Oxytocin: Parallel Processing in the Social Brain?

Untitled work

(1943) · The Nervous child · Cited by 8,870 · see citing works

Does the autistic child have a “theory of mind” ?

Baron-Cohen, S., Leslie, A. M., & Frith, U. (1985) · Cognition · doi:10.1016/0010-0277(85)90022-8 · Cited by 8,599 · see citing works

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014

Baio, J., Wiggins, L., Christensen, D. L., Maenner, M. J., Daniels, J., Warren, Z., Kurzius-Spencer, M., Zahorodny, W., Robinson, C., Rosenberg, et al. (2018) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6706a1 · Cited by 6,078 · see citing works

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999) · Nature Genetics · doi:10.1038/13810 · Cited by 4,990 · see citing works

Visual perception of biological motion and a model for its analysis

Johansson, G. (1973) · Perception & Psychophysics · doi:10.3758/bf03212378 · Cited by 4,547 · see citing works

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2016

Maenner, M. J., Shaw, K. A., Baio, J., EdS1, Washington, A., Patrick, M., DiRienzo, M., Christensen, D. L., Wiggins, L. D., Pettygrove, S., et al. (2020) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6904a1 · Cited by 3,780 · see citing works

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90397-h · Cited by 3,481 · see citing works

An Experimental Study of Apparent Behavior

Heider, F., & Simmel, M. (1944) · The American Journal of Psychology · doi:10.2307/1416950 · Cited by 3,340 · 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

Strong association of de novo copy number mutations with autism

Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., et al. (2007) · Science · doi:10.1126/science.1138659 · Cited by 2,795 · see citing works

Synaptic, transcriptional and chromatin genes disrupted in autism

Study, T. D., De Rubeis, S., Autism, H. M. C. F., UK10K Consortium, The Autism Sequencing Consortium, He, X., Goldberg, A. P., Poultney, C. S., Samocha, K., Ercument Cicek, A., et al. (2014) · Nature · doi:10.1038/nature13772 · Cited by 2,746 · see citing works

The contribution of de novo coding mutations to autism spectrum disorder

Iossifov, I., O’Roak, B. J., Sanders, S. J., Ronemus, M., Krumm, N., Levy, D., Stessman, H. A., Witherspoon, K. T., Vives, L., Patterson, K. E., et al. (2014) · Nature · doi:10.1038/nature13908 · Cited by 2,585 · see citing works

An advanced test of theory of mind: understanding of story characters’ thoughts and feelings by able autistic, mentally handicapped, and normal children and adults

Happé, F. G. E. (1994) · Journal of Autism and Developmental Disorders · doi:10.1007/bf02172093 · Cited by 2,352 · see citing works

Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain

Azevedo, F. A. C., Carvalho, L. R. B., Grinberg, L. T., Farfel, J. M., Ferretti, R. E. L., Leite, R. E. P., Filho, W. J., Lent, R., & Herculano‐Houzel, S. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21974 · Cited by 2,337 · see citing works

People thinking about thinking peopleThe role of the temporo-parietal junction in “theory of mind”

Saxe, R., & Kanwisher, N. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00230-1 · Cited by 2,316 · see citing works

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

O’Roak, B. J., Vives, L., Girirajan, S., Karakoc, E., Krumm, N., Coe, B. P., Levy, R., Ko, A., Lee, C., Smith, J. D., et al. (2012) · Nature · doi:10.1038/nature10989 · Cited by 2,165 · see citing works

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Sanders, S. J., Murtha, M. T., Gupta, A. R., Murdoch, J. D., Raubeson, M. J., Willsey, A. J., Ercan-Sencicek, A. G., DiLullo, N. M., Parikshak, N. N., Stein, J. L., et al. (2012) · Nature · doi:10.1038/nature10945 · Cited by 2,084 · see citing works

The social motivation theory of autism

Chevallier, C., Kohls, G., Troiani, V., Brodkin, E. S., & Schultz, R. T. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.02.007 · Cited by 2,072 · see citing works

Animal models of neuropsychiatric disorders

Nestler, E. J., & Hyman, S. E. (2010) · Nature Neuroscience · doi:10.1038/nn.2647 · Cited by 2,023 · see citing works

Another Advanced Test of Theory of Mind: Evidence from Very High Functioning Adults with Autism or Asperger Syndrome

Baron‐Cohen, S., Jolliffe, T., Mortimore, C., & Robertson, M. (1997) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1997.tb01599.x · Cited by 1,970 · see citing works

Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry

Kravitz, A. V., Freeze, B. S., Parker, P. R. L., Kay, K., Thwin, M. T., Deisseroth, K., & Kreitzer, A. C. (2010) · Nature · doi:10.1038/nature09159 · Cited by 1,885 · see citing works

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Neale, B. M., Kou, Y., Liu, L., Ma’ayan, A., Samocha, K. E., Sabo, A., Lin, C.-F., Stevens, C., Wang, L.-S., Makarov, V., et al. (2012) · Nature · doi:10.1038/nature11011 · Cited by 1,734 · 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

Oxytocin Modulates Neural Circuitry for Social Cognition and Fear in Humans

Kirsch, P., Esslinger, C., Chen, Q., Mier, D., Lis, S., Siddhanti, S., Gruppe, H., Mattay, V. S., Gallhofer, B., & Meyer-Lindenberg, A. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3984-05.2005 · Cited by 1,639 · see citing works

Does the chimpanzee have a theory of mind? 30 years later

Call, J., & Tomasello, M. (2008) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2008.02.010 · Cited by 1,592 · see citing works

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic‐like behavior in mice

Moy, S. S., Nadler, J. J., Perez, A., Barbaro, R. P., Johns, J. M., Magnuson, T. R., Piven, J., & Crawley, J. N. (2004) · Genes, Brain and Behavior · doi:10.1111/j.1601-1848.2004.00076.x · Cited by 1,545 · see citing works

The neurobiology of pair bonding.

