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
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Amygdala and striatum have a well-documented anatomic connectivity (29) and show a tight functional coupling in stimulus–reward association and stimulus–cue devaluation (30).”
From Amygdala damage eliminates monetary loss aversion (2010) · cites this paper as [30]
In the citing paper
“Both the amygdala and hippocampus are known to mediate attentional and learning aspects of emotion (Baxter and Murray, 2002, Calder et al., 2001; Phelps, 2004; Phelps and LeDoux, 2005).”
From Adolescent neurobiological susceptibility to social context (2016) · cites this paper as Baxter and Murray, 2002
Citations
Cites
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
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
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).
Cited by
Sorted by citations
Items 501–600 of 999
Human Neurobiological Approaches to Hedonically Motivated Behaviors
Burger, K. S., Shearrer, G. E., & Sadler, J. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.009 · Cited by 42
Feedback Models for Gambling Control: The Use and Efficacy of Online Responsible Gambling Tools
Griffiths, M. D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.034 · Cited by 42
LUO, S. H., Romero, A., Adam, T. C., Hu, P., Monterosso, J. R., & Page, K. A. (2013) · Obesity · doi:10.1002/oby.20344 · Cited by 42
Interaction of Satiety and Reward Response to Food Stimulation
James, G. A., Gold, M. S., & Liu, Y. (2004) · Journal of Addictive Diseases · doi:10.1300/j069v23n03_03 · Cited by 43
Brain Activation Associated with Pride and Shame
Roth, L., Kaffenberger, T., Herwig, U., & Brühl, A. B. (2014) · Neuropsychobiology · doi:10.1159/000358090 · Cited by 47
Central Amygdala GluA1 Facilitates Associative Learning of Opioid Reward
Cai, Y.-Q., Wang, W., Hou, Y.-Y., Zhang, Z., Xie, J., & Pan, Z. Z. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1749-12.2013 · Cited by 42
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
Effect of Hypoxic Injury in Mood Disorder
Zhao, F., Yang, J., & Cui, R. (2017) · Neural Plasticity · doi:10.1155/2017/6986983 · Cited by 43
Peripheral secretin-induced Fos expression in the rat brain is largely vagal dependent
Yang, H., Wang, L., Wu, S. V., Tay, J., Goulet, M., Boismenu, R., Czimmer, J., Wang, Y., Wu, S. V., Ao, Y., et al. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.027 · Cited by 43
Lanuza, E., Novejarque, A., Martínez‐Ricós, J., Hernández, J. M., Agustín‐Pavón, C., & Martínez‐Garciá, F. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.10.042 · 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
Neural plasticity and depression treatment
Wang, Y., Song, N., Ding, Y., & Zhang, L. (2022) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2022.09.001 · Cited by 48
Stress to inflammation and anhedonia: Mechanistic insights from preclinical and clinical models
Boyle, C. C., Bower, J. E., Eisenberger, N. I., & Irwin, M. R. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105307 · Cited by 45
Olucha-Bordonau, F. E., Fortes-Marco, L., Otero‐García, M., Lanuza, E., & Martínez‐Garciá, F. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00018-8 · Cited by 52
Perland, E., Lekholm, E., Ceder, M. M., Bagchi, S., Arapi, V., & Fredriksson, R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0156912 · Cited by 42
Longitudinal brain volume changes in major depressive disorder
Yüksel, D., Engelen, J., Schuster, V., Dietsche, B., Konrad, C., Jansen, A., Dannlowski, U., Kircher, T. T. J., & Krug, A. (2018) · Journal of Neural Transmission · doi:10.1007/s00702-018-1919-8 · Cited by 45
Simmons, D. A., & Neill, D. B. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.01.026 · Cited by 47
