Dense, Unspecific Connectivity of Neocortical Parvalbumin-Positive Interneurons: A Canonical Microcircuit for Inhibition?

CircStat : A MATLAB Toolbox for Circular Statistics

Berens, P. (2009) · Journal of Statistical Software · doi:10.18637/jss.v031.i10 · Cited by 3,099

NEURONAL CIRCUITS OF THE NEOCORTEX

Douglas, R. J., & Martin, K. A. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144152 · Cited by 1,886

Serial Block-Face Scanning Electron Microscopy to Reconstruct Three-Dimensional Tissue Nanostructure

Denk, W., & Horstmann, H. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020329 · Cited by 1,644

Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex

The Petilla Interneuron Nomenclature Group (PING) (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2402 · Cited by 1,491

Interneuron Migration from Basal Forebrain to Neocortex: Dependence on Dlx Genes

Anderson, S. A., Eisenstat, D. D., Shi, L., & Rubenstein, J. L. R. (1997) · Science · doi:10.1126/science.278.5337.474 · Cited by 1,462

Monosynaptic Restriction of Transsynaptic Tracing from Single, Genetically Targeted Neurons

Wickersham, I. R., Lyon, D. C., Barnard, R. J. O., Mori, T., Finke, S., Conzelmann, K., Young, J. A. T., & Callaway, E. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.033 · Cited by 1,176

Differential signaling via the same axon of neocortical pyramidal neurons

Markram, H., Wang, Y., & Tsodyks, M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.9.5323 · Cited by 1,102

Highly selective receptive fields in mouse visual cortex

Niell, C. M., & Stryker, M. P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.0623-08.2008 · Cited by 1,081

Network anatomy and in vivo physiology of visual cortical neurons

Bock, D. D., Lee, W.-C. A., Kerlin, A., Andermann, M. L., Hood, G., Wetzel, A. W., Yurgenson, S., Soucy, E. R., Kim, H. S., & Reid, R. C. (2011) · Nature · doi:10.1038/nature09802 · Cited by 867

Diverse sources of hippocampal unitary inhibitory postsynaptic potentials and the number of synaptic release sites

Buhl, E. H., Halasy, K., & Somogyi, P. (1994) · Nature · doi:10.1038/368823a0 · Cited by 728

Estrogens and the cognitive symptoms of schizophrenia: Possible neuroprotective mechanisms

McGregor, C., Riordan, A. J., & Thornton, J. E. (2017) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.06.003 · Cited by 90

Optogenetic Activation of an Inhibitory Network Enhances Feedforward Functional Connectivity in Auditory Cortex

Hamilton, L. S., Sohl‐Dickstein, J., Huth, A. G., Carels, V. M., Deisseroth, K. A., & Bao, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.017 · Cited by 85

Molecular Mechanisms of L1 and NCAM Adhesion Molecules in Synaptic Pruning, Plasticity, and Stabilization

Duncan, B. W., Murphy, K. E., & Maness, P. F. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.625340 · Cited by 85

Parvalbumin- and vasoactive intestinal polypeptide-expressing neocortical interneurons impose differential inhibition on Martinotti cells

Walker, F., Möck, M., Feyerabend, M., Guy, J., Wagener, R. J., Schubert, D., Staiger, J. F., & Witte, M. (2016) · Nature Communications · doi:10.1038/ncomms13664 · Cited by 92

Rapid Disinhibition by Adjustment of PV Intrinsic Excitability during Whisker Map Plasticity in Mouse S1

Gainey, M. A., Aman, J. W., & Feldman, D. E. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3628-17.2018 · Cited by 74

Primary visual cortex shows laminar‐specific and balanced circuit organization of excitatory and inhibitory synaptic connectivity

Xu, X., Olivas, N. D., Ikrar, T., Peng, T., Holmes, T. C., Nie, Q., & Shi, Y. (2016) · The Journal of Physiology · doi:10.1113/jp271891 · Cited by 83

