The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Thalamic amplification of cortical connectivity sustains attentional control
Open accessAbstract
Although interactions between the thalamus and cortex are critical for cognitive function, the exact contribution of the thalamus to these interactions remains unclear. Recent studies have shown diverse connectivity patterns across the thalamus, but whether this diversity translates to thalamic functions beyond relaying information to or between cortical regions is unknown. Here we show, by investigating the representation of two rules used to guide attention in the mouse prefrontal cortex (PFC), that the mediodorsal thalamus sustains these representations without relaying categorical information. Specifically, mediodorsal input amplifies local PFC connectivity, enabling rule-specific neural sequences to emerge and thereby maintain rule representations. Consistent with this notion, broadly enhancing PFC excitability diminishes rule specificity and behavioural performance, whereas enhancing mediodorsal excitability improves both. Overall, our results define a previously unknown principle in neuroscience; thalamic control of functional cortical connectivity. This function, which is dissociable from categorical information relay, indicates that the thalamus has a much broader role in cognition than previously thought.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Thalamic input amplifies PFC connectivity, sustaining attentional control 24 and enabling sensory selection in divided attention 25.”
From Mechanisms of synaptic transmission dysregulation in the prefrontal cortex: pathophysiological implications (2022) · cites this paper as [24]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Neocortical excitation/inhibition balance in information processing and social dysfunction
Yizhar, O., Fenno, L. E., Prigge, M., Schneider, F., Davidson, T. J., O’Shea, D. J., Sohal, V. S., Goshen, I., Finkelstein, J., Paz, J. T., et al. (2011) · Nature · doi:10.1038/nature10360 · Cited by 2,454
Context-dependent computation by recurrent dynamics in prefrontal cortex
Mante, V., Sussillo, D., Shenoy, K. V., & Newsome, W. T. (2013) · Nature · doi:10.1038/nature12742 · Cited by 1,910
Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat
Hoover, W. B., & Vertes, R. P. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0150-4 · Cited by 1,365
The MVGC multivariate Granger causality toolbox: A new approach to Granger-causal inference
Barnett, L., & Seth, A. K. (2013) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2013.10.018 · Cited by 1,038
The pulvinar regulates information transmission between cortical areas based on attention demands
Saalmann, Y. B., Pinsk, M. A., Wang, L., Li, X., & Kastner, S. (2012) · Science · doi:10.1126/science.1223082 · Cited by 1,016
Choice-specific sequences in parietal cortex during a virtual-navigation decision task
Harvey, C. D., Coen, P., & Tank, D. W. (2012) · Nature · doi:10.1038/nature10918 · Cited by 951
Barthó, P., Hirase, H., Monconduit, L., Zugaro, M., Harris, K. D., & Buzsáki, G. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01170.2003 · Cited by 912
Gamma and Beta Bursts Underlie Working Memory
Lundqvist, M., Rose, J., Herman, P., Brincat, S. L., Buschman, T. J., & Miller, E. K. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.028 · Cited by 846
Synfire Chains and Cortical Songs: Temporal Modules of Cortical Activity
Ikegaya, Y., Aaron, G., Cossart, R., Aronov, D., Lampl, I., Ferster, D., & Yuste, R. (2004) · Science · doi:10.1126/science.1093173 · Cited by 838
Thalamus plays a central role in ongoing cortical functioning
Sherman, S. M. (2016) · Nature Neuroscience · doi:10.1038/nn.4269 · Cited by 809
Research works printed but not linked: 1
- Duda, R. O ., Hart, P. E. & Stork, D. G. Pattern Classification Vol. 18 (Wiley, 2001)
Cited by
Sorted by citations
Single-trial neural dynamics are dominated by richly varied movements
