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Oxytocin enhances brain function in children with autism
Open accessAbstract
Significance: This article presents our discovery that intranasal administration of oxytocin enhances activity in the brain for socially meaningful stimuli and attenuates its response to nonsocially meaningful stimuli in children with autism spectrum disorder (ASD) as measured via functional MRI. We also identified a relationship between changes in salivary oxytocin following administration and enhancements in brain function. These discoveries are particularly important given the urgent need for treatments that target the core social dysfunction in ASD. The functional neural attunement we demonstrated might facilitate social learning, thus potentially bringing about long-term change in neural systems and subsequent behavioral improvements. Our results illustrate the power of a translational neuroscience approach to facilitate the development of pharmacological interventions for neurodevelopmental disorders like ASD.
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“These results have been supported by functional neuroimaging studies involving persons with autism spectrum disorder, which have shown differences in regional brain activation in response to social stimuli after the administration of intranasal oxytocin, as compared with placebo.11,15–17”
From Intranasal Oxytocin in Children and Adolescents with Autism Spectrum Disorder (2021) · cites this paper as [15]
In the citing paper
“The current finding is consistent with a prior neuroimaging study demonstrating that oxytocin administration enhances STS activity in individuals with autism (37), and with a recent finding that OXTR methylation is associated with STS activity (6).”
From Epigenetic modification of OXT and human sociability (2016) · cites this paper as [37]
In the citing paper
“Oxytocin-enhanced therapy would have the combined benefits of increasing the salience of information coming from the therapist [63,64], promoting synaptic plasticity [65], and facilitating learning by modulating circuit-level neural activity [37*,66].”
From Translational opportunities for circuit-based social neuroscience: advancing 21st century psychiatry (2021) · cites this paper as [63]
In the citing paper
“At the neural networks level, it has been shown that intranasal OXT leads to increased activation in the brain regions known to be involved in perceiving and thinking about social-emotional information and enhances effective connectivity between nodes of the brain’s reward and socioemotional processing systems [87, 88].”
From An Update on Psychopharmacological Treatment of Autism Spectrum Disorder (2022) · cites this paper as [88]
In the citing paper
“our own neuroimaging work demonstrating OT-enhanced neural attunement to visual social cues37”
From Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism (2016) · cites this paper as [37]
In the citing paper
“these results show that in ASD, OT may not only serve to enhance neural activity to “preferred” stimuli, but also improve communication among brain regions involved in social motivation and perception.”
From Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism (2016) · cites this paper as [37]
In the citing paper
“the current results illustrate a discrete aspect of OT’s effect captured by measures of connectivity”
From Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism (2016) · cites this paper as [37]
In the citing paper
“While we have recently reported on OT’s ability to enhance the function of several key nodes of the social brain in ASD37”
From Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism (2016) · cites this paper as [37]
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Citations
Cites
Lord, C., Rutter, M., & Le Couteur, A. (1994) · Journal of Autism and Developmental Disorders · doi:10.1007/bf02172145 · Cited by 9,065
(1943) · The Nervous child · Cited by 8,870
Baron‐Cohen, S., Wheelwright, S., Hill, J., Raste, Y., & Plumb, I. (2001) · Journal of Child Psychology and Psychiatry · doi:10.1111/1469-7610.00715 · Cited by 4,555 · cited 5×
“This is consistent with the empirical record, which shows improvements only on some items from the RMET, according to difficulty level, but not overall (11, 22).”
MethodInfluentialBaron‐Cohen, S., Wheelwright, S. J., Hill, J., Raste, Y., & Plumb, I. (2001) · PubMed · Cited by 4,313
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 · cited 1×
“These neural systems-level findings indicate that OT enhances activity in key nodes of the neural circuits that have been previously implicated in reward (dorsal and ventral striatum, including the NAcc) (29, 30); social attention, perception, and cognition (premotor cortex, posterior cingulate, inferior parietal lobu…”
BackgroundThe reward circuit: linking primate anatomy and human imaging
Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718
Forman, S. D., Cohen, J. D., Fitzgerald, M., Eddy, W. F., Mintun, M. A., & Noll, D. C. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910330508 · Cited by 3,202
The oxytocin receptor system: structure, function, and regulation
Gimpl, G., & Fahrenholz, F. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.629 · Cited by 3,089
Autistic disturbances of affective contact.