Production and organization of neocortical interneurons

Sultan, K. T., Brown, K. N., & Shi, S.-H. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00221 · Cited by 83

Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome

Lovelace, J. W., Rais, M., Palacios, A. R., Shuai, X. S., Bishay, S., Popa, O., Pirbhoy, P. S., Binder, D. K., Nelson, D. L., Ethell, I. M., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz141 · Cited by 82

Coming of age in the frontal cortex: The role of puberty in cortical maturation

Delevich, K. M., Klinger, M., Okada, N. J., & Wilbrecht, L. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.04.021 · Cited by 91

Laminarly Orthogonal Excitation of Fast-Spiking and Low-Threshold-Spiking Interneurons in Mouse Motor Cortex

Apicella, A. J., Wickersham, I. R., Seung, H. S., & Shepherd, G. M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0011-12.2012 · Cited by 86

Functional effects of distinct innervation styles of pyramidal cells by fast spiking cortical interneurons

Kubota, Y., Kondo, S., Nomura, M., Hatada, S., Yamaguchi, N., Mohamed, A. A., Karube, F., Lübke, J. H. R., & Kawaguchi, Y. (2015) · eLife · doi:10.7554/elife.07919 · Cited by 83

Differential tuning of excitation and inhibition shapes direction selectivity in ferret visual cortex

Wilson, D. E., Scholl, B., & Fitzpatrick, D. (2018) · Nature · doi:10.1038/s41586-018-0354-1 · Cited by 82

Functional specificity of recurrent inhibition in visual cortex

Znamenskiy, P., Kim, M.-H., Muir, D. R., Iacaruso, M. F., Hofer, S. B., & Mrsic‐Flogel, T. D. (2024) · Neuron · doi:10.1016/j.neuron.2023.12.013 · Cited by 152

Synaptic Organization of Perisomatic GABAergic Inputs onto the Principal Cells of the Mouse Basolateral Amygdala

Vereczki, V., Veres, J. M., Müller, K., Nagy, G. A., Rácz, B., Barsy, B., & Hájos, N. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00020 · Cited by 79

Dual Function of NRP1 in Axon Guidance and Subcellular Target Recognition in Cerebellum.

Telley, L., Cadilhac, C., Cioni, J.-M., Saywell, V., Jahannault-Talignani, C., Huettl, R., Sarrailh-Faivre, C., Dayer, A., Huber, A. B., & Ango, F. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.015 · Cited by 69

The Synaptic Organization of Layer 6 Circuits Reveals Inhibition as a Major Output of a Neocortical Sublamina

Frandolig, J. E., Matney, C. J., Lee, K., Kim, J., Chevée, M., Kim, S.-J., Bickert, A. A., & Brown, S. P. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.048 · Cited by 78

Selective Functional Interactions between Excitatory and Inhibitory Cortical Neurons and Differential Contribution to Persistent Activity of the Slow Oscillation

Tahvildari, B., Wölfel, M., Duque, A., & McCormick, D. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1181-12.2012 · Cited by 77

Functional Diversity of Subicular Principal Cells during Hippocampal Ripples

Böhm, C., Peng, Y., Maier, N., Winterer, J., Poulet, J. F. A., Geiger, J. R. P., & Schmitz, D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5034-14.2015 · Cited by 78

Functional diversity of supragranular GABAergic neurons in the barrel cortex

Gentet, L. J. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00052 · Cited by 83

Callosal Projections Drive Neuronal-Specific Responses in the Mouse Auditory Cortex

Rock, C., & Apicella, A. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5049-14.2015 · Cited by 76

Axo-dendritic overlap and laminar projection can explain interneuron connectivity to pyramidal cells

Packer, A. M., McConnell, D. J., Fino, E., & Yuste, R. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs210 · Cited by 73

GABAergic Neurons in Ferret Visual Cortex Participate in Functionally Specific Networks

Wilson, D. E., Smith, G. B., Jacob, A., Walker, T., Dimidschstein, J., Fishell, G., & Fitzpatrick, D. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.035 · Cited by 72

