The Cellular Basis of GABA B -Mediated Interhemispheric Inhibition

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 · see citing works

Interhemispheric inhibition of the human motor cortex.

Ferbert, A., Priori, A., Rothwell, J. C., Day, B. L., Colebatch, J. G., & MARSDEN, C. D. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019243 · Cited by 1,490 · see citing works

Channelrhodopsin-2-assisted circuit mapping of long-range callosal projections

Petreanu, L., Huber, D., Sobczyk, A., & Svoboda, K. (2007) · Nature Neuroscience · doi:10.1038/nn1891 · Cited by 930 · see citing works

Molecular Structure and Physiological Functions of GABA B Receptors

Bettler, B., Kaupmann, K., Mosbacher, J., & Gassmann, M. (2004) · Physiological Reviews · doi:10.1152/physrev.00036.2003 · Cited by 927 · see citing works

The Role of the Corpus Callosum in Interhemispheric Transfer of Information: Excitation or Inhibition?

Bloom, J. S., & Hynd, G. W. (2005) · Neuropsychology Review · doi:10.1007/s11065-005-6252-y · Cited by 591 · see citing works

Enhanced visual spatial attention ipsilateral to rTMS-induced 'virtual lesions' of human parietal cortex

Hilgetag, C. C., Théoret, H., & Pascual‐Leone, Á. (2001) · Nature Neuroscience · doi:10.1038/nn0901-953 · Cited by 583 · see citing works

Dendritic organization of sensory input to cortical neurons in vivo

Jia, H., Rochefort, N. L., Chen, X., & Konnerth, A. (2010) · Nature · doi:10.1038/nature08947 · Cited by 508 · see citing works

Horizontal Propagation of Visual Activity in the Synaptic Integration Field of Area 17 Neurons

Bringuier, V., Chavane, F., Glaeser, L., & Frégnac, Y. (1999) · Science · doi:10.1126/science.283.5402.695 · Cited by 507 · see citing works

Frontal lobe neglect in man

Heilman, K. M., & Valenstein, E. (1972) · Neurology · doi:10.1212/wnl.22.6.660 · Cited by 447 · see citing works

Forty-five years of split-brain research and still going strong

Gazzaniga, M. S. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1723 · Cited by 442 · see citing works

Membrane Potential and Firing Rate in Cat Primary Visual Cortex

Carandini, M., & Ferster, D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00470.2000 · Cited by 413 · see citing works

General Organization of Callosal Connections in the Cerebral Cortex

Innocenti, G. M. (1986) · Cerebral cortex · doi:10.1007/978-1-4613-2149-1_9 · Cited by 394 · see citing works

In vivo dendritic calcium dynamics in deep-layer cortical pyramidal neurons

Helmchen, F., Svoboda, K., Denk, W. T., & Tank, D. W. (1999) · Nature Neuroscience · doi:10.1038/14788 · Cited by 380 · see citing works

Dendritic encoding of sensory stimuli controlled by deep cortical interneurons

Murayama, M., Pérez-Garci, E., Nevian, T., Bock, T., Senn, W., & Larkum, M. E. (2009) · Nature · doi:10.1038/nature07663 · Cited by 369 · see citing works

Top-down Dendritic Input Increases the Gain of Layer 5 Pyramidal Neurons

Larkum, M. E. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh065 · Cited by 366 · see citing works

Identified sources and targets of slow inhibition in the neocortex

Tamás, G., Simon, A. L., & Szabadics, J. (2003) · Science · doi:10.1126/science.1082053 · Cited by 359 · see citing works

Direct hyperpolarizing action of baclofen on hippocampal pyramidal cells

Newberry, N. R., & Nicoll, R. A. (1984) · Nature · doi:10.1038/308450a0 · Cited by 337 · see citing works

Mechanisms and consequences of action potential burst firing in rat neocortical pyramidal neurons

Williams, S. R., & Stuart, G. J. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00467.x · Cited by 298 · see citing works

Repetitive TMS of the motor cortex improves ipsilateral sequential simple finger movements