Young, L. J., & Wang, Z. (2004) · Nature Neuroscience · doi:10.1038/nn1327 · Cited by 1,523 · see citing works

Behavioural phenotyping assays for mouse models of autism

Silverman, J. L., Yang, M., Lord, C., & Crawley, J. N. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2851 · Cited by 1,462 · see citing works

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Glessner, J. T., Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., Zhang, H., Estes, A., Brune, C. W., Bradfield, J. P., et al. (2009) · Nature · doi:10.1038/nature07953 · Cited by 1,421 · see citing works

The paraventricular nucleus of the hypothalamus: Cytoarchitectonic subdivisions and organization of projections to the pituitary, dorsal vagal complex, and spinal cord as demonstrated by retrograde fluorescence double‐labeling methods

Swanson, L. W., & Kuypers, H. G. J. M. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901940306 · Cited by 1,413 · 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

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

Intranasal delivery to the central nervous system: Mechanisms and experimental considerations

Dhuria, S. V., Hanson, L. R., & Frey, W. H. (2010) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.21924 · Cited by 1,239 · 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

Immunohistochemical identification of neurons in the paraventricular nucleus of the hypothalamus that project to the medulla or to the spinal cord in the rat

Sawchenko, P. E., & Swanson, L. W. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902050306 · Cited by 1,150 · see citing works

Measuring Social Value OrientationPreprint

Murphy, R. O., Ackermann, K., & Handgraaf, M. (2011) · Social Science Research Network · doi:10.2139/ssrn.1804189 · Cited by 1,099 · see citing works

Evoked axonal oxytocin release in the central amygdala attenuates fear response

Knobloch, H. S., Charlet, A., Hoffmann, L. C., Eliava, M., Khrulev, S., Cetin, A. H., Osten, P., Schwarz, M. K., Seeburg, P. H., Stoop, R., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.030 · Cited by 1,049 · see citing works

The Challenge of Translation in Social Neuroscience: A Review of Oxytocin, Vasopressin, and Affiliative Behavior

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

Oxytocin: The Great Facilitator of Life

Lee, H.-J., Macbeth, A. H., Pagani, J., & Young, W. S. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.04.001 · Cited by 1,037 · see citing works

Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat

Buijs, R. M., Swaab, D. F., Dogterom, J., & van Leeuwen, F. W. (1978) · Cell and Tissue Research · doi:10.1007/bf00224932 · Cited by 1,029 · see citing works

On some physiological actions of ergot

Dale, H. H. (1906) · The Journal of Physiology · doi:10.1113/jphysiol.1906.sp001148 · Cited by 1,011 · see citing works

Intentional Systems

Dennett, D. C., & The Journal of Philosophy, I. (1971) · Journal of Philosophy · doi:10.2307/2025382 · Cited by 994 · see citing works

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., et al. (2009) · Nature · doi:10.1038/nature07999 · Cited by 989 · see citing works

Correction of Fragile X Syndrome in Mice

Dölen, G., Osterweil, E., Rao, B. S. S., Smith, G. B., Auerbach, B. D., Chattarji, S., & Bear, M. F. (2007) · Neuron · doi:10.1016/j.neuron.2007.12.001 · Cited by 979 · see citing works

The hippocampal CA2 region is essential for social memory

Hitti, F. L., & Siegelbaum, S. A. (2014) · Nature · doi:10.1038/nature13028 · Cited by 976 · see citing works

Distinct roles for direct and indirect pathway striatal neurons in reinforcement

Kravitz, A. V., Tye, L. D., & Kreitzer, A. C. (2012) · Nature Neuroscience · doi:10.1038/nn.3100 · Cited by 972 · see citing works

Intranasal oxytocin improves emotion recognition for youth with autism spectrum disorders.

Guastella, A. J., Einfeld, S. L., Gray, K. M., Rinehart, N. J., Tonge, B. J., Lambert, T. J., & Hickie, I. B. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.020 · Cited by 962 · see citing works

Dissociation of cognitive and emotional empathy in adults with Asperger syndrome using the multifaceted empathy test (MET).

Dziobek, I., Rogers, K., Fleck, S., Bahnemann, M., Heekeren, H. R., Wolf, O. T., & Convit, A. (2008) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-007-0486-x · Cited by 951 · see citing works

Measuring Social Value Orientation

Murphy, R. O., Ackermann, K. A., & Handgraaf, M. J. J. (2011) · Judgment and Decision Making · doi:10.1017/s1930297500004204 · Cited by 948 · 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

Empathy and pro-social behavior in rats

Bartal, I. B.-A., Decety, J., & Mason, P. (2011) · Science · doi:10.1126/science.1210789 · Cited by 934 · see citing works

Introducing MASC: A Movie for the Assessment of Social Cognition

Dziobek, I., Fleck, S., Kalbe, E., Rogers, K., Hassenstab, J., Brand, M., Kessler, J., Woike, J. K., Wolf, O. T., & Convit, A. (2006) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-006-0107-0 · Cited by 926 · 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

Oxytocin promotes human ethnocentrism

De Dreu, C. K. W., Greer, L. L., Van Kleef, G. A., Shalvi, S., & Handgraaf, M. J. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015316108 · Cited by 838 · see citing works

Oxytocin increases generosity in humans

Zak, P. J., Stanton, A. A., & Ahmadi, S. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001128 · Cited by 831 · see citing works

Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat

Buijs, R. M. (1978) · Cell and Tissue Research · doi:10.1007/bf00212323 · Cited by 830 · see citing works

Oxytocin receptor genetic variation relates to empathy and stress reactivity in humans

Rodrigues, S. M., Saslow, L. R., Garcia, N., John, O. P., & Keltner, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909579106 · Cited by 812 · see citing works

Neuropeptide Transmission in Brain Circuits

van den Pol, A. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.014 · Cited by 810 · 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

Vasopressin and Oxytocin Excite Distinct Neuronal Populations in the Central Amygdala

Huber, D., Veinante, P., & Stoop, R. (2005) · Science · doi:10.1126/science.1105636 · Cited by 804 · see citing works

Parallel processing strategies of the primate visual system

Nassi, J. J., & Callaway, E. M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2619 · Cited by 802 · see citing works

Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities

Zoghbi, H. Y., & Bear, M. F. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a009886 · Cited by 797 · see citing works

Automated apparatus for quantitation of social approach behaviors in mice

Nadler, J. J., Moy, S. S., Dold, G., Trang, D., Simmons, N., Perez, A., Young, N. B., Barbaro, R. P., Piven, J., Magnuson, T. R., et al. (2004) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2004.00071.x · Cited by 775 · see citing works