Developmentally regulated impairment of parvalbumin interneuron synaptic transmission in an experimental model of Dravet syndrome

Kaneko, K., Currin, C. B., Goff, K. M., Wengert, E. R., Somarowthu, A., Vogels, T. P., & Goldberg, E. M. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110580 · Cited by 72

Decorrelating Action of Inhibition in Neocortical Networks

Sippy, T., & Yuste, R. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4579-12.2013 · Cited by 68

Functional selectivity and specific connectivity of inhibitory neurons in primary visual cortexPreprint

Znamenskiy, P., Kim, M.-H., Muir, D. R., Iacaruso, M. F., Hofer, S. B., & Mrsic‐Flogel, T. D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/294835 · Cited by 72

Learning prediction error neurons in a canonical interneuron circuit

Hertäg, L., & Sprekeler, H. (2020) · eLife · doi:10.7554/elife.57541 · Cited by 72

Amplifying the redistribution of somato-dendritic inhibition by the interplay of three interneuron types

Hertäg, L., & Sprekeler, H. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006999 · Cited by 75

Cell-type-specific inhibitory circuitry from a connectomic census of mouse visual cortexPreprint

Schneider-Mizell, C. M., Bodor, Á. L., Brittain, D., Buchanan, J., Bumbarger, D. J., Elabbady, L., Gamlin, C. R., Kapner, D., Kinn, S., Mahalingam, G., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.23.525290 · Cited by 70

Corticocortical Systems Underlying High-Order Motor Control

Battaglia‐Mayer, A., & Caminiti, R. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2094-18.2019 · Cited by 75

Large-scale functional network overlap is a general property of brain functional organization: Reconciling inconsistent fMRI findings from general-linear-model-based analyses

Xu, J., Potenza, M. N., Calhoun, V. D., Zhang, R., Yip, S. W., Wall, J. T., Pearlson, G. D., Worhunsky, P. D., Garrison, K. A., & Moran, J. M. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.035 · Cited by 68

Enhanced Central Neural Gain Compensates Acoustic Trauma-induced Cochlear Impairment, but Unlikely Correlates with Tinnitus and Hyperacusis

Möhrle, D., Hofmeier, B., Amend, M., Wolpert, S., Ni, K., Bing, D., Klose, U., Pichler, B. J., Knipper, M., & Rüttiger, L. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.12.038 · Cited by 70

Response Selectivity Is Correlated to Dendritic Structure in Parvalbumin-Expressing Inhibitory Neurons in Visual Cortex

Runyan, C. A., & Sur, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2196-12.2013 · Cited by 67

Cortical Circuits of Callosal GABAergic Neurons

Rock, C., Zurita, H., Lebby, S., Wilson, C. J., & Apicella, A. J. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx025 · Cited by 73

A recurrent circuit implements normalization, simulating the dynamics of V1 activity

Heeger, D. J., & Zemlianova, K. O. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005417117 · Cited by 72

Myelination synchronizes cortical oscillations by consolidating parvalbumin-mediated phasic inhibition

Dubey, M., Pascual-Garcia, M., Helmes, K., Wever, D. D., Hamada, M. S., Kushner, S. A., & Kole, M. H. P. (2022) · eLife · doi:10.7554/elife.73827 · Cited by 71

Path Laplacian matrices: Introduction and application to the analysis of consensus in networks

Estrada, E. (2011) · Linear Algebra and its Applications · doi:10.1016/j.laa.2011.11.032 · Cited by 61

Lineage-dependent circuit assembly in the neocortex

Gao, P., Sultan, K. T., Zhang, X., & Shi, S. (2013) · Development · doi:10.1242/dev.087668 · Cited by 68

Mapping Brain-Wide Afferent Inputs of Parvalbumin-Expressing GABAergic Neurons in Barrel Cortex Reveals Local and Long-Range Circuit Motifs

Hafner, G., Witte, M., Guy, J., Subhashini, N., Fenno, L. E., Ramakrishnan, C., Kim, Y. S., Deisseroth, K. A., Callaway, E. M., Oberhuber, M., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.064 · Cited by 63

