Pathways for emotions and attention converge on the thalamic reticular nucleus in primates
Open accessAbstract
How do emotional events readily capture our attention? To address this question we used neural tracers to label pathways linking areas involved in emotional and attentional processes in the primate brain (Macaca mulatta). We report that a novel pathway from the amygdala, the brain's emotional center, targets the inhibitory thalamic reticular nucleus (TRN), a key node in the brain's attentional network. The amygdalar pathway formed unusual synapses close to cell bodies of TRN neurons and had more large and efficient terminals than pathways from the orbitofrontal cortex and the thalamic mediodorsal nucleus, which similarly innervated extensive TRN sites. The robust amygdalar pathway provides a mechanism for rapid shifting of attention to emotional stimuli. Acting synergistically, pathways from the amygdala and orbitofrontal cortex provide a circuit for purposeful assessment of emotional stimuli. The different pathways to TRN suggest distinct mechanisms of attention to external and internal stimuli that may be differentially disrupted in anxiety and mood disorders and may be selectively targeted for therapeutic interventions.
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
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?
This gating mechanism is critically involved in integrating real-time sensory and affective information, assessing value, and regulating passage to the cortex.
“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 [146]
Subgenual ACC and OFC are involved in directing attention to affective stimuli and integrating emotion and cognitive control.
“two regions involved in directing attention to affective stimuli (Zikopoulos and Barbas, 2012) and integrating emotion and cognitive control (Pessoa, 2008).”
From Neurocognitive bases of emotion regulation development in adolescence (2015) · cites this paper as Zikopoulos and Barbas, 2012
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Deep Brain Stimulation for Treatment-Resistant Depression
Mayberg, H. S., Lozano, A. M., Voon, V., McNeely, H. E., Seminowicz, D., Hamani, C., Schwalb, J. M., & Kennedy, S. H. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.014 · Cited by 4,059 · see citing works
Emotion, Decision Making and the Orbitofrontal Cortex
Bechara, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.295 · Cited by 3,589 · see citing works
Stress signalling pathways that impair prefrontal cortex structure and function
Arnsten, A. F. T. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2648 · Cited by 3,299 · see citing works
On the relationship between emotion and cognition
Pessoa, L. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2317 · Cited by 2,350 · see citing works
How brains beware: neural mechanisms of emotional attention
Vuilleumier, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.10.011 · Cited by 2,162 · see citing works
Pessoa, L., & Adolphs, R. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2920 · Cited by 1,794 · see citing works
Primate anterior cingulate cortex: Where motor control, drive and cognition interface
Paus, T. (2001) · Nature Reviews Neuroscience · doi:10.1038/35077500 · Cited by 1,722 · see citing works
Function of the thalamic reticular complex: the searchlight hypothesis
Crick, F. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.14.4586 · Cited by 1,651 · see citing works
Bursts as a unit of neural information: making unreliable synapses reliable
Lisman, J. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10070-9 · Cited by 1,412 · see citing works
A neuromodulatory role for the human amygdala in processing emotional facial expressions
Morris, J. (1998) · Brain · doi:10.1093/brain/121.1.47 · Cited by 1,291 · see citing works
How do emotion and motivation direct executive control?
Pessoa, L. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.01.006 · Cited by 1,286 · see citing works
Anxiety and affective style: role of prefrontal cortex and amygdala
Davidson, R. J. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01328-2 · Cited by 1,139 · see citing works
The human amygdala and the emotional evaluation of sensory stimuli
Zald, D. H. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00248-5 · Cited by 1,062 · see citing works
Targeting abnormal neural circuits in mood and anxiety disorders: from the laboratory to the clinic
Ressler, K. J., & Mayberg, H. S. (2007) · Nature Neuroscience · doi:10.1038/nn1944 · Cited by 1,007 · see citing works
The Anatomical Connections of the Macaque Monkey Orbitofrontal Cortex. A Review
Cavada, C. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.220 · Cited by 917 · see citing works
Reconstruct : a free editor for serial section microscopy
Fiala, J. C. (2005) · Journal of Microscopy · doi:10.1111/j.1365-2818.2005.01466.x · Cited by 884 · see citing works
Organization of projections from the medial nucleus of the amygdala: A PHAL study in the rat
Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903600203 · Cited by 884 · see citing works
Siegle, G. J., Steinhauer, S. R., Thase, M. E., Stenger, V. A., & Carter, C. S. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01314-8 · Cited by 859 · see citing works
Increased Amygdala and Insula Activation During Emotion Processing in Anxiety-Prone Subjects
Stein, M. B., Simmons, A. N., Feinstein, J. S., & Paulus, M. P. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.2.318 · Cited by 851 · see citing works
Ghashghaei, H. T., Hilgetag, C. C., & Barbas, H. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.046 · Cited by 845 · see citing works
