The DOI matches its Crossref record; 131 of the 131 references it cites were found in a registry or an index.
Thalamic subnetworks as units of function
Open accessAbstract
The thalamus engages in various functions including sensory processing, attention, decision making and memory. Classically, this diversity of function has been attributed to the nuclear organization of the thalamus, with each nucleus performing a well-defined function. Here, we highlight recent studies that used state-of-the-art expression profiling, which have revealed gene expression gradients at the single-cell level within and across thalamic nuclei. These gradients, combined with anatomical tracing and physiological analyses, point to previously unappreciated heterogeneity and redefine thalamic units of function on the basis of unique input-output connectivity patterns and gene expression. We propose that thalamic subnetworks, defined by the intersection of genetics, connectivity and computation, provide a more appropriate level of functional description; this notion is supported by behavioral phenotypes resulting from appropriately tailored perturbations. We provide several examples of thalamic subnetworks and suggest how this new perspective may both propel progress in basic neuroscience and reveal unique targets with therapeutic potential.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“subtype 4 specifically targets the thalamus (Fig. 2C), likely participating in the transmission and processing of sensory information to regulate attention, consciousness, and sensory perception [32,33].”
From The Insular Cortex: An Interface Between Sensation, Emotion and Cognition (2024) · cites this paper as [33]
Experimental — accuracy not yet measured
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
Genome-wide atlas of gene expression in the adult mouse brain
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572
Molecular diversity and specializations among the cells of the adult mouse brain
Saunders, A., Macosko, E. Z., Wysoker, A., Goldman, M., Krienen, F. M., de Rivera, H., Bien, E., Baum, M., Bortolin, L., Wang, S., et al. (2018) · Cell · doi:10.1016/j.cell.2018.07.028 · Cited by 1,531
Swanson, L. W., & Hartman, B. K. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630406 · Cited by 1,475
Integrative single-cell analysis
Stuart, T., & Satija, R. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-019-0093-7 · Cited by 1,460
Electrophysiological properties of guinea‐pig thalamic neurones: an in vitro study.
Jahnsen, H., & Llinás, R. R. (1984) · Journal of Physiology · doi:10.1113/jphysiol.1984.sp015153 · Cited by 1,213
Jones, E. G. (1985) · Springer eBooks · doi:10.1007/978-1-4615-1749-8 · Cited by 1,164
Lindvall, O., & Björklund, A. (1974) · PubMed · Cited by 1,131
Immunohistochemical evidence for the existence of adrenaline neurons in the rat brain
Ho¨kfelt, T., Fuxé, K., Goldstein, M., & Johansson, O. (1974) · Brain Research · doi:10.1016/0006-8993(74)90143-7 · Cited by 1,093
Jahnsen, H., & Llinas, R. H. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015154 · Cited by 1,081
Puelles, L., Kuwana, E., Puelles, E., Bulfone, A., Shimamura, K., Keleher, J., Smiga, S., & Rubenstein, J. L. R. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000828)424:3 · Cited by 951
Research works printed but not linked: 3
- Jones, E. G. The Thalamus (Cambridge Univ. Press, 2007).
- Tello, F. Disposicion macroscopica y estructura del cuerpo geniculado externo. Trabajos Lab. Invest. Biol. Madr. 3, 39–62 (1904).
- Lorente de No, R. Cerebral Cortex: Architecture, Intracortical Connections, Motor Projections (Oxford Univ. Press, 1938).
