited by 153
The cognitive neuroscience of visual short-term memory
Postle, B. R. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2014.08.004 · Cited by 149
The Ebbinghaus illusion deceives adults but not young children
DOHERTY, M. J., Campbell, N. M., Tsuji, H., & Phillips, W. A. (2009) · Developmental Science · doi:10.1111/j.1467-7687.2009.00931.x · Cited by 149
Self-citation
Neocortical Layer 1: an elegant solution to top-down and bottom-up integration
Schuman, B., Dellal, S., Prönneke, A., Machold, R., & Rudy, B. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100520-012117 · Cited by 148
The microcircuit concept applied to cortical evolution: from three-layer to six-layer cortex
Shepherd, G. M. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00030 · Cited by 148
Distribution and function of HCN channels in the apical dendritic tuft of neocortical pyramidal neurons
Harnett, M. T., Magee, J. C., & Williams, S. R. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2813-14.2015 · Cited by 148
Visual Perception Disturbances in Schizophrenia: A Unified Model
Silverstein, S. M. (2016) · Nebraska Symposium on Motivation/The Nebraska symposium on motivation · doi:10.1007/978-3-319-30596-7_4 · Cited by 147
Transcranial magnetic stimulation (TMS) inhibits cortical dendrites
Murphy, S. C., Palmer, L. M., Nyffeler, T., Müri, R. M., & Larkum, M. E. (2016) · eLife · doi:10.7554/elife.13598 · Cited by 143
AN fMRI EXAMINATION OF VISUAL INTEGRATION IN SCHIZOPHRENIA
Silverstein, S. M., Berten, S., Essex, B. G., Kovács, I., Susmaras, T. M., & Little, D. M. (2009) · Journal of Integrative Neuroscience · doi:10.1142/s0219635209002113 · Cited by 141
Subcircuit-specific neuromodulation in the prefrontal cortex
Dembrow, N. C., & Johnston, D. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00054 · Cited by 141
Protein kinase A-independent modulation of ion channels in the brain by cyclic AMP.
Pedarzani, P., & Storm, J. F. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.25.11716 · Cited by 138
The role of monoamine oxidase A in the neurobiology of aggressive, antisocial, and violent behavior: A tale of mice and men
Kolla, N. J., & Bortolato, M. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101875 · Cited by 138
Physiology of Layer 5 Pyramidal Neurons in Mouse Primary Visual Cortex: Coincidence Detection through Bursting
Shai, A. S., Anastassiou, C. A., Larkum, M. E., & Koch, C. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004090 · Cited by 137
Constellation of HCN Channels and cAMP Regulating Proteins in Dendritic Spines of the Primate Prefrontal Cortex: Potential Substrate for Working Memory Deficits in Schizophrenia
Paspalas, C. D., Wang, M., & Arnsten, A. F. T. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs152 · Cited by 136
Visual Functions Generating Conscious Seeing
Lamme, V. A. F. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.00083 · Cited by 136
Distinct Feedforward and Feedback Effects of Microstimulation in Visual Cortex Reveal Neural Mechanisms of Texture Segregation
Klink, P. C., Dagnino, B., Gariel-Mathis, M.-A., & Roelfsema, P. R. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.033 · Cited by 135
Spatial working memory alters the efficacy of input to visual cortex
Merrikhi, Y., Clark, K., Albarran, E., Parsa, M., Zirnsak, M., Moore, T., & Noudoost, B. (2017) · Nature Communications · doi:10.1038/ncomms15041 · Cited by 134
Noradrenaline Modulates Visual Perception and Late Visually Evoked Activity
Gelbard-Sagiv, H., Magidov, E., Sharon, H., Hendler, T., & Nir, Y. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.051 · Cited by 134
Visual cortex excitability increases during visual mental imagery—a TMS study in healthy human subjects
Sparing, R., Mottaghy, F. M., Ganis, G., Thompson, W. L., Töpper, R., Kosslyn, S. M., & Pascual‐Leone, Á. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02478-2 · Cited by 133
The discovery of structure by multi-stream networks of local processors with contextual guidance
Phillips, W. A., Kay, J., & Smyth, D. (1995) · Network Computation in Neural Systems · doi:10.1088/0954-898x_6_2_005 · Cited by 133
Self-citation
Anterolateral Motor Cortex Connects with a Medial Subdivision of Ventromedial Thalamus through Cell Type-Specific Circuits, Forming an Excitatory Thalamo-Cortico-Thalamic Loop via Layer 1 Apical Tuft Dendrites of Layer 5B Pyramidal Tract Type Neurons
Guo, K., Yamawaki, N., Svoboda, K., & Shepherd, G. M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1333-18.2018 · Cited by 133
Evidence of Reduced Global Processing in Autism Spectrum Disorder
Booth, R. D. L., & Happe, F. G. E. (2016) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-016-2724-6 · Cited by 131
Bits from Brains for Biologically Inspired Computing
Wibral, M., Lizier, J. T., & Priesemann, V. (2015) · Frontiers in Robotics and AI · doi:10.3389/frobt.2015.00005 · Cited by 131
Towards an integrated view of HCN channel role in epilepsy
Noam, Y., Bernard, C., & Baram, T. Z. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.06.013 · Cited by 130
