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A developmental neurobiological model of motivated behavior: Anatomy, connectivity and ontogeny of the triadic nodes
Open accessAbstract
Adolescence is the transition period that prepares individuals for fulfilling their role as adults. Most conspicuous in this transition period is the peak level of risk-taking behaviors that characterize adolescent motivated behavior. Significant neural remodeling contributes to this change. This review focuses on the functional neuroanatomy underlying motivated behavior, and how ontogenic changes can explain the typical behavioral patterns in adolescence. To help model these changes and provide testable hypotheses, a neural systems-based theory is presented. In short, the Triadic Model proposes that motivated behavior is governed by a carefully orchestrated articulation among three systems, approach, avoidance and regulatory. These three systems map to distinct, but overlapping, neural circuits, whose representatives are the striatum, the amygdala and the medial prefrontal cortex. Each of these system-representatives will be described from a functional anatomy perspective that includes a review of their connectivity and what is known of their ontogenic changes.
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“The combination of heightened activity in reward-related circuits and underdeveloped cognitive control centres contributes to greater emotionality, impulsivity and reward-seeking behaviour174,175.”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [174]
In the citing paper
“with continued maturation in the brain systems that underlie both (Casey, Getz et al. 2008; Ernst and Fudge 2009).”
From Developmental imaging genetics: Linking dopamine function to adolescent behavior (2014) · cites this paper as Ernst and Fudge 2009
In the citing paper
“Adolescence is characterized by developmentally specific changes in reward-related behavior, including initiation of alcohol involvement and increased risk-taking, that are assumed to reflect ongoing changes in the structure and function of reward-related circuitry (Ernst & Fudge, 2009; Forbes & Dahl, 2005; Spear, 2000).”
From Sleep and circadian contributions to adolescent alcohol use disorder (2015) · cites this paper as Ernst & Fudge, 2009
In the citing paper
“The amygdala has been long-recognized as a core node within the mesolimbocortical dopamine system (Berridge, 2004) and serves to modulate ventral striatal activity (Ernst and Fudge, 2009).”
From Neural networks involved in adolescent reward processing: an activation likelihood estimation meta-analysis of functional neuroimaging studies (2015) · cites this paper as Ernst and Fudge, 2009
In the citing paper
“Adding nuance to dual-systems models, the Triadic Model (Ernst and Fudge, 2009, Ernst et al., 2006) proposed that motivated behavior in adolescence results from the coordination of two social-affective neural circuits via cognitive circuitry.”
From Adolescent neurobiological susceptibility to social context (2016) · cites this paper as Ernst and Fudge, 2009
In the citing paper
“It is likely that they have a superordinate function that operates independently of valence, as part of a broad and overlapping affective circuitry (Ernst and Fudge, 2009).”
From Adolescent neurobiological susceptibility to social context (2016) · cites this paper as Ernst and Fudge, 2009
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Citations
Cites
An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803
(1994) · DigitalGeorgetown (Georgetown University Library) · Cited by 10,542
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444
The episodic buffer: a new component of working memory?
Baddeley, A. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01538-2 · Cited by 7,359
Brain development during childhood and adolescence: a longitudinal MRI study
Giedd, J. N., Blumenthal, J., Jeffries, N. O., Castellanos, F. X., Liu, H., Zijdenbos, A., Paus, T., Evans, A. C., & Rapoport, J. L. (1999) · Nature Neuroscience · doi:10.1038/13158 · Cited by 5,552
Handbook of Personality : Theory and Research
Pervin, L. A. (1992) · Cited by 4,543
Functional architecture of basal ganglia circuits: neural substrates of parallel processing
Alexander, G. E., & Crutcher, M. D. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90107-l · Cited by 4,131
Meeting of minds: the medial frontal cortex and social cognition
Amodio, D. M., & Frith, C. D. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1884 · Cited by 3,782
Specific impairments of planning
Shallice, T. (1982) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1982.0082 · Cited by 3,741
Frith, C., & Frith, U. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.041 · Cited by 3,561
Olds, J., & Milner, P. (1954) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0058775 · Cited by 3,176
Synaptic density in human frontal cortex —Developmental changes and effects of aging
Peter R., H. (1979) · Brain Research · doi:10.1016/0006-8993(79)90349-4 · Cited by 2,645
The Prefrontal Cortex: Anatomy, Physiology, and Neuropsychology of the Frontal Lobe
Fuster, J. M. (1980) · Cited by 2,367
Adolphs, R., Tranel, D., Damasio, H., & Damasio, A. (1994) · Nature · doi:10.1038/372669a0 · Cited by 2,360
Descartes’ Error. Emotion, Reason and the Human Brain. New York (Grosset/Putnam) 1994.