Kanner, L. (1968) · PubMed · Cited by 2,282
Lord, C., Rutter, M., Goode, S., Heemsbergen, J., Jordan, H., Mawhood, L., & Schopler, E. (1989) · Journal of Autism and Developmental Disorders · doi:10.1007/bf02211841 · Cited by 2,030
Cited by
Sorted by citations
Robertson, C. E., & Baron-Cohen, S. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.112 · Cited by 1,157
An aberrant precision account of autism
Lawson, R. P., Rees, G., & Friston, K. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00302 · Cited by 641
The serotonin system in autism spectrum disorder: From biomarker to animal models
Muller, C. L., Anacker, A. M. J., & Veenstra-VanderWeele, J. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.010 · Cited by 531
Father’s brain is sensitive to childcare experiences
Abraham, E., Hendler, T., Shapira-Lichter, I., Kanat-Maymon, Y., Zagoory-Sharon, O., & Feldman, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402569111 · Cited by 343
Self-citationIntranasal Oxytocin in Children and Adolescents with Autism Spectrum Disorder
Sikich, L., Kolevzon, A., King, B. H., McDougle, C. J., Sanders, K. B., Kim, S.-J., Spanos, M., Chandrasekhar, T., Trelles, M. D. P., Rockhill, C. M., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2103583 · Cited by 298
Nakajima, M., Görlich, A., & Heintz, N. (2014) · Cell · doi:10.1016/j.cell.2014.09.020 · Cited by 262
In and out of synchrony—Behavioral and physiological dynamics of dyadic interpersonal coordination
Mayo, O., & Gordon, I. (2020) · Psychophysiology · doi:10.1111/psyp.13574 · Cited by 264
Self-citationGuastella, A. J., & Hickie, I. B. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.06.028 · Cited by 223
Mu, Y., Kitayama, S., Han, S., & Gelfand, M. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1509839112 · Cited by 254
Clinical and neural effects of six-week administration of oxytocin on core symptoms of autism
Watanabe, T., Kuroda, M., Kuwabara, H., Aoki, Y., Iwashiro, N., Tatsunobu, N., Takao, H., Nippashi, Y., Kawakubo, Y., Kunimatsu, A., et al. (2015) · Brain · doi:10.1093/brain/awv249 · Cited by 222
Parker, K. J., Garner, J. P., Libove, R. A., Hyde, S. A., Hornbeak, K. B., Carson, D. S., Liao, C.-P., Phillips, J. M., Hallmayer, J. F., & Hardan, A. Y. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402236111 · Cited by 215
An Update on Psychopharmacological Treatment of Autism Spectrum Disorder
Aishworiya, R., Valica, T., Hagerman, R., & Restrepo, B. (2022) · Neurotherapeutics · doi:10.1007/s13311-022-01183-1 · Cited by 233
Baribeau, D. A., & Anagnostou, E. A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00335 · Cited by 241
An update on pharmacotherapy for autism spectrum disorder in children and adolescents
Ji, N. Y., & Findling, R. L. (2015) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000132 · Cited by 217
Genetic origins of social networks in rhesus macaques
Brent, L. J. N., Heilbronner, S. R., Horvath, J. E., Gonzalez-Martinez, J., Ruiz-Lambides, A., Robinson, A. G., Skene, J. H. P., & Platt, M. L. (2013) · Scientific Reports · doi:10.1038/srep01042 · Cited by 220
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
Bolis, D., Balsters, J., Wenderoth, N., Becchio, C., & Schilbach, L. (2017) · Psychopathology · doi:10.1159/000484353 · Cited by 204
Young, L. J., & Barrett, C. E. (2015) · Science · doi:10.1126/science.aaa8120 · Cited by 200
Yamasue, H., Okada, T., Munesue, T., Kuroda, M., Fujioka, T., Uno, Y., Matsumoto, K., Kuwabara, H., Mori, D., Okamoto, Y., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-018-0097-2 · Cited by 185
Martino, J., Pegg, J., & Frates, E. P. (2017) · American Journal of Lifestyle Medicine · doi:10.1177/1559827615608788 · Cited by 192