Cited by
Sorted by citations
Roy, D. S., Park, Y.-G., Kim, M. E., Zhang, Y., Ogawa, S. K., DiNapoli, N., Gu, X., Cho, J. H., Choi, H., Kamentsky, L. D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29384-4 · Cited by 253
Self-citationThe Insular Cortex: An Interface Between Sensation, Emotion and Cognition
Zhang, R., Deng, H., & Xiao, X. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01211-4 · Cited by 158
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-citationHuman high-order thalamic nuclei gate conscious perception through the thalamofrontal loop
Fang, Z., Dang, Y., Ping, A., Wang, C., Zhao, Q., Zhao, H., Li, X., & Zhang, M. (2025) · Science · doi:10.1126/science.adr3675 · Cited by 73
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
Zhao, J., Liu, C., Zhang, F., Zheng, Z., Luo, F., Xia, J., Wang, Y., Zhang, Z., Tang, J., Song, Z., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111824 · Cited by 56
Sleep and vigilance states: Embracing spatiotemporal dynamics
Nir, Y., & de Lecea, L. (2023) · Neuron · doi:10.1016/j.neuron.2023.04.012 · Cited by 52
Molecular and spatial profiling of the paraventricular nucleus of the thalamus
Gao, C., Gohel, C., Leng, Y., Ma, J., Goldman, D. A., Levine, A. J., & Penzo, M. A. (2023) · eLife · doi:10.7554/elife.81818 · Cited by 49
Shin, D. S., Kim, C. N., Ross, J. M., Hennick, K. M., Wu, S., Paranjape, N., Leonard, R., Wang, J. C., Keefe, M. G., Pavlovic, B. J., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.01.010 · Cited by 48
A neural signature for the subjective experience of threat anticipation under uncertainty
Liu, X., Jiao, G., Zhou, F., Kendrick, K. M., Yao, D., Gong, Q., Xiang, S., Jia, T., Zhang, X., Zhang, J., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45433-6 · Cited by 45
Anterior thalamic circuits crucial for working memory
Roy, D. S., Zhang, Y., Aida, T., Shen, C.-J., Skaggs, K. M., Hou, Y., Fleishman, M., Mosto, O., Weninger, A., & Feng, G. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2118712119 · Cited by 42
Self-citationLi, D., Li, Y., Zhu, Z.-Y., Zhang, F., Zhao, Q., Jiang, J.-H., Shen, B., Tang, Y., & Xu, G. (2025) · Neuron · doi:10.1016/j.neuron.2025.04.019 · Cited by 42
Proprioception: A New Era Set in Motion by Emerging Genetic and Bionic Strategies?
Marasco, P. D., & de Nooij, J. C. (2022) · Annual Review of Physiology · doi:10.1146/annurev-physiol-040122-081302 · Cited by 52
Exploring human brain development and disease using assembloids
Wu, S., & Nowakowski, T. J. (2025) · Neuron · doi:10.1016/j.neuron.2025.02.010 · Cited by 36
Yang, W. F. Z., Sparby, T., Wright, M., Kim, E., & Sacchet, M. D. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e31223 · Cited by 34
Thalamocortical architectures for flexible cognition and efficient learning
Scott, D. N., Mukherjee, A., Nassar, M. R., & Halassa, M. M. (2024) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2024.05.006 · Cited by 37
Self-citationA phylogenetically-conserved axis of thalamocortical connectivity in the human brain
Oldham, S., & Ball, G. (2023) · Nature Communications · doi:10.1038/s41467-023-41722-8 · Cited by 34
Shima, Y., Skibbe, H., Sasagawa, Y., Fujimori, N., Iwayama, Y., Isomura-Matoba, A., Yano, M., Ichikawa, T., Nikaido, I., Hattori, N., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113309 · Cited by 34
The thalamic reticular nucleus orchestrates social memory