Damasio, A. R. (1994) · Cited by 2,266
Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex
Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129
Dissociable Roles of Ventral and Dorsal Striatum in Instrumental Conditioning
O'Doherty, J., Dayan, P., Schultz, J., Deichmann, R., Friston, K., & Dolan, R. J. (2004) · Science · doi:10.1126/science.1094285 · Cited by 2,088
Different contributions of the human amygdala and ventromedial prefrontal cortex to decision-making
Bechara, A., Damasio, H., Damasio, A. R., & Lee, G. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05473.1999 · Cited by 2,001
EVOLUTION OF THE BRAIN AND INTELLIGENCE
Radinsky, L., & Jerison, H. J. (1975) · Evolution · doi:10.2307/2407154 · Cited by 1,982
The neural basis of error detection: Conflict monitoring and the error-related negativity
Yeung, N., Botvinick, M. M., & Cohen, J. D. (2004) · Psychological Review · doi:10.1037/0033-295x.111.4.931 · Cited by 1,924
The neural basis of loss aversion in decision-making under risk
Tom, S. M., Fox, C. R., Trepel, C., & Poldrack, R. A. (2007) · Science · doi:10.1126/science.1134239 · Cited by 1,733
Chambers, R. A., Taylor, J. R., & Potenza, M. N. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.6.1041 · Cited by 1,719
(1967) · Medical Entomology and Zoology · Cited by 1,713
Preliminary analysis of functions of the temporal lobes in monkeys
KLÜVER, H. (1939) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1939.02270240017001 · Cited by 1,696
Haber, S. N., Fudge, J. L., & McFarland, N. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02369.2000 · Cited by 1,610
Self-citationFinding the self? An event-related fMRI study
Kelley, W. M., Macrae, C. N., Wyland, C. L., Caglar, S., Inati, S., & Heatherton, T. F. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/08989290260138672 · Cited by 1,606
The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction.
Aggleton, J. P. (1992) · Wiley-Liss eBooks · Cited by 1,536
Other minds in the brain: a functional imaging study of “theory of mind” in story comprehension.
Fletcher, P. (1995) · Cognition · doi:10.1016/0010-0277(95)00692-r · Cited by 1,522
In vivo evidence for post-adolescent brain maturation in frontal and striatal regions
Sowell, E. R., Thompson, P. M., Holmes, C. J., Jernigan, T. L., & Toga, A. W. (1999) · Nature Neuroscience · doi:10.1038/13154 · Cited by 1,439
Functional imaging of neural responses to expectancy and experience of monetary gains and losses
Breiter, H. C., Aharon, I., Kahneman, D., Dale, A., & Shizgal, P. (2001) · Neuron · doi:10.1016/s0896-6273(01)00303-8 · Cited by 1,404
Gallagher, H. L., Happé, F., Brunswick, N., Fletcher, P. C., Frith, U., & Frith, C. D. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00053-6 · Cited by 1,394
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
A mechanism for impaired fear recognition after amygdala damage
Adolphs, R., Gosselin, F., Buchanan, T. W., Tranel, D., Schyns, P., & Damasio, A. R. (2005) · Nature · doi:10.1038/nature03086 · Cited by 1,331
Structural maturation of neural pathways in children and adolescents: in vivo study
Paus, T., Zijdenbos, A., Worsley, K., Collins, D. L., Blumenthal, J., Giedd, J. N., Rapoport, J. L., & Evans, A. C. (1999) · Science · doi:10.1126/science.283.5409.1908 · Cited by 1,322
Sexual dimorphism of brain developmental trajectories during childhood and adolescence
Lenroot, R. K., Gogtay, N., Greenstein, D. K., Wells, E. M., Wallace, G. L., Clasen, L. S., Blumenthal, J. D., Lerch, J., Zijdenbos, A. P., Evans, A. C., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.053 · Cited by 1,309
Dissociation of reward anticipation and outcome with event-related fMRI
Knutson, B., Fong, G. W., Adams, C. M., Varner, J. L., & Hommer, D. (2001) · Neuroreport · doi:10.1097/00001756-200112040-00016 · Cited by 1,300
Galvan, A., Hare, T. A., Parra, C. E., Penn, J., Voss, H., Glover, G., & Casey, B. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1062-06.2006 · Cited by 1,282
Alheid, G. F., & Heimer, L. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90217-5 · Cited by 1,217
NEWMAN, S. W. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09271.x · Cited by 1,189
A philosophical essay on probabilities
Laplace, P. S., & Dale, A. I. (1952) · Journal of the Franklin Institute · doi:10.1016/0016-0032(52)90656-x · Cited by 1,140
Adolphs, R., Tranel, D., Damasio, H., & Damasio, A. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-09-05879.1995 · Cited by 1,138
Tracking the Hemodynamic Responses to Reward and Punishment in the Striatum