Multi-stage mental process for economic choice in capuchins
Padoa‐Schioppa, C., Jandolo, L., & Visalberghi, E. M. (2005) · Cognition · doi:10.1016/j.cognition.2005.04.008 · Cited by 42
Path dependence in risky choice: Affective and deliberative processes in brain and behavior
Hytönen, K., Baltussen, G., van den Assem, M. J., Klucharev, V. A., Sanfey, A. G., & Smidts, A. (2014) · Journal of Economic Behavior & Organization · doi:10.1016/j.jebo.2014.01.016 · Cited by 41
Amygdala–prefrontal connectivity modulates loss aversion bias in anxious individuals
Xu, P., Dam, N. T. V., van Tol, M., Shen, X., Cui, Z., Gu, R., Qin, S., Aleman, A., Fan, J., & Luo, Y. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116957 · Cited by 44
Positive reinforcing effect of oxytocin microinjection in the rat central nucleus of amygdala
László, K., Kovács, A., Zagorácz, O., Ollmann, T., Péczely, L., Kertes, E., Lacy, D. G., & Lénárd, L. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.09.021 · Cited by 43
Pinna, G., Brödel, O., Eravci, M., Stoltenburg, G., Plueckhan, H., Fuxius, S., MEINHOLD, H., & Baumgartner, A. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00414-1 · Cited by 40
Brain Metabolism during Hallucination-Like Auditory Stimulation in Schizophrenia
Horga, G., Fernández-Egea, E., Mané, A., Font, M., Schatz, K. C., Falcón, C., Lomeña, F., Bernardo, M., & Parellada, E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084987 · Cited by 41
Shulman, A., Goldstein, B., & STRASHUN, A. M. (2009) · PubMed · Cited by 40
Dong, G., Liu, X., Zheng, H., Du, X.-X., & Potenza, M. (2019) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2019.03.003 · Cited by 37
Herting, M. M., Azad, A., Kim, R., Tyszka, J. M., Geffner, M. E., & Kim, M. S. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa023 · Cited by 41
Baldo, B. A., Alsene, K. M., Negrón, A., & Kelley, A. E. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.5.1195 · Cited by 42
PAIR BONDING IN THE FEMALE ZEBRA FINCH: A POTENTIAL ROLE FOR THE NUCLEUS TAENIAE
Svec, L. A., Licht, K. M., & Wade, J. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.003 · Cited by 45
Complexity and Competition in Appetitive and Aversive Neural Circuits
Barberini, C. L., Morrison, S. E., Saez, A., Lau, B., & Salzman, C. D. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00170 · Cited by 42
Chemosensory Function of the Amygdala
Gutiérrez‐Castellanos, N., Martı́nez-Marcos, A., Martínez‐Garciá, F., & Lanuza, E. (2010) · Vitamins and hormones · doi:10.1016/s0083-6729(10)83007-9 · Cited by 40
Gansler, D. A., Lee, A. K. W., Emerton, B. C., D’Amato, C., Bhadelia, R. A., Jerram, M. W., & Fulwiler, C. (2010) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2010.09.003 · Cited by 38
Altered functioning of reward circuitry in youth offspring of parents with bipolar disorder
Manelis, A., Ladouceur, C. D., Graur, S., Monk, K., Bonar, L. K., Hickey, M. B., Dwojak, A., Axelson, D., Goldstein, B., Goldstein, T. R., et al. (2015) · Psychological Medicine · doi:10.1017/s003329171500166x · Cited by 42
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
Manuel, A. L., Murray, N. W. G., & Piguet, O. (2019) · Scientific Reports · doi:10.1038/s41598-019-55157-z · Cited by 40
Jasinska, A. J., Chua, H. F., Ho, S.-H. S., Polk, T. A., Rozek, L. S., & Strecher, V. J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.064 · Cited by 41
Amodio, A., Quarantelli, M., Mucci, A., Prinster, A., Soricelli, A., Vignapiano, A., Giordano, G. M., Merlotti, E., Nicita, A., & Galderisi, S. (2017) · Clinical EEG and Neuroscience · doi:10.1177/1550059417745934 · Cited by 41
Cui, Y., Huang, X., Huang, P., Huang, L., Feng, Z., Xiang, X., Chen, X., Li, A., Ren, C., & Li, H. (2022) · Science Advances · doi:10.1126/sciadv.abn0193 · Cited by 38