Wang, F., Sun, H., Chen, M., Feng, B., Lu, Y., Lyu, M., Cui, D., Zhai, Y., Zhang, Y., Zhu, Y., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.04.013 · Cited by 28
Self-citationMukherjee, A., & Halassa, M. M. (2022) · The Neuroscientist · doi:10.1177/10738584221112861 · Cited by 25
Self-citationNeuronal diversity and stereotypy at multiple scales through whole brain morphometry
Liu, Y., Jiang, S., Li, Y., Zhao, S., Yun, Z., Zhao, Z.-H., Zhang, L., Wang, G., Chen, X., Manubens-Gil, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54745-6 · Cited by 26
The Role of the Thalamus in Nociception: Important but Forgotten
Galdino, G., Veras, F. P., & dos Anjos‐Garcia, T. (2024) · Brain Sciences · doi:10.3390/brainsci14080741 · Cited by 24
Halliday, A. R., Vucic, S. N., Georges, B., LaRoche, M., Mendoza Pardo, M. A., Swiggard, L. O., McDonald, K., Olofsson, M., Menon, S. N., Francis, S. M., et al. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1474003 · Cited by 20
Thalamocortical Mechanisms Underlying Real and Imagined Acupuncture
Kong, Q., Saccà, V., Walker, K. L., Hodges, S., & Kong, J. (2023) · Biomedicines · doi:10.3390/biomedicines11071830 · Cited by 20
The Evolved Mind and Modern Education
Geary, D. C. (2024) · Cambridge University Press eBooks · doi:10.1017/9781009454858 · Cited by 19
Deng, J. F., Chen, L., Liu, C., Liu, M., Guo, G., Wei, J., Zhang, J., Fan, H.-T., Zheng, Z., Yan, P., et al. (2024) · Advanced Science · doi:10.1002/advs.202401855 · Cited by 18
Czekus, C., Steullet, P., López, A. O., Bozic, I., Rusterholz, T., Bandarabadi, M., Kim, Q., & Herrera, C. G. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01700-w · Cited by 18
Frustrative Nonreward: Behavior, Circuits, Neurochemistry, and Disorders
Papini, M. R., Green, T. A., Contreras, Y. M. M., Torres, C., Ogawa, M., & Li, Z. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1021-24.2024 · Cited by 18
A prefrontal thalamocortical readout for conflict-related executive dysfunction in schizophrenia
Huang, A., Wimmer, R. D., Lam, N. H., Wang, B., Suresh, S., Roeske, M. J., Pleger, B., Halassa, M. M., & Woodward, N. D. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101802 · Cited by 18
Self-citationChibaatar, E., Watanabe, K., Okamoto, N., Orkhonselenge, N., Natsuyama, T., Hayakawa, G., Ikenouchi, A., Kakeda, S., & Yoshimura, R. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1151551 · Cited by 16
Zhang, Z., Huang, Y., Chen, X., Li, J., Yang, Y., Lv, L., Wang, J., Wang, M., Wang, Y., & Wang, Z. (2024) · Advanced Science · doi:10.1002/advs.202402718 · Cited by 15
Mediodorsal thalamus regulates task uncertainty to enable cognitive flexibility
Zhang, X., Mukherjee, A., Halassa, M. M., & Chen, Z. S. (2025) · Nature Communications · doi:10.1038/s41467-025-58011-1 · Cited by 19
Self-citationDai, L., Mai, J.-W., Deng, J., Chen, L., Fan, H.-T., Zhang, W.-L., Xin, W., Feng, X., Xu, T. S., & Luo, D. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106699 · Cited by 14
Whiteside, D. J., Street, D., Murley, A. G., Jones, P. S., Malpetti, M., Ghosh, B. C. P., Coyle-Gilchrist, I. T. S., Gerhard, A., Hu, M. T., Klein, J. C., et al. (2023) · Human Brain Mapping · doi:10.1002/hbm.26342 · Cited by 14
Yu, T., Zou, Y., Nie, H., Li, Y., Chen, J., Du, Y., Peng, H., & Luo, Q. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.11.074 · Cited by 13
Fredericksen, K. E., & Samuelsen, C. L. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0674-22.2022 · Cited by 15