Delgado, M. R., Nystrom, L. E., Fissell, C., Noll, D. C., & Fiez, J. A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.6.3072 · Cited by 1,116
The neural basis of puberty and adolescence
Sisk, C. L., & Foster, D. L. (2004) · Nature Neuroscience · doi:10.1038/nn1326 · Cited by 1,085
Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey
Selemon, L. D., & Goldman-Rakic, P. S. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-03-00776.1985 · Cited by 1,074
Petrides, M., & Pandya, D. N. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00518.x · Cited by 1,068
Regulation of firing of dopaminergic neurons and control of goal-directed behaviors
Grace, A. A., Floresco, S. B., Goto, Y., & Lodge, D. J. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.003 · Cited by 1,034
Quantitative magnetic resonance imaging of human brain development: ages 4–18
Giedd, J. N., Snell, J. W., Lange, N., Rajapakse, J. C., Casey, B. J., Kozuch, P. L., Vaituzis, A. C., Vauss, Y. C., Hamburger, S. D., Kaysen, D., et al. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.4.551 · Cited by 1,024
Pitkänen, A., Savander, V., & LeDoux, J. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01125-9 · Cited by 980
Quirk, G. J., Likhtik, E., Pelletier, J. G., & Paré, D. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08800.2003 · Cited by 927
Reckless behavior in adolescence: A developmental perspective
ARNETT, J. (1992) · Developmental Review · doi:10.1016/0273-2297(92)90013-r · Cited by 917
Selemon, L. D., & Goldman-Rakic, P. S. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-11-04049.1988 · Cited by 908
An adaptive coding model of neural function in prefrontal cortex
Duncan, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35097575 · Cited by 874
Knutson, B. D., Fong, G., Bennett, S. M., Adams, C. M., & Hommer, D. W. (2003) · NeuroImage · doi:10.1016/s1053-8119(02)00057-5 · Cited by 868
Zald, D. H., & Pardo, J. V. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.8.4119 · Cited by 863
Dopamine neurons and their role in reward mechanisms
Schultz, W. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80007-4 · Cited by 809
THE CORTICO-STRIATE PROJECTION IN THE MONKEY
Kemp, J. M., & Powell, T. P. S. (1970) · Brain · doi:10.1093/brain/93.3.525 · Cited by 798
Ghashghaei, H. T., & Barbas, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00446-3 · Cited by 785
Anterior Prefrontal Function and the Limits of Human Decision-Making
Koechlin, É., & Hyafil, A. (2007) · Science · doi:10.1126/science.1142995 · Cited by 776
Rolls, E. T. (1996) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1996.0128 · Cited by 755
Benes, F. M. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950060041004 · Cited by 744
Daumas‐Duport, C., Scheithauer, B. W., Chodkiewicz, J. P., et al. (1988) · Neurosurgery · doi:10.1227/00006123-198811000-00002 · Cited by 721
Triadic model of the neurobiology of motivated behavior in adolescence.
ERNST, M., PINE, D. S., & HARDIN, M. (2006) · Psychological Medicine · doi:10.1017/s0033291705005891 · Cited by 718
Haber, S. N., Kim, K.-S., Mailly, P., & Calzavara, R. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0271-06.2006 · Cited by 686
Hippocampal Efferents Reach Widespread Areas of Cerebral Cortex and Amygdala in the Rhesus Monkey
Rosene, D. L., & Hoesen, G. W. V. (1977) · Science · doi:10.1126/science.410102 · Cited by 678
James, W. (1977) · Williams & Wilkins eBooks · doi:10.1037/10735-001 · Cited by 661
Architectonic subdivision of the orbital and medial prefrontal cortex in the macaque monkey
Carmichael, S. T., & Price, J. L. (1994) · Journal of Comparative Neurology · doi:10.1002/cne.903460305 · Cited by 656
Development of Cortical Circuitry and Cognitive Function
Goldman-Rakic, P. S. (1987) · Child Development · doi:10.2307/1130201 · Cited by 655
Different types of fear-conditioned behaviour mediated by separate nuclei within amygdala
Killcross, S., Robbins, T. W., & Everitt, B. J. (1997) · Nature · doi:10.1038/41097 · Cited by 652
Fellows, L. K. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh108 · Cited by 646
Yeterian, E. H., & Hoesen, G. W. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90059-8 · Cited by 641
Ernst, M., Nelson, E. E., Jazbec, S., McClure, E. B., Monk, C. S., Leibenluft, E., Blair, J., & Pine, D. S. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.038 · Cited by 635
The domain of supervisory processes and temporal organization of behaviour
Shallice, T., & Burgess, P. W. (1996) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1996.0124 · Cited by 633
