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Parallel incentive processing: an integrated view of amygdala function
Abstract
The amygdala is a heterogeneous structure that has been implicated in a wide variety of functions, most notably in fear conditioning. From this research, an influential serial model of amygdala processes has emerged in which aversive learning is mediated by the amygdala basolateral nucleus whereas performance, in this case of various defensive reflexes, is mediated by the central nucleus. By contrast, recent evidence from appetitive conditioning studies suggests that the basolateral and central nuclei operate in parallel to mediate distinct incentive processes: the basolateral nucleus encodes emotional events with reference to their particular sensory-specific features, whereas the central nucleus encodes their more general motivational or affective significance. Given that there is little if any direct behavioral evidence for the serial model, we suggest that more attention should be given to the claims of the parallel view.
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“In particular, given its access to primary sensory information, the CeA could orchestrate appropriate behavioral responses to salient stimuli with different valences [88,93].”
From Oxytocin Signaling in the Central Amygdala Modulates Emotion Discrimination in Mice (2019) · cites this paper as [88]
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“The data support a parallel model53 whereby, via distinct outputs to the DMS, the amygdala actively gates the nature of learning to regulate the balance of behavioral control strategies.”
From A dual-pathway architecture for stress to disrupt agency and promote habit (2025) · cites this paper as [53]
Citations
Cites
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444
THE AMYGDALA MODULATES THE CONSOLIDATION OF MEMORIES OF EMOTIONALLY AROUSING EXPERIENCES
McGaugh, J. L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144157 · Cited by 2,296
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
Integrative activity of the brain
Konorski, J. (1967) · Cited by 1,372
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Yin, H. H., Knowlton, B. J., & Balleine, B. W. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03095.x · Cited by 1,226
Self-citationMotivational control of goal-directed action
Dickinson, A., & Balleine, B. (1994) · Animal Learning & Behavior · doi:10.3758/bf03199951 · Cited by 995
Self-citationThe Amygdala: a functional analysis
Aggleton, J. P. (2000) · Cited by 966
Reward, Motivation, and Reinforcement Learning
Dayan, P., & Balleine, B. W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00963-7 · Cited by 855
Self-citationCerebral hemisphere regulation of motivated behavior
Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02905-x · Cited by 846
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Items 201–300 of 621
Disrupted cortico‐limbic connectivity during reward processing in remitted bipolar I disorder
Dutra, S. J., Man, V. Y., Hedy Kober, A., Cunningham, W. A., & Gruber, J. (2017) · Bipolar Disorders · doi:10.1111/bdi.12560 · Cited by 58
Neuropharmacology of learned flavor preferences
Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.06.001 · Cited by 57
Evolution of circuits regulating pleasure and happiness with the habenula in control
LOONEN, A. J. M., & Ivanova, S. А. (2017) · CNS Spectrums · doi:10.1017/s1092852917000748 · Cited by 56
Kaul, D., Schwab, S. G., Mechawar, N., & Matosin, N. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.01.025 · Cited by 58
A neuronal mechanism for motivational control of behavior
Courtin, J., Bitterman, Y., Müller, S., Hinz, J., Hagihara, K. M., Müller, C. R., & Lüthi, A. (2022) · Science · doi:10.1126/science.abg7277 · Cited by 55
John, Y. J., Zikopoulos, B., Bullock, D. H., & Barbas, H. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004722 · Cited by 58
Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06829.x · Cited by 53
Pool, E. R., Pauli, W. M., Kress, C. S., & O’Doherty, J. P. (2019) · Nature Human Behaviour · doi:10.1038/s41562-018-0527-9 · Cited by 56
Targeting memory processes with drugs to prevent or cure PTSD
Cain, C. K., Maynard, G. D., & Kehne, J. H. (2012) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2012.704020 · Cited by 50
