Rapid Neocortical Dynamics: Cellular and Network Mechanisms

Haider, Bilal; McCormick, David A.

doi:10.1016/j.neuron.2009.04.008

Cited by 441Neural dynamics and brain functionNeuroscience and Neuropharmacology ResearchFunctional Brain Connectivity Studies

Rapid Neocortical Dynamics: Cellular and Network Mechanisms

Open access

Haider, Bilal, McCormick, David A.·2009·Neuron

DOI 10.1016/j.neuron.2009.04.008PMC PMC3132648

Open this paper in CoChat — free account Open PDF

Abstract

The highly interconnected local and large-scale networks of the neocortical sheet rapidly and dynamically modulate their functional connectivity according to behavioral demands. This basic operating principle of the neocortex is mediated by the continuously changing flow of excitatory and inhibitory synaptic barrages that not only control participation of neurons in networks but also define the networks themselves. The rapid control of neuronal responsiveness via synaptic bombardment is a fundamental property of cortical dynamics that may provide the basis of diverse behaviors, including sensory perception, motor integration, working memory, and attention.

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

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

Integrity signals

Registry

Crossref · 10.1016/j.neuron.2009.04.008

Cites

251 of 251 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

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

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

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cortical GABAergic inhibition has a crucial role in regulating the gain of sensory responses.
“Although recent work has identified some potential mechanisms for excitatory regulation of cortical gain97,98, several lines of evidence suggest that cortical GABAergic inhibition has a crucial role in regulating the gain of sensory responses5,99,100 (FIG. 1).”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [99]

