Cited by 1,200Memory and Neural MechanismsNeural and Behavioral Psychology StudiesNeurotransmitter Receptor Influence on Behavior

The DOI matches its Crossref record; 99 of the 99 references it cites were found in a registry or an index.

The amygdala and reward

Baxter, Mark G., Murray, Elisabeth A.·2002·Nature Reviews Neuroscience

DOI 10.1038/nrn875

Open this paper in CoChat — free account

Abstract

The amygdala -- an almond-shaped group of nuclei at the heart of the telencephalon -- has been associated with a range of cognitive functions, including emotion, learning, memory, attention and perception. Most current views of amygdala function emphasize its role in negative emotions, such as fear, and in linking negative emotions with other aspects of cognition, such as learning and memory. However, recent evidence supports a role for the amygdala in processing positive emotions as well as negative ones, including learning about the beneficial biological value of stimuli. Indeed, the amygdala's role in stimulus-reward learning might be just as important as its role in processing negative affect and fear conditioning.

Integrity signals

Registry

Crossref · 10.1038/nrn875

Cites

99 of 99 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Insensitivity to future consequences following damage to human prefrontal cortex
Bechara, A., Damasio, A. R., Damasio, H., & Anderson, S. W. (1994) · Cognition · doi:10.1016/0010-0277(94)90018-3 · Cited by 6,128
What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience?
Berridge, K. C., & Robinson, T. E. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00019-8 · Cited by 4,127
The amygdala: vigilance and emotion
Davis, M., & Whalen, P. J. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000812 · Cited by 2,882
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
Neural correlates of decision variables in parietal cortex
Platt, M. L., & Glimcher, P. W. (1999) · Nature · doi:10.1038/22268 · Cited by 1,721
The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction.
Aggleton, J. P. (1992) · Wiley-Liss eBooks · Cited by 1,536
The Neuroscience of Natural Rewards: Relevance to Addictive Drugs
Kelley, A. E., & Berridge, K. C. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-09-03306.2002 · Cited by 1,505
What is the amygdala?
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Relative reward preference in primate orbitofrontal cortex
Tremblay, L., & Schultz, W. (1999) · Nature · doi:10.1038/19525 · Cited by 1,314
The amygdala: Neurobiological aspects of emotion, memory and mental dysfunction
Scheel-Krüger, J. (1993) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(93)90037-5 · Cited by 1,281

Flagged first, then by citations

Show all 91 references

Research works printed but not linked: 1

Mishkin, M. & Oubre, J. L. Dissociation of deficits on visual memory tasks after inferior temporal and amygdala lesions in monkeys. Soc. Neurosci. Abstr. 2, 1127 (1976).

