Cortical interneurons that specialize in disinhibitory control

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A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex

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How Inhibition Shapes Cortical Activity

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Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons

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A subpopulation of cortical VIP-expressing interneurons with highly dynamic spines

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Behavioral strategy shapes activation of the Vip-Sst disinhibitory circuit in visual cortex

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Prefrontal Regulation of Social Behavior and Related Deficits: Insights From Rodent Studies

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Alcohol reduces the activity of somatostatin interneurons in the mouse prefrontal cortex: A neural basis for its disinhibitory effect?

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Cognition and the single neuron: How cell types construct the dynamic computations of frontal cortex

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Untangling stability and gain modulation in cortical circuits with multiple interneuron classesPreprint

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Common rules underlying optogenetic and behavioral modulation of responses in multi-cell-type V1 circuitsPreprint

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Information Processing Across Behavioral States: Modes of Operation and Population Dynamics in Rodent Sensory Cortex

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Electrophysiological monitoring of inhibition in mammalian species, from rodents to humans

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Distinct Roles of Parvalbumin- and Somatostatin-Expressing Neurons in Flexible Representation of Task Variables in the Prefrontal Cortex

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Inhibitory plasticity in layer 1 – dynamic gatekeeper of neocortical associations

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Gene-expression correlates of the oscillatory signatures supporting human episodic memory encoding

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Differential Excitability of PV and SST Neurons Results in Distinct Functional Roles in Inhibition Stabilization of Up States

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Longitudinal functional imaging of VIP interneurons reveals sup-population specific effects of stroke that are rescued with chemogenetic therapy

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Cell-type-specific responses to associative learning in the primary motor cortex

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Predictive Mouse Ultrasonic Vocalization Sequences: Uncovering Behavioral Significance, Auditory Cortex Neuronal Preferences, and Social-Experience-Driven Plasticity

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Id2 GABAergic interneurons comprise a neglected fourth major group of cortical inhibitory cells

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Transition dynamics of generalized multiple epileptic seizures associated with thalamic reticular nucleus excitability: A computational study

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Optogenetic targeting of cardiac myocytes and non-myocytes: Tools, challenges and utility

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Critical Periods in Cortical Development

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The influence of locomotion on sensory processing and its underlying neuronal circuits

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Somatostatin receptors (SSTR1-5) on inhibitory interneurons in the barrel cortex

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Increasing endogenous activity of NMDARs on GABAergic neurons increases inhibition, alters sensory processing and prevents noise-induced tinnitus

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Roles and Transcriptional Responses of Inhibitory Neurons in Learning and Memory

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Progressive Circuit Changes during Learning and Disease

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Cortical circuits for integration of self-motion and visual-motion signals

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Inhibitory and disinhibitory VIP IN-mediated circuits in neocortexPreprint

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Fifty shades of inhibition

Maffei, A. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.12.003 · Cited by 23

Dissecting executive control circuits with neuron types

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Closed-Loop Control of Absence Seizures Inspired by Feedback Modulation of Basal Ganglia to the Corticothalamic Circuit

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Barrel cortex VIP/ChAT interneurons suppress sensory responses in vivo

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Open Source Tools for Temporally Controlled Rodent Behavior Suitable for Electrophysiology and Optogenetic Manipulations

Solari, N., Sviatkó, K., Laszlovszky, T., Hegedüs, P., & Hangya, B. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00018 · Cited by 23

Visual processing mode switching regulated by VIP cells

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GABAergic microcircuitry of fear memory encoding

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The local and long‐range input landscape of inhibitory neurons in mouse auditory cortex

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Neocortical somatostatin neuron diversity in cognition and learning

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Potential roles of cholinergic modulation in the neural coding of location and movement speed

Dannenberg, H., Hinman, J. R., & Hasselmo, M. E. (2016) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2016.09.002 · Cited by 22

α4β2 ∗ nicotinic receptors stimulate GABA release onto fast-spiking cells in layer V of mouse prefrontal (Fr2) cortex

Aracri, P., Meneghini, S., Coatti, A., Amadeo, A., & Becchetti, A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.10.045 · Cited by 22