Oxytocin attenuates amygdala responses to emotional faces regardless of valence

Domes, G., Heinrichs, M., Gläscher, J., Büchel, C., Braus, D. F., & Herpertz, S. C. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.03.025 · Cited by 774 · see citing works

Oxytocin enhances amygdala-dependent, socially reinforced learning and emotional empathy in humans

Hurlemann, R., Patin, A., Onur, O. A., Cohen, M. X., Baumgartner, T., Metzler, S., Dziobek, I., Gallinat, J., Wagner, M., Maier, W., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5538-09.2010 · Cited by 771 · see citing works

Identifying autism loci and genes by tracing recent shared ancestry

Morrow, E. M., Yoo, S.-Y., Flavell, S. W., Kim, T.-K., Lin, Y., Hill, R. S., Mukaddes, N. M., Balkhy, S., Gascon, G., Hashmi, A., et al. (2008) · Science · doi:10.1126/science.1157657 · Cited by 737 · see citing works

Oxytocin is required for nursing but is not essential for parturition or reproductive behavior.

Nishimori, K., Young, L. J., Guo, Q., Wang, Z., Insel, T. R., & Matzuk, M. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11699 · Cited by 734 · see citing works

Dopaminergic foundations of schizotypy as measured by the German version of the Oxford-Liverpool Inventory of Feelings and Experiences (O-LIFE)—a suitable endophenotype of schizophrenia

Grant, P. S., Kuepper, Y., Mueller, E. A., Wielpuetz, C., Mason, O. J., & Hennig, J. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00001 · Cited by 719 · see citing works

Naturally occurring variations in maternal behavior in the rat are associated with differences in estrogen-inducible central oxytocin receptors

Champagne, F., Diorio, J., Sharma, S., & Meaney, M. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221224598 · Cited by 707 · see citing works

Oxytocin Increases Retention of Social Cognition in Autism

Hollander, E., Bartz, J., Chaplin, W., Phillips, A., Sumner, J., Soorya, L., Anagnostou, E., & Wasserman, S. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.05.030 · Cited by 693 · see citing works

Oxytocin Infusion Reduces Repetitive Behaviors in Adults with Autistic and Asperger's Disorders

Hollander, E., Novotny, S., Hanratty, M., Yaffe, R., DeCaria, C. M., Aronowitz, B. R., & Mosovich, S. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300021 · Cited by 689 · see citing works

Abnormal functional connectivity of default mode sub-networks in autism spectrum disorder patients

Assaf, M., Jagannathan, K., Calhoun, V. D., Miller, L., Stevens, M. C., Sahl, R., O'Boyle, J. G., Schultz, R. T., & Pearlson, G. D. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.067 · Cited by 680 · see citing works

The safety and efficacy of ±3,4-methylenedioxymethamphetamine-assisted psychotherapy in subjects with chronic, treatment-resistant posttraumatic stress disorder: the first randomized controlled pilot study

Mithoefer, M. C., Wagner, M. T., Mithoefer, A. T., Jerome, L., & Doblin, R. (2011) · Journal of Psychopharmacology · doi:10.1177/0269881110378371 · Cited by 674 · see citing works

Parallel-distributed Processing in Olfactory Cortex: New Insights from Morphological and Physiological Analysis of Neuronal Circuitry

Haberly, L. B. (2001) · Chemical Senses · doi:10.1093/chemse/26.5.551 · Cited by 673 · see citing works

Activity-dependent neuronal signalling and autism spectrum disorder

Ebert, D. H., & Greenberg, M. E. (2013) · Nature · doi:10.1038/nature11860 · Cited by 666 · see citing works

CD38 is critical for social behaviour by regulating oxytocin secretion

Jin, D., Liu, H.-X., Hirai, H., Torashima, T., Nagai, T., Lopatina, O., Shnayder, N. A., Yamada, K., Noda, M., Seike, T., et al. (2007) · Nature · doi:10.1038/nature05526 · Cited by 665 · 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

Feeling, caring, knowing: different types of empathy deficit in boys with psychopathic tendencies and autism spectrum disorder

Bartoli, A. J., Happe, F. G. E., Gilbert, F., Heyes, S. B., & Viding, E. M. (2010) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2010.02280.x · Cited by 640 · see citing works

Structure and expression of a human oxytocin receptor

Kimura, T., Tanizawa, O., Mori, K., Brownstein, M., & Okayama, H. (1992) · Nature · doi:10.1038/356526a0 · Cited by 631 · see citing works

The neurobiology of psychopathic traits in youths

Blair, J. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3577 · Cited by 620 · see citing works

A genome-wide linkage and association scan reveals novel loci for autism

The Gene Discovery Project of Johns Hopkins & the Autism Consortium, Weiss, L. A., & Arking, D. E. (2009) · Nature · doi:10.1038/nature08490 · Cited by 619 · see citing works

Somatosensory processes subserving perception and action

Dijkerman, H. C., & de Haan, E. H. F. (2007) · Behavioral and Brain Sciences · doi:10.1017/s0140525x07001392 · Cited by 609 · see citing works

Evidence That Oxytocin Exerts Anxiolytic Effects via Oxytocin Receptor Expressed in Serotonergic Neurons in Mice

Yoshida, M., Takayanagi, Y., Inoue, K., Kimura, T., Young, L. J., Onaka, T., & Nishimori, K. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5593-08.2009 · Cited by 608 · see citing works

THE SEQUENCE OF AMINO ACIDS IN OXYTOCIN, WITH A PROPOSAL FOR THE STRUCTURE OF OXYTOCIN

du Vigneaud, V., Ressler, C., & Trippett, S. (1953) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)49238-1 · Cited by 603 · see citing works

Effects of experience and social context on prospective caching strategies by scrub jays

Emery, N. J., & Clayton, N. S. (2001) · Nature · doi:10.1038/35106560 · Cited by 565 · see citing works

Plasma oxytocin increases in the human sexual response

CARMICHAEL, M. S., HUMBERT, R., DIXEN, J., PALMISANO, G., GREENLEAF, W., & DAVIDSON, J. M. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-64-1-27 · Cited by 554 · see citing works

