Coordinated developmental recruitment of latent fast spiking interneurons in layer IV barrel cortex

Excitatory actions of gaba during development: the nature of the nurture

Ben-Ari, Y. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn920 · Cited by 2,448 · see citing works

The structural organization of layer IV in the somatosensory region (S I) of mouse cerebral cortex

Woolsey, T. A., & Van der Loos, H. (1970) · Brain Research · doi:10.1016/0006-8993(70)90079-x · Cited by 2,254 · see citing works

Two networks of electrically coupled inhibitory neurons in neocortex

Gibson, J. R., Beierlein, M., & Connors, B. W. (1999) · Nature · doi:10.1038/47035 · Cited by 1,404 · 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

Giant synaptic potentials in immature rat CA3 hippocampal neurones.

Ben‐Ari, Y., Cherubini, E., Corradetti, R., & Gaiarsa, J. L. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017762 · Cited by 1,317 · see citing works

GABA regulates synaptic integration of newly generated neurons in the adult brain

Ge, S., Goh, E. L. K., Sailor, K. A., Kitabatake, Y., Ming, G., & Song, H. (2005) · Nature · doi:10.1038/nature04404 · Cited by 1,261 · see citing works

Is there more to gaba than synaptic inhibition?

Owens, D. F., & Kriegstein, A. R. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn919 · Cited by 1,158 · see citing works

Target-cell-specific facilitation and depression in neocortical circuits

Reyes, A., Lujan, R., Rozov, A., Burnashev, N., Somogyi, P., & Sakmann, B. (1998) · Nature Neuroscience · doi:10.1038/1092 · Cited by 716 · see citing works

Cortex is driven by weak but synchronously active thalamocortical synapses

Bruno, R. M., & Sakmann, B. (2006) · Science · doi:10.1126/science.1124593 · Cited by 714 · see citing works

A critical period for long-term potentiation at thalamocortical synapses

Crair, M. C., & Malenka, R. C. (1995) · Nature · doi:10.1038/375325a0 · Cited by 691 · see citing works

Thalamocortical responses of mouse somatosensory (barrel) cortexin vitro

Agmon, A., & Connors, B. W. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90333-j · Cited by 673 · 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

Two dynamically distinct inhibitory networks in layer 4 of the neocortex

Beierlein, M., Gibson, J. R., & Connors, B. W. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00283.2003 · Cited by 591 · see citing works

Postnatal maturation of the GABAergic system in rat neocortex

Luhmann, H. J., & Prince, D. A. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.2.247 · Cited by 575 · see citing works

Silent synapses during development of thalamocortical inputs

Isaac, J. T. R., Crair, M. C., Nicoll, R. A., & Malenka, R. C. (1997) · Neuron · doi:10.1016/s0896-6273(00)80267-6 · Cited by 507 · see citing works

Novel Hippocampal Interneuronal Subtypes Identified Using Transgenic Mice That Express Green Fluorescent Protein in GABAergic Interneurons

Oliva, A. A., Jiang, M., Lam, T., Smith, K. L., & Swann, J. W. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03354.2000 · Cited by 498 · see citing works

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

Distinct Subtypes of Somatostatin-Containing Neocortical Interneurons Revealed in Transgenic Mice

Ma, Y., Hu, H., Berrebi, A. S., Mathers, P. H., & Agmon, A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0661-06.2006 · Cited by 432 · see citing works

A critical period for experience-dependent synaptic plasticity in rat barrel cortex

Fox, K. D. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-05-01826.1992 · Cited by 420 · see citing works

Ca2+ Oscillations Mediated by the Synergistic Excitatory Actions of GABAA and NMDA Receptors in the Neonatal Hippocampus

Leinekugel, X., Medina, I., Khalilov, I., Ben-Ari, Y., & Khazipov, R. (1997) · Neuron · doi:10.1016/s0896-6273(00)80265-2 · Cited by 407 · see citing works

Coincidence detection and changes of synaptic efficacy in spiny stellate neurons in rat barrel cortex

Egger, V., Feldmeyer, D., & Sakmann, B. J. (1999) · Nature Neuroscience · doi:10.1038/16026 · Cited by 405 · see citing works

Unique features of action potential initiation in cortical neurons

Naundorf, B., Wolf, F., & Volgushev, M. (2006) · Nature · doi:10.1038/nature04610 · Cited by 396 · see citing works

Diverse Types of Interneurons Generate Thalamus-Evoked Feedforward Inhibition in the Mouse Barrel Cortex

Porter, J. T., Johnson, C. K., & Agmon, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02699.2001 · Cited by 344 · see citing works

Neural mechanisms subserving cutaneous sensibility, with special reference to the role of afferent inhibition in sensory perception and discrimination.