Self-citationKim, M. J., Loucks, R. A., Palmer, A. L., Brown, A. C., Solomon, K. M., Marchante, A. N., & Whalen, P. J. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.04.025 · Cited by 838 · see citing works
Ghashghaei, H. T., & Barbas, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00446-3 · Cited by 785 · see citing works
Self-citationAnterior Prefrontal Function and the Limits of Human Decision-Making
Koechlin, É., & Hyafil, A. (2007) · Science · doi:10.1126/science.1142995 · Cited by 750 · see citing works
An autoradiographic study of the projections of the central nucleus of the monkey amygdala
Price, J. L., & Amaral, D. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-11-01242.1981 · Cited by 709 · see citing works
The thalamic reticular nucleus: structure, function and concept
Pinault, D. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.04.008 · Cited by 683 · see citing works
The primate mediodorsal (MD) nucleus and its projection to the frontal lobe
Goldman‐Rakic, P. S., & Porrino, L. J. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420406 · Cited by 666 · see citing works
Inactivity produces increases in neurotransmitter release and synapse size
Murthy, V. N., Schikorski, T., Stevens, C. F., & Zhu, Y. (2001) · Neuron · doi:10.1016/s0896-6273(01)00500-1 · Cited by 612 · see citing works
Heterogeneous Release Properties of Visualized Individual Hippocampal Synapses
Murthy, V. N., B, T. J. S. A., & Stevens, C. F. (1997) · Neuron · doi:10.1016/s0896-6273(00)80301-3 · Cited by 596 · see citing works
Neural Correlates of the Automatic Processing of Threat Facial Signals
Anderson, A. K., Christoff, K., Panitz, D., De Rosa, E., & Gabrieli, J. D. E. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05627.2003 · Cited by 574 · see citing works
Topographic organization of projections from the amygdala to the visual cortex in the macaque monkey
Amaral, D. G., Behniea, H., & Kelly, J. L. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)01001-1 · Cited by 552 · see citing works
Giguere, M., & Goldman-Rakic, P. S. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902770204 · Cited by 529 · see citing works
To what extent are emotional visual stimuli processed without attention and awareness?
Pessoa, L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.002 · Cited by 510 · see citing works
Guarding the gateway to cortex with attention in visual thalamus
McAlonan, K., Cavanaugh, J., & Wurtz, R. H. (2008) · Nature · doi:10.1038/nature07382 · Cited by 503 · see citing works
Direct and indirect pathways from the amygdala to the frontal-lobe in rhesus-monkeys
Porrino, L. J., Crane, A. M., & Goldman‐Rakic, P. S. (1981) · Journal of Comparative Neurology · doi:10.1002/cne.901980111 · Cited by 491 · see citing works
Romanski, L. M., & LeDoux, J. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-11-04501.1992 · Cited by 461 · see citing works
The Interface Between Emotion and Attention: A Review of Evidence From Psychology and Neuroscience
Compton, R. J. (2003) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582303255278 · Cited by 419 · see citing works
Russchen, F. T., Amaral, D. G., & Price, J. L. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902560202 · Cited by 416 · see citing works
Emotion and cognition and the amygdala: From “what is it?” to “what's to be done?”
Pessoa, L. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.06.038 · Cited by 403 · see citing works
Invasive circuitry-based neurotherapeutics: stereotactic ablation and deep brain stimulation for OCD
Greenberg, B. D., Rauch, S. L., & Haber, S. N. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.128 · Cited by 359 · see citing works
Zikopoulos, B., & Barbas, H. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5511-05.2006 · Cited by 344 · see citing works
Self-citationPathway tracing using biotinylated dextran amines
Reiner, A. J., Veenman, C. L., Medina, L. M., Jiao, Y., Mar, N. D., & Honig, M. G. (2000) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(00)00293-4 · Cited by 343 · see citing works
Neural Mechanisms Underlying Selective Attention to Threat
Bishop, S. J. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1417.016 · Cited by 330 · see citing works
Role of Mechanical Factors in the Morphology of the Primate Cerebral Cortex
Hilgetag, C. C., & Barbas, H. (2006) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0020022 · Cited by 310 · see citing works
Self-citationThe forms of non‐pyramidal neurons in the visual cortex of the rat
Feldman, M. L., & Peters, A. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901790406 · Cited by 303 · see citing works
Diverse thalamic projections to the prefrontal cortex in the rhesus monkey
Barbas, H., Henion, T. H. H., & Dermon, C. R. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903130106 · Cited by 292 · see citing works
Self-citationWaiting for spiders: Brain activation during anticipatory anxiety in spider phobics
Straube, T., Mentzel, H.-J., & Miltner, W. H. R. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.06.023 · Cited by 282 · see citing works
Afferent projections to nucleus reuniens of the thalamus
McKenna, J. T., & Vertes, R. P. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20342 · Cited by 272 · see citing works
The reticular nucleus revisited: Intrinsic and network properties of a thalamic pacemaker
FUENTEALBA, P., & STERIADE, M. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.01.002 · Cited by 263 · see citing works
Browning, M., Holmes, E. A., & Harmer, C. J. (2010) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.10.1.8 · Cited by 247 · see citing works
Cognitive biases in anxiety and attention to threat.
