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State-Dependent Architecture of Thalamic Reticular Subnetworks
Open accessAbstract
Behavioral state is known to influence interactions between thalamus and cortex, which are important for sensation, action, and cognition. The thalamic reticular nucleus (TRN) is hypothesized to regulate thalamo-cortical interactions, but the underlying functional architecture of this process and its state dependence are unknown. By combining the first TRN ensemble recording with psychophysics and connectivity-based optogenetic tagging, we found reticular circuits to be composed of distinct subnetworks. While activity of limbic-projecting TRN neurons positively correlates with arousal, sensory-projecting neurons participate in spindles and show elevated synchrony by slow waves during sleep. Sensory-projecting neurons are suppressed by attentional states, demonstrating that their gating of thalamo-cortical interactions is matched to behavioral state. Bidirectional manipulation of attentional performance was achieved through subnetwork-specific optogenetic stimulation. Together, our findings provide evidence for differential inhibition of thalamic nuclei across brain states, where the TRN separately controls external sensory and internal limbic processing facilitating normal cognitive function. PAPERFLICK:
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“Greater mindfulness-based pain relief was also associated with significant extensive, bilateral deactivation of the thalamus, a critical node of ascending nociceptive information from the spinal cord (Fig. 1).49”
From The neural mechanisms of mindfulness-based pain relief: a functional magnetic resonance imaging-based review and primer (2019) · cites this paper as [49]
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“This mechanism is critically involved in integrating real-time sensory and affective information,129 assessing value,49 and regulating “passage to the cortex”.146”
From The neural mechanisms of mindfulness-based pain relief: a functional magnetic resonance imaging-based review and primer (2019) · cites this paper as [49]
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Cites
The Elements of Statistical Learning
Hastie, T., Tibshirani, R., & Friedman, J. (2009) · Springer Series in Statistics · doi:10.1007/978-0-387-84858-7 · Cited by 25,970
The Elements of Statistical Learning: Data Mining, Inference, and Prediction
Lu, Z. Q. J. (2010) · Journal of the Royal Statistical Society Series A (Statistics in Society) · doi:10.1111/j.1467-985x.2010.00646_6.x · Cited by 12,916
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Neural Mechanisms of Selective Visual Attention
Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
Sohal, V. S., Zhang, F., Yizhar, O., & Deisseroth, K. (2009) · Nature · doi:10.1038/nature07991 · Cited by 2,606
Driving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603
Top-Down Versus Bottom-Up Control of Attention in the Prefrontal and Posterior Parietal Cortices
Buschman, T. J., & Miller, E. K. (2007) · Science · doi:10.1126/science.1138071 · Cited by 2,380
Steriade, M., Nunez, A., & Amzica, F. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03252.1993 · Cited by 1,903
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Fernandez, L. M. J., & Lüthi, A. (2020) · Physiological Reviews · doi:10.1152/physrev.00042.2018 · Cited by 716
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Schmitt, L. I., Wimmer, R. D., Nakajima, M., Happ, M., Mofakham, S., & Halassa, M. M. (2017) · Nature · doi:10.1038/nature22073 · Cited by 663
Self-citationThalamic control of sensory selection in divided attention
Wimmer, R. D., Schmitt, L. I., Davidson, T. J., Nakajima, M., Deisseroth, K., & Halassa, M. M. (2015) · Nature · doi:10.1038/nature15398 · Cited by 530
Self-citationThalamic functions in distributed cognitive control
Halassa, M. M., & Kästner, S. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0020-1 · Cited by 540
Self-citationCircuit-based interrogation of sleep control
Weber, F., & Dan, Y. (2016) · Nature · doi:10.1038/nature19773 · Cited by 383
Sleep—A brain-state serving systems memory consolidation
Brodt, S., Inostroza, M., Niethard, N., & Born, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.005 · Cited by 343
