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

Coherence and cognition in the cortex: the fundamental role of parvalbumin, myelin, and the perineuronal net

Bucher, E., Collins, J. M., King, A. E., Vickers, J. C., & Kirkcaldie, M. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02327-3 · Cited by 31

Common excitatory synaptic inputs to electrically connected cortical fast-spiking cell networks

Otsuka, T., & Kawaguchi, Y. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00071.2013 · Cited by 29

A Neural Model of Empathic States in Attachment-Based Psychotherapy

Cittern, D., & Edalat, A. (2017) · Computational Psychiatry · doi:10.1162/cpsy_a_00006 · Cited by 30

The influence of cortical activity on perception depends on behavioral state and sensory context

Russell, L. E., Fişek, M., Yang, Z., Tan, L. P., Packer, A. M., Dalgleish, H. W. P., Chettih, S. N., Harvey, C. D., & Häusser, M. (2024) · Nature Communications · doi:10.1038/s41467-024-46484-5 · Cited by 59

Bringing Anatomical Information into Neuronal Network Models

van Albada, S. J., Morales-Gregorio, A., Dickscheid, T., Goulas, A., Bakker, R., Bludau, S., Palm, G., Hilgetag, C. C., & Diesmann, M. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-89439-9_9 · Cited by 29

Early NMDA Receptor Ablation in Interneurons Causes an Activity-Dependent E/I Imbalance in vivo in Prefrontal Cortex Pyramidal Neurons of a Mouse Model Useful for the Study of Schizophrenia

Pafundo, D. E., Annan, C. A. P., Fulginiti, N. M., & Belforte, J. E. (2021) · Schizophrenia Bulletin · doi:10.1093/schbul/sbab030 · Cited by 27

Chemogenetic Activation of Feed-Forward Inhibitory Parvalbumin-Expressing Interneurons in the Cortico-Thalamocortical Network During Absence Seizures

Panthi, S., & Leitch, B. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.688905 · Cited by 29

Using diffusion anisotropy to characterize neuronal morphology in gray matter: the orientation distribution of axons and dendrites in the NeuroMorpho.org database

Hansen, M. B., Jespersen, S. N., Leigland, L. A., & Kroenke, C. D. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00031 · Cited by 28

Stimulus-Selective Response Plasticity in Primary Visual Cortex: Progress and Puzzles

Montgomery, D. P., Hayden, D. J., Chaloner, F. A., Cooke, S. F., & Bear, M. F. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.815554 · Cited by 31

Optimizing interneuron circuits for compartment-specific feedback inhibition

Keijser, J., & Sprekeler, H. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009933 · Cited by 28

Tightly coupled inhibitory and excitatory functional networks in the developing primary visual cortex

Mulholland, H. N., Hein, B., Kaschube, M., & Smith, G. B. (2021) · eLife · doi:10.7554/elife.72456 · Cited by 25

Net gain and loss: influence of natural rewards and drugs of abuse on perineuronal nets

Brown, T. E., & Sorg, B. A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01337-x · Cited by 25

Inhibition in the Human Auditory Cortex

Inui, K., Nakagawa, K., Nishihara, M., Motomura, E., & Kakigi, R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155972 · Cited by 25

Modeling Inhibitory Interneurons in Efficient Sensory Coding Models

Zhu, M., & Rozell, C. J. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004353 · Cited by 25

PackIO and EphysViewer: software tools for acquisition and analysis of neuroscience dataPreprint

Watson, B. O., Yuste, R., & Packer, A. M. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/054080 · Cited by 25

Structural changes in perineuronal nets and their perforating GABAergic synapses precede motor coordination recovery post stroke

Dzyubenko, E., Willig, K. I., Yin, D., Sardari, M., Tokmak, E., Labus, P., Schmermund, B., & Hermann, D. M. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00971-x · Cited by 24

The role of parvalbumin interneuron dysfunction across neurodegenerative dementias

Smeralda, C. L., Pandit, S., Turrini, S., Reilly, J., Palmisano, A., Sprugnoli, G., Hampel, H. J., Benussi, A., Borroni, B., Press, D. Z., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102509 · Cited by 26

Calcium-permeable AMPA receptors govern PV neuron feature selectivity

Hong, I., Kim, J., Hainmueller, T., Kim, D. W., Keijser, J., Johnson, R. C., Park, S. H., Limjunyawong, N., Yang, Z., Cheon, D., et al. (2024) · Nature · doi:10.1038/s41586-024-08027-2 · Cited by 26