Mathews, A., Mackintosh, B., & Fulcher, E. (1997) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(97)01092-9 · Cited by 245 · see citing works
Neuroimaging studies of attention and the processing of emotion-laden stimuli
Pessoa, L., & Ungerleider, L. G. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)14412-3 · Cited by 236 · see citing works
Williams, L. M., Das, P., Liddell, B. J., Kemp, A. H., Rennie, C. J., & Gordon, E. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1016-06.2006 · Cited by 232 · cited 2× · see citing works
“In primates, pathways that involve high-order thalamic nuclei, association cortices, and amygdala provide another route for the perception and evaluation of complex salient stimuli (Morris et al., 1998; Compton, 2003; Williams et al., 2006; Jones, 2007; Straube et al., 2007; Pessoa, 2008; Pessoa and Adolphs, 2010).”
BackgroundProjections of the amygdala to the thalamus in the cynomolgus monkey
Aggleton, J. P., & Mishkin, M. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902220106 · Cited by 231 · see citing works
Independent Sources of Quantal Variability at Single Glutamatergic Synapses
Franks, K. M., Stevens, C. F., & Sejnowski, T. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03186.2003 · Cited by 224 · cited 2× · see citing works
“However, the proportion of large and small terminals in different pathways varied and can provide useful information about the robustness, efficacy, and level of activity of a pathway (Pierce and Lewin, 1994; Murthy et al., 2001; Franks et al., 2003; Germuska et al., 2006; Zikopoulos and Barbas, 2006, 2007b; Medalla a…”
BackgroundStructure and connections of the thalamic reticular nucleus: Advancing views over half a century
Guillery, R. W., & Harting, J. K. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10738 · Cited by 220 · see citing works
Increased Amygdala and Insula Activation During Emotion Processing in Anxiety-Prone Subjects
Stein, M. B. (2007) · American Journal of Psychiatry · doi:10.1176/appi.ajp.164.2.318 · Cited by 212 · see citing works
Functional neuroimaging in obsessive-compulsive disorder
Del Casale, A., Kotzalidis, G. D., Rapinesi, C., Serata, D., Ambrosi, E., Simonetti, A., Pompili, M., Ferracuti, S., Tatarelli, R., & Girardi, P. (2011) · Neuropsychobiology · doi:10.1159/000325223 · Cited by 210 · see citing works
A comparative analysis of the morphology of corticothalamic projections in mammals
Rouiller, E. M., & Welker, E. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00364-6 · Cited by 203 · see citing works
Amygdalocortical Circuitry in Schizophrenia: From Circuits to Molecules
Benes, F. M. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.116 · Cited by 189 · see citing works
Activation of a Cortical Column by a Thalamocortical Impulse
Swadlow, H. A., Gusev, A. G., & Bezdudnaya, T. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07766.2002 · Cited by 183 · see citing works
McDonald, A. J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902620105 · Cited by 181 · see citing works
The Prefrontal Cortex and Flexible Behavior
Barbas, H., & Zikopoulos, B. (2007) · The Neuroscientist · doi:10.1177/1073858407301369 · Cited by 178 · see citing works
Self-citationFlow of information for emotions through temporal and orbitofrontal pathways
Barbas, H. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00777.x · Cited by 167 · see citing works
Self-citationHöistad, M., & Barbas, H. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.12.043 · Cited by 157 · see citing works
Self-citationAn ultrastructural size principle
Pierce, J. P., & Lewin, G. R. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90071-x · Cited by 157 · see citing works
Ruffini, C., Locatelli, M., Lucca, A., Benedetti, F., Insacco, C., & Smeraldi, E. (2009) · The Primary Care Companion to The Journal of Clinical Psychiatry · doi:10.4088/pcc.08m00663 · Cited by 156 · see citing works
Zikopoulos, B., & Barbas, H. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.6.417 · Cited by 156 · see citing works
Self-citationAste, N., Balthazart, J., Absil, P., Grossmann, R., M�lhbauer, E., Viglietti‐Panzica, C., & Panzica, G. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980629)396:2 · Cited by 147 · see citing works
Medalla, M., & Barbas, H. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.006 · Cited by 146 · see citing works
Self-citationSensory Pathways and Emotional Context for Action in Primate Prefrontal Cortex
Barbas, H., Zikopoulos, B., & Timbie, C. M. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.08.008 · Cited by 145 · see citing works
Self-citationLaminar and modular organization of prefrontal projections to multiple thalamic nuclei
Xiao, D., Zikopoulos, B., & Barbas, H. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.04.034 · Cited by 138 · see citing works
Self-citationAttentional orienting is impaired by unilateral lesions of the thalamic reticular nucleus in the rat
Weese, G. D., Phillips, J. M., & Brown, V. J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-22-10135.1999 · Cited by 132 · see citing works
Anatomical evidence for a mechanism of lateral inhibition in the rat thalamus