Cell Type-Specific Expression of Corticotropin-Releasing Hormone-Binding Protein in GABAergic Interneurons in the Prefrontal Cortex

Ketchesin, K. D., Huang, N. S., & Seasholtz, A. F. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00090 · Cited by 22

Visual Processing by Calretinin Expressing Inhibitory Neurons in Mouse Primary Visual Cortex

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Plasticity of Persistent Activity and Its Constraints

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Complementary Inhibitory Weight Profiles Emerge from Plasticity and Allow Flexible Switching of Receptive Fields

Agnes, E. J., Luppi, A. I., & Vogels, T. P. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0276-20.2020 · Cited by 21

The Spectrum of Asynchronous Dynamics in Spiking Networks as a Model for the Diversity of Non-rhythmic Waking States in the Neocortex

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Identifying roles for peptidergic signaling in mice

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Contrast gain control occurs independently of both parvalbumin-positive interneuron activity and shunting inhibition in auditory cortex

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Region- and Layer-Specific Activation of the Higher Order Auditory Cortex Te2 after Remote Retrieval of Fear or Appetitive Memories

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Differential expression of synaptic and interneuron genes in the aging human prefrontal cortex

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Contribution of Interneuron Subtype-Specific GABAergic Signaling to Emergent Sensory Processing in Mouse Somatosensory Whisker Barrel Cortex

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Direction selectivity of inhibitory interneurons in mouse barrel cortex differs between interneuron subtypes

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Acute alcohol and chronic drinking bidirectionally regulate the excitability of prefrontal cortex vasoactive intestinal peptide interneurons

Thompson, S. M., Fabian, C. B., Ferranti, A. S., & Joffe, M. E. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109638 · Cited by 20

Hypersensitivity to Distractors in Fragile X Syndrome from Loss of Modulation of Cortical VIP Interneurons

Rahmatullah, N., Schmitt, L., Stefano, L. A. D., Post, S., Robledo, J., Chaudhari, G., Pedapati, E. V., Erickson, C. A., Portera‐Cailliau, C., & Goel, A. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0571-23.2023 · Cited by 20

GABAergic dysfunction in postmortem dorsolateral prefrontal cortex: implications for cognitive deficits in schizophrenia and affective disorders

Hughes, H., Brady, L. J., & Schoonover, K. E. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1440834 · Cited by 20

Specific inhibition and disinhibition in the higher-order structure of a cortical connectome

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Unbalanced Peptidergic Inhibition in Superficial Neocortex Underlies Spike and Wave Seizure Activity

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Using Multi-Compartment Ensemble Modeling As an Investigative Tool of Spatially Distributed Biophysical Balances: Application to Hippocampal Oriens-Lacunosum/Moleculare (O-LM) Cells

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Preferential inputs from cholecystokinin-positive neurons to the somatic compartment of parvalbumin-expressing neurons in the mouse primary somatosensory cortex

Hioki, H., Sohn, J., Nakamura, H., Okamoto, S., Hwang, J., Ishida, Y., Takahashi, M., & Kameda, H. (2018) · Brain Research · doi:10.1016/j.brainres.2018.05.029 · Cited by 20

Extended Temporal Association Memory by Modulations of Inhibitory Circuits

Haga, T., & Fukai, T. (2019) · Physical Review Letters · doi:10.1103/physrevlett.123.078101 · Cited by 20

Different coding strategy of sound information between GABAergic and glutamatergic neurons in the auditory midbrain

Ito, T. (2020) · The Journal of Physiology · doi:10.1113/jp279296 · Cited by 20

Learning-induced plasticity in the barrel cortex is disrupted by inhibition of layer 4 somatostatin-containing interneurons

Dobrzański, G., Łukomska, A., Zakrzewska, R., Posluszny, A., Kanigowski, D., Urban‐Ciećko, J., Liguz‐Lecznar, M., & Kossut, M. M. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2021.119146 · Cited by 20

Serotonergic regulation of bipolar cell survival in the developing cerebral cortex

