Emotion processing and the amygdala: from a’low road’to’many roads’ of evaluating biological significance.
Open accessAbstract
A subcortical pathway through the superior colliculus and pulvinar to the amygdala is commonly assumed to mediate the non-conscious processing of affective visual stimuli. We review anatomical and physiological data that argue against the notion that such a pathway plays a prominent part in processing affective visual stimuli in humans. Instead, we propose that the primary role of the amygdala in visual processing, like that of the pulvinar, is to coordinate the function of cortical networks during evaluation of the biological significance of affective visual stimuli. Under this revised framework, the cortex has a more important role in emotion processing than is traditionally assumed.
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Emotion is typically elicited based on one's evaluation of the internal or external stimuli.
“Emotion is typically elicited based on one’s evaluation of the internal or external stimuli (Ellsworth and Scherer, 2003; Pessoa and Adolphs, 2010).”
From Motivational and Affective Factors Underlying Consumer Dropout and Transactional Success in eCommerce: An Overview (2020) · cites this paper as Pessoa and Adolphs, 2010
The Abstract (page not available in our copy) describes assigning biological value to stimuli in an animal’s environment, supporting the claim’s evaluation of external stimuli. The paper focuses on processing affective visual information; the passages do not establish that emotion is typically elicited by evaluating internal stimuli. (LLM, conf=0.78)
Experimental — accuracy not yet measuredMultiple cognitive functions support automatic salience evaluation and detection, including automatic salience evaluation, inhibition or interruption of ongoing activity, alerting, salience-driven switching, and reflexive orienting.
“These include automatic salience evaluation, [ 4 9 8 _ T D $ D I F F ] inhibition/interruption of ongoing activity[ 4 9 9 _ T D $ D I F F ] , alerting, salience-driven switching, and reflexive orienting [40,43,47,48].”
From Anxiety and Threat-Related Attention: Cognitive-Motivational Framework and Treatment (2018) · cites this paper as [47]
Automatic evaluation of the affective and motivational significance of stimuli plays a crucial role in anxiety.
“Another bottom-up process, which plays a crucial role in anxiety, is automatic evaluation of the affective and motivational significance of stimuli (Pessoa & Adolphs, 2010;Pessoa, 2009;Vuilleumier & Driver, 2007;Vuilleumier, 2005); the functions of which are discussed later (Section 4.3.1).”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa & Adolphs, 2010
The primary role of the amygdala is to coordinate and modulate functioning of cortical networks during the evaluation of the biological or motivational significance of stimuli.
“A more recent view, put forward by Pessoa and Adolphs (2010), is that the primary role of the amygdala is to coordinate and modulate functioning of cortical networks during the evaluation of the biological or motivational significance of stimuli.”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa and Adolphs (2010)
The present framework encompasses the view that bottom-up stimulus-salience evaluation processes play an important role in contributing to anxiety, and that evaluation of the motivational importance of a stimulus, which includes its threat value, can occur outside awareness and depends on automatic integration of information from multiple sources.
“Thus, the present framework encompasses the view that bottom-up stimulus-salience evaluation processes play an important role in contributing to anxiety, and that evaluation of the motivational importance of a stimulus, which includes its threat value, can occur outside awareness and depends on automatic integration of information from multiple sources (Pessoa & Adolphs, 2010).”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa & Adolphs, 2010
The amygdala biases the allocation of processing resources to stimuli by modulating other brain networks in order to prioritise selection of motivationally salient information.
“The amygdala consequently biases the allocation of processing resources to stimuli by modulating other brain networks in order to prioritise selection of motivationally salient information (Pessoa & Adolphs, 2010).”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa & Adolphs, 2010
Cortical regions are involved in both conscious and nonconscious processing of emotional information; and these multiple parallel sources of information are automatically integrated in subcortical regions, such as the amygdala and pulvinar.
“They conclude from their review of neuroscience research that cortical regions are involved in both conscious and nonconscious processing of emotional information; and these multiple parallel sources of information are automatically integrated in subcortical regions, such as the amygdala and pulvinar.”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa & Adolphs, 2010
Bottom-up stimulus-salience-evaluation processes play a key role in assessing the motivational importance and threat value of stimuli by integrating multiple sources of information.
“Bottom-up stimulus-salience-evaluation processes play a key role not only in assessing the motivational importance and threat value of stimuli by integrating multiple sources of information”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa & Adolphs, 2010
Bottom-up stimulus-salience-evaluation processes play a key role in modulating activity in other bottom-up and top-down processes to prioritise motivationally salient information.
“but also in modulating activity in other bottom-up and top-down processes to prioritise motivationally salient information (Pessoa & Adolphs, 2010).”
From Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification (2016) · cites this paper as Pessoa & Adolphs, 2010
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Cites
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783 · see citing works
The reorienting system of the human brain: from environment to theory of mind
Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889 · see citing works
(1996) · Cited by 3,692 · see citing works
Speed of processing in the human visual system
Thorpe, S., Fize, D., & Marlot, C. (1996) · Nature · doi:10.1038/381520a0 · Cited by 3,538 · see citing works
Fears, phobias, and preparedness: toward an evolved module of fear and fear learning
Öhman, A., & Mineka, S. (2001) · Psychological Review · doi:10.1037/0033-295x.108.3.483 · Cited by 3,147 · see citing works
The amygdala: vigilance and emotion
Davis, M., & Whalen, P. J. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000812 · Cited by 2,882 · see citing works
A cortical network for directed attention and unilateral neglect
Mesulam, M. ‐. (1981) · Annals of Neurology · doi:10.1002/ana.410100402 · Cited by 2,498 · see citing works
On the relationship between emotion and cognition
Pessoa, L. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2317 · Cited by 2,350 · see citing works
Self-citationThe distinct modes of vision offered by feedforward and recurrent processing
Lamme, V. A. F., & Roelfsema, P. R. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01657-x · Cited by 2,338 · cited 1× · see citing works
“1b ), providing the means for faster information transmission to the inferotemporal corte”
Whalen, P. J., Rauch, S. L., Etcoff, N. L., McInerney, S. C., Lee, M. B., & Jenike, M. A. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00411.1998 · Cited by 2,205 · see citing works
How brains beware: neural mechanisms of emotional attention
Vuilleumier, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.10.011 · Cited by 2,162 · see citing works
Conscious and unconscious emotional learning in the human amygdala
Morris, J. S., Öhman, A., & Dolan, R. J. (1998) · Nature · doi:10.1038/30976 · Cited by 1,665 · see citing works
Retinotopic organization in human visual cortex and the spatial precision of functional MRI
Engel, S. A. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.2.181 · Cited by 1,606 · see citing works
Corbetta, M., Miezin, F. M., Dobmeyer, S., Shulman, G. L., & Petersen, S. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02383.1991 · Cited by 1,590 · see citing works
The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction.