Cell Type-Specific Circuit Mapping Reveals the Presynaptic Connectivity of Developing Cortical Circuits

Cocas, L. A., Fernández, G., Barch, M., Doll, J., Díaz, I., & Pleasure, S. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0375-15.2016 · Cited by 23

Control of excitatory hierarchical circuits by parvalbumin-FS basket cells in layer 5 of the frontal cortex: insights for cortical oscillations

Kawaguchi, Y., Otsuka, T., Morishima, M., Ushimaru, M., & Kubota, Y. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00778.2018 · Cited by 25

Cortical parvalbumin neurons are responsible for homeostatic sleep rebound through CaMKII activation

Kon, K., Ode, K. L., Mano, T., Fujishima, H., Takahashi, R. R., Tone, D., Shimizu, C., Shiono, S., Yada, S., Matsuzawa, K., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50168-5 · Cited by 26

Modulation of parvalbumin interneuron number by developmentally transient neocortical vasopressin receptor 1a (V1aR)

Hammock, E. A. D., & Levitt, P. R. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.07.025 · Cited by 25

Synaptic Conductance Estimates of the Connection Between Local Inhibitor Interneurons and Pyramidal Neurons in Layer 2/3 of a Cortical Column

Hoffmann, J. H. O., Meyer, H. S., Schmitt, A. C., Straehle, J., Weitbrecht, T., Sakmann, B. J., & Helmstaedter, M. N. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv039 · Cited by 26

Precise inhibitory microcircuit assembly of developmentally related neocortical interneurons in clusters

Zhang, X., Li, Z., Han, Z., Sultan, K. T., Huang, K., & Shi, S. (2017) · Nature Communications · doi:10.1038/ncomms16091 · Cited by 26

GABAergic mechanisms involved in the prepulse inhibition of auditory evoked cortical responses in humans

Inui, K., Takeuchi, N., Sugiyama, S., Motomura, E., & Nishihara, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0190481 · Cited by 24

Two-Photon Optogenetic Mapping of Excitatory Synaptic Connectivity and Strength

Izquierdo-Serra, M., Hirtz, J. J., Shababo, B., & Yuste, R. (2018) · iScience · doi:10.1016/j.isci.2018.09.008 · Cited by 23

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

Li, M., Cabrera-García, D., Salling, M. C., Au, E., Yang, G., & Harrison, N. L. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108501 · Cited by 25

Functional properties and short‐term dynamics of unidirectional and reciprocal synaptic connections between layer 2/3 pyramidal cells and fast‐spiking interneurons in juvenile rat prefrontal cortex

Zaitsev, A. V., & Lewis, D. A. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12294 · Cited by 22

Adolescent maturation of inhibitory inputs onto cingulate cortex neurons is cell-type specific and TrkB dependent

Vandenberg, A., Piekarski, D. J., Caporale, N., Munoz-Cuevas, F. J., & Wilbrecht, L. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00005 · Cited by 22

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

Romero-Sosa, J. L., Motanis, H., & Buonomano, D. V. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2830-20.2021 · Cited by 24

Repeated methamphetamine administration produces cognitive deficits through augmentation of GABAergic synaptic transmission in the prefrontal cortex

Armenta-Reséndiz, M., Assali, A., Tsvetkov, E., Cowan, C. W., & Lavín, A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01371-9 · Cited by 25

Multi-scale spiking network model of human cerebral cortex

Pronold, J., van Meegen, A., Shimoura, R. O., Vollenbröker, H., Senden, M., Hilgetag, C. C., Bakker, R., & van Albada, S. J. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae409 · Cited by 26

Inhibition in Simple Cell Receptive Fields Is Broad and OFF-Subregion Biased

Taylor, M. M., Sedigh-Sarvestani, M., Vigeland, L. E., Palmer, L. A., & Contreras, D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2099-17.2017 · Cited by 22

Dysbindin-1, BDNF, and GABAergic Transmission in Schizophrenia

Jun, R. A., Zhang, W., Beacher, N. J., Zhang, Y., Li, Y., & Lin, D. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.876749 · Cited by 23

Differential modulation of repetitive firing and synchronous network activity in neocortical interneurons by inhibition of A-type K+ channels and Ih

Williams, S. B., & Hablitz, J. J. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00089 · Cited by 22

Functional Network Overlap as Revealed by fMRI Using sICA and Its Potential Relationships with Functional Heterogeneity, Balanced Excitation and Inhibition, and Sparseness of Neuron Activity