Kobayashi, M., Hutchinson, S., Théoret, H., Gottfried Schlaug, A., & Pascual‐Leone, Á. (2004) · Neurology · doi:10.1212/wnl.62.1.91 · Cited by 268 · see citing works

The GABAB1b Isoform Mediates Long-Lasting Inhibition of Dendritic Ca2+ Spikes in Layer 5 Somatosensory Pyramidal Neurons

Pérez‐Garci, E., Gassmann, M., Bettler, B., & Larkum, M. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.019 · Cited by 262 · see citing works

Transient Suppression of Ipsilateral Primary Somatosensory Cortex during Tactile Finger Stimulation

Hlushchuk, Y., & Hari, R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5536-05.2006 · Cited by 243 · see citing works

EFFECTS OF TRANSCALLOSAL VOLLEYS ON PYRAMIDAL TRACT CELL ACTIVITY OF CAT

Asanuma, H., & Okuda, O. (1962) · Journal of Neurophysiology · doi:10.1152/jn.1962.25.2.198 · Cited by 208 · see citing works

Bimanual coordination and interhemispheric interaction

Gerloff, C. P., & Andres, F. G. (2002) · Acta Psychologica · doi:10.1016/s0001-6918(02)00032-x · Cited by 202 · see citing works

Synaptic interactions of late-spiking neocortical neurons in layer 1

Chu, Z., Galarreta, M., & Hestrin, S. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00096.2003 · Cited by 172 · see citing works

Interhemispheric control of manual motor activity

Geffen, G. M., Jones, D. L., & Geffen, L. B. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90125-2 · Cited by 163 · see citing works

Increased sensitivity to ipsilateral cutaneous stimuli following transcranial magnetic stimulation of the parietal lobe

Seyal, M., Ro, T., & Rafal, R. D. (1995) · Annals of Neurology · doi:10.1002/ana.410380221 · Cited by 158 · see citing works

Modified activation of somatosensory cortical network in patients with right-hemisphere stroke

Forss, N., Hietanen, M., Salonen, O. L. M., & Hari, R. (1999) · Brain · doi:10.1093/brain/122.10.1889 · Cited by 148 · see citing works

Whisker maps of neuronal subclasses of the rat ventral posterior medial thalamus, identified by whole‐cell voltage recording and morphological reconstruction

Brecht, M., & Sakmann, B. J. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.012334 · Cited by 137 · see citing works

Specificity of synaptic connectivity between layer 1 inhibitory interneurons and layer 2/3 pyramidal neurons in the rat neocortex

Wozny, C., & Williams, S. R. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq257 · Cited by 129 · see citing works

Expression and distribution of metabotropic GABA receptor subtypes GABABR1 and GABABR2 during rat neocortical development

López‐Bendito, G., Shigemoto, R., Kulik, Á., Paulsen, O., Fairén, A. G., & Luján, R. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02032.x · Cited by 113 · see citing works

Transcallosally mediated inhibition of interneurons within human primary motor cortex

Schnitzler, A., Kessler, K. R., & Benecke, R. (1996) · Experimental Brain Research · doi:10.1007/bf00227944 · Cited by 96 · see citing works

Fiberoptic System for Recording Dendritic Calcium Signals in Layer 5 Neocortical Pyramidal Cells in Freely Moving Rats

Murayama, M., Pérez‐Garci, E., Lüscher, H., & Larkum, M. E. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00082.2007 · Cited by 91 · see citing works

Inhibitory control of excitable dendrites in neocortex

Kim, H. G., Beierlein, M., & Connors, B. W. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.4.1810 · Cited by 81 · see citing works

Interhemispheric balance of overt attention: a theta burst stimulation study

Cazzoli, D., Wurtz, P., Müri, R. M., Hess, C. W., & Nyffeler, T. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06665.x · Cited by 78 · see citing works

GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits

Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033 · see citing works

Diaschisis: past, present, future

Carrera, E., & Tononi, G. (2014) · Brain · doi:10.1093/brain/awu101 · Cited by 824 · see citing works

A cellular mechanism for cortical associations: an organizing principle for the cerebral cortex

Larkum, M. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2012.11.006 · Cited by 755 · see citing works