Serotonin selectively influences moral judgment and behavior through effects on harm aversion

Crockett, M. J., Clark, L., Hauser, M. D., & Robbins, T. W. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009396107 · Cited by 526 · see citing works

Not just fear and sadness: Meta-analytic evidence of pervasive emotion recognition deficits for facial and vocal expressions in psychopathy

Dawel, A., O’Kearney, R., McKone, E., & Palermo, R. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.08.006 · Cited by 525 · see citing works

The Intense World Theory – A Unifying Theory of the Neurobiology of Autism

Markram, H., & Markram, H. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00224 · Cited by 522 · see citing works

Rhesus Monkeys Attribute Perceptions to Others

Flombaum, J., & Santos, L. R. (2005) · Current Biology · doi:10.1016/j.cub.2004.12.076 · Cited by 507 · see citing works

Food-Caching Western Scrub-Jays Keep Track of Who Was Watching When

Dally, J. M., Emery, N. J., & Clayton, N. S. (2006) · Science · doi:10.1126/science.1126539 · Cited by 501 · see citing works

Variations in maternal behaviour are associated with differences in oxytocin receptor levels in the rat

Francis, D. D., Champagne, F. C., & Meaney, M. J. (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00599.x · Cited by 496 · see citing works

The translation of translational control by FMRP: therapeutic targets for FXS

Darnell, J. C., & Klann, E. (2013) · Nature Neuroscience · doi:10.1038/nn.3379 · Cited by 491 · see citing works

Empathy toward strangers triggers oxytocin release and subsequent generosity

Barraza, J. A., & Zak, P. J. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04504.x · Cited by 489 · see citing works

Different amygdala subregions mediate valence-related and attentional effects of oxytocin in humans

Gamer, M., Zurowski, B., & Büchel, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000985107 · Cited by 487 · see citing works

Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors

Rothwell, P. E., Fuccillo, M. V., Maxeiner, S., Hayton, S. J., Gokce, O., Lim, B. K., Fowler, S. C., Malenka, R. C., & Südhof, T. C. (2014) · Cell · doi:10.1016/j.cell.2014.04.045 · Cited by 477 · see citing works

Social buffering of the stress response: diversity, mechanisms, and functions

Hennessy, M. B., Kaiser, S., & Sachser, N. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.06.001 · Cited by 477 · see citing works

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients

Shcheglovitov, A., Shcheglovitova, O., Yazawa, M., Portmann, T., Shu, R., Sebastiano, V., Krawisz, A., Froehlich, W., Bernstein, J. A., Hallmayer, J. F., et al. (2013) · Nature · doi:10.1038/nature12618 · Cited by 470 · see citing works

Modulating social behavior with oxytocin: How does it work? What does it mean?

Churchland, P. S., & Winkielman, P. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.003 · Cited by 464 · see citing works

Neural control of maternal and paternal behaviors

Dulac, C., O’Connell, L. A., & Wu, Z. (2014) · Science · doi:10.1126/science.1253291 · Cited by 457 · see citing works

The biology of mammalian parenting and its effect on offspring social development

Rilling, J. K., & Young, L. J. (2014) · Science · doi:10.1126/science.1252723 · Cited by 452 · see citing works

CNS region-specific oxytocin receptor expression: importance in regulation of anxiety and sex behavior

Bale, T. L., Davis, A. M., Auger, A. P., Dorsa, D. M., & McCarthy, M. M. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02546.2001 · Cited by 446 · see citing works

Dendrites of hypothalamic magnocellular neurons release neurohypophysial peptides by exocytosis

Pow, D. V., & Morris, J. F. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90091-2 · Cited by 446 · see citing works

The diencephalon of the albino rat: studies on the brain of the rat. No. 2

Gurdjian, E. S. (1927) · Journal of Comparative Neurology · doi:10.1002/cne.900430102 · Cited by 439 · 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 · see citing works

The Synthesis of Oxytocin1

du Vigneaud, V., Ressler, C., SWAN, J. M., Roberts, C. W., & Katsoyannis, P. G. (1954) · Journal of the American Chemical Society · doi:10.1021/ja01641a004 · Cited by 422 · see citing works

Naturally Occurring Differences in Maternal Care are Associated with the Expression of Oxytocin and Vasopressin (V1a) Receptors: Gender Differences

Francis, D. D., Young, L. J., Meaney, M. J., & Insel, T. R. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.0007-1331.2002.00776.x · Cited by 415 · see citing works

Who Shalt Not Kill? Individual Differences in Working Memory Capacity, Executive Control, and Moral Judgment

Moore, A., Clark, B. A., & Kane, M. J. (2008) · Psychological Science · doi:10.1111/j.1467-9280.2008.02122.x · Cited by 398 · see citing works

Autism Profiles of Males With Fragile X Syndrome

Harris, S. W., Hessl, D., Goodlin-Jones, B., Ferranti, J., Bacalman, S., Barbato, I., Tassone, F., Hagerman, P. J., Herman, K., & Hagerman, R. J. (2008) · American Journal on Mental Retardation · doi:10.1352/2008.113:427-438 · Cited by 396 · see citing works

Systematic analysis of genes required for synapse structure and function

Sieburth, D., Ch'ng, Q.-L., Dybbs, M., et al. (2005) · Nature · doi:10.1038/nature03809 · Cited by 394 · see citing works

THE RÔLE OF FIBER SIZE IN THE ESTABLISHMENT OF A NERVE BLOCK BY PRESSURE OR COCAINE

Gasser, H. S., & Erlanger, J. (1929) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1929.88.4.581 · Cited by 394 · see citing works

Sniffing around oxytocin: Review and meta-analyses of trials in healthy and clinical groups with implications for pharmacotherapy

Bakermans-Kranenburg, M. J., & van IJzendoorn, M. H. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.34 · Cited by 383 · see citing works

Oxytocin Selectively Gates Fear Responses Through Distinct Outputs from the Central Amygdala

Viviani, D., Charlet, A., van den Burg, E., Robinet, C., Hurni, N., Abatis, M., Magara, F., & Stoop, R. (2011) · Science · doi:10.1126/science.1201043 · Cited by 381 · see citing works

The site of origin of the hormones of the posterior pituitary.