Walker, D. L., & Davis, M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09375.1997 · Cited by 627
O'Doherty, J., Critchley, H., Deichmann, R., & Dolan, R. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-21-07931.2003 · Cited by 611
The orbital and medial prefrontal circuit through the primate basal ganglia
Haber, S., Kunishio, K., Mizobuchi, M., & Lynd-Balta, E. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04851.1995 · Cited by 605
Incentive-elicited brain activation in adolescents: Similarities and differences from young adults
Bjork, J. M., Knutson, B., Fong, G. W., Caggiano, D. M., Bennett, S. M., & Hommer, D. W. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4862-03.2004 · Cited by 567
Künzle, H. (2008) · Brain Behavior and Evolution · doi:10.1159/000123779 · Cited by 559
Sowell, E. R., Thompson, P. M., Holmes, C. J., Batth, R., Jernigan, T. L., & Toga, A. W. (1999) · NeuroImage · doi:10.1006/nimg.1999.0436 · Cited by 554
The domain of supervisory processes and the temporal organization of behaviour
Shallice, T., & Burgess, P. W. (1998) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524410.003.0003 · Cited by 551
Künzle, H., & Akert, K. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730108 · Cited by 540
Turner, B. H., Mishkin, M., & Knapp, M. E. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901910402 · Cited by 534
Wilensky, A. E., Schafe, G. E., Kristensen, M. P., & LeDoux, J. E. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4316-06.2006 · Cited by 533
An intricately patterned prefronto‐caudate projection in the rhesus monkey
Goldman, P. S., & Nauta, W. J. H. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901710305 · Cited by 509
Reward Circuitry Activation by Noxious Thermal Stimuli
Becerra, L. R., Breiter, H. C., Wise, R. A., González, R., & Borsook, D. (2001) · Neuron · doi:10.1016/s0896-6273(01)00533-5 · Cited by 501
Newly generated neurons in the amygdala and adjoining cortex of adult primates
Bernier, P. J., Bédard, A., Vinet, J., Lévesque, M., & Parent, A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.172403999 · Cited by 497
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
Differential Encoding of Losses and Gains in the Human Striatum
Seymour, B., Daw, N. D., Dayan, P., Singer, T., & Dolan, R. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0400-07.2007 · Cited by 479
Dorn, L. D., Dahl, R. E., Woodward, H. R., & Biro, F. (2006) · Applied Developmental Science · doi:10.1207/s1532480xads1001_3 · Cited by 477
Adolescent immaturity in attention-related brain engagement to emotional facial expressions
Monk, C. S., McClure, E. B., Nelson, E. E., Zarahn, E., Bilder, R. M., Leibenluft, E., Charney, D. S., Ernst, M., & Pine, D. S. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00355-0 · Cited by 470
Self-citationNeurobiology of Decision Making: A Selective Review from a Neurocognitive and Clinical Perspective
Ernst, M., & Paulus, M. P. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.06.004 · Cited by 469
Self-citationThe Prefrontal CortexExecutive and Cognitive Functions
Roberts, A., Robbins, T. W., & Weiskrantz, L. (1998) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524410.001.0001 · Cited by 468
LUNA, B., & SWEENEY, J. A. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1308.035 · Cited by 467
Lee, Y., & Davis, M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06434.1997 · Cited by 457
Direct Activation of the Ventral Striatum in Anticipation of Aversive Stimuli
Jensen, J., McIntosh, A. R., Crawley, A. P., Mikulis, D. J., Remington, G., & Kapur, S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00724-4 · Cited by 455
Jones, E. G., Coulter, J. D., Burton, H., & Porter, R. W. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730105 · Cited by 436
The accumbens: beyond the core-shell dichotomy
Heimer, L., Alheid, G. F., de Olmos, J. S., Groenewegen, H. J., Haber, S. N., Harlan, R. E., & Zahm, D. S. (1997) · Journal of Neuropsychiatry · doi:10.1176/jnp.9.3.354 · Cited by 429
Decision-making and impulse control after frontal lobe injuries
Bechara, A., & der Linden, M. V. (2005) · Current Opinion in Neurology · doi:10.1097/01.wco.0000194141.56429.3c · Cited by 426
Sánchez, M. M., Young, L. J., Plotsky, P. M., & Insel, T. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04657.2000 · Cited by 420
Rogers, R. D., Ramnani, N., Mackay, C. E., Wilson, J. L., Jezzard, P., Carter, C. S., & Smith, S. M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.11.012 · Cited by 414
Anatomical MRI of the developing human brain: what have we learned?
