An embedded subnetwork of highly active neurons in the neocortex

A gene expression atlas of the central nervous system based on bacterial artificial chromosomes

Gong, S., Zheng, C., Doughty, M. L., Losos, K., Didkovsky, N., Schambra, U. B., Nowak, N. J., Joyner, A., Leblanc, G., Hatten, M. E., et al. (2003) · Nature · doi:10.1038/nature02033 · Cited by 2,108 · see citing works

Expression of c- <i>fos</i> Protein in Brain: Metabolic Mapping at the Cellular Level

Sagar, S. M., Sharp, F. R., & Curran, T. (1988) · Science · doi:10.1126/science.3131879 · Cited by 1,925 · see citing works

A novel slow (&lt; 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

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

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

Synfire Chains and Cortical Songs: Temporal Modules of Cortical Activity

Ikegaya, Y., Aaron, G., Cossart, R., Aronov, D., Lampl, I., Ferster, D., & Yuste, R. (2004) · Science · doi:10.1126/science.1093173 · Cited by 838 · 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

Hebb and homeostasis in neuronal plasticity

Turrigiano, G. G., & Nelson, S. B. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00091-x · Cited by 687 · 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

First spikes in ensembles of human tactile afferents code complex spatial fingertip events

Johansson, R. S., & Birznieks, I. (2004) · Nature Neuroscience · doi:10.1038/nn1177 · Cited by 637 · 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

Sparse Representation of Sounds in the Unanesthetized Auditory Cortex

Hromádka, T., DeWeese, M. R., & Zador, A. M. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060016 · Cited by 572 · 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

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

In vivo, low-resistance, whole-cell recordings from neurons in the anaesthetized and awake mammalian brain

Margrie, T. W., Brecht, M., & Sakmann, B. J. (2002) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-002-0831-z · Cited by 525 · see citing works

Sequential structure of neocortical spontaneous activity <i>in vivo</i>

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

Sensitivity to perturbations in vivo implies high noise and suggests rate coding in cortex

London, M., Roth, A., Beeren, L., Häusser, M., & Latham, P. (2010) · Nature · doi:10.1038/nature09086 · Cited by 494 · 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

Spike times make sense

VanRullen, R., Guyonneau, R., & Thorpe, S. J. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.10.010 · Cited by 473 · 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 · cited 1× · 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

Synaptic connections and small circuits involving excitatory and inhibitory neurons in layers 2-5 of adult rat and cat neocortex: triple intracellular recordings and biocytin labelling in vitro

Thomson, A. M. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.9.936 · Cited by 420 · see citing works

Selective reconfiguration of layer 4 visual cortical circuitry by visual deprivation

Maffei, A., Nelson, S. B., & Turrigiano, G. G. (2004) · Nature Neuroscience · doi:10.1038/nn1351 · Cited by 415 · see citing works

Internal Dynamics Determine the Cortical Response to Thalamic Stimulation

MacLean, J. N., Watson, B. O., Aaron, G. B., & Yuste, R. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.035 · Cited by 373 · see citing works

Lateral competition for cortical space by layer-specific horizontal circuits

Adesnik, H., & Scanziani, M. (2010) · Nature · doi:10.1038/nature08935 · Cited by 356 · 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

Targeted patch-clamp recordings and single-cell electroporation of unlabeled neurons in vivo

Kitamura, K., Judkewitz, B., Kano, M., Denk, W. T., & Häusser, M. (2007) · Nature Methods · doi:10.1038/nmeth1150 · Cited by 331 · see citing works

Efficacy and connectivity of intracolumnar pairs of layer 2/3 pyramidal cells in the barrel cortex of juvenile rats.