Decoding Natural Sounds in Early “Visual” Cortex of Congenitally Blind Individuals
Vetter, P., Bola, Ł., Reich, L., Bennett, M., Muckli, L. F., & Amedi, A. (2020) · Current Biology · doi:10.1016/j.cub.2020.05.071 · Cited by 129
Visual intracortical and transthalamic pathways carry distinct information to cortical areas
Blot, A., Roth, M., Gasler, I. T., Javadzadeh, M., Imhof, F., & Hofer, S. B. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.017 · Cited by 129
A Dendritic Substrate for the Cholinergic Control of Neocortical Output Neurons
Williams, S. R., & Fletcher, L. N. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.035 · Cited by 128
Context-dependent interpretation of words: Evidence for interactive neural processes
Gennari, S. P., MacDonald, M. C., Postle, B. R., & Seidenberg, M. S. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.01.015 · Cited by 127
Transcriptional and imaging-genetic association of cortical interneurons, brain function, and schizophrenia risk
Anderson, K. M., Collins, M. A., Chin, R., Ge, T., Rosenberg, M. D., & Holmes, A. J. (2020) · Nature Communications · doi:10.1038/s41467-020-16710-x · Cited by 123
Normalization and the Cholinergic Microcircuit: A Unified Basis for Attention
Schmitz, T. W., & Duncan, J. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.02.011 · Cited by 119
The disruption of the ‘sense of self’ in schizophrenia: Potential links with disturbances of information processing
Hemsley, D. R. (1998) · British Journal of Medical Psychology · doi:10.1111/j.2044-8341.1998.tb01373.x · Cited by 117
Short-term visual memory
Phillips, W. A. (1983) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1983.0056 · Cited by 117
Self-citation
Functional evolution of new and expanded attention networks in humans
Patel, G. H., Yang, D., Jamerson, E. C., Snyder, L. H., Corbetta, M., & Ferrera, V. P. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1420395112 · Cited by 116
Inhibitory interneurons in visual cortical plasticity
van Versendaal, D., & Levelt, C. N. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2264-4 · Cited by 113
A disinhibitory circuit motif and flexible information routing in the brain
Wang, X.-J., & Yang, G. R. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.01.002 · Cited by 113
The course and clinical correlates of dysfunctions in visual perceptual organization in schizophrenia during the remission of psychotic symptoms
Uhlhaas, P. J., Phillips, W. A., & Silverstein, S. M. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2004.11.005 · Cited by 112
Self-citation
Seizures and Schizophrenia
Hyde, T. M., & Weinberger, D. R. (1997) · Schizophrenia Bulletin · doi:10.1093/schbul/23.4.611 · Cited by 111
It is time to combine the two main traditions in the research on the neural correlates of consciousness: C = L × D
Bachmann, T., & Hudetz, A. G. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00940 · Cited by 111
Why Are No Animal Communication Systems Simple Languages?
Beecher, M. D. (2021) · Frontiers in Psychology · doi:10.3389/fpsyg.2021.602635 · Cited by 111
Precision control for a flexible body representation
Limanowski, J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.023 · Cited by 111
Fast 3D Imaging of Spine, Dendritic, and Neuronal Assemblies in Behaving Animals
Szalay, G., Judák, L., Katona, G., Ócsai, K., Juhász, G., Veress, M., Szadai, Z., Fehér, A., Tompa, T., Chiovini, B., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.002 · Cited by 110
Learning with two sites of synaptic integration
Kording, K. P., & Peter König, B. (2000) · Network Computation in Neural Systems · doi:10.1088/0954-898x_11_1_302 · Cited by 107
Visual Selective Attention in Mice
Wang, L., & Krauzlis, R. J. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.038 · Cited by 107
Cortical and subcortical contributions to context-control learning
Chiu, Y., & Egner, T. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.01.019 · Cited by 107
Reduced depth inversion illusions in schizophrenia are state-specific and occur for multiple object types and viewing conditions.
Keane, B. P., Silverstein, S. M., Wang, Y., & Papathomas, T. V. (2013) · Journal of Abnormal Psychology · doi:10.1037/a0032110 · Cited by 106
Contextually guided unsupervised learning using local multivariate binary processors
Kay, J., Floreano, D., & Phillips, W. A. (1998) · Neural Networks · doi:10.1016/s0893-6080(97)00110-x · Cited by 105
Self-citation
Visual Short-Term Memory Compared in Rhesus Monkeys and Humans
Elmore, L. C., Ma, W. J., Magnotti, J. F., Leising, K. J., Passaro, A. D., Katz, J. S., & Wright, A. A. (2011) · Current Biology · doi:10.1016/j.cub.2011.04.031 · Cited by 104
The Context Sensitivity of Visual Size Perception Varies across Cultures
DOHERTY, M. J., Tsuji, H., & Phillips, W. A. (2008) · Perception · doi:10.1068/p5946 · Cited by 103
Self-citation
Rapid Linguistic Ambiguity Resolution in Young Children with Autism Spectrum Disorder: Eye Tracking Evidence for the Limits of Weak Central Coherence
Hahn, N., Snedeker, J., & Rabagliati, H. (2015) · Autism Research · doi:10.1002/aur.1487 · Cited by 103