DURSTON, S., HULSHOFF POL, H. E., CASEY, B. J., GIEDD, J. N., BUITELAAR, J. K., & VAN ENGELAND, H. (2001) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/00004583-200109000-00009 · Cited by 410
Reynolds, S. M., & Berridge, K. C. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07308.2002 · Cited by 403
The amygdalostriatal projections in the monkey. An anterograde tracing study
Russchen, F. T., Bakst, I., Amaral, D. G., & Price, J. L. (1985) · Brain Research · doi:10.1016/0006-8993(85)90530-x · Cited by 395
The Temporal Lobe and Limbic System
GLOOR, P. (1997) · Medical Entomology and Zoology · Cited by 391
Maternal presence serves as a switch between learning fear and attraction in infancy
Moriceau, S., & Sullivan, R. M. (2006) · Nature Neuroscience · doi:10.1038/nn1733 · Cited by 386
Botvinick, M., & Plaut, D. C. (2004) · Psychological Review · doi:10.1037/0033-295x.111.2.395 · Cited by 375
Encoding Strategies Dissociate Prefrontal Activity from Working Memory Demand
Bor, D., Duncan, J., Wiseman, R. J., & Owen, A. M. (2003) · Neuron · doi:10.1016/s0896-6273(02)01171-6 · Cited by 373
Neural correlates of genetically abnormal social cognition in Williams syndrome
Meyer-Lindenberg, A., Hariri, A. R., Munoz, K. E., Mervis, C. B., Mattay, V. S., Morris, C. A., & Berman, K. F. (2005) · Nature Neuroscience · doi:10.1038/nn1494 · Cited by 357
A developmental examination of amygdala response to facial expressions
Guyer, A. E., Monk, C. S., McClure-Tone, E. B., Nelson, E. E., Roberson-Nay, R., Adler, A. D., Fromm, S. J., Leibenluft, E., Pine, D. S., & Ernst, M. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20114 · Cited by 357
Self-citationThe projection field of the stria terminalis in the rat brain. An experimental study
de Olmos, J. S., & Ingram, W. R. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901460303 · Cited by 355
Prefrontostriatal connections in relation to cortical architectonic organization in rhesus monkeys
Yeterian, E. H., & Pandya, D. N. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903120105 · Cited by 351
Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome
Bellugi, U., Lichtenberger, L., Mills, D. L., Galaburda, A. M., & Korenberg, J. R. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01397-1 · Cited by 351
Hitchcock, J. M., & Davis, M. (1991) · Behavioral Neuroscience · doi:10.1037/0735-7044.105.6.826 · Cited by 345
Flaherty, A. W., & Graybiel, A. M. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.4.1249 · Cited by 344
Hitchcock, J. M., & Davis, M. (1991) · Behavioral Neuroscience · doi:10.1037//0735-7044.105.6.826 · Cited by 342
Extended Amygdala and Basal Forebrain
Alheid, G. F. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07082.x · Cited by 334
Chikama, M., Mcfarland, N. R., Amaral, D., & Haber, S. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-24-09686.1997 · Cited by 333
The neuroscience of personality
Pickering, A. D., & Gray, J. A. (1999) · Medical Entomology and Zoology · Cited by 330
Sullivan, G. M., Apergis, J., Bush, D. E. A., Johnson, L. R., Hou, M., & Ledoux, J. E. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.015 · Cited by 327
Graveland, G. A., & DiFiglia, M. (1985) · Brain Research · doi:10.1016/0006-8993(85)91524-0 · Cited by 323
Medial temporal lobe structures and autism: A review of clinical and experimental findings
Bachevalier, J. (1994) · Neuropsychologia · doi:10.1016/0028-3932(94)90025-6 · Cited by 322
What have we learned about cognitive development from neuroimaging?
Durston, S., & Casey, B. J. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.10.010 · Cited by 319
Good memories of bad events in infancy
Sullivan, R. M., Landers, M., Yeaman, B., & Wilson, D. A. (2000) · Nature · doi:10.1038/35024156 · Cited by 315
Multimodal Amnesic Syndrome Following Bilateral Temporal and Basal Forebrain Damage
Damásio, A. R., Eslinger, P. J., Damasio, H., Hoesen, G. W. V., & Cornell, S. H. (1985) · Archives of Neurology · doi:10.1001/archneur.1985.04060030070012 · Cited by 310
Owen, A. M., Morris, R. G., Sahakian, B. J., Polkey, C. E., & Robbins, T. W. (1996) · Brain · doi:10.1093/brain/119.5.1597 · Cited by 308
Cortical afferents to the extended amygdala
McDONALD, A. J., SHAMMAH‐LAGNADO, S. J., SHI, C., & DAVIS, M. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09275.x · Cited by 306
Romeo, R. D., Bellani, R., Karatsoreos, I. N., Chhua, N., Vernov, M., Conrad, C. D., & McEwen, B. S. (2006) · Endocrinology · doi:10.1210/en.2005-1432 · Cited by 304
Stanton, G. B., Goldberg, M. E., & Bruce, C. J. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902710402 · Cited by 301
The Psychophysiological Nature of Introversion—Extraversion: A Modification of Eysenck's Theory
Gray, J. A. B. (1972) · Elsevier eBooks · doi:10.1016/b978-0-12-515350-8.50017-x · Cited by 297
