A spatiotemporal profile of in vivo cerebral blood flow changes following intranasal oxytocin in humans
Open accessAbstract
BACKGROUND: Animal and human studies highlight the role of oxytocin in social cognition and behavior and the potential of intranasal oxytocin (IN-OT) to treat social impairment in individuals with neuropsychiatric disorders such as autism. However, extensive efforts to evaluate the central actions and therapeutic efficacy of IN-OT may be marred by the absence of data regarding its temporal dynamics and sites of action in the living human brain. METHODS: In a placebo-controlled study, we used arterial spin labeling to measure IN-OT-induced changes in resting regional cerebral blood flow (rCBF) in 32 healthy men. Volunteers were blinded regarding the nature of the compound they received. The rCBF data were acquired 15 min before and up to 78 min after onset of treatment onset (40 IU of IN-OT or placebo). The data were analyzed using mass univariate and multivariate pattern recognition techniques. RESULTS: We obtained robust evidence delineating an oxytocinergic network comprising regions expected to express oxytocin receptors, based on histologic evidence, and including core regions of the brain circuitry underpinning social cognition and emotion processing. Pattern recognition on rCBF maps indicated that IN-OT-induced changes were sustained over the entire posttreatment observation interval (25-78 min) and consistent with a pharmacodynamic profile showing a peak response at 39-51 min. CONCLUSIONS: Our study provides the first visualization and quantification of IN-OT-induced changes in rCBF in the living human brain unaffected by cognitive, affective, or social manipulations. Our findings can inform theoretical and mechanistic models regarding IN-OT effects on typical and atypical social behavior and guide future experiments (e.g., regarding the timing of experimental manipulations).
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?
It is doubtful how far intranasal oxytocin crosses the blood-brain barrier.
“doubt has been cast on the extent to which intranasal OXT crosses the blood-brain barrier (Neumann et al., 2013;Paloyelis et al., 2014;Striepens et al., 2013).”
From Oxytocin increases attention to the eyes and selectively enhances self-reported affective empathy for fear (2017) · cites this paper as Paloyelis et al., 2014
There are uncertainties regarding the site and mechanism of action of exogenous intranasal oxytocin in humans due to lack of suitable radio tracers.
“Furthermore, there are uncertainties regarding the site and mechanism of action of exogenous intranasal oxytocin in humans due to lack of suitable radio tracers (Paloyelis et al., 2016).”
From Meta-analysis of the effects of intranasal oxytocin on interpretation and expression of emotions (2017) · cites this paper as Paloyelis et al., 2016
Intranasal oxytocin modulates neural responses in brain regions involved in threat detection and reward processing.
“intranasal administration of oxytocin has been shown to modulate neural responses in brain regions involved in threat detection and reward processing (Ma et al., 2016b; Paloyelis et al., 2016; Wang et al., 2017; Liu et al., 2019).”
From Oxytocin promotes coordinated out-group attack during intergroup conflict in humans (2019) · cites this paper as Paloyelis et al., 2016
An arterial spin labeling study showed that intranasal oxytocin increases cerebral blood flow in key regions of the social brain network, including ventral striatum, amygdala, hippocampus, caudate nucleus, anterior and middle cingulate cortices, anterior insula, ventral tegmental area, inferior frontal gyrus, inferior parietal cortex, and superior temporal gyrus.
“A recent elegant study using arterial spin labeling showed that IN-OT increases the levels of cerebral blood flow of key regions of the SBN such as ventral striatum, amygdala, hippocampus, caudate nucleus, anterior and middle cingulate cortices, anterior insula, ventral tegmental area (VTA), inferior frontal gyrus, inferior parietal cortex, and superior temporal gyrus (Paloyelis et al. 2016).”
From A precision medicine approach to oxytocin trials (2017) · cites this paper as Paloyelis et al. 2016
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
A Simple Sequentially Rejective Multiple Test Procedure
(1979) · Scandinavian Journal of Statistics · doi:10.2307/4615733 · Cited by 21,526 · see citing works
Gaussian Processes for Machine Learning
Rasmussen, C. E., & Williams, C. K. I. (2005) · doi:10.7551/mitpress/3206.001.0001 · Cited by 11,705 · see citing works
Comparison of Beck Depression Inventories -IA and -II in psychiatric outpatients
Beck, A. T., Steer, R. A., Ball, R., & Ranieri, W. F. (1996) · Journal of Personality Assessment · doi:10.1207/s15327752jpa6703_13 · Cited by 5,965 · 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
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 · see citing works
Glial and neuronal control of brain blood flow
Attwell, D., Buchan, A. M., Charpak, S., Lauritzen, M., MacVicar, B. A., & Newman, E. A. (2010) · Nature · doi:10.1038/nature09613 · Cited by 2,511 · see citing works
A Note on Robust Variance Estimation for Cluster‐Correlated Data
Williams, R. L. (2000) · Biometrics · doi:10.1111/j.0006-341x.2000.00645.x · Cited by 2,501 · see citing works
Beyond mind-reading: multi-voxel pattern analysis of fMRI data
Norman, K. A., Polyn, S. M., Detre, G. J., & Haxby, J. V. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.07.005 · Cited by 2,271 · see citing works
Analysing controlled trials with baseline and follow up measurements
Vickers, A. J., & Altman, D. G. (2001) · BMJ · doi:10.1136/bmj.323.7321.1123 · Cited by 2,116 · see citing works
Neural mechanisms of empathy in humans: a relay from neural systems for imitation to limbic areas
Carr, L., Iacoboni, M., Dubeau, M.-C., Mazziotta, J. C., & Lenzi, G. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0935845100 · Cited by 1,978 · see citing works
A wilcoxon‐type test for trend
Cuzick, J. M. (1985) · Statistics in Medicine · doi:10.1002/sim.4780040112 · Cited by 1,920 · see citing works
The Social Brain: Neural Basis of Social Knowledge
Adolphs, R. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.60.110707.163514 · Cited by 1,827 · see citing works
Pessoa, L., & Adolphs, R. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2920 · Cited by 1,794 · see citing works
Social cognition and the brain: A meta-analysis
Van Overwalle, F. (2009) · Human Brain Mapping · doi:10.1002/hbm.20547 · Cited by 1,792 · see citing works
Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine
Meyer-Lindenberg, A., Domes, G., Kirsch, P., & Heinrichs, M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3044 · Cited by 1,688 · see citing works
Conscious and unconscious emotional learning in the human amygdala
Morris, J. S., Öhman, A., & Dolan, R. J. (1998) · Nature · doi:10.1038/30976 · Cited by 1,665 · see citing works
Oxytocin, 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
Imitation, empathy, and mirror neurons
Iacoboni, M. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.60.110707.163604 · Cited by 1,606 · see citing works
Detre, J. A., LEIGH, J. S. J., Williams, D. S., & Koretsky, A. P. (1992) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910230106 · Cited by 1,606 · see citing works
Social effects of oxytocin in humans: context and person matter
Bartz, J. A., Zaki, J., Bolger, N., & Ochsner, K. N. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.05.002 · Cited by 1,572 · cited 1× · see citing works
“The power of arterial spin labeling to quantify the effects of IN-OT on brain physiology renders it a promising, noninvasive, in vivo method to investigate the impact of genetic (9,143), epigenetic (126), social-environmental (40), and contextual (144) factors on the baseline function of the OT system.”
Magnetic resonance imaging of perfusion using spin inversion of arterial water.