Aggleton, J. P. (1992) · Wiley-Liss eBooks · Cited by 1,536 · see citing works
Neural systems responding to degrees of uncertainty in human decision-making
Hsu, M., Bhatt, M., Adolphs, R., Tranel, D., & Camerer, C. F. (2005) · Science · doi:10.1126/science.1115327 · Cited by 1,411 · see citing works
Self-citationThe face in the crowd revisited: A threat advantage with schematic stimuli.
Öhman, A., Lundqvist, D., & Esteves, F. (2001) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.80.3.381 · Cited by 1,366 · see citing works
A subcortical pathway to the right amygdala mediating “unseen” fear
Morris, J. S., Öhman, A., & Dolan, R. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1680 · Cited by 1,349 · see citing works
A mechanism for impaired fear recognition after amygdala damage
Adolphs, R., Gosselin, F., Buchanan, T. W., Tranel, D., Schyns, P., & Damasio, A. R. (2005) · Nature · doi:10.1038/nature03086 · Cited by 1,331 · cited 1× · see citing works
“Indeed, a study in a patient with bilateral amygdala lesions showed that this patient's impaired recognition of facial expressions of fear was due to impaired processing of the eye region of faces, especially of high-spatial-frequency information about the eye”
Self-citationDistinct spatial frequency sensitivities for processing faces and emotional expressions
Vuilleumier, P., Armony, J. L., Driver, J., & Dolan, R. J. (2003) · Nature Neuroscience · doi:10.1038/nn1057 · Cited by 1,117 · see citing works
Neural bases of the non-conscious perception of emotional signals
Tamietto, M., & de Gelder, B. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2889 · Cited by 1,042 · see citing works
Signal timing across the macaque visual system
Schmolesky, M. T., Wang, Y., Hanes, D. P., Thompson, K. G., Leutgeb, S., Schall, J. D., & Leventhal, A. G. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.6.3272 · Cited by 1,032 · see citing works
Integrated model of visual processing
Bullier, J. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00085-6 · Cited by 1,016 · see citing works
The Amygdala: a functional analysis
Aggleton, J. P. (2000) · Cited by 964 · see citing works
Distant influences of amygdala lesion on visual cortical activation during emotional face processing
Vuilleumier, P., Richardson, M. P., Armony, J. L., Driver, J., & Dolan, R. J. (2004) · Nature Neuroscience · doi:10.1038/nn1341 · Cited by 955 · see citing works
The Human Amygdala: An Evolved System for Relevance Detection
Sander, D., Grafman, J., & Zalla, T. (2003) · Reviews in the Neurosciences · doi:10.1515/revneuro.2003.14.4.303 · Cited by 944 · see citing works
A feedforward architecture accounts for rapid categorization
Serre, T., Oliva, A., & Poggio, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700622104 · Cited by 918 · see citing works
A cortical mechanism for triggering top-down facilitation in visual object recognition
Bar, M. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321662976 · Cited by 900 · see citing works
Fast Readout of Object Identity from Macaque Inferior Temporal Cortex
Hung, C. P., Kreiman, G., Poggio, T., & DiCarlo, J. J. (2005) · Science · doi:10.1126/science.1117593 · Cited by 854 · see citing works
Ghashghaei, H. T., Hilgetag, C. C., & Barbas, H. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.046 · Cited by 845 · see citing works
Dehaene, S., Sergent, C., & Changeux, J.-P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1332574100 · Cited by 838 · see citing works
Rapid natural scene categorization in the near absence of attention
Fei-Fei, L., Rufin Vanrullen, A., Christof Koch, A., & Perona, P. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092277599 · Cited by 833 · see citing works
Fear, Vigilance, and Ambiguity
Whalen, P. J. (1998) · Current Directions in Psychological Science · doi:10.1111/1467-8721.ep10836912 · Cited by 790 · see citing works
Global and fine information coded by single neurons in the temporal visual cortex
Sugase, Y., Yamane, S., Ueno, S., & Kawano, K. (1999) · Nature · doi:10.1038/23703 · Cited by 788 · see citing works
Functional organization of thalamocortical relays
Sherman, S. M., & Guillery, R. W. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.3.1367 · Cited by 762 · see citing works
Transmitting and Decoding Facial Expressions
Smith, M. L., Cottrell, G. W., Gosselin, F., & Schyns, P. G. (2005) · Psychological Science · doi:10.1111/j.0956-7976.2005.00801.x · Cited by 730 · see citing works
Principles of Frontal Lobe Function
(2013) · Oxford University Press eBooks · doi:10.1093/med/9780199837755.001.0001 · Cited by 719 · see citing works
Humans Prefer Curved Visual Objects
Bar, M., & Neta, M. (2006) · Psychological Science · doi:10.1111/j.1467-9280.2006.01759.x · Cited by 680 · see citing works
See it with feeling: affective predictions during object perception
Barrett, L. F., & Bar, M. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0312 · Cited by 632 · see citing works
Bridging emotion theory and neurobiology through dynamic systems modeling
Lewis, M. D. (2005) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0500004x · Cited by 618 · see citing works
Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta)
Aggleton, J. P., Burton, M. J., & Passingham, R. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90279-6 · Cited by 610 · see citing works
Morris, J. S. (2001) · Brain · doi:10.1093/brain/124.6.1241 · Cited by 598 · see citing works
Category-specific visual responses of single neurons in the human medial temporal lobe
Kreiman, G., Christof Koch, A., & Fried, I. (2000) · Nature Neuroscience · doi:10.1038/78868 · Cited by 547 · see citing works
Affect is a form of cognition: A neurobiological analysis
Duncan, S., & Barrett, L. F. (2007) · Cognition & Emotion · doi:10.1080/02699930701437931 · Cited by 533 · see citing works
Recognition memory for a rapid sequence of pictures.
Potter, M. C., & Levy, E. I. (1969) · Journal of Experimental Psychology · doi:10.1037/h0027470 · Cited by 529 · see citing works
To what extent are emotional visual stimuli processed without attention and awareness?
Pessoa, L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.002 · Cited by 510 · see citing works
Self-citationFear, faces, and the human amygdala
Adolphs, R. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.06.006 · Cited by 502 · see citing works
Self-citationThe Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction
Eslinger, P. J. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90106-i · Cited by 498 · see citing works
Bypassing V1: a direct geniculate input to area MT
Sincich, L. C., Park, K. F., Wohlgemuth, M. J., & Horton, J. C. (2004) · Nature Neuroscience · doi:10.1038/nn1318 · Cited by 496 · see citing works
Cognitive Response Profile of the Human Fusiform Face Area as Determined by MEG
Halgren, E. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.1.69 · Cited by 490 · see citing works
Greene, M. R., & Oliva, A. (2009) · Psychological Science · doi:10.1111/j.1467-9280.2009.02316.x · Cited by 483 · see citing works
The subcortical anatomy of human spatial neglect: putamen, caudate nucleus and pulvinar
Karnath, H., Himmelbach, M., & Rorden, C. (2002) · Brain · doi:10.1093/brain/awf032 · Cited by 476 · see citing works
Measuring consciousness: relating behavioural and neurophysiological approaches
Seth, A. K., Dienes, Z., Cleeremans, A., Overgaard, M., & Pessoa, L. (2008) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2008.04.008 · Cited by 458 · see citing works
Self-citationThe timing of information transfer in the visual system
Nowak, L. G., & Bullier, J. (1997) · Cerebral cortex · doi:10.1007/978-1-4757-9625-4_5 · Cited by 444 · see citing works
The functional logic of cortico-pulvinar connections
Shipp, S. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1213 · Cited by 411 · cited 1× · see citing works
“For example, all 20–30 known visual areas connect with the pulvinar, sometimes in a relatively topographic fashio”
Emotion and cognition and the amygdala: From “what is it?” to “what's to be done?”