The prefrontal cortex, pathological anxiety, and anxiety disorders
Kenwood, M. M., Kalin, N. H., & Barbas, H. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01109-z · Cited by 379
IL-17a promotes sociability in mouse models of neurodevelopmental disorders
Reed, M. D., Yim, Y. S., Wimmer, R. D., Kim, H., Ryu, C., Welch, G. M., Andina, M., King, H. O., Waisman, A., Halassa, M. M., et al. (2020) · Nature · doi:10.1038/s41586-019-1843-6 · Cited by 274
Self-citationThe Mediodorsal Thalamus: An Essential Partner of the Prefrontal Cortex for Cognition
Parnaudeau, S., Bolkan, S. S., & Kellendonk, C. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.008 · Cited by 283
Hypothalamic feedforward inhibition of thalamocortical network controls arousal and consciousness
Herrera, C. G., Carús-Cadavieco, M., Jego, S., Ponomarenko, A. A., Korotkova, T. M., & Adamantidis, A. (2015) · Nature Neuroscience · doi:10.1038/nn.4209 · Cited by 286
The Slow Oscillation in Cortical and Thalamic Networks: Mechanisms and Functions
Neske, G. T. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00088 · Cited by 296
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Rauschecker, J. P., May, E. S., Maudoux, A., & Ploner, M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.08.002 · Cited by 261
Thalamic Inhibition: Diverse Sources, Diverse Scales
Halassa, M. M., & Acsády, L. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.08.001 · Cited by 243
Self-citationCohen, S. M., Tsien, R. W., GOFF, D. C., & Halassa, M. M. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.026 · Cited by 249
Self-citationClemente-Perez, A., Makinson, S. R., Higashikubo, B. T., Brovarney, S., Cho, F. S., Urry, A., Holden, S. S., Wimer, M., Dávid, C., Fenno, L. E., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.044 · Cited by 223
Manoach, D. S., Pan, J. Q., Purcell, S., & Stickgold, R. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.10.003 · Cited by 216
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Nakajima, M., Schmitt, L. I., & Halassa, M. M. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.026 · Cited by 218
Self-citationDistinct subnetworks of the thalamic reticular nucleus
Li, Y., López-Huerta, V. G., Adiconis, X., Levandowski, K. M., Choi, S., Simmons, S., Arias-García, M. A., Guo, B., Yao, A. Y., Blosser, T. R., et al. (2020) · Nature · doi:10.1038/s41586-020-2504-5 · Cited by 211
Self-citationThalamic reticular nucleus induces fast and local modulation of arousal state
Lewis, L. D., Voigts, J., Flores, F. J., Schmitt, L. I., Wilson, M. A., Halassa, M. M., & Brown, E. N. (2015) · eLife · doi:10.7554/elife.08760 · Cited by 215
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Thalamic reticular impairment underlies attention deficit in Ptchd1Y/− mice
Wells, M. F., Wimmer, R. D., Schmitt, L. I., Feng, G., & Halassa, M. M. (2016) · Nature · doi:10.1038/nature17427 · Cited by 211
Self-citationModels of psychedelic drug action: modulation of cortical-subcortical circuits
Doss, M. K., Madden, M. B., Gaddis, A., Nebel, M. B., Griffiths, R. R., Mathur, B. N., & Barrett, F. S. (2021) · Brain · doi:10.1093/brain/awab406 · Cited by 217
Thalamic subnetworks as units of function
Roy, D. S., Zhang, Y., Halassa, M. M., & Feng, G. (2022) · Nature Neuroscience · doi:10.1038/s41593-021-00996-1 · Cited by 177
Self-citationNeuronal 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
Steullet, P., Cabungcal, J.-H., Bukhari, S. A., Ardelt, M., Pantazopoulos, H., Hamati, F., Salt, T. E., Cuénod, M., Kim, Q., & Berretta, S. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.230 · Cited by 173
Visual Functions of the Thalamus
Usrey, W. M., & Alitto, H. J. (2015) · Annual Review of Vision Science · doi:10.1146/annurev-vision-082114-035920 · Cited by 175
Abnormal sleep spindles, memory consolidation, and schizophrenia
Manoach, D. S., & Stickgold, R. (2019) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-050718-095754 · Cited by 157
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Fogerson, P. M., & Huguenard, J. R. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.024 · Cited by 155
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Zucca, S., D’Urso, G., Pasquale, V., Vecchia, D., Pica, G., Bovetti, S., Moretti, C., Varani, S., Molano‐Mazón, M., Chiappalone, M., et al. (2017) · eLife · doi:10.7554/elife.26177 · Cited by 160
