Inhibitory Interneurons Regulate Temporal Precision and Correlations in Cortical Circuits

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Analysis of spiking synchrony in visual cortex reveals distinct types of top-down modulation signals for spatial and object-based attention

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Suppression of Low-Frequency Gamma Oscillations by Activation of 40-Hz Oscillation

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Estrogens rapidly shape synaptic and intrinsic properties to regulate the temporal precision of songbird auditory neurons

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Cerebral Cortex Generated from Pluripotent Stem Cells to Model Corticogenesis and Rebuild Cortical Circuits: In Vitro Veritas?

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Neocortical inhibitory interneuron subtypes are differentially attuned to synchrony- and rate-coded information

Prince, L. Y., Tran, M. M., Grey, D., Saad, L., Chasiotis, H., Kwag, J., Kohl, M. M., & Richards, B. A. (2021) · Communications Biology · doi:10.1038/s42003-021-02437-y · Cited by 13

Bidirectional Regulation of GABAA Reversal Potential in the Adult Brain: Physiological and Pathological Implications

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GABAergic interneuron diversity and organization are crucial for the generation of human-specific functional neural networks in cerebral organoids

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Modulation of stress-, pain-, and alcohol-related behaviors by perineuronal nets

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Neocortical long-range inhibition promotes cortical synchrony and sleep

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Distinct recruitment of feedforward and recurrent pathways across higher-order areas of mouse visual cortex

Li, J. Y., Hass, C. A., Matthews, I., Kristl, A. C., & Glickfeld, L. L. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.042 · Cited by 9

Ultrafast (400 Hz) network oscillations induced in mouse barrel cortex by optogenetic activation of thalamocortical axons

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Overexpression of the schizophrenia risk gene C4 in PV cells drives sex-dependent behavioral deficits and circuit dysfunction

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Spine loss in depression impairs dendritic signal integration in human cortical microcircuit models

Yao, H. K., Mazza, F., Prévot, T. D., Sibille, E. L., & Hay, E. (2025) · iScience · doi:10.1016/j.isci.2025.112136 · Cited by 12

Genetically encoded sensors illuminate in vivo detection for neurotransmission: Development, application, and optimization strategies

Zhong, X., Gu, H., Lim, J., Zhang, P., Wang, G., Zhang, K., & Li, X. (2025) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2025.03.003 · Cited by 10

Large-scale coupling of prefrontal activity patterns as a mechanism for cognitive control in health and disease: evidence from rodent models

Negrón-Oyarzo, I., Dib, T., Chacana-Véliz, L., Quilodrán, N. L., & Urrutia-Piñones, J. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1286111 · Cited by 7

Neural activity of heterogeneous inhibitory spiking networks with delay

Luccioli, S., Angulo‐García, D., & Torcini, A. (2019) · Physical review. E · doi:10.1103/physreve.99.052412 · Cited by 9

Memory Prosthesis: Is It Time for a Deep Neuromimetic Computing Approach?

Cutsuridis, V. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00667 · Cited by 10

Brightness illusions drive a neuronal response in the primary visual cortex under top-down modulation

Saeedi, A., Wang, K., Nikpourian, G., Bartels, A., Logothetis, N. K., Totah, N. K. B., & Watanabe, M. (2024) · Nature Communications · doi:10.1038/s41467-024-46885-6 · Cited by 10

Neural Circuit Mapping and Neurotherapy-Based Strategies

Marei, H. E. S. (2025) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-025-01595-5 · Cited by 13

Toward the Identification of Neurophysiological Biomarkers for Alzheimer’s Disease in Down Syndrome: A Potential Role for Cross-Frequency Phase-Amplitude Coupling Analysis

Victorino, D. B., Faber, J., Pinheiro, D. J. L. L., Scorza, F. A., de Almeida, A.-C. G., Costa, A. C. S., & Scorza, C. A. (2022) · Aging and Disease · doi:10.14336/ad.2022.0906 · Cited by 8

Thy Mind, Thy Brain and Time

Drayton, L. A., & Furman, M. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.09.001 · Cited by 7