Mountcastle, V. B., & Powell, T. P. S. (1959) · PubMed · Cited by 334 · see citing works

Anatomical pathways and molecular mechanisms for plasticity in the barrel cortex

Fox, K. D. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00027-1 · Cited by 307 · see citing works

Barrel Cortex Microcircuits: Thalamocortical Feedforward Inhibition in Spiny Stellate Cells Is Mediated by a Small Number of Fast-Spiking Interneurons

Sun, Q., Huguenard, J. R., & Prince, D. A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4727-04.2006 · Cited by 242 · see citing works

Developmental and activity- dependent regulation of kainate receptors at thalamocortical synapses

Kidd, F. L., & Isaac, J. T. R. (1999) · Nature · doi:10.1038/23040 · Cited by 224 · see citing works

Depolarizing GABAergic Conductances Regulate the Balance of Excitation to Inhibition in the Developing Retinotectal Circuit In Vivo

Akerman, C. J., & Cline, H. T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0319-06.2006 · Cited by 189 · see citing works

Developmental changes in NMDA and non-NMDA receptor-mediated synaptic potentials in rat neocortex

Burgard, E. C., & Hablitz, J. J. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.1.230 · Cited by 187 · see citing works

NMDAR EPSC kinetics do not regulate the critical period for LTP at thalamocortical synapses

Barth, A. L., & Malenka, R. C. (2001) · Nature Neuroscience · doi:10.1038/85070 · Cited by 183 · see citing works

Long-Term Depression at Thalamocortical Synapses in Developing Rat Somatosensory Cortex

Feldman, D. E., Nicoll, R. A., Malenka, R. C., & Isaac, J. T. R. (1998) · Neuron · doi:10.1016/s0896-6273(00)80544-9 · Cited by 181 · see citing works

Cellular and synaptic physiology and epileptogenesis of developing rat neocortical neurons in vitro

Kriegstein, A. R., Suppes, T. M., & Prince, D. A. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90206-9 · Cited by 168 · see citing works

NMDA receptor-mediated currents are prominent in the thalamocortical synaptic response before maturation of inhibition

Agmon, A., & O’Dowd, D. K. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.68.1.345 · Cited by 166 · see citing works

Whisker Vibration Information Carried by Rat Barrel Cortex Neurons

Arabzadeh, E., Panzeri, S., & Diamond, M. E. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1389-04.2004 · Cited by 145 · see citing works

Synaptic basis for developmental plasticity in somatosensory cortex

Foeller, E., & Feldman, D. E. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.01.011 · Cited by 136 · see citing works

Synaptic organization of GABAergic neurons in the mouse SmI cortex

Keller, A., & White, E. L. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902620102 · Cited by 129 · see citing works

THALAMOCORTICAL SYNAPSES

Castro‐Alamancos, M. A., & Connors, B. W. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00002-6 · Cited by 114 · see citing works

Thalamocortical Bursts Trigger Recurrent Activity in Neocortical Networks: Layer 4 as a Frequency-Dependent Gate

Beierlein, M., Fall, C. P., Rinzel, J., & Yuste, R. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-22-09885.2002 · Cited by 104 · see citing works

Molecular basis for induction of ocular dominance plasticity

Bear, M. F., & Rittenhouse, C. D. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199910)41:1 · Cited by 99 · see citing works

Distribution of GABAergic elements postsynaptic to ventroposteromedial thalamic projections in layer IV of rat barrel cortex

Staiger, J. F., Zilles, K., & Freund, T. F. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01191.x · Cited by 98 · see citing works

Population coding in somatosensory cortex

Petersen, R. S. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00338-0 · Cited by 95 · see citing works

Functional GABAergic Synaptic Connection in Neonatal Mouse Barrel Cortex

Agmon, A., Hollrigel, G. S., & O’Dowd, D. K. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-15-04684.1996 · Cited by 91 · see citing works

Properties of Excitatory Synaptic Events in Neurons of Primary Somatosensory Cortex of Neonatal Rats

Kim, H. G., Fox, K. D., & Connors, B. W. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.2.148 · Cited by 86 · see citing works

GABAergic Inhibition Suppresses Paroxysmal Network Activity in the Neonatal Rodent Hippocampus and Neocortex

Wells, J. E., Porter, J. T., & Agmon, A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08822.2000 · Cited by 78 · see citing works

Developmental Changes in AMPA and Kainate Receptor-Mediated Quantal Transmission at Thalamocortical Synapses in the Barrel Cortex