Pinault, D., & Deschênes, M. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00362.x · Cited by 121 · see citing works
Parallel driving and modulatory pathways link the prefrontal cortex and thalamus
Zikopoulos, B., & Barbas, H. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000848 · Cited by 114 · see citing works
Self-citationRouiller, E. M., & Welker, E. (1991) · Hearing Research · doi:10.1016/0378-5955(91)90168-9 · Cited by 113 · see citing works
Lanuza, E., Nader, K., & LeDoux, J. E. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.12.034 · Cited by 108 · see citing works
Medalla, M., & Barbas, H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1773-10.2010 · Cited by 102 · see citing works
Self-citationContralateral thalamic projections predominantly reach transitional cortices in the rhesus monkey
Dermon, C. R., & Barbas, H. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903440403 · Cited by 98 · see citing works
Self-citationde Olmos, J. S. (1990) · Elsevier eBooks · doi:10.1016/b978-0-12-547625-6.50025-8 · Cited by 96 · see citing works
Mitchell, D. G. V., Luo, Q., Mondillo, K., Vythilingam, M., Finger, E. C., & Blair, J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.002 · Cited by 93 · see citing works
Montero, V. M. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00417-4 · Cited by 90 · see citing works
Lanuza, E., Moncho-Bogani, J., & LeDoux, J. E. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.06.028 · Cited by 84 · see citing works
Ultrastructure of the stomatogastric ganglion neuropil of the crab, Cancer borealis
Kilman, V. L., & Marder, E. E. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961021)374:3 · Cited by 81 · see citing works
Mackie, J. A. C. (1992) · Asian Studies Review · doi:10.1080/03147539208712844 · Cited by 78 · see citing works
Lam, Y., & Sherman, S. M. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00206.2005 · Cited by 73 · see citing works
Deep Brain Stimulation for Psychiatric Disorders
Holtzheimer, P., & Mayberg, H. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113638 · Cited by 65 · see citing works
Rods and cones project to the inner plexiform layer during development
Johnson, P. T., Williams, R. R., Cusato, K., & Reese, B. E. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991108)414:1 · Cited by 56 · see citing works
Synaptic Distinction of Laminar-specific Prefrontal-temporal Pathways in Primates
Germuska, M. A., Saha, S. G., Fiala, J. C., & Barbas, H. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj030 · Cited by 53 · see citing works
Self-citationUrsu, S., & Carter, C. S. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.03.018 · Cited by 49 · see citing works
Sequential and parallel circuits for emotional processing in primate orbitofrontal cortex
Barbas, H., & Zikopoulos, B. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198565741.003.0004 · Cited by 46 · see citing works
Self-citationNonkes, L. J. P., Tomson, K., Märtin, A., Dederen, J., Maes, J. H. R., & Homberg, J. R. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.04.002 · Cited by 42 · see citing works
Differential modes of termination of amygdalothalamic and amygdalocortical projections in the monkey
Miyashita, T., Ichinohe, N., & Rockland, K. S. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21304 · Cited by 39 · see citing works
The dual pattern of corticothalamic projection of the primary auditory cortex in macaque monkey
Rouiller, E. M., & Durif, C. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.01.008 · Cited by 36 · see citing works
Bunce, J. G., & Barbas, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.064 · Cited by 35 · see citing works
Self-citationChan, S. O., & Chung, K. Y. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990405)406:2 · Cited by 29 · see citing works
Transient features of the thalamic reticular nucleus in the human foetal brain
Ulfig, N., Nickel, J., & Böhl, J. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00390.x · Cited by 25 · see citing works
Petrof, I., & Brown, V. J. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.03.045 · Cited by 11 · see citing works
Neuronal organization of the reticular nucleus of the thalamus in adult humans
Berezhnaya, L. A. (2006) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-006-0049-1 · Cited by 3 · see citing works
Nakatani, T. (1993) · PubMed · Cited by 3 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- De Olmos JS 1990 Amygdala The Human Nervous System Paxinos G 583 710 San Diego Academic Press,Inc.
- Jones EG 2007 The Thalamus New York Cambridge University Press
Cited by
Sorted by citations
The theory of constructed emotion: an active inference account of interoception and categorization
Barrett, L. F. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw154 · Cited by 1,426 · see citing works
“…signal the precision of incoming sensory inputs via their modulation of the reticular nucleus that encircles that thalamus and controls the sensory input that reaches the cortex via thalamocortical pathways [for relevant anatomy, see (Zikopoulos and Barbas, 2006, 2012; John et al. , 2016)].”