Williams, D. S., Detre, J. A., Leigh, J. S., & Koretsky, A. P. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.1.212 · Cited by 1,553 · see citing works
Shamay-Tsoory, S. G., Aharon-Peretz, J., & Perry, D. (2009) · Brain · doi:10.1093/brain/awn279 · Cited by 1,544 · 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
Jeurgen, K., Assheuer, J., & Paxinos, G. (1997) · Medical Entomology and Zoology · Cited by 1,403 · see citing works
Sniffing neuropeptides: A transnasal approach to the human brain
Born, J., Lange, T., Kern, W., McGregor, G. P., Bickel, U., & Fehm, H. L. (2002) · Nature Neuroscience · doi:10.1038/nn0602-849 · Cited by 1,356 · see citing works
Oxytocin improves “mind-reading” in humans
Domes, G., Heinrichs, M., Michel, A., Berger, C., & Herpertz, S. C. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.07.015 · Cited by 1,298 · see citing works
Positron Emission Tomographic Studies of the Processing of Singe Words
Petersen, S. E., Fox, P. T., Posner, M. I., Mintun, M. A., & Raichle, M. E. (1989) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1989.1.2.153 · Cited by 1,284 · see citing works
Oxytocin shapes the neural circuitry of trust and trust adaptation in humans
Baumgartner, T., Heinrichs, M., Vonlanthen, A., Fischbacher, U., & Fehr, E. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.009 · Cited by 1,258 · see citing works
The cerebellum and cognitive function: 25 years of insight from anatomy and neuroimaging
Buckner, R. L. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.044 · Cited by 1,173 · see citing works
The neurobiology of attachment
Insel, T. R., & Young, L. J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35053579 · Cited by 1,173 · see citing works
The human amygdala in social judgment
Adolphs, R., Tranel, D., & Damasio, A. R. (1998) · Nature · doi:10.1038/30982 · Cited by 1,125 · see citing works
Landgraf, R., & Neumann, I. D. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.05.001 · 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
Oxytocin in the Medial Amygdala is Essential for Social Recognition in the Mouse
Ferguson, J. N., Aldag, J. M., Insel, T. R., & Young, L. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-20-08278.2001 · Cited by 1,043 · see citing works
Dai, W., Garcia, D., de BAZELAIRE, C., & Alsop, D. C. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21790 · Cited by 986 · see citing works
Dendritic peptide release and peptide-dependent behaviours
Ludwig, M., & Leng, G. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1845 · Cited by 945 · see citing works
Promoting social behavior with oxytocin in high-functioning autism spectrum disorders.
Andari, E., Duhamel, J.-R., Zalla, T., Herbrecht, E., Leboyer, M., & Sirigu, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910249107 · Cited by 941 · see citing works
Is there a core neural network in empathy? an fMRI based quantitative meta-analysis
Fan, Y., Duncan, N. W., de Greck, M., & Northoff, G. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.009 · Cited by 902 · see citing works
Functional MRI : an introduction to methods
Jezzard, P., Matthews, P. M., & Smith, S. M. (2002) · Cited by 885 · see citing works
The Human Amygdala in Social Judgment
Adolphs, R., Tranel, D., & Damásio, A. R. (2002) · The MIT Press eBooks · doi:10.7551/mitpress/3077.003.0027 · Cited by 882 · see citing works
Statistical analysis of activation images
Worsley, K. J. (2001) · doi:10.1093/acprof:oso/9780192630711.003.0014 · Cited by 825 · see citing works
Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice
Takayanagi, Y., Yoshida, M., Bielsky, I. F., Ross, H. E., Kawamata, M., Onaka, T., Yanagisawa, T., Kimura, T., Matzuk, M. M., Young, L. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505312102 · Cited by 806 · see citing works
The social brain in psychiatric and neurological disorders
Kennedy, D. P., & Adolphs, R. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.09.006 · Cited by 798 · see citing works
On the relationship between the “default mode network” and the “social brain
Mars, R. B., Neubert, F.-X., Noonan, M. P., Sallet, J., Toni, I., & Rushworth, M. F. S. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00189 · Cited by 766 · see citing works
Consensus Paper: Pathological Role of the Cerebellum in Autism
Fatemi, S. H., Aldinger, K. A., Ashwood, P., Bauman, M. L., Blaha, C. D., Blatt, G. J., Chauhan, A., Chauhan, V., Dager, S. R., Dickson, P. E., et al. (2012) · The Cerebellum · doi:10.1007/s12311-012-0355-9 · Cited by 723 · see citing works
The Peptide That Binds: A Systematic Review of Oxytocin and its Prosocial Effects in Humans
MacDonald, K., & MacDonald, T. M. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673220903523615 · Cited by 585 · see citing works
Tost, H., Kolachana, B., Hakimi, S., Lemaitre, H., Verchinski, B. A., Mattay, V. S., Weinberger, D. R., & Meyer–Lindenberg, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003296107 · Cited by 564 · see citing works
Oxytocin Attenuates Amygdala Reactivity to Fear in Generalized Social Anxiety Disorder
Labuschagne, I., Phan, K. L., Wood, A., Angstadt, M., Chua, P., Heinrichs, M., Stout, J. C., & Nathan, P. J. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.123 · Cited by 549 · see citing works
Intranasal Administration of Oxytocin Increases Envy and Schadenfreude (Gloating)
Shamay-Tsoory, S. G., Fischer, M., Dvash, J., Harari, H., Perach-Bloom, N., & Levkovitz, Y. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.06.009 · Cited by 542 · cited 1× · see citing works
“org/j empathy (78,79,81,83,84) or theory of mind and mentalizing (89) (Supplement).”
Effects of intranasal oxytocin on emotional face processing in women
Domes, G., Lischke, A., Berger, C., Grossmann, A., Hauenstein, K., Heinrichs, M., & Herpertz, S. C. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.06.016 · Cited by 521 · cited 3× · see citing works
“Biological P IN-OT on amygdala functional connectivity (105) or amygdala response involving left (92,98,113,114) or right amygdala laterality (97,100,101).”
Increased brain and plasma oxytocin after nasal and peripheral administration in rats and mice
Neumann, I. D., Maloumby, R., Beiderbeck, D. I., Lukas, M., & Landgraf, R. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.03.003 · Cited by 511 · see citing works
Neuromodulation by Oxytocin and Vasopressin
Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works
Correlation Between Regional Cerebral Blood Flow and Oxidative Metabolism
Raichle, M. E. (1976) · Archives of Neurology · doi:10.1001/archneur.1976.00500080001001 · Cited by 485 · see citing works
Williams, J. R., Insel, T. R., Harbaugh, C. R., & Carter, C. S. (1994) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1994.tb00579.x · Cited by 483 · see citing works
Sokoloff, L. (1981) · PubMed · Cited by 480 · see citing works
Handbook of Psychological Assessment in Primary Care Settings
(2000) · Routledge eBooks · doi:10.4324/9781315827346 · Cited by 471 · see citing works
Striepens, N., Kendrick, K. M., Hanking, V., Landgraf, R., Wüllner, U., Maier, W., & Hurlemann, R. (2013) · Scientific Reports · doi:10.1038/srep03440 · Cited by 452 · see citing works
Personal space regulation by the human amygdala
Kennedy, D. P., Gläscher, J., Tyszka, J. M., & Adolphs, R. (2009) · Nature Neuroscience · doi:10.1038/nn.2381 · Cited by 450 · see citing works
Social cognition and the cerebellum: A meta-analysis of over 350 fMRI studies
Overwalle, F. V., Baetens, K., Mariën, P., & Vandekerckhove, M. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.033 · Cited by 428 · see citing works
Oxytocin Attenuates Affective Evaluations of Conditioned Faces and Amygdala Activity
Petrovic, P., Kalisch, R., Singer, T., & Dolan, R. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4572-07.2008 · Cited by 424 · cited 2× · see citing works
“Biological P IN-OT on amygdala functional connectivity (105) or amygdala response involving left (92,98,113,114) or right amygdala laterality (97,100,101).”