Wong, F. K., Selten, M. M., Rosés-Novella, C., Sreenivasan, V., Pallas‐Bazarra, N., Serafeimidou‐Pouliou, E., Hanusz-Godoy, A., Oozeer, F., Edwards, R. H., & Marín, Ó. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111037 · Cited by 20

Targeting prefrontal cortex GABAergic microcircuits for the treatment of alcohol use disorder

Fish, K. N., & Joffe, M. E. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.936911 · Cited by 20

Bidirectional synaptic plasticity rapidly modifies hippocampal representationsPreprint

Milstein, A. D., Li, Y., Bittner, K. C., Grienberger, C., Soltész, I., Magee, J. C., & Romani, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.04.934182 · Cited by 20

Chronic Stress Induces Coordinated Cortical Microcircuit Cell–Type Transcriptomic Changes Consistent With Altered Information Processing

Newton, D. F., Oh, H., Shukla, R., Misquitta, K., Fee, C., Banasr, M., & Sibille, E. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.10.015 · Cited by 19

Hippocampal OLM interneurons regulate CA1 place cell plasticity and remapping

Udakis, M., Claydon, M. D. B., Zhu, H. W., Oakes, E. C., & Mellor, J. R. (2025) · Nature Communications · doi:10.1038/s41467-025-64859-0 · Cited by 19

Rate and oscillatory switching dynamics of a multilayer visual microcircuit model

Hahn, G., Kumar, A., SCHMIDT, H. J., Knösche, T. R., & Deco, G. (2022) · eLife · doi:10.7554/elife.77594 · Cited by 21

Prelimbic area to lateral hypothalamus circuit drives social aggression

Bai, F., Huang, L., Deng, J., Long, Z., Hao, X., Chen, P., Wu, G., Wen, H., Deng, Q., Bao, X., et al. (2023) · iScience · doi:10.1016/j.isci.2023.107718 · Cited by 19

Inhibitory modulation of optogenetically identified neuron subtypes in the rostral solitary nucleus

Chen, Z., Travers, S. P., & Travers, J. B. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00168.2016 · Cited by 19

Brief Stimulus Exposure Fully Remediates Temporal Processing Deficits Induced by Early Hearing Loss

Green, D. B., Mattingly, M. M., Ye, Y., Gay, J. D., & Rosen, M. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0916-17.2017 · Cited by 19

Characterizing the morphology of somatostatin‐expressing interneurons and their synaptic innervation pattern in the barrel cortex of the GFP‐expressing inhibitory neurons mouse

Zhou, X., Mansori, I., Fischer, T., Witte, M., & Staiger, J. F. (2020) · Journal of Comparative Neurology · doi:10.1002/cne.24756 · Cited by 18

Dendritic computation for abstract rule-based flexible decision-making

Zhang, Y., Liu, Y., Hu, Y., Zhenkun, 张. Z., Du, J., Cui, L., Liu, Q., Zhong, L., Xin, Y., Chai, R., et al. (2026) · Science · doi:10.1126/science.adz5323 · Cited by 18

Learning-related congruent and incongruent changes of excitation and inhibition in distinct cortical areas

Esmaeili, V., Oryshchuk, A., Asri, R., Tamura, K., Foustoukos, G., Liu, Y., Guiet, R., Crochet, S., & Petersen, C. C. H. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001667 · Cited by 18

Multimodal gradients of basal forebrain connectivity across the neocortex

Chakraborty, S., Haast, R. A. M., Onuska, K. M., Kanel, P., Prado, M. A. M., Prado, V. F., KHAN, A. R., & Schmitz, T. W. (2024) · Nature Communications · doi:10.1038/s41467-024-53148-x · Cited by 18

Mediodorsal thalamus regulates task uncertainty to enable cognitive flexibility

Zhang, X., Mukherjee, A., Halassa, M. M., & Chen, Z. S. (2025) · Nature Communications · doi:10.1038/s41467-025-58011-1 · Cited by 19

Cell-specific modulation of plasticity and cortical state by cholinergic inputs to the visual cortex

杉原, 弘., Chen, N., & Sur, M. (2016) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2016.11.004 · Cited by 18