TMS and drugs revisited 2014

Ziemann, U., Reis, J., Schwenkreis, P., Rosanova, M., Strafella, A. P., Badawy, R. A. B., & Müller‐Dahlhaus, F. (2014) · Clinical Neurophysiology · doi:10.1016/j.clinph.2014.08.028 · Cited by 678 · see citing works

Dendritic integration: 60 years of progress

Stuart, G. J., & Spruston, N. (2015) · Nature Neuroscience · doi:10.1038/nn.4157 · Cited by 489 · see citing works

Active properties of neocortical pyramidal neuron dendrites

Major, G., Larkum, M. E., & Schiller, J. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150343 · Cited by 443 · see citing works

Active cortical dendrites modulate perception

Takahashi, N., Oertner, T. G., Hegemann, P., & Larkum, M. E. (2016) · Science · doi:10.1126/science.aah6066 · Cited by 419 · see citing works

Somatostatin-expressing neurons in cortical networks

Urban-Ciecko, J., & Barth, A. L. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.53 · Cited by 374 · see citing works

The organization of two new cortical interneuronal circuits

Jiang, X., Wang, G., Lee, A. J., Stornetta, R. L., & Zhu, J. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3305 · Cited by 338 · see citing works

Spontaneous and Therapeutic-Induced Mechanisms of Functional Recovery After Stroke

Cassidy, J. M., & Cramer, S. C. (2017) · Translational Stroke Research · doi:10.1007/s12975-016-0467-5 · Cited by 292 · see citing works

Transcriptomic and morphophysiological evidence for a specialized human cortical GABAergic cell type

Boldog, E., Bakken, T. E., Hodge, R. D., Novotny, M., Aevermann, B. D., Baka, J., Bordé, S., Close, J. L., Diez-Fuertes, F., Ding, S.-L., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0205-2 · Cited by 291 · see citing works

Dendritic channelopathies contribute to neocortical and sensory hyperexcitability in Fmr1−/y mice

Zhang, Y., Bonnan, A., Bony, G., Férézou, I., Pietropaolo, S., Ginger, M. R., Sans, N., Rossier, J., Oostra, B. A., LeMasson, G., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3864 · Cited by 227 · see citing works

Principles Governing the Operation of Synaptic Inhibition in Dendrites

Gidon, A., & Segev, I. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.015 · Cited by 224 · see citing works

Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons

Abs, E., Poorthuis, R. B., Apelblat, D., Muhammad, K., Pardi, M. B., Enke, L., Kushinsky, D., Pu, D.-L., Eizinger, M. F., Conzelmann, K., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.001 · Cited by 212 · see citing works

Thalamic control of layer 1 circuits in prefrontal cortex

Cruikshank, S. J., Ahmed, O. J., Stevens, T. R., Patrick, S. L., Gonzalez, A. N., Elmaleh, M., & Connors, B. W. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3231-12.2012 · Cited by 212 · see citing works

Interneuron Types as Attractors and Controllers

Fishell, G., & Kepecs, Á. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050421 · Cited by 197 · see citing works

Anatomy and physiology of the thick-tufted layer 5 pyramidal neuron

Ramaswamy, S., & Markram, H. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00233 · Cited by 186 · see citing works

Four Unique Interneuron Populations Reside in Neocortical Layer 1

Schuman, B., Machold, R. P., Hashikawa, Y., Fuzik, J., Fishell, G. J., & Rudy, B. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1613-18.2018 · Cited by 184 · see citing works

The Diversity of Cortical Inhibitory Synapses

Kubota, Y., Karube, F., Nomura, M., & Kawaguchi, Y. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00027 · Cited by 180 · see citing works

Untangling GABAergic wiring in the cortical microcircuit

Kubota, Y. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.003 · Cited by 172 · see citing works

Membrane Potential Dynamics of Neocortical Projection Neurons Driving Target-Specific Signals

Yamashita, T., Pala, A., Pedrido, L., Kremer, Y., Welker, E., & Petersen, C. C. H. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.059 · Cited by 172 · see citing works