Oxytocin and Vasopressin Agonists and Antagonists as Research Tools and Potential Therapeutics
Manning, M., Misicka, A., Olma, A., Bankowski, K., Stoev, S., Chini, B., Durroux, T., Mouillac, B., Corbani, M., & Guillon, G. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2012.02303.x · Cited by 423 · see citing works
The SCL-90-R and Brief Symptom Inventory (BSI) in Primary Care
Savitz, L. R. D. A. K. L. (2000) · Routledge eBooks · doi:10.4324/9781315827346-11 · Cited by 384 · see citing works
Bakermans-Kranenburg, M. J., & van IJzendoorn, M. H. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.34 · Cited by 383 · see citing works
Graustella, A. J., & MacLeod, C. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.002 · Cited by 379 · see citing works
Loup, F., Tribollet, E., Dubois-Dauphin, M., & Dreifuss, J. J. (1991) · Brain Research · doi:10.1016/0006-8993(91)90345-v · Cited by 378 · see citing works
Riem, M. M. E., Bakermans-Kranenburg, M. J., Pieper, S., Tops, M., Boksem, M. A. S., Vermeiren, R. R. J. M., van IJzendoorn, M. H., & Rombouts, S. A. R. B. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.006 · Cited by 366 · see citing works
Van IJzendoorn, M. H., & Bakermans-Kranenburg, M. J. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.07.008 · Cited by 365 · see citing works
Mens, W. B. J., Witter, A., & Van Wimersma Greidanus, T. B. (1983) · Brain Research · doi:10.1016/0006-8993(83)90478-x · Cited by 360 · see citing works
Guastella, A. J., Hickie, I. B., McGuinness, M. M., Otis, M., Woods, E. A., Disinger, H. M., Chan, H.-K., Chen, T. F., & Banati, R. B. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.11.019 · Cited by 357 · see citing works
A review of safety, side-effects and subjective reactions to intranasal oxytocin in human research
MacDonald, E., Dadds, M. R., Brennan, J. L., Williams, K., Levy, F., & Cauchi, A. J. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.02.015 · Cited by 352 · cited 3× · see citing works
“, in 14% of studies until 2011 (66) and still being used (15)] to maximize power.”
Anagnostou, E., Soorya, L., Chaplin, W., Bartz, J., Halpern, D., Wasserman, S., Wang, A. T., Pepa, L., Tanel, N., Kushki, A., et al. (2012) · Molecular Autism · doi:10.1186/2040-2392-3-16 · Cited by 350 · see citing works
Oxytocin enhances brain function in children with autism
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. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312857110 · Cited by 336 · see citing works
Ross, H. E., Freeman, S. M., Spiegel, L. L., Ren, X., Terwilliger, E. F., & Young, L. J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5039-08.2009 · Cited by 322 · see citing works
Does mental activity change the oxidative metabolism of the brain?
Roland, P. E., Eriksson, L., Stone‐Elander, S., & Widén, L. (1987) · Europe PMC (PubMed Central) · Cited by 313 · see citing works
Rilling, J. K., DeMarco, A. C., Hackett, P. D., Thompson, R., Ditzen, B., Patel, R., & Pagnoni, G. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.07.013 · Cited by 303 · see citing works
Immunohistochemical localization of oxytocin receptors in human brain
Boccia, M. L., Petrusz, P., Suzuki, K., Marson, L., & Pedersen, C. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.048 · Cited by 276 · see citing works
Russell, T. A., Rubia, K., Bullmore, E. T., Soni, W., John Suckling, A., Brammer, M. J., Simmons, A., Williams, S., & Sharma, T. (2000) · American Journal of Psychiatry · doi:10.1176/appi.ajp.157.12.2040 · Cited by 259 · see citing works
Effects of intranasal oxytocin on the neural basis of face processing in autism spectrum disorder
Domes, G., Heinrichs, M., Kumbier, E., Grossmann, A., Hauenstein, K., & Herpertz, S. C. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.02.007 · Cited by 255 · see citing works
Nasal oxytocin for social deficits in childhood autism: A randomized controlled trial
Dadds, M. R., MacDonald, E., Cauchi, A., Williams, K., Levy, F., & Brennan, J. (2014) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-013-1899-3 · Cited by 250 · see citing works
Oxytocin facilitates protective responses to aversive social stimuli in males
Striepens, N., Scheele, D., Kendrick, K. M., Becker, B., Schäfer, L., Schwalba, K., Reul, J., Maier, W., & Hurlemann, R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208852109 · Cited by 242 · see citing works
Atzil, S., Hendler, T., Zagoory-Sharon, O., Winetraub, Y., & Feldman, R. (2012) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2012.06.008 · Cited by 225 · see citing works
Oxytocin promotes group-serving dishonesty
Shalvi, S., & Dreu, C. K. W. D. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400724111 · Cited by 225 · see citing works
Action Understanding Requires the Left Inferior Frontal Cortex
Pobric, G., & Hamilton, A. F. D. C. (2006) · Current Biology · doi:10.1016/j.cub.2006.01.033 · Cited by 224 · see citing works
Lischke, A., Berger, C., Prehn, K., Heinrichs, M., Herpertz, S. C., & Domes, G. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.07.015 · Cited by 221 · see citing works
A sociability gene? Meta-analysis of oxytocin receptor genotype effects in humans
Bakermans‐Kranenburg, M. J., & van IJzendoorn, M. H. (2013) · Psychiatric Genetics · doi:10.1097/ypg.0b013e3283643684 · Cited by 217 · see citing works
Neural response to specific components of fearful faces in healthy and schizophrenic adults
Raduà, J., Phillips, M. L., Russell, T. A., Lawrence, N., Marshall, N., Kalidindi, S., El‐Hage, W., McDonald, C., Giampietro, V., Brammer, M. J., et al. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.030 · Cited by 214 · see citing works
Kagerbauer, S. M., Martin, J., Schuster, T., Blobner, M., Kochs, E. F., & Landgraf, R. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12038 · Cited by 212 · see citing works
Intact rapid detection of fearful faces in the absence of the amygdala
Tsuchiya, N., Moradi, F., Felsen, C. N., Yamazaki, M., & Adolphs, R. (2009) · Nature Neuroscience · doi:10.1038/nn.2380 · Cited by 210 · see citing works
Skuse, D. H., Lori, A., Cubells, J. F., Lee, I., Conneely, K. N., Puura, K., Lehtimäki, T., Binder, E. B., & Young, L. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302985111 · Cited by 207 · see citing works
Oxytocin enhances resting-state connectivity between amygdala and medial frontal cortex
Sripada, C. S., Phan, K. L., Labuschagne, I., Welsh, R., Nathan, P. J., & Wood, A. G. (2013) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145712000533 · Cited by 197 · see citing works
Oxytocin increases amygdala reactivity to threatening scenes in females
Lischke, A., Gamer, M., Berger, C., Grossmann, A., Hauenstein, K., Heinrichs, M., Herpertz, S. C., & Domes, G. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.01.011 · Cited by 194 · cited 2× · see citing works
“Biological P IN-OT on amygdala functional connectivity (105) or amygdala response involving left (92,98,113,114) or right amygdala laterality (97,100,101).”