A Role for the Human Amygdala in Higher Cognition
Schaefer, A., & Gray, J. R. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.5.355 · Cited by 57
Barreiros, I. V., Panayi, M. C., & Walton, M. E. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.02.017 · Cited by 51
Portal glucose influences the sensory, cortical and reward systems in rats
Delaere, F., Akaoka, H., Vadder, F. D., Duchampt, A., & Mithieux, G. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12354 · Cited by 61
Zhao, Q., Zhou, Z., Xu, H., Chen, S., Xu, F., Fan, W., & Han, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059351 · Cited by 51
Gill, T. M., Castaneda, P. J., & Janak, P. H. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq036 · Cited by 48
Wang, M. Z., & Hayden, B. Y. (2017) · Nature Communications · doi:10.1038/ncomms15821 · Cited by 51
The Human Basolateral Amygdala Is Indispensable for Social Experiential Learning
Rosenberger, L. A., Eisenegger, C., Naef, M., Terburg, D., Fourie, J., Stein, D. J., & van Honk, J. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.078 · Cited by 48
Lucas, M., Frenois, F., Vouillac‐Mendoza, C., Stinus, L., Cador, M., & Moine, C. L. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.006 · Cited by 47
van Steenbergen, H., Watson, P., Wiers, R. W. H. J., Hommel, B., & de Wit, S. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13586 · Cited by 47
Nuclear disconnection within the amygdala reveals a direct pathway to fearPreprint
Jimenez, S. A., & Maren, S. (2009) · Learning & Memory · doi:10.1101/lm.1607109 · Cited by 48
Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.05.009 · Cited by 47
Opposing Effects of Appetitive and Aversive Cues on Go/No-go Behavior and Motor Excitability
Chiu, Y., Cools, R., & Aron, A. R. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00585 · Cited by 52
Neural Correlates of Appetite and Hunger-Related Evaluative Judgments
Piech, R. M., Lewis, J., Parkinson, C. H., Owen, A. M., Roberts, A., Downing, P. E., & Parkinson, J. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006581 · Cited by 47
Bie, B., Zhu, W., & Pan, Z. Z. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.049 · Cited by 46
Sign-tracking is an expectancy-mediated behavior that relies on prediction error mechanismsPreprint
Derman, R. C., Schneider, K. N., Juarez, S., & Delamater, A. R. (2018) · Learning & Memory · doi:10.1101/lm.047365.118 · Cited by 48
The mere exposure effect depends on an odor’s initial pleasantness
Delplanque, S., Coppin, G., Bloesch, L., Cayeux, I., & Sander, D. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.00920 · Cited by 45
Organization of the sensory input to the telencephalon in the fire‐bellied toad, Bombina orientalis
Laberge, F., & Roth, G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21297 · Cited by 45
Increased enkephalin in brain of rats prone to overconsuming a fat-rich diet
Chang, G., Karatayev, O., Barson, J. R., Chang, S. Y. A., & LEIBOWITZ, S. F. (2010) · Physiology & Behavior · doi:10.1016/j.physbeh.2010.06.005 · Cited by 44
Semi-rational models of conditioning:
Daw, N. D., Courville, A. C., & Dayan, P. (2008) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199216093.003.0019 · Cited by 47
Responses to music: Emotional signaling, and learning
Gardiner, M. F. (2008) · Behavioral and Brain Sciences · doi:10.1017/s0140525x08005359 · Cited by 44
McDannald, M. A., & Galarce, E. M. (2010) · Brain Research · doi:10.1016/j.brainres.2010.12.050 · Cited by 44
Mendelsohn, A., Pine, A., & Schiller, D. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.019 · Cited by 45
Bernal, S. Y., Miner, P., Abayev, Y., Kandova, E., Gerges, M., Touzani, K., Sclafani, A. J., & Bodnar, R. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.06.032 · Cited by 43
Apathy blunts neural response to money in Parkinson's disease
Lawrence, A. D., Goerendt, I. K., & Brooks, D. J. (2011) · Social Neuroscience · doi:10.1080/17470919.2011.556821 · Cited by 47
Nonkes, 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
Adult attachment style modulates neural responses in a mentalizing task
Schneider-Haßloff, H., Straube, B., Nuscheler, B., Wemken, G., & Kircher, T. T. J. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.062 · Cited by 44
Modulation of attention and action in the medial prefrontal cortex of rats.