Whole-brain Mapping of Inputs and Outputs of Specific Orbitofrontal Cortical Neurons in Mice
Zhang, Y., Zhang, W., Wang, L., Liu, D., Xie, T., Le, Z., Li, X., Gong, H., Xu, X., Xu, M., et al. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01229-8 · Cited by 12
Self-citationLiu, D., Xu, F.-X., Yu, Z., Huang, X., Zhu, Y.-B., Wang, L.-J., Wu, C., Zhang, X., Cao, J., & Li, J. (2025) · Journal of Clinical Investigation · doi:10.1172/jci191270 · Cited by 14
Distinct subnetworks of the mouse anterior thalamic nuclei
Hintiryan, H., Rudd, M., Nanda, S., Gutierrez, A. E., Lo, D., Boesen, T., Garcia, L., Sun, J., Estrada, C., Mun, H.-S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60774-6 · Cited by 11
Thalamic pathways mediating motor and non-motor symptoms in a Parkinson’s disease model
Xiao, B., & Tan, E. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.09.004 · Cited by 11
Mapping whole brain effects of infrared neural stimulation with positron emission tomography
Meneghetti, M., Gudmundsen, F., Jessen, N. S., Sui, K., Baun, C., Palner, M., & Markos, C. (2023) · Imaging Neuroscience · doi:10.1162/imag_a_00052 · Cited by 12
Non-homogenous axonal bouton distribution in whole-brain single-cell neuronal networks
Qian, P., Manubens-Gil, L., Jiang, S., & Peng, H. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113871 · Cited by 8
Dissection of the long-range circuit of the mouse intermediate retrosplenial cortex
Li, Y., Ren, M., Liu, B., Jiang, T., Jia, X., Zhang, H., Gong, H., & Wang, X. (2025) · Communications Biology · doi:10.1038/s42003-025-07463-8 · Cited by 9
Shiraishi, H., Egawa, K., Murakami, K., Nakajima, M., Ueda, Y., Nakakubo, S., Narugami, M., Kimura, S., Goto, T., Hiramatsu, Y., et al. (2023) · Brain and Development · doi:10.1016/j.braindev.2023.08.007 · Cited by 9
Zhang, P., He, Z., Mao, Y., Sun, R., Qu, Y., Chen, L., Ma, P., Yin, S., Yin, T., & Zeng, F. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1001557 · Cited by 8
Structural network-specific effect of extreme capsule stimulation for drug-resistant focal epilepsy
Cheng, Y., Wang, D., Zhang, X., Jin, G., Wu, D., Wang, Q., Du, J., Qi, L., Xu, C., Qiao, Z., et al. (2025) · Brain · doi:10.1093/brain/awaf097 · Cited by 8
The unique role of the associative thalamus in cognitive processing
Wang, B., Li, S., Halassa, M. M., & Pleger, B. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111432 · Cited by 8
Self-citationDai, Y., Hu, J., Wang, Q., Qiao, J., Tian, Y., Li, C., Chen, J., Zhao, F., Li, X., Liu, C., et al. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70514 · Cited by 8
Zhou, W., Xie, X., Hu, J., Wang, M., Hu, X., Shi, L., Zhou, C., & Sun, X. (2023) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.28781 · Cited by 7
Perinatal development of structural thalamocortical connectivity
Oldham, S., Sina Mansour, L., & Ball, G. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00418 · Cited by 7
Deciphering consciousness: The role of corticothalamocortical interactions in general anesthesia
Zhou, Y., Huang, S., Zhang, T., Deng, D., Huang, L., & Chen, X. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107593 · Cited by 7
Mapping the pain pathway: The VPL–S1HL–ACC circuit's role in central post-stroke pain
Li, P., Lu, C., Wang, M., Mao, Y., Wang, X., Liu, Y., Zhang, J., & Zhao, S. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111406 · Cited by 7