Sorted by citations

Items 701–800 of 999

Developmental Expression of Orphan G Protein-Coupled Receptor 50 in the Mouse Brain
Grünewald, E., Tew, K. D., Porteous, D. J., & Thomson, P. A. (2012) · ACS Chemical Neuroscience · doi:10.1021/cn300008p · Cited by 19
Neuroimaging Studies Reveal the Subtle Difference Among Social Network Size Measurements and Shed Light on New Directions
Liu, X., Liu, S., Huang, R., Chen, X., Xie, Y., Ma, R., Luo, Y., Bu, J., & Zhang, X. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00461 · Cited by 18
Gene expression in the social behavior network of the wire‐tailed manakin ( Pipra filicauda ) brain
Horton, B. M., Ryder, T. B., Moore, I. T., & Balakrishnan, C. N. (2019) · Genes Brain & Behavior · doi:10.1111/gbb.12560 · Cited by 18
The impact of targeted cathodal transcranial direct current stimulation on reward circuitry and affect in Bipolar Disorder
Bertocci, M. A., Chase, H. W., Graur, S., Stiffler, R. S., Edmiston, E. K., Coffman, B. A., Greenberg, B. D., & Phillips, M. L. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0567-1 · Cited by 17
Using deep learning to classify pediatric posttraumatic stress disorder at the individual level
Yang, J., Lei, D., Qin, K., Pinaya, W. H. L., Suo, X., Li, W., Li, L., Kemp, G. J., & Gong, Q. (2021) · BMC Psychiatry · doi:10.1186/s12888-021-03503-9 · Cited by 21
What Can Different Brains Do with Reward
Murray, E., Wise, S., & Rhodes, S. E. (2011) · Frontiers in neuroscience · doi:10.1201/b10776-6 · Cited by 30
Self-citation
Age-related changes in conditioned flavor preference in rats
Renteria, A. F., Silbaugh, B. C., Tolentino, J. C., & Gilbert, P. E. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.10.016 · Cited by 19
A model of preverbal social development and its application to social dysfunctions in autism
Berger, M. (2006) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2005.01586.x · Cited by 20
Neural correlates of positive and negative performance feedback in younger and older adults
Drueke, B., Weichert, L., Forkmann, T., Mainz, V., Gauggel, S., & Boecker, M. (2015) · Behavioral and Brain Functions · doi:10.1186/s12993-015-0062-z · Cited by 26
Cognitive impairment in a young marmoset reveals lateral ventriculomegaly and a mild hippocampal atrophy: a case report
Sadoun, A., Strelnikov, K., Bonté, E., Fonta, C., & Girard, P. (2015) · Scientific Reports · doi:10.1038/srep16046 · Cited by 18
A preliminary study on functional activation and connectivity during frustration in youths with bipolar disorder
Ross, A. J., Roule, A. L., Deveney, C. M., Towbin, K. E., Brotman, M. A., Leibenluft, E., & Tseng, W. (2020) · Bipolar Disorders · doi:10.1111/bdi.12985 · Cited by 18
Endogenous fluorescence imaging of somatosensory cortical activities after discrimination learning in rats
Shibuki, K., Ono, K., Hishida, R., & Kudoh, M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.10.004 · Cited by 18
Neural Substrates of Youth and Adult Antisocial Behavior
Waller, R. E., Dotterer, H. L., Murray, L., & Hyde, L. W. (2018) · Cambridge University Press eBooks · doi:10.1017/9781316847992.040 · Cited by 17
Impact of prenatal marijuana exposure on adolescent brain structural and functional connectivity and behavioural outcomes
Vishnubhotla, R. V., Ahmad, S. T., Zhao, Y., & Radhakrishnan, R. (2024) · Brain Communications · doi:10.1093/braincomms/fcae001 · Cited by 18
Representation of Anticipated Rewards and Punishments in the Human Brain
Ben‐Zion, Z., & Levy, I. (2024) · Annual Review of Psychology · doi:10.1146/annurev-psych-022324-042614 · Cited by 21
Can Understanding Reward Help Illuminate Anhedonia?
Kaya, S., & McCabe, C. (2019) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-019-00186-1 · Cited by 16
Pre-scan state anxiety is associated with greater right amygdala-hippocampal response to fearful versus happy faces among trait-anxious Latina girls
Díaz, D. E., Tseng, W., & Michalska, K. J. (2024) · BMC Psychiatry · doi:10.1186/s12888-023-05403-6 · Cited by 17
Similar Neural Activity during Fear and Disgust in the Rat Basolateral Amygdala
Shabel, S. J., Schairer, W. W., Donahue, R. J., Powell, V. E., & Janak, P. H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027797 · Cited by 18
Trait positive affect is associated with hippocampal volume and change in caudate volume across adolescence
Dennison, M., Whittle, S., Yücel, M., Byrne, M. L., Schwartz, O., Simmons, J. G., & Allen, N. B. (2014) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-014-0319-2 · Cited by 16
Dopamine-Glutamate Interactions in Reward-Related Incentive Learning
Beninger, R. J., & Gerdjikov, T. V. (2005) · Humana Press eBooks · doi:10.1007/978-1-59259-852-6_14 · Cited by 17
Tract-Specific White Matter Correlates of Age-Related Reward Devaluation Deficits in Macaque Monkeys
Gray, D. T., Umapathy, L., Burke, S. N., Trouard, T. P., & Barnes, C. A. (2018) · Journal of Neuroimaging in Psychiatry and Neurology · doi:10.17756/jnpn.2018-023 · Cited by 16