Bargmann, W., & Scharrer, E. (1951) · PubMed · Cited by 379 · 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

Durability of improvement in post-traumatic stress disorder symptoms and absence of harmful effects or drug dependency after 3,4-methylenedioxymethamphetamine-assisted psychotherapy: a prospective long-term follow-up study

Mithoefer, M. C., Wagner, M. T., Mithoefer, A. T., Jerome, L., Martin, S. F., Yazar‐Klosinski, B., Michel, Y., Brewerton, T. D., & Doblin, R. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112456611 · Cited by 376 · see citing works

Pharmacologic rescue of impaired cognitive flexibility, social deficits, increased aggression, and seizure susceptibility in oxytocin receptor null mice: a neurobehavioral model of autism

Sala, M., Braida, D., Lentini, D., Busnelli, M., Bulgheroni, E., Capurro, V., Finardi, A., Donzelli, A., Pattini, L., Rubino, T., et al. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.12.022 · Cited by 375 · see citing works

Stepwise evolution of stable sociality in primates

Shultz, S., Opie, C., & Atkinson, Q. D. (2011) · Nature · doi:10.1038/nature10601 · Cited by 373 · see citing works

Oxytocin improves long-lasting spatial memory during motherhood through MAP kinase cascade

Tomizawa, K., Iga, N., Lü, Y.-F., Moriwaki, A., Matsushita, M., Li, S., Miyamoto, O., Itano, T., & Matsui, H. (2003) · Nature Neuroscience · doi:10.1038/nn1023 · Cited by 372 · see citing works

The Striatal Balancing Act in Drug Addiction: Distinct Roles of Direct and Indirect Pathway Medium Spiny Neurons

Lobo, M. K., & Nestler, E. J. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00041 · Cited by 371 · see citing works

Oxytocin modulates amygdala, insula, and inferior frontal gyrus responses to infant crying: a randomized controlled trial

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

Penetration of neurohypophyseal hormones from plasma into cerebrospinal fluid (CSF): Half-times of disappearance of these neuropeptides from CSF

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

Hypothalamic Oxytocin Mediates Social Buffering of the Stress Response

Smith, A. S., & Wang, Z. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.09.017 · Cited by 359 · see citing works

MDMA enhances emotional empathy and prosocial behavior

Hysek, C. M., Schmid, Y., Simmler, L. D., Domes, G., Heinrichs, M., Eisenegger, C., Preller, K. H., Quednow, B. B., & Liechti, M. E. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst161 · Cited by 356 · see citing works

The hypothalamus of the albino rat

Krieg, W. J. S. (1932) · The Journal of Comparative Neurology · doi:10.1002/cne.900550104 · Cited by 351 · see citing works

Intranasal oxytocin versus placebo in the treatment of adults with Autism Spectrum Disorders: A randomized controlled trial

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 reward system responses in men viewing the face of their female partner

Scheele, D., Wille, A., Kendrick, K. M., Stoffel-Wagner, B., Becker, B., Güntürkün, O., Maier, W., & Hurlemann, R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314190110 · Cited by 345 · see citing works

Rearing effects on cerebrospinal fluid oxytocin concentration and social buffering in rhesus monkeys

Winslow, J. T., Noble, P. L., Lyons, C. K., Sterk, S. M., & Insel, T. R. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300128 · Cited by 345 · see citing works

Oxytocin enhances hippocampal spike transmission by modulating fast-spiking interneurons

Owen, S. F., Tuncdemir, S. N., Bader, P. L., Tirko, N. N., Fishell, G., & Tsien, R. W. (2013) · Nature · doi:10.1038/nature12330 · Cited by 339 · see citing works

Oxytocin and vasopressin release within the supraoptic and paraventricular nuclei of pregnant, parturient and lactating rats: A microdialysis study

Neumann, I., Russell, J. A., & Landgraf, R. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90285-n · Cited by 337 · see citing works

Impaired theory of mind for moral judgment in high-functioning autism

Moran, J. M., Young, L., Saxe, R. R., Lee, S. M., O'Young, D., Mavros, P. L., & Gabrieli, J. D. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011734108 · Cited by 336 · see citing works

The milk-ejection reflex of the rat: a 20-to 40-fold acceleration in the firing of paraventricular neurones during oxytocin release

WAKERLEY, J. B., & LINCOLN, D. W. (1973) · Journal of Endocrinology · doi:10.1677/joe.0.0570477 · Cited by 327 · see citing works

Neurophysin in the hypothalamo-neurohypophysial system. I. Production and characterization of monoclonal antibodies

Ben-Barak, Y., Russell, J., Whitnall, M., Ozato, K., & Gainer, H. (1985) · The Journal of Neuroscience · doi:10.1523/jneurosci.05-01-00081.1985 · Cited by 313 · see citing works

Characterization of the oxytocin system regulating affiliative behavior in female prairie voles

Ross, H. E., Cole, C. D., Smith, Y., Neumann, I. D., Landgraf, R., Murphy, A. Z., & Young, L. J. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.055 · Cited by 309 · see citing works

Comparative Distribution of Vasopressin V1b and Oxytocin Receptor Messenger Ribonucleic Acids in Brain ¹

Vaccari, C., Lolait, S. J., & Ostrowski, N. L. (1998) · Endocrinology · doi:10.1210/endo.139.12.6382 · Cited by 308 · see citing works

Deficiency in mouse oxytocin prevents milk ejection, but not fertility or parturition

Young III, W. S., Shepard, E., Amico, J., Hennighausen, L., Wagner, K., LaMarca, M. E., McKinney, C., & Ginns, E. I. (1996) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1996.05266.x · Cited by 308 · see citing works

Intranasal oxytocin reduces psychotic symptoms and improves Theory of Mind and social perception in schizophrenia

Pedersen, C. A., Gibson, C. M., Rau, S. W., Salimi, K., Smedley, K. L., Casey, R. L., Leserman, J., Jarskog, L. F., & Penn, D. L. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.07.027 · Cited by 305 · see citing works

The effects of a course of intranasal oxytocin on social behaviors in youth diagnosed with autism spectrum disorders: a randomized controlled trial