Feldmeyer, D., Lübke, J., & Sakmann, B. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.105106 · Cited by 314 · see citing works

Internally Mediated Developmental Desynchronization of Neocortical Network Activity

Golshani, P., Gonçalves, J. T., Khoshkhoo, S., Mostany, R., Smirnakis, S., & Portera-Cailliau, C. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2012-09.2009 · Cited by 298 · see citing works

Dynamic Receptive Fields of Reconstructed Pyramidal Cells in Layers 3 and 2 of Rat Somatosensory Barrel Cortex

Brecht, M., Roth, A., & Sakmann, B. J. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.044222 · Cited by 294 · see citing works

Long-term depression induced by sensory deprivation during cortical map plasticity in vivo

Allen, C. B., Celikel, T., & Feldman, D. E. (2003) · Nature Neuroscience · doi:10.1038/nn1012 · Cited by 270 · see citing works

Burst Spiking of a Single Cortical Neuron Modifies Global Brain State

Li, C.-Y. T., Poo, M., & Dan, Y. (2009) · Science · doi:10.1126/science.1169957 · Cited by 257 · see citing works

Alteration of Neuronal Firing Properties afterIn VivoExperience in a FosGFP Transgenic Mouse

Barth, A. L., Gerkin, R. C., & Dean, K. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4737-03.2004 · 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 252 · see citing works

In Vivo Two-Photon Imaging Reveals a Role of Arc in Enhancing Orientation Specificity in Visual Cortex

Wang, K. H., Majewska, A. K., Schummers, J., Farley, B. J., Hu, C., Sur, M., & Tonegawa, S. (2006) · Cell · doi:10.1016/j.cell.2006.06.038 · Cited by 242 · see citing works

Time course of experience-dependent synaptic potentiation and depression in barrel cortex of adolescent rats

Glazewski, S., & Fox, K. D. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.75.4.1714 · Cited by 236 · see citing works

Pathway-Specific Trafficking of Native AMPARs by In Vivo Experience

Clem, R. L., & Barth, A. L. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.019 · Cited by 217 · see citing works

Modulation of spike timing by sensory deprivation during induction of cortical map plasticity

Celikel, T., Szostak, V. A., & Feldman, D. E. (2004) · Nature Neuroscience · doi:10.1038/nn1222 · Cited by 195 · see citing works

Sparse and powerful cortical spikes

Wolfe, J. H., Houweling, A. R., & Brecht, M. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.03.006 · Cited by 163 · see citing works

Ongoing in Vivo Experience Triggers Synaptic Metaplasticity in the Neocortex

Clem, R. L., Celikel, T., & Barth, A. L. (2008) · Science · doi:10.1126/science.1143808 · Cited by 151 · see citing works

A seizure-induced gain-of-function in BK channels is associated with elevated firing activity in neocortical pyramidal neurons

Shruti, S., Clem, R. L., & Barth, A. L. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.02.002 · Cited by 94 · see citing works

Stochastic Emergence of Repeating Cortical Motifs in Spontaneous Membrane Potential Fluctuations In Vivo

Mokeichev, A., Okun, M., Barak, O., Katz, Y., Ben‐Shahar, O., & Lampl, I. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.017 · Cited by 90 · see citing works

Mapping Brain Networks Engaged by, and Changed by, Learning

Gall, C. M., Hess, U. S., & LYNCH, G. S. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3835 · Cited by 77 · see citing works

Ipsilateral Whiskers Suppress Experience-Dependent Plasticity in the Barrel Cortex

Glazewski, S., Benedetti, B. L., & Barth, A. L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0181-07.2007 · Cited by 35 · see citing works

Activity in the Barrel Cortex During Active Behavior and Sleep

Vijayan, S., Hale, G. J., Moore, C. I., Brown, E. N., & Wilson, M. A. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00474.2009 · Cited by 32 · see citing works

Statistical Significance of Precisely Repeated Intracellular Synaptic Patterns

Ikegaya, Y., Matsumoto, W., Chiou, H.-Y., Yuste, R., & Aaron, G. B. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003983 · Cited by 21 · see citing works

Cortical Up State Activity Is Enhanced After Seizures: A Quantitative Analysis

Gerkin, R. C., Clem, R. L., Shruti, S., Kass, R. E., & Barth, A. L. (2010) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0b013e3181fdf8bd · Cited by 9 · see citing works

A taxonomy of transcriptomic cell types across the isocortex and hippocampal formation

Yao, Z., van Velthoven, C. T. J., Nguyen, T. N., Goldy, J., Sedeno-Cortes, A. E., Baftizadeh, F., Bertagnolli, D., Casper, T., Chiang, M., Crichton, K., et al. (2021) · Cell · doi:10.1016/j.cell.2021.04.021 · Cited by 1,065 · see citing works