The theory of constructed emotion: an active inference account of interoception and categorization
Barrett, L. F. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx060 · Cited by 950 · see citing works
“…nucleus that encircles that thalamus and controls the sensory input that reaches the cortex via thalamocortical pathways [for relevant anatomy, see (Zikopoulos and Barbas, 2006, 2012; John et al., 2016)].21 My hypothesis, then, is that cortical limbic regions within the salience network are at the…”
Neurocognitive bases of emotion regulation development in adolescence
Ahmed, S. P., Bittencourt-Hewitt, A., & Sebastian, C. L. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.07.006 · Cited by 621 · see citing works
An active inference theory of allostasis and interoception in depression
Barrett, L. F., Quigley, K. S., & Hamilton, P. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0011 · Cited by 554 · see citing works
General Cortical and Special Prefrontal Connections: Principles from Structure to Function
Barbas, H. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033936 · Cited by 395 · see citing works
Self-citationPulvinar-Cortex Interactions in Vision and Attention
Zhou, H., Schafer, R. J., & Desimone, R. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.034 · Cited by 370 · see citing works
Altered neural connectivity in excitatory and inhibitory cortical circuits in autism
Zikopoulos, B., & Barbas, H. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00609 · Cited by 313 · see citing works
Self-citationAffect-biased attention as emotion regulation
Todd, R. M., Cunningham, W. A., Anderson, A. K., & Thompson, E. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.06.003 · Cited by 336 · see citing works
State-dependent architecture of thalamic reticular subnetworks
Halassa, M. M., Chen, Z., Wimmer, R. D., Brunetti, P. M., Zhao, S., Zikopoulos, B., Wang, F., Brown, E. N., & Wilson, M. A. (2014) · Cell · doi:10.1016/j.cell.2014.06.025 · Cited by 309 · see citing works
Self-citationMitchell, A. S. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.03.001 · Cited by 323 · see citing works
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 339 · see citing works
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 231 · see citing works
Manoach, D. S., Pan, J. Q., Purcell, S., & Stickgold, R. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.10.003 · Cited by 210 · see citing works
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 204 · see citing works
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 204 · see citing works
Malmierca, M. S., Anderson, L. A., & Antunes, F. M. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00019 · Cited by 159 · see citing works
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 · see citing works
Mindfulness-meditation-based pain relief is not mediated by endogenous opioids
Zeidan, F., Adler-Neal, A. L., Wells, R. E., Stagnaro, E., May, L. M., Eisenach, J. C., McHaffie, J. G., & Coghill, R. C. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.4328-15.2016 · Cited by 132 · see citing works
“All feedback connections between the cortex and thalamus must pass through the TRN in a topographically organized fashion (Pinault, 2004; Zikopoulos and Barbas, 2006, 2012).”
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 127 · see citing works
Sanjuan, P. M., Thoma, R., Claus, E. D., Mays, N., & Caprihan, A. (2013) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2013.09.002 · Cited by 125 · see citing works
Zeidan, F., Baumgartner, J. N., & Coghill, R. C. (2019) · PAIN Reports · doi:10.1097/pr9.0000000000000759 · Cited by 115 · see citing works
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 117 · see citing works
Functional Diversity of Thalamic Reticular Subnetworks
Crabtree, J. W. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00041 · Cited by 122 · see citing works
Frontal-thalamic circuits associated with language
Barbas, H., García‐Cabezas, M. Á., & Zikopoulos, B. (2012) · Brain and Language · doi:10.1016/j.bandl.2012.10.001 · Cited by 115 · see citing works
Self-citationA 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 · see citing works
The thalamus: gateway to the mind
Ward, L. M. (2013) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1256 · Cited by 111 · see citing works
Differentiating Cerebellar Impact on Thalamic Nuclei
Gornati, S. V., Schäfer, C. B., Rooda, O. H. J. E., Nigg, A. L., Zeeuw, C. I. D., & Hoebeek, F. E. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.098 · Cited by 107 · see citing works
Ghodrati, M., Khaligh‐Razavi, S., & Lehky, S. R. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.06.002 · Cited by 99 · see citing works
Reduced modulation of thalamocortical connectivity during exposure to sensory stimuli in ASD