Pessoa, L. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.06.038 · Cited by 403 · see citing works
Self-citationThe brain circuitry of attention
Shipp, S. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.03.004 · Cited by 402 · see citing works
Magnocellular Projections as the Trigger of Top-Down Facilitation in Recognition
Kveraga, K., Boshyan, J., & Bar, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3481-07.2007 · Cited by 402 · see citing works
Neurons in the amygdala of the monkey with responses selective for faces.
Leonard, C. M., Rolls, E. T., Wilson, F. A., & Baylis, G. C. (1985) · Behavioural Brain Research · doi:10.1016/0166-4328(85)90062-2 · Cited by 396 · see citing works
Fearful expressions gain preferential access to awareness during continuous flash suppression.
Yang, E., Zald, D. H., & Blake, R. (2007) · Emotion · doi:10.1037/1528-3542.7.4.882 · Cited by 395 · see citing works
Liu, H., Agam, Y., Madsen, J. R., & Kreiman, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.025 · Cited by 388 · see citing works
Pulvinar nuclei of the behaving rhesus monkey: visual responses and their modulation
Petersen, S. E., Robinson, D. L., & Keys, W. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.54.4.867 · Cited by 378 · see citing works
Single-neuron responses to emotional visual stimuli recorded in human ventral prefrontal cortex
Kawasaki, H., Adolphs, R., Kaufman, O., Damásio, H., Damásio, A. R., Granner, M. A., Bakken, H. E., Hori, T., & Howard, M. A. (2001) · Nature Neuroscience · doi:10.1038/82850 · Cited by 367 · see citing works
Self-citationGuillery, R. W. (1995) · Europe PMC (PubMed Central) · Cited by 366 · see citing works
(2001) · Elsevier eBooks · doi:10.1016/b978-0-12-305460-9.x5013-8 · Cited by 355 · see citing works
Positron emission tomographic measurements of pulvinar activity during an attention task
LaBerge, D., & Buchsbaum, M. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00613.1990 · Cited by 353 · see citing works
Rolls, E. T. (2005) · doi:10.1093/acprof:oso/9780198570035.001.0001 · Cited by 339 · see citing works
Blindsight depends on the lateral geniculate nucleus
Schmid, M. C., Mrowka, S. W., Turchi, J. N., Saunders, R. C., Wilke, M., Peters, A. J., Ye, F. Q., & Leopold, D. A. (2010) · Nature · doi:10.1038/nature09179 · Cited by 334 · see citing works
Discriminating emotional faces without primary visual cortices involves the right amygdala
Pegna, A. J., Khateb, A., Lazeyras, F., & Seghier, M. L. (2004) · Nature Neuroscience · doi:10.1038/nn1364 · Cited by 334 · see citing works
Neural Responses to Facial Expression and Face Identity in the Monkey Amygdala
Gothard, K. M., Battaglia, F. P., Erickson, C. A., Spitler, K. M., & Amaral, D. G. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00714.2006 · Cited by 332 · see citing works
Romanski, L. M., Giguere, M., Bates, J. F., & Goldman-Rakic, P. S. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970317)379:3 · Cited by 325 · see citing works
The color-opponent and broad-band channels of the primate visual system
Schiller, P. H., & Logothetis, N. K. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90117-s · Cited by 311 · see citing works
Early Amygdala Reaction to Fear Spreading in Occipital, Temporal, and Frontal Cortex
Krolak‐Salmon, P., Hénaff, M., Vighetto, A., Bertrand, O., & Mauguı̀ere, F. (2004) · Neuron · doi:10.1016/s0896-6273(04)00264-8 · Cited by 307 · see citing works
de Gelder, B., den Stock, J. V., Meeren, H. K. M., Sinke, C. B. A., Kret, M. E., & Tamietto, M. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.10.008 · Cited by 304 · see citing works
Grossberg, S., & Levine, D. S. (1987) · Applied Optics · doi:10.1364/ao.26.005015 · Cited by 302 · see citing works
(2009) · Cited by 294 · see citing works
Diverse thalamic projections to the prefrontal cortex in the rhesus monkey
Barbas, H., Henion, T. H. H., & Dermon, C. R. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903130106 · Cited by 292 · see citing works
The primate pulvinar nuclei: vision and action
Grieve, K. L., Acuña, C., & Cudeiro, J. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01482-4 · Cited by 290 · see citing works
Neural mechanisms of rapid natural scene categorization in human visual cortex
Peelen, M. V., Li, F., & Kästner, S. (2009) · Nature · doi:10.1038/nature08103 · Cited by 287 · see citing works
Network architecture of the long-distance pathways in the macaque brain
Modha, D. S., & Singh, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008054107 · Cited by 283 · see citing works
Rapid emotional face processing in the human right and left brain hemispheres
Pizzagalli, D. A., Regard, M., & Lehmann, D. (1999) · Neuroreport · doi:10.1097/00001756-199909090-00001 · Cited by 277 · see citing works
Yukie, M., & Iwai, E. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902010107 · Cited by 264 · see citing works
Amygdala Automaticity in Emotional Processing
DOLAN, R. J., & VUILLEUMIER, P. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07093.x · Cited by 263 · see citing works
Genetic Gating of Human Fear Learning and Extinction
Lonsdorf, T. B., Weike, A. I., Nikamo, P., Schalling, M., Hamm, A. O., & Öhman, A. (2009) · Psychological Science · doi:10.1111/j.1467-9280.2009.02280.x · Cited by 242 · see citing works
Oya, H., Kawasaki, H., Howard, M. A., & Adolphs, R. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09502.2002 · Cited by 240 · see citing works
Self-citationAttentional Control of Visual Perception: Cortical and Subcortical Mechanisms
Desimone, R., Wessinger, M., Thomas, L., & Schneider, W. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.090 · Cited by 235 · see citing works
(2000) · doi:10.1093/oso/9780198505013.001.0001 · Cited by 229 · see citing works
Functional Imaging of the Human Lateral Geniculate Nucleus and Pulvinar
Kastner, S., O'Connor, D. H., Fukui, M. M., Fehd, H. M., Herwig, U., & Pinsk, M. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00553.2003 · Cited by 228 · see citing works
Changes in connectivity after visual cortical brain damage underlie altered visual function
Bridge, H., Thomas, O., Jbabdi, S., & Cowey, A. (2008) · Brain · doi:10.1093/brain/awn063 · Cited by 228 · see citing works
A Disynaptic Relay from Superior Colliculus to Dorsal Stream Visual Cortex in Macaque Monkey
Lyon, D. C., Nassi, J. J., & Callaway, E. M. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.003 · Cited by 226 · see citing works
A quantitative theory of immediate visual recognition
Serre, T., Kreiman, G., Kouh, M., Cadieu, C. F., Knoblich, U., & Poggio, T. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)65004-8 · Cited by 217 · see citing works