Bannister, N., Benke, T., Mellor, J., Scott, H. L., Gürdal, E., Crabtree, J., & Isaac, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0827-05.2005 · Cited by 50 · see citing works

Rapid, Activity-Dependent Plasticity in Timing Precision in Neonatal Barrel Cortex

Daw, M. I., Bannister, N. V., & Isaac, J. T. R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0150-06.2006 · Cited by 37 · see citing works

Cultured basal forebrain cholinergic neurons in contact with cortical cells display synapses, enhanced morphological features, and decreased dependence on nerve growth factor

Ha, D. H., Robertson, R. T., Ribak, C. E., & Weiss, J. H. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960923)373:3 · Cited by 36 · see citing works

Development and Functional Diversification of Cortical Interneurons

Lim, L., Mi, D., Llorca, A., & Marín, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.009 · Cited by 714 · see citing works

Pathway-Specific Feedforward Circuits between Thalamus and Neocortex Revealed by Selective Optical Stimulation of Axons

Cruikshank, S. J., Urabe, H., Nurmikko, A. V., & Connors, B. W. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.025 · Cited by 459 · see citing works

GABAergic Interneurons Shape the Functional Maturation of the Cortex

Le Magueresse, C., & Monyer, H. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.011 · Cited by 425 · see citing works

Barrel cortex function

Feldmeyer, D., Brecht, M., Helmchen, F., Petersen, C. C. H., Poulet, J. F. A., Staiger, J. F., Luhmann, H. J., & Schwarz, C. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.11.002 · Cited by 354 · see citing works

Input normalization by global feedforward inhibition expands cortical dynamic range

Pouille, F., Marin-Burgin, A., Adesnik, H., Atallah, B. V., & Scanziani, M. (2009) · Nature Neuroscience · doi:10.1038/nn.2441 · Cited by 306 · see citing works

Lateral Sharpening of Cortical Frequency Tuning by Approximately Balanced Inhibition

Wu, G. K., Arbuckle, R., Liu, B., Tao, H. W., & Zhang, L. I. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.035 · Cited by 276 · see citing works

A conserved switch in sensory processing prepares developing neocortex for vision

Colonnese, M. T., Kaminska, A., Minlebaev, M., Milh, M., Bloem, B., Lescure, S., Moriette, G., Chiron, C., Ben-Ari, Y., & Khazipov, R. (2010) · Neuron · doi:10.1016/j.neuron.2010.07.015 · Cited by 273 · see citing works

Early Gamma Oscillations Synchronize Developing Thalamus and Cortex

Minlebaev, M., Colonnese, M., Tsintsadze, T., Sirota, A., & Khazipov, R. (2011) · Science · doi:10.1126/science.1210574 · Cited by 257 · see citing works

Postnatal Differentiation of Basket Cells from Slow to Fast Signaling Devices

Doischer, D., Aurel Hosp, J., Yanagawa, Y., Obata, K., Jonas, P., Vida, I., & Bartos, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2890-08.2008 · Cited by 248 · see citing works

Inhibitory Interneurons Regulate Temporal Precision and Correlations in Cortical Circuits

Cardin, J. A. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.07.015 · Cited by 254 · see citing works

The mediodorsal thalamus drives feedforward inhibition in the anterior cingulate cortex via parvalbumin interneurons

Delevich, K., Tucciarone, J., Huang, Z. J., & Li, B. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4565-14.2015 · Cited by 226 · see citing works

Early somatostatin interneuron connectivity mediates the maturation of deep layer cortical circuits

Tuncdemir, S. N., Wamsley, B., Stam, F. J., Osakada, F., Goulding, M., Callaway, E. M., Rudy, B., & Fishell, G. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.020 · Cited by 224 · see citing works

The Developmental Switch in GABA Polarity Is Delayed in Fragile X Mice

He, Q., Nomura, T., Xu, J., & Contractor, A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4447-13.2014 · Cited by 230 · see citing works

Sensitive and critical periods during neurotypical and aberrant neurodevelopment: A framework for neurodevelopmental disorders

Meredith, R. M. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.001 · Cited by 237 · 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

A transient translaminar GABAergic interneuron circuit connects thalamocortical recipient layers in neonatal somatosensory cortex

Marques-Smith, A., Lyngholm, D., Kaufmann, A.-K., Stacey, J. A., Hoerder-Suabedissen, A., Becker, E. B. E., Wilson, M. C., Molnár, Z., & Butt, S. J. B. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.015 · Cited by 173 · see citing works

The postnatal GABA shift: A developmental perspective

Peerboom, C., & Wierenga, C. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.01.024 · Cited by 174 · 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

Asynchronous Transmitter Release from Cholecystokinin-Containing Inhibitory Interneurons Is Widespread and Target-Cell Independent