Sharpe, M. J., & Killcross, S. (2018) · Psychological Review · doi:10.1037/rev0000118 · Cited by 41
Self-citationThe Role of Value Systems in Decision Making
Dayan, P. (2008) · The MIT Press eBooks · doi:10.7551/mitpress/7735.003.0006 · Cited by 52
Brain activity and infant attachment history in young men during loss and reward processing
Quevedo, K. M., Waters, T. E. A., Scott, H., Roisman, G. I., Shaw, D. S., & Forbes, E. E. (2017) · Development and Psychopathology · doi:10.1017/s0954579417000116 · Cited by 40
Naneix, F., Darlot, F., Coutureau, É., & Cador, M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13149 · Cited by 43
Laminar- and Target-Specific Amygdalar Inputs in Rat Primary Gustatory Cortex
Haley, M. S., Fontanini, A., & Maffei, A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3224-15.2016 · Cited by 37
Dumais, K. M., Alonso, A. G., Bredewold, R., & Veenema, A. H. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.036 · Cited by 42
Klockars, O. A., Klockars, A., Levine, A. S., & Olszewski, P. K. (2018) · Neuroreport · doi:10.1097/wnr.0000000000001005 · Cited by 40
Unzipping empathy in psychopathy: Empathy and facial affect processing in psychopaths
Rijnders, R. J. P., Terburg, D., Bos, P. A., Kempes, M. M., & van Honk, J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.020 · Cited by 39
Optogenetic Long-Term Depression Induction in the PVT-CeL Circuitry Mediates Decreased Fear Memory
Chen, M., & Bi, L. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1407-z · Cited by 45
How does Music Arouse Emotions?
Juslin, P. N. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780198753421.003.0017 · Cited by 37
Multiple Memory Subsystems: Reconsidering Memory in the Mind and Brain
Sherman, B. E., Turk‐Browne, N. B., & Goldfarb, E. V. (2023) · Perspectives on Psychological Science · doi:10.1177/17456916231179146 · Cited by 48
The amygdala: A potential player in timing CS–US intervals
Díaz-Mataix, L., Tallot, L., & Doyère, V. (2013) · Behavioural Processes · doi:10.1016/j.beproc.2013.08.007 · Cited by 42
Neural mechanisms of decision‐making in aging
Lighthall, N. R. (2019) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1519 · Cited by 40
Chapter 3.1 Brain mechanisms of Pavlovian and instrumental aversive conditioning
Cain, C. K., & LeDoux, J. E. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(07)00007-0 · Cited by 41
An active inference perspective for the amygdala complex
Sladky, R., Kargl, D., Haubensak, W. E., & Lamm, C. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.11.004 · Cited by 41
Social Brain Development in Williams Syndrome: The Current Status and Directions for Future Research
Haas, B. W., & Reiss, A. L. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00186 · Cited by 40
Bruijnzeel, A. W., Alexander, J. C., Pérez, P. D., Bauzo-Rodriguez, R., Hall, G., Klausner, R., Guerra, V. M. C. D. O., Zeng, H., Igari, M., & Febo, M. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyu011 · Cited by 37
Amygdala-Cortical Control of Striatal Plasticity Drives the Acquisition of Goal-Directed Action
Fisher, S. D., Ferguson, L. A., Bertran-Gonzalez, J., & Balleine, B. W. (2020) · Current Biology · doi:10.1016/j.cub.2020.08.090 · Cited by 36
Self-citationConditioned associations and economic decision biases.
Guitart-Masip, M., Talmi, D., & Dolan, R. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.021 · Cited by 36
A pavlovian model of the amygdala and its influence within the medial temporal lobe
Carrere, M., & Alexandre, F. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00041 · Cited by 38
Polston, J. E., Rubbinaccio, H. Y., Morra, J. T., Sell, E. M., & Glick, S. D. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.11.024 · Cited by 36
The roles of the amygdala in the affective regulation of body, brain, and behaviour
Mirolli, M., Mannella, F., & Baldassarre, G. (2010) · Connection Science · doi:10.1080/09540091003682553 · Cited by 36
Prior cocaine exposure disrupts extinction of fear conditioningPreprint
Burke, K. A., Franz, T. M., Gugsa, N., & Schoenbaum, G. M. (2006) · Learning & Memory · doi:10.1101/lm.216206 · Cited by 36
Vicario, A., Abellán, A., Desfilis, E., & Medina, L. M. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00090 · Cited by 35
Neurotrophin signalling in amygdala-dependent cued fear learning
Meis, S., Endres, T., & Leßmann, V. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03260-3 · Cited by 40
FitzGerald, T. H. B., Schwartenbeck, P., & Dolan, R. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4389-13.2014 · Cited by 36
FOS expression induced by an ethanol-paired conditioned stimulus
Hill, K., Ryabinin, A. E., & Cunningham, C. L. (2007) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2007.04.017 · Cited by 35
Salling, M. C., Hodge, C. J., Psilos, K. E., Eastman, V. R., Faccidomo, S., & Hodge, C. W. (2017) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.10.011 · Cited by 29
The Roles of Basolateral Amygdala Parvalbumin Neurons in Fear Learning
Yau, J. O.-Y., Chaichim, C., Power, J., & McNally, G. P. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2461-20.2021 · Cited by 40
Towards an integrative theory of consciousness: Part 1 (Neurobiological and cognitive models)
De Sousa, A. (2013) · Mens Sana Monographs · doi:10.4103/0973-1229.109335 · Cited by 33
What Can Different Brains Do with Reward?