Neuronal circuits in barrel cortex for whisker sensory perception

Staiger, J. F., & Petersen, C. C. H. (2021) · Physiological Reviews · doi:10.1152/physrev.00019.2019 · Cited by 165 · see citing works

Engagement of Pulvino-cortical Feedforward and Feedback Pathways in Cognitive Computations

Jaramillo, J., Mejías, J. F., & Wang, X. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.023 · Cited by 160 · see citing works

Theta burst stimulation reduces disability during the activities of daily living in spatial neglect

Cazzoli, D., Müri, R. M., Schumacher, R., von Arx, S., Chaves, S., Gutbrod, K., Bohlhalter, S., Bauer, D., Vanbellingen, T., Bertschi, M., et al. (2012) · Brain · doi:10.1093/brain/aws182 · Cited by 161 · see citing works

Perirhinal input to neocortical layer 1 controls learning

Doron, G., Shin, J. N., Takahashi, N., Drüke, M., Bocklisch, C., Skenderi, S., de Mont, L., Toumazou, M., Ledderose, J., Brecht, M., et al. (2020) · Science · doi:10.1126/science.aaz3136 · Cited by 160 · see citing works

All-Optical Electrophysiology Reveals the Role of Lateral Inhibition in Sensory Processing in Cortical Layer 1

Fan, L. Z., Kheifets, S., Böhm, U. L., Wu, H., Piatkevich, K. D., Xie, M. E., Parot, V., Ha, Y., Evans, K. E., Boyden, E. S., et al. (2020) · Cell · doi:10.1016/j.cell.2020.01.001 · Cited by 155 · see citing works

Diversity of layer 5 projection neurons in the mouse motor cortex

Oswald, M. J., Tantirigama, M. L. S., Sonntag, I., Hughes, S. M., & Empson, R. M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00174 · Cited by 155 · see citing works

Neocortical Layer 1: an elegant solution to top-down and bottom-up integration

Schuman, B., Dellal, S., Prönneke, A., Machold, R., & Rudy, B. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100520-012117 · Cited by 148 · see citing works

The Neurobiological Grounding of Persistent Stuttering: from Structure to Function

Neef, N. E., Anwander, A., & Friederici, A. D. (2015) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-015-0579-4 · Cited by 146 · see citing works

Pathway- and Cell-Specific Kappa-Opioid Receptor Modulation of Excitation-Inhibition Balance Differentially Gates D1 and D2 Accumbens Neuron Activity

Tejeda, H. A., Wu, J., Kornspun, A. R., Pignatelli, M., Kashtelyan, V., Krashes, M. J., Lowell, B. B., Carlezon, W. A., & Bonci, A. (2017) · Neuron · doi:10.1016/j.neuron.2016.12.005 · Cited by 134 · see citing works

A Laminar Organization for Selective Cortico-Cortical Communication

D’Souza, R. D., & Burkhalter, A. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00071 · Cited by 138 · see citing works

Mediodorsal and Ventromedial Thalamus Engage Distinct L1 Circuits in the Prefrontal Cortex

Anastasiades, P. G., Collins, D. P., & Carter, A. G. (2020) · Neuron · doi:10.1016/j.neuron.2020.10.031 · Cited by 135 · see citing works

Transcranial magnetic stimulation (TMS) inhibits cortical dendrites

Murphy, S. C., Palmer, L. M., Nyffeler, T., Müri, R. M., & Larkum, M. E. (2016) · eLife · doi:10.7554/elife.13598 · Cited by 136 · see citing works

Neocortical Somatostatin Neurons Reversibly Silence Excitatory Transmission via GABAb Receptors

Urban‐Ciećko, J., Fanselow, E. E., & Barth, A. L. (2015) · Current Biology · doi:10.1016/j.cub.2015.01.035 · Cited by 126 · see citing works

Inhibitory Circuits in Cortical Layer 5

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

Effects of controlled germination on selected physicochemical and functional properties of whole-wheat flour and enhanced γ-aminobutyric acid accumulation by ultrasonication

