Steroidal/neuropeptide interactions in hypothalamus and amygdala related to social anxiety

Emotion circuits in the brain

LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444 · see citing works

Cloning of a novel receptor expressed in rat prostate and ovary.

Kuiper, G. G. J. M., Enmark, E., Pelto‐Huikko, M., Nilsson, S., & Gustafsson, J.-Α. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.12.5925 · Cited by 4,792 · see citing works

Contributions of the Amygdala to Emotion Processing: From Animal Models to Human Behavior

Phelps, E. A., & LeDoux, J. E. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.025 · Cited by 3,203 · 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

Serotonin transporter genetic variation and the response of the human amygdala.

Hariri, A. R., Mattay, V. S., Tessitore, A., Kolachana, B., Fera, F., Goldman, D., Egan, M. F., & Weinberger, D. R. (2002) · Science · doi:10.1126/science.1071829 · Cited by 2,340 · see citing works

Estrogen Receptor Null Mice: What Have We Learned and Where Will They Lead Us?

Couse, J. F., & Korach, K. S. (1999) · Endocrine Reviews · doi:10.1210/edrv.20.3.0370 · Cited by 2,045 · see citing works

Estrogen receptors: how do they signal and what are their targets

Heldring, N., Pike, A., Andersson, S., Matthews, J., Cheng, G., Hartman, J., Tujague, M., Ström, A., Treuter, E., Warner, M., et al. (2007) · Physiological Reviews · doi:10.1152/physrev.00026.2006 · Cited by 1,857 · 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

Gaze fixation and the neural circuitry of face processing in autism

Dalton, K. M., Nacewicz, B. M., Johnstone, T., Schaefer, H. S., Gernsbacher, M. A., Goldsmith, H. H., Alexander, A. L., & Davidson, R. J. (2005) · Nature Neuroscience · doi:10.1038/nn1421 · Cited by 1,543 · see citing works

The neural correlates of maternal and romantic love

Bartels, A., & Zeki, S. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.003 · Cited by 1,448 · see citing works

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

The Autism Genome Project Consortium (2007) · Nature Genetics · doi:10.1038/ng1985 · Cited by 1,402 · see citing works

A mechanism for impaired fear recognition after amygdala damage

Adolphs, R., Gosselin, F., Buchanan, T. W., Tranel, D., Schyns, P., & Damasio, A. R. (2005) · Nature · doi:10.1038/nature03086 · Cited by 1,331 · see citing works

Social amnesia in mice lacking the oxytocin gene

Ferguson, J. N., Young, L. J., Hearn, E. F., Matzuk, M. M., Insel, T. R., & Winslow, J. T. (2000) · Nature Genetics · doi:10.1038/77040 · Cited by 1,130 · see citing works

Cognitive Enhancers as Adjuncts to Psychotherapy: Use of D-Cycloserine in Phobic Individuals to Facilitate Extinctionof Fear

Ressler, K. J., Rothbaum, B. O., Tannenbaum, L., Anderson, P., Graap, K., Zimand, E., Hodges, L., & Davis, M. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.11.1136 · Cited by 1,063 · see citing works

Vasopressin and oxytocin release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication

Landgraf, R., & Neumann, I. D. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.05.001 · Cited by 1,059 · 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

Autoradiographic differentiation of mu, delta and kappa opioid receptors in the rat forebrain and midbrain

Mansour, A., Khachaturian, H., Lewis, M. E. S., Akil, H., & Watson, S. J. (1988) · Pain · doi:10.1016/0304-3959(88)90103-0 · Cited by 973 · see citing works

The primate amygdala represents the positive and negative value of visual stimuli during learning

Paton, J. J., Belova, M. A., Morrison, S. E., & Salzman, C. D. (2006) · Nature · doi:10.1038/nature04490 · Cited by 917 · see citing works

Immunolocalization of Estrogen Receptor β in the Mouse Brain: Comparison with Estrogen Receptor α

Mitra, S. W., Hoskin, E., Yudkovitz, J., Pear, L., Wilkinson, H. A., Hayashi, S., Pfaff, D. W., Ogawa, S., Rohrer, S. P., Schaeffer, J. M., et al. (2003) · Endocrinology · doi:10.1210/en.2002-221069 · Cited by 856 · see citing works

Estrogen signaling: a subtle balance between ER alpha and ER beta.