Gottfried, J. A. (2011) · CRC Press eBooks · doi:10.1201/b10776-10 · Cited by 33
Ortiz, J. P., Heinricher, M. M., & Selden, N. R. W. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.003 · Cited by 33
Translational neuroscience of basolateral amygdala lesions: Studies of urbach‐wiethe disease
Koen, N., Fourie, J., Terburg, D., Stoop, R., Morgan, B. E., Stein, D. J., & van Honk, J. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23731 · Cited by 36
The rational use of causal inference to guide reinforcement learning strengthens with age
Cohen, A. O., Nussenbaum, K., Dorfman, H. M., Gershman, S. J., & Hartley, C. A. (2020) · npj Science of Learning · doi:10.1038/s41539-020-00075-3 · Cited by 36
Parallel and hierarchical neural mechanisms for adaptive and predictive behavioral control
Macpherson, T., Matsumoto, M., Gomi, H., Morimoto, J., Uchibe, E., & Hikida, T. (2021) · Neural Networks · doi:10.1016/j.neunet.2021.09.009 · Cited by 30
Amygdala Intercalated Cells: Gate Keepers and Conveyors of Internal State to the Circuits of Emotion
Asede, D., Doddapaneni, D., & Bolton, M. M. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1176-22.2022 · Cited by 31
Holmes, N. M., Raipuria, M., Qureshi, O. A., Killcross, S., & Westbrook, R. F. (2018) · eNeuro · doi:10.1523/eneuro.0381-17.2017 · Cited by 31
Self-citationManassero, E., Renna, A., Milano, L., & Sacchetti, B. (2018) · Scientific Reports · doi:10.1038/s41598-017-19074-3 · Cited by 33
van Holstein, M., MacLeod, P. E., & Floresco, S. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109830 · Cited by 31
Engaging endogenous opioid circuits in pain affective processes
Kimmey, B. A., McCall, N. M., Wooldridge, L. M., Satterthwaite, T. D., & Corder, G. F. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24762 · Cited by 31
The effects of amphetamine exposure on outcome-selective Pavlovian-instrumental transfer in rats
Shiflett, M. W. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2724-y · Cited by 30
Haney, R. Z., Calu, D. J., Takahashi, Y. K., Hughes, B. W., & Schoenbaum, G. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0054-10.2010 · Cited by 31
Goal-Directed Behavior and Instrumental Devaluation: A Neural System-Level Computational Model
Mannella, F., Mirolli, M., & Baldassarre, G. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00181 · Cited by 33
Goal-Driven Cognition in the Brain: A Computational FrameworkPreprint
O’Reilly, R. C., Hazy, T. E., Mollick, J., Mackie, P., & Herd, S. A. (2014) · arXiv (Cornell University) · doi:10.48550/arxiv.1404.7591 · Cited by 54
A dual-pathway architecture for stress to disrupt agency and promote habit
Giovanniello, J. R., Paredes, N., Wiener, A., Ramírez-Armenta, K., Oragwam, C., Uwadia, H. O., Yu, A. L., Lim, K., Pimenta, J. S., Vilchez, G. E., et al. (2025) · Nature · doi:10.1038/s41586-024-08580-w · Cited by 30
The Neural Foundations of Reaction and Action in Aversive Motivation
Campese, V. D., Sears, R. M., Moscarello, J. M., Díaz-Mataix, L., Cain, C. K., & LeDoux, J. E. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_401 · Cited by 33
Brain activation patterns during classical conditioning with appetitive or aversive UCS
Cybulska-Kłosowicz, A., Zakrzewska, R., & Kossut, M. M. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.05.024 · Cited by 29
Stress Transiently Affects Pavlovian-to-Instrumental Transfer
Morgado, P. F., Silva, M., Sousa, N., & Cerqueira, J. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00093 · Cited by 30
Associative structure of fear memory after basolateral amygdala lesions in rats.