Zheng, Y., Wang, P., Yao, C., Wang, J., Wang, J., & Xue, S. (2025) · Human Brain Mapping · doi:10.1002/hbm.70249 · Cited by 7
Learning Temporal Relationships Between Symbols with Laplace Neural Manifolds
Howard, M. W., Esfahani, Z. G., Le, B., & Sederberg, P. B. (2024) · Computational Brain & Behavior · doi:10.1007/s42113-024-00230-8 · Cited by 11
Haubrich, J., Vera, L. D., & Manahan‐Vaughan, D. (2025) · Scientific Reports · doi:10.1038/s41598-025-93263-3 · Cited by 7
Ma, L., Tao, Q., Dang, J., Sun, J., Niu, X., Zhang, M., Kang, Y., Wang, W., Cheng, J., & Zhang, Y. (2025) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2025.1403604 · Cited by 7
Self-citationA parallel tonotopically arranged thalamocortical circuit for sound processing
Zhao, Z., Tang, X., Chen, Y., Tao, J., Polat, M., Yang, Z., Yang, L., Wang, M., Liang, S., Zhang, K., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.03.022 · Cited by 6
Self-citationLuo, S., Wang, Y., He, M., Wen, Q., Wang, S., Cao, J., & Chen, Q. (2025) · BMJ Mental Health · doi:10.1136/bmjment-2024-301142 · Cited by 7
Gustatory thalamic neurons mediate aversive behaviors
Cao, F., Park, S., Pauli, J. L., Seo, E. Y., Nguyen, A.-D., & Palmiter, R. D. (2025) · Nature Communications · doi:10.1038/s41467-025-63464-5 · Cited by 8
An opposing molecular gradient axis underlies primate cortical organization
Huang, Z. R., Yang, Q., Li, S., Zhu, X., Wang, H., Lin, J., Zhan, Y., Wu, Y. H., Wang, Z.-H., Majka, P., et al. (2026) · Science · doi:10.1126/science.aea2673 · Cited by 8
Functional connectivity alterations in the thalamus among patients with bronchial asthma
Wang, T., Huang, X., Dai, L., Zhan, K.-M., & Wang, J. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1378362 · Cited by 6
Campbell, P. W., Govindaiah, G., & Guido, W. (2024) · Neural Development · doi:10.1186/s13064-024-00183-5 · Cited by 6
Chen, Z., Cai, Y., Liu, Y., Liu, H., Wei, X., Lin, C., Liu, D., Xiao, L., & Rong, L. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1388213 · Cited by 6
Ventral posteromedial nucleus of the thalamus gates the spread of trigeminal neuropathic pain
Du, Y., Lin, S.-D., Wu, X., Xue, B.-Y., Ding, Y.-L., Zhang, J.-H., Tan, B., Lou, G., Hu, W., Chen, Z., et al. (2024) · The Journal of Headache and Pain · doi:10.1186/s10194-024-01849-5 · Cited by 8
Long‐range inputome of prefrontal GABAergic interneurons in the Alzheimer's disease mouse
Ren, M., Li, Y., Jiang, T., Liu, B., Li, X., Jia, X., Li, A., Luo, Q., Gong, H., & Li, X. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.14552 · Cited by 5
Bordin, V., Pirastru, A., Bergsland, N., Cazzoli, M., Baselli, G., & Baglio, F. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120272 · Cited by 6
Yokoyama, H., Kaneko, N., Usuda, N., Kato, T., Khoo, H. M., Fukuma, R., Oshino, S., Tani, N., Kishima, H., Yanagisawa, T., et al. (2024) · APL Bioengineering · doi:10.1063/5.0226457 · Cited by 6
A neural signature for the subjective experience of threat anticipation under uncertaintyPreprint
Liu, X., Jiao, G., Zhou, F., Kendrick, K. M., Yao, D., Xiang, S., Jia, T., Zhang, X., Zhang, J., Feng, J., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.20.558716 · Cited by 6
The potential of laminar functional MRI in refining the understanding of epilepsy in humans
Aitken, F., Winston, J. S., O’Muircheartaigh, J., & Carmichael, D. W. (2025) · Brain · doi:10.1093/brain/awaf320 · Cited by 5
Acosta-Mejia, M. T., & Villalobos, N. (2023) · Diagnostics · doi:10.3390/diagnostics13142394 · Cited by 5