Oxytocin increases anxiety to unpredictable threat
Grillon, C., Krimsky, M., Charney, D. R., Vytal, K., Ernst, M., & Cornwell, B. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.156 · Cited by 192 · see citing works
DNA methylation of the oxytocin receptor gene predicts neural response to ambiguous social stimuli
Jack, A., Connelly, J. J., & Morris, J. P. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00280 · Cited by 192 · cited 2× · see citing works
“, anterior cingulate cortex) (123,127) or predominantly left hemisphere (122,125,126,128,130) and right cerebellum effects (Supplement) (127).”
Riem, M. M. E., van IJzendoorn, M. H., Tops, M., Boksem, M. A. S., Rombouts, S. A. R. B., & Bakermans-Kranenburg, M. J. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.313 · Cited by 191 · see citing works
Sabatier, N., Caquineau, C., Dayanithi, G., Bull, P., Douglas, A. J., Guan, X. M. M., Jiang, M., Van der Ploeg, L., & Leng, G. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10351.2003 · Cited by 190 · see citing works
MRI atlas of the human hypothalamus
Baroncini, M., Jissendi, P., Balland, É., Besson, P., Pruvo, J., Francke, J.-P., Dewailly, D., Blond, S., & Prévot, V. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.013 · Cited by 190 · see citing works
Oxytocin increases recognition of masked emotional faces
Schulze, L., Lischke, A., Greif, J., Herpertz, S. C., Heinrichs, M., & Domes, G. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.03.011 · Cited by 180 · see citing works
Human neuroimaging of oxytocin and vasopressin in social cognition
Zink, C. F., & Meyer-Lindenberg, A. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.016 · Cited by 176 · see citing works
Handbook of Psychological Assessment in Primary Care Settings, Second Edition
(2017) · Routledge eBooks · doi:10.4324/9781315658407 · Cited by 173 · see citing works
Association between the oxytocin receptor gene and amygdalar volume in healthy adults
Inoue, H., Yamasue, H., Tochigi, M., Abe, O., Liu, X., Kawamura, Y., Takei, K., Suga, M., Yamada, H., Rogers, M. A., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.07.019 · Cited by 164 · see citing works
Oxytocin receptor density is associated with male mating tactics and social monogamy
Ophir, A. G., Gessel, A., Zheng, D.-J., & Phelps, S. M. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.007 · Cited by 161 · see citing works
Inability to empathize: brain lesions that disrupt sharing and understanding another’s emotions.
Hillis, A. E. (2014) · Brain · doi:10.1093/brain/awt317 · Cited by 158 · see citing works
Variant in oxytocin receptor gene is associated with amygdala volume
Furman, D. J., Chen, M. C., & Gotlib, I. H. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2010.12.004 · Cited by 151 · see citing works
Low CSF oxytocin reflects high intent in suicide attempters
Jokinen, J., Chatzittofis, A., Hellström, C., Nordström, P., Uvnäs-Moberg, K., & Åsberg, M. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.07.016 · Cited by 143 · see citing works
MacDonald, K., MacDonald, T. M., Brüne, M., Lamb, K., Wilson, M. P., Golshan, S., & Feifel, D. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.05.014 · Cited by 140 · see citing works
Oxytocin׳s role in anxiety: A critical appraisal
MacDonald, K., & Feifel, D. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.025 · Cited by 139 · see citing works
Labuschagne, I., Phan, K. L., WOOD, A. G., Angstadt, M., Chua, P. M.-L., Heinrichs, M., Stout, J. C., & Nathan, P. J. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711001489 · Cited by 139 · see citing works
Oxytocin Modulates Neural Reactivity to Children's Faces as a Function of Social Salience
Wittfoth-Schardt, D., Gründing, J., Wittfoth, M., Lanfermann, H., Heinrichs, M., Domes, G., Buchheim, A., Gündel, H., & Waller, C. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.47 · Cited by 139 · see citing works
Elevated salivary levels of oxytocin persist more than 7 h after intranasal administration
van IJzendoorn, M. H., Bhandari, R., van der Veen, R., Grewen, K. M., & Bakermans-Kranenburg, M. J. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00174 · Cited by 137 · see citing works
Loup, F., Tribollet, E., Dubois-Dauphin, M., Pizzolato, G., & Dreifuss, J. J. (1989) · Brain Research · doi:10.1016/0006-8993(89)90317-x · Cited by 136 · see citing works
Aerosolized oxytocin increases cerebrospinal fluid oxytocin in rhesus macaques
Modi, M. E., Connor-Stroud, F., Landgraf, R., Young, L. J., & Parr, L. A. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.02.011 · Cited by 129 · see citing works
Wang, D., Buckner, R. L., & Liu, H. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00598.2012 · Cited by 124 · see citing works
Spatiotemporal Evolution of the Functional Magnetic Resonance Imaging Response to Ultrashort Stimuli
Hirano, Y., Stefanovic, B., & Silva, A. C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3986-10.2011 · Cited by 122 · see citing works
Intranasal oxytocin administration is reflected in human saliva
Weisman, O., Zagoory-Sharon, O., & Feldman, R. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.02.014 · Cited by 120 · see citing works
Sex, Receptors, and Attachment: A Review of Individual Factors Influencing Response to Oxytocin
MacDonald, K. S. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00194 · Cited by 119 · see citing works
Doyle, O., Simoni, S. D., Schwarz, A. J., Brittain, C., O’Daly, O., Williams, S., & Mehta, M. A. (2013) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.112.201665 · Cited by 117 · see citing works
A Time-Dependent Peak of Oxytocin Exists in Cerebrospinal Fluid but Not in Plasma of Humans
Amico, J. A., Tenicela, R., Johnston, J., & ROBINSON, A. G. (1983) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-57-5-947 · Cited by 116 · see citing works
Oxytocin mediates acquisition of maternally associated odor preferences in preweanling rat pups.
Nelson, E. E., & Panksepp, J. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.3.583 · Cited by 113 · see citing works
Oxytocin mediates acquisition of maternally associated odor preferences in preweanling rat pups.