The Role of Callous-Unemotional Traits on Adolescent Positive and Negative Emotional Reactivity: A Longitudinal Community-Based Study
Truedsson, E., Fawcett, C. A., Wesevich, V. G., Gredebäck, G., & Wåhlstedt, C. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00573 · Cited by 17
Functional neuroimaging applications in marketing: some methodological and statistical considerations
Mostafa, M. M. (2014) · Qualitative Market Research An International Journal · doi:10.1108/qmr-06-2011-0003 · Cited by 21
It’s in the eye of the beholder: selective attention to drink properties during tasting influences brain activation in gustatory and reward regions
van Rijn, I., de Graaf, C., & Smeets, P. A. M. (2017) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9710-2 · Cited by 17
Affective memory rehearsal with temporal sequences in amygdala neurons
Reitich-Stolero, T., & Paz, R. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0542-9 · Cited by 17
Nutritional factors affecting wound healing.
Thomas, D. R. (1996) · PubMed · Cited by 17
The projection from dorsal medial prefrontal cortex to basolateral amygdala promotes behaviors of negative emotion in rats
Cai, Y.-Q., Ge, J., & Pan, Z.-Z. Z. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1331864 · Cited by 16
Pathophysiological aspects of complex PTSD – a neurobiological account in comparison to classic posttraumatic stress disorder and borderline personality disorder
Stopyra, M. A., Simon, J. J., Rheude, C., & Nikendei, C. (2022) · Reviews in the Neurosciences · doi:10.1515/revneuro-2022-0014 · Cited by 17
A randomized controlled trial investigating the effect of liraglutide on self-reported liking and neural responses to food stimuli in participants with obesity
Coppin, G., Tord, D. M., Pool, E. R., Locatelli, L., Achaïbou, A., Erdemli, A., Pérez, L. L., Wuensch, L., Cereghetti, D. M., Golay, A., et al. (2023) · International Journal of Obesity · doi:10.1038/s41366-023-01370-w · Cited by 16
Multimodal MRI evaluation of parkinsonian limbic pathologies
Wang, E. W., Du, G., Lewis, M. M., Lee, E.-Y., Jesus, S. D., Kanekar, S. G., Kong, L., & Huang, X. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.01.004 · Cited by 16
Long time-scales in primate amygdala neurons support aversive learning
Taub, A. H., Reitich-Stolero, T., Livneh, U., Shohat, Y., & Paz, R. (2018) · Nature Communications · doi:10.1038/s41467-018-07020-4 · Cited by 16
Restructuring of amygdala subregion apportion across adolescence
Campbell, C. E., Mezher, A. F., Eckel, S. P., Tyszka, J. M., Pauli, W. M., Nagel, B. J., & Herting, M. M. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2020.100883 · Cited by 16
Differences in resting-state functional connectivity according to the level of impulsiveness in patients with internet gaming disorder
Kim, S., Kim, M.-K., Shin, Y., Kim, H. E., Kwon, J. H., & Kim, J. (2021) · Journal of Behavioral Addictions · doi:10.1556/2006.2021.00005 · Cited by 16
Cortical depression in the mouse auditory cortex after sound discrimination learning
Ohshima, S., Tsukano, H., Kubota, Y., Takahashi, K., Hishida, R., Takahashi, S., & Shibuki, K. (2010) · Neuroscience Research · doi:10.1016/j.neures.2010.01.005 · Cited by 17
Effects of interaction of an early experience of reward through maternal contact or its denial with social stress during adolescence on the serotonergic system and the stress responsiveness of adult female rats
Raftogianni, A., Diamantopoulou, A., Alikaridis, F., Stamatakis, A., & Stylianopoulou, F. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.01.032 · Cited by 16
Relationship between Personality Traits and Brain Reward Responses when Playing on a Team
Morawetz, C., Kirilina, E. P., Baudewig, J., & Heekeren, H. R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087277 · Cited by 16
Rewarding images do not invoke the reward positivity: They inflate it
Brown, D. R., & Cavanagh, J. F. (2018) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2018.02.012 · Cited by 18
Repetitive transcranial magnetic stimulation: Re-wiring the alcoholic human brain
Diana, M., Bolloni, C., Antonelli, M., Giuda, D. D., Cocciolillo, F., Fattore, L., & Addolorato, G. (2018) · Alcohol · doi:10.1016/j.alcohol.2018.05.011 · Cited by 16
Pain imaging: future applications to integrative clinical and basic neurobiology
Borsook, D., & Becerra, L. R. (2003) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(03)00099-1 · Cited by 16
GluA1 in central amygdala increases pain but inhibits opioid withdrawal-induced aversion
Cai, Y.-Q., Hou, Y.-Y., & Pan, Z. Z. (2020) · Molecular Pain · doi:10.1177/1744806920911543 · Cited by 15
Selectively predicting the onset of ADHD, oppositional defiant disorder, and conduct disorder in early adolescence with high accuracy
de Lacy, N., & Ramshaw, M. J. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1280326 · Cited by 16