The log-dynamic brain: how skewed distributions affect network operations

Buzsáki, G., & Mizuseki, K. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3687 · Cited by 964 · see citing works

Finding the engram

Josselyn, S. A., Köhler, S., & Frankland, P. W. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn4000 · Cited by 687 · see citing works

Activity-Regulated Transcription: Bridging the Gap between Neural Activity and Behavior

Yap, E.-L., & Greenberg, M. E. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.013 · Cited by 626 · see citing works

Slow dynamics and high variability in balanced cortical networks with clustered connections

Litwin-Kumar, A., & Doiron, B. (2012) · Nature Neuroscience · doi:10.1038/nn.3220 · Cited by 545 · see citing works

Projections from neocortex mediate top-down control of memory retrieval

Rajasethupathy, P., Sankaran, S., Marshel, J. H., Kim, C. K., Ferenczi, E., Lee, S. Y., Berndt, A., Ramakrishnan, C., Jaffe, A., Lo, M., et al. (2015) · Nature · doi:10.1038/nature15389 · Cited by 509 · see citing works

Role of Immediate-Early Genes in Synaptic Plasticity and Neuronal Ensembles Underlying the Memory Trace

Minatohara, K., Akiyoshi, M., & Okuno, H. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00078 · Cited by 507 · see citing works

Nuclear RNA-seq of single neurons reveals molecular signatures of activation

Lacar, B., Linker, S. B., Jaeger, B. N., Krishnaswami, S. R., Barron, J. J., Kelder, M. J. E., Parylak, S. L., Paquola, A. C. M., Venepally, P., Novotny, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11022 · Cited by 405 · see citing works

Increased excitation-inhibition ratio stabilizes synapse and circuit excitability in four autism mouse models

Antoine, M. W., Langberg, T., Schnepel, P., & Feldman, D. E. (2019) · Neuron · doi:10.1016/j.neuron.2018.12.026 · Cited by 413 · 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

The Brain from Inside Out

Buzsáki, G. (2019) · doi:10.1093/oso/9780190905385.001.0001 · Cited by 358 · see citing works

Cerebellar modules operate at different frequencies

Zhou, H., Lin, Z., Voges, K., Ju, C., Gao, Z., Bosman, L. W. J., Ruigrok, T. J. H., Hoebeek, F. E., Zeeuw, C. I. D., & Schonewille, M. (2014) · eLife · doi:10.7554/elife.02536 · Cited by 335 · see citing works

Identification of a Functional Connectome for Long-Term Fear Memory in Mice

Wheeler, A. L., Teixeira, C. M., Wang, A. H., Xiong, X., Kovacevic, N., Lerch, J. P., McIntosh, A. R., Parkinson, J., & Frankland, P. W. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002853 · Cited by 315 · see citing works

Preconfigured, Skewed Distribution of Firing Rates in the Hippocampus and Entorhinal Cortex

Mizuseki, K., & Buzsáki, G. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.07.039 · Cited by 319 · 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

Functional and structural underpinnings of neuronal assembly formation in learning

Holtmaat, A., & Caroni, P. (2016) · Nature Neuroscience · doi:10.1038/nn.4418 · Cited by 239 · see citing works

New technologies for examining the role of neuronal ensembles in drug addiction and fear

Cruz, F. C., Koya, E., Guez‐Barber, D., Bossert, J. M., Lupica, C. R., Shaham, Y., & Hope, B. T. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3597 · Cited by 241 · see citing works

Synaptic Computation and Sensory Processing in Neocortical Layer 2/3

Petersen, C. C. H., & Crochet, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.020 · Cited by 239 · see citing works

Neural Computation and the Computational Theory of Cognition

Piccinini, G., & Bahar, S. (2012) · Cognitive Science · doi:10.1111/cogs.12012 · Cited by 225 · see citing works

Reorganization of cortical population activity imaged throughout long-term sensory deprivation

Margolis, D. J., Lütcke, H., Schulz, K., Haiss, F., Weber, B., Kügler, S., Hasan, M. T., & Helmchen, F. (2012) · Nature Neuroscience · doi:10.1038/nn.3240 · Cited by 203 · see citing works