Rabinak, C. A., & Maren, S. (2008) · Behavioral Neuroscience · doi:10.1037/a0012903 · Cited by 30
Alcaraz, F., Marchand, A. R., Vidal, E., Guillou, A., Faugère, A., Coutureau, É., & Wolff, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1237-15.2015 · Cited by 29
Altered amygdala functional connectivity in adult Tourette’s syndrome
Werner, C. J., Stöcker, T., Kellermann, T., Wegener, H. P., Schneider, F. W., Shah, N. J., & Neuner, I. (2010) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-010-0161-7 · Cited by 31
Development of an aversive Pavlovian-to-instrumental transfer task in rat
Campese, V. D., McCue, M. G., Lázaro‐Muñoz, G., LeDoux, J. E., & Cain, C. K. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00176 · Cited by 32
Bercovici, D. A., Princz-Lebel, O., Tse, M. T., Moorman, D. E., & Floresco, S. B. (2018) · eneuro · doi:10.1523/eneuro.0422-18.2018 · Cited by 33
The Role of Value Systems in Decision Making
Dayan, P. (2008) · The MIT Press eBooks · doi:10.7551/mitpress/9780262195805.003.0003 · Cited by 29
The Effect of Ratio and Interval Training on Pavlovian-Instrumental Transfer in Mice
Wiltgen, B. J., Sinclair, C., Lane, C., Barrows, F., Molina, M., & Chabanon-Hicks, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048227 · Cited by 28
Environmental enrichment for pregnant sows modulates HPA-axis and behavior in the offspring
Tatemoto, P., Bernardino, T., Alves, L. R., Souza, A. C. D. O., Palme, R., & Zanella, A. J. (2019) · Applied Animal Behaviour Science · doi:10.1016/j.applanim.2019.104854 · Cited by 28
Toward a systems-oriented approach to the role of the extended amygdala in adaptive responding
Waraczynski, M. A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.015 · Cited by 28
Orsini, C. A., Hernandez, C. M., Bizon, J. L., & Setlow, B. (2018) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-018-00649-0 · Cited by 28
Plasticity of Fear and Safety Neurons of the Amygdala in Response to Fear Extinction
Sangha, S. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00354 · Cited by 28
Primate amygdala neurons evaluate the progress of self-defined economic choice sequences
Fabian Grabenhorst, B., Hernádi, I., & Schultz, W. (2016) · eLife · doi:10.7554/elife.18731 · Cited by 26
Interpersonal dysfunction in borderline personality: a decision neuroscience perspective
Hallquist, M. N., Hall, N. T., Schreiber, A., & Dombrovski, A. Y. (2017) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2017.09.011 · Cited by 28
Involvement of central amygdala NMDA receptor mechanism in morphine state-dependent memory retrieval
Ardjmand, A., Rezayof, A., & Zarrindast, M. (2010) · Neuroscience Research · doi:10.1016/j.neures.2010.09.005 · Cited by 26
Ousdal, O. T., Brown, A. A., Jensen, J., Nakstad, P., Melle, I. S., Agartz, I., Djurovic, S., Bogdan, R., Hariri, A. R., & Andreassen, O. A. (2012) · Twin Research and Human Genetics · doi:10.1017/thg.2012.5 · Cited by 25
Parsing Reward and Aversion in the Amygdala
Maren, S. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.011 · Cited by 28
Holmes, N. M., & Westbrook, R. F. (2017) · Learning & Memory · doi:10.1101/lm.044297.116 · Cited by 25
Metadata
- Authors
- Balleine, B. W., & Killcross, S.
- Affiliations
- University of California, Los Angeles (US)
- Cardiff University (GB)
- Corresponding author
- Balleine, Bernard W.
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2006-05
- Volume
- 29
- Issue
- 5
- Pages
- 272-279
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W2145286440
- Cited by
- 622
- References
- 72
- Citations by year
- 2026: 5 · 2025: 15 · 2024: 15 · 2023: 15 · 2022: 25 · 2021: 33 · 2020: 18 · 2019: 68 · 2018: 25 · 2017: 31 · 2016: 27 · 2015: 41 · 2014: 34 · 2013: 43 · 2012: 40
- FWCI
- 3.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- Funders
- National Institutes of Health
- U.S. Public Health Service (NIH 56446)
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- amygdala, parallel computing, serial model, basolateral amygdala, central amygdala, incentive processing, appetitive conditioning, fear conditioning, aversive learning, emotional meaning, defensive reflex
- MeSH terms
- Amygdala, Animals, Appetitive Behavior, Association Learning, Avoidance Learning, Conditioning, Classical, Conditioning, Operant, Humans, Models, Neurological, Motivation, Reward
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 ›
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