Musall, S., Kaufman, M. T., Juavinett, A., Gluf, S., & Churchland, A. K. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0502-4 · Cited by 1,102
Predictive Processing: A Canonical Cortical Computation
Keller, G. B., & Mrsic-Flogel, T. D. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.003 · Cited by 836
Miller, E. K., Lundqvist, M., & Bastos, A. M. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.023 · Cited by 797
Ferguson, B. R., & Gao, W.-J. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00037 · Cited by 594
Thalamic projections sustain prefrontal activity during working memory maintenance
Bolkan, S. S., Stujenske, J. M., Parnaudeau, S., Spellman, T., Rauffenbart, C., Abbas, A. I., Harris, A. Z., Gordon, J. A., & Kellendonk, C. (2017) · Nature Neuroscience · doi:10.1038/nn.4568 · Cited by 547
Thalamic functions in distributed cognitive control
Halassa, M. M., & Kästner, S. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0020-1 · Cited by 540
Self-citationThalamus Modulates Consciousness via Layer-Specific Control of Cortex
Redinbaugh, M. J., Phillips, J. M., Kambi, N. A., Mohanta, S., Andryk, S., Dooley, G. L., Afrasiabi, M., Raz, A., & Saalmann, Y. B. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.005 · Cited by 391
General anesthesia decouples cortical pyramidal neurons
Suzuki, M., & Larkum, M. E. (2020) · Cell · doi:10.1016/j.cell.2020.01.024 · Cited by 348
Neural mechanisms of movement planning: motor cortex and beyond
Svoboda, K., & Li, N. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.10.023 · Cited by 347
The Cognitive Thalamus as a Gateway to Mental Representations
Wolff, M., & Vann, S. D. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0479-18.2018 · Cited by 364
Thalamocortical Circuit Motifs: A General Framework
Halassa, M. M., & Sherman, S. M. (2019) · Neuron · doi:10.1016/j.neuron.2019.06.005 · Cited by 322
Self-citationCircuit organization of the rodent medial prefrontal cortex
Anastasiades, P. G., & Carter, A. G. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.03.006 · Cited by 314
The impact of the human thalamus on brain-wide information processing
Shine, J. M., Lewis, L. D., Garrett, D. D., & Hwang, K. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00701-0 · Cited by 335
Thalamic regulation of switching between cortical representations enables cognitive flexibility
Rikhye, R. V., Gilra, A., & Halassa, M. M. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0269-z · Cited by 324
Self-citationYan, Z., & Rein, B. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01092-3 · Cited by 300
Working Memory: Delay Activity, Yes! Persistent Activity? Maybe Not
Lundqvist, M., Herman, P. A., & Miller, E. K. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2485-17.2018 · Cited by 298
The 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
The form and function of channelrhodopsin
Deisseroth, K. A., & Hegemann, P. (2017) · Science · doi:10.1126/science.aan5544 · Cited by 297
Flexible Sensorimotor Computations through Rapid Reconfiguration of Cortical Dynamics
Remington, E. D., Narain, D., Hosseini, E. A., & Jazayeri, M. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.020 · Cited by 257
Thalamic dual control of sleep and wakefulness
Gent, T. C., Bandarabadi, M., Herrera, C. G., & Adamantidis, A. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0164-7 · Cited by 255
The role of population structure in computations through neural dynamics
Dubreuil, A., Valente, A., Beiran, M., Mastrogiuseppe, F., & Ostojic, S. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01088-4 · Cited by 237
Thalamic control of functional cortical connectivity
Nakajima, M., & Halassa, M. M. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.04.001 · Cited by 237
Self-citationReciprocal Circuits Linking the Prefrontal Cortex with Dorsal and Ventral Thalamic Nuclei
Collins, D. P., Anastasiades, P. G., Marlin, J. J., & Carter, A. G. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.024 · Cited by 247