Self-check

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

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

An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803 · see citing works
Neural Mechanisms of Selective Visual Attention
Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388 · see citing works
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576 · 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
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 4,831 · 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
LTP and LTD
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968 · see citing works
Visual Feature Integration and the Temporal Correlation Hypothesis
Singer, W., & Gray, C. M. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.003011 · Cited by 3,157 · see citing works
Interneurons of the neocortical inhibitory system
Markram, H., Toledo-Rodriguez, M., Wang, Y., Gupta, A., Silberberg, G., & Wu, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1519 · Cited by 2,954 · see citing works
Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention
Fries, P., Reynolds, J. H., Rorie, A. E., & Desimone, R. (2001) · Science · doi:10.1126/science.1055465 · Cited by 2,786 · see citing works
Neurodegenerative Disorders: Parkinson's Disease and Huntington's Disease
Hague, S., Klaffke, S., & Bandmann, O. (2006) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781860948961_0007 · Cited by 2,767 · see citing works
Channelrhodopsin-2, a directly light-gated cation-selective membrane channel
Nagel, G., Szellas, T., Huhn, W., Kateriya, S., Adeishvili, N., Berthold, P. R., Ollig, D., Hegemann, P., & Bamberg, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1936192100 · Cited by 2,672 · see citing works
High Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex
Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., Berger, M. S., Barbaro, N. M., & Knight, R. T. (2006) · Science · doi:10.1126/science.1128115 · Cited by 2,650 · see citing works
Driving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603 · see citing works
Single-channel currents recorded from membrane of denervated frog muscle fibres
Neher, E., & Sakmann, B. J. (1976) · Nature · doi:10.1038/260799a0 · Cited by 2,577 · see citing works
The Intrinsic Electrophysiological Properties of Mammalian Neurons: Insights into Central Nervous System Function
Llinás, R. R. (1988) · Science · doi:10.1126/science.3059497 · Cited by 2,285 · see citing works
The Variable Discharge of Cortical Neurons: Implications for Connectivity, Computation, and Information Coding
Shadlen, M. N., & Newsome, W. T. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03870.1998 · Cited by 2,178 · see citing works
Spike Timing–Dependent Plasticity: A Hebbian Learning Rule
Caporale, N., & Dan, Y. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125639 · Cited by 1,997 · see citing works
Reliability of spike timing in neocortical neurons
Mainen, Z. F., & Sejnowski, T. J. (1995) · Science · doi:10.1126/science.7770778 · Cited by 1,950 · see citing works
Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex
McCormick, D. A., Connors, B. W., Lighthall, J. W., & Prince, D. A. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.54.4.782 · Cited by 1,935 · see citing works
Self-citation
A novel slow (< 1 Hz) oscillation of neocortical neurons in vivo: depolarizing and hyperpolarizing components
Steriade, M., Nunez, A., & Amzica, F. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03252.1993 · Cited by 1,903 · see citing works
Large-scale recording of neuronal ensembles
Buzsáki, G. (2004) · Nature Neuroscience · doi:10.1038/nn1233 · Cited by 1,875 · see citing works
Chaos in Neuronal Networks with Balanced Excitatory and Inhibitory Activity
van Vreeswijk, C., & Sompolinsky, H. (1996) · Science · doi:10.1126/science.274.5293.1724 · Cited by 1,831 · see citing works
The action potential in mammalian central neurons
Bean, B. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2148 · Cited by 1,785 · see citing works
The highly irregular firing of cortical cells is inconsistent with temporal integration of random epsps.
Softky, W., & Koch, C. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-01-00334.1993 · Cited by 1,689 · see citing works
Dynamics of ongoing activity: explanation of the large variability in evoked cortical responses
Arieli, A., Sterkin, A., Grinvald, A., & Aertsen, A. (1996) · Science · doi:10.1126/science.273.5283.1868 · Cited by 1,660 · 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
Cellular and network mechanisms of rhythmic recurrent activity in neocortex
Sanchez-Vives, M. V., & McCormick, D. A. (2000) · Nature Neuroscience · doi:10.1038/79848 · Cited by 1,539 · see citing works
Self-citation
Highly nonrandom features of synaptic connectivity in local cortical circuits
Song, S., Sjöström, P. J., Reigl, M., Nelson, S., & Chklovskii, D. B. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030068 · Cited by 1,512 · see citing works
Feature-based attention influences motion processing gain in macaque visual cortex
Treue, S., & Trujillo, J. C. M. (1999) · Nature · doi:10.1038/21176 · Cited by 1,465 · see citing works
The Normalization Model of Attention
Reynolds, J. H., & Heeger, D. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.002 · Cited by 1,457 · see citing works
Intrinsic firing patterns of diverse neocortical neurons
Connors, B. W., & Gutnick, M. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90185-d · Cited by 1,440 · see citing works
Sparse coding of sensory inputs
Olshausen, B. A., & Field, D. J. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.07.007 · Cited by 1,404 · see citing works
Modulation of Neuronal Interactions Through Neuronal Synchronization
Womelsdorf, T., Schoffelen, J.-M., Oostenveld, R., Singer, W., Desimone, R., Engel, A. K., & Fries, P. (2007) · Science · doi:10.1126/science.1139597 · Cited by 1,367 · see citing works
Balanced inhibition underlies tuning and sharpens spike timing in auditory cortex
Wehr, M., & Zador, A. M. (2003) · Nature · doi:10.1038/nature02116 · Cited by 1,363 · see citing works
Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo
Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345 · see citing works
Neural substrates of awakening probed with optogenetic control of hypocretin neurons
Adamantidis, A. R., Zhang, F., Aravanis, A. M., Deisseroth, K., & de Lecea, L. (2007) · Nature · doi:10.1038/nature06310 · Cited by 1,341 · see citing works
Correlated neuronal activity and the flow of neural information
Salinas, E., & Sejnowski, T. J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35086012 · Cited by 1,333 · see citing works
Natural waking and sleep states: a view from inside neocortical neurons
Steriade, M., Timofeev, I., & Grenier, F. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.5.1969 · Cited by 1,296 · see citing works
Effects of Attention on Orientation-Tuning Functions of Single Neurons in Macaque Cortical Area V4
McAdams, C. J., & Maunsell, J. H. R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00431.1999 · Cited by 1,214 · see citing works
Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex
Ohki, K., Chung, S., Ch'ng, Y. H., Kara, P., & Reid, R. C. (2005) · Nature · doi:10.1038/nature03274 · Cited by 1,191 · see citing works
Attentional modulation of visual processing
Reynolds, J. H., & Chelazzi, L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131039 · Cited by 1,158 · see citing works
DENDRITIC COMPUTATION
London, M., & Häusser, M. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135703 · Cited by 1,149 · see citing works
Neurotransmitter actions in the thalamus and cerebral cortex and their role in neuromodulation of thalamocortical activity
McCormick, D. A. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90012-4 · Cited by 1,117 · see citing works
Self-citation
Enforcement of Temporal Fidelity in Pyramidal Cells by Somatic Feed-Forward Inhibition
Pouille, F., & Scanziani, M. (2001) · Science · doi:10.1126/science.1060342 · Cited by 1,097 · see citing works
The high-conductance state of neocortical neurons in vivo
Alain Destexhe, A., Rudolph, M., & Paré, D. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1198 · Cited by 1,077 · see citing works
Turning on and off recurrent balanced cortical activity
Shu, Y., Hasenstaub, A., & McCormick, D. A. (2003) · Nature · doi:10.1038/nature01616 · Cited by 1,054 · see citing works
Self-citation
The subcellular organization of neocortical excitatory connections
Petreanu, L., Mao, T., Sternson, S. M., & Svoboda, K. (2009) · Nature · doi:10.1038/nature07709 · Cited by 1,047 · see citing works
The gamma cycle.
Fries, P., Nikolić, D., & Singer, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.05.005 · Cited by 1,044 · see citing works
Temporal structure in neuronal activity during working memory in macaque parietal cortex
Pesaran, B., Pezaris, J. S., Sahani, M., Mitra, P. P., & Andersen, R. A. (2002) · Nature Neuroscience · doi:10.1038/nn890 · Cited by 1,029 · see citing works
Principles of two-photon excitation microscopy and its applications to neuroscience
Svoboda, K., & Yasuda, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.05.019 · Cited by 1,027 · see citing works
Attention Increases Sensitivity of V4 Neurons
Reynolds, J. H., Pasternak, T., & Desimone, R. (2000) · Neuron · doi:10.1016/s0896-6273(00)81206-4 · Cited by 1,017 · see citing works
Entrainment of Neocortical Neurons and Gamma Oscillations by the Hippocampal Theta Rhythm
Sirota, A., Montgomery, S., Fujisawa, S., Isomura, Y., Zugaro, M., & Buzsáki, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.014 · Cited by 1,015 · see citing works
Gain Modulation from Background Synaptic Input
Chance, F. S., Abbott, L. F., & Reyes, A. D. (2002) · Neuron · doi:10.1016/s0896-6273(02)00820-6 · Cited by 1,012 · see citing works
On The Cellular and Network Bases of Epileptic Seizures
McCormick, D. A., & Contreras, D. (2001) · Annual Review of Physiology · doi:10.1146/annurev.physiol.63.1.815 · Cited by 1,006 · see citing works
Self-citation
Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat
Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 990 · see citing works
Oscillatory coupling of hippocampal pyramidal cells and interneurons in the behaving rat
Csicsvari, J., Hirase, H., Czurkó, A., Mamiya, A., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00274.1999 · Cited by 966 · see citing works