The case against specialized visual-spatial short-term memory
Morey, C. C. (2018) · Psychological Bulletin · doi:10.1037/bul0000155 · Cited by 103
Cell-type specific innervation of cortical pyramidal cells at their apical dendrites
Karimi, A., Odenthal, J., Drawitsch, F., Boergens, K. M., & Helmstaedter, M. (2020) · eLife · doi:10.7554/elife.46876 · Cited by 103
A perspective on cortical layering and layer-spanning neuronal elements
Larkum, M. E., Petro, L. S., Sachdev, R. N. S., & Muckli, L. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00056 · Cited by 102
Context-dependent signaling of coincident auditory and visual events in primary visual cortex
Deneux, T., Harrell, E. R., Kempf, A., Ceballo, S., Filipchuk, A., & Bathellier, B. (2019) · eLife · doi:10.7554/elife.44006 · Cited by 98
Adrenergic Modulation Regulates the Dendritic Excitability of Layer 5 Pyramidal Neurons In Vivo
Labarrera, C., Deitcher, Y., Dudai, A., Weiner, B., Amichai, A. K., Zylbermann, N., & London, M. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.103 · Cited by 98
An Augmented Two-Layer Model Captures Nonlinear Analog Spatial Integration Effects in Pyramidal Neuron Dendrites
Jadi, M. P., Behabadi, B. F., Poleg-Polsky, A., Schiller, J., & Mel, B. W. (2014) · Proceedings of the IEEE · doi:10.1109/jproc.2014.2312671 · Cited by 96
Homologous Mechanisms of Visuospatial Working Memory Maintenance in Macaque and Human: Properties and Sources
Reinhart, R. M. G., Heitz, R. P., Purcell, B. A., Weigand, P. K., Schall, J. D., & Woodman, G. F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0215-12.2012 · Cited by 95
The spark of life: Darwin and the primeval soup
(2000) · Choice Reviews Online · doi:10.5860/choice.38-2160 · Cited by 95
On the functions, mechanisms, and malfunctions of intracortical contextual modulation
Phillips, W. A., Clark, A., & Silverstein, S. M. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.02.010 · Cited by 94
Self-citation
The Phenomenology and Neurobiology of Visual Distortions and Hallucinations in Schizophrenia: An Update
Silverstein, S. M., & Lai, A. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.684720 · Cited by 94
Human Teaching and Cumulative Cultural Evolution
Caldwell, C. A., Renner, E., & Atkinson, M. (2017) · Review of Philosophy and Psychology · doi:10.1007/s13164-017-0346-3 · Cited by 93
FROM CHANGE BLINDNESS TO CHOICE BLINDNESS
Johansson, P., Lars, H. A. L. L., & Sikström, S. (2008) · PSYCHOLOGIA · doi:10.2117/psysoc.2008.142 · Cited by 93
The Modulation of Orexin A on HCN Currents of Pyramidal Neurons in Mouse Prelimbic Cortex
Li, B., Chen, F., Ye, J., Chen, X., Yan, J., Li, Y., Xiong, Y., Zhou, Z., Xia, J., & Hu, Z. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp241 · Cited by 92
The Effects of Context and Attention on Spiking Activity in Human Early Visual Cortex
Self, M. W., Peters, J. C., Possel, J. K., Reithler, J., Goebel, R., Ris, P., Jeurissen, D., Reddy, L., Claus, S., Baayen, J. C., et al. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002420 · Cited by 92
Size Perception is Less Context-Sensitive in Males
Phillips, W. A., Chapman, K. L. S., & Berry, P. D. (2004) · Perception · doi:10.1068/p5110 · Cited by 90
Self-citation
Activity-Dependent Modulation of Layer 1 Inhibitory Neocortical Circuits by Acetylcholine
Brombas, A., Fletcher, L. N., & Williams, S. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4470-13.2014 · Cited by 90
Feature Binding in the Feedback Layers of Area V2
Shipp, S. D., Adams, D. L., Moutoussis, K., & Zeki, S. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn243 · Cited by 89
Precision and False Perceptual Inference
Parr, T., Benrimoh, D. A., Vincent, P., & Friston, K. J. (2018) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2018.00039 · Cited by 87
Visual Context Integration is Not Fully Developed in 4-Year-Old Children
Káldy, Z., & Kovács, I. (2003) · Perception · doi:10.1068/p3473 · Cited by 87
A Noradrenergic Mechanism Functions to Couple Motor Behavior with Arousal State
Burgess, C. R., & Peever, J. H. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.014 · Cited by 85
Integration of local features into global shapes: monkey and human fMRI studies
Kourtzi, Z., Tolias, A. S., Altmann, C. F., Augath, M. A., & Logothetis, N. K. (2010) · Journal of Vision · doi:10.1167/3.9.191 · Cited by 85
Pyramidal Neurons Are Not Generalizable Building Blocks of Cortical Networks
Luebke, J. I. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00011 · Cited by 84
Neocortical Topology Governs the Dendritic Integrative Capacity of Layer 5 Pyramidal Neurons
Fletcher, L. N., & Williams, S. R. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.048 · Cited by 84
The circuit architecture of cortical multisensory processing: Distinct functions jointly operating within a common anatomical network
Meijer, G. T., Mertens, P. E. C., Pennartz, C. M. A., Olcese, U., & Lansink, C. S. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.01.004 · Cited by 84
Autism and talent: the cognitive and neural basis of systemizing