Green, S. A., Hernandez, L. M., Bookheimer, S. Y., & Dapretto, M. (2016) · Autism Research · doi:10.1002/aur.1726 · Cited by 96 · see citing works
Abivardi, A., & Bach, D. R. (2017) · Human Brain Mapping · doi:10.1002/hbm.23639 · Cited by 93 · see citing works
Auditory thalamic circuits and GABAA receptor function: Putative mechanisms in tinnitus pathology
Caspary, D. M., & Llano, D. A. (2016) · Hearing Research · doi:10.1016/j.heares.2016.08.009 · Cited by 90 · see citing works
CGRP receptor antagonist MK-8825 attenuates cortical spreading depression induced pain behavior
Filiz, A., Tepe, N., Eftekhari, S., Boran, H. E., Dileköz, E., Edvinsson, L. I., & Bolay, H. (2017) · Cephalalgia · doi:10.1177/0333102417735845 · Cited by 88 · see citing works
Borgomaneri, S., Battaglia, S., Sciamanna, G., Tortora, F., & Laricchiuta, D. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.04.036 · Cited by 90 · see citing works
Précis on <i>The Cognitive-Emotional Brain</i>
Pessoa, L. (2015) · Behavioral and Brain Sciences · doi:10.1017/s0140525x14000120 · Cited by 84 · see citing works
Pratt, J. A., & MORRIS, B. J. (2015) · Journal of Psychopharmacology · doi:10.1177/0269881114565805 · Cited by 83 · see citing works
How the prefrontal executive got its stripes
Barbas, H., & García‐Cabezas, M. Á. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.07.003 · Cited by 81 · see citing works
Self-citationSebastian, C. L., McCrory, E. J., Dadds, M. R., Cecil, C. A. M., Lockwood, P. L., Hyde, Z. H., De Brito, S. A., & Viding, E. (2014) · Psychological Medicine · doi:10.1017/s0033291713000482 · Cited by 75 · see citing works
The involvement of limbic structures in typical and atypical absence epilepsy
Onat, F., van Luijtelaar, G., Nehlig, A., & Snead, O. C. (2012) · Epilepsy Research · doi:10.1016/j.eplepsyres.2012.08.008 · Cited by 74 · see citing works
Disentangling the influences of multiple thalamic nuclei on prefrontal cortex and cognitive control
Phillips, J. M., Kambi, N. A., Redinbaugh, M. J., Mohanta, S., & Saalmann, Y. B. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.06.042 · Cited by 70 · see citing works
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 · see citing works
Zikopoulos, B., García‐Cabezas, M. Á., & Barbas, H. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2004559 · Cited by 63 · see citing works
Self-citationLee, D. J., Dallapiazza, R. F., Vloo, P. D., Elias, G. J. B., Fomenko, A., Boutet, A., Giacobbe, P., & Lozano, A. M. (2018) · Brain stimulation · doi:10.1016/j.brs.2018.11.012 · Cited by 64 · see citing works
Antal, M., Beneduce, B. M., & Regehr, W. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0236-14.2014 · Cited by 63 · see citing works
Associative Learning Beyond the Medial Temporal Lobe: Many Actors on the Memory Stage
Pergola, G., & Boris Suchan, A. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00162 · Cited by 65 · see citing works
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 · see citing works
Tepe, N., Filiz, A., Dileköz, E., Akçalı, D. T., Sara, Y., Charles, A. C., & Bolay, H. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12753 · Cited by 62 · see citing works
On the Diverse Functions of Electrical Synapses
Vaughn, M. J., & Haas, J. S. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.910015 · Cited by 59 · see citing works
Anatomy and computational modeling of networks underlying cognitive-emotional interaction
John, Y. J., Bullock, D. H., Zikopoulos, B., & Barbas, H. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00101 · Cited by 59 · see citing works
Self-citationRamírez-Mahaluf, J. P., Roxin, A., Mayberg, H. S., & Compte, A. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv249 · Cited by 58 · see citing works
Medalla, M., & Barbas, H. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2339-12.2012 · Cited by 57 · see citing works
Self-citationSenova, S., Clair, A.-H., Palfi, S., Yelnik, J., Domenech, P., & Mallet, L. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00905 · Cited by 57 · see citing works
Mediodorsal thalamus and cognition in non-human primates
Baxter, M. G. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00038 · Cited by 54 · see citing works
John, Y. J., Zikopoulos, B., Bullock, D. H., & Barbas, H. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004722 · Cited by 54 · see citing works
Self-citationProjection from the Amygdala to the Thalamic Reticular Nucleus Amplifies Cortical Sound Responses
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 · see citing works
Varela, C., & Wilson, M. A. (2020) · eLife · doi:10.7554/elife.48881 · Cited by 52 · see citing works
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 · see citing works
The intercalated nuclear complex of the primate amygdala
Zikopoulos, B., John, Y. J., García‐Cabezas, M. Á., Bunce, J. G., & Barbas, H. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.052 · Cited by 51 · see citing works