Daw, M. I., Tricoire, L., Erdelyi, F., Szabo, G., & McBain, C. J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5760-08.2009 · Cited by 151 · see citing works

Robust but delayed thalamocortical activation of dendritic-targeting inhibitory interneurons

Tan, Z., Hu, H., Huang, Z. J., & Agmon, A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710628105 · Cited by 155 · see citing works

Neuronal Activity Patterns in the Developing Barrel Cortex

Luhmann, H. J., & Khazipov, R. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.025 · Cited by 149 · see citing works

Fast-spiking parvalbumin-positive interneurons in brain physiology and Alzheimer’s disease

Hijazi, S., Smit, A. B., & van Kesteren, R. E. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02168-y · Cited by 144 · see citing works

Developmental Changes in Electrophysiological Properties and a Transition from Electrical to Chemical Coupling between Excitatory Layer 4 Neurons in the Rat Barrel Cortex

Valiullina, F., Akhmetshina, D., Nasretdinov, A., Mukhtarov, M. R., Valeeva, G. R., Khazipov, R., & Rozov, A. V. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00001 · Cited by 147 · see citing works

Excitatory GABA in Rodent Developing Neocortex In Vitro

Rheims, S., Minlebaev, M., Ivanov, A., Represa, A., Khazipov, R., Holmes, G. L., Ben-Ari, Y., & Zilberter, Y. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90402.2008 · Cited by 138 · see citing works

Experience-dependent regulation of NG2 progenitors in the developing barrel cortex

Mangin, J., Li, P., Scafidi, J., & Gallo, V. (2012) · Nature Neuroscience · doi:10.1038/nn.3190 · Cited by 139 · see citing works

Somatostatin and Somatostatin-Containing Neurons in Shaping Neuronal Activity and Plasticity

Liguz‐Lecznar, M., Urban‐Ciećko, J., & Kossut, M. M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00048 · Cited by 141 · see citing works

Manipulating critical period closure across different sectors of the primary auditory cortex

de Villers-Sidani, E., Simpson, K. L., Lu, Y.-F., Lin, R. C. S., & Merzenich, M. M. (2008) · Nature Neuroscience · doi:10.1038/nn.2144 · Cited by 137 · 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

Sensory Processing Phenotypes in Fragile X Syndrome

Rais, M., Binder, D. K., Razak, K. A., & Ethell, I. M. (2018) · ASN NEURO · doi:10.1177/1759091418801092 · Cited by 128 · see citing works

Inhibitory Circuits in Cortical Layer 5

Naka, A., & Adesnik, H. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00035 · Cited by 130 · see citing works

Myelination of parvalbumin interneurons shapes the function of cortical sensory inhibitory circuits

Benamer, N., Vidal, M., Balia, M., & Angulo, M. C. (2020) · Nature Communications · doi:10.1038/s41467-020-18984-7 · Cited by 124 · see citing works

Many specialists for suppressing cortical excitation

Burkhalter, A. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.026.2008 · Cited by 122 · see citing works

How development sculpts hippocampal circuits and function

Cossart, R., & Khazipov, R. (2021) · Physiological Reviews · doi:10.1152/physrev.00044.2020 · Cited by 119 · see citing works

Parvalbumin‐containing neurons, perineuronal nets and experience‐dependent plasticity in murine barrel cortex

Nowicka, D., Soulsby, S., Skangiel‐Kramska, J., & Glazewski, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06996.x · Cited by 110 · see citing works

Interneurons and oligodendrocyte progenitors form a structured synaptic network in the developing neocortex

Orduz, D., Maldonado, P. P., Balia, M., Vélez‐Fort, M., de Sars, V., Yanagawa, Y., Emiliani, V., & Angulo, M. C. (2015) · eLife · doi:10.7554/elife.06953 · Cited by 115 · see citing works

Cortical Plasticity, Excitatory–Inhibitory Balance, and Sensory Perception

Carcea, I., & Froemke, R. C. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00003-5 · Cited by 110 · see citing works

Children With Autism Show Reduced Somatosensory Response: An MEG Study

Marco, E. J., Khatibi, K., Hill, S. S., Siegel, B., Arroyo, M. S., Dowling, A. F., Neuhaus, J. M., Sherr, E. H., Hinkley, L. B. N., & Nagarajan, S. S. (2012) · Autism Research · doi:10.1002/aur.1247 · Cited by 110 · see citing works

Postnatal erythropoietin treatment mitigates neural cell loss after systemic prenatal hypoxic-ischemic injury