Baron‐Cohen, S., & Lombardo, M. V. (2017) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2017.19.4/sbaroncohen · Cited by 84
Reevaluating the Role of Persistent Neural Activity in Short-Term Memory
Masse, N. Y., Rosen, M. C., & Freedman, D. J. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.12.014 · Cited by 84
Are Dendrites Conceptually Useful?
Larkum, M. E. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.03.008 · Cited by 84
Schizophrenia: A Very Short Introduction
Frith, C., & Johnstone, E. C. (2003) · UCL Discovery (University College London) · Cited by 83
Enhanced dendritic activity in awake rats
Murayama, M., & Larkum, M. E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910379106 · Cited by 83
Contextual signals in visual cortex
Khan, A. G., & Hofer, S. B. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.05.003 · Cited by 83
Between Perfectly Critical and Fully Irregular: A Reverberating Model Captures and Predicts Cortical Spike Propagation
Wilting, J., & Priesemann, V. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz049 · Cited by 82
Coherent Infomax as a Computational Goal for Neural Systems
Kay, J., & Phillips, W. A. (2010) · Bulletin of Mathematical Biology · doi:10.1007/s11538-010-9564-x · Cited by 80
Self-citation
Quantifying Information Modification in Developing Neural Networks via Partial Information Decomposition
Wibral, M., Finn, C., Wollstadt, P., Lizier, J. T., & Priesemann, V. (2017) · Entropy · doi:10.3390/e19090494 · Cited by 80
Intellectual realism in children's drawings of cubes
Phillips, W. A., Hobbs, S. B., & Pratt, F. R. (1978) · Cognition · doi:10.1016/0010-0277(78)90007-0 · Cited by 78
Self-citation
The role of temporal cortex in the control of attention
Ramezanpour, H., & Fallah, M. (2022) · Current Research in Neurobiology · doi:10.1016/j.crneur.2022.100038 · Cited by 76
The effects of arousal on apical amplification and conscious state
Phillips, W. A., Larkum, M. E., Harley, C. W., & Silverstein, S. M. (2016) · Neuroscience of Consciousness · doi:10.1093/nc/niw015 · Cited by 75
Self-citation
The coherent organization of mental life depends on mechanisms for context-sensitive gain-control that are impaired in schizophrenia
Phillips, W. A., & Silverstein, S. M. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00307 · Cited by 75
Self-citation
Cortico-Thalamo-Cortical Circuits of Mouse Forelimb S1 Are Organized Primarily as Recurrent Loops
Guo, K., Yamawaki, N., Barrett, J. M., Tapies, M. G. R., & Shepherd, G. M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2277-19.2020 · Cited by 75
Dendritic ion channelopathy in acquired epilepsy
Poolos, N. P., & Johnston, D. (2012) · Epilepsia · doi:10.1111/epi.12033 · Cited by 75
Amplifying the redistribution of somato-dendritic inhibition by the interplay of three interneuron types
Hertäg, L., & Sprekeler, H. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006999 · Cited by 75
Apical drive-A cellular mechanism of dreaming?
Aru, J., Siclari, F., Phillips, W. A., & Storm, J. F. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.09.018 · Cited by 74
Self-citation
Ebbinghaus illusion: Context, contour, and age influence the judged size of a circle amidst circles.
Weintraub, D. J. (1979) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037//0096-1523.5.2.353 · Cited by 74
United we sense, divided we fail: context-driven perception of ambiguous visual stimuli
Klink, P. C., Wezel, R. J. A. V., & van Ee, R. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2011.0358 · Cited by 74
Ion channels in EEG: isolating channel dysfunction in NMDA receptor antibody encephalitis
Symmonds, M., Moran, C., Leite, M. I., Buckley, C. J., Irani, S. R., Stephan, K. E., Friston, K. J., & Moran, R. (2018) · Brain · doi:10.1093/brain/awy107 · Cited by 74
Autoimmune encephalitis: a case series and comprehensive review of the literature
Wingfield, T., McHugh, C., Vas, A. L., Richardson, A. M. T., Wilkins, E., Bonington, A., & Varma, A. R. (2011) · QJM · doi:10.1093/qjmed/hcr111 · Cited by 73
The anatomical problem posed by brain complexity and size: a potential solution
DeFelipe, J. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00104 · Cited by 72
A recurrent circuit implements normalization, simulating the dynamics of V1 activity
Heeger, D. J., & Zemlianova, K. O. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005417117 · Cited by 72
Early Exposure to Alcohol Leads to Permanent Impairment of Dendritic Excitability in Neocortical Pyramidal Neurons
Granato, A., Palmer, L. M., Giorgio, A. D., Tavian, D., & Larkum, M. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5520-11.2012 · Cited by 72
The neuroecology of the water-to-land transition and the evolution of the vertebrate brain
MacIver, M. A., & Finlay, B. L. (2021) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2020.0523 · Cited by 71
Postnatal Development of Dendritic Synaptic Integration in Rat Neocortical Pyramidal Neurons
Atkinson, S. E., & Williams, S. R. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00083.2009 · Cited by 70
Intelligence as a Developing Function: A Neuroconstructivist Approach