Amplitude modulations of cortical sensory responses in pulsatile evidence accumulation

Koay, S. A., Thiberge, S. Y., Brody, C. D., & Tank, D. W. (2020) · eLife · doi:10.7554/elife.60628 · Cited by 18

Control and analysis of epilepsy waveforms in a disinhibition model of cortex network

Shen, Z., Deng, Z., Du, L., Zhang, H., Yan, L., & Xiao, P. (2021) · Nonlinear Dynamics · doi:10.1007/s11071-020-06131-2 · Cited by 18

Spinal GABAergic neurons are under feed-forward inhibitory control driven by A δ and C fibers in Gad2 td-Tomato mice

Liu, P., Zhang, X., He, X., Jiang, Z., Wang, Q., & Lü, Y. (2021) · Molecular Pain · doi:10.1177/1744806921992620 · Cited by 18

Neurophysiological basis of the N400 deflection, from Mismatch Negativity to Semantic Prediction Potentials and late positive components

Almeida, V. N. (2021) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2021.06.001 · Cited by 18

Cholinergic modulation of sensory processing in awake mouse cortex

Jiménez-Martín, J., Потапов, Д. О., Potapov, K., Knöpfel, T., & Empson, R. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-96696-8 · Cited by 18

GABA B receptor-mediated, layer-specific synaptic plasticity reorganizes gamma-frequency neocortical response to stimulation

Ainsworth, M., Lee, S., Kaiser, M., Simonotto, J. D., Kopell, N., & Whittington, M. A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605243113 · Cited by 18

Orexin facilitates GABAergic IPSCs via postsynaptic OX1 receptors coupling to the intracellular PKC signalling cascade in the rat cerebral cortex

Usui, M., Kaneko, K., Oi, Y., & Kobayashi, M. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.02.012 · Cited by 18

Amygdala circuit transitions supporting developmentally-appropriate social behavior

Ferrara, N. C., & Opendak, M. M. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107762 · Cited by 17

Advances in the understanding of the pathophysiology of schizophrenia and bipolar disorder through induced pluripotent stem cell models

Perrottelli, A., Marzocchi, F. F., Caporusso, E., Giordano, G. M., Giuliani, L., Melillo, A., Pezzella, P., Bucci, P., Mucci, A., & Galderisi, S. (2024) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.230112 · Cited by 17

Transition to seizure in focal epilepsy: From SEEG phenomenology to underlying mechanisms

Kayabas, M. A., Ersöz, E. K., Yochum, M., Bartoloméi, F., Benquet, P., & Wendling, F. (2024) · Epilepsia · doi:10.1111/epi.18173 · Cited by 17

Spike‐timing dependent inhibitory plasticity to learn a selective gating of backpropagating action potentials

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A Reward-Based Behavioral Platform to Measure Neural Activity during Head-Fixed Behavior

Micallef, A. H., Takahashi, N., Larkum, M. E., & Palmer, L. M. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00156 · Cited by 17

5-HTR2A and 5-HTR3A but not 5-HTR1A antagonism impairs the cross-modal reactivation of deprived visual cortex in adulthood

Lombaert, N., Hennes, M., Gilissen, S. R. J., Schevenels, G., Aerts, L., Vanlaer, R., Geenen, L., Eeckhaut, A. V., Smolders, I. J., Nys, J., et al. (2018) · Molecular Brain · doi:10.1186/s13041-018-0404-5 · Cited by 17

Cortical VIP+/ChAT+ interneurons: From genetics to function

Dudai, A., Yayon, N., Soreq, H., & London, M. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15263 · Cited by 18

Corticofugal VIP Gabaergic Projection Neurons in the Mouse Auditory and Motor Cortex

Bertero, A., Garcia, C., & Apicella, A. J. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.714780 · Cited by 17

Transition dynamics and optogenetic controls of generalized periodic epileptiform discharges

Shen, Z., Zhang, H., Cao, Z., Yan, L., Zhao, Y., Du, L., & Deng, Z. (2022) · Neural Networks · doi:10.1016/j.neunet.2022.01.022 · Cited by 17