Dual function of thalamic low-vigilance state oscillations: rhythm-regulation and plasticity
Crunelli, V., Lörincz, M. L., Connelly, W. M., David, F., Hughes, S. W., Lambert, R. C., Leresche, N., & Errington, A. C. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.151 · Cited by 131
ErbB4 regulation of a thalamic reticular nucleus circuit for sensory selection
Ahrens, S., Jaramillo, S., Yu, K., Ghosh, S., Hwang, G., Paik, R., Lai, C., He, M., Huang, Z. J., & Li, B. (2014) · Nature Neuroscience · doi:10.1038/nn.3897 · Cited by 129
McCafferty, C. P., David, F., Venzi, M., Lörincz, M. L., Delicata, F., Atherton, Z., Recchia, G. E., Orbán, G., Lambert, R. C., Giovanni, G. D., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0130-4 · Cited by 125
Optogenetic feedback control of neural activity
Newman, J. P., Fong, M., Millard, D. C., Whitmire, C. J., Stanley, G. B., & Potter, S. M. (2015) · eLife · doi:10.7554/elife.07192 · Cited by 123
Zeidan, F., Baumgartner, J. N., & Coghill, R. C. (2019) · PAIN Reports · doi:10.1097/pr9.0000000000000759 · Cited by 115
Thalamic Reticular Dysfunction as a Circuit Endophenotype in Neurodevelopmental Disorders
Krol, A., Wimmer, R. D., Halassa, M. M., & Feng, G. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.021 · Cited by 121
Self-citationFunctional Diversity of Thalamic Reticular Subnetworks
Crabtree, J. W. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00041 · Cited by 124
Reduced sleep spindle activity point to a TRN-MD thalamus-PFC circuit dysfunction in schizophrenia
Ferrarelli, F., & Tononi, G. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.05.023 · Cited by 109
A thalamic bridge from sensory perception to cognition
Wolff, M., Morceau, S., Folkard, R., Martín-Cortecero, J., & Groh, A. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.013 · Cited by 114
Not a single but multiple populations of GABAergic neurons control sleep
Luppi, P., Peyron, C., & Fort, P. (2016) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.03.002 · Cited by 110
Ghodrati, M., Khaligh‐Razavi, S., & Lehky, S. R. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.06.002 · Cited by 107
Regulation of Local Sleep by the Thalamic Reticular Nucleus
Vantomme, G., Osorio-Forero, A., Lüthi, A., & Fernandez, L. M. J. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00576 · Cited by 101
Microglia modulate stable wakefulness via the thalamic reticular nucleus in mice
Liu, H., Wang, X., Chen, L., Chen, L., Tsirka, S. E., Ge, S., & Xiong, Q. (2021) · Nature Communications · doi:10.1038/s41467-021-24915-x · Cited by 99
Turning a Negative into a Positive: Ascending GABAergic Control of Cortical Activation and Arousal
Brown, R. E., & McKenna, J. T. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00135 · Cited by 95
Human neural correlates of sevoflurane-induced unconsciousness
Palanca, B. J. A., Avidan, M. S., & Mashour, G. A. (2017) · British Journal of Anaesthesia · doi:10.1093/bja/aex244 · Cited by 97
A role for spindles in the onset of rapid eye movement sleep
Bandarabadi, M., Herrera, C. G., Gent, T. C., Bassetti, C. L., Schindler, K. A., & Adamantidis, A. (2020) · Nature Communications · doi:10.1038/s41467-020-19076-2 · Cited by 95
Thalamic reticular control of local sleep in mouse sensory cortex
Fernandez, L. M. J., Vantomme, G., Osorio-Forero, A., Cardis, R., Béard, E., & Lüthi, A. (2018) · eLife · doi:10.7554/elife.39111 · Cited by 88
Thankachan, S., Katsuki, F., McKenna, J. T., Yang, C. Z., Shukla, C., Deisseroth, K. A., Uygun, D. S., Strecker, R. E., Brown, R. E., McNally, J. M., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-40398-9 · Cited by 93
The mediodorsal thalamus in executive control
Wolff, M., & Halassa, M. M. (2024) · Neuron · doi:10.1016/j.neuron.2024.01.002 · Cited by 110
Self-citationThe Challenge of Understanding the Brain: Where We Stand in 2015
Lisman, J. E. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.032 · Cited by 92
Ferraris, M., Cassel, J., de Vasconcelos, A. P., Stéphan, A., & Quilichini, P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.025 · Cited by 92
Pratt, J. A., & MORRIS, B. J. (2015) · Journal of Psychopharmacology · doi:10.1177/0269881114565805 · Cited by 83
Baran, B., Karahanoğlu, F. I., Mylonas, D., Demanuele, C., Vangel, M. G., Stickgold, R., Anticevic, A., & Manoach, D. S. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.04.012 · Cited by 82