Oxytocin improves behavioural and neural deficits in inferring others’ social emotions in autism
Aoki, Y., Yahata, N., Watanabe, T., Takano, Y., Kawakubo, Y., Kuwabara, H., Iwashiro, N., Natsubori, T., Inoue, H., Suga, M., et al. (2014) · Brain · doi:10.1093/brain/awu231 · Cited by 187
Oxytocin, testosterone, and human social cognition
Crespi, B. J. (2015) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12175 · Cited by 183
Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics
Kazdoba, T. M., Leach, P. T., Yang, M., Silverman, J. L., Solomon, M., & Crawley, J. N. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_5003 · Cited by 185
Feng, C., Hackett, P. D., DeMarco, A. C., Chen, X., Stair, S., Haroon, E., Ditzen, B., Pagnoni, G., & Rilling, J. K. (2015) · Brain Imaging and Behavior · doi:10.1007/s11682-014-9333-9 · Cited by 157
Neural mechanisms of social decision-making in the primate amygdala
Chang, S. W. C., Fagan, N. A., Toda, K., Utevsky, A. V., Pearson, J. M., & Platt, M. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1514761112 · Cited by 157
Intranasal oxytocin, social cognition and neurodevelopmental disorders: A meta-analysis
Keech, B., Crowe, S., & Hocking, D. R. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.09.022 · Cited by 145
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
Pharmacological therapies for autism spectrum disorder: a review.
(2015) · PubMed Central · Cited by 150
Quintana, D. S., Alvares, G. A., Hickie, I. B., & Guastella, A. J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.011 · Cited by 149
Ma, Y., Shamay-Tsoory, S., Han, S., & Zink, C. F. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.10.009 · Cited by 131
Cortical variability in the sensory-evoked response in autism
Haigh, S. M., Heeger, D. J., Dinstein, I., Minshew, N., & Behrmann, M. (2015) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-014-2276-6 · Cited by 113
Grace, S. A., Rossell, S. L., Heinrichs, M., Kordsachia, C., & Labuschagne, I. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.05.031 · Cited by 120
Gordon, I., Jack, A., Pretzsch, C. M., Vander Wyk, B., Leckman, J. F., Feldman, R., & Pelphrey, K. A. (2016) · Scientific Reports · doi:10.1038/srep35054 · Cited by 114
Self-citationThe Eyes as Windows Into Other Minds
Großmann, T. (2017) · Perspectives on Psychological Science · doi:10.1177/1745691616654457 · Cited by 127
Hormonal Physiology of Childbearing: Evidence and Implications for Women, Babies, and Maternity Care
Buckley, S. J. (2015) · Issue Lab (Candid) · Cited by 113
Oxytocin and Autism Spectrum Disorders
Yamasue, H., & Domes, G. (2017) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2017_24 · Cited by 109
Bernaerts, S., Boets, B., Bosmans, G., Steyaert, J., & Alaerts, K. (2020) · Molecular Autism · doi:10.1186/s13229-020-0313-1 · Cited by 102
Zürcher, N. R., Bhanot, A., McDougle, C. J., & Hooker, J. M. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.02.002 · Cited by 105
Insular function in autism: Update and future directions in neuroimaging and interventions
Nomi, J. S., Molnar-Szakacs, I., & Uddin, L. Q. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.10.015 · Cited by 98
Aoki, Y., Watanabe, T., Abe, O., Kuwabara, H., Yahata, N., Takano, Y., Iwashiro, N., Natsubori, T., Takao, H., Kawakubo, Y., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2014.74 · Cited by 95
Structural, Functional, and Molecular Imaging of Autism Spectrum Disorder
Li, X., Zhang, K., He, X., Zhou, J., Jin, C., Shen, L., Gao, Y., Tian, M., & Zhang, H. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00673-0 · Cited by 94
