Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys
Abstract
Sensory and premotor inputs to the orbital and medial prefrontal cortex (OMPFC) were studied with retrograde axonal tracers. Restricted areas of the lateral and posterior orbital cortex had specific connections with visual-, somatosensory-, olfactory-, gustatory-, and visceral-related structures. More medial areas received few direct sensory inputs. Within the lateral and posterior orbital cortex, area 12l received a substantial projection from visual areas in the inferior temporal cortex (TE). Area 12m received somatosensory input from face, digit, or forelimb regions in the opercular part of area 1-2, in area 7b, in the second somatosensory area (SII), and in the anterior infraparietal area (AIP). Areas 13m and 13l also received a projection from the opercular part of areas 1-2 and 3b. The posteromedial and lateral agranular insular areas (Iapm and Ial, respectively) received fibers from the ventral part of the parvicellular division of the ventroposterior medial nucleus of the thalamus (VPMpc) that may represent a visceral afferent system. The dorsal part of VPMpc projected to the adjacent gustatory cortex. These restricted inputs from several sensory modalities and the convergent corticocortical connections to orbital areas 13l and 13m suggest a network related to feeding. The OMPFC was also connected to premotor cortex in ventral area 6 (areas 6va and 6vb), in cingulate area 24c, and probably in the supplementary eye field. Area 6va projected to area 12m, whereas a regio…
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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 orbitofrontal cortex is anatomically well suited to integrate exteroceptive and interoceptive sensory information to guide behavior, given lateral orbitofrontal cortex connections to sensory modalities and medial orbitofrontal cortex connections to visceral control areas.
“With the lateral OFC's connections to sensory modalities (e.g., Barbas 1988; Rolls 1999, see Kringelbach & Rolls 2004) and the medial OFC's connections to areas involved in visceral control (e.g., Carmichael & Price 1995; Eblen & Graybiel 1995; Ongür & Price 1998; 2000; Rempel-Clower & Barbas 1998; see Kringelbach & Rolls 2004 for a review), the OFC is anatomically well suited to perform this role”
From The brain basis of emotion: a meta-analytic review (2012) · cites this paper as Carmichael & Price 1995
The orbital network has specific connections with sensory cortex, including primary olfactory and gustatory cortex, visual inferior temporal areas, the ventral bank of the superior temporal sulcus, and somatic sensory areas in the dysgranular insula and frontal operculum.
“These include primary olfactory and gustatory cortex, visual areas in the inferior temporal cortex (TEa), and the ventral bank of the superior temporal sulcus, somatic sensory areas in the dysgranular insula (Id) and the frontal operculum (Carmichael and Price, 1995b;Saleem et al, 2008).”
From Neurocircuitry of Mood Disorders (2010) · cites this paper as Carmichael and Price, 1995b
Cites
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783 · see citing works
Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685 · see citing works
Evidence for a viscerotopic sensory representation in the cortex and thalamus in the rat
Cechetto, D. F., & Saper, C. B. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620104 · Cited by 703 · see citing works
‘‘Taste-smell confusions” and the duality of the olfactory sense
Rozin, P. (1982) · Perception & Psychophysics · doi:10.3758/bf03202667 · Cited by 627 · see citing works
Ray, J. P., & Price, J. L. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903370102 · Cited by 402 · see citing works
Self-citationTaste and olfaction: Independence vs interaction
Murphy, C., & Cain, W. S. (1980) · Physiology & Behavior · doi:10.1016/0031-9384(80)90257-7 · Cited by 270 · see citing works
Distribution of visual and somatic functions in the parietal associative area 7 of the monkey
Hyvärinen, J., & Shelepin, Y. (1979) · Brain Research · doi:10.1016/0006-8993(79)90404-9 · Cited by 142 · see citing works
SOME RESPIRATORY, VASCULAR AND THERMAL RESPONSES TO STIMULATION OF ORBITAL SURFACE OF FRONTAL LOBE
Delgado, J. M. R., & Livingston, R. B. (1948) · Journal of Neurophysiology · doi:10.1152/jn.1948.11.1.39 · Cited by 119 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
How do you feel? Interoception: The sense of the physiological condition of the body
Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006 · see citing works
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472 · see citing works
Gusnard, D. A., Akbudak, E., Shulman, G. L., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071043098 · Cited by 2,997 · see citing works
Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · see citing works
“Kringelbach & Rolls 2004) and the mOFC’s connections to areas involved in visceral control (e.g., Carmichael & Price 1995; Eblen & Graybiel 1995; Ongür & Price 1998; 2000; Rempel-Clower & Barbas 1998; see Kringelbach & Rolls [2004] for a review), the OFC is anatomically well suited to perform this…”
BackgroundThe human orbitofrontal cortex: linking reward to hedonic experience
Kringelbach, M. L. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1747 · Cited by 2,180 · see citing works
KRINGELBACH, M. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.006 · Cited by 1,977 · see citing works
Synaptic plasticity and depression: new insights from stress and rapid-acting antidepressants
Duman, R. S., Aghajanian, G. K., Sanacora, G., & Krystal, J. H. (2016) · Nature Medicine · doi:10.1038/nm.4050 · Cited by 1,750 · see citing works
Neurocircuitry of Mood Disorders
Price, J. L., & Drevets, W. C. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.104 · Cited by 1,606 · see citing works
Self-citationThe Orbitofrontal Cortex and Reward
Rolls, E. T. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.284 · Cited by 1,595 · see citing works
The primate basal ganglia: Parallel and integrative networks
Haber, S. N. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.10.003 · Cited by 1,479 · see citing works
An opportunity cost model of subjective effort and task performance
Kurzban, R., Duckworth, A., Kable, J. W., & Myers, J. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x12003196 · Cited by 1,381 · see citing works
Ridderinkhof, K. R., van den Wildenberg, W. P. M., Segalowitz, S. J., & Carter, C. S. (2004) · Brain and Cognition · doi:10.1016/j.bandc.2004.09.016 · Cited by 1,407 · see citing works
The functions of the orbitofrontal cortex
Rolls, E. T. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00277-x · Cited by 1,327 · see citing works
Cortical pathways to the mammalian amygdala
McDonald, A. J. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00003-3 · Cited by 1,303 · see citing works
Lateral prefrontal cortex: architectonic and functional organization
Petrides, M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1631 · Cited by 1,212 · see citing works
Limbic connections of the orbital and medial prefrontal cortex in macaque monkeys
Carmichael, S. T., & Price, J. L. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903630408 · Cited by 1,197 · see citing works
Self-citationFrontal cortex and reward-guided learning and decision-making
Rushworth, M. F. S., Noonan, M. P., Boorman, E. D., Walton, M. E., & Behrens, T. E. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.014 · Cited by 1,111 · see citing works
Goldman-Rakic, P. S. (1996) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1996.0129 · Cited by 1,072 · see citing works
Orbitofrontal Cortex as a Cognitive Map of Task Space
Wilson, R. C., Takahashi, Y. K., Schoenbaum, G., & Niv, Y. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.005 · Cited by 885 · see citing works
Architectonic subdivision of the human orbital and medial prefrontal cortex
Öngür, D., Ferry, A. T., & Price, J. L. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10609 · Cited by 944 · see citing works
Self-citationThe 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
Petrides, M., & Pandya, D. N. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2001.02090.x · Cited by 882 · see citing works
Ghashghaei, H. T., & Barbas, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00446-3 · Cited by 785 · see citing works
Informatic parcellation of the network involved in the computation of subjective value
Clithero, J. A., & Rangel, A. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst106 · Cited by 706 · see citing works
Impulsivity, frontal lobes and risk for addiction
Crews, F. T., & Boettiger, C. A. (2009) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2009.04.018 · Cited by 679 · see citing works
“The dlPFC and OFC is associated with behavioral regulation owing to its unique capacity to maintain and integrate sensory, affective, and associative information (Carmichael and Price, 1995a, b).”