Neighborhood Resources Associated With Psychological Trajectories and Neural Reactivity to Reward After Trauma
Webb, E. K., Stevens, J. S., Ely, T. D., Lebois, L. A. M., van Rooij, S. J. H., Bruce, S. E., House, S. L., Beaudoin, F. L., An, X., Neylan, T. C., et al. (2024) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2024.2148 · Cited by 16
The Algorithmic Agent Perspective and Computational Neuropsychiatry: From Etiology to Advanced Therapy in Major Depressive Disorder
Ruffini, G., Castaldo, F., Lopez-Sola, E., Sanchez-Todo, R., & Vohryzek, J. (2024) · Entropy · doi:10.3390/e26110953 · Cited by 20
Neural Correlates of the Formation and Retention of Cocaine-Induced Stimulus–Reward Associations
Nelissen, K., Jarraya, B., Arsenault, J. T., Rosen, B. R., Wald, L. L., Mandeville, J. B., Marota, J. J. A., & Vanduffel, W. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.02.021 · Cited by 15
Separating analgesia from reward within the ventral tegmental area
Schifirnet, E., Bowen, S. E., & Borszcz, G. S. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.009 · Cited by 15
Social processing by the primate medial frontal cortex
Putnam, P. T., & Chang, S. W. C. (2021) · International review of neurobiology · doi:10.1016/bs.irn.2020.12.003 · Cited by 18
Affect Regulation in Pediatric Bipolar Disorder
Dickstein, D. P., Brazel, A. C., Goldberg, L. D., & Hunt, J. (2009) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2008.12.003 · Cited by 15
Task-Dependent Spatial Selectivity in the Primate Amygdala
Peck, E. L., Peck, C. J., & Salzman, C. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3217-14.2014 · Cited by 15
The central amygdala regulates sodium intake in sodium-depleted rats: Role of 5-HT3 and 5-HT2C receptors
Luz, C. P. N., Souza, A. B. D. S., Reis, R., Mineiro, P. C. D. O., Ferreira, H. S., Fregoneze, J. B., & Silva, E. D. C. E. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.012 · Cited by 15
The amygdalostriatal and corticostriatal effective connectivity in anticipation and evaluation of facial attractiveness
Yu, H., Zhou, Z., & Zhou, X. (2013) · Brain and Cognition · doi:10.1016/j.bandc.2013.04.011 · Cited by 15
Mutual Influence of Reward Anticipation and Emotion on Brain Activity during Memory Retrieval
Yan, C., Liu, F., Li, Y., Zhang, Q., & Cui, L. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01873 · Cited by 15
A Heuristic Pathophysiological Model of Tinnitus
Ridder, D. D. (2010) · Springer eBooks · doi:10.1007/978-1-60761-145-5_21 · Cited by 15
Hydration level is an internal variable for computing motivation to obtain water rewards in monkeys
Minamimoto, T., Yamada, H., Hori, Y., & Suhara, T. (2012) · Experimental Brain Research · doi:10.1007/s00221-012-3054-3 · Cited by 15
Blaming the Parts Instead of the Person: Understanding and Applying Neurobiological Factors Associated with Psychopathy
Freedman, L. F., & Verdun‐Jones, S. N. (2010) · Canadian Journal of Criminology and Criminal Justice/La Revue canadienne de criminologie et de justice pénale · doi:10.3138/cjccj.52.1.29 · Cited by 15
Involvement of NMDA and AMPA/KA receptors in the nucleus accumbens core in instrumental learning guided by reward‐predictive cues
Giertler, C., Bohn, I., & Hauber, W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03983.x · Cited by 16
Excessive Sensory Stimulation during Development Alters Neural Plasticity and Vulnerability to Cocaine in Mice
Ravinder, S., Donckels, E. A., Ramirez, J. S. B., Christakis, D., Ramirez, J., & Ferguson, S. M. (2016) · eNeuro · doi:10.1523/eneuro.0199-16.2016 · Cited by 19
Acquisition of specific response–outcome associations requires NMDA receptor activation in the basolateral amygdala but not in the insular cortex
Parkes, S. L., Ferreira, G., & Coutureau, É. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.12.005 · Cited by 14
‘Proactive’ use of cue-context congruence for building reinforcement learning’s reward function
Zsuga, J., Bíró, K., Tajti, G., Szilasi, M. E., Papp, C., Juhász, B., & Gesztelyi, R. (2016) · BMC Neuroscience · doi:10.1186/s12868-016-0302-7 · Cited by 13
Trauma Affects Prospective Relationships Between Reward-Related Ventral Striatal and Amygdala Activation and 1-Year Future Hypo/Mania Trajectories
Eckstrand, K., Forbes, E. E., Bertocci, M. A., Chase, H. W., Greenberg, T., Lockovich, J., Stiffler, R., Aslam, H. A., Graur, S., Bebko, G. M., et al. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.11.017 · Cited by 14
Medial Prefrontal Cortex Activity to Reward Outcome Moderates the Association Between Victimization Due to Sexual Orientation and Depression in Youth
Eckstrand, K., Silk, J. S., Nance, M., Wallace, M. L., Buckley, N., Lindenmuth, M., Flores, L. E., Alarcón, G., Quevedo, K. M., Phillips, M. L., et al. (2022) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2022.08.009 · Cited by 15
Complementary roles for the amygdala and hippocampus during different phases of appetitive information processing