New dimensions of interneuronal specialization unmasked by principal cell heterogeneity

Krook-Magnuson, E., Varga, C., Lee, S.-H., & Soltesz, I. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.10.005 · Cited by 63

The excitatory-inhibitory balance as a target for the development of novel drugs to treat schizophrenia

Uliana, D. L., Lisboa, J. R., Gomes, F. V., & Grace, A. A. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116298 · Cited by 71

GABAergic synapses: their plasticity and role in sensory cortex - See more at: http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00091/abstract#sthash.l5jGe6MC.dpuf

Griffen, T. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00091 · Cited by 64

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 62

Operant Conditioning of Synaptic and Spiking Activity Patterns in Single Hippocampal Neurons

Ishikawa, D., Matsumoto, N., Sakaguchi, T., Matsuki, N., & Ikegaya, Y. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5298-13.2014 · Cited by 55

Learning excitatory-inhibitory neuronal assemblies in recurrent networks

Mackwood, O., Naumann, L., & Sprekeler, H. (2021) · eLife · doi:10.7554/elife.59715 · Cited by 64

Parvalbumin-positive interneurons regulate cortical sensory plasticity in adulthood and development through shared mechanisms

Rupert, D. D., & Shea, S. D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.886629 · Cited by 58

Prediction-error neurons in circuits with multiple neuron types: Formation, refinement, and functional implications

Hertäg, L., & Clopath, C. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2115699119 · Cited by 57

Theory of neuronal perturbome in cortical networks

Sadeh, S., & Clopath, C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2004568117 · Cited by 53

Quantitative Relationship Between Cerebrovascular Network and Neuronal Cell Types in Mice

Wu, Y.-T., Bennett, H. C., Chon, U., Vanselow, D. J., Zhang, Q., Muñoz-Castañeda, R., Cheng, K. C., Osten, P., Drew, P. J., & Kim, Y. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110978 · Cited by 61

Diurnal changes in perineuronal nets and parvalbumin neurons in the rat medial prefrontal cortex

Harkness, J. H., Gonzalez, A. E., Bushana, P. N., Jorgensen, E. T., Hegarty, D. M., Nardo, A. A. D., Prochiantz, A., Wisor, J. P., Aicher, S. A., Brown, T. E., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02229-4 · Cited by 55

Mapping pathologic circuitry in schizophrenia

Glausier, J. R., & Lewis, D. A. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63639-3.00025-6 · Cited by 53

Opposed hemodynamic responses following increased excitation and parvalbumin-based inhibition

Lee, J., Stile, C. L., Bice, A. R., Rosenthal, Z. P., Yan, P., Snyder, A. Z., Lee, J., & Bauer, A. Q. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20930831 · Cited by 51

Distinct Spatiotemporal Response Properties of Excitatory Versus Inhibitory Neurons in the Mouse Auditory Cortex

Maor, I., Shalev, A., & Mizrahi, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw266 · Cited by 58

Altered Markers of Cortical γ-Aminobutyric Acid Neuronal Activity in Schizophrenia

Kimoto, S., Zaki, M. M., Bazmi, H. H., & Lewis, D. A. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.0533 · Cited by 53

Local Connectivity and Synaptic Dynamics in Mouse and Human NeocortexPreprint

Campagnola, L., Seeman, S. C., Chartrand, T., Kim, L., Hoggarth, A., Gamlin, C. R., Ito, S., Trinh, J., Davoudian, P. A., Radaelli, C., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.31.437553 · Cited by 53

Generation of diverse cortical inhibitory interneurons

Sultan, K. T., & Shi, S. (2017) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.306 · Cited by 57

Connectivity concepts in neuronal network modeling

Senk, J., Kriener, B., Djurfeldt, M., Voges, N., Jiang, H.-J., Schüttler, L., Gramelsberger, G., Diesmann, M., Pleßer, H. E., & van Albada, S. J. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010086 · Cited by 52