Rinaldi, L., & Karmiloff‐Smith, A. (2017) · Journal of Intelligence · doi:10.3390/jintelligence5020018 · Cited by 70
An event-related potential examination of contour integration deficits in schizophrenia
Butler, P. D., Abeles, I. Y., Silverstein, S. M., Dias, E. C., Weiskopf, N. G., Calderone, D., & Sehatpour, P. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00132 · Cited by 69
A Theory of Predictive Dissonance: Predictive Processing Presents a New Take on Cognitive Dissonance
Kaaronen, R. O. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02218 · Cited by 69
Scene Representations Conveyed by Cortical Feedback to Early Visual Cortex Can Be Described by Line Drawings
Morgan, A., Petro, L. S., & Muckli, L. F. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0852-19.2019 · Cited by 69
Modern theories of human evolution foreshadowed by Darwin’s Descent of Man
Richerson, P. J., Gavrilets, S., & de Waal, F. B. M. (2021) · Science · doi:10.1126/science.aba3776 · Cited by 69
Shakespeare's Philosophy: Discovering the Meaning Behind the Plays
McGinn, C. (2006) · Cited by 67
Visual persistence at both onset and offset of stimulation
Wilson, L. (1981) · Perception & Psychophysics · doi:10.3758/bf03206150 · Cited by 66
Some further ideas regarding the neuronal basis of awareness.
Koch, C., & Crick, F. (1994) · Cited by 65
Computing with a Canonical Neural Circuits Model with Pool Normalization and Modulating Feedback
Brosch, T., & Heiko Neumann, B. (2014) · Neural Computation · doi:10.1162/neco_a_00675 · Cited by 64
Practopoiesis: Or how life fosters a mind
Nikolić, D. (2015) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2015.03.003 · Cited by 64
Local Choices: Rationality and the Contextuality of Decision-Making
Vlaev, I. (2018) · Brain Sciences · doi:10.3390/brainsci8010008 · Cited by 64
Altered organization of cortical interneurons in rats exposed to ethanol during neonatal life
Granato, A. (2005) · Brain Research · doi:10.1016/j.brainres.2005.11.024 · Cited by 62
Cognitive functions of intracellular mechanisms for contextual amplification
Phillips, W. A. (2017) · Brain and Cognition · doi:10.1016/j.bandc.2015.09.005 · Cited by 62
Self-citation
Apical function in neocortical pyramidal cells: a common pathway by which general anesthetics can affect mental state
Phillips, W. A., Bachmann, T., & Storm, J. F. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00050 · Cited by 62
Self-citation
Organization of cortico-cortical associative projections in rats exposed to ethanol during early postnatal life
Granato, A., Rocco, F. D., Zumbo, A., Toesca, A., & Giannetti, S. (2003) · Brain Research Bulletin · doi:10.1016/s0361-9230(03)00052-2 · Cited by 61
An efficient analytical reduction of detailed nonlinear neuron models
Amsalem, O., Eyal, G., Rogozinski, N., Gevaert, M., Kumbhar, P., Schürmann, F., & Segev, I. (2020) · Nature Communications · doi:10.1038/s41467-019-13932-6 · Cited by 61
Dendritic integration theory: A thalamo-cortical theory of state and content of consciousness
Bachmann, T., Suzuki, M., & Aru, J. (2020) · Philosophy and the Mind Sciences · doi:10.33735/phimisci.2020.ii.52 · Cited by 61
Distinct “driving” versus “modulatory” influences of different visual corticothalamic pathways
Kirchgessner, M. A., Franklin, A. D., & Callaway, E. M. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.025 · Cited by 59
On the working memory of humans and great apes: Strikingly similar or remarkably different?
Read, D., Manrique, H. M., & WALKER, M. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.12.019 · Cited by 58
Segregation by onset asynchrony
Hancock, P., Walton, L., Mitchell, G., Plenderleith, Y., & Phillips, W. A. (2008) · Journal of Vision · doi:10.1167/8.7.21 · Cited by 57
Self-citation
Serotonin Differentially Regulates L5 Pyramidal Cell Classes of the Medial Prefrontal Cortex in Rats and Mice
Elliott, M. C., Tanaka, P. M., Schwark, R., & Andrade, R. (2018) · eNeuro · doi:10.1523/eneuro.0305-17.2018 · Cited by 57
Rapid contour integration in macaque monkeys
Mandon, S., & Kreiter, A. K. (2004) · Vision Research · doi:10.1016/j.visres.2004.08.010 · Cited by 56
Dendritic integration in pyramidal neurons during network activity and disease
Palmer, L. M. (2013) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.09.010 · Cited by 56
Apical dendrite activity in cognition and consciousness
LaBerge, D. (2005) · Consciousness and Cognition · doi:10.1016/j.concog.2005.09.007 · Cited by 55
Non-Conscious Prediction and a Role for Consciousness in Correcting Prediction Errors
Pally, R. (2005) · Cortex · doi:10.1016/s0010-9452(08)70282-x · Cited by 55
Oscillatory recurrent gated neural integrator circuits (ORGaNICs), a unifying theoretical framework for neural dynamics
Heeger, D. J., & Mackey, W. E. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1911633116 · Cited by 55
The ascending arousal system promotes optimal performance through mesoscale network integration in a visuospatial attentional task
Wainstein, G., Rojas‐Líbano, D., Medel, V., Alnæs, D., Kolskår, K. K., Endestad, T., Laeng, B., Ossandón, T., Crossley, N. A., Matar, E., et al. (2021) · Network Neuroscience · doi:10.1162/netn_a_00205 · Cited by 55