Mechanisms of specificity in neuronal activity-regulated gene transcription

Lyons, M. R., & West, A. E. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.05.003 · Cited by 199 · see citing works

Functional labeling of neurons and their projections using the synthetic activity–dependent promoter E-SARE

Kawashima, T., Kitamura, K., Suzuki, K., Nonaka, M., Kamijo, S., Takemoto‐Kimura, S., Kano, M., Okuno, H., Ohki, K., & Bito, H. (2013) · Nature Methods · doi:10.1038/nmeth.2559 · Cited by 189 · see citing works

Rich-Club Organization in Effective Connectivity among Cortical Neurons

Nigam, S., Shimono, M., Ito, S., Yeh, F.-C., Timme, N. M., Myroshnychenko, M., Lapish, C. C., Tosi, Z., Hottowy, P., Smith, W. C., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2177-15.2016 · Cited by 180 · see citing works

A new era for functional labeling of neurons: activity-dependent promoters have come of age

Kawashima, T., Okuno, H., & Bito, H. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00037 · Cited by 165 · see citing works

Using c-fos to study neuronal ensembles in corticostriatal circuitry of addiction

Cruz, F. C., Rubio, F. J., & Hope, B. T. (2014) · Brain Research · doi:10.1016/j.brainres.2014.11.005 · Cited by 162 · see citing works

Orchestrated ensemble activities constitute a hippocampal memory engram

Ghandour, K., Ohkawa, N., Fung, C. C. A., Asai, H., Saitoh, Y., Takekawa, T., Okubo-Suzuki, R., Soya, S., Nishizono, H., Matsuo, M., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10683-2 · Cited by 162 · see citing works

The supramammillary nucleus and the claustrum activate the cortex during REM sleep

Renouard, L., Billwiller, F., Ogawa, K., Clément, O., Camargo, N., Abdelkarim, M., Gay, N., Scoté-Blachon, C., Touré, R., Libourel, P.-A., et al. (2015) · Science Advances · doi:10.1126/sciadv.1400177 · Cited by 152 · see citing works

Stimulus-dependent representational drift in primary visual cortex

Marks, T. D., & Goard, M. J. (2021) · Nature Communications · doi:10.1038/s41467-021-25436-3 · Cited by 175 · see citing works

Genetic strategies to access activated neurons

DeNardo, L. A., & Luo, L. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.05.014 · Cited by 139 · 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

POm Thalamocortical Input Drives Layer-Specific Microcircuits in Somatosensory Cortex

Audette, N. J., Urban‐Ciećko, J., Matsushita, M. T., & Barth, A. L. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx044 · Cited by 136 · see citing works

Neocortical Somatostatin Neurons Reversibly Silence Excitatory Transmission via GABAb Receptors

Urban‐Ciećko, J., Fanselow, E. E., & Barth, A. L. (2015) · Current Biology · doi:10.1016/j.cub.2015.01.035 · Cited by 126 · see citing works

Functional Clusters, Hubs, and Communities in the Cortical Microconnectome

Shimono, M., & Beggs, J. M. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu252 · Cited by 128 · see citing works

Subnetwork-Specific Homeostatic Plasticity in Mouse Visual Cortex In Vivo

Barnes, S. J., Sammons, R. P., Jacobsen, R. I., Mackie, J., Keller, G. B., & Keck, T. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.010 · Cited by 123 · see citing works

Micro-connectomics: probing the organization of neuronal networks at the cellular scale

Schröter, M. S., Paulsen, O., & Bullmore, E. T. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.182 · Cited by 123 · see citing works

Associative Fear Learning Enhances Sparse Network Coding in Primary Sensory Cortex

Gdalyahu, A., Tring, E., Polack, P., Gruver, R., Golshani, P., Fanselow, M. S., Silva, A. J., & Trachtenberg, J. T. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.035 · Cited by 109 · see citing works

Reprogramming reactive glia into interneurons reduces chronic seizure activity in a mouse model of mesial temporal lobe epilepsy

Lentini, C., d’Orange, M., Marichal, N., Trottmann, M.-M., Vignoles, R., Foucault, L., Verrier, C., Massera, C., Raineteau, O., Conzelmann, K.-K., et al. (2021) · Cell Stem Cell · doi:10.1016/j.stem.2021.09.002 · Cited by 114 · see citing works