Addiction to Food and Brain Reward Systems
Joranby, L., Frost-Pineda, K., & Gold, M. S. (2005) · Sexual Addiction & Compulsivity The Journal of Treatment and Prevention · doi:10.1080/10720160500203765 · Cited by 44
Differential modes of termination of amygdalothalamic and amygdalocortical projections in the monkey
Miyashita, T., Ichinohe, N., & Rockland, K. S. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21304 · Cited by 38
Bases neurales de la toma de decisiones
Broche‐Pérez, Y., Jiménez, L. F. H., & Martínez, E. O. (2015) · Neurología · doi:10.1016/j.nrl.2015.03.001 · Cited by 51
State of expectancy modulates the neural response to visual food stimuli in humans
Malik, S., McGlone, F., & Dagher, A. (2011) · Appetite · doi:10.1016/j.appet.2011.01.005 · Cited by 38
FTO gene variant modulates the neural correlates of visual food perception
Kühn, A. B., Feis, D., Schilbach, L., Kracht, L., Hess, M. E., Mauer, J., Brüning, J. C., & Tittgemeyer, M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.12.049 · Cited by 38
Pedersen, W. S., Muftuler, L. T., & Larson, C. L. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx133 · Cited by 38
Novel Perspectives on the Development of the Amygdala in Rodents
Aerts, T., & Seuntjens, E. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.786679 · Cited by 36
Sex differences in brain control of prosody
Rymarczyk, K., & Grabowska, A. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.08.021 · Cited by 40
Social appraisal in chronic psychosis: Role of medial frontal and occipital networks
Taylor, S. F., Chen, A. C., Tso, I. F., Liberzon, I., & Welsh, R. C. (2010) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.08.004 · Cited by 39
Amygdala Mechanisms of Pavlovian Psychostimulant Conditioning and Relapse
Buffalari, D. M., & See, R. E. (2009) · Current topics in behavioral neurosciences · doi:10.1007/7854_2009_18 · Cited by 36
Aal-Aaboda, M. S., Alhaddad, H., Osowik, F. A., Nauli, S. M., & Sari, Y. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23554 · Cited by 37
Wilson, F. A. W., & Rolls, E. T. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.03.022 · Cited by 37
Ostrander, S., Cazares, V. A., Kim, C. R., Cheung, S., Gonzalez, I., & Izquierdo, A. (2011) · Behavioral Neuroscience · doi:10.1037/a0023574 · Cited by 41
Mineur, Y. S., Garcia‐Rivas, V., Thomas, M. A., Soares, A. R., McKee, S. A., & Picciotto, M. R. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06120-w · Cited by 34
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
Long‐term cognitive enrichment affects opioid receptor expression in the amygdala of domestic pigs
Kalbe, C., & Puppe, B. (2009) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2009.00536.x · Cited by 36
Structural connectivity and risk for anhedonia after trauma: A prospective study and replication
Fani, N., Michopoulos, V., van Rooij, S. J. H., Clendinen, C., Hardy, R. A., Jovanović, T., ROTHBAUM, B. O., Ressler, K. J., & Stevens, J. S. (2019) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2019.05.009 · Cited by 34
Multidimensional Neural Selectivity in the Primate Amygdala
Putnam, P. T., & Gothard, K. M. (2019) · eNeuro · doi:10.1523/eneuro.0153-19.2019 · Cited by 37
Francesco, P. N. D., Valdivia, S., Cabral, A., Reynaldo, M., Raingo, J., Sakata, I., Osborne-Lawrence, S. L., Zigman, J. M., & Perelló, M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.006 · Cited by 33
Damiano, C. R., Cockrell, D. C., Dunlap, K., Hanna, E. K., Miller, S., Bizzell, J., Kovac, M., Turner‐Brown, L., Sideris, J. H., Kinard, J. L., et al. (2015) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-015-9107-8 · Cited by 37
Pathological anxiety and function/dysfunction in the brain's fear/defense circuitry