Prenatal Ethanol Exposure Leads to Attention Deficits in Both Male and Female Rats
Wang, R., Martin, C. D., Lei, A. L., Hausknecht, K. A., Ishiwari, K., Richards, J. B., Haj‐Dahmane, S., & Shen, R. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00012 · Cited by 55
Dendritic Integration Dysfunction in Neurodevelopmental Disorders
Nelson, A. D., & Bender, K. J. (2021) · Developmental Neuroscience · doi:10.1159/000516657 · Cited by 54
The Role of Dendritic Signaling in the Anesthetic Suppression of Consciousness
Meyer, K. (2015) · Anesthesiology · doi:10.1097/aln.0000000000000673 · Cited by 53
Timing and Precision of Spike Initiation in Layer V Pyramidal Cells of the Rat Somatosensory Cortex
Berger, T. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.274 · Cited by 53
A feedback model of perceptual learning and categorization
Spratling, M., & Johnson, M. H. (2006) · Visual Cognition · doi:10.1080/13506280500168562 · Cited by 53
The role of NMDA receptor and neuroligin rare variants in synaptic dysfunction underlying neurodevelopmental disorders
Vieira, M. M., Jeong, J., & Roche, K. W. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.03.001 · Cited by 51
Invariant Components of Synergy, Redundancy, and Unique Information among Three Variables
Pica, G., Piasini, E., Chicharro, D., & Panzeri, S. (2017) · Entropy · doi:10.3390/e19090451 · Cited by 51
Cortical feedback signals generalise across different spatial frequencies of feedforward inputs
Revina, Y., Petro, L. S., & Muckli, L. F. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.09.047 · Cited by 50
How a (sub)Cellular Coincidence Detection Mechanism Featuring Layer-5 Pyramidal Cells May Help Produce Various Visual Phenomena
Bachmann, T. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01947 · Cited by 49
Mining the jewels of the cortex’s crowning mystery
Ibrahim, L. A., Schuman, B., Bandler, R. C., Rudy, B., & Fishell, G. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.04.005 · Cited by 49
The integrated information theory of consciousness: A case of mistaken identity
Merker, B., Williford, K., & Rudrauf, D. (2022) · Behavioral and Brain Sciences · doi:10.1017/s0140525x21000881 · Cited by 49
Global disruption in excitation-inhibition balance can cause localized network dysfunction and Schizophrenia-like context-integration deficits
Calvin, O. L., & Redish, A. D. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008985 · Cited by 49
The structure of executive functions in preschool children and chimpanzees
Völter, C. J., Reindl, E., Felsche, E., Civelek, Z., Whalen, A., Lugosi, Z., Duncan, L., Herrmann, E., Call, J., & Seed, A. M. (2022) · Scientific Reports · doi:10.1038/s41598-022-08406-7 · Cited by 49
Layer-specific high-frequency action potential spiking in the prefrontal cortex of awake rats
Boudewijns, Z. S. R. M., Groen, M. R., Lodder, B., McMaster, M. T. B., Kalogreades, L., de Haan, R., Narayanan, R. T., Meredith, R. M., Mansvelder, H. D., & de Kock, C. P. J. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00099 · Cited by 48
Sapiens: A Brief History of Humankind
Pfeiffer, J. R. (2017) · Utopian Studies · doi:10.5325/utopianstudies.28.1.0214 · Cited by 48
Interaction of feedforward and feedback streams in visual cortex in a firing-rate model of columnar computations
Brosch, T., & Heiko Neumann, B. (2014) · Neural Networks · doi:10.1016/j.neunet.2014.02.005 · Cited by 46
Decoding Schizophrenia
Javitt, D. C., & Coyle, J. T. (2004) · Scientific American · doi:10.1038/scientificamerican0104-48 · Cited by 45
Apical amplification—a cellular mechanism of conscious perception?
Marvan, T., Polák, M., Bachmann, T., & Phillips, W. A. (2021) · Neuroscience of Consciousness · doi:10.1093/nc/niab036 · Cited by 45
Self-citation
Layer-specific regulation of cortical neurons by interhemispheric inhibition
Palmer, L. M., Schulz, J. M., & Larkum, M. E. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.23545 · Cited by 44
Beyond the Classical Receptive Field: Contextual Modulation of V1 Responses
Lamme, V. A. F. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/7131.003.0053 · Cited by 44
Partial and Entropic Information Decompositions of a Neuronal Modulatory Interaction
Kay, J., Ince, R. A. A., Dering, B. R., & Phillips, W. (2017) · Entropy · doi:10.3390/e19110560 · Cited by 44
Self-citation
Excitatory and inhibitory effects of HCN channel modulation on excitability of layer V pyramidal cells
Mäki‐Marttunen, T., & Mäki-Marttunen, V. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010506 · Cited by 44
Dynamic Coordination in Brain and Mind
Phillips, W. A., von der Malsburg, C., & Singer, W. (2010) · The MIT Press eBooks · doi:10.7551/mitpress/8797.003.0004 · Cited by 44
Self-citation
SINBAD: A neocortical mechanism for discovering environmental variables and regularities hidden in sensory input
Favorov, O. V., & Ryder, D. (2004) · Biological Cybernetics · doi:10.1007/s00422-004-0464-8 · Cited by 43
Dendritic processing of spontaneous neuronal sequences for single-trial learning