Probabilistic Inference in General Graphical Models through Sampling in Stochastic Networks of Spiking Neurons

Pecevski, D., Buesing, L., & Maass, W. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002294 · Cited by 107 · see citing works

Steady or changing? Long-term monitoring of neuronal population activity

Lütcke, H., Margolis, D. J., & Helmchen, F. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.03.008 · Cited by 104 · see citing works

Electrical Responses and Spontaneous Activity of Human iPS-Derived Neuronal Networks Characterized for 3-month Culture with 4096-Electrode Arrays

Amin, H., Maccione, A., Marinaro, F., Zordan, S., Nieus, T. R., & Berdondini, L. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00121 · Cited by 98 · see citing works

Sleep regulation of the distribution of cortical firing rates

Levenstein, D., Watson, B. O., Rinzel, J., & Buzsáki, G. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.02.013 · Cited by 96 · see citing works

Dense functional and molecular readout of a circuit hub in sensory cortex

Condylis, C., Ghanbari, A., Manjrekar, N., Bistrong, K., Yao, S., Yao, Z., Nguyen, T. N., Zeng, H., Tasic, B., & Chen, J. L. (2022) · Science · doi:10.1126/science.abl5981 · Cited by 81 · see citing works

Serotonergic Regulation of Excitability of Principal Cells of the Dorsal Cochlear Nucleus

Tang, Z., & Trussell, L. O. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4825-14.2015 · Cited by 80 · see citing works

Self-Organization of Microcircuits in Networks of Spiking Neurons with Plastic Synapses

Ocker, G. K., Litwin-Kumar, A., & Doiron, B. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004458 · Cited by 84 · see citing works

Structure of a Single Whisker Representation in Layer 2 of Mouse Somatosensory Cortex

Clancy, K. B., Schnepel, P., Rao, A. T., & Feldman, D. E. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3887-14.2015 · Cited by 82 · see citing works

Temporal correlations among functionally specialized striatal neural ensembles in reward-conditioned mice

Bakhurin, K. I., Mac, V., Golshani, P., & Masmanidis, S. C. (2016) · Journal of Neurophysiology · doi:10.1152/jn.01037.2015 · Cited by 73 · see citing works

Cortical fosGFP Expression Reveals Broad Receptive Field Excitatory Neurons Targeted by POm

Jouhanneau, J.-S., Ferrarese, L., Estebanez, L., Audette, N. J., Brecht, M., Barth, A. L., & Poulet, J. F. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.014 · Cited by 72 · see citing works

Somatosensory maps

Harding-Forrester, S., & Feldman, D. E. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00004-8 · Cited by 72 · see citing works

Decreasing-Rate Pruning Optimizes the Construction of Efficient and Robust Distributed Networks

Navlakha, S., Barth, A. L., & Bar‐Joseph, Z. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004347 · Cited by 68 · see citing works

Default activity patterns at the neocortical microcircuit level

Luczak, A., & MacLean, J. N. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00030 · Cited by 67 · see citing works

Neural coding: A single neuron’s perspective

Azarfar, A., Calcini, N., Huang, C., Zeldenrust, F., & Celikel, T. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.007 · Cited by 67 · see citing works

Hysteresis, neural avalanches, and critical behavior near a first-order transition of a spiking neural network

Scarpetta, S., Apicella, I., Minati, L., & CANDIA, A. D. (2018) · Physical review. E · doi:10.1103/physreve.97.062305 · Cited by 65 · see citing works

Active dendrites enable strong but sparse inputs to determine orientation selectivity

Goetz, L., Roth, A., & Häusser, M. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017339118 · Cited by 72 · see citing works

Neural synchrony in cortical networks: mechanisms and implications for neural information processing and coding

Gansel, K. S. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.900715 · Cited by 62 · see citing works

Medial Prefrontal Cortex Neuronal Activation and Synaptic Alterations after Stress-Induced Reinstatement of Palatable Food Seeking: A Study Using c-fos-GFP Transgenic Female Rats