Ding, J., Hou, G. G., Nemzer, B. V., Xiong, S., Dubat, A., & Feng, H. (2017) · Food Chemistry · doi:10.1016/j.foodchem.2017.09.128 · Cited by 129 · see citing works

Functional integration across oscillation frequencies by cross‐frequency phase synchronization

Palva, J. M., & Palva, S. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13767 · Cited by 131 · see citing works

Inhibitory Gating of Input Comparison in the CA1 Microcircuit

Milstein, A. D., Bloss, E. B., Apostolides, P. F., Vaidya, S. P., Dilly, G. A., Zemelman, B. V., & Magee, J. C. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.025 · Cited by 126 · see citing works

Spatiotemporal specificity in cholinergic control of neocortical function

Muñoz, W., & Rudy, B. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.02.015 · Cited by 122 · see citing works

A Dendritic Substrate for the Cholinergic Control of Neocortical Output Neurons

Williams, S. R., & Fletcher, L. N. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.035 · Cited by 125 · see citing works

An integrative, multiscale view on neural theories of consciousness

Storm, J. F., Klink, P. C., Aru, J., Senn, W., Goebel, R., Pigorini, A., Avanzini, P., Vanduffel, W., Roelfsema, P. R., Massimini, M., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.02.004 · Cited by 114 · see citing works

Variable Dendritic Integration in Hippocampal CA3 Pyramidal Neurons

Makara, J. K., & Magee, J. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.033 · Cited by 114 · see citing works

Sensory inputs control the integration of neurogliaform interneurons into cortical circuits

De Marco García, N. V., Priya, R., Tuncdemir, S. N., Fishell, G., & Karayannis, T. (2015) · Nature Neuroscience · doi:10.1038/nn.3946 · Cited by 117 · see citing works

Enhancement of gama-aminobutyric acid (GABA) and other health-related metabolites in germinated red rice (Oryza sativa L.) by ultrasonication

Ding, J., ULANOV, A. V., Dong, M., Yang, T., Nemzer, B. V., Xiong, S., Zhao, S., & Feng, H. (2017) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2017.08.029 · Cited by 113 · see citing works

Inter‐hemispheric inhibition sculpts the output of neural circuits by co‐opting the two cerebral hemispheres

Carson, R. G. (2020) · The Journal of Physiology · doi:10.1113/jp279793 · Cited by 111 · see citing works

Inhibitory interneurons in visual cortical plasticity

van Versendaal, D., & Levelt, C. N. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2264-4 · Cited by 102 · see citing works

The Contribution of the Corpus Callosum to Language Lateralization

Hinkley, L. B. N., Marco, E. J., Brown, E. G., Bukshpun, P., Gold, J., Hill, S. S., Findlay, A. M., Jeremy, R. J., Wakahiro, M. L. J., Barkovich, A. J., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3850-14.2016 · Cited by 103 · see citing works

Inhibitory Modulation of Orbitofrontal Cortex on Medial Prefrontal Cortex–Amygdala Information Flow

Chang, C., & Grace, A. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw342 · Cited by 105 · see citing works

Theta burst stimulation in neglect after stroke: functional outcome and response variability origins

Nyffeler, T., Vanbellingen, T., Kaufmann, B. C., Pflugshaupt, T., Bauer, D., Frey, J. N., Chechlacz, M., Bohlhalter, S., Müri, R. M., Nef, T., et al. (2019) · Brain · doi:10.1093/brain/awz029 · Cited by 97 · see citing works

Dendritic function in vivo

Grienberger, C., Chen, X., & Konnerth, A. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.11.002 · Cited by 97 · see citing works

It is time to combine the two main traditions in the research on the neural correlates of consciousness: C = L × D

Bachmann, T., & Hudetz, A. G. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00940 · Cited by 104 · see citing works

Multisensory stimulation improves functional recovery and resting-state functional connectivity in the mouse brain after stroke

Hakon, J., Quattromani, M. J., Sjölund, C., Tomasevic, G., Carey, L. M., Lee, J., Ruscher, K., Wieloch, T. W., & Bauer, A. Q. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.11.022 · Cited by 97 · see citing works