Xu, J., Calhoun, V. D., Worhunsky, P. D., Xiang, H., Li, J., Wall, J. T., Pearlson, G. D., & Potenza, M. N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117029 · Cited by 21

Extensive Structural Remodeling of the Axonal Arbors of Parvalbumin Basket Cells during Development in Mouse Neocortex

Micheva, K. D., Király, M., Perez, M. M., & Madison, D. V. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0871-21.2021 · Cited by 23

Dysregulation of prefrontal parvalbumin interneurons leads to adult aggression induced by social isolation stress during adolescence

Li, X., Sun, H., Zhu, Y., Wang, F., Wang, X., Han, L., Cui, D., Luo, D., Zhai, Y., Zhuo, L., et al. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1010152 · Cited by 25

3D Clustering of GABAergic Neurons Enhances Inhibitory Actions on Excitatory Neurons in the Mouse Visual Cortex

Ebina, T., Sohya, K., Imayoshi, I., Yin, S., Kimura, R., Yanagawa, Y., Kameda, H., Hioki, H., Kaneko, T., & Tsumoto, T. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.057 · Cited by 20

Developmental Reduction of Asynchronous GABA Release from Neocortical Fast-Spiking Neurons

Jiang, M., Yang, M., Yin, L., Zhang, X. H., & Shu, Y. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht236 · Cited by 20

NMDA receptors regulate the firing rate set point of hippocampal circuits without altering single-cell dynamics

Ruggiero, A., Heim, L. R., Susman, L., Hreaky, D., Shapira, I., Katsenelson, M., Rosenblum, K., & Slutsky, I. (2024) · Neuron · doi:10.1016/j.neuron.2024.10.014 · Cited by 19

Circuit Mechanisms Underlying Epileptogenesis in a Mouse Model of Focal Cortical Malformation

Yang, W., Williams, A. J., & Sun, Q. (2020) · Current Biology · doi:10.1016/j.cub.2020.10.029 · Cited by 17

Spatially structured inhibition defined by polarized parvalbumin interneuron axons promotes head direction tuning

Peng, Y., Tomás, F. J. B., Pfeiffer, P., Drangmeister, M., Schreiber, S., Vida, I., & Geiger, J. R. P. (2021) · Science Advances · doi:10.1126/sciadv.abg4693 · Cited by 20

Synaptic Basis for Differential Orientation Selectivity between Complex and Simple Cells in Mouse Visual Cortex

Li, Y.-T., Liu, B.-H., Chou, X.-L., Zhang, L., & Tao, H. W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5246-14.2015 · Cited by 19

Perisomatic Features Enable Efficient and Dataset Wide Cell-Type Classifications Across Large-Scale Electron Microscopy VolumesPreprint

Elabbady, L., Seshamani, S., Mu, S., Mahalingam, G., Schneider-Mizell, C. M., Bodor, Á. L., Bae, J. A., Brittain, D., Buchanan, J., Bumbarger, D. J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.20.499976 · Cited by 19

Rapid learning of neural circuitry from holographic ensemble stimulation enabled by model-based compressed sensing

Triplett, M. A., Gajowa, M. A., Antin, B., Sadahiro, M., Adesnik, H., & Paninski, L. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02053-7 · Cited by 17

Implications of cortical balanced excitation and inhibition, functional heterogeneity, and sparseness of neuronal activity in fMRI

Xu, J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.08.018 · Cited by 17

Motor Cortex Microcircuit Simulation Based on Brain Activity Mapping

Chadderdon, G. L., Mohan, A., Suter, B. A., Neymotin, S. A., Kerr, C. C., Francis, J. T., Shepherd, G. M., & Lytton, W. W. (2014) · Neural Computation · doi:10.1162/neco_a_00602 · Cited by 19

Thalamic microcircuits: presynaptic dendrites form two feedforward inhibitory pathways in thalamus

Crandall, S. R., & Cox, C. L. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00559.2012 · Cited by 18

Developmental time windows for axon growth influence neuronal network topology

Lim, S. I., & Kaiser, M. (2015) · Biological Cybernetics · doi:10.1007/s00422-014-0641-3 · Cited by 18

Cell-type specific function of GABAergic neurons in layers 2 and 3 of mouse barrel cortex

Petersen, C. C. H. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.004 · Cited by 19

Functional Logic of Layer 2/3 Inhibitory Connectivity in the Ferret Visual Cortex