Nelson, E., & Panksepp, J. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.3.583 · Cited by 113 · see citing works
Handley, R., Zelaya, F. O., Reinders, A. A. T. S., Marques, T. R., Mehta, M. A., Tuura, R., Alsop, D. C., Taylor, H., Johnston, A. E., Williams, S., et al. (2012) · Human Brain Mapping · doi:10.1002/hbm.21436 · Cited by 108 · see citing works
Potentials and Challenges for Arterial Spin Labeling in Pharmacological Magnetic Resonance Imaging
Wang, D. J. J., Chen, Y., Fernández‐Seara, M. A., & Detre, J. A. (2011) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.110.172577 · Cited by 105 · see citing works
Lowbridge, J., Manning, M., Haldar, J., & Sawyer, W. H. (1977) · Journal of Medicinal Chemistry · doi:10.1021/jm00211a025 · Cited by 98 · see citing works
Geissler, D. B., & Ehret, G. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03205.x · Cited by 95 · see citing works
Oxytocin effects on complex brain networks are moderated by experiences of maternal love withdrawal
Riem, M. M. E., van IJzendoorn, M. H., Tops, M., Boksem, M. A. S., Rombouts, S. A. R. B., & Bakermans-Kranenburg, M. J. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.01.011 · Cited by 91 · see citing works
Pincus, D. (2010) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2010.00134 · Cited by 91 · see citing works
Rocchetti, M., Radua, J., Paloyelis, Y., Xenaki, L., Frascarelli, M., Caverzasi, E., Politi, P., & Fusar‐Poli, P. (2014) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12185 · Cited by 83 · see citing works
Changes in cerebrospinal fluid neurochemistry during pregnancy
Altemus, M., Fong, J., Yang, R., Damast, S., Luine, V., & Ferguson, D. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.06.002 · Cited by 83 · see citing works
Chen, Y., Wan, H. I., O’Reardon, J. P., Wang, D. J. J., Wang, Z., Korczykowski, M., & Detre, J. A. (2010) · Clinical Pharmacology & Therapeutics · doi:10.1038/clpt.2010.296 · Cited by 78 · see citing works
Neurogenetic effects of OXTR rs2254298 in the extended limbic system of healthy Caucasian adults
Tost, H., Kolachana, B., Verchinski, B. A., Bilek, E., Goldman, A. L., Mattay, V. S., Weinberger, D. R., & Meyer-Lindenberg, A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.06.034 · Cited by 77 · see citing works
Michalska, K. J., Decety, J., Liu, C., Chen, Q., Martz, M. E., Jacob, S., Hipwell, A. E., Lee, S. S., Chronis-Tuscano, A., Waldman, I. D., et al. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00021 · Cited by 76 · see citing works
Marquand, A. F., O’Daly, O., Simoni, S. D., Alsop, D. C., Maguire, R. P., Williams, S., Zelaya, F. O., & Mehta, M. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.058 · Cited by 72 · see citing works
Loth, E., Poline, J.-B., Thyreau, B., Jia, T., Tao, C., Lourdusamy, A., Stacey, D., Cattrell, A., Desrivières, S., Ruggeri, B., et al. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.07.043 · Cited by 65 · see citing works
Regional Correlation between Resting State FDG PET and pCASL Perfusion MRI
Cha, Y.-H. K., Jog, M., Kim, Y., Chakrapani, S., Kraman, S. M., & Wang, D. J. J. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.147 · Cited by 58 · see citing works
Association between the oxytocin receptor (OXTR) gene and mesolimbic responses to rewards
Damiano, C. R., Aloi, J. M., Dunlap, K., Burrus, C. J., Mosner, M. G., Kozink, R. V., McLaurin, R. E., Mullette-Gillman, O. A., Carter, R., Huettel, S. A., et al. (2014) · Molecular Autism · doi:10.1186/2040-2392-5-7 · Cited by 54 · see citing works
Costandi, M. (2015) · Springer eBooks · doi:10.1007/978-3-662-44191-6_41 · Cited by 53 · see citing works
Kim, Y., Kim, C., Park, S. J., Pyo, J., & Treasure, J. L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090721 · Cited by 53 · see citing works
Hodkinson, D. J., Krause, K., Khawaja, N., Renton, T. F., Huggins, J. P., Vennart, W., Thacker, M. A., Mehta, M. A., Zelaya, F. O., Williams, S., et al. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.09.004 · Cited by 48 · see citing works
Variant in OXTR gene and functional connectivity of the hypothalamus in normal subjects
Wang, J., Qin, W., Liu, B., Wang, D., Zhang, Y., Jiang, T., & Yu, C. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.029 · Cited by 42 · see citing works
Central release of oxytocin and the ventromedial hypothalamus
Sabatier, N., Rowe, I. C. M., & Leng, G. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351247 · Cited by 40 · see citing works
Lin, I.-F., Kashino, M., Ohta, H., Yamada, T., Tani, M., Watanabe, H., Kanai, C., Ohno, T., Takayama, Y., Iwanami, A., et al. (2014) · Molecular Autism · doi:10.1186/2040-2392-5-20 · Cited by 40 · see citing works
Tsubokawa, T., Katayama, Y., Kondo, T., Ueno, Y., Hayashi, N., & MORIYASU, N. (1980) · Brain Research · doi:10.1016/0006-8993(80)91159-2 · Cited by 35 · see citing works
Montag, C., Sauer, C., Reuter, M., & Kirsch, P. (2013) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-013-0452-x · Cited by 32 · see citing works
Murphy, K., Harris, A. D., Diukova, A., Evans, J., Lythgoe, D. J., Zelaya, F. O., & Wise, R. G. (2011) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2011.02.030 · Cited by 32 · see citing works
Multivariate decoding of brain images using ordinal regression
Doyle, O., Ashburner, J., Zelaya, F. O., Williams, S., Mehta, M. A., & Marquand, A. F. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.036 · Cited by 29 · see citing works
Zelaya, F. O., Zois, E., Muller-Pollard, C., Lythgoe, D. J., Lee, S., Andrews, C., Smart, T. S., Conrod, P., Vennart, W., Williams, S., et al. (2011) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-011-0293-4 · Cited by 26 · see citing works
Effect of paroxetine and bupropion on human resting brain perfusion: An arterial spin labeling study
Viviani, R., Abler, B., Seeringer, A., & Stingl, J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.014 · Cited by 25 · see citing works
When too much of a good thing is bad: chronic oxytocin, development, and social impairments
Young, L. J. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.015 · Cited by 22 · see citing works
Social Cognition, the Male Brain and the Autism Spectrum
Hall, J., Philip, R. C. M., Marwick, K. F. M., Whalley, H. C., Romaniuk, L., McIntosh, A. M., Santos, I. M., Sprengelmeyer, R., Johnstone, E. C., Stanfield, A. C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049033 · Cited by 22 · see citing works
Yamasue, H., Suga, M., Yahata, N., Inoue, H., Tochigi, M., Abe, O., Liu, X., Kawamura, Y., Rogers, M. A., Takei, K., et al. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.021 · Cited by 22 · see citing works
Nordin, L. E., Li, T., Brogren, J., Johansson, P., Sjögren, N., Hannesdóttir, K., Björk, C., Segerdahl, M., Wang, D. J. J., & Julin, P. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.11.035 · Cited by 20 · see citing works
Distribution of vasopressin and oxytocin in rat brain.
HASHIMOTO, H., FUKUI, K., NOTO, T., NAKAJIMA, T., & KATO, N. (1985) · Endocrinologia Japonica · doi:10.1507/endocrj1954.32.89 · Cited by 17 · see citing works
Does the Amygdala Mediate Oxytocin Effects on Socially Reinforced Learning?
Gamer, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2847-10.2010 · Cited by 9 · see citing works
Flagged first, then by citations
2 of the 154 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Rogers LR, Vallortigara G, Andrew RJ (2013): Divided Brains. Cam- bridge: Cambridge University Press. 120.