Thalamic Circuit Mechanisms Link Sensory Processing in Sleep and Attention
Chen, Z. S., Wimmer, R. D., Wilson, M. A., & Halassa, M. M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00083 · Cited by 79
Self-citationCognitive and Physiologic Impacts of the Infraslow Oscillation
Watson, B. O. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00044 · Cited by 74
Electrophysiological signatures of memory reactivation in humans
Schreiner, T., & Staudigl, T. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0293 · Cited by 87
Lack of Intrinsic GABAergic Connections in the Thalamic Reticular Nucleus of the Mouse
Hou, G., Smith, A. G., & Zhang, Z. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0607-16.2016 · Cited by 75
Basal forebrain subcortical projections
Agostinelli, L. J., Geerling, J. C., & Scammell, T. E. (2019) · Brain Structure and Function · doi:10.1007/s00429-018-01820-6 · Cited by 77
A novel cortico-intrathalamic circuit for flight behavior
Dong, P., Wang, H., Shen, X., Jiang, P., Zhu, X., Li, Y., Gao, J., Lin, S., Huang, Y., He, X., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0391-6 · Cited by 71
Yang, M., Logothetis, N. K., & Eschenko, O. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.2107-18.2018 · Cited by 57
Neuroscience: A Distributed Neural Network Controls REM Sleep
Peever, J. H., & Fuller, P. M. (2016) · Current Biology · doi:10.1016/j.cub.2015.11.011 · Cited by 74
Open-loop organization of thalamic reticular nucleus and dorsal thalamus: a computational model
Willis, A. M., Slater, B. J., Gribkova, E., & Llano, D. A. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00926.2014 · Cited by 63
Validation of an automated sleep spindle detection method for mouse electroencephalography
Uygun, D. S., Katsuki, F., Bolortuya, Y., Aguilar, D. D., McKenna, J. T., Thankachan, S., McCarley, R. W., Basheer, R., Brown, R. E., Strecker, R. E., et al. (2018) · SLEEP · doi:10.1093/sleep/zsy218 · Cited by 60
Generation of ventralized human thalamic organoids with thalamic reticular nucleus
Kiral, F. R., Çakır, B., Tanaka, Y., Kim, J., Yang, W. S., Wehbe, F., Kang, Y., Zhong, M., Sancer, G., Lee, S.-H., et al. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.03.007 · Cited by 64
Sleep restores an optimal computational regime in cortical networks
Xu, Y., Schneider, A. M., Weßel, R., & Hengen, K. B. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01536-9 · Cited by 62
Cephalopod Behavior: From Neural Plasticity to Consciousness
Ponte, G., Chiandetti, C., Edelman, D. B., Imperadore, P., Pieroni, E. M., & Fiorito, G. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.787139 · Cited by 66
Corticothalamic feedback sculpts visual spatial integration in mouse thalamus
Born, G., Schneider-Soupiadis, F. A., Erisken, S., Vaičeliūnaitė, A., Lao, C. L., Mobarhan, M. H., Spacek, M. A., Einevoll, G. T., & Busse, L. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00943-0 · Cited by 62
Luppi, P., & Fort, P. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64032-1.00023-0 · Cited by 58
Precise coupling of the thalamic head-direction system to hippocampal ripples
Viejo, G. D., & Peyrache, A. (2020) · Nature Communications · doi:10.1038/s41467-020-15842-4 · Cited by 57
Circuits and components of delta wave regulation
Uygun, D. S., & Basheer, R. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.06.006 · Cited by 60
Campbell, P. W., Govindaiah, G., Masterson, S. P., Bickford, M. E., & Guido, W. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00757.2019 · Cited by 63
Information Coding through Adaptive Gating of Synchronized Thalamic Bursting
Whitmire, C. J., Waiblinger, C., Schwarz, C., & Stanley, G. B. (2016) · Cell Reports · doi:10.1016/j.celrep.2015.12.068 · Cited by 55
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Aizenberg, M., Rolón‐Martínez, S., Pham, T. D., Rao, W., Haas, J. S., & Geffen, M. N. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.050 · Cited by 52
The Contribution of Thalamic Nuclei in Salience Processing
Zhou, K., Zhu, L. L., Hou, G., Chen, X., Chen, B., Yang, C., & Zhu, Y. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.634618 · Cited by 53
Region-selective control of the thalamic reticular nucleus via cortical layer 5 pyramidal cells