VIP interneurons selectively enhance weak but behaviorally-relevant stimuliPreprint

Millman, D. J., Ocker, G. K., Caldejon, S., Kato, I., Larkin, J. D., Lee, E., Luviano, J., Nayan, C., Nguyen, T. V., North, K., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/858001 · Cited by 7

A dendritic substrate for temporal diversity of cortical inhibitionPreprint

Morabito, A., Zerlaut, Y., Dhanasobhon, D., Berthaux, E., Tzilivaki, A., Moneron, G., Cathala, L., Poirazi, P., Bacci, A., DiGregorio, D. A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.09.602783 · Cited by 7

State modulation in spatial networks with three interneuron subtypesPreprint

Edwards, M., Jonathan Rubin, A., & Huang, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.23.609417 · Cited by 7

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

Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2025) · eLife · doi:10.7554/elife.99808.4 · Cited by 9

Stage-Dependent Neural Mechanisms in Human Methamphetamine Abstinence: Insights From the Digital Twin Brain Model

Zhang, J., Du, Y., Jin, L., Yang, W., Cao, D., Luo, N., Yang, Z., Tang, K., Chu, C., Xiao, X., et al. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.05.010 · Cited by 8

Excitatory/inhibitory ratio disruption modulates neural synchrony and flow directions in a cortical microcircuit

Wagatsuma, N., Nobukawa, S., & Kurikawa, T. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013306 · Cited by 6

Auditory brainstem response in autistic children

Cardon, G. J., Cate, M., Cordingley, S. A., & Bown, B. (2023) · Hearing Balance and Communication · doi:10.1080/21695717.2023.2181558 · Cited by 6

Selective Deletion of Methyl CpG Binding Protein 2 from Parvalbumin Interneurons in the Auditory Cortex Delays the Onset of Maternal Retrieval in Mice

Rupert, D. D., Pagliaro, A. H., Choe, J., & Shea, S. D. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0838-23.2023 · Cited by 7

Contraindicated Drug Responses in Dravet Syndrome Brain Organoids Utilizing Micro Electrode Array Assessment Methods

Yokoi, R., Nagafuku, N., Ishibashi, Y., Matsuda, N., & Suzuki, I. (2023) · Organoids · doi:10.3390/organoids2040014 · Cited by 8

State modulation in spatial networks with three interneuron subtypes

Edwards, M. M., Rubin, J. E., & Huang, C. (2025) · Science Advances · doi:10.1126/sciadv.ads9134 · Cited by 13

Sexual dimorphism of inhibitory synaptic transmission in RA projection neurons of songbirds

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Somatostatin interneurons exhibit enhanced functional output and resilience to axotomy after mild traumatic brain injury

Harris, A. C., Jin, X., Greer, J. E., Povlishock, J. T., & Jacobs, K. M. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105801 · Cited by 8

Constraints on the design of neuromorphic circuits set by the properties of neural population codes

Panzeri, S., Janotte, E., Pequeño-Zurro, A., Bonato, J., & Bartolozzi, C. (2023) · Neuromorphic Computing and Engineering · doi:10.1088/2634-4386/acaf9c · Cited by 9

Thy Mind, Thy Brain and Time

Drayton, L. A., & Furman, M. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.08.007 · Cited by 6

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

Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2024) · eLife · doi:10.7554/elife.99808 · Cited by 8

Evidence for the involvement of a fronto-striatal pathway in the processing of social reward

Lin, K., & Coutellier, L. D. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102834 · Cited by 6

Multimodal Temporal Pattern Discrimination Is Encoded in Visual Cortical Dynamics

Post, S., Mol, W., Abu-Wishah, O., Ali, S., Rahmatullah, N., & Goel, A. (2023) · eNeuro · doi:10.1523/eneuro.0047-23.2023 · Cited by 4

Dynamic electrical synapses rewire brain networks for persistent oscillations and epileptogenesis

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Velocity of conduction between columns and layers in barrel cortex reported by parvalbumin interneurons