Smucny, J., Dienel, S. J., Lewis, D. A., & Carter, C. S. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01089-0 · Cited by 231
Dynamic salience processing in paraventricular thalamus gates associative learning
Zhu, Y., Nachtrab, G. T., Keyes, P. C., Allen, W. E., Luo, L., & Chen, X. (2018) · Science · doi:10.1126/science.aat0481 · Cited by 220
Distinct 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-citationThe mouse prefrontal cortex: Unity in diversity
Le Merre, P., Ährlund-Richter, S., & Carlén, M. (2021) · Neuron · doi:10.1016/j.neuron.2021.03.035 · Cited by 207
A midbrain-thalamus-cortex circuit reorganizes cortical dynamics to initiate movement
Inagaki, H., Chen, S., Ridder, M. C., Sah, P., Li, N., Yang, Z., Hasanbegović, H., Gao, Z., Gerfen, C. R., & Svoboda, K. (2022) · Cell · doi:10.1016/j.cell.2022.02.006 · Cited by 209
The Regulatory Role of the Human Mediodorsal Thalamus
Pergola, G., Danet, L., Pitel, A., Carlesimo, G. A., Segobin, S. H., Pariente, J., Boris Suchan, A., Mitchell, A. S., & Barbeau, E. J. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.08.006 · Cited by 213
Clinical and experimental insight into pathophysiology, comorbidity and therapy of absence seizures
Crunelli, V., Lörincz, M. L., McCafferty, C. P., Lambert, R. C., Leresche, N., Giovanni, G. D., & David, F. (2020) · Brain · doi:10.1093/brain/awaa072 · Cited by 213
Prefrontal Cortex Regulates Sensory Filtering through a Basal Ganglia-to-Thalamus Pathway
Nakajima, M., Schmitt, L. I., & Halassa, M. M. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.026 · Cited by 218
Self-citationPrefrontal-Thalamic Anatomical Connectivity and Executive Cognitive Function in Schizophrenia
Giraldo‐Chica, M., Rogers, B. P., Damon, S. M., Landman, B. A., & Woodward, N. D. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.09.022 · Cited by 194
Ferguson, B. R., & Gao, W.-J. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.033 · Cited by 186
How do memory systems detect and respond to novelty?
Kafkas, A., & Montaldi, D. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.01.053 · Cited by 207
Brain-wide Electrical Spatiotemporal Dynamics Encode Depression Vulnerability
Hultman, R., Ulrich, K., Sachs, B. D., Blount, C., Carlson, D. E., Ndubuizu, N., Bagot, R. C., Parise, E. M., Vu, M.-A. T., Gallagher, N. M., et al. (2018) · Cell · doi:10.1016/j.cell.2018.02.012 · Cited by 183
Abbas, A. I., Sundiang, M. J. M., Henoch, B., Morton, M. P., Bolkan, S. S., Park, A. J., Harris, A. Z., Kellendonk, C., & Gordon, J. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.029 · Cited by 183
Cerebellar contribution to preparatory activity in motor neocortex
Chabrol, F. P., Blot, A., & Mrsic-Flogel, T. D. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.022 · Cited by 182
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-citationMeda, K., Patel, T., Braz, J. M., Malik, R., Turner, M., Seifikar, H., Basbaum, A. I., & Sohal, V. S. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.042 · Cited by 180
Thalamic control of cortical dynamics in a model of flexible motor sequencing
Logiaco, L., Abbott, L. F., & Escola, G. S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109090 · Cited by 173
The locus coeruleus drives disinhibition in the midline thalamus via a dopaminergic mechanism
Beas, B. S., Wright, B. J., Skirzewski, M., Leng, Y., Hyun, J. H., Koita, O., Ringelberg, N. W., Kwon, H., Buonanno, A., & Penzo, M. A. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0167-4 · Cited by 163
Subset of Cortical Layer 6b Neurons Selectively Innervates Higher Order Thalamic Nuclei in Mice
Hoerder‐Suabedissen, A., Hayashi, S., Upton, L., Nolan, Z. T., Casas-Torremocha, D., Grant, E., Viswanathan, S., Kanold, P. O., Clascá, F., Kim, Y., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy036 · Cited by 162
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 166
Shine, J. M. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101951 · Cited by 171