Haga, T., & Fukai, T. (2018) · Scientific Reports · doi:10.1038/s41598-018-33513-9 · Cited by 43
Confidence Drives a Neural Confirmation Bias
Rollwage, M., Hauser, T. U., Loosen, A. M., Moran, R., Dolan, R. J., & Fleming, S. M. (2019) · Conference on Cognitive Computational Neuroscience (CCN) · doi:10.32470/ccn.2019.1064-0 · Cited by 43
Alterations of Neocortical Pyramidal Neurons: Turning Points in the Genesis of Mental Retardation
Granato, A., & Giorgio, A. D. (2014) · Frontiers in Pediatrics · doi:10.3389/fped.2014.00086 · Cited by 41
What makes a simple partial seizure complex?
Cavanna, A. E., Rickards, H. E., & Ali, F. (2011) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2011.10.003 · Cited by 40
Self-Organized Complexity and Coherent Infomax from the Viewpoint of Jaynes’s Probability Theory
Phillips, W. A. (2012) · Information · doi:10.3390/info3010001 · Cited by 40
Self-citation
Top-Down Suppression of Sensory Cortex in an NMDAR Hypofunction Model of Psychosis
Ranson, A., Broom, E., Powell, A. L., Chen, F., Major, G., & Hall, J. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sby190 · Cited by 40
All-or-None Context Dependence Delineates Limits of FEF Visual Target Selection
Scerra, V. E., Costello, M. G., Salinas, E., & Stanford, T. R. (2019) · Current Biology · doi:10.1016/j.cub.2018.12.013 · Cited by 39
Dendritic Compartmentalization of Learning-Related Plasticity
Godenzini, L., Shai, A. S., & Palmer, L. M. (2022) · eNeuro · doi:10.1523/eneuro.0060-22.2022 · Cited by 39
A Comparison of Partial Information Decompositions Using Data from Real and Simulated Layer 5b Pyramidal Cells
Kay, J., Schulz, J. M., & Phillips, W. A. (2022) · Entropy · doi:10.3390/e24081021 · Cited by 39
Self-citation
Contour interpolation: A case study in Modularity of Mind
Keane, B. P. (2017) · Journal of Vision · doi:10.1167/17.10.1366 · Cited by 38
Reduced density of dendritic spines in pyramidal neurons of rats exposed to alcohol during early postnatal life
Giorgio, A. D., & Granato, A. (2015) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2015.01.005 · Cited by 36
Collinear facilitation and contour integration in autism: evidence for atypical visual integration
Jachim, S., Warren, P. A., McLoughlin, N. P., & Gowen, E. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00115 · Cited by 35
Going Beyond the Point Neuron: Active Dendrites and Sparse Representations for Continual LearningPreprint
Grewal, K., Forest, J., Cohen, B. P., & Ahmad, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.25.465651 · Cited by 35
Measures for investigating the contextual modulation of information transmission
Smyth, D., Phillips, W., & Kay, J. (1996) · Network Computation in Neural Systems · doi:10.1088/0954-898x/7/2/011 · Cited by 34
Self-citation
Visual mental imagery engages the left fusiform gyrus, but not the early visual cortex: A meta-analysis of neuroimaging evidence
Spagna, A., Hajhajate, D., Liu, J., & Bartolomeo, P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.12.029 · Cited by 33
Perspective on the Multiple Pathways to Changing Brain States
Tantirigama, M. L. S., Zolnik, T. A., Judkewitz, B., Larkum, M. E., & Sachdev, R. N. S. (2020) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.00023 · Cited by 32
Differences in Noradrenaline Receptor Expression Across Different Neuronal Subtypes in Macaque Frontal Eye Field
Lee, M. L., Mueller, A. L., & Moore, T. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.574130 · Cited by 32
Unlocking the Potential of Two-Point Cells for Energy-Efficient and Resilient Training of Deep Nets
Adeel, A., Adetomi, A., Ahmed, K., Hussain, A., Arslan, T., & Phillips, W. A. (2023) · IEEE Transactions on Emerging Topics in Computational Intelligence · doi:10.1109/tetci.2022.3228537 · Cited by 32
Self-citation
A model of non-linear interactions between cortical top-down and horizontal connections explains the attentional gating of collinear facilitation
Meyer, K. D., & Spratling, M. (2009) · Vision Research · doi:10.1016/j.visres.2008.12.017 · Cited by 31
Contextual Modulation in Mammalian Neocortex is Asymmetric
Kay, J., & Phillips, W. A. (2020) · Symmetry · doi:10.3390/sym12050815 · Cited by 30
Self-citation
How to Mitigate the Hard Problem by Adopting the Dual Theory of Phenomenal Consciousness
Polák, M., & Marvan, T. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.02837 · Cited by 30
Glutamate and norepinephrine interaction: Relevance to higher cognitive operations and psychopathology
Abdallah, C. G., Averill, L. A., Krystal, J. H., Southwick, S. M., & Arnsten, A. F. T. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15001727 · Cited by 30
Challenging the point neuron dogma: FS basket cells as 2-stage nonlinear integratorsPreprint
Tzilivaki, A., Kastellakis, G., & Poirazi, P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/251314 · Cited by 30
Visual short-term memory of local information in briefly viewed natural scenes: Configural and non-configural factors
Velisavljevic, L., & Elder, J. H. (2008) · Journal of Vision · doi:10.1167/8.16.8 · Cited by 29