Scheuer, K. S., Judge, J. M., Zhao, X., & Jackson, M. B. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad254 · Cited by 6

Cortical excitation:inhibition imbalance causes abnormal brain network dynamics as observed in neurodevelopmental disordersPreprint

Markicevic, M., Fulcher, B. D., Lewis, C., Helmchen, F., Rudin, M., Zerbi, V., & Wenderoth, N. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/492108 · Cited by 7

Tonic GABAergic activity facilitates dendritic calcium signaling and short-term plasticityPreprint

Chiu, C. Q., Morse, T. M., Nani, F., Knoflach, F., Hernandez, M., Jadi, M. P., & Higley, M. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.22.055137 · Cited by 5

Infralimbic parvalbumin neural activity facilitates cued threat avoidancePreprint

Ho, Y.-Y., Yang, Q., Boddu, P., Bulkin, D. A., & Warden, M. R. (2023) · eLife · doi:10.7554/elife.91221 · Cited by 9

Combining gamma neuromodulation and robotic rehabilitation after a stroke restores parvalbumin interneuron dynamics and improves motor recovery in mice

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Reliable and dynamic monitoring changes in cortical excitation and inhibition balance using aperiodic 1/f slope: functions, diseases and drug effects

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Contribution of spike timing to the neural code: from fast to slow timescales

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Evaluating the Diagnostic Value of Electrovestibulography (EVestG) in Alzheimer’s Patients with Mixed Pathology: A Pilot Study

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Developmental Inhibitory Changes in the Primary Somatosensory Cortex of the Stargazer Mouse Model of Absence Epilepsy

Hassan, M. J., Grattan, D. R., & Leitch, B. (2023) · Biomolecules · doi:10.3390/biom13010186 · Cited by 3

What's New on Alzheimer's Disease? Insights From AD Mouse Models

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Neocortical inhibitory interneuron subtypes display distinct responses to synchrony and rate of inputsPreprint

Tran, M. M., Prince, L. Y., Gray, D., Saad, L., Chasiotis, H., Kwag, J., Kohl, M. M., & Richards, B. A. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/671248 · Cited by 4

Neonatal immune challenge induces female-specific changes in social behavior and somatostatin cell number, independent of microglial inflammatory signalingPreprint

Smith, C. J. W., Kingsbury, M. A., Dziabis, J. E., Hanamsagar, R. M., Malacon, K. E., Tran, J. N., Norris, H. A., Gulino, M., & Bilbo, S. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.30.068924 · Cited by 4

Excitation-Inhibition Balance in Absence Seizure Ictogenesis

Lörincz, M. L., Crunelli, V., & David, F. (2024) · doi:10.1093/med/9780197549469.003.0020 · Cited by 3

Luminance invariant encoding in mouse primary visual cortex

O’Shea, R. T., Nauhaus, I., Wei, X.-X., & Priebe, N. J. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115217 · Cited by 3

Prefrontal cortex interneurons and their contributions to attention, working memory, and adaptive behavior

Boroujeni, K. B., Balaram, P., Tiesinga, P. H. E., & Womelsdorf, T. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102873 · Cited by 4

Neuroanatomical Substrates of Circuit-Specific Cholinergic Modulation across the Primate Anterior Cingulate Cortex

Tsolias, A., Zhou, Y., Mojica, C. A., Sakharkar, M., Tsolias, M., Moore, T. L., Rosene, D. L., & Medalla, M. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0953-23.2024 · Cited by 3

Auditory evoked delta brushes involve stimulus-specific cortical networks in preterm infants

Kamińska, A., Arzounian, D., Delattre, V., Laschet, J. J., Magny, J., Hovhannisyan, S., Mokhtari, M., Manresa, A., Boissel, A., Ouss, L., et al. (2025) · iScience · doi:10.1016/j.isci.2025.112313 · Cited by 5

Behavioral and Neuroanatomical Consequences of Cell-Type Specific Loss of Dopamine D2 Receptors in the Mouse Cerebral Cortex