Changes in cell-cycle kinetics during the development and evolution of primate neocortex
Kornack, D. R., & RAKIC, P. T. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.1242 · Cited by 292
Primate cingulostriatal projection: Limbic striatal versus sensorimotor striatal input
Kunishio, K., & Haber, S. N. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500302 · Cited by 290
Anxiety, Fears, and Phobias in Persons With Williams Syndrome
Dykens, E. M. (2003) · Developmental Neuropsychology · doi:10.1080/87565641.2003.9651896 · Cited by 289
The Intrinsic Organization of the Central Extended Amygdala
Cassell, M. D., Freedman, L. J., & Shi, C. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09270.x · Cited by 287
Reynolds, S. M., & Berridge, K. C. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-09-03261.2001 · Cited by 281
Crosby, E. C., & Humphrey, T. (1941) · The Journal of Comparative Neurology · doi:10.1002/cne.900740209 · Cited by 275
Emery, N. J., Capitanio, J. P., Mason, W. A., Machado, C. J., Mendoza, S. P., & Amaral, D. G. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.3.515 · Cited by 273
Estrogen receptors in the human forebrain and the relation to neuropsychiatric disorders
Österlund, M. K., & Hurd, Y. L. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00059-9 · Cited by 267
An Experiment of Nature: Brain Anatomy Parallels Cognition and Behavior in Williams Syndrome
Reiss, A. L., Eckert, M. A., Rose, F. E., Karchemskiy, A., Kesler, S. R., Chang, M., Reynolds-May, M. F., Kwon, H., & Galaburda, A. M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5272-03.2004 · Cited by 266
Widespread corticostriate projections from temporal cortex of the rhesus monkey
Hoesen, G. W. V., Yeterian, E. H., & Lavizzo‐Mourey, R. J. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901990205 · Cited by 264
Functional and Biochemical Alterations of the Medial Frontal Cortex in Obsessive-Compulsive Disorder
Yücel, M., Harrison, B. J., Wood, S. J., Fornito, A., Wellard, R. M., Pujol, J., Clarke, K., Phillips, M. L., Kyrios, M., Velakoulis, D., et al. (2007) · Archives of General Psychiatry · doi:10.1001/archpsyc.64.8.946 · Cited by 263
The human frontal lobes: Transcending the default mode through contingent encoding.
Mesulam, M.-M. (2002) · Principles of Frontal Lobe Function · doi:10.1093/acprof:oso/9780195134971.003.0002 · Cited by 262
Influence of psychological variables on the activity of the hypothalamic–pituitary–adrenal axis
Levine, S. D. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00548-3 · Cited by 257
Social Stress in Hamsters: Defeat Activates Specific Neurocircuits within the Brain
Kollack‐Walker, S., Watson, S. J., & Akil, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-22-08842.1997 · Cited by 253
Increased social fear and decreased fear of objects in monkeys with neonatal amygdala lesions
Prather, M. D., Lavenex, P., Mauldin-Jourdain, M. L., Mason, W. A., Capitanio, J. P., Mendoza, S. P., & Amaral, D. G. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00445-6 · Cited by 248
Brain Mechanisms of Serial and Parallel Processing during Dual-Task Performance
Sigman, M., & Dehaene, S. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0948-08.2008 · Cited by 242
Distinctive Personality Characteristics of 8-, 9-, and 10-Year-Olds With Williams Syndrome
Klein-Tasman, B., & Mervis, C. Β. (2003) · Developmental Neuropsychology · doi:10.1080/87565641.2003.9651895 · Cited by 238
Preliminary analysis of functions of the temporal lobes in monkeys. 1939 [classical article]
Klüver, H., & Bucy, P. C. (1997) · Journal of Neuropsychiatry · doi:10.1176/jnp.9.4.606 · Cited by 234
Kalin, N. H., Shelton, S. E., Davidson, R. J., & Kelley, A. E. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-06-02067.2001 · Cited by 227
Amygdaloid projections to ventromedial striatal subterritories in the primate
Fudge, J. L., Kunishio, K., Walsh, P., Richard, C., & Haber, S. N. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00546-2 · Cited by 226
Self-citationNeuropsychological Correlates of Bilateral Amygdala Damage
Tranel, D., & Hyman, B. T. (1990) · Archives of Neurology · doi:10.1001/archneur.1990.00530030131029 · Cited by 226
Infralimbic cortex activation increases c-fos expression in intercalated neurons of the amygdala
Berretta, S., Pantazopoulos, H., Caldera, M., Pantazopoulos, P., & Paré, D. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.01.020 · Cited by 223
Neuropsychological and neuropathological sequelae of cerebral anoxia: A critical review
Caine, D., & Watson, J. D. G. (2000) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617700611116 · Cited by 214
O’Doherty, J. P. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.036 · Cited by 206