Toward an Integrative Theory of Thalamic Function
Rikhye, R. V., Wimmer, R. D., & Halassa, M. M. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080317-062144 · Cited by 164
Self-citationThe what, where and how of delay activity
Sreenivasan, K. K., & D’Esposito, M. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0176-7 · Cited by 168
Higher-Order Thalamic Circuits Channel Parallel Streams of Visual Information in Mice
Bennett, C., Gale, S. D., Garrett, M., Newton, M. L., Callaway, E. M., Murphy, G. J., & Olsen, S. R. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.010 · Cited by 166
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
Ouhaz, Z., Fleming, H., & Mitchell, A. S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00033 · Cited by 142
Beyond Trial-Based Paradigms: Continuous Behavior, Ongoing Neural Activity, and Natural Stimuli
Huk, A. C., Bonnen, K., & He, B. J. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1920-17.2018 · Cited by 149
A diverse range of factors affect the nature of neural representations underlying short-term memory
Orhan, A. E., & Ma, W. J. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0314-y · Cited by 136
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 139
Advances in understanding neural mechanisms of social dominance
Zhou, T., Sandi, C., & Hu, H. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.01.006 · Cited by 133
Thalamic circuits for independent control of prefrontal signal and noise
Mukherjee, A., Lam, N. H., Wimmer, R. D., & Halassa, M. M. (2021) · Nature · doi:10.1038/s41586-021-04056-3 · Cited by 128
Self-citationMcCafferty, 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
Functional Diversity of Thalamic Reticular Subnetworks
Crabtree, J. W. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00041 · Cited by 124
Differential Encoding in Prefrontal Cortex Projection Neuron Classes Across Cognitive Tasks
Lui, J. H., Nguyen, N. D., Grutzner, S. M., Darmanis, S., Peixoto, D., Wagner, M. J., Allen, W. E., Kebschull, J. M., Richman, E. B., Ren, J., et al. (2020) · Cell · doi:10.1016/j.cell.2020.11.046 · Cited by 124
Regulation of cortical activity and arousal by the matrix cells of the ventromedial thalamic nucleus
Honjoh, S., Sasai, S., Schiereck, S. S., Nagai, H., Tononi, G., & Cirelli, C. (2018) · Nature Communications · doi:10.1038/s41467-018-04497-x · Cited by 118
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-citationCore and matrix thalamic sub-populations relate to spatio-temporal cortical connectivity gradients
Müller, E. J., Munn, B., Hearne, L. J., Smith, J. B., Fulcher, B., Arnatkevičiūtė, A., Lurie, D. J., Cocchi, L., & Shine, J. M. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117224 · Cited by 119
White matter tracts and executive functions: a review of causal and correlation evidence
Ribeiro, M., Yordanova, Y. N., Noblet, V., Herbet, G., & Ricard, D. (2023) · Brain · doi:10.1093/brain/awad308 · Cited by 125
Prefrontal deep projection neurons enable cognitive flexibility via persistent feedback monitoring
Spellman, T., Svei, M., Kaminsky, J. C., Manzano-Nieves, G., & Liston, C. M. (2021) · Cell · doi:10.1016/j.cell.2021.03.047 · Cited by 123
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
The Parvalbumin Hypothesis of Autism Spectrum Disorder
Filice, F., Janickova, L., Henzi, T., Bilella, A., & Schwaller, B. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.577525 · Cited by 118
Low-dimensional and monotonic preparatory activity in mouse anterior lateral motor cortex
Inagaki, H. K., Inagaki, M., Romani, S., & Svoboda, K. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.3152-17.2018 · Cited by 111
“Such sequences have been reported during motor planning and other kinds of short-term memory in the premotor cortex, the mPFC, the posterior parietal cortex, and the hippocampus of rodents (Harvey et al., 2012; Buzsáki and Moser, 2013; Murakami et al., 2014; Schmitt et al., 2017).”