Cifani, C., Koya, E., Navarre, B. M., Calu, D. J., Baumann, M. H., Marchant, N. J., Liu, Q., Khuc, T., Pickel, J. M., Lupica, C. R., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5895-11.2012 · Cited by 63 · see citing works

Self-organization in Balanced State Networks by STDP and Homeostatic Plasticity

Effenberger, F., Jost, J., & Levina, A. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004420 · Cited by 61 · see citing works

Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero

Salmi, M., Bruneau, N., Cillario, J., Lozovaya, N., Massacrier, A., Buhler, E., Cloarec, R., Tsintsadze, T. S., Françoise Watrin, A., Tsintsadze, V., et al. (2013) · Brain · doi:10.1093/brain/awt161 · Cited by 59 · see citing works

Neuronal firing rates diverge during REM and homogenize during non-REM

Miyawaki, H., Watson, B. O., & Diba, K. (2019) · Scientific Reports · doi:10.1038/s41598-018-36710-8 · Cited by 59 · see citing works

Cux1 and Cux2 selectively target basal and apical dendritic compartments of layer II‐III cortical neurons

Cubelos, B., Briz, C. G., Esteban-Ortega, G. M., & Nieto, M. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22215 · Cited by 56 · see citing works

Hippocampal information processing across sleep/wake cycles.

Mizuseki, K., & Miyawaki, H. (2017) · Neurosciences research · doi:10.1016/j.neures.2017.04.018 · Cited by 52 · see citing works

Dense Neuron Clustering Explains Connectivity Statistics in Cortical Microcircuits

Klinshov, V. V., Teramae, J.-N., Nekorkin, V. I., & Fukai, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094292 · Cited by 52 · see citing works

Emergence of Slow-Switching Assemblies in Structured Neuronal Networks

Schaub, M. T., Billeh, Y. N., Anastassiou, C. A., Christof Koch, A., & Barahona, M. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004196 · Cited by 49 · see citing works

Genetic tagging of active neurons in auditory cortex reveals maternal plasticity of coding ultrasonic vocalizations

Tasaka, G., Guenthner, C. J., Shalev, A., Gilday, O. D., Luo, L., & Mizrahi, A. (2018) · Nature Communications · doi:10.1038/s41467-018-03183-2 · Cited by 52 · see citing works

Genetic Basis of Neuronal Individuality in the Mammalian Brain

Yagi, T. (2013) · Journal of Neurogenetics · doi:10.3109/01677063.2013.801969 · Cited by 49 · see citing works

Diverse levels of an inwardly rectifying potassium conductance generate heterogeneous neuronal behavior in a population of dorsal cochlear nucleus pyramidal neurons

Leão, R. M., Li, S., Doiron, B., & Tzounopoulos, T. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00660.2011 · Cited by 47 · see citing works

Autonomous emergence of connectivity assemblies via spike triplet interactions

Montangie, L., Miehl, C., & Gjorgjieva, J. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007835 · Cited by 48 · see citing works

Balanced neural architecture and the idling brain

Doiron, B., & Litwin-Kumar, A. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00056 · Cited by 43 · see citing works

Stimulation triggers endogenous activity patterns in cultured cortical networks

Pasquale, V., Sergio Martinoia, A., & Chiappalone, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-08369-0 · Cited by 46 · see citing works

Encoding of long-term associations through neural unitization in the human medial temporal lobe

Rey, H. G., Falco, E. D., Ison, M. J., Valentı́n, A., Alarcón, G., Selway, R., Richardson, M. P., & Quiroga, R. Q. (2018) · Nature Communications · doi:10.1038/s41467-018-06870-2 · Cited by 46 · see citing works

Challenges of understanding brain function by selective modulation of neuronal subpopulations

Kumar, A., Vlachos, I., Aertsen, A., & Boucsein, C. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.06.005 · Cited by 43 · see citing works

Neurogenesis during Abstinence Is Necessary for Context-Driven Methamphetamine-Related Memory

Galinato, M. H., Takashima, Y., Fannon, M. J., Quach, L. W., Silva, R. J. M., Mysore, K. K., Terranova, M. J., Dutta, R. R., Ostrom, R. W., Somkuwar, S. S., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2011-17.2018 · Cited by 42 · see citing works