BackgroundDevelopment of Anterior Cingulate Functional Connectivity from Late Childhood to Early Adulthood
Kelly, A. M. C., Di Martino, A., Uddin, L. Q., Shehzad, Z., Gee, D. G., Reiss, P. T., Margulies, D. S., Castellanos, F. X., & Milham, M. P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn117 · Cited by 572 · see citing works
Johansen-Berg, H., Gutman, D. A., Behrens, T. E. J., Matthews, P. M., Rushworth, M. F. S., Katz, E., Lozano, A. M., & Mayberg, H. S. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm167 · Cited by 561 · see citing works
Representations of Pleasant and Painful Touch in the Human Orbitofrontal and Cingulate Cortices
Rolls, E. T. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.308 · Cited by 535 · see citing works
Flexible control of mutual inhibition: a neural model of two-interval discrimination
Machens, C. K., Romo, R., & Brody, C. D. (2005) · Science · doi:10.1126/science.1104171 · Cited by 535 · see citing works
van der Meer, L., Costafreda, S., Aleman, A., & David, A. S. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.12.004 · Cited by 520 · see citing works
The orbitofrontal cortex: reward, emotion and depression
Rolls, E. T., Cheng, W., & Feng, J. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa196 · Cited by 474 · see citing works
Differential neural responses evoked by orthonasal versus retronasal odorant perception in humans
Small, D. M., Gerber, J. C., Mak, Y. E., & Hummel, T. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.022 · Cited by 463 · see citing works
Avery, J. A., Drevets, W. C., Moseman, S. E., Bodurka, J., Barcalow, J. C., & Simmons, W. K. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.11.027 · Cited by 442 · see citing works
Neurons in the frontal lobe encode the value of multiple decision variables
Kennerley, S. W., Dahmubed, A. F., Lara, A. H., & Wallis, J. D. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21100 · Cited by 453 · see citing works
Comparative aspects of amygdala connectivity
PRICE, J. L. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07070.x · Cited by 442 · see citing works
Self-citationWalton, M. E., Behrens, T. E. J., Buckley, M. J., Rudebeck, P. H., & Rushworth, M. F. S. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.027 · Cited by 397 · see citing works
Neural and behavioral substrates of mood and mood regulation
Davidson, R. J., Lewis, D. A., Alloy, L. B., Amaral, D. G., Bush, G., Cohen, J. D., Drevets, W. C., Farah, M. J., Kagan, J., McClelland, J. L., et al. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01458-0 · Cited by 411 · see citing works
Neural representations of subjective reward value
Peters, J., & Büchel, C. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.04.031 · Cited by 405 · see citing works
PRICE, J. L. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.008 · Cited by 395 · see citing works
Self-citationRudebeck, P. H., & Murray, E. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.049 · Cited by 405 · see citing works
Neuronal correlates of decision-making in secondary somatosensory cortex
Romo, R., Hernández, A., Zainos, A., Lemus, L., & Brody, C. D. (2002) · Nature Neuroscience · doi:10.1038/nn950 · Cited by 387 · see citing works
Dissociable components of rule-guided behavior depend on distinct medial and prefrontal regions
Buckley, M. J., Mansouri, F. A., Hoda, H., Mahboubi, M., Browning, P. G. F., Kwok, S. C., Phillips, A., & Tanaka, K. (2009) · Science · doi:10.1126/science.1172377 · Cited by 319 · see citing works
Saleem, K. S., Kondo, H., & Price, J. L. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21577 · Cited by 315 · see citing works
Self-citationPrimary somatosensory cortex discriminates affective significance in social touch
Gazzola, V., Spezio, M. L., Etzel, J. A., Castelli, F., Adolphs, R., & Keysers, C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1113211109 · Cited by 323 · see citing works
Vision Modulates Somatosensory Cortical Processing
Taylor-Clarke, M., Kennett, S., & Haggard, P. (2002) · Current Biology · doi:10.1016/s0960-9822(01)00681-9 · Cited by 309 · see citing works
Connectivity-based parcellation of the human orbitofrontal cortex
Kahnt, T., Chang, L. J., Park, S. Q., Heinzle, J., & Haynes, J.-D. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0257-12.2012 · Cited by 299 · see citing works
Neurobiological mechanisms of anhedonia
Gorwood, P. (2008) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2008.10.3/pgorwood · Cited by 285 · see citing works