Mormann, F., Kornblith, S., Quiroga, R. Q., Kraskov, A., Cerf, M., Fried, I., & Christof Koch, A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1640-08.2008 · Cited by 212 · see citing works
The modular organization of projections from areas V1 and V2 to areas V4 and TEO in macaques
Nakamura, H., Gattass, R., Desimone, R., & Ungerleider, L. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-09-03681.1993 · Cited by 211 · cited 1× · see citing works
“However, important 'short-cut' connections link areas V1 to V4 (Ref”
Intact rapid detection of fearful faces in the absence of the amygdala
Tsuchiya, N., Moradi, F., Felsen, C. N., Yamazaki, M., & Adolphs, R. (2009) · Nature Neuroscience · doi:10.1038/nn.2380 · Cited by 210 · see citing works
Self-citationEger, E., Jedynak, A., Iwaki, T., & Skrandies, W. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00287-7 · Cited by 208 · see citing works
Functional Identification of a Pulvinar Path from Superior Colliculus to Cortical Area MT
Berman, R. A., & Wurtz, R. H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6176-09.2010 · Cited by 204 · see citing works
Rempel-Clower, N. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.851 · Cited by 203 · see citing works
Effects of Low-Spatial Frequency Components of Fearful Faces on Fusiform Cortex Activity
Winston, J. S., Vuilleumier, P. O., & Dolan, R. J. (2003) · Current Biology · doi:10.1016/j.cub.2003.09.038 · Cited by 194 · see citing works
A projection from the medial pulvinar to the amygdala in primates
Jones, E. G., & Burton, H. (1976) · Brain Research · doi:10.1016/0006-8993(76)90654-5 · Cited by 181 · see citing works
Shi, C., & Davis, M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09844.2001 · Cited by 179 · see citing works
Amygdala damage affects event‐related potentials for fearful faces at specific time windows
Rotshtein, P., Richardson, M. P., Winston, J. S., Kiebel, S. J., Vuilleumier, P. O., Martin Eimer, A., Driver, J., & Dolan, R. J. (2009) · Human Brain Mapping · doi:10.1002/hbm.20921 · Cited by 179 · see citing works
On the importance of the transient visual response in the superior colliculus
Boehnke, S. E., & Munoz, D. P. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.11.004 · Cited by 177 · see citing works
Lim, S.-L., Padmala, S., & Pessoa, L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904551106 · Cited by 166 · see citing works
Self-citationUnraveling the principles of auditory cortical processing: can we learn from the visual system?
King, A. J., & Nelken, I. (2009) · Nature Neuroscience · doi:10.1038/nn.2308 · Cited by 164 · see citing works
Smile Through Your Fear and Sadness
Smith, F. W., & Schyns, P. G. (2009) · Psychological Science · doi:10.1111/j.1467-9280.2009.02427.x · Cited by 162 · see citing works
Unconscious processing of orientation and color without primary visual cortex
Boyer, J. L., Harrison, S. A., & Ro, T. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505332102 · Cited by 159 · see citing works
Functional anatomy and interaction of fast and slow visual pathways in macaque monkeys
Chen, C.-M., Lakatos, P., Shah, A. S., Mehta, A. D., Givre, S. J., Javitt, D. C., & Schroeder, C. E. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl067 · Cited by 155 · see citing works
Rosenberg, D. S., Mauguı̀ere, F., Catenoix, H., Faillenot, I., & Magnin, M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn185 · Cited by 154 · see citing works
Receptive fields in human visual cortex mapped with surface electrodes
Yoshor, D., Bosking, W. H., Ghose, G. M., & Maunsell, J. H. R. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl138 · Cited by 152 · see citing works
Projection of the lateral geniculate nucleus onto cortical area V2 in the macaque monkey
Bullier, J., & Kennedy, H. (1983) · Experimental Brain Research · doi:10.1007/bf00239409 · Cited by 151 · see citing works
Visual activation of neurons in the primate pulvinar depends on cortex but not colliculus
Bender, D. B. (1983) · Brain Research · doi:10.1016/0006-8993(83)90188-9 · Cited by 146 · see citing works
Rudrauf, D., Olivier David, A., Lachaux, J.-P., Kovach, C. K., Martinerie, J. M., Renault, B., & Damásio, A. R. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3476-07.2008 · Cited by 145 · see citing works
Neural activity in the visual thalamus reflects perceptual suppression
Wilke, M., Mueller, K.-M., & Leopold, D. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900714106 · Cited by 144 · see citing works
Neural Correlates of Change Detection and Change Blindness in a Working Memory Task
Pessoa, L. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh013 · Cited by 138 · see citing works
Self-citationActivity of single neurons in the monkey amygdala during performance of a visual discrimination task
Nakamura, K., Mikami, A., & Kubota, K. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.6.1447 · Cited by 135 · see citing works
Ward, R., Danziger, S., Owen, V., & Rafal, R. (2002) · Nature Neuroscience · doi:10.1038/nn794 · Cited by 124 · see citing works
The Connectivity of the Human Pulvinar: A Diffusion Tensor Imaging Tractography Study
Leh, S. E., Chakravarty, M. M., & Ptito, A. (2007) · International Journal of Biomedical Imaging · doi:10.1155/2008/789539 · Cited by 120 · see citing works
THE CONTRIBUTION OF THE ‘SECOND’ VISUAL SYSTEM TO DIRECTED VISUAL ATTENTION IN MAN
ZIHL, J., & CRAMON, D. V. (1979) · Brain · doi:10.1093/brain/102.4.835 · Cited by 120 · see citing works
The 30th Sir Frederick Bartlett Lecture: Fact, Artefact, and Myth about Blindsight
Cowey, A. (2004) · The Quarterly Journal of Experimental Psychology Section A · doi:10.1080/02724980343000882 · Cited by 118 · see citing works
The Statistical Neuroanatomy of Frontal Networks in the Macaque
Averbeck, B. B., & Seo, M. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000050 · Cited by 112 · see citing works
Tovée, M. J., & Rolls, E. T. (1995) · Visual Cognition · doi:10.1080/13506289508401721 · Cited by 112 · see citing works
Emotion recognition following human pulvinar damage
Ward, R. D., Calder, A. J., Parker, M., & Arend, I. C. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.09.017 · Cited by 100 · see citing works
Distinct and Convergent Visual Processing of High and Low Spatial Frequency Information in Faces
Rotshtein, P., Vuilleumier, P. O., Winston, J. S., Driver, J., & Dolan, R. J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl180 · Cited by 100 · see citing works
(2003) · CRC Press eBooks · doi:10.1201/9780203507599 · Cited by 98 · see citing works