Holahan, M. R. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.06.001 · Cited by 14
Cannabinoid receptors in the basolateral amygdala are involved in the potentiation of morphine rewarding properties in the acquisition, but not expression of conditioned place preference in rats
Haghparast, A., Shamsizadeh, A., Samandari, R., Omranifard, A., Vaziri, A., & Razavi, Y. (2014) · Brain Research · doi:10.1016/j.brainres.2014.04.003 · Cited by 14
Understanding decision neuroscience: A multidisciplinary perspective and neural substrates
Miyapuram, K. P., & Pammi, V. S. C. (2013) · Progress in brain research · doi:10.1016/b978-0-444-62604-2.00014-9 · Cited by 18
Social Saliency
Wang, S., & Adolphs, R. (2016) · Cognitive science and technology · doi:10.1007/978-981-10-0213-7_8 · Cited by 14
The influence of social signals on the self-experience of pain: A neuroimaging review
Sharvit, G., & Schweinhardt, P. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.856874 · Cited by 11
Childhood abuse influences clinical features of major depressive disorder by modulating the functional network of the right amygdala subregions
Chen, S., Yin, Y., Zhang, Y., Jiang, W., Hou, Z., & Yuan, Y. (2024) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2024.103946 · Cited by 12
Amygdala in Action: Functional Connectivity during Approach and Avoidance Behaviors
Leitão, J., Burckhardt, M., & Vuilleumier, P. O. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01800 · Cited by 16
Brain Activation in Response to Low-Calorie Food Pictures: An Explorative Analysis of a Randomized Trial With Dapagliflozin and Exenatide
van Ruiten, C. C., Veltman, D. J., Nieuwdorp, M., & IJzerman, R. G. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.863592 · Cited by 13
GABAergic inactivation of basolateral amygdala alters behavioral processes other than primary reward of ventral tegmental self-stimulation
Simmons, D. A., Brooks, B. M., & Neill, D. B. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.03.034 · Cited by 13
Reward, Context, and Human Behaviour
Blaukopf, C. L., & DiGirolamo, G. J. (2007) · The Scientific World JOURNAL · doi:10.1100/tsw.2007.122 · Cited by 15
Can beneficial ends justify lying? Neural responses to the passive reception of lies and truth-telling with beneficial and harmful monetary outcomes
Yin, L., & Weber, B. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv127 · Cited by 14
Establishing aversive, but not safe, taste memories requires lateralized pontine–cortical connections
Clark, E. W., & Bernstein, I. L. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.030 · Cited by 13
Working and Reference Memory in Seizure-Prone and Seizure-Resistant Rats: Impact of Amygdala Kindling.
McIntyre, D., McLeod, W., & Anisman, H. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.2.314 · Cited by 13
Mental processes and strategic equilibration: An fMRI study of selling strategies in second price auctions
Grether, D. M., Plott, C. R., Rowe, D. B., Sereno, M. I., & Allman, J. M. (2007) · Experimental Economics · doi:10.1007/s10683-006-9135-z · Cited by 13
Appetitive Needs and Addiction
Sussman, S. Y., & Pakdaman, S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.004 · Cited by 12
The Dark and Gloomy Brain: Grey Matter Volume Alterations in Major Depressive Disorder–Fine-Grained Meta-Analyses
Romeo, Z., Biondi, M., Oltedal, L., & Spironelli, C. (2024) · Depression and Anxiety · doi:10.1155/2024/6673522 · Cited by 12
Neural Responses to Smoking Stimuli Are Influenced by Smokers' Attitudes towards Their Own Smoking Behaviour
Stippekohl, B., Winkler, M. H., Walter, B., Kagerer, S., Mucha, R. F., Pauli, P., Vaitl, D., & Stark, R. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046782 · Cited by 13
Lesions of the nucleus accumbens disrupt reinforcement omission effects in rats
Judice-Daher, D. M., & Bueno, J. L. O. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.06.028 · Cited by 12
Executive Functions Of Persistent Violent Offenders: A Critical Review Of The Literature
Brito, S. A. D., & Hodgins, S. (2009) · Oxford University Press eBooks · doi:10.1093/oso/9780199543533.003.0010 · Cited by 13
Context-Dependent and Context-Independent Effects of D1 Receptor Antagonism in the Basolateral and Central Amygdala during Cocaine Self-Administration
Kim, E. S., & Lattal, K. M. (2019) · eNeuro · doi:10.1523/eneuro.0203-19.2019 · Cited by 11
Characteristic Alteration of Subcortical Nuclei Shape in Medication-Free Patients with Obsessive-Compulsive Disorder
Zhang, L., Hu, X., Li, H., Lu, L., Li, B., Hu, X., Bu, X., Tang, S., Tang, W., Liu, N., et al. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.102040 · Cited by 12
Dynamic functional connectivity between nucleus accumbens and the central executive network relates to chronic cannabis use
Yoo, H. B., Moya, B. E., & Filbey, F. M. (2020) · Human Brain Mapping · doi:10.1002/hbm.25036 · Cited by 12
