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 101–200 of 999
The Cognitive Neuroscience of Human Decision Making: A Review and Conceptual Framework
Fellows, L. K. (2004) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582304273251 · Cited by 285
Fine Cuts of Empathy and the Amygdala: Dissociable Deficits in Psychopathy and Autism
Blair, J. (2007) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470210701508855 · Cited by 286
Fundamental contribution by the basolateral amygdala to different forms of decision making
Ghods-Sharifi, S., St. Onge, J. R., & Floresco, S. B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0315-09.2009 · Cited by 257
Integrating automatic and controlled processes into neurocognitive models of social cognition
Satpute, A. B., & Lieberman, M. D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.01.005 · Cited by 347
Adolescent neurobiological susceptibility to social context
Schriber, R. A., & Guyer, A. E. (2016) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.12.009 · Cited by 246
Reduced Amygdalar Gray Matter Volume in Familial Pediatric Bipolar Disorder
Chang, K., Karchemskiy, A., Barnea‐Goraly, N., Garrett, A. S., Simeonova, D. I., & Reiss, A. L. (2005) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/01.chi.0000159948.75136.0d · Cited by 253
Uncertainty during anticipation modulates neural responses to aversion in human insula and amygdala
Sarinopoulos, I., Grupe, D. W., Mackiewicz, K. L., Herrington, J. D., Lor, M., Steege, E. E., & Nitschke, J. B. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp155 · Cited by 241
Ventral pallidum firing codes hedonic reward: when a bad taste turns good
Tindell, A. J., Smith, K. S., Peciña, S., Berridge, K. C., & Aldridge, J. W. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00576.2006 · Cited by 241
Neural substrates of cue reactivity: association with treatment outcomes and relapse
Courtney, K. E., Schacht, J. P., Hutchison, K. E., Roche, D. J. O., & Ray, L. A. (2015) · Addiction Biology · doi:10.1111/adb.12314 · Cited by 256
Prefrontal–amygdala circuits in social decision-making
Gangopadhyay, P., Chawla, M., Monte, O. D., & Chang, S. W. C. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00738-9 · Cited by 266
Neural systems underlying approach and avoidance in anxiety disorders
Robin L., A., & Martin, P. P. (2010) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2010.12.4/raupperle · Cited by 227
Temperament and Anxiety Disorders
Pérez‐Edgar, K. E., & Fox, N. A. (2005) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2005.05.008 · Cited by 252
Role of stress, corticotrophin releasing factor (CRF) and amygdala plasticity in chronic anxiety
Shekhar, A., Truitt, W., Rainnie, D., & Sajdyk, T. (2005) · Stress · doi:10.1080/10253890500504557 · Cited by 237
The Nucleus Accumbens and Pavlovian Reward Learning
Day, J. J., & Carelli, R. M. (2007) · The Neuroscientist · doi:10.1177/1073858406295854 · Cited by 235
Behavioral disinhibition requires dopamine receptor activation
van Gaalen, M. M., Brueggeman, R. J., Bronius, P. F. C., Schoffelmeer, A. N. M., & Vanderschuren, L. J. M. J. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0396-1 · Cited by 240
Psychopathy, frustration, and reactive aggression: The role of ventromedial prefrontal cortex
Blair, J. (2009) · British Journal of Psychology · doi:10.1348/000712609x418480 · Cited by 258
Estimation of Current and Future Physiological States in Insular Cortex
Livneh, Y., Sugden, A. U., Madara, J. C., Essner, R. A., Flores, V. I., Sugden, L. A., Resch, J. M., Lowell, B. B., & Andermann, M. L. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.027 · Cited by 209
Moment-to-moment tracking of state value in the amygdala
Belova, M. A., Paton, J. J., & Salzman, C. D. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1400-08.2008 · Cited by 221
Sensing the invisible: differential sensitivity of visual cortex and amygdala to traumatic context
Hendler, T., Rotshtein, P., Yeshurun, Y., Weizmann, T., Kahn, I., Bashat, D. B., Malach, R., & Bleich, A. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00141-1 · Cited by 228
Is a bird in the hand worth two in the future? The neuroeconomics of intertemporal decision-making
Kalenscher, T., & Pennartz, C. M. A. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.11.004 · Cited by 227
The neurobiological basis of temperament: Towards a better understanding of psychopathology
Whittle, S., Allen, N. B., Lubman, D. I., & Yücel, M. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.09.003 · Cited by 235
Identity-specific coding of future rewards in the human orbitofrontal cortex
Howard, J. D., Gottfried, J. A., Tobler, P. N., & Kahnt, T. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503550112 · Cited by 231
Rosen, J. B. (2004) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582304265945 · Cited by 219
Blair, J. (2006) · Cognition · doi:10.1016/j.cognition.2006.04.005 · Cited by 230
Amygdala responses to nonlinguistic emotional vocalizations
Fecteau, S., Belin, P., Joanette, Y., & Armony, J. L. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.043 · Cited by 228
Holland, P. C., & Gallagher, M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02585.x · Cited by 236
Brain Mechanisms for Inferring Deceit in the Actions of Others
Grèzes, J., Frith, C., & Passingham, R. E. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0219-04.2004 · Cited by 222