Response to Visual Threat Following Damage to the Pulvinar
Ward, R. D., Danziger, S., & Bamford, S. (2005) · Current Biology · doi:10.1016/j.cub.2005.01.056 · Cited by 95 · see citing works
Benevento, L. A., & Port, J. D. (1995) · Visual Neuroscience · doi:10.1017/s0952523800008439 · Cited by 86 · see citing works
Visually Driven Activation in Macaque Areas V2 and V3 without Input from the Primary Visual Cortex
Schmid, M. C., Panagiotaropoulos, T. I., Augath, M. A., Logothetis, N. K., & Smirnakis, S. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005527 · Cited by 82 · see citing works
Mackie, J. A. C. (1992) · Asian Studies Review · doi:10.1080/03147539208712844 · Cited by 78 · see citing works
Pulvinar lesions in monkeys produce abnormal scanning of a complex visual array
Ungerleider, L. G., & Christensen, C. A. (1979) · Neuropsychologia · doi:10.1016/0028-3932(79)90056-3 · Cited by 65 · see citing works
Arend, I. C., Machado, L., Ward, R. D., McGrath, M., Ro, T., & Rafal, R. D. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00669-9 · Cited by 64 · see citing works
Pulvinar and affective significance: responses track moment-to-moment stimulus visibility
Padmala, S. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00064 · Cited by 61 · see citing works
Sherman, S. M. (2006) · Scholarpedia · doi:10.4249/scholarpedia.1583 · Cited by 59 · see citing works
Gilaie‐Dotan, S., Perry, A., Bonneh, Y. S., Malach, R., & Shlomo Bentin, A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn205 · Cited by 56 · see citing works
Responses of single neurons in monkey amygdala to facial and vocal emotions.
Kuraoka, K., & Nakamura, K. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00464.2006 · Cited by 52 · see citing works
Individual differences in valence modulation of face-selective m170 response.
JAPEE, S. A., Crocker, L., Carver, F. W., Pessoa, L., & Ungerleider, L. G. (2009) · Emotion · doi:10.1037/a0014487 · Cited by 46 · see citing works
Self-citationRepresenting the Forest before the Trees: A Global Advantage Effect in Monkey Inferotemporal Cortex
Sripati, A. P., & Olson, C. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5766-08.2009 · Cited by 41 · see citing works
Electrophysiological correlates of affective blindsight
Andino, S. L. G., GRAVEDEPERALTAMENENDEZ, R., Khateb, A., Landis, T., & Pegna, A. J. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.002 · Cited by 40 · see citing works
Ouellette, B. G., & Casanova, C. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0555-y · Cited by 34 · see citing works
Fear-enhanced visual search persists after amygdala lesions
Piech, R. M., McHugo, M., Smith, S. D., Dukic, M. S., Meer, J. V. D., Abou-Khalil, B. W., & Zald, D. H. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.07.009 · Cited by 29 · see citing works
Combining Structural Connectivity and Response Latencies to Model the Structure of the Visual System
Capalbo, M., Postma, E. O., & Goebel, R. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000159 · Cited by 26 · see citing works
Pessoa, L. (2010) · Scholarpedia · doi:10.4249/scholarpedia.6314 · Cited by 13 · see citing works
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Research works printed but not linked: 2
- [39]Pessoa L Oliveira L Pereira MG Armony JL Vuilleumier P Handbook of Human Affective Neuroscience 2011 Cambridge, UK Cambridge Univ. Press
- [45]Robinson DL Cowie RJ McCormick D The Thalamus 1997 New York Elsevier 53 92
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Sorted by citations
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · see citing works
“Thus, visual processing takes place within a context that is defined by signals occurring in the amygdala (as well as the orbitofrontal cortex, pulvinar, and other regions), including those linked to affective significance (Pessoa & Adolphs 2010).”
BackgroundInfluentialCognitive Reappraisal of Emotion: A Meta-Analysis of Human Neuroimaging Studies
Buhle, J. T., Silvers, J. A., Wager, T. D., Lopez, R., Onyemekwu, C., Kober, H., Weber, J., & Ochsner, K. N. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht154 · Cited by 1,896 · see citing works
The ventral visual pathway: an expanded neural framework for the processing of object quality
Kravitz, D. J., Saleem, K. S., Baker, C. I., Ungerleider, L. G., & Mishkin, M. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.10.011 · Cited by 1,154 · see citing works
Ventromedial hypothalamic neurons control a defensive emotion state
Kunwar, P. S., Zelikowsky, M., Remedios, R., Cai, H., Balban, M. Y., Meister, M., & Anderson, D. J. (2015) · eLife · doi:10.7554/elife.06633 · Cited by 1,112 · see citing works
LeDoux, J. E. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400335111 · Cited by 891 · see citing works
Hamilton, J. P., Etkin, A., Furman, D. J., Lemus, M. G., Johnson, R. F., & Gotlib, I. H. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.11071105 · Cited by 866 · see citing works
Compound facial expressions of emotion
Du, S., Tao, Y., & Martinez, A. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322355111 · Cited by 806 · see citing works
Anterior insular cortex and emotional awareness
Gu, X., Hof, P. R., Friston, K. J., & Fan, J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23368 · Cited by 712 · see citing works
Mather, M., Clewett, D., Sakaki, M., & Harley, C. W. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15000667 · Cited by 695 · see citing works
Brain mechanisms for emotional influences on perception and attention: What is magic and what is not
Pourtois, G., Schettino, A., & Vuilleumier, P. (2013) · Biological Psychology · doi:10.1016/j.biopsycho.2012.02.007 · Cited by 687 · see citing works
Venkatraman, V., Dimoka, A., Pavlou, P. A., Vo, K. D., Hampton, W. H., Bollinger, B. K., Ersner-Hershfield, H., Ishihara, M., & Winer, R. S. (2014) · Journal of Marketing Research · doi:10.1509/jmr.13.0593 · Cited by 554 · see citing works
Dynamic Facial Expressions of Emotion Transmit an Evolving Hierarchy of Signals over Time
Jack, R. E., Garrod, O., & Schyns, P. G. (2014) · Current Biology · doi:10.1016/j.cub.2013.11.064 · Cited by 529 · see citing works
Adolphs, R. (2013) · Current Biology · doi:10.1016/j.cub.2012.11.055 · Cited by 524 · see citing works
Self-citationThe hierarchical basis of neurovisceral integration
Smith, R., Thayer, J. F., Khalsa, S. S., & Lane, R. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.003 · Cited by 523 · see citing works
A quantitative meta-analysis of neurocognitive functioning in posttraumatic stress disorder.