Guastella, A. J., Gray, K. M., Rinehart, N. J., Alvares, G. A., Tonge, B. J., Hickie, I. B., Keating, C. M., Cacciotti‐Saija, C., & Einfeld, S. L. (2015) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12305 · Cited by 299 · see citing works

Capacitance steps and fusion pores of small and large-dense-core vesicles in nerve terminals

Klyachko, V. A., & Jackson, M. B. (2002) · Nature · doi:10.1038/nature00852 · Cited by 294 · see citing works

Oxytocin receptors in the nucleus accumbens facilitate “spontaneous” maternal behavior in adult female prairie voles

Olazábal, D. E., & Young, L. J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.04.017 · Cited by 289 · see citing works

THE ACTIVE PRINCIPLES OF THE POSTERIOR LOBE OF THE PITUITARY GLAND. 1 I. THE DEMONSTRATION OF THE PRESENCE OF TWO ACTIVE PRINCIPLES. II. THE SEPARATION OF THE TWO PRINCIPLES AND THEIR CONCENTRATION IN THE FORM OF POTENT SOLID PREPARATIONS

Kamm, O., Aldrich, T. B., Grote, I. W., Rowe, L. W., & BUGBEE, E. P. (1928) · Journal of the American Chemical Society · doi:10.1021/ja01389a050 · Cited by 270 · see citing works

A conditional knockout mouse line of the oxytocin receptor

Lee, H.-J., Caldwell, H. K., Macbeth, A. H., Tolu, S. G., & Young, W. S. (2008) · Endocrinology · doi:10.1210/en.2007-1710 · Cited by 269 · see citing works

PKC-1 regulates secretion of neuropeptides

Sieburth, D., Madison, J. M., & Kaplan, J. M. (2006) · Nature Neuroscience · doi:10.1038/nn1810 · Cited by 268 · see citing works

Chronic intranasal oxytocin causes long-term impairments in partner preference formation in male prairie voles

Bales, K. L., Perkeybile, A. M., Conley, O. G., Lee, M. H., Guoynes, C. D., Downing, G. M., Yun, C. R., Solomon, M., Jacob, S., & Mendoza, S. P. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.08.025 · Cited by 265 · see citing works

Overview of the most prevalent hypothalamus-specific mRNAs, as identified by directional tag PCR subtraction.

Gautvik, K. M., de Lecea, L., Gautvik, V. T., Danielson, P. E., Tranque, P., Dopazo, A., Bloom, F. E., & Sutcliffe, J. G. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8733 · Cited by 264 · see citing works

Fine Cuts of Empathy and the Amygdala: Dissociable Deficits in Psychopathy and Autism

Blair, J. (2007) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470210701508855 · Cited by 263 · see citing works

Comparative genomics of autism and schizophrenia

Crespi, B., Stead, P., & Elliot, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906080106 · Cited by 262 · see citing works

Centrally released oxytocin mediates mating-induced anxiolysis in male rats

Waldherr, M., & Neumann, I. D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705860104 · Cited by 261 · see citing works

Evolution of oxytocin pathways in the brain of vertebrates

Knobloch, H. S., & Grinevich, V. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00031 · Cited by 259 · see citing works

Electrophysiological evidence for the activation of supraoptic neurones during the release of oxytocin

LINCOLN, D. W., & Wakerley, J. B. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010722 · Cited by 252 · 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

Effects of oxytocin and prosocial behavior on brain responses to direct and vicariously experienced pain.

Singer, T., Snozzi, R., Bird, G., Petrovic, P., Silani, G., Heinrichs, M., & Dolan, R. J. (2008) · Emotion · doi:10.1037/a0014195 · Cited by 248 · see citing works

Is Ecstasy an “Empathogen”? Effects of +/- 3,4-Methylenedioxymethamphetamine on Prosocial Feelings and Identification of Emotional States in Others

Bedi, G., Hyman, D., & de Wit, H. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.08.003 · Cited by 247 · see citing works

Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome

Portmann, T., Yang, M., Mao, R., Panagiotakos, G., Ellegood, J., Dolen, G., Bader, P. L., Grueter, B. A., Goold, C., Fisher, E., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.036 · Cited by 245 · see citing works

The human oxytocin gene promoter is regulated by estrogens

Richard, S., & Zingg, H. H. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)39297-x · Cited by 242 · see citing works

Neurodevelopmental effects of the FMR-1 full mutation in humans

Reiss, A. L., Abrams, M. T., Greenlaw, R., Freund, L., & Denckla, M. B. (1995) · Nature Medicine · doi:10.1038/nm0295-159 · Cited by 242 · see citing works

Opposing actions of prostaglandins and oxytocin determine the onset of murine labor

Gross, G. A., Imamura, T., Luedke, C., Vogt, S. K., Olson, L. M., Nelson, D. M., Sadovsky, Y., & Muglia, L. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.20.11875 · Cited by 238 · see citing works

Increased oxytocin concentrations and prosocial feelings in humans after ecstasy (3,4-methylenedioxymethamphetamine) administration

Dumont, G. J. H., Sweep, F. C. G. J., van der Steen, R., Hermsen, R., Donders, A. R. T., Touw, D. J., van Gerven, J. M. A., Buitelaar, J. K., & Verkes, R. J. (2009) · Social Neuroscience · doi:10.1080/17470910802649470 · Cited by 238 · see citing works

Simultaneous microdialysis in blood and brain: oxytocin and vasopressin release in response to central and peripheral osmotic stimulation and suckling in the rat

Neumann, I., Ludwig, M., Engelmann, M., Pittman, Q. J., & Landgraf, R. (2008) · Neuroendocrinology · doi:10.1159/000126604 · Cited by 236 · see citing works

Brain regions for perceiving and reasoning about other people in school-aged children

Saxe, R. R., Whitfield-Gabrieli, S., Scholz, J., & Pelphrey, K. A. (2009) · Child Development · doi:10.1111/j.1467-8624.2009.01325.x · Cited by 234 · see citing works

Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies

Grabrucker, A. M., Schmeisser, M. J., Schoen, M., & Boeckers, T. M. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.07.003 · Cited by 233 · see citing works