Bolton, J. L., Molet, J., Regev, L., Chen, Y., Rismanchi, N., Haddad, E., Yang, D. Z., Obenaus, A., & Baram, T. Z. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.08.023 · Cited by 222
Contributions of the Amygdala to Reward Expectancy and Choice Signals in Human Prefrontal Cortex
Hampton, A. N., Adolphs, R., Tyszka, J. M., & O'Doherty, J. P. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.022 · Cited by 213
Fairness and Cooperation Are Rewarding: Evidence from Social Cognitive Neuroscience
TABIBNIA, G., & LIEBERMAN, M. D. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1412.001 · Cited by 211
Abstract context representations in primate amygdala and prefrontal cortex
Saez, A., Rigotti, M., Ostojic, S., Fusi, S., & Salzman, C. D. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.024 · Cited by 183
Caetano, S. C., Hatch, J. P., Brambilla, P., Sassi, R. B., Nicoletti, M., Mallinger, A. G., Frank, E., Kupfer, D. J., Keshavan, M. S., & Soares, J. C. (2004) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2004.08.002 · Cited by 214
Unsupervised identification of the internal states that shape natural behavior
Calhoun, A. J., Pillow, J. W., & Murthy, M. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0533-x · Cited by 205
Emotional imagery: Assessing pleasure and arousal in the brain's reward circuitry
Costa, V. D., Lang, P. J., Sabatinelli, D., Versace, F., & Bradley, M. M. (2010) · Human Brain Mapping · doi:10.1002/hbm.20948 · Cited by 202
The neurobiology of punishment
Seymour, B., Singer, T., & Dolan, R. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2119 · Cited by 240
Attention alters neural responses to evocative faces in behaviorally inhibited adolescents
Pérez-Edgar, K., Roberson-Nay, R., Hardin, M. G., Poeth, K., Guyer, A. E., Nelson, E. E., McClure, E. B., Henderson, H. A., Fox, N. A., Pine, D. S., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.006 · Cited by 198
Efficient coding of subjective value
Polanía, R., Woodford, M., & Ruff, C. C. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0292-0 · Cited by 205
Functional connectivity with anterior cingulate and orbitofrontal cortices during decision-making
Cohen, M. X., Heller, A. S., & Ranganath, C. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2005.01.010 · Cited by 205
A cognitive architecture that combines internal simulation with a global workspace
Shanahan, M. (2005) · Consciousness and Cognition · doi:10.1016/j.concog.2005.11.005 · Cited by 206
Amygdala–prefrontal interactions in (mal)adaptive learning
Likhtik, E., & Paz, R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.12.007 · Cited by 198
Neural substrates of approach‐avoidance conflict decision‐making
Aupperle, R. L., Melrose, A. J., Francisco, A. J., Paulus, M. P., & Stein, M. B. (2014) · Human Brain Mapping · doi:10.1002/hbm.22639 · Cited by 209
Endocannabinoids in Amygdala and Nucleus Accumbens Mediate Social Play Reward in Adolescent Rats
Trezza, V., Damsteegt, R., Manduca, A., Petrosino, S., Van Kerkhof, L. W. M., Pasterkamp, R. J., Zhou, Y., Campolongo, P., Cuomo, V., Di Marzo, V., et al. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0114-12.2012 · Cited by 190
Shabel, S. J., & Janak, P. H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905580106 · Cited by 194
Separable Substrates for Anticipatory and Consummatory Food Chemosensation
Small, D. M., Veldhuizen, M. G., Felsted, J. A., Mak, Y. E., & McGlone, F. P. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.021 · Cited by 190
Self-related awareness and emotion regulation
Herwig, U., Kaffenberger, T., Jäncke, L., & Brühl, A. B. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.089 · Cited by 189
The Emergence and Representation of Knowledge about Social and Nonsocial Hierarchies
Kumaran, D., Melo, H., & Düzel, E. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.035 · Cited by 198
The rhinal cortices: a wall of inhibition between the neocortex and the hippocampus
DECURTIS, M., & Paré, D. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.08.005 · Cited by 186
ALE meta-analysis on facial judgments of trustworthiness and attractiveness
Bzdok, D., Langner, R., Caspers, S., Kurth, F., Habel, U., Zilles, K., Laird, A., & Eickhoff, S. B. (2011) · Brain Structure and Function · doi:10.1007/s00429-010-0287-4 · Cited by 183
Robinson, M. J. F., Warlow, S. M., & Berridge, K. C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2013-14.2014 · Cited by 190
Adaptive decision making and value in the anterior cingulate cortex
Walton, M. E., Croxson, P. L., Behrens, T. E. J., Kennerley, S. W., & Rushworth, M. F. S. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.029 · Cited by 191
The amygdala and decision-making
Gupta, R., Koscik, T. R., Bechara, A., & Tranel, D. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.09.029 · Cited by 205
Solway, A., & Botvinick, M. (2012) · Psychological Review · doi:10.1037/a0026435 · Cited by 194
Deafness to fear in boys with psychopathic tendencies
Blair, J., Budhani, S., Colledge, E., & Scott, S. K. (2004) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2004.00356.x · Cited by 191
Lateral Asymmetry in the Hippocampal Response to the Remoteness of Autobiographical Memories
Maguire, E. A., & Frith, C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05302.2003 · Cited by 181
Neurobehavioral foundation of environmental reactivity.