Lee, G. S., Graham, D. L., Noble, B. L., Trammell, T. S., McCarthy, D. M., Anderson, L., Rubinstein, M., Bhide, P. G., & Stanwood, G. D. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.815713 · Cited by 4

The Therapeutic Potential of Restoring Gamma Oscillations in Alzheimer’s Disease

Ferretti, A., Rogers-Healion, K., & Fotros, A. (2022) · Advances in Psychiatry and Behavioral Health · doi:10.1016/j.ypsc.2022.05.002 · Cited by 3

Infralimbic parvalbumin neural activity facilitates cued threat avoidance

Ho, Y.-Y., Yang, Q., Boddu, P., Bulkin, D. A., & Warden, M. R. (2025) · eLife · doi:10.7554/elife.91221.3 · Cited by 4

Structural changes in the neocortex as correlates of variations in EEG spectra and seizure susceptibility in rat brains with different degrees of dysplasia

Setkowicz, Z., Gzieło, K., Kiełbiński, M., & Janeczko, K. J. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25282 · Cited by 3

Inhibitory inputs to an inhibitory interneuron: Spontaneous postsynaptic currents and GABA A receptors of A17 amacrine cells in the rat retina

Beltrán‐Matas, P., Castilho, Á., Tencer, B., Veruki, M. L., & Hartveit, E. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15634 · Cited by 2

Inhibitory Feedback Enables Predictive Learning of Multiple Sequences in Neural Networks

Saponati, M., & Vinck, M. A. (2026) · Neural Computation · doi:10.1162/neco.a.1504 · Cited by 3

Voluntary alcohol consumption disrupts coupling of prefrontal cortical activity to arousalPreprint

Sipe, G. O., Linares-García, I., Nguyen, M. H., Vazey, E. M., & Huda, R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.01.429229 · Cited by 3

Disorganized Inhibitory Dynamics in Hippocampal area CA1 of 22q11.2 Deletion Mutant MicePreprint

Herrlinger, S. A., Rao, B. Y., Paredes, M. E. C., Tuttman, A. L., Arain, H., Varol, E., Gogos, J. A., & Losonczy, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.28.591464 · Cited by 3

Middle-aged CBA/CaJ mice exhibit auditory dysfunction in background noise

Fabrizio-Stover, E. M., Wu, J., Lang, H., & Harris, K. C. (2025) · Hearing Research · doi:10.1016/j.heares.2025.109259 · Cited by 2

Single Circuit in V1 Capable of Switching Contexts During Movement Using an Inhibitory Population as a Switch

Voina, D., Recanatesi, S., Hu, B., Shea‐Brown, E., & Mihalaş, Ş. (2022) · Neural Computation · doi:10.1162/neco_a_01472 · Cited by 3

Reciprocal Connections between Parvalbumin-Expressing Cells and Adjacent Pyramidal Cells Are Regulated by Clustered Protocadherin γ

Kawamura, N., Osuka, T., Kaneko, R., Kishi, E., Higuchi, R., Yoshimura, Y., Hirabayashi, T., Yagi, T., & Tarusawa, E. (2023) · eNeuro · doi:10.1523/eneuro.0250-23.2023 · Cited by 2

Discovering functional interactions among schizophrenia-risk genes by combining behavioral genetics with cell biology

Ma, D., & Gu, C. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105897 · Cited by 2

Brainstem inhibitory neurons enhance behavioral feature selectivity by sharpening the tuning of excitatory neurons

He, Y., Chou, X.-L., Lavoie, A., Liu, J., Russo, M., & Liu, B. (2024) · Current Biology · doi:10.1016/j.cub.2024.08.037 · Cited by 2

Gamma oscillations and auditory perception: A cluster-based statistic investigation in infants at higher likelihood of autism and developmental language disorder

Polver, S., Cantiani, C., Bulf, H., Piazza, C., Turati, C., Molteni, M., & Riva, V. (2024) · Journal of Experimental Child Psychology · doi:10.1016/j.jecp.2024.106132 · Cited by 3