Cited by
Sorted by citations
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
Does Oxytocin Increase Trust in Humans? A Critical Review of Research
Nave, G., Camerer, C., & McCullough, M. (2015) · Perspectives on Psychological Science · doi:10.1177/1745691615600138 · Cited by 309 · see citing works
Quintana, D. S., Lischke, A., Grace, S., Scheele, D., Ma, Y., & Becker, B. (2021) · Molecular Psychiatry · doi:10.1038/s41380-020-00864-7 · Cited by 263 · see citing works
Kinetics and dose dependency of intranasal oxytocin effects on amygdala reactivity
Spengler, F. B., Schultz, J., Scheele, D., Essel, M., Maier, W., Heinrichs, M., & Hurlemann, R. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.04.015 · Cited by 229 · see citing works
Why empathy has a beneficial impact on others in medicine: unifying theories
Jean Decety, A., & Fotopoulou, A. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00457 · Cited by 240 · see citing works
Meta-analysis of the effects of intranasal oxytocin on interpretation and expression of emotions
Leppanen, J., Ng, K. W., Tchanturia, K., & Treasure, J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.04.010 · Cited by 188 · see citing works
Brain oxytocin: how puzzle stones from animal studies translate into psychiatry
Grinevich, V., & Neumann, I. D. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0802-9 · Cited by 189 · see citing works
Walker, S. C., Trotter, P. D., Swaney, W. T., Marshall, A. G., & McGlone, F. P. (2017) · Neuropeptides · doi:10.1016/j.npep.2017.01.001 · Cited by 193 · see citing works
Advances in human oxytocin measurement: challenges and proposed solutions
Tabak, B. A., Leng, G., Szeto, A., Parker, K. J., Verbalis, J. G., Ziegler, T. E., Lee, M. R., Neumann, I. D., & Mendez, A. J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-022-01719-z · Cited by 170 · see citing works
Intranasal Oxytocin Normalizes Amygdala Functional Connectivity in Posttraumatic Stress Disorder
Koch, S. B. J., van Zuiden, M., Nawijn, L., Frijling, J. L., Veltman, D. J., & Olff, M. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.1 · Cited by 132 · see citing works
Labeled oxytocin administered via the intranasal route reaches the brain in rhesus macaques
Lee, M. R., Shnitko, T. A., Blue, S. W., Kaucher, A. V., Winchell, A. J., Erikson, D. W., Grant, K. A., & Leggio, L. (2020) · Nature Communications · doi:10.1038/s41467-020-15942-1 · Cited by 132 · see citing works
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 · see citing works
Martins, D., Mazibuko, N., Zelaya, F. O., Vasilakopoulou, S., Loveridge, J., Oates, A. E., Maltezos, S., Mehta, M. A., Wastling, S. J., Howard, M. A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14845-5 · Cited by 130 · see citing works
Overview of human oxytocin research
Kendrick, K. M., Guastella, A. J., & Becker, B. (2017) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2017_19 · Cited by 121 · see citing works
Preventive Treatments for Psychosis: Umbrella Review (Just the Evidence)
Fusar-Poli, P., Davies, C., Solmi, M., Brondino, N., De Micheli, A., Kotlicka-Antczak, M., Shin, J. I., & Radua, J. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00764 · Cited by 108 · see citing works
Quintana, D. S., Guastella, A. J., Westlye, L. T., & Andreassen, O. A. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.166 · Cited by 107 · see citing works
Detection, processing and reinforcement of social cues: regulation by the oxytocin system
Menon, R., & Neumann, I. D. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00759-w · Cited by 100 · see citing works
Koch, S. B., van Zuiden, M., Nawijn, L., Frijling, J. L., Veltman, D. J., & Olff, M. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.299 · Cited by 98 · see citing works
Daughters, K., Manstead, A. S. R., Hubble, K., Rees, A., Thapar, A., & van Goozen, S. H. M. (2015) · PLOS ONE · doi:10.1371/journal.pone.0145104 · Cited by 92 · see citing works
“[27] demonstrated that IN-OT also crosses the blood-brain barrier in human males, providing further evidence that IN-OT has direct effects on the brain.”
BackgroundOxytocin modulates social value representations in the amygdala
Liu, Y., Li, S., Lin, W., Li, W., Yan, X., Wang, X., Pan, X., Rutledge, R. B., & Ma, Y. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0351-1 · Cited by 89 · see citing works
Oxytocin promotes coordinated out-group attack during intergroup conflict in humans
Zhang, H., Gross, J., De Dreu, C., & Ma, Y. (2019) · eLife · doi:10.7554/elife.40698 · Cited by 87 · see citing works
Frijling, J. L. (2017) · European Journal of Psychotraumatology · doi:10.1080/20008198.2017.1302652 · Cited by 84 · see citing works
Cai, Q., Feng, L., & Yap, K. Z. (2017) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12627 · Cited by 77 · see citing works
Numan, M. (2020) · doi:10.1093/oso/9780190848675.001.0001 · Cited by 101 · see citing works
Oxytocin promotes intuitive rather than deliberated cooperation with the in-group
Ten Velden, F. S., Daughters, K., & De Dreu, C. K. W. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.06.005 · Cited by 66 · see citing works
Khalili‐Mahani, N., Rombouts, S. A. R. B., van Osch, M. J. P., Duff, E. P., Carbonell, F., Nickerson, L. D. H., Becerra, L. R., Dahan, A., Evans, A. C., Soucy, J., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23516 · Cited by 61 · see citing works
Sex- and context-dependent effects of oxytocin on social sharing
Ma, X., Zhao, W., Luo, R., Zhou, F., Geng, Y., Xu, L., Gao, Z., Zheng, X., Becker, B., & Kendrick, K. M. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.08.004 · Cited by 64 · see citing works
Improving the precision of intranasal oxytocin research
Winterton, A., Westlye, L. T., Steen, N. E., Andreassen, O. A., & Quintana, D. S. (2020) · Nature Human Behaviour · doi:10.1038/s41562-020-00996-4 · Cited by 62 · see citing works
Kou, J., Zhang, Y., Zhou, F., Sindermann, C., Montag, C., Becker, B., & Kendrick, K. M. (2020) · Psychological Medicine · doi:10.1017/s0033291720003803 · Cited by 63 · see citing works
Paloyelis, Y., Krahé, C., Maltezos, S., Williams, S. C., Howard, M. A., & Fotopoulou, A. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12347 · Cited by 61 · see citing works
Frijling, J. L., van Zuiden, M., Koch, S. B. J., Nawijn, L., Veltman, D. J., & Olff, M. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.278 · Cited by 60 · see citing works
What's Love Got to do with it: Role of oxytocin in trauma, attachment and resilience
Sharma, S. R., Gonda, X., Dome, P., & Tarazi, F. I. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107602 · Cited by 61 · see citing works
Ebert, A., & Brüne, M. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2017_21 · Cited by 62 · see citing works
Nawijn, L., van Zuiden, M., Koch, S. B. J., Frijling, J. L., Veltman, D. J., & Olff, M. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.01.020 · Cited by 59 · see citing works
Zhao, Z., Ma, X., Geng, Y., Zhao, W., Zhou, F., Wang, J., Markett, S. A., Biswal, B. B., Ma, Y., Kendrick, K. M., et al. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.09.067 · Cited by 55 · see citing works
Sniff and mimic–Intranasal oxytocin increases facial mimicry in a sample of men
Korb, S., Malsert, J., Strathearn, L., Vuilleumier, P., & Niedenthal, P. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.06.003 · Cited by 54 · see citing works
Kou, J., Zhang, Y., Zhou, F., Gao, Z., Yao, S., Zhao, W., Li, H., Lei, Y., Gao, S., Kendrick, K. M., et al. (2022) · Psychotherapy and Psychosomatics · doi:10.1159/000521348 · Cited by 54 · see citing works
Yao, S., & Kendrick, K. M. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14020323 · Cited by 52 · see citing works
Fragkaki, I., Cima, M., & Granic, I. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.11.005 · Cited by 52 · see citing works
The oxytocin receptor gene predicts brain activity during an emotion recognition task in autism
Uzefovsky, F., Bethlehem, R. A. I., Shamay-Tsoory, S., Ruigrok, A., Holt, R., Spencer, M., Chura, L., Warrier, V., Chakrabarti, B., Bullmore, E., et al. (2019) · Molecular Autism · doi:10.1186/s13229-019-0258-4 · Cited by 49 · see citing works
How does oxytocin modulate human behavior?