Excitatory-inhibitory balance modulates the formation and dynamics of neuronal assemblies in cortical networks

Sadeh, S., & Clopath, C. (2021) · Science Advances · doi:10.1126/sciadv.abg8411 · Cited by 57

Dynamical models of cortical circuits

Wolf, F., Engelken, R., Touzel, M. P., Weidinger, J. D. F., & Neef, A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.017 · Cited by 56

Mild Traumatic Brain Injury Induces Structural and Functional Disconnection of Local Neocortical Inhibitory Networks via Parvalbumin Interneuron Diffuse Axonal Injury

Vascak, M., Jin, X., Jacobs, K. M., & Povlishock, J. T. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx058 · Cited by 50

Structured inhibitory activity dynamics in new virtual environments

Arriaga, M. A., & Han, E. B. (2019) · eLife · doi:10.7554/elife.47611 · Cited by 49

Neural mechanisms of auditory categorization: from across brain areas to within local microcircuits

Tsunada, J., & Cohen, Y. E. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00161 · Cited by 47

Strength and duration of perisomatic GABAergic inhibition depend on distance between synaptically connected cells

Strüber, M., Jonas, P., & Bartos, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412996112 · Cited by 43

Parvalbumin-Positive Neuron Loss and Amyloid-β Deposits in the Frontal Cortex of Alzheimer’s Disease-Related Mice

Ali, F., Baringer, S. L., Neal, A., Choi, E. Y., & Kwan, A. C. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181190 · Cited by 43

Hyperexcitable Neurons Enable Precise and Persistent Information Encoding in the Superficial Retrosplenial Cortex

Brennan, E. K. W., Sudhakar, S., Jedrasiak‐Cape, I., John, T. T., & Ahmed, O. J. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.093 · Cited by 46

Segregated Excitatory–Inhibitory Recurrent Subnetworks in Layer 5 of the Rat Frontal Cortex

Morishima, M., Kobayashi, K., Kato, S., Kobayashi, K., & Kawaguchi, Y. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx276 · Cited by 43

Primate Neuronal Connections are Sparse as Compared to Mouse

Wildenberg, G. A., Rosen, M. C., Lundell, J., Paukner, D., Freedman, D. J., & Kasthuri, N. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109709 · Cited by 49

A Computer-assisted Multi-electrode Patch-clamp System

Perin, R., & Markram, H. (2013) · Journal of Visualized Experiments · doi:10.3791/50630 · Cited by 42

Routes to, from and within the subiculum

Böhm, C., Peng, Y., Geiger, J. R. P., & Schmitz, D. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2848-4 · Cited by 44

Fast and reversible neural inactivation in macaque cortex by optogenetic stimulation of GABAergic neurons

De, A., El-Shamayleh, Y., & Horwitz, G. D. (2020) · eLife · doi:10.7554/elife.52658 · Cited by 45

Parvalbumin - Positive Neurons in the Neocortex: A Review

Druga, R., Salaj, M., & Al‐Redouan, A. (2023) · Physiological Research · doi:10.33549/physiolres.935005 · Cited by 47

Target‐selectivity of parvalbumin‐positive interneurons in layer II of medial entorhinal cortex in normal and epileptic animals

Armstrong, C., Wang, J. J., Lee, S. Y., Broderick, J., Bezaire, M. J., Lee, S.-H., & Soltész, I. (2015) · Hippocampus · doi:10.1002/hipo.22559 · Cited by 43

Intersectional monosynaptic tracing for dissecting subtype-specific organization of GABAergic interneuron inputs

Yetman, M. J., Washburn, E. K., Hyun, J. H., Osakada, F., Hayano, Y., Zeng, H., Callaway, E. M., Kwon, H., & Taniguchi, H. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0322-y · Cited by 39

Cholinergic modulation of neuronal excitability and recurrent excitation‐inhibition in prefrontal cortex circuits: implications for gamma oscillations