Scholl, B., Wilson, D. E., Jaepel, J., & Fitzpatrick, D. (2019) · Neuron · doi:10.1016/j.neuron.2019.08.004 · Cited by 18

Aging But Not Age-Related Hearing Loss Dominates the Decrease of Parvalbumin Immunoreactivity in the Primary Auditory Cortex of Mice

Rogalla, M. M., & Hildebrandt, K. J. (2020) · eNeuro · doi:10.1523/eneuro.0511-19.2020 · Cited by 18

Orientation Selectivity in Inhibition-Dominated Networks of Spiking Neurons: Effect of Single Neuron Properties and Network Dynamics

Sadeh, S., & Rotter, S. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004045 · Cited by 18

Reward Timing and Its Expression by Inhibitory Interneurons in the Mouse Primary Visual Cortex

Monk, K. J., Allard, S., & Shuler, M. G. H. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa068 · Cited by 18

Organization of Cortical and Thalamic Input to Inhibitory Neurons in Mouse Motor Cortex

Okoro, S. U., Goz, R. U., Njeri, B. W., Harish, M., Ruff, C. F., Ross, S. E., Gerfen, C. R., & Hooks, B. M. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0950-22.2022 · Cited by 25

Foramen lacerum impingement of trigeminal nerve root as a rodent model for trigeminal neuralgia

Ding, W., Yang, L., Chen, Q., Hu, K., Liu, Y., Bao, E., Wang, C., Mao, J., & Shen, S. (2023) · JCI Insight · doi:10.1172/jci.insight.168046 · Cited by 17

Emergence of co-tuning in inhibitory neurons as a network phenomenon mediated by randomness, correlations, and homeostatic plasticity

Lagzi, F., & Fairhall, A. L. (2024) · Science Advances · doi:10.1126/sciadv.adi4350 · Cited by 27

Brain (Hyper)Excitability Revealed by Optimal Electrical Stimulation of GABAergic Interneurons

Wendling, F., Gerber, U. R., Cosandier‐Rimélé, D., Nica, A., de Montigny, J., Raineteau, O., Kalitzin, S., Lopes, F. H. D. S., & Benquet, P. (2016) · Brain stimulation · doi:10.1016/j.brs.2016.07.001 · Cited by 20

Reconciliation of weak pairwise spike–train correlations and highly coherent local field potentials across space

Senk, J., Hagen, E., van Albada, S. J., & Diesmann, M. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae405 · Cited by 21

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

Interplay of Intrinsic and Synaptic Conductances in the Generation of High-Frequency Oscillations in Interneuronal Networks with Irregular Spiking

Baroni, F., Burkitt, A. N., & Grayden, D. B. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003574 · Cited by 16

Spiking attractor model of motor cortex explains modulation of neural and behavioral variability by prior target informationPreprint

Rostami, V., Rost, T., Schmitt, F. J., van Albada, S. J., Riehle, A., & Nawrot, M. P. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.27.968339 · Cited by 15

Synaptic promiscuity in brain development

Wolterhoff, N., & Hiesinger, P. R. (2024) · Current Biology · doi:10.1016/j.cub.2023.12.037 · Cited by 18

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

Reimann, M., Santander, D. E., Ecker, A., & Muller, E. B. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae433 · Cited by 20

Voluntary Wheel Running Exercise Evoked by Food-Restriction Stress Exacerbates Weight Loss of Adolescent Female Rats But Also Promotes Resilience by Enhancing GABAergic Inhibition of Pyramidal Neurons in the Dorsal Hippocampus

Chowdhury, T. G., Wable, G. S., Chen, Y.-W., Tateyama, K., Yu, I., Wang, J., Reyes, A. D., & Aoki, C. J. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy283 · Cited by 14

Impaired long-range synchronization of gamma oscillations in the neocortex of a mouse lacking Kv3.2 potassium channels

Harvey, M., Lau, D., Civillico, E. F., Rudy, B., & Contreras, D. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00102.2012 · Cited by 16

A network model of the barrel cortex combined with a differentiator detector reproduces features of the behavioral response to single-neuron stimulation

Bernardi, D., Doron, G., Brecht, M., & Lindner, B. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007831 · Cited by 16

Perineuronal Nets in the Rat Medial Prefrontal Cortex Alter Hippocampal–Prefrontal Oscillations and Reshape Cocaine Self-Administration Memories