Yao, S., & Kendrick, K. M. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-02898-1 · Cited by 55 · see citing works
Gryksa, K., & Neumann, I. D. (2021) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2021.105601 · Cited by 49 · see citing works
Xin, F., Zhou, X., Dong, D., Zhao, Z., Yang, X., Wang, Q., Gu, Y., Kendrick, K. M., Chen, A., & Becker, B. (2020) · Advanced Science · doi:10.1002/advs.202001077 · Cited by 46 · see citing works
Leppänen, J., Cardi, V., Ng, K. W., Paloyelis, Y., Stein, D., Tchanturia, K., & Treasure, J. L. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.01.017 · Cited by 46 · see citing works
Oxytocin promotes face-sensitive neural responses to infant and adult faces in mothers
Peltola, M. J., Strathearn, L., & Puura, K. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.02.012 · Cited by 43 · see citing works
Seeley, S. H., Chou, Y., & O'Connor, M. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.011 · Cited by 42 · see citing works
Koch, S. B. J., van Zuiden, M., Nawijn, L., Frijling, J. L., Veltman, D. J., & Olff, M. (2018) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2018.12.002 · Cited by 45 · see citing works
Oxytocin Modulates the Intrinsic Dynamics Between Attention-Related Large-Scale Networks
Xin, F., Zhou, F., Zhou, X., Ma, X., Geng, Y., Zhao, W., Yao, S., Dong, D., Biswal, B. B., Kendrick, K. M., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy295 · Cited by 39 · see citing works
Hubble, K., Daughters, K., Manstead, A. S. R., Rees, A., Thapar, A., & van Goozen, S. H. M. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.10.019 · Cited by 41 · see citing works
Intrinsic, dynamic and effective connectivity among large-scale brain networks modulated by oxytocin
Jiang, X., Ma, X., Geng, Y., Zhao, Z., Zhou, F., Zhao, W., Yao, S., Yang, S., Zhao, Z., Becker, B., et al. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117668 · Cited by 39 · see citing works
The role of machine learning in neuroimaging for drug discovery and development
Doyle, O., Mehta, M. A., & Brammer, M. J. (2015) · Psychopharmacology · doi:10.1007/s00213-015-3968-0 · Cited by 41 · see citing works
A precision medicine approach to oxytocin trials
Andari, E., Hurlemann, R., & Young, L. J. (2017) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2017_29 · Cited by 40 · see citing works
Oxytocin modulates meta-mood as a function of age and sex
Ebner, N. C., Horta, M., Lin, T., Feifel, D., Fischer, H., & Cohen, R. A. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00175 · Cited by 40 · see citing works
Intranasal Oxytocin and Vasopressin Modulate Divergent Brainwide Functional Substrates
Galbusera, A., Felice, A. D., Girardi, S., Bassetto, G., Maschietto, M., Nishimori, K., Chini, B., Papaleo, F., Vassanelli, S., & Gozzi, A. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.283 · Cited by 38 · see citing works
Alaerts, K., Bernaerts, S., Vanaudenaerde, B. M., Daniëls, N., & Wenderoth, N. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.01.008 · Cited by 40 · see citing works
Geng, Y., Zhao, W., Zhou, F., Ma, X., Yao, S., Becker, B., & Kendrick, K. M. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00572 · Cited by 40 · see citing works
“Less is more”: A dose-response account of intranasal oxytocin pharmacodynamics in the human brain
Martins, D., Brodmann, K., Veronese, M., Dipasquale, O., Mazibuko, N., Schuschnig, U., Zelaya, F. O., Fotopoulou, A., & Paloyelis, Y. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102239 · Cited by 42 · see citing works
A dose-finding study of oxytocin using neurophysiological measures of social processing
Wynn, J. K., Green, M. F., Hellemann, G., Reavis, E. A., & Marder, S. R. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0165-y · Cited by 39 · see citing works
Chen, Y., Becker, B., Zhang, Y., Cui, H., Du, J. R., Wernicke, J., Montag, C., Kendrick, K. M., & Yao, S. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2020.08.003 · Cited by 39 · see citing works
Sniffing oxytocin: Nose to brain or nose to blood?
Yao, S., Chen, Y., Zhuang, Q., Zhang, Y., Lan, C., Zhu, S., Becker, B., & Kendrick, K. M. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02075-2 · Cited by 38 · see citing works
Kou, J., Lan, C., Zhang, Y., Wang, Q., Zhou, F., Zhao, Z., Montag, C., Yao, S., Becker, B., & Kendrick, K. M. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01241-w · Cited by 37 · see citing works
Intranasal Oxytocin Selectively Modulates Large-Scale Brain Networks in Humans
Brodmann, K., Gruber, O., & Goya‐Maldonado, R. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0528 · Cited by 34 · see citing works
Zunhammer, M., Geis, S., Busch, V., Eichhammer, P., & Greenlee, M. W. (2016) · Scientific Reports · doi:10.1038/srep31606 · Cited by 35 · see citing works
Daughters, K., Manstead, A. S. R., Velden, F. S. T., & Dreu, C. K. W. D. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.11.039 · Cited by 35 · see citing works
Oxytocin and Facial Emotion Recognition
Ellenbogen, M. A. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2017_20 · Cited by 33 · see citing works
Alaerts, K., Bernaerts, S., Prinsen, J., Dillen, C., Steyaert, J. G., & Wenderoth, N. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0653-8 · Cited by 35 · see citing works
Cui, F., Huang, X., Jing, Y., Luo, Y., Liu, J., & Gu, R. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac017 · Cited by 32 · see citing works
Impact of intranasal oxytocin on interoceptive accuracy in alcohol users: an attentional mechanism?