Mazur, M. D., Miller, R. H., & Robinson, S. (2010) · Journal of Neurosurgery Pediatrics · doi:10.3171/2010.5.peds1032 · Cited by 99 · see citing works

GABAergic interneurons form transient layer-specific circuits in early postnatal neocortex

Anastasiades, P. G., Marques-Smith, A., Lyngholm, D., Lickiss, T., Raffiq, S., Kätzel, D., Miesenböck, G., & Butt, S. J. B. (2016) · Nature Communications · doi:10.1038/ncomms10584 · Cited by 87 · see citing works

Postnatal connectomic development of inhibition in mouse barrel cortex

Gour, A., Boergens, K. M., Heike, N., Hua, Y., Laserstein, P., Song, K., & Helmstaedter, M. N. (2020) · Science · doi:10.1126/science.abb4534 · Cited by 97 · see citing works

Progressive synaptic pathology of motor cortical neurons in a BAC transgenic mouse model of Huntington's disease

Spampanato, J. G., Gu, X., Yang, X. W., & Módy, I. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.09.020 · Cited by 87 · see citing works

Synaptogenesis of Electrical and GABAergic Synapses of Fast-Spiking Inhibitory Neurons in the Neocortex

Pangratz-Fuehrer, S., & Hestrin, S. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6655-10.2011 · Cited by 83 · see citing works

Emergence of cortical inhibition by coordinated sensory-driven plasticity at distinct synaptic loci

Chittajallu, R., & Isaac, J. T. R. (2010) · Nature Neuroscience · doi:10.1038/nn.2639 · Cited by 81 · see citing works

Postnatal Erythropoietin Mitigates Impaired Cerebral Cortical Development Following Subplate Loss from Prenatal Hypoxia–Ischemia

Jantzie, L. L., Corbett, C. J., Firl, D. J., & Robinson, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu066 · Cited by 81 · see citing works

Assemblies of Perisomatic GABAergic Neurons in the Developing Barrel Cortex

Mòdol, L., Bollmann, Y., Tressard, T., Baude, A., Che, A., Duan, Z. R. S., Babij, R., García, N. V. D. M., & Cossart, R. (2019) · Neuron · doi:10.1016/j.neuron.2019.10.007 · Cited by 80 · see citing works

Cortical Adenylyl Cyclase 1 Is Required for Thalamocortical Synapse Maturation and Aspects of Layer IV Barrel Development

Iwasato, T., Inan, M., Kanki, H., Erzurumlu, R. S., Itohara, S., & Crair, M. C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0815-08.2008 · Cited by 78 · see citing works

Thalamocortical Inputs Show Post-Critical-Period Plasticity

Yu, X., Chung, S., Chen, D.-Y., Wang, S., Dodd, S. J., Walters, J. R., Isaac, J. T. R., & Koretsky, A. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.024 · Cited by 78 · see citing works

Control of CA3 Output by Feedforward Inhibition Despite Developmental Changes in the Excitation–Inhibition Balance

Torborg, C. L., Nakashiba, T., Tonegawa, S., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3099-10.2010 · Cited by 76 · see citing works

Thalamocortical Long-Term Potentiation Becomes Gated after the Early Critical Period in the Auditory Cortex

Chun, S., Bayazitov, I. T., Blundon, J. A., & Zakharenko, S. S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4500-12.2013 · Cited by 75 · see citing works

Critical period inhibition of NKCC1 rectifies synapse plasticity in the somatosensory cortex and restores adult tactile response maps in fragile X mice

He, Q., Arroyo, E. D., Smukowski, S. N., Xu, J., Piochon, C., Savas, J. N., Portera‐Cailliau, C., & Contractor, A. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0048-y · Cited by 73 · see citing works

The Nature of the Sensory Input to the Neonatal Rat Barrel Cortex

Akhmetshina, D., Nasretdinov, A., Zakharov, A., Valeeva, G. R., & Khazipov, R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1781-16.2016 · Cited by 73 · see citing works

Delayed maturation of fast-spiking interneurons is rectified by activation of the TrkB receptor in the mouse model of fragile X syndrome.