Periodic Organization of a Major Subtype of Pyramidal Neurons in Neocortical Layer V

Maruoka, H., Kubota, K., Kurokawa, R., Tsuruno, S., & Hosoya, T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3117-11.2011 · Cited by 43 · see citing works

Simultaneous visualization of multiple neuronal properties with single-cell resolution in the living rodent brain

Ako, R., Wakimoto, M., Ebisu, H., Tanno, K., Hira, R., Kasai, H., Matsuzaki, M., & Kawasaki, H. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.08.005 · Cited by 41 · see citing works

Multiple Two-Photon Targeted Whole-Cell Patch-Clamp Recordings From Monosynaptically Connected Neurons in vivo

Jouhanneau, J.-S., & Poulet, J. F. A. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00015 · Cited by 41 · see citing works

Arc Regulates Experience-Dependent Persistent Firing Patterns in Frontal Cortex

Ren, M., Cao, V. Y., Ye, Y., Manji, H. K., & Wang, K. H. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0167-14.2014 · Cited by 39 · see citing works

Distinct Roles of SOM and VIP Interneurons during Cortical Up States

Neske, G. T., & Connors, B. W. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00052 · Cited by 38 · see citing works

The Noonan Syndrome-linked Raf1L613V mutation drives increased glial number in the mouse cortex and enhanced learning

Holter, M. C., Hewitt, L. T., Koebele, S. V., Judd, J. M., Xing, L., Bimonte‐Nelson, H. A., Conrad, C. D., Araki, T., Neel, B. G., Snider, W. D., et al. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008108 · Cited by 38 · see citing works

Activity labeling in vivo using CaMPARI2 reveals intrinsic and synaptic differences between neurons with high and low firing rate set points

Trojanowski, N. F., Bottorff, J., & Turrigiano, G. G. (2020) · Neuron · doi:10.1016/j.neuron.2020.11.027 · Cited by 38 · see citing works

Engram cell connectivity: an evolving substrate for information storage

Ryan, T. J., Luis, C. O. S., Pezzoli, M., & Sen, S. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.01.006 · Cited by 38 · see citing works

ΔFosB accumulation in hippocampal granule cells drives cFos pattern separation during spatial learning

Lamothe‐Molina, P. J., Franzelin, A., Beck, L., Li, D., Auksutat, L., Fieblinger, T., Laprell, L., Ahlbeck, J., Gee, C. E., Kneussel, M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33947-w · Cited by 46 · see citing works

Computational capability of liquid state machines with spike-timing-dependent plasticity

Xue, F., Hou, Z., & Li, X. (2013) · Neurocomputing · doi:10.1016/j.neucom.2013.06.019 · Cited by 37 · see citing works

Local MEG networks: The missing link between protein expression and epilepsy in glioma patients?

Douw, L., de Groot, M., van Dellen, E., Aronica, E., Heimans, J. J., Klein, M., Stam, C. J., Reijneveld, J. C., & Hillebrand, A. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.02.067 · Cited by 35 · see citing works

Postnatal maturation of the spinal-bulbo-spinal loop

Schwaller, F., Kwok, C. H. T., & Fitzgerald, M. (2015) · Pain · doi:10.1097/j.pain.0000000000000420 · Cited by 35 · see citing works

RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex

Cho, J.-H., Huang, B. S., & Gray, J. M. (2016) · Scientific Reports · doi:10.1038/srep31753 · Cited by 32 · see citing works

Rich-club connectivity, diverse population coupling, and dynamical activity patterns emerging from local cortical circuits

Gu, Y., Qi, Y., & Gong, P. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006902 · Cited by 33 · see citing works

Associative memory model with long-tail-distributed Hebbian synaptic connections

Hiratani, N., Teramae, J.-N., & Fukai, T. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00102 · Cited by 35 · see citing works

Neural mechanisms of social learning in the female mouse

Gao, Y., Budlong, C. H., Durlacher, E., & Davison, I. G. (2017) · eLife · doi:10.7554/elife.25421 · Cited by 34 · see citing works

Exploring Memory Representations with Activity-Based GeneticsPreprint

Mayford, M. R., & Reijmers, L. G. J. E. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021832 · Cited by 34 · see citing works