Wingert, J. C., Ramos, J. D., Reynolds, S., Gonzalez, A. E., Rose, R. M., Hegarty, D. M., Aicher, S. A., Bailey, L. G., Brown, T. E., Abbas, A. I., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0468-24.2024 · Cited by 16

Chaotic recurrent neural networks for brain modelling: A review

Mattera, A., Alfieri, V., Granato, G., & Baldassarre, G. (2024) · Neural Networks · doi:10.1016/j.neunet.2024.107079 · Cited by 19

Cadherins orchestrate specific patterns of perisomatic inhibition onto distinct pyramidal cell populations

Jézéquel, J., Condomitti, G., Kroon, T., Hamid, F., Sanalidou, S., Garcés, T., Maeso, P. A., Balia, M., Hu, Z., Sahara, S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59635-z · Cited by 13

Differential effects of group III metabotropic glutamate receptors on spontaneous inhibitory synaptic currents in spine-innervating double bouquet and parvalbumin-expressing dendrite-targeting GABAergic interneurons in human neocortex

Lukacs, I. P., Francavilla, R., Field, M., Hunter, E., Howarth, M., Horie, S., Plaha, P., Stacey, R. J., Livermore, L. J., Ansorge, O., et al. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac195 · Cited by 14

Regulation of epileptiform discharges in rat neocortex by HCN channels

Albertson, A. J., Williams, S. B., & Hablitz, J. J. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00955.2012 · Cited by 17

Alterations in Prefrontal Cortical Circuitry and Cognitive Dysfunction in Schizophrenia

Lewis, D. A., & Glausier, J. R. (2016) · Nebraska Symposium on Motivation/The Nebraska symposium on motivation · doi:10.1007/978-3-319-30596-7_3 · Cited by 15

Synaptic mechanisms underlying the intense firing of neocortical layer 5B pyramidal neurons in response to cortico-cortical inputs

Sempere-Ferràndez, A., Martı́nez, S., & Geijo‐Barrientos, E. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01842-8 · Cited by 16

Increased matrix metalloproteinase levels and perineuronal net proteolysis in the HIV-infected brain; relevance to altered neuronal population dynamics

Bozzelli, P. L., Caccavano, A., Avdoshina, V., Mocchetti, I., Wu, J., & Conant, K. E. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113077 · Cited by 15

Cortical Representation of Touch in Silico

Huang, C., Zeldenrust, F., & Celikel, T. (2022) · Neuroinformatics · doi:10.1007/s12021-022-09576-5 · Cited by 15

A latent pool of neurons silenced by sensory-evoked inhibition can be recruited to enhance perception

Gauld, O. M., Packer, A. M., Russell, L. E., Dalgleish, H. W. P., Iuga, M., Sacadura, F., Roth, A., Clark, B. A., & Häusser, M. (2024) · Neuron · doi:10.1016/j.neuron.2024.04.015 · Cited by 18

Mean-field analysis of orientation selectivity in inhibition-dominated networks of spiking neurons

Sadeh, S., Cardanobile, S., & Rotter, S. (2014) · SpringerPlus · doi:10.1186/2193-1801-3-148 · Cited by 14

Cell Type Specific Representation of Vibro-tactile Stimuli in the Mouse Primary Somatosensory Cortex

Hayashi, A., Yoshida, T., & Ohki, K. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00109 · Cited by 14

Increasing the Excitatory Drive Rescues Excitatory/Inhibitory Imbalance and Mismatch Negativity Deficit Caused by Parvalbumin Specific GluA1 Deletion

Chen-Engerer, H.-J., Jaeger, S., Bondarenko, R., Sprengel, R., Hengerer, B., Rosenbrock, H., Mack, V., & Schuelert, N. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.06.027 · Cited by 13

Oxidative Stress-mediated Loss of Hippocampal Parvalbumin Interneurons Contributes to Memory Precision Decline After Acute Sleep Deprivation

Gao, Y.-Z., Liu, K., Wu, X., Shi, C., He, Q., Wu, H., Yang, J., Yao, H., & Ji, M. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04628-0 · Cited by 15

Unravelling the early photochemical behavior of (8-substituted-7-hydroxyquinolinyl)methyl acetates through electronic structure theory and ultrafast transient absorption spectroscopy

Ma, J., Mewes, J., Harris, K. T., Dore, T. M., Phillips, D. L., & Dreuw, A. (2016) · Physical Chemistry Chemical Physics · doi:10.1039/c6cp05499d · Cited by 13