Nomura, T., Musial, T. F., Marshall, J. J., Zhu, Y., Remmers, C. L., Xu, J., Nicholson, D. A., & Contractor, A. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2893-16.2017 · Cited by 64 · see citing works

Postnatal Development of 2 Microcircuits Involving Fast-Spiking Interneurons in the Mouse Prefrontal Cortex

Yang, J., Zhang, J., Yu, Y., Duan, S., & Li, X. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs291 · Cited by 67 · see citing works

Early patterns of activity in the developing cortex: Focus on the sensorimotor system

Khazipov, R., & Milh, M. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.014 · Cited by 64 · see citing works

Early gamma oscillations

Khazipov, R., Minlebaev, M., & Valeeva, G. R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.019 · Cited by 65 · see citing works

Disruption of Transient Serotonin Accumulation by Non-Serotonin-Producing Neurons Impairs Cortical Map Development

Chen, X., Ye, R., Gargus, J. J., Blakely, R., Dobrenis, K., & Sze, J. Y. (2015) · Cell Reports · doi:10.1016/j.celrep.2014.12.033 · Cited by 65 · see citing works

mGluR5 in Cortical Excitatory Neurons Exerts Both Cell-Autonomous and -Nonautonomous Influences on Cortical Somatosensory Circuit Formation

Ballester‐Rosado, C. J., Albright, M. J., Wu, C., Liao, C.-C., Zhu, J., Xu, J., Lee, L., & Lu, H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2462-10.2010 · Cited by 65 · see citing works

Gabaergic Interneurons in Early Brain Development: Conducting and Orchestrated by Cortical Network Activity

Warm, D., Schroer, J., & Sinning, A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.807969 · Cited by 60 · see citing works

A role for GABAergic interneuron diversity in circuit development and plasticity of the neonatal cerebral cortex

Butt, S. J. B., Stacey, J. A., Teramoto, Y., & Vagnoni, C. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.011 · Cited by 61 · see citing works

What can we get from ‘barrels’: the rodent barrel cortex as a model for studying the establishment of neural circuits

Wu, C., Ballester‐Rosado, C. J., & Lu, H. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07892.x · Cited by 61 · see citing works

Early GABAergic circuitry in the cerebral cortex

Luhmann, H. J., Kirischuk, S., Sinning, A., & Kilb, W. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.014 · Cited by 59 · see citing works

Erythropoietin attenuates loss of potassium chloride co-transporters following prenatal brain injury

Jantzie, L. L., Getsy, P. M., Firl, D. J., Wilson, C. G., Miller, R. H., & Robinson, S. (2014) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2014.06.009 · Cited by 58 · see citing works

Emergence of Coordinated Activity in the Developing Entorhinal–Hippocampal Network

Valeeva, G. R., Janáčková, S., Nasretdinov, A., Rychkova, V., Makarov, R., Holmes, G. L., Khazipov, R., & Lenck‐Santini, P. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy309 · Cited by 56 · see citing works

Cellular and synaptic phenotypes lead to disrupted information processing in Fmr1-KO mouse layer 4 barrel cortex

Domanski, A. P. F., Booker, S. A., Wyllie, D. J. A., Isaac, J. T. R., & Kind, P. C. (2019) · Nature Communications · doi:10.1038/s41467-019-12736-y · Cited by 56 · see citing works

Network state transitions during cortical development

Wu, M. W., Kourdougli, N., & Portera‐Cailliau, C. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00824-y · Cited by 55 · see citing works

The Organization and Development of Cortical Interneuron Presynaptic Circuits is Area Specific

Pouchelon, G., Dwivedi, D., Bollmann, Y., Agba, C. K., Xu, Q., Mirow, A. M., Kim, S., Qiu, Y., Sevier, E., Ritola, K., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109993 · Cited by 52 · see citing works

Imprecise Whisker Map in the Neonatal Rat Barrel Cortex

Mitrukhina, O., Suchkov, D., Khazipov, R., & Minlebaev, M. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu169 · Cited by 50 · see citing works

Step by step: cells with multiple functions in cortical circuit assembly

Cossart, R., & Garel, S. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00585-6 · Cited by 48 · see citing works

Loss of Cation-Chloride Cotransporter Expression in Preterm Infants With White Matter Lesions: Implications for the Pathogenesis of Epilepsy

Robinson, S., Mikolaenko, I., Thompson, I., Cohen, M. L., & Goyal, M. (2010) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3181dd25bc · Cited by 49 · see citing works

Developmental mechanisms for the generation of telencephalic interneurons

Corbin, J. G., & Butt, S. J. B. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20890 · Cited by 49 · see citing works

Thalamic inhibitory circuits and network activity development

Murata, Y., & Colonnese, M. T. (2018) · Brain Research · doi:10.1016/j.brainres.2018.10.024 · Cited by 49 · see citing works

Rapid Developmental Emergence of Stable Depolarization during Wakefulness by Inhibitory Balancing of Cortical Network Excitability

Colonnese, M. T. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3659-13.2014 · Cited by 47 · see citing works

Identification of altered brain metabolites associated with TNAP activity in a mouse model of hypophosphatasia using untargeted NMR ‐based metabolomics analysis