Moore, S. R., & Depue, R. A. (2015) · Psychological Bulletin · doi:10.1037/bul0000028 · Cited by 183
Basolateral Amygdala Lesions Abolish Orbitofrontal-Dependent Reversal Impairments
Stalnaker, T. A., Franz, T. M., Singh, T., & Schoenbaum, G. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.014 · Cited by 180
Motivational neural circuits underlying reinforcement learning
Averbeck, B. B., & Costa, V. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4506 · Cited by 181
Effects of Amygdala Lesions on Reward-Value Coding in Orbital and Medial Prefrontal Cortex
Rudebeck, P. H., Mitz, A. R., Chacko, R. V., & Murray, E. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.036 · Cited by 178
Self-citationRe-evaluating the role of the orbitofrontal cortex in reward and reinforcement
Noonan, M. P., Kolling, N., Walton, M. E., & Rushworth, M. F. S. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08023.x · Cited by 169
A review of white matter microstructure alterations of pathways of the reward circuit in depression
Bracht, T., Linden, D. E. J., & Keedwell, P. A. (2015) · Journal of Affective Disorders · doi:10.1016/j.jad.2015.06.041 · Cited by 178
Different neural systems adjust motor behavior in response to reward and punishment
Wrase, J., Kahnt, T., Schlagenhauf, F., Beck, A., Cohen, M. X., Knutson, B., & Heinz, A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.04.001 · Cited by 172
Neural mechanisms underlying food motivation in children and adolescents
Holsen, L. M., Zarcone, J. R., Thompson, T., Brooks, W., Anderson, M. F., Ahluwalia, J., Nollen, N., & Savage, C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.04.043 · Cited by 164
Laviolette, S. R., & Grace, A. A. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-006-6027-5 · Cited by 172
Modulation of anticipatory emotion and perception processing by cognitive control
Herwig, U., Baumgärtner, T., Kaffenberger, T., Brühl, A. B., Kottlow, M., Schreiter-Gasser, U., Abler, B., Jäncke, L., & Rufer, M. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.023 · Cited by 170
Effects of early life stress on amygdala and striatal development
Fareri, D. S., & Tottenham, N. (2016) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.04.005 · Cited by 177
Izquierdo, A., & Murray, E. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00968.2003 · Cited by 167
Self-citationEmotional enhancement of memory via amygdala-driven facilitation of rhinal interactions
Paz, R., Pelletier, J. G., Bauer, E. P., & Paré, D. (2006) · Nature Neuroscience · doi:10.1038/nn1771 · Cited by 167
Wang, S., Leri, F., & Rizvi, S. J. (2021) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2021.110289 · Cited by 171
Laviolette, S. (2007) · Schizophrenia bulletin · doi:10.1093/schbul/sbm048 · Cited by 177
Kipps, C., Duggins, A., McCusker, E. A., & Calder, A. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.7.1206 · Cited by 171
Neural mechanisms of social decision-making in the primate amygdala
Chang, S. W. C., Fagan, N. A., Toda, K., Utevsky, A. V., Pearson, J. M., & Platt, M. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1514761112 · Cited by 157
What’s in a word? How instructions, suggestions, and social information change pain and emotion
Koban, L., Jepma, M., Geuter, S., & Wager, T. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.014 · Cited by 166
PromisingInterventions, O’Connell, M. E., Boat, T. F., & Warner, K. E. (2009) · Cited by 159
Basal Ganglia Mechanisms of Reward‐Oriented Eye Movement
Hikosaka, O. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.012 · Cited by 159
Keltner, D. J., & Lerner, J. S. (2010) · Wiley eBooks · doi:10.1002/9780470561119.socpsy001009 · Cited by 164
Pardo‐Bellver, C., Cádiz‐Moretti, B., Novejarque, A., Martínez‐Garciá, F., & Lanuza, E. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00033 · Cited by 166
Being liked activates primary reward and midline self‐related brain regions
Davey, C. G., Allen, N. B., Harrison, B. J., Dwyer, D. B., & Yücel, M. (2010) · Human Brain Mapping · doi:10.1002/hbm.20895 · Cited by 155