Betka, S., van Praag, C. G., Paloyelis, Y., Bond, R., Pfeifer, G., Sequeira, H., Duka, T., & Critchley, H. (2018) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsy027 · Cited by 30 · see citing works
The Role of Intranasal Oxytocin on Social Cognition: an Integrative Human Lifespan Approach
Horta, M., Pehlivanoglu, D., & Ebner, N. C. (2020) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-020-00214-5 · Cited by 30 · see citing works
The Neuropeptide Oxytocin Enhances Information Sharing and Group Decision Making Quality
de Wilde, T. R. W., Velden, F. S. T., & Dreu, C. K. W. D. (2017) · Scientific Reports · doi:10.1038/srep40622 · Cited by 30 · see citing works
Grace, S., Labuschagne, I., Castle, D. J., & Rossell, S. L. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.05.022 · Cited by 30 · see citing works
Oxytocin modulates hippocampal perfusion in people at clinical high risk for psychosis
Davies, C., Paloyelis, Y., Rutigliano, G., Cappucciati, M., Micheli, A. D., Ramella‐Cravaro, V., Provenzani, U., Antoniades, M., Modinos, G., Oliver, D., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-018-0311-6 · Cited by 28 · see citing works
Acute and Repeated Intranasal Oxytocin Differentially Modulate Brain-wide Functional Connectivity
Pagani, M., Felice, A. D., Montani, C., Galbusera, A., Papaleo, F., & Gozzi, A. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2019.12.036 · Cited by 27 · see citing works
Oxytocin receptor binding sites in the periphery of the neonatal mouse
Greenwood, M. A., & Hammock, E. A. D. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172904 · Cited by 27 · see citing works
Leslie, M. R., Leppänen, J., Paloyelis, Y., & Treasure, J. L. (2018) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2018.12.014 · Cited by 27 · see citing works
Berends, Y. R., Tulen, J. H. M., Wierdsma, A. I., PELT, J. V., Feldman, R., Zagoory‐Sharon, O., de Rijke, Y. B., Kushner, S. A., & Marle, H. J. C. V. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.03.027 · Cited by 27 · see citing works
Oral Administration of Oxytocin, Like Intranasal Administration, Decreases Top-Down Social Attention
Zhuang, Q., Zheng, X., Yao, S., Zhao, W., Becker, B., Xu, X., & Kendrick, K. M. (2022) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyac059 · Cited by 26 · see citing works
Oxytocin amplifies sex differences in human mate choice
Xu, L., Becker, B., Luo, R., Zheng, X., Zhao, W., Zhang, Q., & Kendrick, K. M. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104483 · Cited by 25 · see citing works
Straccia, M. A., Teed, A. R., Katzman, P. L., Tan, K. M., Parrish, M. H., Irwin, M. R., Eisenberger, N. I., Lieberman, M. D., & Tabak, B. A. (2021) · Psychological Medicine · doi:10.1017/s0033291721004104 · Cited by 25 · see citing works
Zhuang, Q., Zhu, S., Yang, X., Zhou, X., Xu, X., Chen, Z., Lan, C., Zhao, W., Becker, B., Yao, S., et al. (2020) · Journal of Psychopharmacology · doi:10.1177/0269881120972347 · Cited by 23 · see citing works
Can intranasal oxytocin reduce craving in automated addictive behaviours? A systematic review
Houghton, B., Kouimtsidis, C., Duka, T., Paloyelis, Y., & Bailey, A. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15617 · Cited by 23 · see citing works
Effects of intranasal oxytocin in food intake and craving: A meta-analysis of clinical trials
Chen, C., Chiang, Y.-C., Kuo, T., Tam, K., & Loh, E. (2021) · Clinical Nutrition · doi:10.1016/j.clnu.2021.08.011 · Cited by 22 · see citing works
Martins, D., Davies, C., Micheli, A. D., Oliver, D., Krawczun-Rygmaczewska, A., Fusar‐Poli, P., & Paloyelis, Y. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-00890-7 · Cited by 24 · see citing works
Chen, Y., Li, Q., Zhang, Q., Kou, J., Zhang, Y., Cui, H., Wernicke, J., Montag, C., Becker, B., Kendrick, K. M., et al. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.589878 · Cited by 23 · see citing works
Lussier, D., Cruz‐Almeida, Y., & Ebner, N. C. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00338 · Cited by 20 · see citing works
Shcherbinin, S., Doyle, O., Zelaya, F. O., Simoni, S. D., Mehta, M. A., & Schwarz, A. J. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4021-z · Cited by 21 · see citing works
Martins, D., Leslie, M. R., Rodan, S., Zelaya, F. O., Treasure, J. L., & Paloyelis, Y. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-00871-w · Cited by 21 · see citing works
Imaging clinically relevant pain states using arterial spin labeling
Loggia, M. L., Segerdahl, A. R., Howard, M. A., & Tracey, I. (2019) · PAIN Reports · doi:10.1097/pr9.0000000000000750 · Cited by 21 · see citing works
Zhao, W., Geng, Y., Luo, L., Zhao, Z., Ma, X., Xu, L., Yao, S., & Kendrick, K. M. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00272 · Cited by 20 · see citing works
Schultebraucks, K., Maslahati, T., Wingenfeld, K., Hellmann‐Regen, J., Kraft, J., Kownatzki, M., Behnia, B., Ripke, S., Otte, C., & Roepke, S. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01247-4 · Cited by 20 · see citing works
Leslie, M. R., Leppänen, J., Paloyelis, Y., Nazar, B. P., & Treasure, J. L. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12771 · Cited by 20 · see citing works
Tully, J., Sethi, A., Griem, J., Paloyelis, Y., Craig, M., Williams, S., Murphy, D., Blair, J., & Blackwood, N. (2023) · Nature Mental Health · doi:10.1038/s44220-023-00067-3 · Cited by 18 · see citing works
Embodied Precision: Intranasal Oxytocin Modulates Multisensory Integration
Crucianelli, L., Paloyelis, Y., Ricciardi, L., Jenkinson, P. M., & Fotopoulou, A. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01366 · Cited by 19 · see citing works
Victory is its own reward: oxytocin increases costly competitive behavior in schizophrenia
Bradley, E., Brustkern, J., Coster, L. D., van den Bos, W., McClure, S. M., Seitz, A., & Woolley, J. D. (2019) · Psychological Medicine · doi:10.1017/s0033291719000552 · Cited by 19 · see citing works
Mekhael, A. A., Bent, J. E., Fawcett, J. M., Campbell, T. S., Aguirre‐Camacho, A., Farrell, A., & Rash, J. A. (2023) · Canadian Journal of Pain · doi:10.1080/24740527.2023.2191114 · Cited by 19 · see citing works
A phase II randomised controlled trial of intranasal oxytocin in anorexia nervosa
Maguire, S., Kesby, A., Brownlow, R. S., Hunt, G. E., Kim, M., McAulay, C., Grisham, J. R., McGregor, I. S., Suraev, A. S., Kevin, R. C., et al. (2024) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2024.107032 · Cited by 17 · see citing works
Chen, Y., Zou, H., Hou, X., Lan, C., Wang, J., Qing, Y., Chen, W., Yao, S., & Kendrick, K. M. (2023) · eLife · doi:10.7554/elife.85847 · Cited by 18 · see citing works
Lan, C., Liu, C., Li, K., Zhao, Z., Yang, J., Ma, Y., Scheele, D., Yao, S., Kendrick, K. M., & Becker, B. (2022) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyac037 · Cited by 16 · see citing works
Ali, Z. A., Yasseen, A. A., Al-Dujaili, A. H., Al-Karaqully, A. J., McAllister, K. A., & Jumaah, A. S. (2022) · PLoS ONE · doi:10.1371/journal.pone.0265217 · Cited by 16 · see citing works
The effect of intranasal oxytocin on social reward processing in humans: a systematic review
Kraus, J., Výborová, E., & Silani, G. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1244027 · Cited by 16 · see citing works
- Authors
- Paloyelis, Y., Doyle, O. M., Zelaya, F. O., Maltezos, S., Williams, S. C., Fotopoulou, A., & Howard, M. A.
- Affiliations
- King's College London (GB)
- University College London (GB)
- Corresponding author
- Paloyelis, Yannis
- ORCID
- Venue
- Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2016-04
- Volume
- 79
- Issue
- 8
- Pages
- 693-705
- ISSN
- 0006-3223 (ISSN-L)
- OpenAlex
- W2021223630
- Cited by
- 187
- References
- 154
- Citations by year
- 2026: 10 · 2025: 6 · 2024: 12 · 2023: 10 · 2022: 12 · 2021: 16 · 2020: 41 · 2019: 20 · 2018: 14 · 2017: 19 · 2016: 13 · 2015: 14
- FWCI
- 22.75
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Biological Psychiatry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Research Portal (King's College London) (publishedVersion, cc-by)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Economic and Social Research Council fellowship (ES/K009400/1)
- Volkswagen Foundation “European Platform for Life Sciences, Mind Sciences and Humanities” (II/85 069)
- Institute for the Study of Affective Neuroscience/Hope for Depression Research Foundation (to AF)
- European Research Council Starting Investigator Award (ERC-2012-STG GA313755)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- intranasal oxytocin, regional cerebral blood flow, arterial spin labeling, oxytocin receptor, social cognition, emotional processing, pharmacodynamics, autism spectrum disorder, social dysfunction, spatiotemporal dynamics
- MeSH terms
- Administration, Intranasal, Brain, Brain Mapping, Central Nervous System Agents, Cerebrovascular Circulation, Humans, Magnetic Resonance Imaging, Male, Oxytocin, Pattern Recognition, Automated, Rest, Multivariate Analysis, Single-Blind Method, Young Adult
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