Cruz, T., Gleizes, M., Balayssac, S., Mornet, É., Marsal, G., Millán, J. L., Malet‐Martino, M., Nowak, L. G., Gilard, V., & Fonta, C. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.13950 · Cited by 47 · see citing works

Cortical Auditory-Evoked Responses in Preterm Neonates: Revisited by Spectral and Temporal Analyses

Kamińska, A., Delattre, V., Laschet, J. J., Dubois, J., Labidurie, M., Duval, A., Manresa, A., Magny, J., Hovhannisyan, S., Mokhtari, M., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx206 · Cited by 46 · see citing works

Principles of GABAergic signaling in developing cortical network dynamics

Kirmse, K., & Zhang, C. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110568 · Cited by 46 · see citing works

Development of the whisker-to-barrel cortex system

Yang, J., Kilb, W., Kirischuk, S., Unichenko, P., Stüttgen, M. C., & Luhmann, H. J. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.04.023 · Cited by 41 · see citing works

Fast activation of feedforward inhibitory neurons from thalamic input and its relevance to the regulation of spike sequences in the barrel cortex

Kimura, F., Itami, C., Ikezoe, K., Tamura, H., Fujita, I., Yanagawa, Y., Obata, K., & Ohshima, M. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.188177 · Cited by 40 · see citing works

Ethanol and the Developing Brain: Inhibition of Neuronal Activity and Neuroapoptosis

Lotfullina, N., & Khazipov, R. (2017) · The Neuroscientist · doi:10.1177/1073858417712667 · Cited by 40 · see citing works

Cerebral Cortical Circuitry Formation Requires Functional Glycine Receptors

Morelli, G., Ávila, A., Ravanidis, S., Aourz, N., Neve, R. L., Smolders, I. J., Harvey, R. J., Rigo, J., Nguyen, L., & Brône, B. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw025 · Cited by 39 · see citing works

Erythropoietin Modulates Cerebral and Serum Degradation Products from Excess Calpain Activation following Prenatal Hypoxia-Ischemia

Jantzie, L. L., Winer, J. L., Corbett, C. J., & Robinson, S. (2015) · Developmental Neuroscience · doi:10.1159/000441024 · Cited by 38 · see citing works

Reduced Inhibition within Layer IV of Sert Knockout Rat Barrel Cortex is Associated with Faster Sensory Integration

Miceli, S., Kasri, N. N., Joosten, J., Huang, C., Kepser, L.-J., Proville, R. D., Selten, M. M., van Eijs, F., Azarfar, A., Homberg, J. R., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx016 · Cited by 38 · see citing works

Peripheral Sensory Deprivation Restores Critical-Period-like Plasticity to Adult Somatosensory Thalamocortical Inputs

Chung, S., Jeong, J., Ko, S., Yu, X., Kim, Y.-H., Isaac, J. T. R., & Koretsky, A. P. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.06.018 · Cited by 37 · see citing works

Early Development of the Thalamic Inhibitory Feedback Loop in the Primary Somatosensory System of the Newborn Mice

Evrard, A., & Ropert, N. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1671-09.2009 · Cited by 37 · see citing works

A postnatal molecular switch drives activity-dependent maturation of parvalbumin interneurons

Moissidis, M., Abbasova, L., Selten, M. M., Alis, R., Bernard, C., Domínguez-Canterla, Y., Oozeer, F., Qin, S., Kelly, A., Mòdol, L., et al. (2025) · Cell · doi:10.1016/j.cell.2025.06.029 · Cited by 34 · see citing works

Prenatal Hypoxia–Ischemia Induces Abnormalities in CA3 Microstructure, Potassium Chloride Co-Transporter 2 Expression and Inhibitory Tone

Jantzie, L. L., Getsy, P. M., Denson, J. L., Firl, D. J., Maxwell, J. R., Rogers, D. A., Wilson, C. G., & Robinson, S. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00347 · Cited by 35 · see citing works

Postnatal maturation of somatostatin-expressing inhibitory cells in the somatosensory cortex of GIN mice

Kinnischtzke, A. K., Sewall, A. M., Berkepile, J. M., & Fanselow, E. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00033 · Cited by 32 · see citing works

Organization of Sensory Feature Selectivity in the Whisker System

Bale, M. R., & Maravall, M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.014 · Cited by 31 · see citing works

Anterior thalamic lesions produce chronic and profuse transcriptional deregulation in retrosplenial cortex: a model of retrosplenial hypoactivity and covert pathology

Poirier, G. L., Shires, K. L., Sugden, D., Amin, E., Thomas, K. L., Carter, D., & Aggleton, J. P. (2008) · Thalamus & Related Systems · doi:10.1017/s1472928808000368 · Cited by 33 · see citing works