Chiba, T., Kayahara, T., & Nakano, K. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03013-4 · Cited by 290 · see citing works
Responses to the Sensory Properties of Fat of Neurons in the Primate Orbitofrontal Cortex
Rolls, E. T., Critchley, H. D., Browning, A. S., Hernadi, I., & Lenard, L. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-04-01532.1999 · Cited by 278 · see citing works
Emotion-induced changes in human medial prefrontal cortex: I. During cognitive task performance
Simpson, J. R., Snyder, A. Z., Gusnard, D. A., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.683 · Cited by 278 · see citing works
Kondo, H., Saleem, K. S., & Price, J. L. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20796 · Cited by 236 · see citing works
Self-citationWarm pleasant feelings in the brain
Rolls, E. T., Grabenhorst, F., & Parris, B. A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.005 · Cited by 227 · see citing works
Price, J. L., Carmichael, S. T., & Drevets, W. C. (1996) · Progress in Brain Research · doi:10.1016/s0079-6123(08)61885-3 · Cited by 222 · see citing works
Self-citationRinaldi, T. (2008) · Frontiers in Neural Circuits · doi:10.3389/neuro.04.004.2008 · Cited by 210 · see citing works
Yao, Z., Wang, L., Lu, Q., Liu, H., & Teng, G. (2009) · Journal of Affective Disorders · doi:10.1016/j.jad.2008.10.013 · Cited by 205 · see citing works
Specializations for reward-guided decision-making in the primate ventral prefrontal cortex
Murray, E. A., & Rudebeck, P. H. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0013-4 · Cited by 169 · see citing works
Heterogeneous reward signals in prefrontal cortex
Wallis, J. D., & Kennerley, S. W. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.02.009 · Cited by 186 · see citing works
Rudebeck, P. H., Saunders, R. C., Lundgren, D. A., & Murray, E. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.042 · Cited by 170 · see citing works
Re-evaluating the role of the orbitofrontal cortex in reward and reinforcement
Noonan, M. P., Kolling, N., Walton, M. E., & Rushworth, M. F. S. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08023.x · Cited by 169 · see citing works
Noonan, M. P., Chau, B. K. H., Rushworth, M. F. S., & Fellows, L. K. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.0692-17.2017 · Cited by 167 · see citing works
Neural basis of interpersonal traits in neurodegenerative diseases
Sollberger, M., Stanley, C. M., Wilson, S. M., Gyurak, A., Beckman, V., Growdon, M., Jang, J., Weiner, M. W., Miller, B. L., & Rankin, K. P. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.06.006 · Cited by 167 · see citing works
Chau, B. K. H., Sallet, J., Papageorgiou, G. K., Noonan, M. P., Bell, A. H., Walton, M. E., & Rushworth, M. F. S. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.018 · Cited by 159 · see citing works
Disgust sensitivity predicts the insula and pallidal response to pictures of disgusting foods.
Calder, A. J., Beaver, J. D., Davis, M. H., Van Ditzhuijzen, J., Keane, J., & Lawrence, A. D. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05604.x · Cited by 154 · see citing works
Neuroethology of primate social behavior
Chang, S. W. C., Brent, L. J. N., Adams, G. K., Klein, J. T., Pearson, J. M., Watson, K. K., & Platt, M. L. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301213110 · Cited by 157 · see citing works
The Control of Mimicry by Eye Contact Is Mediated by Medial Prefrontal Cortex
Wang, Y., Ramsey, R., & de C. Hamilton, A. F. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0845-11.2011 · Cited by 141 · see citing works
De Raedt, R., Leyman, L., Baeken, C., Van Schuerbeek, P., Luypaert, R., Vanderhasselt, M.-A., & Dannlowski, U. (2010) · Biological Psychology · doi:10.1016/j.biopsycho.2010.09.015 · Cited by 135 · see citing works
Prefrontal connectomics: From anatomy to human imaging
Haber, S. N., Liu, H., Seidlitz, J., & Bullmore, E. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01156-6 · Cited by 129 · see citing works
Symptom Differences in Moderate to Severe Ibs Patients Based on Predominant Bowel Habit
Schmulson, M., Lee, O.-Y., Chang, L., Naliboff, B., & Mayer, E. A. (1999) · American Journal of Gastroenterology · doi:10.1111/j.1572-0241.1999.01440.x · Cited by 134 · see citing works
The human basal forebrain. Part II
Heimer, L., de Olmos, J. S., Alheid, G. F., Pearson, J., Sakamoto, N., Shinoda, K., Marksteiner, J., & Switzer, R. C. (1999) · Handbook of Chemical Neuroanatomy · doi:10.1016/s0924-8196(99)80024-4 · Cited by 125 · see citing works