Social approach behaviors in oxytocin knockout mice: comparison of two independent lines tested in different laboratory environments

Crawley, J. N., Chen, T., Puri, A., Washburn, R., Sullivan, T. L., Hill, J. M., Young, N. B., Nadler, J. J., Moy, S. S., Young, L. J., et al. (2007) · Neuropeptides · doi:10.1016/j.npep.2007.02.002 · Cited by 232 · see citing works

Species and individual differences in juvenile female alloparental care are associated with oxytocin receptor density in the striatum and the lateral septum

Olazábal, D. E., & Young, L. J. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.12.010 · Cited by 230 · see citing works

Menstrual cycle-related changes in plasma oxytocin are relevant to normal sexual function in healthy women

Salonia, A., Nappi, R. E., Pontillo, M., Daverio, R., Smeraldi, A., Briganti, A., Fabbri, F., Zanni, G. E., Rigatti, P., & Montorsi, F. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.10.002 · Cited by 229 · see citing works

The magnocellular and parvocellular paraventricular nucleus of rat: intrinsic organization

Van Den Pol, A. N. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902060402 · Cited by 228 · see citing works

Similar Brain Activation during False Belief Tasks in a Large Sample of Adults with and without Autism

Dufour, N., Redcay, E., Young, L., Mavros, P. L., Moran, J. M., Triantafyllou, C., Gabrieli, J. D. E., & Saxe, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075468 · Cited by 228 · see citing works

Verbal, Facial and Autonomic Responses to Empathy-Eliciting Film Clips by Disruptive Male Adolescents with High Versus Low Callous-Unemotional Traits

de Wied, M. A., Boxtel, A. V., Matthys, W., & Meeus, W. (2011) · Research on Child and Adolescent Psychopathology · doi:10.1007/s10802-011-9557-8 · Cited by 224 · see citing works

The association between oxytocin receptor gene polymorphism (OXTR) and trait empathy

Wu, N., Li, Z., & Su, Y. (2012) · Journal of Affective Disorders · doi:10.1016/j.jad.2012.01.009 · 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

Fear-enhancing effects of septal oxytocin receptors

Guzmán, Y. F., Tronson, N. C., Jovasevic, V., Sato, K., Guedea, A. L., Mizukami, H., Nishimori, K., & Radulovic, J. (2013) · Nature Neuroscience · doi:10.1038/nn.3465 · Cited by 215 · see citing works

An intrinsic vasopressin system in the olfactory bulb is involved in social recognition

Tobin, V. A., Hashimoto, H., Wacker, D. W., Takayanagi, Y., Langnaese, K., Caquineau, C., Noack, J., Landgraf, R., Onaka, T., Leng, G., et al. (2010) · Nature · doi:10.1038/nature08826 · Cited by 213 · see citing works

Oxytocin facilitates the extinction of conditioned fear in humans

Eckstein, M., Becker, B., Scheele, D., Scholz, C., Preckel, K., Schlaepfer, T. E., Grinevich, V., Kendrick, K. M., Maier, W., & Hurlemann, R. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.10.015 · Cited by 210 · see citing works

Neurophysin in the hypothalamo-neurohypophysial system. II. Immunocytochemical studies of the ontogeny of oxytocinergic and vasopressinergic neurons

Whitnall, M., Key, S., Ben-Barak, Y., Ozato, K., & Gainer, H. (1985) · The Journal of Neuroscience · doi:10.1523/jneurosci.05-01-00098.1985 · Cited by 209 · see citing works

The comparative distribution of forebrain receptors for neurohypophyseal peptides in monogamous and polygamous mice

Insel, T. R., Gelhard, R., & Shapiro, L. E. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90321-e · Cited by 209 · see citing works

Neuropeptide exocytosis involving synaptotagmin-4 and oxytocin in hypothalamic programming of body weight and energy balance

Zhang, G., Bai, H., Zhang, H., Dean, C., Wu, Q., Li, J., Guariglia, S., Meng, Q., & Cai, D. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.036 · Cited by 208 · see citing works

Vasopressin-immunoreactive cell bodies in the bed nucleus of the stria terminalis of the rat

van Leeuwen, F., & Caffé, R. (1983) · Cell and Tissue Research · doi:10.1007/bf00211473 · Cited by 206 · see citing works

Selective amnesic effects of oxytocin on human memory

Heinrichs, M., Meinlschmidt, G., Wippich, W., Ehlert, U., & Hellhammer, D. H. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.07.020 · Cited by 205 · see citing works

Cyto- and chemoarchitecture of the hypothalamic paraventricular nucleus in the C57BL/6J male mouse: a study of immunostaining and multiple fluorescent tract tracing

Biag, J., Huang, Y., Gou, L., Hintiryan, H., Askarinam, A., Hahn, J. D., Toga, A. W., & Dong, H. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.22698 · Cited by 205 · see citing works

MDMA-Assisted Psychotherapy Using Low Doses in a Small Sample of Women with Chronic Posttraumatic Stress Disorder

Bouso, J. C., Doblin, R., Farré, M., Alcázar‐Córcoles, M. Á., & Gómez-Jarabo, G. (2008) · Journal of Psychoactive Drugs · doi:10.1080/02791072.2008.10400637 · Cited by 205 · see citing works

Selective amnesic effects of oxytocin on human memory.

HEINRICHS, M., MEINLSCHMIDT, G., WIPPICH, W., EHLERT, U., & HELLHAMMER, D. (2004) · Physiology &amp; Behavior · doi:10.1016/s0031-9384(04)00346-4 · Cited by 205 · see citing works

A rise in the intracellular Ca2+ concentration of isolated rat supraoptic cells in response to oxytocin.

Lambert, R. C., Dayanithi, G., Moos, F., & Richard, P. (1994) · The Journal of Physiology · doi:10.1113/jphysiol.1994.sp020249 · Cited by 202 · see citing works

Can oxytocin treat autism?