The serotonin reuptake inhibitor citalopram suppresses activity in the neonatal rat barrel cortex in vivo

Akhmetshina, D., Zakharov, A., Vinokurova, D. A., Nasretdinov, A., Valeeva, G. R., & Khazipov, R. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.03.011 · Cited by 31 · see citing works

Plasticity-Related Gene 1 Affects Mouse Barrel Cortex Function via Strengthening of Glutamatergic Thalamocortical Transmission

Unichenko, P., Kirischuk, S., Yang, J., Baumgart, J., Roskoden, T., Schneider, P., Sommer, A. M., Horta, G., Radyushkin, K., Nitsch, R., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw066 · Cited by 30 · see citing works

It's about time for thalamocortical circuits

Hull, C., & Scanziani, M. (2007) · Nature Neuroscience · doi:10.1038/nn0407-400 · Cited by 30 · see citing works

Suppression of cortical seizures by optic stimulation of the reticular thalamus in PV-mhChR2-YFP BAC transgenic mice

Chang, W., Chang, W. P., & Shyu, B. (2017) · Molecular Brain · doi:10.1186/s13041-017-0320-0 · Cited by 29 · see citing works

The Logic of Developing Neocortical Circuits in Health and Disease

Hanganu‐Opatz, I. L., Butt, S. J. B., Hippenmeyer, S., García, N. V. D. M., Cardin, J. A., Voytek, B., & Muotri, A. R. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1655-20.2020 · Cited by 27 · see citing works

A transient postnatal quiescent period precedes emergence of mature cortical dynamics

Domínguez, S., Ma, L., Yu, H. Y., Pouchelon, G., Mayer, C., Spyropoulos, G. D., Cea, C., Buzsáki, G., Fishell, G., Khodagholy, D., et al. (2021) · eLife · doi:10.7554/elife.69011 · Cited by 27 · see citing works

Experience-Dependent, Layer-Specific Development of Divergent Thalamocortical Connectivity

Crocker-Buque, A., Brown, S. M., Kind, P. C., Isaac, J. T. R., & Daw, M. I. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu031 · Cited by 27 · see citing works

Ontogeny of kainate-induced gamma oscillations in the rat CA3 hippocampus in vitro

Tsintsadze, V., Minlebaev, M., Suchkov, D., Cunningham, M. O., & Khazipov, R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00195 · Cited by 26 · see citing works

Synaptic biology of barrel cortex circuit assembly

Vitali, I., & Jabaudon, D. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.07.009 · Cited by 25 · see citing works

Cross-Modal Reinstatement of Thalamocortical Plasticity Accelerates Ocular Dominance Plasticity in Adult Mice

Rodrı́guez, G., Chakraborty, D., Schrode, K. M., Saha, R., Uribe, I. R., Lauer, A. M., & Lee, H. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.08.072 · Cited by 25 · see citing works

A sensory-motor-sensory circuit underlies antinociception ignited by primary motor cortex in mice

Wang, F., Tian, Z., Ding, H., Yang, X. W., Wang, F., Ji, R.-X., Xu, L., Cao, Z.-X., Ma, S., Zhang, M., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.03.027 · Cited by 24 · see citing works

Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome.

Rais, M., Lovelace, J., Shuai, X. S., Woodard, W., Bishay, S., Estrada, L., Sharma, A. R., Nguy, A., Kulinich, A., Pirbhoy, P. S., et al. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105577 · Cited by 23 · see citing works

Functional GABAergic Synaptic Connection in Neonatal Mouse Barrel Cortex

Agmon, A., Hollrigel, G. S., & O’Dowd, D. K. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-15-04684.1996 · Cited by 91 · see citing works

A transient translaminar GABAergic interneuron circuit connects thalamocortical recipient layers in neonatal somatosensory cortex

Marques-Smith, A., Lyngholm, D., Kaufmann, A.-K., Stacey, J. A., Hoerder-Suabedissen, A., Becker, E. B. E., Wilson, M. C., Molnár, Z., & Butt, S. J. B. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.015 · Cited by 173 · see citing works

Postnatal development of GABAergic signalling in the rat lateral geniculate nucleus: presynaptic dendritic mechanisms

Perreault, M., Qin, Y., Heggelund, P., & Zhu, J. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.030643 · Cited by 30 · see citing works

Postnatal maturation of the GABAergic system in rat neocortex

Luhmann, H. J., & Prince, D. A. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.2.247 · Cited by 575 · see citing works

Principles of GABAergic signaling in developing cortical network dynamics

Kirmse, K., & Zhang, C. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110568 · Cited by 46 · see citing works