Wang, D., Yan, X., Li, M., & Ma, Y. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx085 · Cited by 86
Epigenetic modification of OXT and human sociability
Haas, B. W., Filkowski, M. M., Cochran, R. N., Denison, L., Ishak, A., Nishitani, S., & Smith, A. K. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602809113 · Cited by 91
Alvares, G. A., Quintana, D. S., & Whitehouse, A. J. O. (2017) · Autism Research · doi:10.1002/aur.1692 · Cited by 91
Neural bases of atypical emotional face processing in autism: A meta-analysis of fMRI studies
Aoki, Y. Y., Cortese, S., & Tansella, M. (2014) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2014.957719 · Cited by 103
Abraham, E., Hendler, T., Zagoory‐Sharon, O., & Feldman, R. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw090 · Cited by 91
Self-citationLe, J., Zhang, L., Zhao, W., Zhu, S., Lan, C., Kou, J., Zhang, Q., Zhang, Y., Li, Q., Chen, Z., et al. (2022) · Psychotherapy and Psychosomatics · doi:10.1159/000524543 · Cited by 86
The many faces of oxytocin: Implications for psychiatry
Zik, J. B., & Roberts, D. L. (2014) · Psychiatry Research · doi:10.1016/j.psychres.2014.11.048 · Cited by 91
Parent–child interaction and oxytocin production in pre-schoolers with autism spectrum disorder
Feldman, R., Golan, O., Hirschler‐Guttenberg, Y., Ostfeld‐Etzion, S., & Zagoory‐Sharon, O. (2014) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.113.137513 · Cited by 86
Self-citationWhy Autism Must be Taken Apart
Waterhouse, L. H., & Gillberg, C. (2014) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-013-2030-5 · Cited by 92
Oxytocin increases empathy to pain when adopting the other-but not the self-perspective
Abu-Akel, A., Palgi, S., Klein, E., Decety, J., & Shamay-Tsoory, S. (2015) · Social Neuroscience · doi:10.1080/17470919.2014.948637 · Cited by 83
Sex differences in cortical volume and gyrification in autism
Schaer, M., Kochalka, J., Padmanabhan, A., Supekar, K., & Menon, V. (2015) · Molecular Autism · doi:10.1186/s13229-015-0035-y · Cited by 90
Brain responses to biological motion predict treatment outcome in young children with autism
Yang, D. Y. ‐., Pelphrey, K. A., Sukhodolsky, D. G., Crowley, M. J., Dayan, E., Dvornek, N. C., Venkataraman, A., Duncan, J. S., Staib, L. H., & Ventola, P. E. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.213 · Cited by 81
Self-citationModi, M. E., Inoue, K., Barrett, C. E., Kittelberger, K. A., Smith, D. G., Landgraf, R., & Young, L. J. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.35 · Cited by 82
Inhaled oxytocin increases positive social behaviors in newborn macaques
Simpson, E. A., Sclafani, V., Paukner, A., Hamel, A. F., Novak, M. A., Meyer, J. S., Suomi, S. J., & Ferrari, P. F. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402471111 · Cited by 82
Vitamin A and vitamin D deficiencies exacerbate symptoms in children with autism spectrum disorders
Guo, M., Zhu, J., Yang, T., Lai, X., Lei, Y., Chen, J., & Li, T. (2018) · Nutritional Neuroscience · doi:10.1080/1028415x.2017.1423268 · Cited by 84
Li, Q., Becker, B., Wernicke, J., Chen, Y., Zhang, Y., Li, R., Le, J., Kou, J., Zhao, W., & Kendrick, K. M. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.11.016 · Cited by 88
Oxytocin during Development: Possible Organizational Effects on Behavior
Miller, T. V., & Caldwell, H. K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00076 · Cited by 79
Oxytocin attenuates neural reactivity to masked threat cues from the eyes
Kanat, M., Heinrichs, M., Schwarzwald, R., & Domes, G. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.183 · Cited by 77