Lang, P. J., McTeague, L. M., & Bradley, M. M. (2014) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-139012 · Cited by 36
Consideration of a Unified Model of Amygdalar Associative Functions
Gabriel, M., Burhans, L. B., & Kashef, A. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07083.x · Cited by 35
Bohn, I. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.9.968 · Cited by 35
Livneh, U., & Paz, R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0323-12.2012 · Cited by 36
Xiao, T., Zhang, S., Lee, L.-E., Chao, H. H., van Dyck, C. H., & Li, C.-S. R. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00209 · Cited by 32
Wang, S.-C., Lin, C.-C., Tzeng, N., Tung, C., & Liu, Y. (2019) · Journal of Biomedical Science · doi:10.1186/s12929-019-0514-0 · Cited by 35
Lesions of the rat basolateral amygdala reduce the behavioral response to ultrasonic vocalizations
Schönfeld, L.-M., Zech, M.-P., Schäble, S., Wöhr, M., & Kalenscher, T. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112274 · Cited by 34
Bernardi, S., & Salzman, C. D. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902293116 · Cited by 34
Genetic and Structural Analysis of the Basolateral Amygdala Complex in BXD Recombinant Inbred Mice
Mozhui, K., Hamre, K. M., Holmes, A., Lu, L., & Williams, R. W. (2006) · Behavior Genetics · doi:10.1007/s10519-006-9122-3 · Cited by 35
Gelez, H., Archer, E., Chesneau, D., Magallon, T., & Fabre‐Nys, C. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03261.x · Cited by 34
What Can Different Brains Do with Reward?
Gottfried, J. A. (2011) · CRC Press eBooks · doi:10.1201/b10776-10 · Cited by 33
Burke, S., Thomé, A., Plange, K., Engle, J. R., Trouard, T., Gothard, K., & Barnes, C. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3918-13.2014 · Cited by 29
Ding, Z., Wu, P., Luo, Y., Shi, H., Shen, H., Wang, S., & Lü, L. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3050-8 · Cited by 35
Engelen, T., Zhan, M., Sack, A. T., & de Gelder, B. (2018) · eNeuro · doi:10.1523/eneuro.0408-17.2018 · Cited by 32
Gao, C., Weber, C. E., & Shinkareva, S. V. (2019) · Cortex · doi:10.1016/j.cortex.2019.05.016 · Cited by 35
Neurological imaging as evidence in political science: a review, critique, and guiding assessment
Tingley, D. H. (2006) · Social Science Information · doi:10.1177/0539018406061100 · Cited by 34
LTP in the lateral amygdala during cocaine withdrawal
Goussakov, I. V., Chartoff, E. H., Tsvetkov, E., Gerety, L. P., Meloni, E. G., Carlezon, W. A., & Bolshakov, V. Y. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04538.x · Cited by 33
Prediction errors to emotional expressions: the roles of the amygdala in social referencing
Meffert, H., Brislin, S. J., White, S. F., & Blair, J. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu085 · Cited by 33
The Actin Cytoskeleton as a Therapeutic Target for the Prevention of Relapse to Methamphetamine Use
Young, E. J., Briggs, S. B., & Miller, C. A. (2015) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527314666150529145531 · Cited by 31
Ben‐Zion, Z., Korem, N., Fine, N. B., Katz, S., Siddhanta, M., Funaro, M. C., Duek, O. A., Spiller, T. R., Danböck, S. K., Levy, I., et al. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.07.001 · Cited by 38
Ely, A. V., Wierenga, C., Bischoff-Grethe, A., Bailer, U., Berner, L. A., Fudge, J., Paulus, M., & Kaye, W. (2017) · Journal of Abnormal Psychology · doi:10.1037/abn0000218 · Cited by 30
Subtype-selective GABAergic drugs facilitate extinction of mouse operant behaviour
McCabe, C., Shaw, D., Atack, J. R., Street, L. J., Wafford, K. A., Dawson, G. R., Reynolds, D. S., & Leslie, J. C. (2003) · Neuropharmacology · doi:10.1016/j.neuropharm.2003.09.004 · Cited by 32