Matthews, J., & Gustafsson, J. (2003) · Molecular Interventions · doi:10.1124/mi.3.5.281 · Cited by 844 · see citing works

The amygdala is enlarged in children but not adolescents with autism; the hippocampus is enlarged at all ages

Schumann, C. M., Hamstra, J., Goodlin-Jones, B. L., Lotspeich, L. J., Kwon, H., Buonocore, M. H., Lammers, C. R., Reiss, A. L., & Amaral, D. G. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1297-04.2004 · Cited by 840 · 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

Plasma oxytocin levels in autistic children

Modahl, C., Green, L. A., Fein, D., Morris, M., Waterhouse, L., Feinstein, C., & Levin, H. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(97)00439-3 · Cited by 728 · see citing works

Amygdala-prefrontal coupling depends on a genetic variation of the serotonin transporter

Heinz, A., Braus, D. F., Smolka, M. N., Wrase, J., Puls, I., Hermann, D., Vollstädt‐Klein, S., Grüsser, S. M., Flor, H., Schumann, G., et al. (2004) · Nature Neuroscience · doi:10.1038/nn1366 · Cited by 700 · 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

Molecular detection of pheromone signals in mammals: from genes to behaviour

Dulac, C. G., & Torello, A. T. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1140 · Cited by 662 · see citing works

Enhanced partner preference in a promiscuous species by manipulating the expression of a single gene.

Lim, M. M., Wang, Z., Olazábal, D. E., Ren, X., Terwilliger, E. F., & Young, L. J. (2004) · Nature · doi:10.1038/nature02539 · Cited by 628 · see citing works

The effects of oxytocin and vasopressin on partner preferences in male and female prairie voles (Microtus ochrogaster)

Cho, M. M., DeVries, A. C., Williams, J. R., & Carter, C. S. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.5.1071 · Cited by 529 · see citing works

A gender-specific mechanism for pair bonding: oxytocin and partner preference formation in monogamous voles

Insel, T. R., & Hulihan, T. J. (1995) · Behavioral Neuroscience · doi:10.1037/0735-7044.109.4.782 · Cited by 528 · see citing works

Oxytocin activates the postpartum onset of rat maternal behavior in the ventral tegmental and medial preoptic areas.

Pedersen, C. A., Caldwell, J. D., Walker, C., Ayers, G., & Mason, G. A. (1994) · Behavioral Neuroscience · doi:10.1037/0735-7044.108.6.1163 · Cited by 475 · see citing works

Brain Oxytocin Inhibits Basal and Stress‐Induced Activity of the Hypothalamo‐Pituitary‐Adrenal Axis in Male and Female Rats: Partial Action Within the Paraventricular Nucleus

Neumann, Wigger, Torner, Holsboer, & Landgraf (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00442.x · Cited by 452 · see citing works

Deficit in Attachment Behavior in Mice Lacking the µ-Opioid Receptor Gene

Moles, A., Kieffer, B. L., & D'Amato, F. R. (2004) · Science · doi:10.1126/science.1095943 · Cited by 449 · see citing works

Cellular Mechanisms of Infralimbic and Prelimbic Prefrontal Cortical Inhibition and Dopaminergic Modulation of Basolateral Amygdala Neurons In Vivo

Rosenkranz, J., & Grace, A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00324.2002 · Cited by 422 · see citing works

Oxytocin and sexual behavior

Carter, C. S. (1992) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(05)80176-9 · Cited by 417 · see citing works

The Role of the Central Nucleus of the Amygdala in Mediating Fear and Anxiety in the Primate

Kalin, N. H., Shelton, S. E., & Davidson, R. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0292-04.2004 · Cited by 406 · see citing works