Local connections among excitatory neurons underlie characteristics of enriched environment exposure-induced neuronal response modulation in layers 2/3 of the mouse V1

Wagatsuma, N., Terada, Y., Okuno, H., & Ageta‐Ishihara, N. (2025) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2025.1525717 · Cited by 2

Auditory regulation of hippocampal locomotion circuits by a non-canonical reticulo-limbic pathway

Winne, J., Nascimento, G., Pedrosa, R., Nogueira, M., Simões, C. S., Kullander, K., Leão, K. E., & Leão, R. N. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102811 · Cited by 2

Nos1+ neurons are critical for motor learning and post-stroke motor recovery

Lin, Y., Xu, X.-M., Lin, L., Deng, X.-H., Chen, W., Chen, M., Hou, Y.-L., Gao, F., Zhang, C.-J., Wu, H., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116322 · Cited by 2

Neocortical Cell Classes: Essential Contributions from Electrophysiology

Womelsdorf, T. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.005 · Cited by 2

Changes of EEG spectra in rat brains with different patterns of dysplasia in response to pilocarpine-induced seizures

Setkowicz, Z., Kiełbiński, M., Gzieło, K., Węglarz, W. P., & Janeczko, K. J. (2020) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2020.107288 · Cited by 2

Paired Feed-Forward Excitation With Delayed Inhibition Allows High Frequency Computations Across Brain Regions

Cao, A. S., & Hooser, S. D. V. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.803065 · Cited by 2

Dual impact of PTEN mutation on CSF dynamics and cortical networks via the dysregulation of neural precursors and their interneuron descendantsPreprint

DeSpenza, T., Kiziltug, E., Allington, G., Barson, D. G., O’Connor, D. A., Robert, S. M., Mekbib, K. Y., Nanda, P., Greenberg, A. B. W., Singh, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.18.533275 · Cited by 2

Cholinergic recruitment of Chandelier cells during arousalPreprint

Martinez-Marquez, E., Reyes-León, S., Garcia-San-Jose, F., López-Begines, S., Nieto-González, J. L., & García‐Junco‐Clemente, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.18.633708 · Cited by 2

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

Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2025) · eLife · doi:10.7554/elife.99808.3 · Cited by 2

The Neural Basis of AgingPreprint

Jackson, B. (2025) · doi:10.33774/coe-2025-fcg76-v3 · Cited by 1

Dissecting Epileptic and Cognitive Network Dysfunction in Epilepsy

Lenck‐Santini, P., & Holmes, G. L. (2024) · Oxford University Press eBooks · doi:10.1093/med/9780197549469.003.0057 · Cited by 1

Inhibitory cell type heterogeneity in a spatially structured mean-field model of V1

Kim, S. H., & Choi, H. (2026) · Physical review. E · doi:10.1101/2025.03.13.643046 · Cited by 1

A disinhibitory microcircuit in the temporal association cortex for fear retrieval to pure tones

Cheng, R., Zhong, W., Yan, Y., Yao, L., Yin, P., Xu, Z., Qin, X., Tan, J., Zeng, Y., Liu, J., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-05566-0 · Cited by 2

A mean-field model of neural networks with PV and SOM interneurons reveals connectivity-based mechanisms of gamma oscillations

Tahvili, F., Vinck, M. A., & di Volo, M. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1014378 · Cited by 2

Temporal discrimination at the neck region is associated with severity of cervical dystonia

Odorfer, T., Junge, A., Volkmann, J., & Zeller, D. (2025) · Scientific Reports · doi:10.1038/s41598-025-31139-2 · Cited by 1

Heterosynaptic Plasticity: History and Evolution of the Concept in Aplysia and Vertebrates

Malyshev, A. Y., Смирнов, И. В., & Volgushev, M. (2025) · The Neuroscientist · doi:10.1177/10738584251390787 · Cited by 1

Molecular and neurochemical underpinnings of altered intrinsic neural timescales in Parkinson’s disease: a multimodal imaging and transcriptomics study