Neocortical Network ActivityIn VivoIs Generated through a Dynamic Balance of Excitation and Inhibition
Haider, B., Duque, A., Hasenstaub, A. R., & McCormick, D. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5297-05.2006 · Cited by 962 · see citing works
Self-citation
Physiology and anatomy of synaptic connections between thick tufted pyramidal neurones in the developing rat neocortex.
Markram, H., Lübke, J., Frotscher, M., Roth, A., & Sakmann, B. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp022031 · Cited by 960 · see citing works
Feature-based attention in visual cortex
Maunsell, J. H. R., & Treue, S. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.04.001 · Cited by 960 · see citing works
Brain States: Top-Down Influences in Sensory Processing
Gilbert, C. D., & Sigman, M. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.019 · Cited by 936 · see citing works
Channelrhodopsin-2-assisted circuit mapping of long-range callosal projections
Petreanu, L., Huber, D., Sobczyk, A., & Svoboda, K. (2007) · Nature Neuroscience · doi:10.1038/nn1891 · Cited by 930 · see citing works
Spontaneously emerging cortical representations of visual attributes
Kenet, T., Bibitchkov, D., Tsodyks, M., Grinvald, A., & Arieli, A. (2003) · Nature · doi:10.1038/nature02078 · Cited by 924 · see citing works
Intracellular analysis of relations between the slow (< 1 Hz) neocortical oscillation and other sleep rhythms of the electroencephalogram
Steriade, M., Nunez, A., & Amzica, F. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03266.1993 · Cited by 894 · see citing works
A Quantitative Map of the Circuit of Cat Primary Visual Cortex
Binzegger, T., Douglas, R. J., & Martin, K. A. C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1400-04.2004 · Cited by 879 · see citing works
Temporal structure in spatially organized neuronal ensembles: a role for interneuronal networks
Buzsáki, G., & Chrobak, J. J. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80012-3 · Cited by 878 · see citing works
The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons
Wilson, C. J., & Kawaguchi, Y. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-07-02397.1996 · Cited by 798 · see citing works
Internal brain state regulates membrane potential synchrony in barrel cortex of behaving mice
Poulet, J. F. A., & Petersen, C. C. H. (2008) · Nature · doi:10.1038/nature07150 · Cited by 796 · see citing works
ELECTRICAL SYNAPSES IN THE MAMMALIAN BRAIN
Connors, B. W., & Long, M. A. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131128 · Cited by 784 · see citing works
Disynaptic Inhibition between Neocortical Pyramidal Cells Mediated by Martinotti Cells
Silberberg, G., & Markram, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.012 · Cited by 768 · see citing works
Genetic Dissection of Neural Circuits
Luo, L., Callaway, E. M., & Svoboda, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.002 · Cited by 754 · see citing works
Intrinsic Fluctuations within Cortical Systems Account for Intertrial Variability in Human Behavior
Fox, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.023 · Cited by 753 · see citing works
Dendritic integration of excitatory synaptic input
Magee, J. C. (2000) · Nature reviews. Neuroscience · doi:10.1038/35044552 · Cited by 737 · see citing works
Dendritic Excitability and Synaptic Plasticity
Sjöström, P. J., Rancz, E. A., Roth, A., & Häusser, M. (2008) · Physiological Reviews · doi:10.1152/physrev.00016.2007 · Cited by 721 · see citing works
Origin of Slow Cortical Oscillations in Deafferented Cortical Slabs
Timofeev, I. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1185 · Cited by 710 · see citing works
Action potential generation requires a high sodium channel density in the axon initial segment
Kole, M. H. P., Ilschner, S. U., Kampa, B. M., Williams, S. R., Ruben, P. C., & Stuart, G. J. (2008) · Nature Neuroscience · doi:10.1038/nn2040 · Cited by 703 · see citing works
Instantaneous correlation of excitation and inhibition during ongoing and sensory-evoked activities
Okun, M., & Lampl, I. (2008) · Nature Neuroscience · doi:10.1038/nn.2105 · Cited by 701 · see citing works
Cellular basis of EEG slow rhythms: a study of dynamic corticothalamic relationships
Contreras, D., & Steriade, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00604.1995 · Cited by 700 · see citing works
Feature-Based Attention Increases the Selectivity of Population Responses in Primate Visual Cortex
Martinez-Trujillo, J. C., & Treue, S. (2004) · Current Biology · doi:10.1016/j.cub.2004.04.028 · Cited by 697 · see citing works
Spatiotemporal Dynamics of Cortical Sensorimotor Integration in Behaving Mice
Férézou, I., Haiss, F., Gentet, L. J., Aronoff, R., Weber, B., & Petersen, C. C. H. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.007 · Cited by 692 · see citing works
Microstructure of the neocortex: comparative aspects
DeFelipe, J., Alonso-Nanclares, L., & Arellano, J. I. (2002) · Journal of Neurocytology · doi:10.1023/a:1024130211265 · Cited by 686 · see citing works
Behavior-dependent short-term assembly dynamics in the medial prefrontal cortex
Fujisawa, S., Amarasingham, A., Harrison, M. T., & Buzsáki, G. (2008) · Nature Neuroscience · doi:10.1038/nn.2134 · Cited by 679 · see citing works
Decision Making in Recurrent Neuronal Circuits
Wang, X.-J. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.034 · Cited by 679 · see citing works
Prefrontal cortex and decision making in a mixed-strategy game
Barraclough, D. J., Conroy, M. L., & Lee, D. (2004) · Nature Neuroscience · doi:10.1038/nn1209 · Cited by 678 · see citing works
Spike Timing-Dependent Plasticity: From Synapse to Perception
Dan, Y., & Poo, M.-M. (2006) · Physiological Reviews · doi:10.1152/physrev.00030.2005 · Cited by 675 · see citing works
Interaction of sensory responses with spontaneous depolarization in layer 2/3 barrel cortex
Petersen, C. C. H., Hahn, T. T. G., Mehta, M. R., Grinvald, A., & Sakmann, B. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2235811100 · Cited by 673 · see citing works
Visual input evokes transient and strong shunting inhibition in visual cortical neurons
Graham, L. J., Monier, C., & Frégnac, Y. (1998) · Nature · doi:10.1038/30735 · Cited by 669 · see citing works
Differential attention-dependent response modulation across cell classes in macaque visual area V4
Mitchell, J. F., Sundberg, K. A., & Reynolds, J. H. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.018 · Cited by 665 · see citing works
Attractor dynamics of network UP states in the neocortex
Cossart, R., Aronov, D., & Yuste, R. (2003) · Nature · doi:10.1038/nature01614 · Cited by 659 · see citing works
Inhibitory Postsynaptic Potentials Carry Synchronized Frequency Information in Active Cortical Networks
Hasenstaub, A. R., Shu, Y., Haider, B., Kraushaar, U., Duque, A., & McCormick, D. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.016 · Cited by 654 · see citing works
Self-citation
Fluctuating synaptic conductances recreate in vivo-like activity in neocortical neurons
Destexhe, A., Rudolph, M., Fellous, J.-M., & Sejnowski, T. J. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00344-x · Cited by 642 · see citing works
Anatomical and Physiological Plasticity of Dendritic Spines
Alvarez, V. A., & Sabatini, B. L. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094222 · Cited by 629 · see citing works
Circuit-breakers: optical technologies for probing neural signals and systems
Zhang, F., Aravanis, A. M., Adamantidis, A., de Lecea, L., & Deisseroth, K. A. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2192 · Cited by 623 · see citing works
VSDI: a new era in functional imaging of cortical dynamics
Grinvald, A., & Hildesheim, R. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1536 · Cited by 618 · see citing works
Silent synapses and the emergence of a postsynaptic mechanism for LTP
Kerchner, G. A., & Nicoll, R. A. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2501 · Cited by 602 · see citing works
Excitatory cortical neurons form fine-scale functional networks
Yoshimura, Y., Dantzker, J. L. M., & Callaway, E. M. (2005) · Nature · doi:10.1038/nature03252 · Cited by 601 · see citing works
Somatosensory integration controlled by dynamic thalamocortical feed-forward inhibition
Gabernet, L., Jadhav, S. P., Feldman, D. E., Carandini, M., & Scanziani, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.022 · Cited by 599 · see citing works
Action potential initiation and propagation in rat neocortical pyramidal neurons
Stuart, G. J., Schiller, J., & Sakmann, B. J. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.617ba.x · Cited by 585 · see citing works
Effects of sleep and arousal on the processing of visual information in the cat
Livingstone, M. S., & Hubel, D. H. (1981) · Nature · doi:10.1038/291554a0 · Cited by 583 · see citing works
Spatiotemporal analysis of local field potentials and unit discharges in cat cerebral cortex during natural wake and sleep states
Destexhe, A., Contreras, D., & Steriade, M. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04595.1999 · Cited by 573 · see citing works
Ca2+ buffering and action potential-evoked Ca2+ signaling in dendrites of pyramidal neurons
Helmchen, F., Imoto, K., & Sakmann, B. (1996) · Biophysical Journal · doi:10.1016/s0006-3495(96)79653-4 · Cited by 559 · see citing works
Synaptic basis for intense thalamocortical activation of feedforward inhibitory cells in neocortex
Cruikshank, S. J., Lewis, T. J., & Connors, B. W. (2007) · Nature Neuroscience · doi:10.1038/nn1861 · Cited by 558 · see citing works
Correlating whisker behavior with membrane potential in barrel cortex of awake mice
Crochet, S., & Petersen, C. (2006) · Nature Neuroscience · doi:10.1038/nn1690 · Cited by 556 · see citing works
Differential regulation of neocortical synapses by neuromodulators and activity
Gil, Z., Connors, B. W., & Amitai, Y. (1997) · Neuron · doi:10.1016/s0896-6273(00)80380-3 · Cited by 553 · see citing works
Sparse optical microstimulation in barrel cortex drives learned behaviour in freely moving mice
Huber, D., Petreanu, L., Ghitani, N., Ranade, S., Hromádka, T., Mainen, Z., & Svoboda, K. (2008) · Nature · doi:10.1038/nature06445 · Cited by 539 · see citing works
Cellular and Network Mechanisms of Slow Oscillatory Activity (<1 Hz) and Wave Propagations in a Cortical Network Model