Enhancement of γ-aminobutyric acid, avenanthramides, and other health-promoting metabolites in germinating oats (Avena sativa L.) treated with and without power ultrasound

Ding, J., Johnson, J., Chu, Y. F., & Feng, H. (2019) · Food Chemistry · doi:10.1016/j.foodchem.2018.12.136 · Cited by 95 · see citing works

Canonical Organization of Layer 1 Neuron-Led Cortical Inhibitory and Disinhibitory Interneuronal Circuits

Lee, A. J., Wang, G., Jiang, X., Johnson, S. M., Hoang, E. T., Lanté, F., Stornetta, R. L., Beenhakker, M. P., Shen, Y., & Julius Zhu, J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu020 · Cited by 94 · see citing works

NDNF interneurons in layer 1 gain-modulate whole cortical columns according to an animal’s behavioral state

Malina, K. C.-K., Tsivourakis, E., Kushinsky, D., Apelblat, D., Shtiglitz, S., Zohar, E., Sokoletsky, M., Tasaka, G., Mizrahi, A., Lampl, I., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.05.001 · Cited by 99 · see citing works

Enhancing Contents of γ-Aminobutyric Acid (GABA) and Other Micronutrients in Dehulled Rice during Germination under Normoxic and Hypoxic Conditions

Ding, J., Yang, T., Feng, H., Dong, M., Slavin, M., Xiong, S., & Zhao, S. (2016) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5b04859 · Cited by 88 · see citing works

Cortical neural populations can guide behavior by integrating inputs linearly, independent of synchrony

Histed, M. H., & Maunsell, J. H. R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1318750111 · Cited by 84 · see citing works

Activity-Dependent Modulation of Layer 1 Inhibitory Neocortical Circuits by Acetylcholine

Brombas, A., Fletcher, L. N., & Williams, S. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4470-13.2014 · Cited by 88 · see citing works

Inhibitory Regulation of Dendritic Activity in vivo

Palmer, L. M., Murayama, M., & Larkum, M. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00026 · Cited by 82 · see citing works

The functional characterization of callosal connections

Innocenti, G. M., Schmidt, K. E., Milleret, C., Mara Fabri, C., Knyazeva, M. G., Battaglia‐Mayer, A., Aboitiz, F., Ptito, M., Caleo, M., Marzi, C. A., et al. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102186 · Cited by 81 · see citing works

GABA-A Receptor Inhibition of Local Calcium Signaling in Spines and Dendrites

Marlin, J. J., & Carter, A. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0869-13.2014 · Cited by 75 · see citing works

Temporal Dynamics of L5 Dendrites in Medial Prefrontal Cortex Regulate Integration Versus Coincidence Detection of Afferent Inputs

Dembrow, N. C., Zemelman, B. V., & Johnston, D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4673-14.2015 · Cited by 75 · see citing works

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 76 · see citing works

Antagonism of the 5-HT 6 receptor – Preclinical rationale for the treatment of Alzheimer's disease

de Jong, I. E. M., & Mørk, A. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.07.010 · Cited by 76 · see citing works

Apical drive-A cellular mechanism of dreaming?

Aru, J., Siclari, F., Phillips, W. A., & Storm, J. F. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.09.018 · Cited by 74 · see citing works

Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs

Naskar, S., Qi, J., Pereira, F., Gerfen, C. R., & Lee, S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108774 · Cited by 72 · see citing works

Rapid Neuromodulation of Layer 1 Interneurons in Human Neocortex

Poorthuis, R. B., Muhammad, K., Wang, M., Verhoog, M. B., Junek, S., Wrana, A., Mansvelder, H. D., & Letzkus, J. J. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.111 · Cited by 70 · see citing works

Inhibition of dendritic Ca2+ spikes by GABAB receptors in cortical pyramidal neurons is mediated by a direct Gi/o‐βγ‐subunit interaction with Cav1 channels

Pérez‐Garci, E., Larkum, M. E., & Nevian, T. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.245464 · Cited by 66 · see citing works

Dendritic calcium spikes are clearly detectable at the cortical surface

Suzuki, M., & Larkum, M. E. (2017) · Nature Communications · doi:10.1038/s41467-017-00282-4 · Cited by 70 · see citing works

Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex

Muralidhar, S., Wang, Y., & Markram, H. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00052 · Cited by 67 · see citing works

Distribution of serotonin receptor 5-HT6 mRNA in rat neuronal subpopulations: A double in situ hybridization study

Helboe, L., Egebjerg, J., & de Jong, I. E. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.09.064 · Cited by 66 · see citing works

The contribution of synaptic location to inhibitory gain control in pyramidal cells

Pouille, F., Watkinson, O., Scanziani, M., & Trevelyan, A. J. (2013) · Physiological Reports · doi:10.1002/phy2.67 · Cited by 65 · see citing works

Sublinear integration underlies binocular processing in primary visual cortex

Longordo, F., To, M., Ikeda, K., & Stuart, G. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3394 · Cited by 63 · see citing works

Cognitive functions of intracellular mechanisms for contextual amplification

Phillips, W. A. (2017) · Brain and Cognition · doi:10.1016/j.bandc.2015.09.005 · Cited by 62 · see citing works

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 62 · see citing works

The Current Status of Somatostatin-Interneurons in Inhibitory Control of Brain Function and Plasticity

Scheyltjens, I., & Arckens, L. (2016) · Neural Plasticity · doi:10.1155/2016/8723623 · Cited by 60 · see citing works

GABAB receptors: modulation of thalamocortical dynamics and synaptic plasticity

Sanchez-Vives, M. V., Barbero‐Castillo, A., Pérez‐Zabalza, M., & Reig, R. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.03.011 · Cited by 61 · see citing works

Impact of functional synapse clusters on neuronal response selectivity

Ujfalussy, B. B., & Makara, J. K. (2020) · Nature Communications · doi:10.1038/s41467-020-15147-6 · Cited by 58 · see citing works

Bottom-up inputs are required for establishment of top-down connectivity onto cortical layer 1 neurogliaform cells

Ibrahim, L. A., Huang, S., Fernández-Otero, M., Sherer, M., Qiu, Y., Vemuri, S., Xu, Q., Machold, R. P., Pouchelon, G., Rudy, B., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.004 · Cited by 60 · see citing works

Neural mechanisms of economic choices in mice

Kuwabara, M., Kang, N., Holy, T. E., & Padoa-Schioppa, C. (2020) · eLife · doi:10.7554/elife.49669 · Cited by 56 · see citing works

Distinct roles of GABA B1a ‐ and GABA B1b ‐containing GABA B receptors in spontaneous and evoked termination of persistent cortical activity

Craig, M. T., Mayne, E. W., Bettler, B., Paulsen, O., & McBain, C. J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.248088 · Cited by 56 · see citing works

Modulation of cortical circuits by top-down processing and arousal state in health and disease

Batista‐Brito, R., Zagha, E., Ratliff, J. M., & Vinck, M. A. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.06.008 · Cited by 57 · see citing works

Neurogliaform cortical interneurons derive from cells in the preoptic area

Niquille, M., Limoni, G., Markopoulos, F., Cadilhac, C., Prados, J., Holtmaat, A., & Dayer, A. (2018) · eLife · doi:10.7554/elife.32017 · Cited by 55 · see citing works

Dendritic Excitability and Gain Control in Recurrent Cortical Microcircuits

Hay, E., & Segev, I. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu200 · Cited by 52 · see citing works

Combining robotic training and inactivation of the healthy hemisphere restores pre-stroke motor patterns in mice

Spalletti, C., Alia, C., Lai, S., Panarese, A., Conti, S., Micera, S., & Caleo, M. (2017) · eLife · doi:10.7554/elife.28662 · Cited by 53 · see citing works

Stimulation of antioxidant activity and γ-aminobutyric acid synthesis in germinated wheat grain Triticum aestivum L. by ultrasound: Increasing the nutritional value of the product

Науменко, Н. В., Потороко, И. Ю., & Kalinina, I. V. (2022) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2022.106000 · Cited by 54 · see citing works

Dendritic integration in pyramidal neurons during network activity and disease

Palmer, L. M. (2013) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.09.010 · Cited by 52 · see citing works

Impact of GABA A and GABA B Inhibition on Cortical Dynamics and Perturbational Complexity during Synchronous and Desynchronized States

Barbero‐Castillo, A., Mateos‐Aparicio, P., Porta, L. D., Camassa, A., Perez-Mendez, L., & Sanchez-Vives, M. V. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1837-20.2021 · Cited by 53 · see citing works

The emerging role of GABAB receptors as regulators of network dynamics: fast actions from a ‘slow’ receptor?