Pafundo, D. E., Miyamae, T., Lewis, D. A., & González‐Burgos, G. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.253823 · Cited by 43

Spatial distribution of neurons innervated by chandelier cells

Blázquez‐Llorca, L., Woodruff, A. R., Inan, M., Anderson, S. A., Yuste, R., DeFelipe, J., & Merchán-Pérez, Á. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0828-3 · Cited by 36

Anterior Thalamic Excitation and Feedforward Inhibition of Presubicular Neurons Projecting to Medial Entorhinal Cortex

Nassar, M., Simonnet, J., Huang, L.-W., Mathon, B., Cohen, I., Bendels, M. H. K., Beraneck, M., Miles, R., & Fricker, D. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0014-18.2018 · Cited by 36

Emergence of Functional Specificity in Balanced Networks with Synaptic Plasticity

Sadeh, S., Clopath, C., & Rotter, S. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004307 · Cited by 35

Mild Traumatic Brain Injury Evokes Pyramidal Neuron Axon Initial Segment Plasticity and Diffuse Presynaptic Inhibitory Terminal Loss

Vascak, M., Sun, J., Baer, M. L., Jacobs, K. M., & Povlishock, J. T. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00157 · Cited by 39

Chandelier cell anatomy and function reveal a variably distributed but common signalPreprint

Schneider-Mizell, C. M., Bodor, Á. L., Collman, F., Brittain, D., Bleckert, A., Dorkenwald, S., Turner, N. L., Macrina, T., Lee, K., Lu, R., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.31.018952 · Cited by 37

Large-Scale Simulation of a Layered Cortical Sheet of Spiking Network Model Using a Tile Partitioning Method

Igarashi, J., YAMAURA, H., & Yamazaki, T. (2019) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2019.00071 · Cited by 36

Choice selective inhibition drives stability and competition in decision circuits

Roach, J. P., Churchland, A. K., & Engel, T. A. (2023) · Nature Communications · doi:10.1038/s41467-023-35822-8 · Cited by 37

Excitatory-Inhibitory Homeostasis and Diaschisis: Tying the Local and Global Scales in the Post-stroke Cortex

dos Santos, F. P., & Verschure, P. F. M. J. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.806544 · Cited by 35

Input-specific maturation of synaptic dynamics of parvalbumin interneurons in primary visual cortex

Lu, J., Tucciarone, J., Lin, Y., & Huang, Z. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400694111 · Cited by 35

Computation of the electroencephalogram (EEG) from network models of point neurons

Martínez‐Cañada, P., Ness, T. V., Einevoll, G. T., Fellin, T., & Panzeri, S. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008893 · Cited by 39

Dopamine Differentially Regulates Response Dynamics of Prefrontal Cortical Principal Neurons and Interneurons to Optogenetic Stimulation of Inputs from Ventral Tegmental Area

Zhong, P., Qin, L., & Yan, Z. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa027 · Cited by 34

Age- and sex-specific effects of stress on parvalbumin interneurons in preclinical models: Relevance to sex differences in clinical neuropsychiatric and neurodevelopmental disorders

Woodward, E. M., & Coutellier, L. D. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.031 · Cited by 37

Regulation of the E/I-balance by the neural matrisome

Mueller-Buehl, C., Wegrzyn, D., Bauch, J., & Faissner, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1102334 · Cited by 35

Thalamic Input to Orbitofrontal Cortex Drives Brain-wide, Frequency-Dependent Inhibition Mediated by GABA and Zona Incerta

Weitz, A. J., Lee, H. J., Choy, M., & Lee, J. H. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.023 · Cited by 33

Regulation of Synapse Development byVgatDeletion from ErbB4-Positive Interneurons

Lin, T. W., Tan, Z., Barik, A., Yin, D., Brudvik, E., Wang, H., Xiong, W., & Mei, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0669-17.2018 · Cited by 37

Conduction Velocity Along the Local Axons of Parvalbumin Interneurons Correlates With the Degree of Axonal Myelination

Micheva, K. D., Király, M., Perez, M. M., & Madison, D. V. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab018 · Cited by 33