Semantic processing and neurobiology in Alzheimer's disease and Mild Cognitive Impairment

Almeida, V. N., & Radanovic, M. (2022) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2022.108337 · Cited by 17

Memory formation and retrieval of neuronal silencing in the auditory cortex

Nomura, H., Hara, K., Abe, R., HitoraーImamura, N., Nakayama, R., Sasaki, T., Matsuki, N., & Ikegaya, Y. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1500869112 · Cited by 17

On how correlations between excitatory and inhibitory synaptic inputs maximize the information rate of neuronal firing

Puzerey, P. A., & Galán, R. F. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00059 · Cited by 17

Feedforward motor information enhances somatosensory responses and sharpens angular tuning of rat S1 barrel cortex neurons

Khateb, M., Schiller, J., & Schiller, Y. (2017) · eLife · doi:10.7554/elife.21843 · Cited by 17

Excitatory versus inhibitory feedback in Bayesian formulations of scene construction

Abadi, A. K., Yahya, K., Amini, M., Friston, K. J., & Heinke, D. G. (2019) · Journal of The Royal Society Interface · doi:10.1098/rsif.2018.0344 · Cited by 17

Neural Correlates of Cognition in Primary Visual versus Neighboring Posterior Cortices during Visual Evidence-Accumulation-based NavigationPreprint

Koay, S. A., Thiberge, S. Y., Brody, C. D., & Tank, D. W. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/568766 · Cited by 17

Increased pyramidal and VIP neuronal excitability in rat primary auditory cortex directly correlates with tinnitus behaviour

Ghimire, M., Cai, R., Ling, L. L., Brownell, K. A., Hackett, T. A., Llano, D. A., & Caspary, D. M. (2023) · The Journal of Physiology · doi:10.1113/jp284675 · Cited by 16

Psychiatric risk gene Transcription Factor 4 (TCF4) regulates the density and connectivity of distinct inhibitory interneuron subtypes

Chen, H.-Y., Phan, B. N., Shim, G., Hamersky, G. R., Sadowski, N., O’Donnell, T. S., Sripathy, S. R., Bohlen, J. F., Pfenning, A. R., & Maher, B. J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02248-z · Cited by 17

Fear extinction rescuing effects of dopamine and L-DOPA in the ventromedial prefrontal cortex

Sartori, S. B., Keil, T. M. V., Kummer, K. K., Murphy, C. P., Gunduz‐Cinar, O., Kress, M., Ebner, K., Holmes, A., & Singewald, N. (2024) · Translational Psychiatry · doi:10.1038/s41398-023-02708-8 · Cited by 16

A connectome manipulation framework for the systematic and reproducible study of structure–function relationships through simulations

Pokorny, C., Awile, O., Isbister, J. B., Kurban, K., Wolf, M., & Reimann, M. (2024) · Network Neuroscience · doi:10.1162/netn_a_00429 · Cited by 16

Cortical interneurons that specialize in disinhibitory control. Nature

Pi, H.-J., Hangya, B., Kvitsiani, D., S, J. I., Huang, Z. J., & Kepecs, Á. (2013)

Inhibitory neurons: VIP neurons expect rewards

Zou, J., & Hires, S. A. (2023) · Current Biology · doi:10.1016/j.cub.2023.07.059 · Cited by 2

Common Principles in Functional Organization of VIP/Calretinin Cell-Driven Disinhibitory Circuits Across Cortical Areas

Guet-McCreight, A., Skinner, F. K., & Topolnik, L. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00032 · Cited by 66

Cortical disinhibitory circuits: cell types, connectivity and function

Kullander, K., & Topolnik, L. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.04.009 · Cited by 86

Cortex-wide response mode of VIP-expressing inhibitory neurons by reward and punishment

Szadai, Z., Pi, H.-J., Chevy, Q., Ócsai, K., Albeanu, D. F., Chiovini, B., Szalay, G., Katona, G., Kepecs, Á., & Rózsa, B. J. (2022) · eLife · doi:10.7554/elife.78815 · Cited by 47