Compte, A., Sanchez-Vives, M. V., McCormick, D. A., & Wang, X. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00845.2002 · Cited by 536 · see citing works
Self-citation
Spontaneous firing patterns and axonal projections of single corticostriatal neurons in the rat medial agranular cortex
Cowan, R. L., & Wilson, C. J. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.71.1.17 · Cited by 535 · see citing works
PHYSIOLOGY OF THE NERVOUS SYSTEM
(1952) · The Lancet · doi:10.1016/s0140-6736(52)90957-4 · Cited by 526 · see citing works
Synaptic background activity influences spatiotemporal integration in single pyramidal cells.
Bernander, Ö., Douglas, R. J., Martin, K. A. C., & Koch, C. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.24.11569 · Cited by 518 · see citing works
Sequential structure of neocortical spontaneous activity in vivo
Luczak, A., Barthó, P., Marguet, S. L., Buzsáki, G., & Harris, K. D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605643104 · Cited by 515 · see citing works
Selective Photostimulation of Genetically ChARGed Neurons
Zemelman, B. V., Lee, G. A., Ng, M., & Miesenböck, G. (2002) · Neuron · doi:10.1016/s0896-6273(01)00574-8 · Cited by 507 · see citing works
NEURAL NETWORK DYNAMICS
Vogels, T. P., Rajan, K., & Abbott, L. F. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135637 · Cited by 497 · see citing works
Behavioural report of single neuron stimulation in somatosensory cortex
Houweling, A., & Brecht, M. (2008) · Nature · doi:10.1038/nature06447 · Cited by 492 · see citing works
Neural Variability in Premotor Cortex Provides a Signature of Motor Preparation
Churchland, M. M., Yu, B. M., Ryu, S. I., Santhanam, G., & Shenoy, K. V. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3762-05.2006 · Cited by 484 · see citing works
Free choice activates a decision circuit between frontal and parietal cortex
Pesaran, B., Nelson, M., & Andersen, R. (2008) · Nature · doi:10.1038/nature06849 · Cited by 479 · see citing works
Imaging input and output of neocortical networks in vivo
Kerr, J. N. D., Greenberg, D., & Helmchen, F. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506029102 · Cited by 474 · see citing works
Targeting and Readout Strategies for Fast Optical Neural ControlIn VitroandIn Vivo
Gradinaru, V., Thompson, K. R., Zhang, F., Mogri, M., Kay, K., Schneider, M. B., & Deisseroth, K. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3578-07.2007 · Cited by 466 · see citing works
Visualizing the Cortical Representation of Whisker Touch: Voltage-Sensitive Dye Imaging in Freely Moving Mice
Ferezou, I., Bolea, S., & Petersen, C. C. H. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.043 · Cited by 466 · see citing works
Disfacilitation and active inhibition in the neocortex during the natural sleep-wake cycle: An intracellular study
Timofeev, I., Grenier, F., & Steriade, M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.4.1924 · Cited by 455 · see citing works
Impact of Spontaneous Synaptic Activity on the Resting Properties of Cat Neocortical Pyramidal Neurons In Vivo
Paré, D., Shink, É., Gaudreau, H., Alain Destexhe, A., & Lang, E. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.3.1450 · Cited by 453 · see citing works
Neural signatures of cell assembly organization
Harris, K. D. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1669 · Cited by 443 · see citing works
Electrophysiological Classes of Cat Primary Visual Cortical Neurons In Vivo as Revealed by Quantitative Analyses
Nowak, L. G., Azouz, R., Sanchez-Vives, M. V., Gray, C. M., & McCormick, D. A. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00580.2002 · Cited by 443 · see citing works
Self-citation
Reliable synaptic connections between pairs of excitatory layer 4 neurones within a single ‘barrel’ of developing rat somatosensory cortex
Feldmeyer, D., Egger, V., Lübke, J., & Sakmann, B. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00169.x · Cited by 441 · see citing works
Frequency-dependent synaptic depression and the balance of excitation and inhibition in the neocortex
Galarreta, M., & Hestrin, S. (1998) · Nature Neuroscience · doi:10.1038/2822 · Cited by 436 · see citing works
Synchronous Membrane Potential Fluctuations in Neurons of the Cat Visual Cortex
Lampl, I., Reichova, I., & Ferster, D. (1999) · Neuron · doi:10.1016/s0896-6273(00)81096-x · Cited by 434 · see citing works
Targets of horizontal connections in macaque primary visual cortex
McGuire, B. A., Gilbert, C. D., Rivlin, P. K., & Wiesel, T. N. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903050303 · Cited by 432 · see citing works
Whisker movements evoked by stimulation of single pyramidal cells in rat motor cortex
Brecht, M., Schneider, M., Sakmann, B. J., & Margrie, T. W. (2004) · Nature · doi:10.1038/nature02266 · Cited by 429 · see citing works
Supralinear increase of recurrent inhibition during sparse activity in the somatosensory cortex
Kapfer, C., Glickfeld, L. L., Atallah, B. V., & Scanziani, M. (2007) · Nature Neuroscience · doi:10.1038/nn1909 · Cited by 427 · see citing works
The Contribution of Noise to Contrast Invariance of Orientation Tuning in Cat Visual Cortex
Anderson, J. S., Lampl, I., Gillespie, D. C., & Ferster, D. (2000) · Science · doi:10.1126/science.290.5498.1968 · Cited by 422 · see citing works
Membrane Potential and Firing Rate in Cat Primary Visual Cortex
Carandini, M., & Ferster, D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00470.2000 · Cited by 413 · see citing works
Cellular Mechanisms Contributing to Response Variability of Cortical NeuronsIn Vivo
Azouz, R., & Gray, C. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02209.1999 · Cited by 408 · see citing works
Population imaging of ongoing neuronal activity in the visual cortex of awake rats
Greenberg, D. S., Houweling, A. R., & Kerr, J. N. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2140 · Cited by 408 · see citing works
Properties of basal dendrites of layer 5 pyramidal neurons: a direct patch-clamp recording study.
Nevian, T., Larkum, M. E., Polsky, A., & Schiller, J. (2007) · Nature Neuroscience · doi:10.1038/nn1826 · Cited by 406 · see citing works
Modulation of intracortical synaptic potentials by presynaptic somatic membrane potential
Shu, Y., Hasenstaub, A. R., Duque, A., Yu, Y., & McCormick, D. A. (2006) · Nature · doi:10.1038/nature04720 · Cited by 397 · see citing works
Self-citation
A central source of movement variability
Churchland, M. M., Afshar, A., & Shenoy, K. V. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.034 · Cited by 393 · see citing works
Gating multiple signals through detailed balance of excitation and inhibition in spiking networks
Vogels, T. P., & Abbott, L. F. (2009) · Nature Neuroscience · doi:10.1038/nn.2276 · Cited by 375 · see citing works
Single units and conscious vision
The American Association for Research into Nervous and Mental Diseases, & Logothetis, N. K. (1998) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1998.0333 · Cited by 375 · see citing works
Dendritic encoding of sensory stimuli controlled by deep cortical interneurons
Murayama, M., Pérez-Garci, E., Nevian, T., Bock, T., Senn, W., & Larkum, M. E. (2009) · Nature · doi:10.1038/nature07663 · Cited by 369 · see citing works
Top-down Dendritic Input Increases the Gain of Layer 5 Pyramidal Neurons
Larkum, M. E. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh065 · Cited by 366 · see citing works
Spontaneous Subthreshold Membrane Potential Fluctuations and Action Potential Variability of Rat Corticostriatal and Striatal Neurons In Vivo
Stern, E. A., Kincaid, A. E., & Wilson, C. J. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.4.1697 · Cited by 362 · see citing works
Inhibition, Spike Threshold, and Stimulus Selectivity in Primary Visual Cortex
Priebe, N. J., & Ferster, D. (2008) · Neuron · doi:10.1016/j.neuron.2008.02.005 · Cited by 359 · see citing works
Mapping the Matrix: The Ways of Neocortex
Douglas, R. J., & Martin, K. A. C. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.017 · Cited by 355 · see citing works
Are corticothalamic ‘up’ states fragments of wakefulness?
Destexhe, A., Hughes, S. W., Rudolph, M., & Crunelli, V. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.04.006 · Cited by 355 · see citing works
Recurrent neuronal circuits in the neocortex
Douglas, R. J., & Martin, K. A. C. (2007) · Current Biology · doi:10.1016/j.cub.2007.04.024 · Cited by 354 · see citing works
Effects of Spatial Attention on Contrast Response Functions in Macaque Area V4
Williford, T., & Maunsell, J. H. R. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01207.2005 · Cited by 353 · see citing works
Regulation of spike timing in visual cortical circuits
Tiesinga, P. H. E., Fellous, J., & B, T. J. S. A. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2315 · Cited by 352 · see citing works
Contextual Influences on Visual Processing
Albright, T. D., & Stoner, G. R. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142900 · Cited by 350 · see citing works
Layer‐ and cell‐type‐specific suprathreshold stimulus representation in rat primary somatosensory cortex
de Kock, C. P. J., Bruno, R. M., Spors, H., & Sakmann, B. J. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.124321 · Cited by 344 · see citing works
Balanced Amplification: A New Mechanism of Selective Amplification of Neural Activity Patterns
Murphy, B. K., & Miller, K. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.005 · Cited by 338 · see citing works
Gain Modulation by Nicotine in Macaque V1
Disney, A. A., Aoki, C., & Hawken, M. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.034 · Cited by 331 · see citing works
Persistent neural activity: prevalence and mechanisms
Major, G., & Tank, D. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.10.017 · Cited by 320 · see citing works
A model of multiplicative neural responses in parietal cortex.
Salinas, E., & Abbott, L. F. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11956 · Cited by 319 · see citing works
Membrane Mechanisms Underlying Contrast Adaptation in Cat Area 17In Vivo
Sanchez-Vives, M. V., Nowak, L. G., & McCormick, D. A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04267.2000 · Cited by 315 · see citing works
Self-citation
Top-Down Control of Motor Cortex Ensembles by Dorsomedial Prefrontal Cortex
Narayanan, N. S., & Laubach, M. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.021 · Cited by 311 · see citing works
Invariant computations in local cortical networks with balanced excitation and inhibition