BackgroundGrodd, W., Kumar, V., Schüz, A., Lindig, T. M., & Scheffler, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-67770-4 · Cited by 115
Paradoxical somatodendritic decoupling supports cortical plasticity during REM sleep
Aime, M., Calcini, N., Borsa, M., Campelo, T., Rusterholz, T., Sattin, A., Fellin, T., & Adamantidis, A. (2022) · Science · doi:10.1126/science.abk2734 · Cited by 106
Thalamic contributions to the state and contents of consciousness
Whyte, C. J., Redinbaugh, M. J., Shine, J. M., & Saalmann, Y. B. (2024) · Neuron · doi:10.1016/j.neuron.2024.04.019 · Cited by 105
Thalamocortical excitability modulation guides human perception under uncertainty
Kosciessa, J. Q., Lindenberger, U., & Garrett, D. D. (2021) · Nature Communications · doi:10.1038/s41467-021-22511-7 · Cited by 102
Alcaraz, F., Fresno, V., Marchand, A. R., Kremer, E. J., Coutureau, É., & Wolff, M. (2018) · eLife · doi:10.7554/elife.32517 · Cited by 108
Theodorakopoulos, L., Theodoropoulou, A., & Klavdianos, C. (2025) · Journal of theoretical and applied electronic commerce research · doi:10.3390/jtaer20020115 · Cited by 111
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-citationKang, L., Zhang, A., Sun, N., Liu, P., Yang, C., Li, G., Liu, Z., Wang, Y., & Zhang, K. (2018) · BMC Psychiatry · doi:10.1186/s12888-018-1913-6 · Cited by 94
Consciousness depends on integration between parietal cortex, striatum, and thalamus
Afrasiabi, M., Redinbaugh, M. J., Phillips, J. M., Kambi, N. A., Mohanta, S., Raz, A., Haun, A., & Saalmann, Y. B. (2021) · Cell Systems · doi:10.1016/j.cels.2021.02.003 · Cited by 95
Thalamus-related anomalies as candidate mechanism-based biomarkers for psychosis
Steullet, P. (2019) · Schizophrenia Research · doi:10.1016/j.schres.2019.05.027 · Cited by 90
Liu, J., Chen, L., Chen, X., Hu, K., Tu, Y., Lin, M., Huang, J., Liu, W., Wu, J., Qiu, Z., et al. (2019) · British Journal of Anaesthesia · doi:10.1016/j.bja.2019.06.017 · Cited by 90
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
Dopamine tunes prefrontal outputs to orchestrate aversive processing
Weele, C. M. V., Siciliano, C. A., & Tye, K. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.044 · Cited by 98
de Kloet, S. F., Bruinsma, B., Terra, H., Heistek, T. S., Passchier, E. M. J., van den Berg, A. R., Luchicchi, A., Min, R., Pattij, T., & Mansvelder, H. D. (2021) · Nature Communications · doi:10.1038/s41467-021-22260-7 · Cited by 100
Thalamus-driven functional populations in frontal cortex support decision-making
Yang, W., Tipparaju, S. L., Chen, G., & Li, N. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01171-w · Cited by 82
Anastasiades, P. G., Marlin, J. J., & Carter, A. G. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.073 · Cited by 90
Thalamus and focal to bilateral seizures
Caciagli, L., Allen, L. A., He, X., Trimmel, K., Vos, S. B., Centeno, M., Galovic, M., Sidhu, M. K., Thompson, P. J., Bassett, D. S., et al. (2020) · Neurology · doi:10.1212/wnl.0000000000010645 · Cited by 85
Chen, P., Ye, E., Jin, X., Zhu, Y., & Wang, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-39367-z · Cited by 85
Decision-making behaviors: weighing ethology, complexity, and sensorimotor compatibility
Juavinett, A. L., Erlich, J. C., & Churchland, A. K. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.11.001 · Cited by 82
Contextual signals in visual cortex
Khan, A. G., & Hofer, S. B. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.05.003 · Cited by 83
Neural Algorithms and Circuits for Motor Planning