Craig, M. T., & McBain, C. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.002 · Cited by 56 · see citing works

The yin and yang of cortical layer 1

Larkum, M. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3317 · Cited by 50 · see citing works

Behavioral consequences of GABAergic neuronal diversity

Lovett-Barron, M., & Losonczy, A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.002 · Cited by 48 · see citing works

Sublinear binocular integration preserves orientation selectivity in mouse visual cortex

Zhao, X., Liu, M., & Cang, J. (2013) · Nature Communications · doi:10.1038/ncomms3088 · Cited by 48 · see citing works

Pursuing personalized medicine for depression by targeting the lateral or medial prefrontal cortex with Deep TMS

Zangen, A., Zibman, S., Tendler, A., Barnea‐Ygael, N., Alyagon, U., Blumberger, D. M., Grammer, G. G., Shalev, H., Gulevsky, T., Vapnik, T., et al. (2023) · JCI Insight · doi:10.1172/jci.insight.165271 · Cited by 48 · see citing works

Mining the jewels of the cortex’s crowning mystery

Ibrahim, L. A., Schuman, B., Bandler, R. C., Rudy, B., & Fishell, G. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.04.005 · Cited by 48 · see citing works

Principles of GABAergic signaling in developing cortical network dynamics

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

Optogenetic Approaches to Target Specific Neural Circuits in Post-stroke Recovery

Cheng, M., Aswendt, M., & Steinberg, G. K. (2015) · Neurotherapeutics · doi:10.1007/s13311-015-0411-5 · Cited by 43 · see citing works

Development of cortical motor circuits between childhood and adulthood: A navigated TMS‐HdEEG study

Määttä, S., Könönen, M., Kallioniemi, E., Lakka, T. A., Lintu, N., Lindi, V., Ferreri, F., Ponzo, D., & Säïsänen, L. (2017) · Human Brain Mapping · doi:10.1002/hbm.23545 · Cited by 45 · see citing works

Pharmacological mechanisms of interhemispheric signal propagation: a TMS-EEG study

Hui, J., Zomorrodi, R., Lioumis, P., Salavati, B., Rajji, T. K., Chen, R. E., Blumberger, D. M., & Daskalakis, Z. J. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0468-7 · Cited by 42 · see citing works

Layer-specific regulation of cortical neurons by interhemispheric inhibition

Palmer, L. M., Schulz, J. M., & Larkum, M. E. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.23545 · Cited by 44 · see citing works

Compartmental distribution of GABAB receptor-mediated currents along the somatodendritic axis of hippocampal principal cells

Degro, C. E., Kulik, Á., Booker, S. A., & Vida, I. (2015) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2015.00006 · Cited by 43 · see citing works

Layer-specific regulation of cortical neurons by interhemispheric inhibition

Palmer, L. M., Schulz, J. M., & Larkum, M. E. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.23545 · Cited by 44 · see citing works

Layer-specific regulation of cortical neurons by

(2016)

GABA-A Receptor Inhibition of Local Calcium Signaling in Spines and Dendrites

Marlin, J. J., & Carter, A. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0869-13.2014 · Cited by 75 · see citing works

Dendritic GABA B receptors control nonlinear information transfer along the dendro-somatic axis in layer 5 pyramidal neuronsPreprint

Schulz, J. M., & Larkum, M. E. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/762625

GABAA-mediated IPSCs in piriform cortex have fast and slow components with different properties and locations on pyramidal cells.

Kapur, A., Pearce, R. A., Lytton, W. W., & Haberly, L. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.5.2531 · Cited by 91 · see citing works