Large‐scale analysis reveals populational contributions of cortical spike rate and synchrony to behavioural functions

Kimura, R., Saiki, A., Fujiwara‐Tsukamoto, Y., Sakai, Y., & Isomura, Y. (2016) · The Journal of Physiology · doi:10.1113/jp272794 · Cited by 32 · see citing works

Algorithms of whisker-mediated touch perception

Maravall, M., & Diamond, M. E. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.014 · Cited by 31 · see citing works

Sparse, reliable, and long-term stable representation of periodic whisker deflections in the mouse barrel cortex

Mayrhofer, J. M., Haiss, F., Helmchen, F., & Weber, B. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.045 · Cited by 31 · see citing works

FosGFP expression does not capture a sensory learning-related engram in superficial layers of mouse barrel cortex

Lee, J., Urban‐Ciećko, J., Park, E., Zhu, M., Myal, S. E., Margolis, D. J., & Barth, A. L. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2112212118 · Cited by 31 · see citing works

Thalamocortical Connections Drive Intracortical Activation of Functional Columns in the MislaminatedReelerSomatosensory Cortex

Wagener, R. J., Witte, M., Guy, J., Mingo-Moreno, N., Kügler, S., & Staiger, J. F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv257 · Cited by 31 · see citing works

Degree Correlations Optimize Neuronal Network Sensitivity to Sub-Threshold Stimuli

Schmeltzer, C., Kihara, A. H., Sokolov, I. M., & Rüdiger, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121794 · Cited by 30 · see citing works

Microcircuit dynamics of map plasticity in barrel cortex

Margolis, D. J., Lütcke, H., & Helmchen, F. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.08.019 · Cited by 29 · see citing works

Fluorescence-Based Quantitative Synapse Analysis for Cell Type-Specific Connectomics

Kuljis, D. A., Park, E., Telmer, C. A., Lee, J., Ackerman, D. S., Bruchez, M. P., Barth, A. L., Watkins, S. C., Arnold, D. B., Bruchez, M. P., et al. (2019) · eNeuro · doi:10.1523/eneuro.0193-19.2019 · Cited by 31 · see citing works

Computational modeling of spiking neural network with learning rules from STDP and intrinsic plasticity

Li, X., Wang, W. J., Xue, F., & Song, Y. (2017) · Physica A Statistical Mechanics and its Applications · doi:10.1016/j.physa.2017.08.053 · Cited by 29 · see citing works

Induction and modulation of persistent activity in a layer V PFC microcircuit model

Papoutsi, A., Sidiropoulou, K., Vassilis Cutsuridis, A., & Poirazi, P. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00161 · Cited by 29 · see citing works

Nonuniform allocation of hippocampal neurons to place fields across all hippocampal subfields

Witharana, W. K. L., Cardiff, J. W., Chawla, M. K., Xie, J., Alme, C. B., Eckert, M. J., Lapointe, V., Demchuk, A. M., Maurer, A. P., Trivedi, V., et al. (2016) · Hippocampus · doi:10.1002/hipo.22609 · Cited by 28 · see citing works

The relevance of network micro-structure for neural dynamics

Pernice, V., Deger, M., Cardanobile, S., & Rotter, S. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00072 · Cited by 28 · see citing works

Differential Wiring of Layer 2/3 Neurons Drives Sparse and Reliable Firing During Neocortical Development

Benedetti, B. L., Takashima, Y., Wen, J. A., Urban‐Ciećko, J., & Barth, A. L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs257 · Cited by 25 · 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

Spatial clusters of constitutively active neurons in mouse visual cortex

Makino, K., Funayama, K., & Ikegaya, Y. (2015) · Anatomical Science International · doi:10.1007/s12565-015-0284-z · Cited by 11 · see citing works

Functional and Structural Properties of Highly Responsive Somatosensory Neurons in Mouse Barrel Cortex

Barz, C. S., Gardères, P.-M., Ganea, D. A., Reischauer, S., Feldmeyer, D., & Haiss, F. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab104 · Cited by 8 · see citing works

A network of fast-spiking cells in the neocortex connected by electrical synapses

Galarreta, M., & Hestrin, S. (1999) · Nature · doi:10.1038/47029 · Cited by 960 · see citing works