Mariño, J., Schummers, J., Lyon, D. C., Schwabe, L., Beck, O., Wiesing, P., Obermayer, K., & Sur, M. (2005) · Nature Neuroscience · doi:10.1038/nn1391 · Cited by 308 · see citing works
Barrages of Synaptic Activity Control the Gain and Sensitivity of Cortical Neurons
Shu, Y., Hasenstaub, A., Badoual, M., Bal, T., & McCormick, D. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10388.2003 · Cited by 298 · see citing works
Self-citation
Gamma frequency oscillation in the hippocampus of the rat: intracellular analysis in vivo
Penttonen, M., Kamondi, A., Acsády, L., & Buzsáki, G. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00096.x · Cited by 296 · see citing works
Cortical activity flips among quasi-stationary states.
Abeles, M., Bergman, H., Gat, I., Meilijson, I., Seidemann, E., Tishby, N., & Vaadia, E. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8616 · Cited by 295 · see citing works
Precise Long-Range Synchronization of Activity and Silence in Neocortical Neurons during Slow-Wave Sleep
Volgushev, M., Chauvette, S., Mukovski, M., & Timofeev, I. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0279-06.2006 · Cited by 289 · see citing works
Dynamics of excitation and inhibition underlying stimulus selectivity in rat somatosensory cortex
Wilent, W. B., & Contreras, D. (2005) · Nature Neuroscience · doi:10.1038/nn1545 · Cited by 288 · see citing works
Synaptic Background Activity Enhances the Responsiveness of Neocortical Pyramidal Neurons
Hô, N., & Destexhe, A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1488 · Cited by 281 · see citing works
Adaptive Coincidence Detection and Dynamic Gain Control in Visual Cortical Neurons In Vivo
Azouz, R., & Gray, C. M. (2003) · Neuron · doi:10.1016/s0896-6273(02)01186-8 · Cited by 278 · see citing works
Response variability of neurons in primary visual cortex (V1) of alert monkeys
Gur, M., Beylin, A., & Snodderly, D. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02914.1997 · Cited by 277 · see citing works
Dendritic morphology of pyramidal neurones of the visual cortex of the rat: III. Spine distributions
Larkman, A. U. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903060209 · Cited by 274 · see citing works
Influence of low and high frequency inputs on spike timing in visual cortical neurons
Nowak, L. G. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.487 · Cited by 272 · see citing works
Balanced Excitation and Inhibition Determine Spike Timing during Frequency Adaptation
Higley, M. J., & Contreras, D. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3506-05.2006 · Cited by 270 · see citing works
Escape Behavior Elicited by Single, Channelrhodopsin-2-Evoked Spikes in Zebrafish Somatosensory Neurons
Douglass, A. D., Kraves, S., Deisseroth, K. A., Schier, A. F., & Engert, F. (2008) · Current Biology · doi:10.1016/j.cub.2008.06.077 · Cited by 257 · see citing works
A Normalization Model of Attentional Modulation of Single Unit Responses
Lee, J., & Maunsell, J. H. R. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004651 · Cited by 257 · see citing works
Temporally Irregular Mnemonic Persistent Activity in Prefrontal Neurons of Monkeys During a Delayed Response Task
Compte, A., Constantinidis, C., Tegner, J. N., Raghavachari, S., Chafee, M. V., Goldman, P. S., & Wang, X. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00949.2002 · Cited by 256 · see citing works
Ivy Cells: A Population of Nitric-Oxide-Producing, Slow-Spiking GABAergic Neurons and Their Involvement in Hippocampal Network Activity
Fuentealba, P., Begum, R., Capogna, M., Jinno, S., Márton, L. F., Csicsvari, J., Thomson, A., Somogyi, P., & Klausberger, T. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.034 · Cited by 255 · see citing works
Context-Dependent Changes in Functional Circuitry in Visual Area MT
Cohen, M. R., & Newsome, W. T. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.007 · Cited by 255 · see citing works
Spatial Organization of Neuronal Population Responses in Layer 2/3 of Rat Barrel Cortex
Kerr, J. N. D., de Kock, C. P. J., Greenberg, D. S., Bruno, R. M., Sakmann, B. J., & Helmchen, F. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2210-07.2007 · Cited by 254 · see citing works
Whole-Cell Recordings in Freely Moving Rats
Lee, A. K., Manns, I. D., Sakmann, B. J., & Brecht, M. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.004 · Cited by 253 · see citing works
The Emergence of Up and Down States in Cortical Networks
Holcman, D., & Tsodyks, M. V. (2006) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0020023 · Cited by 252 · see citing works
Selective Cholinergic Modulation of Cortical GABAergic Cell Subtypes
Kawaguchi, Y. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.3.1743 · Cited by 250 · see citing works
Shunting Inhibition Does Not Have a Divisive Effect on Firing Rates
Holt, G. R., & Koch, C. (1997) · Neural Computation · doi:10.1162/neco.1997.9.5.1001 · Cited by 250 · see citing works
Inhibition Determines Membrane Potential Dynamics and Controls Action Potential Generation in Awake and Sleeping Cat Cortex
Rudolph, M., Pospischil, M., Timofeev, I., & Destexhe, A. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4652-06.2007 · Cited by 247 · see citing works
Neural codes for perceptual discrimination in primary somatosensory cortex
Luna, R., Hernández, A., Brody, C. D., & Romo, R. (2005) · Nature Neuroscience · doi:10.1038/nn1513 · Cited by 246 · see citing works
How silent is the brain: is there a “dark matter” problem in neuroscience?
Shoham, S., O’Connor, D. H., & Segev, R. (2006) · Journal of Comparative Physiology A · doi:10.1007/s00359-006-0117-6 · Cited by 238 · see citing works
Action potential threshold of hippocampal pyramidal cells in vivo is increased by recent spiking activity
Henze, D. A., & Buzsáki, G. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00167-1 · Cited by 237 · see citing works
Laminar and Columnar Organization of Ascending Excitatory Projections to Layer 2/3 Pyramidal Neurons in Rat Barrel Cortex
Shepherd, G. M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1173-05.2005 · Cited by 236 · see citing works
Targeted bulk-loading of fluorescent indicators for two-photon brain imaging in vivo
Garaschuk, O., Milos, R., & Konnerth, A. (2006) · Nature Protocols · doi:10.1038/nprot.2006.58 · Cited by 235 · see citing works
PHYSIOLOGY OF THE NERVOUS SYSTEM
Fulton, J. F. (1939) · Science · doi:10.1126/science.90.2327.110 · Cited by 227 · see citing works
GABAergic Neurons Are Less Selective to Stimulus Orientation than Excitatory Neurons in Layer II/III of Visual Cortex, as Revealed byIn VivoFunctional Ca2+Imaging in Transgenic Mice
Sohya, K., Kameyama, K., Yanagawa, Y., Obata, K., & Tsumoto, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4641-06.2007 · Cited by 227 · see citing works
Gain control of firing rate by shunting inhibition: Roles of synaptic noise and dendritic saturation
Prescott, S. A., & De Koninck, Y. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337591100 · Cited by 226 · see citing works
Spatiotemporally Graded NMDA Spike/Plateau Potentials in Basal Dendrites of Neocortical Pyramidal Neurons
Major, G., Poleg-Polsky, A., Denk, W. T., Schiller, J., & Tank, D. W. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00011.2008 · Cited by 222 · see citing works
Properties of Action-Potential Initiation in Neocortical Pyramidal Cells: Evidence From Whole Cell Axon Recordings
Shu, Y., Duque, A., Yu, Y., Haider, B., & McCormick, D. A. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00922.2006 · Cited by 221 · see citing works
Self-citation
The contribution of spike threshold to the dichotomy of cortical simple and complex cells
Priebe, N. J., Mechler, F., Carandini, M., & Ferster, D. (2004) · Nature Neuroscience · doi:10.1038/nn1310 · Cited by 217 · see citing works
The Functional Microarchitecture of the Mouse Barrel Cortex
Sato, T., Gray, N. W., Mainen, Z. F., & Svoboda, K. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050189 · Cited by 211 · see citing works
Neural Noise Can Explain Expansive, Power-Law Nonlinearities in Neural Response Functions
Miller, K. D., & Troyer, T. W. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00425.2001 · Cited by 207 · see citing works
Prefrontal Cortex Activity Related to Abstract Response Strategies
Genovesio, A., Brasted, P. J., Mitz, A. R., & Wise, S. P. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.006 · Cited by 205 · see citing works
Neural circuit dynamics underlying accumulation of time-varying evidence during perceptual decision-making
Wong, K.-F. (2007) · Frontiers in Computational Neuroscience · doi:10.3389/neuro.10.006.2007 · Cited by 204 · see citing works
Attention Modulates the Responses of Simple Cells in Monkey Primary Visual Cortex
McAdams, C. J., & Reid, R. C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2904-05.2005 · Cited by 203 · see citing works
Neuronal Integration of Synaptic Input in the Fluctuation-Driven Regime
Kuhn, A., Aertsen, A., & Rotter, S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3349-03.2004 · Cited by 200 · see citing works
Cortical Action Potential Backpropagation Explains Spike Threshold Variability and Rapid-Onset Kinetics
Yu, Y., Shu, Y., & McCormick, D. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1613-08.2008 · Cited by 199 · see citing works
Self-citation
State changes rapidly modulate cortical neuronal responsiveness
Hasenstaub, A., Sachdev, R. N. S., & McCormick, D. A. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2184-07.2007 · Cited by 196 · see citing works
Self-citation
State-dependent receptive-field restructuring in the visual cortex
Wörgötter, F., Suder, K., Zhao, Y., Kerscher, N., Eysel, U. T., & Funke, K. (1998) · Nature · doi:10.1038/24157 · Cited by 192 · see citing works
Stimulus feature selectivity in excitatory and inhibitory neurons in primary visual cortex
Cardin, J. A., Palmer, L. A., & Contreras, D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1692-07.2007 · Cited by 185 · see citing works
Intracellular Correlates of Fast (>200 Hz) Electrical Oscillations in Rat Somatosensory Cortex
Jones, M. S., MacDonald, K. D., Choi, B., Dudek, F. E., & Barth, D. S. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1505 · Cited by 184 · see citing works
Problems of the Keimbahn. New work on mammalian germ cell lineage.
Sturrock, R. R. (1983) · PubMed · Cited by 182 · see citing works