Wen, Z., He, Y.-Z., Hu, Z.-X., Huang, X., & Xie, B. (2025) · Brain Research · doi:10.1016/j.brainres.2025.150133 · Cited by 1

Autonomous Learning from Intrinsic Sensory Dependencies Yields Generalizable Representations in Cortical-Like Networks

Rongala, U. B., & Jörntell, H. (2026) · PRX Life · doi:10.1103/wkwq-r8hk · Cited by 3

Disinhibitory circuit mediated by connections from vasoactive intestinal polypeptide to somatostatin interneurons underlies the paradoxical decrease in spike synchrony with increased border ownership selective neuron firing rate

Wagatsuma, N., Shimomura, H., & Nobukawa, S. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.988715 · Cited by 1

Self-adaptation of networks of nonidentical pulse-coupled excitatory and inhibitory oscillators in the presence of distance-related delays to achieve frequency synchronization

Gil, L. (2023) · Physical review. E · doi:10.1103/physreve.108.034211 · Cited by 1

Vasoactive intestinal peptide-expressing interneurons modulate the effect of behavioral state on cortical activity

Sabri, E., & Batista‐Brito, R. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1465836 · Cited by 2

Fxr1 Deletion from Cortical Parvalbumin Interneurons Modifies Their Excitatory Synaptic Responses

Scheuer, K. S., Jansson, A. M., Shen, M., Zhao, X., & Jackson, M. B. (2025) · eNeuro · doi:10.1523/eneuro.0363-24.2024 · Cited by 1

Bicuculline restores frequency-dependent hippocampal I/E ratio and circuit function in PGC-1ɑ null mice

Bhattacharya, D., Bartley, A. F., Li, Q., & Dobrunz, L. E. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.07.003 · Cited by 1

Single circuit in V1 capable of switching contexts during movement using VIP population as a switchPreprint

Voina, D., Recanatesi, S., Hu, B., Shea‐Brown, E., & Mihalaş, Ş. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.24.309500 · Cited by 1

The interaction between endogenous GABA, functional connectivity and behavioral flexibility is critically altered with advanced agePreprint

Heise, K.-F., Rueda‐Delgado, L. M., Chalavi, S., King, B. R., Monteiro, T. S., Edden, R. A. E., Mantini, D., & Swinnen, S. P. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.08.331637 · Cited by 1

Luminance invariant encoding in primary visual cortexPreprint

O’Shea, R. T., Nauhaus, I., Wei, X.-X., & Priebe, N. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.18.590073 · Cited by 1

Infralimbic parvalbumin neural activity facilitates cued threat avoidancePreprint

Ho, Y.-Y., Yang, Q., Boddu, P., Bulkin, D. A., & Warden, M. R. (2024) · eLife · doi:10.7554/elife.91221.2 · Cited by 1

Combining Gamma Neuromodulation and Robotic Rehabilitation Restores Parvalbimin-mediated Gamma Function and Boosts Motor Recovery in Stroke MicePreprint

Vignozzi, L., Macchi, F., Montagni, E., Pasquini, M., Martello, A., Minetti, A., Coulomb, É., Mascaro, A. L. A., Micera, S., Caleo, M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.15.608060 · Cited by 1

Cell types associated with human brain functional connectomes and their implications in psychiatric diseasesPreprint

Nie, P., Zhan, Y., Chen, R., Qi, R., Liu, C., & Wang, G.-Z. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.11.627878 · Cited by 1

Keeping Inhibition Timely

Mann, E. O., & Paulsen, O. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.015 · Cited by 12

GABAB Inhibition through Feedback Is Involved in the Synchronization of Interictal Spikes in the Cortex

Марченко, В. Г., & Зайченко, М. И. (2023) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-023-01381-0

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

Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons

Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O., & Somogyi, P. (1995) · Nature · doi:10.1038/378075a0 · Cited by 1,498

Role of GABAergic inhibition in hippocampal network oscillations

Mann, E. O., & Paulsen, O. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.05.003 · Cited by 405