Oxytocin-augmented labor and risk for autism in males
Weisman, O., Agerbo, E., Carter, C. S., Harris, J. C., Uldbjerg, N., Henriksen, T. B., Thygesen, M., Mortensen, P. B., Leckman, J. F., & Dalsgaard, S. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.02.028 · Cited by 78
Self-citationKruppa, J. A., Gossen, A., Oberwelland Weiß, E., Kohls, G., Großheinrich, N., Cholemkery, H., Freitag, C. M., Karges, W., Wölfle, E., Sinzig, J., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-018-0258-7 · Cited by 69
Tsuji, S., Yuhi, T., Furuhara, K., Ohta, S., Shimizu, Y., & Higashida, H. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00058 · Cited by 75
Peled‐Avron, L., Abu-Akel, A. M., & Shamay‐Tsoory, S. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.023 · Cited by 79
Restoring effects of oxytocin on the attentional preference for faces in autism
Kanat, M., Spenthof, I., Riedel, A., van Elst, L. T., Heinrichs, M., & Domes, G. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.67 · Cited by 70
Oxytocin and vasopressin: signalling, behavioural modulation and potential therapeutic effects
Rae, M., Lemos Duarte, M., Gomes, I., Camarini, R., & Devi, L. A. (2022) · British Journal of Pharmacology · doi:10.1111/bph.15481 · Cited by 72
Havránek, T., Zatkova, M., Lestanova, Z., Bačová, Z., Mravec, B., Hodosy, J., Štrbák, V., & Bakoš, J. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23559 · Cited by 71
Singletary, W. M. (2015) · Neuropsychoanalysis · doi:10.1080/15294145.2015.1092334 · Cited by 73
DeMayo, M. M., Song, Y. J. C., Hickie, I. B., & Guastella, A. J. (2017) · Pediatric Drugs · doi:10.1007/s40272-017-0248-y · Cited by 71
Oxytocin and Vasopressin Receptor Gene Polymorphisms: Role in Social and Psychiatric Traits
Aspé-Sánchez, M., Moreno, M., Rivera, M. I., Rossi, A., & Ewer, J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00510 · Cited by 71
The Role of Vitamins in Autism Spectrum Disorder: What Do We Know?
Bjørklund, G., Waly, M. I., Al-Farsi, Y. M., Saad, K., Dadar, M., Rahman, M. M., Elhoufey, A. A., Chirumbolo, S., Jóźwik-Pruska, J., & Kałużna‐Czaplińska, J. (2019) · Journal of Molecular Neuroscience · doi:10.1007/s12031-018-1237-5 · Cited by 72
Oxytocin modulates fMRI responses to facial expression in macaques
Liu, N., Hadj-Bouziane, F., Jones, K. B., Turchi, J. N., Averbeck, B. B., & Ungerleider, L. G. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508097112 · Cited by 65
Adaptive coding of the value of social cues with oxytocin, an fMRI study in autism spectrum disorder
Andari, E., Richard, N., Leboyer, M., & Sirigu, A. (2016) · Cortex · doi:10.1016/j.cortex.2015.12.010 · Cited by 62
Krol, K. M., Monakhov, M. V., Lai, P. S., Ebstein, R. P., & Großmann, T. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506352112 · Cited by 65
Variable sensory perception in autism
Haigh, S. M. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13601 · Cited by 61
GABA and glycine in the developing brain
Ito, S. (2016) · The Journal of Physiological Sciences · doi:10.1007/s12576-016-0442-7 · Cited by 68
Regulation of neuronal chloride homeostasis by neuromodulators
Mahadevan, V., & Woodin, M. A. (2016) · The Journal of Physiology · doi:10.1113/jp271593 · Cited by 61
Fujisawa, T. X., Tanaka, S., Saito, D. N., Kosaka, H., & Tomoda, A. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00295 · Cited by 59
Yang, D. Y. ‐., Sukhodolsky, D. G., Lei, J., Dayan, E., Pelphrey, K. A., & Ventola, P. E. (2017) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-017-9183-z · Cited by 64