Zhang, X., Asim, M., Fang, W., Monir, H. M., Wang, H., Kim, K., Feng, H., Wang, S., Gao, Q., Lai, Y., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02127-7 · Cited by 32
Yang, C., Wang, X.-K., Ma, S., Lee, N. Y., Zhang, Q.-R., Dong, W., Zang, Y., & Yuan, L. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.12.013 · Cited by 33
Experience-dependent changes in human brain activation during contingency learning
Schlund, M. W., & Ortu, D. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.10.014 · Cited by 31
Scheuer, H., Alarcón, G., Demeter, D. V., Earl, E., Fair, D. A., & Nagel, B. J. (2017) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2017.05.012 · Cited by 32
Amygdala functioning during threat acquisition and extinction differentiates antisocial subtypes
Fanti, K. A., Konikkou, K., Cohn, M. D., Popma, A., & Brazil, I. A. (2019) · Journal of Neuropsychology · doi:10.1111/jnp.12183 · 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
van Ruiten, C. C., ten Kulve, J. S., van Bloemendaal, L., Nieuwdorp, M., Veltman, D. J., & IJzerman, R. G. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105667 · Cited by 36
Kang, O.-S., Kim, S., Jahng, G., Kim, H., Kim, J.-W., Chung, S.-Y., Kim, J. W., Yang, S.-I., Park, H., Lee, H., et al. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3015-y · Cited by 30
Effects of drugs that potentiate GABA on extinction of positively-reinforced operant behaviour
Leslie, J. C., Shaw, D., McCabe, C., Reynolds, D. S., & Dawson, G. R. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.01.003 · Cited by 31
Pollmann, S. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh049 · Cited by 31
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
Klug, M., Enneking, V., Borgers, T., Jacobs, C. M., Dohm, K., Kraus, A., Grotegerd, D., Opel, N., Repple, J., Suslow, T., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02429-4 · Cited by 41
Hierarchical Brain Systems Support Multiple Representations of Valence and Mixed Affect
Man, V. Y., Nohlen, H. U., Melo, H., & Cunningham, W. A. (2017) · Emotion Review · doi:10.1177/1754073916667237 · Cited by 33
Asim, M., Wang, H., & Waris, A. (2023) · Neuropeptides · doi:10.1016/j.npep.2023.102322 · Cited by 31
Hensler, J. G. (2010) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(10)70090-4 · Cited by 31
Rezayof, A., Khajehpour, L., & Zarrindast, M. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.069 · Cited by 30
Neural Encoding in the Orbitofrontal Cortex Related to Goal‐Directed Behavior
Furuyashiki, T., & Gallagher, M. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.037 · Cited by 31
Near-Death Experiences in patients with locked-in syndrome: Not always a blissful journey
Charland‐Verville, V., Lugo, Z., Jourdan, J.-P., Donneau, A., & Laureys, S. (2015) · Consciousness and Cognition · doi:10.1016/j.concog.2015.03.011 · Cited by 29
Interactions of timing and prediction error learning
Kirkpatrick, K. (2013) · Behavioural Processes · doi:10.1016/j.beproc.2013.08.005 · Cited by 29
Drug-Induced Glucocorticoids and Memory for Substance Use
Goldfarb, E. V., & Sinha, R. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.08.005 · Cited by 30
Girven, K. S., Aroni, S., Navarrete, J. S., Marino, R. A. M., McKeon, P. N., Cheer, J. F., & Sparta, D. R. (2020) · Addiction Biology · doi:10.1111/adb.12961 · Cited by 28
Metadata
- Authors
- Baxter, M. G., & Murray, E. A.
- Affiliations
- Harvard University (US)
- National Institutes of Health (US)
- Venue
- Nature Reviews Neuroscience
- Published
- 2002-07-01
- Volume
- 3
- Issue
- 7
- Pages
- 563-573
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- 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
- 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