A multimodal characterization of low-dimensional thalamocortical structural connectivity patterns
John, A., Hettwer, M. D., Schaare, H. L., Saberi, A., Bayrak, Ş., Wan, B., Royer, J., Bernhardt, B. C., & Valk, S. L. (2025) · Communications Biology · doi:10.1038/s42003-025-07528-8 · Cited by 8
Gao, W., Zhang, K., Jiao, Q., Su, L., Cui, D., Lu, S., & Yang, R. (2025) · BMC Psychiatry · doi:10.1186/s12888-025-07018-5 · Cited by 5
Anterior thalamic nuclei: A critical substrate for non‐spatial paired‐associate memory in rats
Hamilton, J. J., & Dalrymple‐Alford, J. C. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15802 · Cited by 5
Naik, A. A., Ma, X., Munyeshyaka, M., Leibenluft, E., & Li, Z. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.28.530477 · Cited by 5
Howell, A. M., Warrington, S., Fonteneau, C., Cho, Y., Sotiropoulos, S. N., Murray, J. D., & Anticevic, A. (2024) · eLife · doi:10.7554/elife.95018 · Cited by 5
Kalchev, E. (2023) · Journal of medical imaging and radiation sciences · doi:10.1016/j.jmir.2023.08.012 · Cited by 4
Zhou, S., Kuang, Q., Huang, H.-Q., She, S., Zheng, Y., & Li, X. (2025) · BMC Psychiatry · doi:10.1186/s12888-025-06535-7 · Cited by 4
Developing algorithmic psychiatry via multi-level spanning computational models
Halassa, M. M., Frank, M. J., Garety, P. A., Öngür, D., Airan, R. D., Sanacora, G., Dzirasa, K., Suresh, S., Fitzpatrick, S. M., & Rothman, D. L. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102094 · Cited by 6
Self-citationKelemen, K., Orbán-Kis, K., Szentes, Á., Nagy, Z., Kelemen, H., Fehér, A., Bába, L.-I., Gáll, Z., Horváth, E., Katona, I., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104906 · Cited by 4
Ye, J., Xu, C., Guo, H., Huang, W., Xie, G., & Liang, J. (2025) · Scientific Reports · doi:10.1038/s41598-025-00431-6 · Cited by 3
Xie, B., Ni, H., Yao, J., Xu, Z., Bian, S., Wang, H., Zhu, K., Wu, X., Song, P., Wu, Y., et al. (2025) · Communications Medicine · doi:10.1038/s43856-025-00909-4 · Cited by 3
Corticothalamic communication for action coordination in a skilled motor behavior
Li, Y., An, X., Mulcahey, P. J., Qian, Y., Xu, X. H., Zhao, S., Mohan, H., Suryanarayana, S. M., Bachschmid-Romano, L., Brunel, N., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-025-02195-8 · Cited by 10
Brihmat, N., Saleh, S., Zhang, F., Carnahan, J., Bayram, M. B., Yue, G. H., & Forrest, G. F. (2026) · Scientific Reports · doi:10.1038/s41598-026-36187-w · Cited by 3
Reevaluating thalamic contributions to pain: A translational framework for precision neuromodulation
Li, Z., Zhang, F., Ren, J., Lu, X., & Hu, L. (2026) · Physics of Life Reviews · doi:10.1016/j.plrev.2026.02.001 · Cited by 5
Yasuno, F., Kimura, Y., Nihashi, T., Minami, H., Minami, H., Takeda, A., Sakurai, T., & Kato, T. (2026) · International Psychogeriatrics · doi:10.1016/j.inpsyc.2026.100199 · Cited by 3
Wu, J., Zhang, Q., Ma, M., Dong, Y., Sun, P.-F., Gao, M. J., Liu, P., & Wu, X. (2024) · NeuroToxicology · doi:10.1016/j.neuro.2024.07.002 · Cited by 3
Zhang, L., He, C., Liu, X., Fan, D., Haisan, Z., Hongxing, Z., & Xie, C. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70116 · Cited by 3
Roy, E. R., Wang, Q., Huang, K., Li, S., Fan, Y., Escobar, E., Atkins, C. L., Huang, S., Herrera, J. J., Li, W., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-12869-9 · Cited by 5
Sparse memory ensembles set brain-wide network states to sustain learned associations