Saunders, R. C., Rosene, D. L., & Hoesen, G. W. V. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902710203 · Cited by 206
Roth, T. L., & Sullivan, R. M. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.01.032 · Cited by 204
The intercalated cells of the amygdala
Millhouse, O. E. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902470209 · Cited by 204
The impact of early and late damage to the human amygdala on ‘theory of mind’ reasoning
Shaw, P., Lawrence, E., Radbourne, C., Bramham, J., Polkey, C. E., & David, A. S. (2004) · Brain · doi:10.1093/brain/awh168 · Cited by 203
Cavada, C., & Goldman-Rakic, P. S. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90037-o · Cited by 201
Functional modularity of the medial prefrontal cortex: involvement in human empathy
Seitz, R. J., Nickel, J., & Azari, N. P. (2006) · Neuropsychology · doi:10.1037/0894-4105.20.6.743 · Cited by 194
A hierarchical neuronal network for planning behavior
Dehaene, S., & Changeux, J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.24.13293 · Cited by 190
Neurobiological mechanisms of puberty in higher primates
Plant, T. M. (2004) · Human Reproduction Update · doi:10.1093/humupd/dmh001 · Cited by 188
Retrograde transport of D-[3H]-aspartate injected into the monkey amygdaloid complex
Amaral, D. G., & Insausti, R. (1992) · Experimental Brain Research · doi:10.1007/bf02259113 · Cited by 187
Izquierdo, A., Suda, R. K., & Murray, E. A. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1232-05.2005 · Cited by 186
Effects of aspiration versus neurotoxic lesions of the amygdala on emotional responses in monkeys
Meunier, M., Bachevalier, J., Murray, E. A., Málková, L., & Mishkin, M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00854.x · Cited by 179
Blanchard, D. C., Canteras, N. S., Markham, C. M., Pentkowski, N. S., & Blanchard, R. J. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.04.019 · Cited by 179
Machado, C. J., & Bachevalier, J. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.4.761 · Cited by 178
Convergence of sensory systems in the orbitofrontal cortex in primates and brain design for emotion.
Rolls, E. (2004) · Anatomical Record Part A-discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20126 · Cited by 170
Perlman, W. R., Webster, M. J., Kleinman, J. E., & Weickert, C. S. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.09.006 · Cited by 163
Reynolds, S. M., & Berridge, K. C. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02642.x · Cited by 163
Johnson, L. R., Aylward, R. L. M., Hussain, Z., & Totterdell, S. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90408-1 · Cited by 162
Amygdalohippocampal and Amygdalocortical Projections in the Primate Brain
Amaral, D. G. (1986) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-7971-3_1 · Cited by 158
Zirlinger, M., Kreiman, G., & Anderson, D. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.091094698 · Cited by 157
Zalla, T., Koechlin, É., Pietrini, P., Basso, G., Aquino, P., Sirigu, A., & Grafman, J. H. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00064.x · Cited by 154
Schoenbaum, G. M., Saddoris, M. P., & Stalnaker, T. A. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.001 · Cited by 152
Camp, L. L., & Rudy, J. W. (1988) · Developmental Psychobiology · doi:10.1002/dev.420210103 · Cited by 147
Insular and gustatory inputs to the caudal ventral striatum in primates
Fudge, J. L., Breitbart, M. A., Danish, M., & Pannoni, V. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20660 · Cited by 146
Self-citationWirth, M. M., & Schultheiss, O. C. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.08.003 · Cited by 145
The central nucleus of the amygdala projection to dopamine subpopulations in primates
Fudge, J. L., & Haber, S. N. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00092-0 · Cited by 138
Self-citationJames, F. O., Cermakian, N., & Boivin, D. B. (2007) · Sleep · doi:10.1093/sleep/30.11.1427 · Cited by 135
Passive cable properties of dendritic spines and spiny neurons
Wilson, C. J. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-01-00281.1984 · Cited by 134
Vaucher, E., Tong, X., Cholet, N., Lantin, S., & Hamel, É. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000529)421:2 · Cited by 126
Cortical input to parvalbumin-immunoreactive neurones in the putamen of the squirrel monkey
Lapper, S. R., Smith, Y., Sadikot, A. F., Parent, A., & Bolam, J. P. (1992) · Brain Research · doi:10.1016/0006-8993(92)90947-8 · Cited by 125
Goldman-Rakic, P. S. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-07-00721.1981 · Cited by 124
Albert, D., & Walsh, M. (1984) · Neuroscience and Biobehavioral Reviews · doi:10.1016/0149-7634(84)90017-4 · Cited by 124
Dysembryoplastic neuroepithelial tumors: CT, MR findings and imaging follow-up: a study of 53 cases.