Hádinger, N., Bősz, E., Tóth, B., Vantomme, G., Lüthi, A., & Acsády, L. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01217-z · Cited by 54
Wang, X.-Y., Xu, X., Chen, R., Jia, W.-B., Xu, P., Liu, X.-Q., Zhang, Y., Liu, X., & Zhang, Y. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113170 · Cited by 50
Li, J., Li, Z., Wang, X., Liu, Y., Wang, S., Wang, X., Li, Y., & Qin, L. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1166-23.2023 · Cited by 49
Thalamic inhibitory circuits and network activity development
Murata, Y., & Colonnese, M. T. (2018) · Brain Research · doi:10.1016/j.brainres.2018.10.024 · Cited by 53
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Vantomme, G., Rovó, Z., Cardis, R., Béard, E., Katsioudi, G., Guadagno, A., Perrenoud, V., Fernandez, L. M. J., & Lüthi, A. (2019) · Cell Reports · doi:10.1016/j.celrep.2020.107747 · Cited by 45
Variation of connectivity across exemplar sensory and associative thalamocortical loops in the mouse
Mukherjee, A., Bajwa, N., Lam, N. H., Porrero, C., Clascá, F., & Halassa, M. M. (2020) · eLife · doi:10.7554/elife.62554 · Cited by 49
Self-citationCingulate-basal ganglia-thalamo-cortical aspects of catatonia and implications for treatment
Fricchione, G. L., & Beach, S. R. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00012-1 · Cited by 48
Ghoshal, A., Uygun, D. S., Yang, L., McNally, J. M., López-Huerta, V. G., Arias-García, M. A., Báez-Nieto, D., Allen, A., Fitzgerald, M. L., Choi, S., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0685-1 · Cited by 44
Subcortical syntax: Reconsidering the neural dynamics of language
Murphy, E., Hoshi, K., & Benítez‐Burraco, A. (2022) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2022.101062 · Cited by 46
Ang, G., McKillop, L. E., Purple, R. J., Blanco‐Duque, C., Peirson, S. N., Foster, F., Harrison, P. J., Sprengel, R., Davies, K. E., Oliver, P. L., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0199-2 · Cited by 44
Thalamus Controls Development and Expression of Arousal States in Visual Cortex
Murata, Y., & Colonnese, M. T. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1519-18.2018 · Cited by 44
Asymmetric neural dynamics characterize loss and recovery of consciousness
Huang, Z., Tarnal, V., Vlisides, P. E., Janke, E., McKinney, A., Picton, P., Mashour, G. A., & Hudetz, A. G. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118042 · Cited by 43
Heuermann, R. J., Jaramillo, T. C., Ying, S.-W., Suter, B. A., Lyman, K. A., Han, Y. S., Lewis, A. S., Hampton, T., Shepherd, G. M., Goldstein, P. A., et al. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.10.005 · Cited by 44
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Metadata
- Authors
- Halassa, M. M., Chen, Z., Wimmer, R. D., Brunetti, P. M., Zhao, S., Zikopoulos, B., Wang, F., Brown, E. N., & Wilson, M. A.
- Affiliations
- NYU Langone Health (US)
- Massachusetts Institute of Technology (US)
- Duke University (US)
- Boston University (US)
- Harvard University (US)
- Corresponding author
- Halassa, Michael M.
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2014-08
- Volume
- 158
- Issue
- 4
- Pages
- 808-821
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC4205482
- OpenAlex
- W2111911706
- Cited by
- 309
- References
- 79
- Citations by year
- 2026: 28 · 2025: 23 · 2024: 31 · 2023: 22 · 2022: 20 · 2021: 27 · 2020: 24 · 2019: 36 · 2018: 19 · 2017: 28 · 2016: 26 · 2015: 22 · 2014: 3
- FWCI
- 14.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-nd)
- Funders
- National Science Foundation
- National Alliance for Research on Schizophrenia and Depression
- National Institutes of Health
- National Institute of Mental Health (R01MH057414, R25MH094612, R01MH061976, R01MH101209, DP1MH103908)
- National Institute of General Medical Sciences (R01GM104948, TR01-GM10498)
- National Institute of Neurological Disorders and Stroke (R00NS078115, R01NS077986, K99NS078115)
- National Center for Chronic Disease Prevention and Health Promotion (DP1MH103908)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- thalamic reticular nucleus, behavioral state, arousal, sleep spindles, slow waves, attention, sensory projections, neuronal synchronization
- MeSH terms
- Animals, Attention, Behavior, Animal, Cognition, Limbic System, Male, Mice, Inbred C57BL, Thalamic Nuclei, Visual Perception, Mice
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