Haubrich, J., Russo, G., & Manahan‐Vaughan, D. (2025) · iScience · doi:10.1016/j.isci.2025.113574 · Cited by 3
Nuclei and tracts in the thalamus of crocodiles
Pritz, M. B. (2024) · The Journal of Comparative Neurology · doi:10.1002/cne.25595 · Cited by 3
Preconfigured cortico-thalamic neural dynamics constrain movement-associated thalamic activity
González-Pereyra, P., Sánchez-Lobato, O., Martínez-Montalvo, M. G., Ortega-Romero, D. I., Pérez-Díaz, C. I., Merchant, H., Téllez, L. A., & Rueda‐Orozco, P. E. (2024) · Nature Communications · doi:10.1038/s41467-024-54742-9 · Cited by 5
Govek, K. W., Chen, S., Sgourdou, P., Yao, Y., Woodhouse, S., Chen, T., Fuccillo, M. V., Epstein, D. J., & Cámara, P. G. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.18.481097 · Cited by 3
Howell, A. M., Warrington, S., Fonteneau, C., Cho, Y., Sotiropoulos, S. N., Murray, J. D., & Anticevic, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.22.550168 · Cited by 4
Cortico-thalamic communication for action coordination in a skilled motor sequencePreprint
Li, Y., An, X., Mulcahey, P. J., Qian, Y., Xu, X. H., Zhao, S., Mohan, H., Suryanarayana, S. M., Bachschmid-Romano, L., Brunel, N., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.25.563871 · Cited by 3
Fang, Z., Dang, Y., Ping, A., Wang, C., Zhao, Q., Zhao, H., Xiaoli Li, A., & Zhang, M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.02.587714 · Cited by 3
Hierarchical sensory processing in zebrafish thalamocortical-like circuits
Trinh, A.-T., Ostenrath, A. M., del Castillo-Berges, I., Cachin, F., Koç, M., Kraus, S., Serneels, B., Kawakami, K., & Yaksi, E. (2026) · Science · doi:10.1126/science.aec2171 · Cited by 5
The Role of Layer 6 Corticothalamic Circuits in Vision: Plasticity, Sensory Processing, and Behavior
Katzner, S., Rose, T., Tchumatchenko, T., & Busse, L. (2025) · Annual Review of Vision Science · doi:10.1146/annurev-vision-101322-012348 · Cited by 2
Qin, M., Jin, X., Yang, Y., Gong, F., Wan, J., Wei, J., Sun, B., Li, X., & Hao, Y. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-07171-1 · Cited by 2
Weyer, C., Sarisik, E., Tovar-Perdomo, S., Vetter, C. S., Dwyer, D. B., Antonucci, L. A., Lichtenstein, T., Kambeitz‐Ilankovic, L., Kambeitz, J. P., Ruhrmann, S., et al. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.03.994 · Cited by 2
Thompson, S. J., Miao, Q., Sonig, A., & Noebels, J. L. (2026) · Neuron · doi:10.1016/j.neuron.2026.03.015 · Cited by 2
Metadata
- Authors
- Roy, D. S., Zhang, Y., Halassa, M. M., & Feng, G.
- Affiliations
- Broad Institute (US)
- McGovern Institute for Brain Research (US)
- Corresponding author
- Roy, Dheeraj S.
- Feng, Guoping
- Venue
- Nature Neuroscience
- Published
- 2022-01-31
- Volume
- 25
- Issue
- 2
- Pages
- 140-153
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC9400132
- OpenAlex
- W4221072568
- Cited by
- 177
- References
- 129
- Citations by year
- 2026: 35 · 2025: 54 · 2024: 47 · 2023: 27 · 2022: 14
- FWCI
- 3.69
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-sa)
- Funders
- National Institute of Mental Health (U01MH114819)
- National Institute of Neurological Disorders and Stroke (R01NS113245)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- thalamus, thalamic nuclei, behavioral phenotypes, therapeutic target
- MeSH terms
- Attention, Neural Pathways, Thalamic Nuclei, Thalamus
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