Self-citationAnterior Cingulate Pathways May Affect Emotions Through Orbitofrontal Cortex
García‐Cabezas, M. Á., & Barbas, H. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw284 · Cited by 50 · see citing works
Self-citationZikopoulos, B., Höistad, M., John, Y. J., & Barbas, H. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3940-16.2017 · Cited by 49 · see citing works
Self-citationOrganization of primate amygdalar–thalamic pathways for emotions
Timbie, C. M., García‐Cabezas, M. Á., Zikopoulos, B., & Barbas, H. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000639 · Cited by 48 · see citing works
Self-citationBunce, J. G., Zikopoulos, B., Feinberg, M. D., & Barbas, H. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23413 · Cited by 46 · see citing works
Self-citationA Thalamic Reticular Circuit for Head Direction Cell Tuning and Spatial Navigation
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 47 · see citing works
Mak-McCully, R. A., Deiss, S. R., Rosen, B. Q., Jung, K.-Y., B, T. J. S. A., Bastuji, H., Rey, M. F., Cash, S. S., Bazhenov, M., & Halgren, E. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003855 · Cited by 46 · see citing works
Neural Plasticity in the Brain during Neuropathic Pain
Bak, M. S., Park, H., & Kim, S. K. (2021) · Biomedicines · doi:10.3390/biomedicines9060624 · Cited by 46 · see citing works
Specialized Pathways from the Primate Amygdala to Posterior Orbitofrontal Cortex
Timbie, C. M., & Barbas, H. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5014-13.2014 · Cited by 45 · see citing works
Self-citationInserra, A., Gregorio, D. D., Rezai, T., López-Canul, M., Comai, S., & Gobbi, G. (2021) · Journal of Psychopharmacology · doi:10.1177/0269881121991569 · Cited by 41 · see citing works
Troyano‐Rodriguez, E., Lladó-Pelfort, L., Santana, N., Teruel‐Martí, V., Celada, P., & Artigas, F. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.05.019 · Cited by 40 · see citing works
Interrogating the mouse thalamus to correct human neurodevelopmental disorders
Schmitt, L. I., & Halassa, M. M. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.183 · Cited by 41 · see citing works
Thalamic Bursts Down-regulate Cortical Theta and Nociceptive Behavior
LeBlanc, B. W., Cross, B., Smith, K. A., Roach, C., Xia, J. J., Chao, Y.-C., Levitt, J., Koyama, S., Moore, C. I., & Saab, C. Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-02753-6 · Cited by 40 · see citing works
Opposite development of short- and long-range anterior cingulate pathways in autism
Zikopoulos, B., Liu, X., Tepe, J., Trutzer, I., John, Y. J., & Barbas, H. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1904-1 · Cited by 38 · see citing works
Self-citationNeuroanatomical Basis of Consciousness
Blumenfeld, H. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800948-2.00001-7 · Cited by 39 · see citing works
Amygdala responses to valence and its interaction by arousal revealed by MEG
Styliadis, C., Ioannides, A. A., Bamidis, P. D., & Papadelis, C. L. (2013) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2013.05.006 · Cited by 38 · see citing works
Pathway mechanism for excitatory and inhibitory control in working memory
Barbas, H., Wang, J., Joyce, M. K. P., & García‐Cabezas, M. Á. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00936.2017 · Cited by 38 · see citing works
Self-citationThe rostroventral part of the thalamic reticular nucleus modulates fear extinction
Lee, J.-H., Latchoumane, C.-F. V., Park, J.-J., Kim, J., Jeong, J., Lee, K.-H., & Shin, H. (2019) · Nature Communications · doi:10.1038/s41467-019-12496-9 · Cited by 38 · see citing works
Theoretical Tinnitus Framework: A Neurofunctional Model
Ghodratitoostani, I., Zana, Y., Delbem, A. C. B., Sani, S. S., Ekhtiari, H., & Sánchez, T. G. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00370 · Cited by 37 · see citing works
Death is common, so is understanding it: the concept of death in other species
Monsó, S., & Osuna‐Mascaró, A. J. (2020) · Synthese · doi:10.1007/s11229-020-02882-y · Cited by 36 · see citing works
Targeting the Limbic System: Insights into Its Involvement in Tinnitus
Singh, A., Smith, P. F., & Zheng, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129889 · Cited by 38 · see citing works
García‐Cabezas, M. Á., & Barbas, H. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0598-3 · Cited by 33 · see citing works
Self-citationMagrou, L., Joyce, M. K. P., Froudist‐Walsh, S., Datta, D., Wang, X., Martínez-Trujillo, J., & Arnsten, A. F. T. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae174 · Cited by 32 · see citing works
Sonomura, T., Furuta, T., Nakatani, I., Yamamoto, Y., Unzai, T., Matsuda, W., Iwai, H., Yamanaka, A., Uemura, M., & Kaneko, T. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00026 · Cited by 31 · see citing works