Scott, J. C., Matt, G. E., Wrocklage, K. M., Crnich, C., Jordan, J., Southwick, S. M., Krystal, J. H., & Schweinsburg, B. C. (2015) · Psychological Bulletin · doi:10.1037/a0038039 · Cited by 513 · see citing works
N170 sensitivity to facial expression: A meta-analysis
Hinojosa, J. A., Mercado, F., & Carretié, L. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.06.002 · Cited by 494 · see citing works
Quantitative meta-analysis of neural activity in posttraumatic stress disorder
Hayes, J. P., Hayes, S. M., & Mikedis, A. M. (2012) · Biology of Mood & Anxiety Disorders · doi:10.1186/2045-5380-2-9 · Cited by 452 · see citing works
A meta-analysis of neurofunctional imaging studies of emotion and cognition in major depression
Diener, C., Kuehner, C., Brusniak, W., Ubl, B., Wessa, M., & Flor, H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.04.005 · Cited by 420 · see citing works
Exogenous (automatic) attention to emotional stimuli: a review
Carretié, L. (2014) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-014-0270-2 · Cited by 412 · see citing works
Neural Substrate of the Late Positive Potential in Emotional Processing
Liu, Y., Huang, H., Deweese, M. M., Keil, A., & Ding, M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3109-12.2012 · Cited by 415 · see citing works
Emotion and cognition and the amygdala: From “what is it?” to “what's to be done?”
Pessoa, L. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.06.038 · Cited by 403 · see citing works
Self-citationA fast pathway for fear in human amygdala
Méndez‐Bértolo, C., Moratti, S., Toledano, R., López-Sosa, F., Martínez-Alvarez, R., Mah, Y., Vuilleumier, P. O., Gil‐Nagel, A., & Strange, B. A. (2016) · Nature Neuroscience · doi:10.1038/nn.4324 · Cited by 396 · see citing works
Processing of visually evoked innate fear by a non-canonical thalamic pathway
Wei, P., Liu, N., Zhang, Z., Liu, X., Tang, Y., He, X., Wu, B., Zhou, Z., Liu, Y., Li, J., et al. (2015) · Nature Communications · doi:10.1038/ncomms7756 · Cited by 387 · see citing works
Emotion Perception from Face, Voice, and Touch: Comparisons and Convergence
Schirmer, A., & Adolphs, R. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.01.001 · Cited by 383 · see citing works
Self-citationGabard-Durnam, L. J., Flannery, J., Goff, B., Gee, D. G., Humphreys, K. L., Telzer, E., Hare, T., & Tottenham, N. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.038 · Cited by 372 · see citing works
Okon-Singer, H., Hendler, T., Pessoa, L., & Shackman, A. J. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00058 · Cited by 371 · see citing works
Self-citationViding, E., Sebastian, C. L., Dadds, M. R., Lockwood, P. L., Cecil, C. A. M., De Brito, S. A., & McCrory, E. J. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12020191 · Cited by 368 · see citing works
Developmental pathways to functional brain networks: emerging principles
Menon, V. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.015 · Cited by 342 · see citing works
Schulze, L., Schmahl, C., & Niedtfeld, I. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.03.027 · Cited by 48 · see citing works
Di Martino, A., Zuo, X.-N., Kelly, C., Grzadzinski, R., Mennes, M., Schvarcz, A., Rodman, J., Lord, C., Castellanos, F. X., & Milham, M. P. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.02.011 · Cited by 345 · see citing works
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Todd, R. M., Cunningham, W. A., Anderson, A. K., & Thompson, E. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.06.003 · Cited by 336 · see citing works
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Kenwood, M. M., Kalin, N. H., & Barbas, H. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01109-z · Cited by 338 · see citing works
Anxiety and attention to threat: cognitive mechanisms and treatment with attention bias modification
Mogg, K., & Bradley, B. P. (2016) · Behaviour Research and Therapy · doi:10.1016/j.brat.2016.08.001 · Cited by 313 · see citing works
Goschke, T. (2014) · International Journal of Methods in Psychiatric Research · doi:10.1002/mpr.1410 · Cited by 293 · see citing works
Johnson, M. H., Senju, A., & Tomalski, P. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.10.009 · Cited by 294 · see citing works
Should a Few Null Findings Falsify Prefrontal Theories of Conscious Perception?
Odegaard, B., Knight, R. T., & Lau, H. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3217-16.2017 · Cited by 316 · see citing works
Cross-Subject Emotion Recognition Using Flexible Analytic Wavelet Transform From EEG Signals
Gupta, V., Chopda, M. D., & Pachori, R. B. (2018) · IEEE Sensors Journal · doi:10.1109/jsen.2018.2883497 · Cited by 292 · see citing works
Hamilton, J. P., Chen, M. C., & Gotlib, I. H. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.01.015 · Cited by 293 · see citing works
Pulvinar neurons reveal neurobiological evidence of past selection for rapid detection of snakes
Le, Q. V., Isbell, L. A., Matsumoto, J., Nguyen, M. N., Hori, E., Maior, R. S., Tomaz, C. A. B., Tran, A. H., Ono, T., & Nishijo, H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312648110 · Cited by 270 · see citing works
Individual Variation in Functional Topography of Association Networks in Youth
Cui, Z., Li, H., Xia, C. H., Larsen, B., Adebimpe, A., Baum, G. L., Cieslak, M., Gur, R. E., Gur, R. C., Moore, T. M., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.029 · Cited by 269 · see citing works
The muted sense: neurocognitive limitations of olfactory language
Olofsson, J., & Gottfried, J. A. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.04.007 · Cited by 268 · see citing works
Predicting treatment response in social anxiety disorder from functional magnetic resonance imaging.
Doehrmann, O., Ghosh, S. S., Polli, F. E., Reynolds, G. O., Horn, F., Keshavan, A., Triantafyllou, C., Saygin, Z. M., Whitfield-Gabrieli, S., Hofmann, S. G., et al. (2013) · JAMA Psychiatry · doi:10.1001/2013.jamapsychiatry.5 · Cited by 262 · see citing works
Jing Sui (Beijing Normal University), my correct affiliation is beijing normal university, N. Q. U. O. S. A. T., Pearlson, G. D., Caprihan, A., Adalı, T., Kiehl, K. A., Liu, J., Yamamoto, J., & Calhoun, V. D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.055 · Cited by 260 · see citing works
Effects of intranasal oxytocin on the neural basis of face processing in autism spectrum disorder
Domes, G., Heinrichs, M., Kumbier, E., Grossmann, A., Hauenstein, K., & Herpertz, S. C. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.02.007 · Cited by 255 · see citing works
Adolfi, F., Couto, B., Richter, F., Decety, J., Lopez, J., Sigman, M., Manes, F., & Ibáñez, A. (2017) · Cortex · doi:10.1016/j.cortex.2016.12.019 · Cited by 238 · see citing works
Qin, S., Young, C. B., Duan, X., Chen, T., Supekar, K., & Menon, V. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.006 · Cited by 249 · see citing works
Inherently Ambiguous: Facial Expressions of Emotions, in Context
Hassin, R. R., Aviezer, H., & Shlomo Bentin, A. (2013) · Emotion Review · doi:10.1177/1754073912451331 · Cited by 245 · see citing works
Subcortical Connections to Human Amygdala and Changes following Destruction of the Visual Cortex
Tamietto, M., Pullens, P., de Gelder, B., Weiskrantz, L., & Goebel, R. (2012) · Current Biology · doi:10.1016/j.cub.2012.06.006 · Cited by 243 · see citing works
The neural basis of one's own conscious and unconscious emotional states
Smith, R. S., & Lane, R. D. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.08.003 · Cited by 240 · see citing works
The neural basis of humour processing
Vrtička, P., Black, J. M., & Reiss, A. L. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3566 · Cited by 245 · see citing works
Brain circuits for pain and its treatment
Lindsay, N. M., Chen, C., Gilam, G., Mackey, S., & Scherrer, G. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abj7360 · Cited by 234 · see citing works
Delvecchio, G., Fossati, P., Boyer, P., Brambilla, P., Falkai, P., Gruber, O., Hietala, J. A., Lawrie, S. M., Martinot, J., McIntosh, A. M., et al. (2011) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2011.07.003 · Cited by 230 · see citing works
Attention biases, anxiety, and development: toward or away from threats or rewards?
Shechner, T., Britton, J. C., Pérez‐Edgar, K. E., Bar‐Haim, Y., Monique Ernst, D., Fox, N. A., Leibenluft, E., & Pine, D. S. (2011) · Depression and Anxiety · doi:10.1002/da.20914 · Cited by 231 · see citing works
Pace-Schott, E. F., Amole, M. C., Aue, T., Balconi, M., Bylsma, L. M., Critchley, H., Demaree, H. A., Friedman, B. H., Gooding, A. E. K., Gosseries, O., et al. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.05.002 · Cited by 221 · see citing works
“, visual versus auditory) may have substantial effects on the neural processing streams, especially as they relate to emotion (Pessoa and Adolphs, 2010).”
Schilbach, L., Bzdok, D., Timmermans, B., Fox, P. T., Laird, A. R., Vogeley, K. T., & Eickhoff, S. B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030920 · Cited by 227 · see citing works
Motomura, Y., Kitamura, S., Oba, K., Terasawa, Y., Enomoto, M., Katayose, Y., Hida, A., Moriguchi, Y., Higuchi, S., & Mishima, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056578 · Cited by 226 · see citing works
Sexual dimorphism in the human brain: evidence from neuroimaging
Sacher, J., Neumann, J., Okon-Singer, H., Gotowiec, S., & Villringer, A. (2013) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2012.06.007 · Cited by 221 · see citing works
Turning a blind eye to temptation: How cognitive load can facilitate self-regulation.
van Dillen, L. F., Papies, E. K., & Hofmann, W. (2012) · Journal of Personality and Social Psychology · doi:10.1037/a0031262 · Cited by 221 · see citing works
Dolcos, F., Katsumi, Y., Moore, M., Berggren, N., de Gelder, B., Derakshan, N., Hamm, A. O., Koster, E. H. W., Ladouceur, C. D., Okon‐Singer, H., et al. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.08.017 · Cited by 222 · see citing works
Mogg, K., Waters, A. M., & Bradley, B. P. (2017) · Clinical Psychological Science · doi:10.1177/2167702617696359 · Cited by 215 · see citing works
Sabatinelli, D., Keil, A., Frank, D. W., & Lang, P. J. (2012) · Biological Psychology · doi:10.1016/j.biopsycho.2012.04.005 · Cited by 212 · see citing works
Does Language Do More Than Communicate Emotion?
Lindquist, K. A., Satpute, A. B., & Gendron, M. (2015) · Current Directions in Psychological Science · doi:10.1177/0963721414553440 · Cited by 221 · see citing works
Anxiety and Threat-Related Attention: Cognitive-Motivational Framework and Treatment
Mogg, K., & Bradley, B. P. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.01.001 · Cited by 210 · see citing works
Emotional Responses to Multisensory Environmental Stimuli
Schreuder, E., van Erp, J. B. F., Toet, A., & Kallen, V. (2016) · SAGE Open · doi:10.1177/2158244016630591 · Cited by 210 · see citing works
Emotion schemas are embedded in the human visual system
Kragel, P. A., Reddan, M. C., LaBar, K. S., & Wager, T. D. (2019) · Science Advances · doi:10.1126/sciadv.aaw4358 · Cited by 191 · see citing works
The sound of emotions—Towards a unifying neural network perspective of affective sound processing
Frühholz, S., Trost, W. J., & Kotz, S. A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.002 · Cited by 196 · see citing works
The face inversion effect in infants is driven by high, and not low, spatial frequencies
Dobkins, K. R., & Harms, R. (2014) · Journal of Vision · doi:10.1167/14.1.1 · Cited by 195 · see citing works
Pathways for emotions and attention converge on the thalamic reticular nucleus in primates
Zikopoulos, B., & Barbas, H. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4793-11.2012 · Cited by 193 · see citing works
Kumfor, F., & Piguet, O. (2012) · Neuropsychology Review · doi:10.1007/s11065-012-9201-6 · Cited by 191 · see citing works
Paloyelis, Y., Doyle, O. M., Zelaya, F. O., Maltezos, S., Williams, S. C., Fotopoulou, A., & Howard, M. A. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.10.005 · Cited by 187 · see citing works
The Neurobiology of Depression: an Integrated Overview from Biological Theories to Clinical Evidence
Ferrari, F., & Villa, R. F. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0032-y · Cited by 186 · see citing works
Cognition–Emotion Integration in the Anterior Insular Cortex
Gu, X., Liu, X., Dam, N. T. V., Hof, P. R., & Fan, J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr367 · Cited by 183 · see citing works
Vainik, U., García‐García, I., & Dagher, A. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14352 · Cited by 182 · see citing works
Reward processing in obesity, substance addiction and non‐substance addiction
García‐García, I., Horstmann, A., Jurado, M. Á., Garolera, M., Chaudhry, S. J., Margulies, D. S., Villringer, A., & Neumann, J. (2014) · Obesity Reviews · doi:10.1111/obr.12221 · Cited by 180 · see citing works
Learning Race from Face: A Survey
Fu, S., He, H., & Hou, Z.-G. (2014) · IEEE Transactions on Pattern Analysis and Machine Intelligence · doi:10.1109/tpami.2014.2321570 · Cited by 178 · see citing works
Revise the revised? New dimensions of the neuroanatomical hypothesis of panic disorder
Dresler, T., Guhn, A., Tupak, S. V., Ehlis, A., Herrmann, M. J., Fallgatter, A. J., Deckert, J., & Domschke, K. (2012) · Journal of Neural Transmission · doi:10.1007/s00702-012-0811-1 · Cited by 177 · see citing works
Three stages of emotional word processing: an ERP study with rapid serial visual presentation
Zhang, D., He, W., Wang, T., Luo, W., Zhu, X., Gu, R., Li, H., & Luo, Y. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst188 · Cited by 176 · see citing works
Thorsen, A. L., Hagland, P., Raduà, J., Mataix‐Cols, D., Kvale, G., Hansen, B. K. A., & van den Heuvel, O. A. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.01.009 · Cited by 175 · see citing works
Shiota, M. N., & Levenson, R. W. (2012) · Journal of Personality and Social Psychology · doi:10.1037/a0029208 · Cited by 174 · see citing works
Attentional capture by signals of threat
Schmidt, L. J., Belopolsky, A. V., & Theeuwes, J. (2015) · Cognition and Emotion · doi:10.1080/02699931.2014.924484 · Cited by 173 · see citing works
Sex differences in physiological reactivity to acute psychosocial stress in adolescence
Ordaz, S. J., & Luna, B. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.01.002 · Cited by 173 · see citing works
A category-specific response to animals in the right human amygdala
Mormann, F., Dubois, J., Kornblith, S., Milosavljevic, M., Cerf, M., Ison, M. J., Tsuchiya, N., Kraskov, A., Quiroga, R. Q., Adolphs, R., et al. (2011) · Nature Neuroscience · doi:10.1038/nn.2899 · Cited by 168 · see citing works
Self-citationSerotonin and decision making processes
Homberg, J. R. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.06.001 · Cited by 167 · see citing works
Predictions penetrate perception: Converging insights from brain, behaviour and disorder
O’Callaghan, C., Kveraga, K., Shine, J. M., Adams, R. B., & Bar, M. (2016) · Consciousness and Cognition · doi:10.1016/j.concog.2016.05.003 · Cited by 162 · see citing works
I'll take the low road: the evolutionary underpinnings of visually triggered fear
Carr, J. A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00414 · Cited by 162 · see citing works
Neural processing of visual information under interocular suppression: a critical review
Sterzer, P., Stein, T., Ludwig, K., Rothkirch, M., & Hesselmann, G. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00453 · Cited by 157 · see citing works
Pulvinar: Associative role in cortical function and clinical correlations
Benarroch, E. E. (2015) · Neurology · doi:10.1212/wnl.0000000000001276 · Cited by 160 · see citing works
The amygdala: An agent of change in adolescent neural networks
Scherf, K. S., Smyth, J. M., & Delgado, M. R. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.05.011 · Cited by 159 · see citing works
Cortical route for facelike pattern processing in human newborns
Buiatti, M., Giorgio, E. D., Manuela Piazza, A., Polloni, C., Menna, G., Taddei, F., Baldo, E., & Vallortígara, G. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812419116 · Cited by 162 · see citing works
Krusemark, E. A., & Li, W. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4394-10.2011 · Cited by 157 · see citing works
Dynamic modulation of emotional processing.
Okon-Singer, H., Lichtenstein-Vidne, L., & Cohen, N. (2013) · Biological Psychology · doi:10.1016/j.biopsycho.2012.05.010 · Cited by 147 · see citing works
Exploring the unconscious using faces
Axelrod, V., Bar, M., & Rees, G. E. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.11.003 · Cited by 159 · see citing works
Delvecchio, G., Sugranyes, G., & Frangou, S. (2012) · Psychological Medicine · doi:10.1017/s0033291712001432 · Cited by 156 · see citing works
Olfactory systems and neural circuits that modulate predator odor fear
Takahashi, L. K. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00072 · Cited by 162 · see citing works
Schweizer, S., Satpute, A. B., Atzil, S., Field, A. P., Hitchcock, C., Black, M., Barrett, L. F., & Dalgleish, T. (2019) · Psychological Bulletin · doi:10.1037/bul0000193 · Cited by 152 · see citing works
Electrical fingerprint of the amygdala guides neurofeedback training for stress resilience
Keynan, J. N., Cohen, A., Jackont, G., Green, N., Goldway, N., Davidov, A., Meir-Hasson, Y., Raz, G., Intrator, N., Fruchter, E., et al. (2018) · Nature Human Behaviour · doi:10.1038/s41562-018-0484-3 · Cited by 148 · see citing works
Mapping anhedonia-specific dysfunction in a transdiagnostic approach: an ALE meta-analysis
Zhang, B., Lin, P., Shi, H., Öngür, D., Auerbach, R. P., Wang, X., Yao, S., & Wang, X. (2016) · Brain Imaging and Behavior · doi:10.1007/s11682-015-9457-6 · Cited by 152 · see citing works
Faces and awareness: Low-level, not emotional factors determine perceptual dominance.
Gray, K. L. H., Adams, W. J., Hedger, N., Newton, K. E., & Garner, M. J. (2013) · Emotion · doi:10.1037/a0031403 · Cited by 151 · see citing works
Algorithms for survival: a comparative perspective on emotions
Bach, D. R., & Dayan, P. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.35 · Cited by 144 · see citing works
Markovic, J., Anderson, A., & Todd, R. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.11.018 · Cited by 132 · see citing works
- Authors
- Pessoa, L., & Adolphs, R.
- Affiliations
- Indiana University Bloomington (US)
- California Institute of Technology (US)
- Corresponding author
- Pessoa, Luiz
- Adolphs, Ralph
- Venue
- Nature Reviews Neuroscience
- Published
- 2010-11
- Volume
- 11
- Issue
- 11
- Pages
- 773-782
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- PMC
- PMC3025529
- OpenAlex
- W2083433785
- Cited by
- 1,794
- References
- 141
- Citations by year
- 2026: 95 · 2025: 106 · 2024: 87 · 2023: 79 · 2022: 99 · 2021: 100 · 2020: 118 · 2019: 122 · 2018: 112 · 2017: 154 · 2016: 132 · 2015: 116 · 2014: 161 · 2013: 126 · 2012: 120
- FWCI
- 7.28
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Funders
- National Science Foundation
- Simons Foundation
- National Institutes of Health
- National Institute of Mental Health (R01MH071589, R01MH080721)
- National Institute of Neurological Disorders and Stroke (P01NS019632)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- amygdala, emotional processing, subcortical pathways, superior colliculus, pulvinar, unconscious processes, cortical networks, primate brain
- MeSH terms
- Amygdala, Animals, Cerebral Cortex, Emotions, Biological Evolution, Humans, Models, Biological, Neural Pathways, Photic Stimulation, Pulvinar
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