Inagaki, H., Chen, S., Daie, K., Finkelstein, A., Fontolan, L., Romani, S., & Svoboda, K. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092021-121730 · Cited by 77
Pyramidal Cell Subtypes and Their Synaptic Connections in Layer 5 of Rat Frontal Cortex
Kawaguchi, Y. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx252 · Cited by 85
Sensation during Active Behaviors
Busse, L., Cardin, J. A., Chiappe, M. E., Halassa, M. M., McGinley, M. J., Yamashita, T., & Saleem, A. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1828-17.2017 · Cited by 84
Self-citationHow deep is the brain? The shallow brain hypothesis
Suzuki, M., Pennartz, C. M. A., & Aru, J. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00756-z · Cited by 79
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
Solved problems for Granger causality in neuroscience: A response to Stokes and Purdon
Barnett, L., Barrett, A. B., & Seth, A. K. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.05.067 · Cited by 73
Metastable attractors explain the variable timing of stable behavioral action sequences
Recanatesi, S., Pereira, U., Murakami, M., Mainen, Z. F., & Mazzucato, L. (2021) · Neuron · doi:10.1016/j.neuron.2021.10.011 · Cited by 76
Towards a pluralistic neurobiological understanding of consciousness
He, B. J. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.02.001 · Cited by 78
Resolving the prefrontal mechanisms of adaptive cognitive behaviors: A cross-species perspective
Hanganu‐Opatz, I. L., Klausberger, T., Sigurdsson, T., Nieder, A., Jacob, S. N., Bartos, M., Sauer, J., Durstewitz, D., Leibold, C., & Diester, I. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.017 · Cited by 79
Corticocortical Systems Underlying High-Order Motor Control
Battaglia‐Mayer, A., & Caminiti, R. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2094-18.2019 · Cited by 75
He, L., Li, H., Wang, J., Chen, M., Gozdas, E., Dillman, J. R., & Parikh, N. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-71914-x · Cited by 75
Cortical-subcortical interactions in goal-directed behavior
Cruz, K. G., Leow, Y. N., Le, N. M., Adam, E. M., Huda, R., & Sur, M. (2022) · Physiological Reviews · doi:10.1152/physrev.00048.2021 · Cited by 76
Nguyen, R., Venkatesan, S., Binko, M. A., Bang, J. Y., Cajanding, J. D., Briggs, C., Sargin, D., Imayoshi, I., Lambe, E. K., & Kim, J. C. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1919-19.2020 · Cited by 72
Antunes, F. M., & Malmierca, M. S. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.721186 · Cited by 71
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
Metadata
- Authors
- Schmitt, L. I., Wimmer, R. D., Nakajima, M., Happ, M., Mofakham, S., & Halassa, M. M.
- Affiliations
- NYU Langone Health (US)
- Corresponding author
- Halassa, Michael M.
- Venue
- Nature
- Published
- 2017-05
- Volume
- 545
- Issue
- 7653
- Pages
- 219-223
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5570520
- OpenAlex
- W2611485120
- Cited by
- 663
- References
- 42
- Citations by year
- 2026: 51 · 2025: 64 · 2024: 62 · 2023: 64 · 2022: 72 · 2021: 90 · 2020: 66 · 2019: 64 · 2018: 105 · 2017: 24
- FWCI
- 40.67
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Mental Health (R01MH107680)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- mediodorsal thalamus, prefrontal cortex, cortical connectivity, attentional control, rule representation, thalamocortical interactions, neural sequences, persistent activity
- MeSH terms
- Animals, Attention, Cognition, Male, Neural Pathways, Thalamus, Prefrontal Cortex, Mice, Optogenetics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review