Chau, L., & Galvez, R. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00092 · Cited by 30 · see citing works
Magdaleno-Madrigal, V. M., Contreras-Murillo, G., Camacho‐Abrego, I., Negrete‐Díaz, J. V., Valdés‐Cruz, A., Fernández‐Mas, R., Almazán‐Alvarado, S., & Flores, G. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.035 · Cited by 29 · see citing works
Marusak, H. A., Zundel, C. G., Brown, S., Rabinak, C. A., & Thomason, M. E. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw182 · Cited by 29 · see citing works
Necula, D., Cho, F. S., He, A., & Paz, J. T. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25259 · Cited by 26 · see citing works
The role of thalamic nuclei in genetic generalized epilepsies
Lüttjohann, A., & van Luijtelaar, G. (2022) · Epilepsy Research · doi:10.1016/j.eplepsyres.2022.106918 · Cited by 26 · see citing works
Amemori, S., Graybiel, A. M., & Amemori, K. (2024) · Nature Communications · doi:10.1038/s41467-024-48375-1 · Cited by 24 · see citing works
Li, Y., Yu, M., Xu, M., Yang, J., Sha, D., Liu, Q., & Yang, C. P. (2019) · Springer eBooks · doi:10.1007/978-981-32-9915-3_9 · Cited by 25 · see citing works
Hoseini, M. S., Higashikubo, B. T., Cho, F. S., Chang, A. H., Clemente-Perez, A., Lew, I., Ciesielska, A., Stryker, M. P., & Paz, J. T. (2021) · eLife · doi:10.7554/elife.61437 · Cited by 24 · see citing works
Antonucci, L. A., Taurisano, P., Fazio, L., Gelao, B., Romano, R., Quarto, T., Porcelli, A., Mancini, M., Giorgio, A. D., Caforio, G., et al. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.03.014 · Cited by 25 · see citing works
Thalamic Bursts and the Epic Pain Model
Saab, C. Y., & Barrett, L. F. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00147 · Cited by 25 · see citing works
Kim, H. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00281 · Cited by 25 · see citing works
Corticothalamic network dysfunction and Alzheimer’s disease
Jagirdar, R., & Chin, J. (2017) · Brain Research · doi:10.1016/j.brainres.2017.09.014 · Cited by 24 · see citing works
Joyce, M. K. P., Marshall, L. G., Banik, S. L., Wang, J., Xiao, D., Bunce, J. G., & Barbas, H. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1724-21.2021 · Cited by 24 · see citing works
Self-citationThe thalamus and tinnitus: Bridging the gap between animal data and findings in humans
Koops, E. A., & Eggermont, J. J. (2021) · Hearing Research · doi:10.1016/j.heares.2021.108280 · Cited by 22 · see citing works
León-Domínguez, U., Vela‐Bueno, A., Froufe, M., & León‐Carrión, J. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.03.012 · Cited by 23 · see citing works
Hintze, P., Junghöfer, M., & Bruchmann, M. (2014) · Biological Psychology · doi:10.1016/j.biopsycho.2014.03.010 · Cited by 22 · see citing works
Spatially generalizable representations of facial expressions: Decoding across partial face samples
Greening, S. G., Mitchell, D. G. V., & Smith, F. W. (2017) · Cortex · doi:10.1016/j.cortex.2017.11.016 · Cited by 20 · see citing works
Hinton, K. E., Lahey, B. B., Villalta‐Gil, V., Meyer, F. A. C., Burgess, L. L., Chodes, L. K., Applegate, B. E., Hulle, C. A. V., Landman, B. A., & Zald, D. H. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101705 · Cited by 21 · see citing works
Prefrontal neural dynamics in consciousness
León-Domínguez, U., & León‐Carrión, J. (2019) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2019.05.018 · Cited by 22 · see citing works
Frӧhlich, F., & Lustenberger, C. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.04.003 · Cited by 20 · see citing works
- Authors
- Zikopoulos, B., & Barbas, H.
- Affiliations
- Boston University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-04-11
- Volume
- 32
- Issue
- 15
- Pages
- 5338-5350
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3342673
- OpenAlex
- W2019751136
- Cited by
- 193
- References
- 98
- Citations by year
- 2026: 11 · 2025: 14 · 2024: 11 · 2023: 10 · 2022: 8 · 2021: 16 · 2020: 15 · 2019: 16 · 2018: 11 · 2017: 14 · 2016: 20 · 2015: 14 · 2014: 11 · 2013: 15 · 2012: 7
- FWCI
- 7.69
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (R01MH057414)
- National Institute of Neurological Disorders and Stroke (R01NS024760)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- thalamic reticular nucleus, amygdala, attention, emotional attention, orbitofrontal cortex, mediodorsal thalamus, primate brain, synaptic terminals, anxiety disorders, mood disorders, emotional stimuli
- MeSH terms
- Amygdala, Animals, Attention, Emotions, Female, Frontal Lobe, Humans, Image Processing, Computer-Assisted, Immunohistochemistry, Functional Laterality, Macaca mulatta, Magnetic Resonance Imaging, Male, Microscopy, Electron, Neural Pathways, Thalamic Nuclei, Presynaptic Terminals, Microscopy, Confocal, Mediodorsal Thalamic Nucleus
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