Research works printed but not linked: 52

2022, Context-sensitivity transforms the effectiveness and efficiency of neural information processing., Arxiv
2000, Precis of neural organization: Structure, function, and dynamics., Behavioral and Brain Sciences
2009, Stress signaling pathways that impair prefrontal cortex structure and function., Nature Reviews Neuroscience
2008, Journal of Neurophysiology
2003, Journal of Neurophysiology
2016, Brain Research Reviews
2007, Alpha2-noradrenergic receptors activation enhances excitability and synaptic integration in rat prefrontal cortex pyramidal neurons via inhibition of HCN currents., Journal of Physiology
2014, Differential distribution of voltage-gated ion channels in cortical neurons. Implications for epilepsy., Neurology
2016, The selfish gene
2007, More accurate size contrast judgements in the Ebbinghaus illusion by a remote culture., Journal of Experimental Psychology: Human Perception and Performance
2004, Freedom evolves
2008, Computing the mind
1983, The modularity of mind
1989, Studies in the way of words
2015, Structural-functional connectivity deficits of neocortical circuits in the Fmr1 (−/y) mouse model of autism., Science Advances
2009, REM sleep and dreaming: Toward a theory of protoconsciousness., Nature Reviews Neuroscience
2011, Thinking, fast and slow
2015, Cell type-specific channelopathies in the prefrontal cortex of the fmr1-/y mouse model of Fragile X syndrome., eNeuro
2009, Nativism vs neuroconstructivism: Rethinking developmental disorders., Developmental Psychology
Contextual signals in visual cortex., Current Opinion in Neurobiology
1927, The Kingsway Shakespeare
2020, Molecular Autism
2004, Cortex,
2003, Synaptically activated Ca2+ waves in layer 2/3 and layer 5 rat neocortical pyramidal neurons., Journal of Physiology
2015, Deep learning., Nature
2012, The time window for generation of dendritic pikes by coincidence of action potentials and EPSPs is layer specific in somatosensory cortex., PLoS One
2002, Synaptic self
2019, Computational modelling of genetic contributions to excitability and neural coding in layer V pyramidal cells: Applications to schizophrenia pathology., Frontiers in Computational Neuroscience
2006, Enhanced perceptual functioning in autism: An updated model, and eight principle of autistic perception., Journal of Autism and Developmental Disorders
2019, Attention or salience?, Current Opinion in Psychology
2014, Animal Cognition
2007, Journal of Comparative Psychology
1974, Function and interaction of on and off transients in vision: 1. Psychophysics., Experimental Brain Research
1999, Physiology of perception: Cortical stimulation and recording in humans., Neurology
1996, The origins of virtue
2009, The neuropsychopharmacology of frontoexecutive function: Monoaminergic modulation., Annual Review of Neuroscience
2009, Thalamic input to apical dendrites in neocortical layer 1 is massive and highly convergent., Cerebral Cortex
2001, Gain modulation in the central nervous system: Where behavior, neurophysiology, and computation meet., Neuroscientist
2021, Frontiers in Cellular Neuroscience
1995, The theoretical foundation of dendritic function: Selected papers of Wilfrid Rall
2000, Integrating top-down and bottom-up sensory processing by somato-dendritic interactions., Journal of Computational Neuroscience
2013, Frontiers in Psychology
1974, Function and interaction of on and off transients in vision: 2. Neurophysiology., Experimental Brain Research
2008, Précis of neuroconstructivism: How the brain constructs cognition., Behavioral and Brain Sciences
2019, Neuron
2013, In vivo cholinergic modulation of the cellular properties of medial entorhinal cortex neurons., Journal of Physiology
2012, Neuron
2017, Why we sleep
1983, Animal thought
2007, Alpha2A-adrenoceptors strengthen working memory networks b inhibiting cAMP-HCN channel signaling in prefrontal cortex., Cell
1961, Culture and society 1780–1050
2000, Maturation of layer 5 neocortical pyramidal neurons: Amplifying salient layer 1 and layer 4 inputs by Ca2+ action potentials in adult rat tuft dendrites., Journal of Physiology

Sorted by citations

An integrative, multiscale view on neural theories of consciousness
Storm, J. F., Klink, P. C., Aru, J., Senn, W., Goebel, R., Pigorini, A., Avanzini, P., Vanduffel, W., Roelfsema, P. R., Massimini, M., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.02.004 · Cited by 114
Context-Sensitive Processing in a Model Neocortical Pyramidal Cell With Two Sites of Input Integration
Graham, B. P., Kay, J., & Phillips, W. A. (2025) · Neural Computation · doi:10.1162/neco_a_01739 · Cited by 9
Self-citation
Simplified two-compartment neuron with calcium dynamics capturing brain-state specific apical-amplification, -isolation and -drive
Pastorelli, E., Yegenoglu, A., Kolodziej, N., Wybo, W. A. M., Simula, F., Diaz-Pier, S., Storm, J. F., & Paolucci, P. S. (2025) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2025.1566196 · Cited by 5
A model of thalamo-cortical interaction for incremental binding in mental contour-tracing
Schmid, D., & Heiko Neumann, B. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012835 · Cited by 7
Semantization of memories in a hippocampal–cortical spiking neural network
D’Alba, F., Kushawaha, N., Fruzzetti, L., Paolucci, P. S., & Falotico, E. (2025) · Neurocomputing · doi:10.1016/j.neucom.2025.130323 · Cited by 4

See all 13

Authors: Phillips, W. A.
Affiliations: University of Stirling (GB)
Corresponding author: Phillips, William A.
ORCID: Phillips, William A.
Publisher: Oxford University PressOxford
Published: 2023-04-20
DOI: 10.1093/oso/9780198876984.001.0001
OpenAlex: W4377022295
Cited by: 13
References: 428
Citations by year: 2026: 4 · 2025: 8 · 2023: 1
FWCI: 3.83
Type: book
Language: en
Open access: closed
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords: neocortex, information amplification, information theory, perception, selective attention, working memory, imagery, cognitive control, learning, philosophy of mind, systems neuroscience

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

The Cooperative Neuron: Cellular Foundations of Mental Life

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Citations

Cites

Cited by

Related

Metadata

Record

About these checks