Biophysical Kv3 channel alterations dampen excitability of cortical PV interneurons and contribute to network hyperexcitability in early Alzheimer’s

Oláh, V. J., Goettemoeller, A. M., Rayaprolu, S., Dammer, E. B., Seyfried, N. T., Rangaraju, S., Dimidschstein, J., & Rowan, M. J. (2022) · eLife · doi:10.7554/elife.75316 · Cited by 34

Functional interactions among neurons within single columns of macaque V1

Trepka, E. B., Zhu, S., Xia, R., Chen, X., & Moore, T. (2022) · eLife · doi:10.7554/elife.79322 · Cited by 35

Studies of cortical connectivity using optical circuit mapping methods

Anastasiades, P. G., Marques–Smith, A., & Butt, S. J. B. (2017) · The Journal of Physiology · doi:10.1113/jp273463 · Cited by 32

Interneuron NMDA Receptor Ablation Induces Hippocampus-Prefrontal Cortex Functional Hypoconnectivity after Adolescence in a Mouse Model of Schizophrenia

Alvarez, R. J., Pafundo, D. E., Zold, C. L., & Belforte, J. E. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1897-19.2020 · Cited by 31

Auditory Cortical Local Subnetworks Are Characterized by Sharply Synchronous Activity

Atencio, C. A., & Schreiner, C. E. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2014-13.2013 · Cited by 31

Bayesian Inference and Online Experimental Design for Mapping Neural Microcircuits

Shababo, B., Paige, B., Pakman, A., & Paninski, L. (2013) · Cited by 29

Feedback Inhibition Shapes Emergent Computational Properties of Cortical Microcircuit Motifs

Jonke, Z., Legenstein, R. A., Habenschuss, S., & Maass, W. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2078-16.2017 · Cited by 29

Classification of neocortical interneurons using affinity propagation

Santana, R., McGarry, L. M., Bielza, C., Larrañaga, P., & Yuste, R. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00185 · Cited by 30

The influence of visual cortex on perception is modulated by behavioural statePreprint

Russell, L. E., Yang, Z., Tan, P. L., Fişek, M., Packer, A. M., Dalgleish, H. W. P., Chettih, S. N., Harvey, C. D., & Häusser, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/706010 · Cited by 30

Physiological features of parvalbumin-expressing GABAergic interneurons contributing to high-frequency oscillations in the cerebral cortex

Milicevic, K. D., Barbeau, B. L., Lovic, D. D., Patel, A. A., Ivanova, V. O., & Antic, S. D. (2023) · Current Research in Neurobiology · doi:10.1016/j.crneur.2023.100121 · Cited by 35

Parvalbumin-expressing interneurons can act solo while somatostatin-expressing interneurons act in chorus in most cases on cortical pyramidal cells

Safari, M.-S., Mirnajafi‐Zadeh, J., Hioki, H., & Tsumoto, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-12958-4 · Cited by 29

Parvalbumin - Positive Neurons in the Neocortex: A Review

Druga, R., Salaj, M., & Al‐Redouan, A. (2023) · Physiological Research · doi:10.33549/physiolres.935005 · Cited by 47

Axo-dendritic overlap and laminar projection can explain interneuron connectivity to pyramidal cells

Packer, A. M., McConnell, D. J., Fino, E., & Yuste, R. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs210 · Cited by 73

Local Connections of Pyramidal Neurons to Parvalbumin-Producing Interneurons in Motor-Associated Cortical Areas of Mice

Kuramoto, E., Tanaka, Y. R., Hioki, H., Goto, T., & Kaneko, T. (2021) · eNeuro · doi:10.1523/eneuro.0567-20.2021 · Cited by 9

Dense Inhibitory Connectivity in Neocortex

Fino, E., & Yuste, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.025 · Cited by 532

A blanket of inhibition: functional inferences from dense inhibitory connectivity

Karnani, M. M., Agetsuma, M., & Yuste, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.015 · Cited by 188