Young, L. J., & Barrett, C. E. (2015) · Science · doi:10.1126/science.aaa8120 · Cited by 200 · see citing works

Vasopressin-immunoreactive cells in the dorsomedial hypothalamic region, medial amygdaloid nucleus and locus coeruleus of the rat

Caffe´, A. R., & van Leeuwen, F. W. (1983) · Cell and Tissue Research · doi:10.1007/bf00222229 · Cited by 199 · see citing works

Chronic and acute intranasal oxytocin produce divergent social effects in mice

Huang, H., Michetti, C., Busnelli, M., Managò, F., Sannino, S., Scheggia, D., Giancardo, L., Sona, D., Murino, V., Chini, B., et al. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2013.310 · Cited by 199 · see citing works

Neuropeptide families and their receptors: evolutionary perspectives

Hoyle, C. H. V. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01975-7 · Cited by 198 · see citing works

Functional Magnetic Resonance Imaging Shows Oxytocin Activates Brain Regions Associated with Mother–Pup Bonding during Suckling

Febo, M., Numan, M., & Ferris, C. F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3604-05.2005 · Cited by 197 · see citing works

Dynamic changes in oxytocin receptor expression and activation at parturition in the rat brain

Meddle, S. L., Bishop, V. R., Gkoumassi, E., van Leeuwen, F. W., & Douglas, A. J. (2007) · Endocrinology · doi:10.1210/en.2007-0615 · Cited by 195 · see citing works

Oxytocin receptor gene variation predicts empathic concern and autonomic arousal while perceiving harm to others

Smith, K. E., Porges, E. C., Norman, G. J., Connelly, J. J., & Decety, J. (2014) · Social Neuroscience · doi:10.1080/17470919.2013.863223 · Cited by 195 · see citing works

The Action of Extracts of the Pituitary Body

Dale, H. H. (1909) · Biochemical Journal · doi:10.1042/bj0040427 · Cited by 195 · see citing works

Maternal behavior deficits in nulliparous oxytocin knockout mice

Pedersen, C. A., Vadlamudi, S. V., Boccia, M. L., & Amico, J. A. (2006) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2005.00162.x · Cited by 190 · see citing works

Striatal microcircuitry and movement disorders

Gittis, A. H., & Kreitzer, A. C. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.06.008 · Cited by 188 · see citing works

Recent gene conversion involving bovine vasopressin and oxytocin precursor genes suggested by nucleotide sequence

Ruppert, S., Scherer, G., & Schütz, G. (1984) · Nature · doi:10.1038/308554a0 · Cited by 188 · see citing works

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 · see citing works

The role of oxytocin in relation to female sexual arousal

Blaicher, W., Gruber, D., Bieglmayer, C., Blaicher, A. M., Knogler, W., & Huber, J. C. (1999) · Gynecologic and Obstetric Investigation · doi:10.1159/000010075 · Cited by 186 · see citing works

FMRP Acts as a Key Messenger for Dopamine Modulation in the Forebrain

Wang, H., Wu, L.-J., Kim, S. S., Lee, F. J. S., Gong, B., Toyoda, H., Ren, M., Shang, Y.-Z., Xu, H., Liu, F., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.06.027 · Cited by 186 · see citing works

Microparticle-based delivery of oxytocin receptor antisense DNA in the medial amygdala blocks social recognition in female mice

Choleris, E., Little, S. R., Mong, J. A., Puram, S. V., Langer, R., & Pfaff, D. W. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700670104 · Cited by 183 · see citing works

Mitigation of Sociocommunicational Deficits of Autism Through Oxytocin-Induced Recovery of Medial Prefrontal Activity: A Randomized Trial

Watanabe, T., Abe, O., Kuwabara, H., Yahata, N., Takano, Y., Iwashiro, N., Natsubori, T., Aoki, Y., Takao, H., Kawakubo, Y., et al. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.3181 · Cited by 183 · see citing works

Serotonin Receptors Involved in Vasopressin and Oxytocin Secretion

Jørgensen, H., Riis, M., Knigge, U., Kjær, A., & Warberg, J. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.00978.x · Cited by 182 · see citing works

Oxytocin-dependent reopening of a social reward learning critical period with MDMA

Nardou, R., Lewis, E. M., Rothhaas, R., Xu, R., Yang, A., Boyden, E., & Dölen, G. (2019) · Nature · doi:10.1038/s41586-019-1075-9 · Cited by 334 · see citing works

Neural circuitry for maternal oxytocin release induced by infant cries

Valtcheva, S., Issa, H. A., Bair-Marshall, C. J., Martin, K. A., Jung, K., Zhang, Y., Kwon, H.-B., & Froemke, R. C. (2023) · Nature · doi:10.1038/s41586-023-06540-4 · Cited by 115 · see citing works

Parallel social information processing circuits are differentially impacted in autism

Lewis, E. M., Stein-O’Brien, G. L., Patino, A. V., Nardou, R., Grossman, C. D., Brown, M., Bangamwabo, B., Ndiaye, N., Giovinazzo, D., Dardani, I., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.10.002 · Cited by 72 · see citing works

Oxytocin

Winokur, S. B., Caslin, A. Y., Davis, F. M., & Froemke, R. C. (2025) · Current Biology · doi:10.1016/j.cub.2025.08.059 · Cited by 7 · see citing works

The Study of Discriminant Validity for the Sensory Processing Scale for Children (SPS-C) of Children with and without Sensory Processing Disorder

조교수, 동. 작., Bae, W.-J., & Jung, N. (2022) · Journal of Korean Society of Sensory Integration Therapists · doi:10.18064/jkasi.2022.20.2.36

Sensory processing disorders in children with cerebral palsy

Pavão, S. L., & Rocha, N. A. C. F. (2016) · Infant Behavior and Development · doi:10.1016/j.infbeh.2016.10.007 · Cited by 107 · see citing works

The convergent validity of two sensory processing scales used with school - age children : comparing the sensory profile and the sensory processing measure

Brown, T., Morrison, I. C., & Stagnitti, K. E. (2010) · Deakin Research Online (Deakin University) · Cited by 32 · see citing works

Specifics of sensory processing in individuals with autism spectrum disorder

Novaković, N., & Pejović-Milovančević, M. (2019) · Engrami · doi:10.5937/engrami1901032n · Cited by 3 · see citing works

Management of Hemiplegic Children with Peripheral Sensory Loss

Jones, M. H. (1960) · Pediatric Clinics of North America · doi:10.1016/s0031-3955(16)30984-1 · Cited by 7 · see citing works