Toward a holistic view of value and social processing in the amygdala: Insights from primate behavioral neurophysiology
Putnam, P. T., & Chang, S. W. C. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113356 · Cited by 11
Amygdala or hippocampus damage only minimally impacts affective responding to threat.
Charbonneau, J. A., Bennett, J. L., & Bliss‐Moreau, E. (2021) · Behavioral Neuroscience · doi:10.1037/bne0000491 · Cited by 11
Development of Reward Circuitry During Adolescence: Depression, Social Context, and Considerations for Future Research on Disparities in Sexual and Gender Minority Youth
Eckstrand, K., Lenniger, C. J., & Forbes, E. E. (2022) · Annual Review of Developmental Psychology · doi:10.1146/annurev-devpsych-120920-040820 · Cited by 13
Engagement of basal amygdala‐nucleus accumbens glutamate neurons in the processing of rewarding or aversive social stimuli
Poggi, G., Bergamini, G., Dulinskas, R., Madur, L., Greter, A., Ineichen, C., Dagostino, A., Kúkeľová, D., Sigrist, H., Bornemann, K. D., et al. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16272 · Cited by 12
Anhedonia and Reward System: Psychobiology, Evaluation, and Clinical Features
Martinotti, G., Hatzigiakoumis, D. S., Vita, O. D., Clerici, M., Petruccelli, F., Giannantonio, M. D., & Janiri, L. (2012) · International Journal of Clinical Medicine · doi:10.4236/ijcm.2012.37125 · Cited by 13
Activation of extracellular signal‐regulated kinase is critical for the discriminative stimulus effects induced by U‐50,488H
Yoshizawa, K., Narita, M., Saeki, M., Narita, M., Isotani, K., Horiuchi, H., Imai, S., Kuzumaki, N., & Suzuki, T. (2011) · Synapse · doi:10.1002/syn.20937 · Cited by 12
Effects of serum response factor (SRF) deletion on conditioned reinforcement
Johnson, A. W., Crombag, H. S., Smith, D. R., & Ramanan, N. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.02.015 · Cited by 12
α‐Synuclein staging in the amygdala of a P arkinson's disease model: cell types involved
Flores‐Cuadrado, A., Úbeda‐Bañón, I., Saiz‐Sánchez, D., de la Rosa‐Prieto, C., & Martı́nez-Marcos, A. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12763 · Cited by 12
Amygdala activation in response to 2D and 3D emotion-inducing stimuli
Dores, A. R., Barbosa, F., Monteiro, L. M. C., Reis, M., Coelho, C. M., Ribeiro, E., Leitão, M., Carvalho, I. P., de Sousa, L., & Castro‐Caldas, A. (2022) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.26537/r4983 · Cited by 12
Prenatal stress suppresses the prefrontal and amygdaline EEG changes associated with a sexually-motivated state in male rats
González, M. H., Hernández‐Arteaga, E., Guevara, M. Á., Almanza-Sepúlveda, M. L., Ramírez‐Rentería, M. L., Arteaga‐Silva, M., & Bonilla‐Jaime, H. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.10.003 · Cited by 12
Layer-specific pyramidal neuron properties underlie diverse anterior cingulate cortical motor and limbic networks
Medalla, M., Chang, W., Ibañez, S., Guillamón-Vivancos, T., Nittmann, M., Kapitonava, A., Busch, S. E., Moore, T. L., Rosene, D. L., & Luebke, J. I. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab347 · Cited by 13
Dark Control: Towards a Unified Account of Default Mode Function by Markov Decision ProcessesPreprint
Dohmatob, E., Dumas, G., & Bzdok, D. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/148890 · Cited by 12
The Neurobiology of Emotion Regulation
Sebastian, C. L., & Ahmed, S. P. (2018) · Wiley eBooks · doi:10.1002/9781118650868.ch6 · Cited by 14
Cocaine-conditioned odor cues without chronic exposure: implications for the development of addiction vulnerability
Lowen, S. B., Rohan, M. L., Gillis, T. E., Thompson, B. S., Wellons, C. B. W., & Andersen, S. L. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.06.012 · Cited by 11
Transcriptomic diversity of amygdalar subdivisions across humans and nonhuman primates
Totty, M. S., Cervera‐Juanes, R. P., Bach, S. V., Ameur, L. B., Valentine, M. R., Simons, E. A., Romac, M. D., Trinh, H., Henderson, K., Rosario, I. D., et al. (2025) · Science Advances · doi:10.1126/sciadv.adw1029 · Cited by 11
GABAB receptors in prelimbic cortex and basolateral amygdala differentially influence intertemporal decision making and decline with age
Hernandez, C. M., McQuail, J. A., Eyck, T. W. T., Wheeler, A.-R., Labiste, C. C., Setlow, B., & Bizon, J. L. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109001 · Cited by 10
Approaching or Decentering? Differential Neural Networks Underlying Experiential Emotion Regulation and Cognitive Defusion
Wang, Y., Vantieghem, I., Dong, D., Nemegeer, J., Mey, J. D., Schuerbeek, P. V., Marinazzo, D., & Vandekerckhove, M. M. P. (2022) · Brain Sciences · doi:10.3390/brainsci12091215 · Cited by 11
The circadian neurobiology of reward
Olejniczak, I., Begemann, K., Wilhelm, I., & Oster, H. (2023) · Acta Physiologica · doi:10.1111/apha.13928 · Cited by 13