Flagged first, then by citations

Research works printed but not linked: 1

Peters A Peters A Jones EG Chandelier Cells In Cerebral Cortex. Cellular Components of the Cerebral Cortex 1984 New York Plenum Press 361 379

Sorted by citations

Mechanisms of Gamma Oscillations
Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796 · see citing works
Neurophysiological and Computational Principles of Cortical Rhythms in Cognition
Wang, X.-J. (2010) · Physiological Reviews · doi:10.1152/physrev.00035.2008 · Cited by 1,939 · see citing works
Modulation of visual responses by behavioral state in mouse visual cortex
Niell, C. M., & Stryker, M. P. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.033 · Cited by 1,483 · see citing works
“Regardless of the mechanism of activation, it is apparent that the state of the cortical network has a profound impact on the response to sensory inputs (Fontanini and Katz, 2008; Haider and McCormick, 2009; Otazu et al., 2009; Poulet and Petersen, 2008).”
Relationships between Pupil Diameter and Neuronal Activity in the Locus Coeruleus, Colliculi, and Cingulate Cortex
Joshi, S., Li, Y., Kalwani, R. M., & Gold, J. I. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.028 · Cited by 1,387 · see citing works
Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons
Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420 · see citing works
Spectral fingerprints of large-scale neuronal interactions
Siegel, M., Donner, T. H., & Engel, A. K. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3137 · Cited by 1,295 · see citing works
Cortical activity in the null space: permitting preparation without movement
Kaufman, M. T., Churchland, M. M., Ryu, S. I., & Shenoy, K. V. (2014) · Nature Neuroscience · doi:10.1038/nn.3643 · Cited by 831 · see citing works
Endogenous electric fields may guide neocortical network activity
Fröhlich, F., & McCormick, D. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.005 · Cited by 913 · see citing works
Self-citation
Equalizing excitation-inhibition ratios across visual cortical neurons
Xue, M., Atallah, B. V., & Scanziani, M. (2014) · Nature · doi:10.1038/nature13321 · Cited by 722 · see citing works
The benefits of noise in neural systems: bridging theory and experiment
McDonnell, M. D., & Ward, L. M. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3061 · Cited by 778 · see citing works
Cation-chloride cotransporters in neuronal development, plasticity and disease
Kaila, K., Price, T. J., Payne, J. A., Puskarjov, M., & Voipio, J. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3819 · Cited by 750 · see citing works
Resting-state networks show dynamic functional connectivity in awake humans and anesthetized macaques
Hutchison, R. M., Womelsdorf, T., Gati, J. S., Everling, S., & Menon, R. S. (2012) · Human Brain Mapping · doi:10.1002/hbm.22058 · Cited by 715 · see citing works
Ephaptic coupling of cortical neurons
Anastassiou, C. A., Perin, R., Markram, H., & Koch, C. (2011) · Nature Neuroscience · doi:10.1038/nn.2727 · Cited by 628 · see citing works
Oscillatory synchronization in large-scale cortical networks predicts perception
Hipp, J. F., Engel, A. K., & Siegel, M. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.027 · Cited by 599 · see citing works
Dynamic Network Communication as a Unifying Neural Basis for Cognition, Development, Aging, and Disease
Voytek, B., & Knight, R. T. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.04.016 · Cited by 556 · see citing works
Phase-dependent neuronal coding of objects in short-term memory
Siegel, M., Warden, M. R., & Miller, E. K. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908193106 · Cited by 573 · see citing works
Inhibition dominates sensory responses in the awake cortex
Haider, B., Häusser, M., & Carandini, M. (2012) · Nature · doi:10.1038/nature11665 · Cited by 541 · see citing works
Self-citation
Neuronal arithmetic
Silver, R. A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2864 · Cited by 481 · see citing works
Transcranial Alternating Current Stimulation Modulates Large-Scale Cortical Network Activity by Network Resonance
Ali, M. M., Sellers, K. K., & Frӧhlich, F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5867-12.2013 · Cited by 476 · see citing works
Membrane potential dynamics of GABAergic neurons in the barrel cortex of behaving mice
Gentet, L. J., Avermann, M., Matyas, F., Staiger, J. F., & Petersen, C. C. H. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.006 · Cited by 429 · see citing works
The effects of neural gain on attention and learning
Eldar, E., Cohen, J. D., & Niv, Y. (2013) · Nature Neuroscience · doi:10.1038/nn.3428 · Cited by 402 · see citing works
Cortical Enlightenment: Are Attentional Gamma Oscillations Driven by ING or PING?
Tiesinga, P. H. E., & B, T. J. S. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.009 · Cited by 421 · see citing works
Experimental evidence for sparse firing in the neocortex
Barth, A. L., & Poulet, J. F. A. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.03.008 · Cited by 364 · see citing works
Shifts in gamma phase–amplitude coupling frequency from theta to alpha over posterior cortex during visual tasks
Voytek, B. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00191 · Cited by 401 · see citing works
Effects and Mechanisms of Wakefulness on Local Cortical Networks
Constantinople, C. M., & Bruno, R. M. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.040 · Cited by 387 · see citing works
Closed-Loop and Activity-Guided Optogenetic Control
Grosenick, L., Marshel, J. H., & Deisseroth, K. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.034 · Cited by 384 · see citing works
Neuromodulation of brain state and behavior
McCormick, D. A., Nestvogel, D. B., & He, B. J. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100219-105424 · Cited by 303 · see citing works
Self-citation
Mechanisms underlying gain modulation in the cortex
Ferguson, K. A., & Cardin, J. A. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0253-y · Cited by 327 · see citing works
Statistical learning research: A critical review and possible new directions.
Frost, R., Armstrong, B. C., & Christiansen, M. H. (2019) · Psychological Bulletin · doi:10.1037/bul0000210 · Cited by 314 · see citing works
Thalamic control of cortical states
Poulet, J. F. A., Fernandez, L. M. J., Crochet, S., & Petersen, C. C. H. (2012) · Nature Neuroscience · doi:10.1038/nn.3035 · Cited by 312 · see citing works
Assessing the mechanisms of brain plasticity by transcranial magnetic stimulation
Jannati, A., Oberman, L. M., Rotenberg, A., & Pascual‐Leone, Á. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01453-8 · Cited by 303 · see citing works
Traveling Waves in Visual Cortex
Sato, T. K., Nauhaus, I., & Carandini, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.029 · Cited by 288 · see citing works
Optogenetic stimulation of infralimbic PFC reproduces ketamine’s rapid and sustained antidepressant actions
Fuchikami, M., Thomas, A., Liu, R., Wohleb, E. S., Land, B. B., DiLeone, R. J., Aghajanian, G. K., & Duman, R. S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414728112 · Cited by 265 · see citing works
The Slow Oscillation in Cortical and Thalamic Networks: Mechanisms and Functions
Neske, G. T. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00088 · Cited by 283 · see citing works
Frequency-invariant temporal ordering of interneuronal discharges during hippocampal oscillations in awake mice
Varga, C., Golshani, P., & Soltesz, I. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210929109 · Cited by 253 · see citing works
Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome
Tai, C., Abe, Y., Westenbroek, R. E., Scheuer, T., & Catterall, W. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411131111 · Cited by 266 · see citing works
Motor cortex feedback influences sensory processing by modulating network state
Zagha, E., Casale, A. E., Sachdev, R. N. S., McGinley, M. J., & McCormick, D. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.008 · Cited by 268 · see citing works
Self-citation
Synaptic and Network Mechanisms of Sparse and Reliable Visual Cortical Activity during Nonclassical Receptive Field Stimulation
Haider, B., Krause, M. R., Duque, A., Yu, Y., Touryan, J., Mazer, J. A., & McCormick, D. A. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.005 · Cited by 263 · see citing works
Self-citation
Disrupted Homer scaffolds mediate abnormal mGluR5 function in a mouse model of fragile X syndrome
Ronesi, J. A., Collins, K. A., Hays, S. A., Tsai, N.-P., Guo, W., Birnbaum, S. G., Hu, J.-H., Worley, P. F., Gibson, J. R., & Huber, K. M. (2012) · Nature Neuroscience · doi:10.1038/nn.3033 · Cited by 251 · see citing works
Mirrored Bilateral Slow-Wave Cortical Activity within Local Circuits Revealed by Fast Bihemispheric Voltage-Sensitive Dye Imaging in Anesthetized and Awake Mice
Mohajerani, M. H., McVea, D. A., Fingas, M., & Murphy, T. H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6437-09.2010 · Cited by 246 · see citing works
Metabolic cost as a unifying principle governing neuronal biophysics.
Hasenstaub, A., Otte, S., Callaway, E., & Sejnowski, T. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914886107 · Cited by 246 · see citing works
A Systems Neuroscience Approach to Migraine
Brennan, K. C., & Pietrobon, D. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.029 · Cited by 243 · see citing works
Oscillations and Neuronal Dynamics in Schizophrenia: The Search for Basic Symptoms and Translational Opportunities
Uhlhaas, P. J., & Singer, W. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.11.019 · Cited by 243 · see citing works
Facilitation of epileptic activity during sleep is mediated by high amplitude slow waves
Frauscher, B., von Ellenrieder, N., Ferrari-Marinho, T., Avoli, M., Dubeau, F., & Gotman, J. (2015) · Brain : a journal of neurology · doi:10.1093/brain/awv073 · Cited by 228 · see citing works
Characterizing VIP neurons in the barrel cortex of VIPcre/tdTomato mice reveals layer-specific differences
Prönneke, A., Scheuer, B., Wagener, R. J., Möck, M., Witte, M., & Staiger, J. F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv202 · Cited by 204 · see citing works
Theta-activity in anterior cingulate cortex predicts task rules and their adjustments following errors
Womelsdorf, T., Johnston, K., Vinck, M. A., & Everling, S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906194107 · Cited by 230 · see citing works
GABA actions and ionic plasticity in epilepsy
Kaila, K., Ruusuvuori, E., Seja, P., Voipio, J., & Puskarjov, M. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.004 · Cited by 232 · see citing works
Microcircuits of excitatory and inhibitory neurons in layer 2/3 of mouse barrel cortex
Avermann, M., Tomm, C., Matéo, C., Wulfram Gerstner, B., & Petersen, C. C. H. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00917.2011 · Cited by 222 · see citing works
The decade of the dendritic nmda spike
Antic, S. D., Zhou, W., Moore, A. R., Short, S. M., & Ikonomu, K. D. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22444 · Cited by 222 · see citing works
Balanced cortical microcircuitry for maintaining information in working memory
Lim, S., & Goldman, M. S. (2013) · Nature Neuroscience · doi:10.1038/nn.3492 · Cited by 208 · see citing works
Astrocytic regulation of cortical UP states
Poskanzer, K. E., & Yuste, R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112378108 · Cited by 207 · see citing works
Mechanisms of Neuronal Computation in Mammalian Visual Cortex
Priebe, N. J., & Ferster, D. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.011 · Cited by 209 · see citing works
Neuronal circuits underlying persistent representations despite time varying activity
Druckmann, S., & Chklovskii, D. B. (2012) · Current Biology · doi:10.1016/j.cub.2012.08.058 · Cited by 174 · see citing works
High-frequency oscillations and the neurobiology of schizophrenia
Uhlhaas, P. J., & Singer, W. (2013) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2013.15.3/puhlhaas · Cited by 196 · see citing works
Large-Scale Microelectrode Recordings of High-Frequency Gamma Oscillations in Human Cortex during Sleep
Le Van Quyen, M., Staba, R., Bragin, A., Dickson, C., Valderrama, M., Fried, I., & Engel, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5049-09.2010 · Cited by 189 · see citing works
Neural control of brain state
Zagha, E., & McCormick, D. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.010 · Cited by 184 · see citing works
Self-citation
Inhibitory stabilization and cortical computation
Sadeh, S., & Clopath, C. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00390-z · Cited by 183 · see citing works
The Locus Coeruleus Is a Complex and Differentiated Neuromodulatory System
Totah, N. K., Neves, R. M., Panzeri, S., Logothetis, N. K., & Eschenko, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.037 · Cited by 179 · see citing works
Development and specification of GABAergic cortical interneurons
Kelsom, C., & Lu, W. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-19 · Cited by 171 · see citing works
Altered Neocortical Rhythmic Activity States inFmr1KO Mice Are Due to Enhanced mGluR5 Signaling and Involve Changes in Excitatory Circuitry
Hays, S. A., Huber, K. M., & Gibson, J. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3157-11.2011 · Cited by 167 · see citing works
Whole-Neuron Synaptic Mapping Reveals Spatially Precise Excitatory/Inhibitory Balance Limiting Dendritic and Somatic Spiking
Iascone, D. M., Li, Y., Sümbül, U., Doron, M., Chen, H., Andreu, V., Goudy, F., Blockus, H., Abbott, L. F., Segev, I., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.02.015 · Cited by 165 · see citing works
UP-DOWN cortical dynamics reflect state transitions in a bistable network
Jercog, D., Roxin, A., Barthó, P., Luczak, A., Compte, A., & de la Rocha, J. (2017) · eLife · doi:10.7554/elife.22425 · Cited by 159 · see citing works
Cortical Network Dynamics of Perceptual Decision-Making in the Human Brain
Siegel, M., Engel, A. K., & Donner, T. H. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00021 · Cited by 159 · see citing works
The roles of alpha oscillation in working memory retention
Wianda, E., & Roß, B. (2019) · Brain and Behavior · doi:10.1002/brb3.1263 · Cited by 157 · see citing works
The Aging Motor System as a Model for Plastic Changes of GABA-Mediated Intracortical Inhibition and Their Behavioral Relevance
Heise, K.-F., Zimerman, M., Hoppe, J., Gerloff, C. P., Wegscheider, K., & Hummel, F. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4094-12.2013 · Cited by 149 · see citing works
Optical probing of neuronal ensemble activity
Grewe, B. F., & Helmchen, F. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.09.003 · Cited by 145 · see citing works
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 144 · see citing works
State-Dependent Population Coding in Primary Auditory Cortex
Pachitariu, M., Lyamzin, D. R., Sahani, M., & Lesica, N. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3318-14.2015 · Cited by 142 · see citing works
Membrane Potential Dynamics of Spontaneous and Visually Evoked Gamma Activity in V1 of Awake Mice
Perrenoud, Q., Pennartz, C. M. A., & Gentet, L. J. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002383 · Cited by 136 · see citing works
Locus coeruleus-norepinephrine modulation of sensory processing and perception: A focused review
McBurney-Lin, J., Lu, J., Zuo, Y., & Yang, H. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.009 · Cited by 137 · see citing works
Neurophysiological Basis of Multi-Scale Entropy of Brain Complexity and Its Relationship With Functional Connectivity
Wang, D. J. J., Jann, K., Fan, C., Qiao, Y., Zang, Y., Lu, H., & Yang, Y. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00352 · Cited by 133 · see citing works
Rapid Developmental Maturation of Neocortical FS Cell Intrinsic Excitability
Goldberg, E. M., Jeong, H.-Y., Kruglikov, I., Tremblay, R., Lazarenko, R. M., & Rudy, B. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq138 · Cited by 132 · see citing works
Orientation selectivity and noise correlation in awake monkey area V1 are modulated by the gamma cycle
Womelsdorf, T., Lima, B., Vinck, M., Oostenveld, R., Singer, W., Neuenschwander, S., & Fries, P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114223109 · Cited by 119 · see citing works
Coupling of Thalamocortical Sleep Oscillations Are Important for Memory Consolidation in Humans
Niknazar, M., Krishnan, G., Bazhenov, M., & Mednick, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144720 · Cited by 138 · see citing works
Three-dimensional imaging and photostimulation by remote-focusing and holographic light patterning
Anselmi, F., Ventalon, C., Bègue, A., Ogden, D., & Emiliani, V. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109111108 · Cited by 134 · see citing works
Unmasking Latent Inhibitory Connections in Human Cortex to Reveal Dormant Cortical Memories
Barron, H. C., Vogels, T. P., Emir, U. E., Makin, T. R., O’Shea, J., Clare, S., Jbabdi, S., Dolan, R. J., & Behrens, T. E. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.031 · Cited by 127 · see citing works
Asymmetric effects of activating and inactivating cortical interneurons
Phillips, E. A. K., & Hasenstaub, A. R. (2016) · eLife · doi:10.7554/elife.18383 · Cited by 127 · see citing works
Phase–Amplitude Coupling in Human Electrocorticography Is Spatially Distributed and Phase Diverse
van der Meij, R., Kahana, M. J., & Maris, E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4816-11.2012 · Cited by 127 · see citing works
Mechanisms of Orientation Selectivity in the Primary Visual Cortex
Priebe, N. J. (2016) · Annual Review of Vision Science · doi:10.1146/annurev-vision-111815-114456 · Cited by 125 · see citing works
An Adenosine-Mediated Glial-Neuronal Circuit for Homeostatic Sleep
Bjorness, T. E., Dale, N., Mettlach, G., Sonneborn, A., Sahin, B., Fienberg, A. A., Yanagisawa, M., Bibb, J. A., & Greene, R. W. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3906-15.2016 · Cited by 124 · see citing works
Dissection of Cortical Microcircuits by Single-Neuron Stimulation In Vivo
Kwan, A. C., & Dan, Y. (2012) · Current Biology · doi:10.1016/j.cub.2012.06.007 · Cited by 127 · see citing works
How many neurons are sufficient for perception of cortical activity?
Dalgleish, H. W. P., Russell, L. E., Packer, A. M., Roth, A., Gauld, O. M., Greenstreet, F., Thompson, E. J., & Häusser, M. (2020) · eLife · doi:10.7554/elife.58889 · Cited by 121 · see citing works
Slow Wave Sleep Is a Promising Intervention Target for Alzheimer’s Disease
Lee, Y. F., Gerashchenko, D., Timofeev, I., Bacskai, B. J., & Kastanenka, K. V. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00705 · Cited by 119 · see citing works
Interstitial ions: A key regulator of state-dependent neural activity?
Rasmussen, R. N., O’Donnell, J., Ding, F., & Nedergaard, M. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101802 · Cited by 113 · see citing works
CaV2.1 ablation in cortical interneurons selectively impairs fast‐spiking basket cells and causes generalized seizures
Rossignol, E., Kruglikov, I., van den Maagdenberg, A. M. J. M., Rudy, B., & Fishell, G. (2013) · Annals of Neurology · doi:10.1002/ana.23913 · Cited by 112 · see citing works
Developmental maturation of excitation and inhibition balance in principal neurons across four layers of somatosensory cortex
Zhang, Z., Jiao, Y.-Y., & Sun, Q. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.11.045 · Cited by 113 · see citing works
Sleep, oscillations, interictal discharges, and seizures in human focal epilepsy
Frauscher, B., & Gotman, J. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.04.007 · Cited by 108 · see citing works
Neocortical Interneurons: From Diversity, Strength
Moore, C. I., Carlén, M., Knoblich, U., & Cardin, J. A. (2010) · Cell · doi:10.1016/j.cell.2010.07.005 · Cited by 104 · see citing works
Too Little and Too Much: Hypoactivation and Disinhibition of Medial Prefrontal Cortex Cause Attentional Deficits
Pezze, M. A., McGarrity, S., Mason, R., Fone, K. C. F., & Bast, T. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3450-13.2014 · Cited by 106 · see citing works
Local cortical desynchronization and pupil-linked arousal differentially shape brain states for optimal sensory performance
Waschke, L., Tune, S., & Obleser, J. (2019) · eLife · doi:10.7554/elife.51501 · Cited by 105 · see citing works
Keeping Your Brain in Balance: Homeostatic Regulation of Network Function
Wen, W., & Turrigiano, G. G. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092523-110001 · Cited by 115 · see citing works
In Vivo Optogenetic Stimulation of Neocortical Excitatory Neurons Drives Brain-State-Dependent Inhibition
Matéo, C., Avermann, M., Gentet, L. J., Zhang, F., Deisseroth, K. A., & Petersen, C. C. H. (2011) · Current Biology · doi:10.1016/j.cub.2011.08.028 · Cited by 100 · see citing works
Human Gamma Oscillations during Slow Wave Sleep
Valderrama, M. A., Crépon, B., Botella‐Soler, V., Martinerie, J. M., Hasboun, D., Alvarado‐Rojas, C., Baulac, M., Adam, C., Navarro, V., & Quyen, M. L. V. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033477 · Cited by 102 · see citing works
Evidence for dysregulated high-frequency oscillations during sensory processing in medication-naïve, first episode schizophrenia
Sun, L., Castellanos, N., Grützner, C., Koethe, D., Rivolta, D., Wibral, M., Kranaster, L., Singer, W., Leweke, M. F., & Uhlhaas, P. J. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.08.023 · Cited by 96 · see citing works
Cell-Type-Specific Optical Recording of Membrane Voltage Dynamics in Freely Moving Mice
Marshall, J. D., Li, J. Z., Zhang, Y., Gong, Y., St-Pierre, F., Lin, M. Z., & Schnitzer, M. J. (2016) · Cell · doi:10.1016/j.cell.2016.11.021 · Cited by 97 · see citing works
Dysregulation of group-I metabotropic glutamate (mGlu) receptor mediated signalling in disorders associated with Intellectual Disability and Autism
D’Antoni, S., Spatuzza, M., Bonaccorso, C. M., Musumeci, S. A., Ciranna, L., Nicoletti, F., Huber, K. M., & Catania, M. V. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.003 · Cited by 94 · see citing works
Spontaneous activity in developing sensory circuits: Implications for resting state fMRI
Colonnese, M. T., & Khazipov, R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.046 · Cited by 95 · see citing works
Persistent Interneuronopathy in the Prefrontal Cortex of Young Adult Offspring Exposed to Ethanol In Utero
Skorput, A. G. J., Gupta, V. P., Yeh, P. W. L., & Yeh, H. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1462-15.2015 · Cited by 92 · see citing works
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 93 · see citing works
Shifting the spotlight of attention: evidence for discrete computations in cognition
Buschman, T. J., & Miller, E. K. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00194 · Cited by 87 · see citing works

Authors: Haider, B., & McCormick, D. A.
Affiliations: Yale University (US)
Corresponding author: McCormick, David A.
ORCID: Haider, Bilal
McCormick, David A.
Venue: Neuron
Publisher: Elsevier BV
Published: 2009-04
Volume: 62
Issue: 2
Pages: 171-189
ISSN: 0896-6273 (ISSN-L)
DOI: 10.1016/j.neuron.2009.04.008
PMC: PMC3132648
OpenAlex: W2067485452
Cited by: 441
References: 251
Citations by year: 2026: 12 · 2025: 23 · 2024: 13 · 2023: 18 · 2022: 19 · 2021: 18 · 2020: 28 · 2019: 27 · 2018: 28 · 2017: 23 · 2016: 32 · 2015: 28 · 2014: 39 · 2013: 32 · 2012: 37
FWCI: 2.38
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/open-access/userlicense/1.0/ (vor, 1568 d)
Locations: Neuron (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute of Neurological Disorders and Stroke (R37NS026143)
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 › Functional Brain Connectivity Studies
Keywords: neocortex, cortical dynamics, functional connectivity, excitatory and inhibitory synapses, neuronal networks, network modulation, sensory perception, working memory, attention, motor integration
MeSH terms: Animals, Humans, Membrane Potentials, Models, Neurological, Nerve Net, Neurons, Nonlinear Dynamics, Neocortex, Synaptic Potentials

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

Rapid Neocortical Dynamics: Cellular and Network Mechanisms

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Self-check

Cites

Cited by

Related

Record

About these checks