Cosson, R., Varlet, P., Beuvon, F., et al. (2001) · PubMed · Cited by 123
The Development of Mother-Infant Interactions after Neonatal Amygdala Lesions in Rhesus Monkeys
Bauman, M. D., Lavenex, P., Mason, W. A., Capitanio, J. P., & Amaral, D. G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3263-03.2004 · Cited by 122
Direct comparison of projections from the central amygdaloid region and nucleus accumbens shell
Zahm, D. S., Jensen, S. L., Williams, E. S., & Martin, J. R. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00524.x · Cited by 121
Neural Circuitry Underlying Rule Use in Humans and Nonhuman Primates: Figure 1.
Bunge, S. A., Wallis, J. D., Parker, A. J., Braß, M., Crone, E. A., Hoshi, E., & Sakai, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2937-05.2005 · Cited by 116
Contextual Inhibitory Gating of Impulse Traffic in the Intra‐amygdaloid Network
Paré, D., Royer, S., Smith, Y., & Lang, E. J. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07073.x · Cited by 114
The functional effects of amygdala lesions in humans: A comparison with findings from monkeys.
Aggleton, J. P. (1992) · Cited by 108
Elliott, R., & Deakin, J. F. W. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(04)65004-5 · Cited by 105
Amygdala contribution to selective dimensions of emotion
Berntson, G. G., Bechara, A., Damásio, H., Tranel, D., & Cacioppo, J. T. (2007) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsm008 · Cited by 105
Emergence of Interoceptive and Exteroceptive Control of Behavior in Rats
Haroutunian, V. H., & Campbell, B. A. (1979) · Science · doi:10.1126/science.472715 · Cited by 105
Role of Amygdalo-Nigral Circuitry in Conditioning of a Visual Stimulus Paired with Food
Lee, H. J., Groshek, F., Petrovich, G. D., Cantalini, J. P., Gallagher, M., & Holland, P. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0416-05.2005 · Cited by 101
Jentsch, J. D., Roth, R. H., & Taylor, J. R. (2000) · Progress in Brain Research · doi:10.1016/s0079-6123(00)26028-7 · Cited by 99
Shaw, P., Bramham, J., Lawrence, E. J., Morris, R., Baron-Cohen, S., & David, A. S. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929054985491 · Cited by 96
Roselli, C. E., Klosterman, S., & Resko, J. A. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1343 · Cited by 91
Meyer, G., González‐Hernández, T., Carrillo-Padilla, F. J., & Ferres-Torres, R. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902840308 · Cited by 88
The expression of the clock protein PER2 in the limbic forebrain is modulated by the estrous cycle
Perrin, J. S., Segall, L. A., Harbour, V. L., Woodside, B., & Amir, S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601310103 · Cited by 88
Sarrieau, A., Dussaillant, M., Javoy-Agid, F., Philibert, D., Agid, Y., & Rostène, W. H. (1986) · Journal of Steroid Biochemistry · doi:10.1016/0022-4731(86)90300-6 · Cited by 86
Research works printed but not linked: 3
- Hemphill M Holm G Crutcher M Delong M Hedreen J Chronister R DeFrance J 1981 Afferent connections of the nucleus accumbens in the monkey Neurobiology of the Nucleus Accumbens Oxford University Press Oxford 75 81
- Robbins TW Everitt BJ 1992 Seminars in the neurosciences Saunders London, UK
- Steinberg L Belsky J Cicchetti D Toth S 1996 A sociobiological perspective on psychopathology in adolescence Rochester Symposium on Developmental Psychopathology University of Rochester Press Rochester, NY 93 124
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Background
Metadata
- Authors
- Ernst, M., & Fudge, J. L.
- Affiliations
- University of Rochester Medicine (US)
- ORCID
- Fudge, Julie L.
- Venue
- Neuroscience & Biobehavioral Reviews
- Publisher
- Elsevier BV
- Published
- 2009-03
- Volume
- 33
- Issue
- 3
- Pages
- 367-382
- ISSN
- 0149-7634 (ISSN-L)
- PMC
- PMC2696617
- OpenAlex
- W1970734866
- Cited by
- 358
- References
- 235
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 12 · 2023: 10 · 2022: 14 · 2021: 8 · 2020: 19 · 2019: 12 · 2018: 22 · 2017: 16 · 2016: 29 · 2015: 45 · 2014: 26 · 2013: 48 · 2012: 38
- FWCI
- 8.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Neuroscience & Biobehavioral Reviews (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (Z99 MH999999)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Social Sciences › Psychology › Clinical Psychology › Child and Adolescent Psychosocial and Emotional Development
- Keywords
- motivated behavior, adolescence, triadic model, regulatory regimes, striatum, amygdala, medial prefrontal cortex, neuronal connectivity, brain reorganization, risk-taking, functional neuroanatomy
- MeSH terms
- Adolescent, Amygdala, Animals, Brain Mapping, Corpus Striatum, Humans, Magnetic Resonance Imaging, Models, Biological, Motivation, Neural Pathways, Prefrontal Cortex
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