Authors: Baxter, M. G., & Murray, E. A.
Affiliations: Harvard University (US)
National Institutes of Health (US)
ORCID: Baxter, Mark G.
Murray, Elisabeth A.
Venue: Nature Reviews Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2002-07-01
Volume: 3
Issue: 7
Pages: 563-573
ISSN: 1471-003X (ISSN-L)
1471-0048
DOI: 10.1038/nrn875
OpenAlex: W2085971650
Cited by: 1,200
References: 91
Citations by year: 2026: 20 · 2025: 27 · 2024: 39 · 2023: 31 · 2022: 46 · 2021: 44 · 2020: 80 · 2019: 48 · 2018: 45 · 2017: 45 · 2016: 40 · 2015: 59 · 2014: 75 · 2013: 59 · 2012: 58
FWCI: 3.97
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
www.springer.com/tdm (vor)
Locations: Nature reviews. Neuroscience (publishedVersion)
PubMed (publishedVersion)
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, reward, positive emotions, fear conditioning, emotional learning, memory, emotion and cognition
MeSH terms: Amygdala, Animals, Haplorhini, Association, Behavior, Animal, Choice Behavior, Discrimination Learning, Photic Stimulation, Reward, Smell, Prefrontal Cortex, Rats

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

The amygdala and reward

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks