An insular view of the social decision-making network
Open accessAbstract
Social animals must detect, evaluate and respond to the emotional states of other individuals in their group. A constellation of gestures, vocalizations, and chemosignals enable animals to convey affect and arousal to others in nuanced, multisensory ways. Observers integrate social information with environmental and internal factors to select behavioral responses to others via a process call social decision-making. The Social Decision Making Network (SDMN) is a system of brain structures and neurochemicals that are conserved across species (mammals, reptiles, amphibians, birds) that are the proximal mediators of most social behaviors. However, how sensory information reaches the SDMN to shape behavioral responses during a social encounter is not well known. Here we review the empirical data that demonstrate the necessity of sensory systems in detecting social stimuli, as well as the anatomical connectivity of sensory systems with each node of the SDMN. We conclude that the insular cortex is positioned to link integrated social sensory cues to this network to produce flexible and appropriate behavioral responses to socioemotional cues.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The insula is involved in social decision-making, involving empathy and fairness.
“The insula is also involved in social decision-making, involving empathy and fairness [97,98].”
From The Insular Cortex: An Interface Between Sensation, Emotion and Cognition (2024) · cites this paper as [98]
Cortical regions involved in emotional processing and decision-making, including the medial prefrontal cortex, anterior cingulate cortex, and insular cortex, have been implicated in social function in rodents and humans alike.
“Cortical regions involved in emotional processing and decision-making, including the mPFC, ACC, and IC, have also been implicated in social function in rodents and humans alike [81,82,83].”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [83]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The expression of the emotions in man and animals.
Darwin, C. D. (1872) · J. Murray eBooks · doi:10.1037/10001-000 · Cited by 12,120 · see citing works
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444 · see citing works
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426 · see citing works
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · cited 4× · see citing works
“…addition to integrating external sensory stimuli, IC is thought to be a locus of interoception because inputs from visceral thalamic nuclei allow IC to detect internal physiological changes (Damasio, 2003; Damasio & Carvalho, 2013; Craig, 2009; Craig 2011, Seth, 2013; and Strigo & Craig, 2016).”
BackgroundInfluentialCore affect and the psychological construction of emotion.
Russell, J. A. (2003) · Psychological Review · doi:10.1037/0033-295x.110.1.145 · Cited by 6,113 · see citing works
Saliency, switching, attention and control: a network model of insula function
Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592 · see citing works
Meeting of minds: the medial frontal cortex and social cognition
Amodio, D. M., & Frith, C. D. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1884 · Cited by 3,782 · see citing works
Functional neuroanatomy of emotion: A meta-analysis of emotion activation studies in PET and fMRI
Phan, K. L., Wager, T., Taylor, S. F., & Liberzon, I. (2002) · NeuroImage · doi:10.1006/nimg.2002.1087 · Cited by 3,502 · see citing works
Mesulam, M. (1998) · Brain · doi:10.1093/brain/121.6.1013 · Cited by 3,072 · see citing works
Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works
Dopamine in motivational control: rewarding, aversive, and alerting
Bromberg-Martin, E. S., Matsumoto, M., & Hikosaka, O. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.022 · Cited by 2,396 · see citing works
Development and neurophysiology of mentalizing
Frith, U., & Frith, C. D. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1218 · Cited by 2,306 · see citing works
Salience processing and insular cortical function and dysfunction
Uddin, L. Q. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3857 · Cited by 2,083 · see citing works
Interoceptive inference, emotion, and the embodied self
Seth, A. K. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.007 · Cited by 1,816 · cited 2× · see citing works
“…addition to integrating external sensory stimuli, IC is thought to be a locus of interoception because inputs from visceral thalamic nuclei allow IC to detect internal physiological changes (Damasio, 2003; Damasio & Carvalho, 2013; Craig, 2009; Craig 2011, Seth, 2013; and Strigo & Craig, 2016).”
BackgroundResultEmpathic neural responses are modulated by the perceived fairness of others
Singer, T., Seymour, B., O'Doherty, J. P., Stephan, K. E., Dolan, R. J., & Frith, C. D. (2006) · Nature · doi:10.1038/nature04271 · Cited by 1,726 · cited 1× · see citing works
“NAc encodes reward value and decision-making, and, as noted, both IC and NAc are implicated in rodent and human social behaviors (Lamm & Singer, 2010; Trezza et al., 2011; Singer et al., 2006; Lichtenberg et al., 2018).”
BackgroundOxytocin, vasopressin, and the neurogenetics of sociality
Donaldson, Z. R., & Young, L. J. (2008) · Science · doi:10.1126/science.1158668 · Cited by 1,645 · see citing works
Herman, J. P., Figueiredo, H., Mueller, N. K., Ulrich-Lai, Y., Ostrander, M. M., Choi, D. C., & Cullinan, W. E. (2003) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2003.07.001 · Cited by 1,586 · see citing works
The polyvagal theory: phylogenetic substrates of a social nervous system.
Porges, S. W. (2001) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(01)00162-3 · Cited by 1,582 · see citing works
The neurobiology of social cognition
Adolphs, R. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00202-6 · Cited by 1,432 · see citing works
What does the retrosplenial cortex do?
Vann, S. D., Aggleton, J. P., & Maguire, E. A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2733 · Cited by 1,409 · see citing works
Paulus, M. P., & Stein, M. B. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.03.042 · Cited by 1,325 · see citing works
Kurth, F., Zilles, K., Fox, P. T., Laird, A. R., & Eickhoff, S. B. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0255-z · Cited by 1,293 · see citing works
The nature of feelings: evolutionary and neurobiological origins
Damasio, A., & Carvalho, G. B. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3403 · Cited by 1,280 · see citing works
A common role of insula in feelings, empathy and uncertainty
Singer, T., Critchley, H. D., & Preuschoff, K. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.05.001 · Cited by 1,270 · see citing works
Ekman, P., & Oster, H. (1979) · Annual Review of Psychology · doi:10.1146/annurev.ps.30.020179.002523 · Cited by 1,197 · see citing works
NEWMAN, S. W. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09271.x · Cited by 1,189 · see citing works
Visceral influences on brain and behavior
Critchley, H. D., & Harrison, N. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.008 · Cited by 1,177 · see citing works
Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin
Dölen, G., Darvishzadeh, A., Huang, K. W., & Malenka, R. C. (2013) · Nature · doi:10.1038/nature12518 · Cited by 1,161 · see citing works
Brog, J. S., Salyapongse, A., Deutch, A. Y., & Zahm, D. S. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903380209 · Cited by 1,102 · see citing works
Shamay-Tsoory, S. G. (2011) · The Neuroscientist · doi:10.1177/1073858410379268 · Cited by 1,059 · see citing works
Insel, T. R. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.005 · Cited by 1,044 · see citing works
Medial prefrontal cortex as an action-outcome predictor
Alexander, W. H., & Brown, J. W. (2011) · Nature Neuroscience · doi:10.1038/nn.2921 · Cited by 1,000 · see citing works
The Vertebrate mesolimbic reward system and social behavior network: A comparative synthesis
O'Connell, L. A., & Hofmann, H. A. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22735 · Cited by 986 · see citing works
Hiser, J., & Koenigs, M. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.10.030 · Cited by 972 · see citing works
Bernhardt, B. C., & Singer, T. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150536 · Cited by 952 · see citing works
Elliott, R. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.308 · Cited by 887 · see citing works
Production of subject-verb agreement, tense, mood, and negation in Italian agrammatic aphasia.
Valantis, F., Semenza, C., Rita, C., Marialuisa, G., Serena, D. P., Giorgio, A., Francesca, B., Anna, M., Nicola, S., & Gabriele, M. (2015) · Frontiers in Psychology · doi:10.3389/conf.fpsyg.2015.65.00011 · Cited by 872 · see citing works
Social Modulation of Pain as Evidence for Empathy in Mice
Langford, D. J., Crager, S. E., Shehzad, Z., Smith, S. B., Sotocinal, S. G., Levenstadt, J. S., Chanda, M. L., Levitin, D. J., & Mogil, J. S. (2006) · Science · doi:10.1126/science.1128322 · Cited by 865 · see citing works
Sotocinal, S., Sorge, R., Zaloum, A., Tuttle, A. H., Martin, L. J., Wieskopf, J. S., Mapplebeck, J. C. S., Wei, P., Zhan, S., Zhang, S., et al. (2011) · Molecular Pain · doi:10.1186/1744-8069-7-55 · Cited by 816 · see citing works
The Neuroscience of Social Decision-Making
Rilling, J. K., & Sanfey, A. G. (2011) · Annual Review of Psychology · doi:10.1146/annurev.psych.121208.131647 · Cited by 775 · see citing works
The vertebrate social behavior network: Evolutionary themes and variations
Goodson, J. L. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.02.003 · Cited by 771 · see citing works
Synaptic and Behavioral Profile of Multiple Glutamatergic Inputs to the Nucleus Accumbens
Britt, J. P., Benaliouad, F., McDevitt, R. A., Stuber, G. D., Wise, R. A., & Bonci, A. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.040 · Cited by 716 · see citing works
Emotion recognition via facial expression and affective prosody in schizophrenia
Edwards, J., Jackson, H. J., & Pattison, P. E. (2002) · Clinical Psychology Review · doi:10.1016/s0272-7358(02)00130-7 · Cited by 714 · 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 · cited 1× · see citing works
“, 2012), social motivation of others (Schreuders, 2018) and emotional awareness (Gu et al., 2013).”
BackgroundEvidence for a viscerotopic sensory representation in the cortex and thalamus in the rat
Cechetto, D. F., & Saper, C. B. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620104 · Cited by 703 · see citing works
Oxytocin-dependent consolation behavior in rodents
Burkett, J. P., Andari, E., Johnson, Z. V., Curry, D. C., de Waal, F. B. M., & Young, L. J. (2016) · Science · doi:10.1126/science.aac4785 · Cited by 692 · see citing works
Partan, S. R., & Marler, P. (1999) · Science · doi:10.1126/science.283.5406.1272 · Cited by 689 · see citing works
Mesulam, M. M., & Mufson, E. J. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902120102 · Cited by 654 · see citing works
Cabanac, M. (2002) · Behavioural Processes · doi:10.1016/s0376-6357(02)00078-5 · Cited by 652 · see citing works
Observational fear learning involves affective pain system and Cav1.2 Ca2+ channels in ACC
Jeon, D., Kim, S., Chetana, M., Jo, D., Ruley, H. E., Lin, S.-Y., Rabah, D., Kinet, J.-P., & Shin, H.-S. (2010) · Nature Neuroscience · doi:10.1038/nn.2504 · Cited by 651 · see citing works
Significance of the insula for the evolution of human awareness of feelings from the body
(Bud) Craig, A. D. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.05990.x · Cited by 646 · see citing works
Differential effects of insular and ventromedial prefrontal cortex lesions on risky decision-making
Clark, L., Bechara, A., Damasio, H., Aitken, M. R. F., Sahakian, B. J., & Robbins, T. W. (2008) · Brain · doi:10.1093/brain/awn066 · Cited by 613 · see citing works
Evolution of a Vertebrate Social Decision-Making Network
O’Connell, L. A., & Hofmann, H. A. (2012) · Science · doi:10.1126/science.1218889 · Cited by 608 · see citing works
Gating of social reward by oxytocin in the ventral tegmental area
Hung, L. W., Neuner, S., Polepalli, J. S., Beier, K. T., Wright, M., Walsh, J. J., Lewis, E. M., Luo, L., Deisseroth, K., Dölen, G., et al. (2017) · Science · doi:10.1126/science.aan4994 · Cited by 578 · see citing works
The Expression of the Emotions in Man and Animals
Darwin, C. R. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511694110 · Cited by 569 · see citing works
The role of anterior insular cortex in social emotions
Lamm, C., & Singer, T. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0251-3 · Cited by 566 · see citing works
The Anterior Cingulate Gyrus and Social Cognition: Tracking the Motivation of Others
Apps, M. A. J., Rushworth, M. F. S., & Chang, S. W. C. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.018 · Cited by 559 · see citing works
HOW THE BRAIN PROCESSES SOCIAL INFORMATION: Searching for the Social Brain
Insel, T. R., & Fernald, R. D. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144148 · Cited by 556 · see citing works
Ventral pallidum roles in reward and motivation
Smith, K. S., Tindell, A. J., Aldridge, J. W., & Berridge, K. C. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.038 · Cited by 548 · see citing works
A comprehensive excitatory input map of the striatum reveals novel functional organization
Hunnicutt, B. J., Jongbloets, B. C., Birdsong, W. T., Gertz, K. J., Zhong, H., & Mao, T. (2016) · eLife · doi:10.7554/elife.19103 · Cited by 536 · see citing works
Bidirectional control of social hierarchy by synaptic efficacy in medial prefrontal cortex
Wang, F., Zhu, J., Zhu, H., Zhang, Q., Lin, Z., & Hu, H. (2011) · Science · doi:10.1126/science.1209951 · Cited by 528 · see citing works
The organization of neural inputs to the medial preoptic nucleus of the rat
Simerly, R. B., & Swanson, L. W. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902460304 · Cited by 523 · see citing works
Dumais, K. M., & Veenema, A. H. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.04.003 · Cited by 520 · see citing works
Rearing complexity affects branching of dendrites in the visual cortex of the rat
Volkmar, F. R., & Greenough, W. T. (1972) · Science · doi:10.1126/science.176.4042.1445 · Cited by 513 · see citing works
Prefrontal Cortex and Social Cognition in Mouse and Man
Bicks, L. K., Koike, H., Akbarian, S., & Morishita, H. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01805 · Cited by 491 · see citing works
Scalable control of mounting and attack by Esr1+ neurons in the ventromedial hypothalamus
Lee, H., Kim, D.-W., Remedios, R., Anthony, T. E., Chang, A., Madisen, L., Zeng, H., & Anderson, D. J. (2014) · Nature · doi:10.1038/nature13169 · Cited by 479 · see citing works
Groenewegen, H. J., Berendse, H. W., & Haber, S. N. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90115-v · Cited by 456 · see citing works
The anterior insula in autism: Under-connected and under-examined
Uddin, L. Q., & Menon, V. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.06.002 · Cited by 424 · see citing works
The Social Dimension of Stress Reactivity
von Dawans, B., Fischbacher, U., Kirschbaum, C., Fehr, E., & Heinrichs, M. (2012) · Psychological Science · doi:10.1177/0956797611431576 · Cited by 418 · see citing works
Ethotransmission: communication of emotional states through ultrasonic vocalization in rats.
Brudzynski, S. M. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.01.014 · Cited by 416 · see citing works
Felix‐Ortiz, A. C., Burgos-Robles, A., Bhagat, N. D., Leppla, C. A., & Tye, K. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.041 · Cited by 414 · see citing works
Feelings of Emotion and the Self
Damásio, A. R. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1279.014 · Cited by 411 · see citing works
Hong, W., Kim, D.-W., & Anderson, D. J. (2014) · Cell · doi:10.1016/j.cell.2014.07.049 · Cited by 405 · see citing works
Galef, B. G., & Wigmore, S. W. (1983) · Animal Behaviour · doi:10.1016/s0003-3472(83)80232-2 · Cited by 404 · see citing works
Romanski, L. M., & LeDoux, J. E. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.6.515 · Cited by 398 · see citing works
Development of multisensory integration from the perspective of the individual neuron
Stein, B. E., Stanford, T. R., & Rowland, B. A. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3742 · Cited by 394 · see citing works
Stein, B. E., Meredith, M. A., Huneycutt, W. S., & McDade, L. (1989) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1989.1.1.12 · Cited by 394 · see citing works
Autism, oxytocin and interoception
Quattrocki, E., & Friston, K. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.09.012 · Cited by 393 · see citing works
Exogenous and evoked oxytocin restores social behavior in the <i>Cntnap2</i> mouse model of autism
Peñagarikano, O., Lázaro, M. T., Lu, X.-H., Gordon, A., Dong, H., Lam, H. A., Peles, E., Maidment, N. T., Murphy, N. P., Yang, X. W., et al. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.3010257 · Cited by 378 · see citing works
Johnson, D. M. G., Illig, K. R., Behan, M., & Haberly, L. B. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-06974.2000 · Cited by 373 · see citing works
Development and critical period plasticity of the barrel cortex
Erzurumlu, R. S., & Gaspar, P. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08075.x · Cited by 344 · see citing works
Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.5.762 · Cited by 343 · see citing works
Dopaminergic-neuropeptide interactions in the social brain
Skuse, D. H., & Gallagher, L. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2008.09.007 · Cited by 340 · see citing works
The neurobiology of social play and its rewarding value in rats
Vanderschuren, L. J. M. J., Achterberg, E. J. M., & Trezza, V. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.07.025 · Cited by 329 · see citing works
Maternal responses to infant vocalizations and olfactory cues in rats and mice
Smotherman, W. P., Bell, R. W., Starzec, J. J., Elias, J. W., & Zachman, T. A. (1974) · Behavioral Biology · doi:10.1016/s0091-6773(74)91026-8 · Cited by 324 · see citing works
Do early sensory cortices integrate cross-modal information?
Kayser, C., & Logothetis, N. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0154-0 · Cited by 319 · see citing works
Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.5.762 · Cited by 317 · see citing works
An autoradiographic study of the efferent connections of the entorhinal cortex in the rat
Wyss, J. M. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901990405 · Cited by 312 · see citing works
The role of the striatum in social behavior
Báez-Mendoza, R., & Schultz, W. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00233 · Cited by 312 · see citing works
Sensory Integration in Mouse Insular Cortex Reflects GABA Circuit Maturation
Gogolla, N., Takesian, A. E., Feng, G., Fagiolini, M., & Hensch, T. K. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.033 · Cited by 310 · see citing works
Organization of valence-encoding and projection-defined neurons in the basolateral amygdala
Beyeler, A., Chang, C.-J., Silvestre, M., Lévêque, C., Namburi, P., Wildes, C. P., & Tye, K. M. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.097 · Cited by 306 · cited 10× · see citing works
“Abbreviations: MeA: Medial amygdala; AH: Anterior hypothalamus; VMH: Ventromedial hypothalamus; mPOA: Medial preoptic area; BNST: Bed nucleus stria terminalis; LS: Lateral septum; Hipp: Hippocampus; VTA: Ventral tegmental area; VP: Ventral pallidum; NAc: Nucleus accumbens core; PAG: Periaqueductal grey; BLA: Basolater…”
BackgroundInfluentialA distributed network for social cognition enriched for oxytocin receptors
Mitre, M., Marlin, B. J., Schiavo, J. K., Morina, E., Norden, S. E., Hackett, T. A., Aoki, C. J., Chao, M. V., & Froemke, R. C. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2409-15.2016 · Cited by 305 · see citing works
Impairments in facial affect recognition associated with autism spectrum disorders: A meta-analysis
Lozier, L. M., VanMeter, J. W., & Marsh, A. A. (2014) · Development and Psychopathology · doi:10.1017/s0954579414000479 · Cited by 299 · see citing works
Dong, H., & Swanson, L. W. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20002 · Cited by 294 · see citing works
Afferent connections to the bed nucleus of the stria terminalis
Weller, K. L., & Smith, D. A. (1982) · Brain Research · doi:10.1016/0006-8993(82)90272-4 · Cited by 293 · see citing works
Liberles, S. D. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021113-170334 · Cited by 292 · see citing works
Pro-social behavior in rats is modulated by social experience
Ben-Ami Bartal, I., Rodgers, D. A., Bernardez Sarria, M. S., Decety, J., & Mason, P. (2014) · eLife · doi:10.7554/elife.01385 · Cited by 286 · see citing works
Medial Nucleus of the Amygdala Mediates Chemosensory Control of Male Hamster Sexual Behavior
Lehman, M. N., Winans, S. S., & Powers, J. B. (1980) · Science · doi:10.1126/science.7423209 · Cited by 282 · see citing works
Furtak, S. C., Wei, S., Agster, K. L., & Burwell, R. D. (2007) · Hippocampus · doi:10.1002/hipo.20314 · Cited by 282 · see citing works
Interoception, homeostatic emotions and sympathovagal balance
Strigo, I. A., & Craig, A. D. (. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0010 · Cited by 281 · see citing works
Insular cortex mediates approach and avoidance responses to social affective stimuli
Rogers-Carter, M. M., Varela, J. A., Gribbons, K. B., Pierce, A. F., McGoey, M. T., Ritchey, M., & Christianson, J. P. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0071-y · Cited by 277 · see citing works
Self-citationBekoff, M. (1972) · The Quarterly Review of Biology · doi:10.1086/407400 · Cited by 271 · see citing works
Nucleus Accumbens μ-Opioid Receptors Mediate Social Reward
Trezza, V., Damsteegt, R., Achterberg, E. J. M., & Vanderschuren, L. J. M. J. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5492-10.2011 · Cited by 263 · see citing works
LeDoux, J. E., Farb, C. R., & Romanski, L. M. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90526-y · Cited by 261 · see citing works
Dong, H., & Swanson, L. W. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20790 · Cited by 249 · see citing works
CHEMICAL COMMUNICATION IN RODENTS: FROM PHEROMONES TO INDIVIDUAL RECOGNITION
Johnston, R. E. (2003) · Journal of Mammalogy · doi:10.1644/ble-010 · Cited by 249 · see citing works
Fleming, A. S., & Rosenblatt, J. S. (1974) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0035936 · Cited by 247 · see citing works
Reynolds, S. M., & Zahm, D. S. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3432-05.2005 · Cited by 239 · see citing works
Mogenson, G. J., & Yang, C. R. (1991) · Advances in experimental medicine and biology · doi:10.1007/978-1-4757-0145-6_14 · Cited by 238 · see citing works
Thalamus provides layer 4 of primary visual cortex with orientation- and direction-tuned inputs
Sun, W., Tan, Z., Mensh, B. D., & Ji, N. (2015) · Nature Neuroscience · doi:10.1038/nn.4196 · Cited by 231 · see citing works
Scent marking behavior as an odorant communication in mice
Arakawa, H., Blanchard, D. C., Arakawa, K., Dunlap, C., & Blanchard, R. J. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.05.012 · Cited by 229 · see citing works
Female mice ultrasonically interact with males during courtship displays
Neunuebel, J. P., Taylor, A. L., Arthur, B. J., & Egnor, S. R. (2015) · eLife · doi:10.7554/elife.06203 · Cited by 224 · see citing works
Anterior insular cortex is necessary for empathetic pain perception
Gu, X., Gao, Z., Wang, X., Liu, X., Knight, R. T., Hof, P. R., & Fan, J. (2012) · Brain · doi:10.1093/brain/aws199 · Cited by 223 · see citing works
Neural mechanisms for voice recognition
Andics, A., McQueen, J. M., Petersson, K. M., Gál, V., Rudas, G., & Vidnyánszky, Z. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.048 · Cited by 222 · see citing works
Neafsey, E. J., Hurley-Gius, K. M., & Arvanitis, D. L. (1986) · Brain Research · doi:10.1016/0006-8993(86)90867-x · Cited by 219 · see citing works
Social Transmission of Fear in Rats: The Role of 22-kHz Ultrasonic Distress Vocalization
Kim, E. J., Kim, E. S., Covey, E., & Kim, J. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015077 · Cited by 216 · see citing works
Oxytocin and vasopressin: powerful regulators of social behavior
Caldwell, H. K. (2017) · The Neuroscientist · doi:10.1177/1073858417708284 · Cited by 216 · see citing works
Effective modulation of male aggression through lateral septum to medial hypothalamus projection
Wong, L. C., Wang, L., D’Amour, J. A., Yumita, T., Chen, G., Yamaguchi, T., Chang, B. C., Bernstein, H., You, X., Feng, J. E., et al. (2016) · Current Biology · doi:10.1016/j.cub.2015.12.065 · Cited by 213 · see citing works
Empathy is moderated by genetic background in mice
Chen, Q., Panksepp, J. B., & Lahvis, G. P. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004387 · Cited by 211 · see citing works
Sexually Dimorphic Control of Parenting Behavior by the Medial Amygdala
Chen, P. B., Hu, R. K., Wu, Y. E., Pan, L., Huang, S., Micevych, P. E., & Hong, W. (2019) · Cell · doi:10.1016/j.cell.2019.01.024 · Cited by 209 · see citing works
Interacting neural ensembles in orbitofrontal cortex for social and feeding behaviour
Jennings, J. H., Kim, C. K., Marshel, J. H., Raffiee, M., Li, Y., Quirin, S., Pak, S., Ramakrishnan, C., & Deisseroth, K. A. (2019) · Nature · doi:10.1038/s41586-018-0866-8 · Cited by 208 · see citing works
Coolen, L. M., & Wood, R. I. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980921)399:2 · Cited by 207 · see citing works
Rewards of beauty: the opioid system mediates social motivation in humans
Chelnokova, O., Laeng, B., Eikemo, M., Riegels, J., Løseth, G. E., Maurud, H., Willoch, F., & Leknes, S. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.1 · Cited by 204 · see citing works
Rice, G. E., & Gainer, P. (1962) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0042276 · Cited by 201 · see citing works
Dopamine and noradrenaline neurons projecting to the septal area in the rat
Lindvall, O., & Stenevi, U. (1978) · Cell and Tissue Research · doi:10.1007/bf00219554 · Cited by 195 · see citing works
Beach, F. A., & Jaynes, J. (1956) · Behaviour · doi:10.1163/156853956x00129 · Cited by 192 · see citing works
Multisensory Integration of Natural Odors and Sounds in the Auditory Cortex
Cohen, L., Rothschild, G., & Mizrahi, A. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.019 · Cited by 192 · see citing works
Complementary codes for odor identity and intensity in olfactory cortex
Bolding, K. A., & Franks, K. M. (2017) · eLife · doi:10.7554/elife.22630 · Cited by 191 · see citing works
The Ultimatum Game and the brain: A meta-analysis of neuroimaging studies
Gabay, A. S., Raduà, J., Kempton, M. J., & Mehta, M. A. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.10.014 · Cited by 185 · see citing works
Cortical and thalamic afferent connections of the insular and adjacent cortex of the rat
Guldin, W. O., & Markowitsch, H. J. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902150203 · Cited by 181 · see citing works
Afferent Inputs to Neurotransmitter-Defined Cell Types in the Ventral Tegmental Area
Faget, L. C., Osakada, F., Duan, J., Ressler, R. L., Johnson, A. B., Proudfoot, J., Yoo, J. H., Callaway, E. M., & Hnasko, T. S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.05.057 · Cited by 180 · see citing works
Social transmission and buffering of synaptic changes after stress
Sterley, T.-L., Baimoukhametova, D., Füzesi, T., Zurek, A. A., Daviu, N., Rasiah, N. P., Rosenegger, D., & Bains, J. S. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0044-6 · Cited by 179 · see citing works
Accumbens dopamine-acetylcholine balance in approach and avoidance
Hoebel, B. G., Avena, N. M., & Rada, P. V. (2007) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2007.10.014 · Cited by 178 · see citing works
Social Cognition through the Lens of Cognitive and Clinical Neuroscience
Arioli, M., Crespi, C., & Canessa, N. (2018) · BioMed Research International · doi:10.1155/2018/4283427 · Cited by 176 · see citing works
Enhanced Neuronal Activity in the Medial Prefrontal Cortex during Social Approach Behavior
Lee, E., Rhim, I., Lee, J. W., Ghim, J.-W., Lee, S., Kim, E., & Jung, M. W. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0307-16.2016 · Cited by 170 · see citing works
Neurobiological mechanisms of social attachment and pair bonding
Johnson, Z. V., & Young, L. J. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.01.009 · Cited by 169 · see citing works
Reep, R. L., & Winans, S. S. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90087-2 · Cited by 169 · see citing works
Sadananda, M., Wöhr, M., & Schwarting, R. K. W. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.02.002 · Cited by 169 · see citing works
The neural correlates of the affective response to unreciprocated cooperation
Rilling, J. K., Goldsmith, D. R., Glenn, A. L., Jairam, M. R., Elfenbein, H. A., Dagenais, J. E., Murdock, C. D., & Pagnoni, G. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.11.033 · Cited by 169 · see citing works
Subcortical sites mediating sympathetic responses from insular cortex in rats
Cechetto, D. F., & Chen, S. J. (1990) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1990.258.1.r245 · Cited by 168 · see citing works
The neural basis of maternal responsiveness to infants: an fMRI study
Ranote, S., Elliott, R., Abel, K. M., Mitchell, R., Deakin, J. F. W., & Appleby, L. (2004) · NeuroReport · doi:10.1097/01.wnr.0000137078.64128.6a · Cited by 167 · see citing works
Marsh, A. A. (2018) · Annual Review of Psychology · doi:10.1146/annurev-psych-010418-103010 · Cited by 164 · see citing works
Auditory, Somatosensory, and Multisensory Insular Cortex in the Rat
Rodgers, K. M., Benison, A. M., Klein, A., & Barth, D. S. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn054 · Cited by 163 · see citing works
Green, S. A., Hernandez, L. M., Bookheimer, S. Y., & Dapretto, M. (2016) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2016.04.013 · Cited by 161 · see citing works
Social modulation of learning in ratsPreprint
Knapska, E., Mikosz, M., Werka, T., & Maren, S. (2009) · Learning & Memory · doi:10.1101/lm.1670910 · Cited by 158 · see citing works
Social Control of Hypothalamus-Mediated Male Aggression
Yang, T., Yang, C. F., Chizari, M., Maheswaranathan, N., Burke, K. J., Borius, M., Inoue, S., Chiang, M. C., Bender, K. J., Ganguli, S., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.046 · Cited by 158 · see citing works
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 157 · see citing works
Viaene, A. N., Petrof, I., & Sherman, S. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114828108 · Cited by 157 · see citing works
The role of ultrasonic vocalizations in mouse communication
Portfors, C., & Perkel, D. J. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.07.002 · Cited by 154 · see citing works
Oxytocin signaling in the medial amygdala is required for sex discrimination of social cues
Yao, S., Bergan, J., Lanjuin, A., & Dulac, C. (2017) · eLife · doi:10.7554/elife.31373 · Cited by 151 · see citing works
The modulatory role of the lateral septum on neuroendocrine and behavioral stress responses
Singewald, G. M., Rjabokon, A., Singewald, N., & Ebner, K. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.213 · Cited by 149 · see citing works
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 149 · see citing works
Wright, C. I., & Groenewegen, H. J. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00592-7 · Cited by 148 · see citing works
Social recognition does not involve vasopressinergic neurotransmission in female rats
Bluthe´, R.-M., & Dantzer, R. (1990) · Brain Research · doi:10.1016/0006-8993(90)91613-l · Cited by 147 · see citing works
Creutz, L. M., & Kritzer, M. (2004) · The Journal of comparative neurology · doi:10.1002/cne.20229 · Cited by 144 · see citing works
Aransay, A., Rodríguez-López, C., García‐Amado, M., Clascá, F., & Prensa, L. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00059 · Cited by 143 · see citing works
Desire for social contact, not empathy, may explain “rescue” behavior in rats
Silberberg, A., Allouch, C., Sandfort, S., Kearns, D., Karpel, H., & Slotnick, B. (2014) · Animal Cognition · doi:10.1007/s10071-013-0692-1 · Cited by 142 · see citing works
The Dalila effect: C57BL6 mice barber whiskers by plucking.
Sarna, J. R., Dyck, R., & Whishaw, I. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00137-0 · Cited by 136 · see citing works
Role of the Primate Orbitofrontal Cortex in Mediating Anxious Temperament
Kalin, N. H., Shelton, S. E., & Davidson, R. J. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.04.004 · Cited by 135 · see citing works
Krushel, L. A., & van der Kooy, D. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902700105 · Cited by 132 · see citing works
Modulation of value representation by social context in the primate orbitofrontal cortex
Azzi, J. C. B., Angela Sirigu, B., & Duhamel, J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111715109 · Cited by 129 · see citing works
Analysis of the stimuli adequate to elicit mating behavior in the sexually inexperienced rat.
Beach, F. A. (1942) · Journal of comparative psychology · doi:10.1037/h0061692 · Cited by 129 · see citing works
Gallo, M., Roldán, G., & Bureš, J. (1992) · Behavioural Brain Research · doi:10.1016/s0166-4328(05)80328-6 · Cited by 129 · see citing works
Hammerschmidt, K., Radyushkin, K., Ehrenreich, H., & Fischer, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041133 · Cited by 127 · see citing works
Efferent connections of the hypothalamic “aggression area” in the rat
Roeling, T. A. P., Veening, J. G., Kruk, M. R., Peters, J. P. W., Vermelis, M. E. J., & Nieuwenhuys, R. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90302-6 · Cited by 126 · see citing works
Oxytocin mediates entrainment of sensory stimuli to social cues of opposing valence
Choe, H. K., Reed, M. D., Benavidez, N., Montgomery, D., Soares, N., Yim, Y. S., & Choi, G. B. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.022 · Cited by 124 · see citing works
Kiyokawa, Y., Honda, A., Takeuchi, Y., & Mori, Y. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.03.043 · Cited by 122 · see citing works
Neural Basis of Self and Other Representation in Autism: An fMRI Study of Self-Face Recognition
Uddin, L. Q., Davies, M. S., Scott, A. A., Zaidel, E., Bookheimer, S. Y., Iacoboni, M., & Dapretto, M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003526 · Cited by 118 · see citing works
Man, K., Kaplan, J., Damásio, H., & Damásio, A. R. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23408 · Cited by 116 · see citing works
Inputs to the ventrolateral bed nucleus of the stria terminalis
Shin, J., Geerling, J. C., & Loewy, A. D. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21870 · Cited by 115 · see citing works
Olfactory Conditioned Partner Preference in the Female Rat.
Coria‐Ávila, G. A., Ouimet, A. J., Pacheco, P., Manzo, J. G., & Pfaus, J. G. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.3.716 · Cited by 115 · see citing works
Schoenbaum, G., Setlow, B., & Ramus, S. J. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.013 · Cited by 113 · see citing works
Neural correlates of pair-bonding in a monogamous primate
Bales, K. L., Mason, W. A., Catana, C., Cherry, S. R., & Mendoza, S. P. (2007) · Brain Research · doi:10.1016/j.brainres.2007.09.087 · Cited by 112 · see citing works
Estrogen regulates responses of dopamine neurons in the ventral tegmental area to cocaine
Zhang, D., Yang, S., Yang, C., Jin, G.-Z., & Zhen, X. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1188-6 · Cited by 110 · see citing works
Consiglio, A. R., Borsoi, A., Pereira, G. A. M., & Lucion, A. B. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.05.002 · Cited by 106 · see citing works
Social Decision-Making and the Brain: A Comparative Perspective
Tremblay, S., Sharika, K. M., & Platt, M. L. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.01.007 · Cited by 105 · see citing works
Christianson, J. P., Jennings, J. H., Ragole, T., Flyer, J. G. N., Benison, A. M., Barth, D. S., Watkins, L. R., & Maier, S. F. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.04.004 · Cited by 104 · see citing works
Self-citationHow social cognition can inform social decision making
Lee, V. K., & Harris, L. T. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00259 · Cited by 104 · see citing works
Expression of c-fos gene activation during rough and tumble play in juvenile rats
Gordon, N. S., Kollack-Walker, S., Akil, H., & Panksepp, J. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00762-6 · Cited by 103 · see citing works
Budinger, E., Laszcz, A., Lison, H., Scheich, H., & Ohl, F. W. (2007) · Brain Research · doi:10.1016/j.brainres.2007.07.084 · Cited by 102 · see citing works
Galef, B. G., Kennett, D. J., & Stein, M. (1985) · Animal Learning & Behavior · doi:10.3758/bf03213361 · Cited by 100 · see citing works
Li, Z., Lü, Y.-F., Li, C.-L., Wang, Y., Sun, W., He, T., Chen, X.-F., Wang, X., & Chen, J. (2014) · Pain · doi:10.1016/j.pain.2014.03.019 · Cited by 100 · see citing works
Social information processing following resection of the insular cortex
Boucher, O., Rouleau, I., Lassonde, M. C., Leporé, F., Bouthillier, A., & Nguyen, D. K. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.03.008 · Cited by 99 · see citing works
Facial Indicators of Positive Emotions in Rats
Finlayson, K., Lampe, J. F., Hintze, S., Würbel, H., & Melotti, L. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166446 · Cited by 97 · see citing works
Altered functional connectivity networks in acallosal and socially impaired BTBR mice
Sforazzini, F., Bertero, A., Dodero, L., Dávid, G., Galbusera, A., Scattoni, M. L., Pasqualetti, M., & Gozzi, A. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0948-9 · Cited by 95 · see citing works
Social memory engram in the hippocampus
Okuyama, T. (2018) · Neuroscience Research · doi:10.1016/j.neures.2017.05.007 · Cited by 95 · see citing works
The Effects of Social Context and Acute Stress on Decision Making Under Uncertainty
FeldmanHall, O., Raio, C. M., Kubota, J. T., Seiler, M. G., & Phelps, E. A. (2015) · Psychological Science · doi:10.1177/0956797615605807 · Cited by 94 · see citing works
Linke, R. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.8.753 · Cited by 91 · see citing works
Facial expressions of mice in aggressive and fearful contexts
Defensor, E. B., Corley, M. J., Blanchard, R. J., & Blanchard, D. C. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.03.024 · Cited by 90 · see citing works
Aversion or Salience Signaling by Ventral Tegmental Area Glutamate Neurons
Root, D. H., Estrin, D. J., & Morales, M. (2018) · iScience · doi:10.1016/j.isci.2018.03.008 · Cited by 89 · see citing works
Teles, M. C., Almeida, O., Lopes, J. S., & Oliveira, R. F. (2015) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2015.1099 · Cited by 87 · see citing works
Siegel, A., & Tassoni, J. P. (2008) · Brain Behavior and Evolution · doi:10.1159/000125434 · Cited by 86 · see citing works
Multisensory regulation of maternal behavior and masculine sexual behavior: A revised view
Stern, J. M. (1990) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(05)80219-2 · Cited by 86 · see citing works
Individual differences in socioemotional sensitivity are an index of salience network function
Toller, G., Brown, J. A., Sollberger, M. A., Shdo, S. M., Bouvet, L., Sukhanov, P., Seeley, W. W., Miller, B. L., & Rankin, K. P. (2018) · Cortex · doi:10.1016/j.cortex.2018.02.012 · Cited by 86 · see citing works
Reep, R. L., & Winans, S. S. (1982) · Neuroscience · doi:10.1016/0306-4522(82)91133-2 · Cited by 86 · see citing works
Social modeling of conditioned fear in mice by non-fearful conspecifics
Guzmán, Y. F., Tronson, N. C., Guedea, A., Huh, K. H., Gao, C., & Radulovic, J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.02.024 · Cited by 85 · see citing works
Increased neural responses to unfairness in a loss context
Guo, X., Zheng, L., Zhu, L., Li, J., Wang, Q., Dienes, Z. P., & Yang, Z. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.048 · Cited by 85 · see citing works
Disrupted prediction errors index social deficits in autism spectrum disorder
Balsters, J. H., Apps, M. A. J., Bolis, D., Lehner, R., Gallagher, L., & Wenderoth, N. (2017) · Brain · doi:10.1093/brain/aww287 · Cited by 85 · see citing works
Phase-Specific Vocalizations of Male Mice at the Initial Encounter during the Courtship Sequence
Matsumoto, Y. K., & Okanoya, K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147102 · Cited by 83 · see citing works
Androgens modulate song effort and aggression in Neotropical singing mice
Pasch, B. S., George, A. S., Hamlin, H. J., Guillette, L. J., & Phelps, S. M. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.10.011 · Cited by 82 · see citing works
Flagged first, then by citations
Research works printed but not linked: 3
- Amodio DM, & Frith CD (2006b). Meeting of minds: the medial frontal cortex and social cognition. Nat Rev Neurosci, 7(4), 268– 277. doi: 10.1038/nrn1884 16552413 · DOI · Paper page
- Chevalier-Skolnikoff S (1973). Facial expression of emotion in nonhuman primates. Darwin and facial expression: A century of research in review, 11– 89.
- Dölen G, Darvishzadeh A, Huang KW, & Malenka RC (2013b). Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin. Nature, 501(7466), 179– 184. doi: 10.1038/nature12518 24025838 PMC4091761 · DOI · Paper page
Cited by
Sorted by citations
Is oxytocin “nature’s medicine”
Carter, C. S., Kenkel, W. M., MacLean, E. L., Wilson, S. R., Perkeybile, A. M., Yee, J. R., Ferris, C. F., Nazarloo, H. P., Porges, S. W., Davis, J. M., et al. (2020) · Pharmacological Reviews · doi:10.1124/pr.120.019398 · Cited by 394 · see citing works
The Insular Cortex: An Interface Between Sensation, Emotion and Cognition
Zhang, R., Deng, H., & Xiao, X. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01211-4 · Cited by 158 · see citing works
Benarroch, E. E. (2019) · Neurology · doi:10.1212/wnl.0000000000008525 · Cited by 146 · see citing works
Social circuits and their dysfunction in autism spectrum disorder
Sato, M., Nakai, N., Fujima, S., Choe, K. Y., & Takumi, T. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02201-0 · Cited by 142 · see citing works
Livneh, Y., & Andermann, M. L. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.036 · Cited by 106 · see citing works
The Neuropsychology of Anxiety
McNaughton, N., & Gray, J. A. (2024) · doi:10.1093/oso/9780198843313.001.0001 · Cited by 98 · see citing works
Rogers-Carter, M. M., Djerdjaj, A., Gribbons, K. B., Varela, J. A., & Christianson, J. P. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.0316-19.2019 · Cited by 79 · see citing works
Self-citationLoth, M. K., & Donaldson, Z. R. (2020) · Endocrinology · doi:10.1210/endocr/bqaa223 · Cited by 74 · see citing works
The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives
Blumenthal, S. A., & Young, L. J. (2023) · Biology · doi:10.3390/biology12060844 · Cited by 59 · see citing works
Ike, K. G. O., de Boer, S. F., Buwalda, B., & Kas, M. J. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.06.030 · Cited by 61 · see citing works
Keep your interoceptive streams under control: An active inference perspective on anorexia nervosa
Barca, L., & Pezzulo, G. (2020) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-020-00777-6 · Cited by 54 · see citing works
Rieger, N. S., Varela, J. A., Ng, A. J., Granata, L. E., Djerdjaj, A., Brenhouse, H. C., & Christianson, J. P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01292-7 · Cited by 47 · see citing works
Self-citationEncoding of social exploration by neural ensembles in the insular cortex
Miura, I., Sato, M., Kunori, N., Overton, E. T. N., Nakai, J., Kawamata, T., Nakai, N., & Takumi, T. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000584 · Cited by 43 · see citing works
Inoue, K., Ford, C. L., Horie, K., & Young, L. J. (2022) · Journal of Comparative Neurology · doi:10.1002/cne.25382 · Cited by 45 · see citing works
One cranium, two brains not yet introduced: Distinct but complementary views of the social brain
Prounis, G. S., & Ophir, A. G. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.11.011 · Cited by 46 · see citing works
Haskal, S., Netser, S., Magalnik, H., Briller, M., Marzan, D., Glatt, S., Abergel, Y., & Wagner, S. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105859 · Cited by 43 · see citing works
Expanding the concept of social behavior to interspecific interactions
Oliveira, R. F., & Bshary, R. (2021) · Ethology · doi:10.1111/eth.13194 · Cited by 38 · see citing works
Matsumoto, M., Yoshida, M., Jayathilake, B. W., Inutsuka, A., Nishimori, K., Takayanagi, Y., & Onaka, T. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.12980 · Cited by 32 · see citing works
The role of the anterior insula during targeted helping behavior in male rats
Cox, S. S., Kearns, A. M., Woods, S. K., Brown, B. J., Brown, S., & Reichel, C. M. (2022) · Scientific Reports · doi:10.1038/s41598-022-07365-3 · Cited by 30 · see citing works
Kietzman, H. W., & Gourley, S. L. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105075 · Cited by 30 · see citing works
Pathogens, odors, and disgust in rodents
Kavaliers, M., Ossenkopp, K., & Choleris, E. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.09.037 · Cited by 29 · see citing works
A social cognition perspective on misophonia
Berger, J. I., Gander, P. E., & Kumar, S. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0257 · Cited by 28 · see citing works
Limongi, R., Silva, A., Mackinley, M., Ford, S. D., & Palaniyappan, L. K. (2023) · Schizophrenia Bulletin · doi:10.1093/schbul/sbac125 · Cited by 27 · see citing works
Zhai, J., Li, X., Zhou, Y. F., Fan, L., Xia, W., Wang, X., Li, Y., Hou, M., Wang, J., & Wu, L. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1056051 · Cited by 27 · see citing works
What do you hear what do you say? Ultrasonic calls as signals during play fighting in rats
Burke, C. J., Euston, D. R., & Pellis, S. M. (2020) · International Journal of Play · doi:10.1080/21594937.2020.1720126 · Cited by 23 · see citing works
Role of Habenula in Social and Reproductive Behaviors in Fish: Comparison With Mammals
Ogawa, S., & Parhar, I. S. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.818782 · Cited by 24 · see citing works
Suyama, H., Egger, V., & Lukas, M. (2021) · Communications Biology · doi:10.1038/s42003-021-02129-7 · Cited by 21 · see citing works
Insular cortex modulates social avoidance of sick rats
Rieger, N. S., Worley, N. B., Ng, A. J., & Christianson, J. P. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113541 · Cited by 21 · see citing works
Self-citationQu, Y., Zhang, L., Hou, W., Liu, L., Liu, J., Li, L., Guo, X., Yin, L., Huang, C., He, Z., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51652-8 · Cited by 21 · see citing works
Shi, T., Feng, S., Zhou, Z., Li, F., Fu, Y., & Zhou, W. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1094808 · Cited by 21 · see citing works
Giordano, G. M., Pezzella, P., Quarantelli, M., Bucci, P., Prinster, A., Soricelli, A., Perrottelli, A., Giuliani, L., Fabrazzo, M., & Galderisi, S. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm11010061 · Cited by 20 · see citing works
Tomek, S. E., Stegmann, G., Leyrer‐Jackson, J. M., Piña, J., & Olive, M. F. (2020) · Social Neuroscience · doi:10.1080/17470919.2020.1746394 · Cited by 19 · see citing works
Pribut, H. J., Vázquez, D., Brockett, A. T., Wei, A. D., Tennyson, S. S., & Roesch, M. R. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.3025-20.2021 · Cited by 19 · see citing works
Hearing, touching, and multisensory integration during mate choice
Lenschow, C., Mendes, A. R. P., & Lima, S. Q. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.943888 · Cited by 17 · see citing works
Fateh, A. A., Huang, W., Mo, T., Wang, X., Luo, Y., Yang, B., Smahi, A., Fang, D., Zhang, L., Meng, X., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.890596 · Cited by 17 · see citing works
Physiological Needs: Sensations and Predictions in the Insular Cortex
Prilutski, Y., & Livneh, Y. (2022) · Physiology · doi:10.1152/physiol.00019.2022 · Cited by 17 · see citing works
Glangetas, C., Guillaumin, A., Ladevèze, E., Braine, A., Gauthier, M., Bonamy, L., Doudnikoff, É., Dhellemmes, T., Landry, M., Bézard, E., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51389-4 · Cited by 15 · see citing works
Paletta, P., Bass, N., Kavaliers, M., & Choleris, E. (2022) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2021.0058 · Cited by 15 · see citing works
Djerdjaj, A., Ng, A. J., Rieger, N. S., & Christianson, J. P. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114050 · Cited by 14 · see citing works
Self-citationSocial affective behaviors among female rats involve the basolateral amygdala and insular cortex
Djerdjaj, A., Rieger, N. S., Brady, B. H., Carey, B. N., Ng, A. J., & Christianson, J. P. (2023) · PLoS ONE · doi:10.1371/journal.pone.0281794 · Cited by 14 · see citing works
Self-citationGan, R., Qiu, Y.-D., Liao, J., Zhang, Y.-T., Wu, J., Peng, X., Lee, T. M., & Huang, R. (2024) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105918 · Cited by 14 · see citing works
Bourret, M., Ratelle, C., Plamondon, A., & Châteauvert, G. B. (2022) · Journal of Vocational Behavior · doi:10.1016/j.jvb.2022.103837 · Cited by 13 · see citing works
Petersen, C. L., Davis, S. E. D., Patel, B., & Hurley, L. M. (2021) · eNeuro · doi:10.1523/eneuro.0247-20.2021 · Cited by 11 · see citing works
High frequency heart rate variability is associated with sensitivity to affective touch
Pawling, R., McGlone, F., & Walker, S. C. (2024) · Physiology & Behavior · doi:10.1016/j.physbeh.2024.114600 · Cited by 10 · see citing works
Barretto‐de‐Souza, L., Joseph, S. A., Lynch, F. M., Ng, A. J., Crestani, C. C., & Christianson, J. P. (2023) · Psychopharmacology · doi:10.1007/s00213-023-06408-5 · Cited by 10 · see citing works
Self-citationModelling sexual violence in male rats: the sexual aggression test (SxAT)
Oliveira, V. E. D. M., A, T. R. D. J., & Neumann, I. D. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01973-3 · Cited by 10 · see citing works
Cupid’s quiver: Integrating sensory cues in rodent mating systems
Hoglen, N. E. G., & Manoli, D. S. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.944895 · Cited by 8 · see citing works
The parental umwelt: Effects of parenthood on sensory processing in rodents
Wilson, K. M., Arquilla, A. M., & Wendy Saltzman, A. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13237 · Cited by 9 · see citing works
Serotonin modulates social responses to stressed conspecifics via insular 5-HT 2C receptors in rat
Ng, A. J., Vincelette, L. K., Li, J., Brady, B. H., & Christianson, J. P. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109598 · Cited by 9 · see citing works
Self-citationLoss of oxytocin receptors in hilar mossy cells impairs social discrimination
Hung, Y.-C., Wu, Y., Chien, M.-E., Lin, Y., Tsai, C., & Hsu, K. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106311 · Cited by 9 · see citing works
Haskal, S., Netser, S., Magalnik, H., Briller, M., Marzan, D., Glatt, S., Abergel, Y., & Wagner, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.05.078139 · Cited by 9 · see citing works
Lee, H., Oh, S., Ha, E., Joo, Y., Suh, C., Kim, Y., Jeong, H. S., Lyoo, I. K., Yoon, S. J., & Hong, H. (2023) · Psychiatry Research · doi:10.1016/j.psychres.2023.115345 · Cited by 7 · see citing works
Parvalbumin interneurons in the insular cortex control social familiarity and emotion recognition
Fujima, S., Sato, M., Nakai, N., & Takumi, T. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116085 · Cited by 7 · see citing works
Zhang, Z., Peng, Y., Jiang, Y., & Chen, T. (2023) · Behavior Research Methods · doi:10.3758/s13428-023-02168-4 · Cited by 6 · see citing works
Are older adults less generous? Age differences in emotion-related social decision making
Xu, H.-Z., Peng, X.-R., Huan, S.-Y., Xu, J.-J., Yu, J., & Ma, Q. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120756 · Cited by 6 · see citing works
Rieger, N. S., Ng, A. J., Lee, S., Brady, B. H., & Christianson, J. P. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2023.105313 · Cited by 6 · see citing works
Self-citationZonca, V., Marizzoni, M., Saleri, S., Mazzelli, M., Petrillo, G., Benedetto, M. G. D., Cillis, F. D., Riva, M. A., & Cattaneo, A. (2025) · Neurobiology of Stress · doi:10.1016/j.ynstr.2025.100761 · Cited by 5 · see citing works
Pan, N., Gao, R., Ma, K., Qiao, L., Ni, D., Yu, T., & Wang, Y. (2025) · Advanced Science · doi:10.1002/advs.202411790 · Cited by 5 · see citing works
Neural control of sex differences in affiliative and prosocial behaviors
Mikulovic, S., & Lenschow, C. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106039 · Cited by 5 · see citing works
Pathogen and Toxin Disgust in Rodents
Kavaliers, M., Ossenkopp, K., & Choleris, E. (2021) · Springer eBooks · doi:10.1007/978-3-030-84486-8_4 · Cited by 5 · see citing works
Jung, C. J., Kim, J., Choi, S.-Y., Seo, Y. K., Park, K.-S., Choi, Y., Choi, S. M., Kwon, O., Song, Y., Kim, J., et al. (2023) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103380 · Cited by 5 · see citing works
Neurobiology of Pathogen Avoidance and Mate Choice: Current and Future Directions
Cantini, D., Choleris, E., & Kavaliers, M. (2024) · Animals · doi:10.3390/ani14020296 · Cited by 5 · see citing works
Exploring rodent prosociality: A conceptual framework
Charron, V., Talbot, J., & Plamondon, H. (2025) · Translational Neuroscience · doi:10.1515/tnsci-2025-0375 · Cited by 4 · see citing works
Hazani, R., Breton, J., Trachtenberg, E., Kantor, B., Maman, A., Bigelman, E., Cole, S. W., Weller, A., & Bartal, I. B.-A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.06.592793 · Cited by 4 · see citing works
Female rats prefer to forage food from males, an effect that is not influenced by stress
Zhou, S.-F., Li, S.-J., Zhao, T.-S., Liu, Y., Li, F., Cui, Y., & Li, F. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114597 · Cited by 4 · see citing works
Oxytocin and Social Isolation: Nonapeptide Regulation of Social Homeostasis
Kareklas, K., & Oliveira, R. F. (2024) · Masterclass in neuroendocrinology · doi:10.1007/978-3-031-51112-7_8 · Cited by 3 · see citing works
Varied impacts of social relationships on neuroendocrine state
Prior, N. H., Haakenson, C. M., Clough, S., Ball, G. F., & Sandkam, B. A. (2023) · Hormones and Behavior · doi:10.1016/j.yhbeh.2023.105403 · Cited by 3 · see citing works
Modulation of social valence by insular cortex activity during acute social isolation in mice
Hiyoshi, K., Matsushita, D., & Watabe, A. M. (2025) · Molecular Brain · doi:10.1186/s13041-025-01236-4 · Cited by 2 · see citing works
Giant Fusiform Cells of the Brain: Discovery, Identification, and Probable Functions
Medvediev, V. V., Черкасов, В. Г., Marushchenko, M. O., Vaslovych, V. V., & Цымбалюк, В. И. (2024) · Cytology and Genetics · doi:10.3103/s0095452724050098 · Cited by 2 · see citing works
Slamin, M. M., Bishnoi, I. R., Bankowski, I. M., Norris, H. A., & Bordt, E. A. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.101034 · Cited by 2 · see citing works
Sato, M., Overton, E. T. N., Fujima, S., & Takumi, T. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70190 · Cited by 2 · see citing works
Christianson, J. P. (2023) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20230110 · Cited by 2 · see citing works
Self-citationMcNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0012 · Cited by 2 · see citing works
Structural connectivity of the fore- and mid-brain in prairie voles
Gossman, K. R., Andrews, E., Dykstra, B., Ta, K., Ashourvan, A., & Smith, A. S. (2025) · iScience · doi:10.1016/j.isci.2025.112065 · Cited by 1 · see citing works
Vitale, E. M., Tbaba, A. H., Tam, K., Gossman, K. R., & Smith, A. S. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15363 · Cited by 1 · see citing works
Epigenetic manipulation of anterior insular cortex alters neural signals and cognitive control
Perry, S., Sharalla, P., Sarubin, D. R., Li, X., Roesch, M. R., & Brockett, A. T. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02181-5 · Cited by 1 · see citing works
Insular Input to the Prelimbic Cortex Underlies Social Affective Behavior in Rats
Chun, E. K., Djerdjaj, A., Matulis, T., Ng, A. J., Rogers-Carter, M. M., & Christianson, J. P. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.1747-25.2026 · Cited by 1 · see citing works
Self-citationLi, S., Yang, J., Cai, M., Zhao, Z., Zhao, X., Li, H., Ning, S., Yang, G., Shen, W., Wang, H., et al. (2026) · Neuron · doi:10.1016/j.neuron.2026.02.015 · Cited by 1 · see citing works
Aholt, M. L., Jacobs, J. T., Adjei, M. P., Mojahed, N., Qasem, E., Athul, S. W., Ellsworth, B. S., & Nordman, J. C. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02432-z · Cited by 1 · see citing works
Fundamentals of the septo-hippocampal system
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0009 · Cited by 1 · see citing works
Memory and the septo-hippocampal system
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0008 · Cited by 1 · see citing works
Encoding social preference by interhemispheric neurons in the InsulaPreprint
Glangetas, C., Ladevèze, E., Guillaumin, A., Gauthier, M., Doudnikoff, É., Bézard, E., Taupignon, A., Baufreton, J., & Georges, F. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.15.520538 · Cited by 1 · see citing works
A cortical basis for perception of internal gut sensationsPreprint
Rafael-Izhaki, O., Shtiglitz, S., Miller, J., Prilutski, Y., Talpir, I., Lavi, A., & Livneh, Y. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.11.705298 · Cited by 1 · see citing works
Human primary auditory cortex and insula encode perceptual decisions, not stimulus featuresPreprint
Lauriers, C. D., Pruvost‐Robieux, E., Zanello, M., Filipescu, C., Moiraghi, A., Landré, E., Pallud, J., Defrance, G., Sharshar, T., Aucouturier, J., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.03.736338 · Cited by 1 · see citing works
Gädeke, M., Willems, T., Ahmed, O. S., Weber, B., Hurlemann, R., & Schultz, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.25.107300
The endocannabinoid system: Signaling and social motivation
Cysneiros, R. M., & Ribeiro, F. T. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-90877-1.00012-7
Dynamic population coding of social novelty in the insular cortexPreprint
Sato, M., Overton, E. T. N., Fujima, S., & Takumi, T. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.01.587524
What do hippocampal cell fields represent?
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0007
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0001
The neurology of anxiety—planning circuits
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0011
A theory of the septo-hippocampal system (SHS)
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0010
Symptoms and syndromes of anxiety
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0013
The neurology of anxiety—survival circuits
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0006
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0002
The treatment of anxiety and fear disorders
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0014
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0011
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0015
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0009
The anxiolytic drugs—our key tool
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0004
McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0003
- Authors
- Rogers-Carter, M. M., & Christianson, J. P.
- Affiliations
- Boston College (US)
- Corresponding author
- Rogers-Carter, Morgan M.
- Venue
- Neuroscience & Biobehavioral Reviews
- Publisher
- Elsevier BV
- Published
- 2019-08
- Volume
- 103
- Pages
- 119-132
- ISSN
- 0149-7634 (ISSN-L)
- PMC
- PMC6699879
- OpenAlex
- W2952020761
- Cited by
- 121
- References
- 315
- Citations by year
- 2026: 13 · 2025: 14 · 2024: 38 · 2023: 18 · 2022: 15 · 2021: 10 · 2020: 10 · 2019: 3
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuroscience & Biobehavioral Reviews (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation
- National Institute of Mental Health (MH110907, MH109545)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Social Sciences › Psychology › Social Psychology › Primate Behavior and Ecology
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Keywords
- social decision-making, insula, chemosignals, vocalizations, social behavior, sensory integration, neuronal connectivity, animal social behavior
- MeSH terms
- Animals, Behavior, Animal, Cerebral Cortex, Decision Making, Emotions, Humans, Nerve Net, Social Behavior, Social Perception
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