Self-citationGreene, R. K., Spanos, M., Alderman, C., Walsh, E., Bizzell, J., Mosner, M. G., Kinard, J. L., Stuber, G. D., Chandrasekhar, T., Politte, L. C., et al. (2018) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-018-9228-y · Cited by 55
Yamasue, H. (2016) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12364 · Cited by 58
New Opportunities in Vasopressin and Oxytocin Research: A Perspective from the Amygdala
Stoop, R., Hegoburu, C., & van den Burg, E. H. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033904 · Cited by 61
Opposing Oxytocin Effects on Intergroup Cooperative Behavior in Intuitive and Reflective Minds
Ma, Y., Liu, Y., Rand, D. G., Heatherton, T. F., & Han, S. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.87 · Cited by 55
Frantz, M., Pellissier, L. P., Pflimlin, E., Loison, S., Gandía, J., MARSOL, C., Durroux, T., Mouillac, B., Becker, J. A. J., Merrer, J. L., et al. (2018) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.8b00697 · Cited by 58
Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity
Hernandez, L. M., Lawrence, K. E., Padgaonkar, N. T., Inada, M., Hoekstra, J. N., Lowe, J. K., Eilbott, J., Jack, A., Aylward, E., Gaab, N., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0750-9 · Cited by 54
Self-citationOxytocin receptor gene variations predict neural and behavioral response to oxytocin in autism
Watanabe, T., Otowa, T., Abe, O., Kuwabara, H., Aoki, Y., Natsubori, T., Takao, H., Kakiuchi, C., Kondo, K., Ikeda, M., et al. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw150 · Cited by 54
Anterior insular cortex regulation in autism spectrum disorders
Carìa, A., & de Falco, S. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00038 · Cited by 60
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Peñagarikano, O. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22449 · Cited by 56
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Metadata
- Authors
- Gordon, I., Vander Wyk, B. C., Bennett, R. H., Cordeaux, C., Lucas, M. V., Eilbott, J. A., Zagoory-Sharon, O., Leckman, J. F., Feldman, R., & Pelphrey, K. A.
- Affiliations
- Yale University (US)
- Center for Translational Developmental Neuroscience, Yale Child Study Center, Yale University, New Haven, CT 06520;
- The Gonda Multidisciplinary Brain Research Center, Bar-Ilan University, Ramat Gan 52900, Israel; and
- Bar-Ilan University (IL)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2013-12-02
- Volume
- 110
- Issue
- 52
- Pages
- 20953-20958
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3876263
- OpenAlex
- W2007655600
- Cited by
- 336
- References
- 74
- Citations by year
- 2026: 14 · 2025: 13 · 2024: 13 · 2023: 26 · 2022: 24 · 2021: 32 · 2020: 20 · 2019: 16 · 2018: 20 · 2017: 34 · 2016: 34 · 2015: 47 · 2014: 39 · 2013: 4
- FWCI
- 62.36
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Yale University
- Lee Foundation
- National Institute of Mental Health (R01MH084080, K01MH071284, L40 MH071890)
- National Institute of Neurological Disorders and Stroke (R56NS035193, R01NS035193)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Social Sciences › Psychology › Social Psychology › Action Observation and Synchronization
- Keywords
- oxytocin, autism spectrum disorder, high-functioning autism, social cognition, social judgment, intranasal administration, brain activity, striatum, nucleus accumbens, amygdala, orbitofrontal cortex, superior temporal sulcus, salience, social attunement, children
- MeSH terms
- Administration, Intranasal, Adolescent, Amygdala, Child, Child Development Disorders, Pervasive, Female, Frontal Lobe, Humans, Judgment, Magnetic Resonance Imaging, Male, Oxytocin, Saliva, Social Adjustment
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