Altered Neurotransmitter Expression in the Corticothalamocortical Network of an Absence Epilepsy Model with impaired Feedforward Inhibition

Adotevi, N. K., Su, A., Peiris, D., Hassan, M. J., & Leitch, B. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.05.024 · Cited by 13

Inhibitory control of synaptic signals preceding locomotion in mouse frontal cortex

Zhang, C.-L., Koukouli, F., Allegra, M., Ortiz, C., Kao, H.-L., Maskos, U., Changeux, J., & Schmidt‐Hieber, C. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110035 · Cited by 13

Local circuit inhibition in the cerebral cortex as the source of gain control and untuned suppression

Shapley, R. M., & Xing, D. (2012) · Neural Networks · doi:10.1016/j.neunet.2012.09.005 · Cited by 13

NeuroPath2Path: Classification and elastic morphing between neuronal arbors using path-wise similarity

Batabyal, T., Condron, B. G., & Acton, S. T. (2020) · Neuroinformatics · doi:10.1007/s12021-019-09450-x · Cited by 12

Inhibitory Units: An Organizing Nidus for Feature-Selective SubNetworks in Area V1

Palagina, G., Meyer, J. F., & Smirnakis, S. M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2275-18.2019 · Cited by 12

Age- and movement-related modulation of cortical oscillations in a mouse model of presbycusis

Rumschlag, J. A., Lovelace, J. W., & Razak, K. A. (2020) · Hearing Research · doi:10.1016/j.heares.2020.108095 · Cited by 15

Serotonergic Modulation of the Excitation/Inhibition Balance in the Visual Cortex

Carlos-Lima, E., Higa, G. S. V., Viana, F. J. C., Tamais, A. M., Cruvinel, E., Borges, F. S., de Oliveira, J. F., Ulrich, H., & Pasquale, R. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010519 · Cited by 12

Choice impulsivity after repeated social stress is associated with increased perineuronal nets in the medial prefrontal cortex

Martinez, C. A., Pantazopoulos, H., Gisabella, B., Stephens, E. T., Garteiser, J., & Arco, A. D. (2024) · Scientific Reports · doi:10.1038/s41598-024-57599-6 · Cited by 11

Stimulus-dependent differences in cortical versus subcortical contributions to visual detection in mice

Cone, J. J., Mitchell, A. O., Parker, R. K., & Maunsell, J. H. R. (2024) · Current Biology · doi:10.1016/j.cub.2024.03.061 · Cited by 12

Network-Centered Homeostasis Through Inhibition Maintains Hippocampal Spatial Map and Cortical Circuit Function

Kaleb, K., Pedrosa, V., & Clopath, C. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109577 · Cited by 12

Perceptual Weighting of V1 Spikes Revealed by Optogenetic White Noise Stimulation

Day-Cooney, J. R., Cone, J. J., & Maunsell, J. H. R. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1736-21.2022 · Cited by 9

The p75 Neurotrophin Receptor in Preadolescent Prefrontal Parvalbumin Interneurons Promotes Cognitive Flexibility in Adult Mice

Chehrazi, P., Lee, K. K. Y., Lavertu-Jolin, M., Abbasnejad, Z., Carreño-Muñoz, M. I., Chattopadhyaya, B., & Cristo, G. D. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.04.019 · Cited by 16

Whisker Deprivation Drives Two Phases of Inhibitory Synapse Weakening in Layer 4 of Rat Somatosensory Cortex

Gainey, M. A., Wolfe, R., Pourzia, O., & Feldman, D. E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148227 · Cited by 12

Self-organization of a doubly asynchronous irregular network state for spikes and bursts

Vercruysse, F., Naud, R., & Sprekeler, H. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009478 · Cited by 13

Possible Role of Parvalbumin Interneurons in Meditation and Psychiatric Illness

Thippaiah, S. M., Pradhan, B., Voyiaziakis, E., Shetty, R., Iyengar, S., Olson, C., & Tang, Y. (2022) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.21050136 · Cited by 12

Effects of homeostatic constraints on associative memory storage and synaptic connectivity of cortical circuits

Chapeton, J. I., Gala, R., & Stepanyants, A. (2015) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2015.00074 · Cited by 11

Anatomical Correlates of Local, Translaminar, and Transcolumnar Inhibition by Layer 6 GABAergic Interneurons in Somatosensory Cortex

Arzt, M., Sakmann, B. J., & Meyer, H. S. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx156 · Cited by 11

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