Budhani, S., Richell, R. A., & Blair, J. (2006) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.115.3.552 · Cited by 151
van Bloemendaal, L., Veltman, D. J., ten Kulve, J. S., Groot, P. F. C., Ruhé, H. G., Barkhof, F., Sloan, J. H., Diamant, M., & Ijzerman, R. G. (2015) · Diabetes, Obesity and Metabolism · doi:10.1111/dom.12506 · Cited by 151
Casebeer, W. D., & Churchland, P. S. (2003) · Biology & Philosophy · doi:10.1023/a:1023380907603 · Cited by 156
Human amygdala development in the absence of species‐expected caregiving
Tottenham, N. (2012) · Developmental Psychobiology · doi:10.1002/dev.20531 · Cited by 149
The human amygdala and orbital prefrontal cortex in behavioural regulation
Dolan, R. J. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2088 · Cited by 150
Knapska, E., Radwańska, K., Werka, T., & Kaczmarek, L. (2007) · Physiological Reviews · doi:10.1152/physrev.00037.2006 · Cited by 161
Neural responses to acute cocaine administration in the human brain detected by fMRI
Kufahl, P. R., Li, Z., Risinger, R. C., Rainey, C. J., Wu, G., Bloom, A. S., & Li, S.-J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.039 · Cited by 151
Plichta, M. M., Gerdes, A. B. M., Alpers, G. W., Harnisch, W., Brill, S. M., Wieser, M. J., & Fallgatter, A. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.011 · Cited by 148
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
Temporal isolation of neural processes underlying face preference decisions
Kim, H., Adolphs, R., O’Doherty, J. P., & Shinsuke Shimojo, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703101104 · Cited by 150
Between-subject transfer of emotional information evokes specific pattern of amygdala activation
Knapska, E., Nikolaev, E., Boguszewski, P. M., Walasek, G., Błaszczyk, J. W., Kaczmarek, L., & Werka, T. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511302103 · Cited by 158
Sun, X., Kroemer, N. B., Veldhuizen, M. G., Babbs, A. E., de Araújo, I. E., Gitelman, D. R., Sherwin, R. S., Sinha, R., & Small, D. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3884-14.2015 · Cited by 147
Ghods-Sharifi, S., & Floresco, S. (2010) · Behavioral Neuroscience · doi:10.1037/a0018932 · Cited by 155
Andrewes, D. G., & Jenkins, L. M. (2019) · Neuropsychology Review · doi:10.1007/s11065-019-09398-4 · Cited by 169
Johnson, A. W., Gallagher, M., & Holland, P. C. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3758-08.2009 · Cited by 132
Blair, J., Mitchell, D. G. V., Leonard, A., Budhani, S., Peschardt, K. S., & Newman, C. G. J. (2004) · Personality and Individual Differences · doi:10.1016/j.paid.2003.12.001 · Cited by 146
Irritability in pediatric mania and other childhood psychopathology
LEIBENLUFT, E., BLAIR, R. J. R., CHARNEY, D. S., & PINE, D. S. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1301.022 · Cited by 145
Distinct Roles of Three Frontal Cortical Areas in Reward-Guided Behavior
Noonan, M. P., Mars, R. B., & Rushworth, M. F. S. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6456-10.2011 · Cited by 151
Brain activation during sight gags and language-dependent humor.
Watson, K., Matthews, B., & Allman, J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhj149 · Cited by 143
The endocannabinoid system: An emotional buffer in the modulation of memory function
Morena, M., & Campolongo, P. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.12.010 · Cited by 153
The Amygdala as a Locus of Pathologic Misfolding in Neurodegenerative Diseases
Nelson, P. T., Abner, E. L., Patel, E., Anderson, S., Wilcock, D. M., Kryscio, R. J., Eldik, L. J. V., Jicha, G. A., Gal, Z. T., Nelson, R. S., et al. (2017) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlx099 · Cited by 141
Motivating forces of human actions
Walter, H., Abler, B., Ciaramidaro, A., & Erk, S. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.06.016 · Cited by 149
Prefrontal dopamine in associative learning and memory
Puig, M. V., Antzoulatos, E. G., & Miller, E. K. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.09.026 · Cited by 148
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