Kennerley, S. W., & Wallis, J. D. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00273.2009 · Cited by 108 · see citing works
Hsu, D. T., & Price, J. L. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21440 · Cited by 97 · see citing works
Self-citationPardo, J. V., Sheikh, S. A., Schwindt, G. C., Lee, J. T., Kuskowski, M. A., Surerus, C., Lewis, S. M., Abuzzahab, F. S., Adson, D. E., & Rittberg, B. R. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.267 · Cited by 79 · see citing works
Conway, C. R., Chibnall, J. T., Gebara, M. A., Price, J. L., Snyder, A. Z., Mintun, M. A., Craig, A. D. (., Cornell, M. E., Perantie, D. C., Giuffra, L. A., et al. (2013) · Brain Stimulation · doi:10.1016/j.brs.2012.11.006 · Cited by 75 · see citing works
Self-citationCorticocortical and thalamocortical projections to layer I of the frontal neocortex in rats
Mitchell, B. D., & Cauller, L. J. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03084-0 · Cited by 71 · see citing works
Baxter, M. G., Gaffan, D., Kyriazis, D. A., & Mitchell, A. S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06740.x · Cited by 65 · see citing works
Hyperthermia-induced disruption of functional connectivity in the human brain network
Sun, G., Qian, S., Jiang, Q., Liu, K., Li, B., Li, M., Zhao, L., Zhou, Z., von Deneen, K. M., & Liu, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061157 · Cited by 58 · see citing works
Exploring the cortical evidence of a sensory-discrimination process
Romo, R., Hernández, A., Zainos, A., Brody, C., & Salinas, E. (2002) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1100 · Cited by 58 · see citing works
Sinclair, D., Webster, M. J., Fullerton, J. M., & Weickert, C. S. (2012) · BMC Psychiatry · doi:10.1186/1471-244x-12-84 · Cited by 55 · see citing works
Satiety-responsive neurons in the medial orbitofrontal cortex of the macaque.
Pritchard, T. C., Nedderman, E. N., Edwards, E. M., Petticoffer, A. C., Schwartz, G. J., & Scott, T. R. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.1.174 · Cited by 40 · see citing works
Vaidya, A. R., & Fellows, L. K. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1607-15.2015 · Cited by 37 · see citing works
“This region is connected robustly with subcortical regions involved in reward processing (Carmichael and Price, 1995a; Eblen and Graybiel, 1995; Cavada et al., 2000; Price, 2007) and has reciprocal connections with diverse sensory systems (Carmichael and Price, 1995b).”
BackgroundLittle, K., Olsson, C. A., Whittle, S., Youssef, G. J., Byrne, M. L., Simmons, J. G., Yücel, M., Foley, D. L., & Allen, N. B. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.85 · Cited by 29 · see citing works
Visual memory uniquely predicts anhedonia in schizophrenia but not bipolar disorder
Bodapati, A. S., Jenkins, L. M., Sharma, R. P., & Rosen, C. (2019) · Journal of Neuropsychology · doi:10.1111/jnp.12124 · Cited by 22 · see citing works
Comparing brain connections in different species using diffusion weighted imaging
Rushworth, M. F. S., Boorman, E., & Mars, R. B. (2009) · Diffusion MRI · doi:10.1016/b978-0-12-374709-9.00020-1 · Cited by 5 · see citing works
- Authors
- Carmichael, S. T., & Price, J. L.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Price, Joseph L.
- ORCID
- Carmichael, S. T.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1995-12-25
- Volume
- 363
- Issue
- 4
- Pages
- 642-664
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2095350455
- Cited by
- 678
- References
- 8
- Citations by year
- 2026: 9 · 2025: 12 · 2024: 14 · 2023: 28 · 2022: 17 · 2021: 22 · 2020: 23 · 2019: 23 · 2018: 18 · 2017: 20 · 2016: 15 · 2015: 28 · 2014: 29 · 2013: 36 · 2012: 32
- FWCI
- 3.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute on Deafness and Other Communication Disorders (DC00093)
- National Institute of Neurological Disorders and Stroke (NS-07057)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- orbitofrontal cortex, medial prefrontal cortex, sensory projections, corticocortical connections, inferior temporal cortex, somatosensory cortex, gustatory cortex, visceral afferents, agranular insular cortex, supplementary eye field, feeding network, macaque
- MeSH terms
- Animals, Female, Histocytochemistry, Macaca fascicularis, Macaca nemestrina, Male, Motor Cortex, Neural Pathways, Somatosensory Cortex, Temporal Lobe, Visual Cortex, Prefrontal Cortex
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