Oxytocin and autistic disorder: alterations in peptide forms

Green, L., Fein, D., Modahl, C., Feinstein, C., Waterhouse, L., & Morris, M. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01139-8 · Cited by 404 · see citing works

Brain oxytocin: differential inhibition of neuroendocrine stress responses and anxiety-related behaviour in virgin, pregnant and lactating rats

Neumann, I. D., Torner, L., & Wigger, A. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00433-9 · Cited by 402 · see citing works

Survival of reproductive behaviors in estrogen receptor β gene-deficient (βERKO) male and female mice

Ogawa, S., Chan, J. S. W., Chester, A. E., Gustafsson, J.-Α., Korach, K. S., & Pfaff, D. W. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12887 · Cited by 399 · see citing works

The endocrinology of sexual arousal

Bancroft, J. (2005) · Journal of Endocrinology · doi:10.1677/joe.1.06233 · Cited by 398 · see citing works

An estrogen-dependent four-gene micronet regulating social recognition: A study with oxytocin and estrogen receptor-α and -β knockout mice

Choleris, E., Gustafsson, J.-Å., Korach, K. S., Muglia, L. J., Pfaff, D. W., & Ogawa, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0631699100 · Cited by 386 · see citing works

A female advantage in the recognition of emotional facial expressions: test of an evolutionary hypothesis

Hampson, E., VANANDERS, S., & Mullin, L. C. (2006) · Evolution and Human Behavior · doi:10.1016/j.evolhumbehav.2006.05.002 · Cited by 383 · see citing works

Glucocorticoids interact with emotion-induced noradrenergic activation in influencing different memory functions

Roozendaal, B., Okuda, S., de Quervain, D. J.-F., & McGaugh, J. L. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.049 · Cited by 382 · see citing works

Sex differences in the perception of affective facial expressions: Do men really lack emotional sensitivity?

Montagne, B., Kessels, R. P. C., Frigerio, E., de Haan, E. H. F., & Perrett, D. I. (2005) · Cognitive Processing · doi:10.1007/s10339-005-0050-6 · Cited by 379 · see citing works

Localization of high-affinity binding sites for oxytocin and vasopressin in the human brain. An autoradiographic study

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

Morphology of vasopressin and oxytocin neurones and their central and vascular projections

Sofroniew, M. V. (1983) · Progress in Brain Research · doi:10.1016/s0079-6123(08)64378-2 · Cited by 370 · see citing works

The V1a Vasopressin Receptor Is Necessary and Sufficient for Normal Social Recognition: A Gene Replacement Study

Bielsky, I. F., Hu, S.-B., Ren, X., Terwilliger, E. F., & Young, L. J. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.031 · Cited by 367 · see citing works

Infant vocalization, adult aggression, and fear behavior of an oxytocin null mutant mouse

Winslow, J. T., Hearn, E. F., Ferguson, J., Young, L. J., Matzuk, M. M., & Insel, T. R. (2000) · Hormones and Behavior · doi:10.1006/hbeh.1999.1566 · Cited by 348 · see citing works

The Prefrontal Cortex Regulates Lateral Amygdala Neuronal Plasticity and Responses to Previously Conditioned Stimuli

Rosenkranz, J. A., Moore, H., & Grace, A. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11054.2003 · Cited by 344 · see citing works

Dopamine Attenuates Prefrontal Cortical Suppression of Sensory Inputs to the Basolateral Amygdala of Rats

Rosenkranz, J. A., & Grace, A. A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-11-04090.2001 · Cited by 334 · see citing works

An Anxiolytic Action of Oxytocin is Enhanced by Estrogen in the Mouse

MCCARTHY, M. M., MCDONALD, C. H., BROOKS, P. J., & GOLDMAN, D. (1996) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00212-0 · Cited by 328 · see citing works

Heritability of Autistic Traits in the General Population

Hoekstra, R. A., Bartels, M., Verweij, C. J. H., & Boomsma, D. I. (2007) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.161.4.372 · Cited by 321 · see citing works

Glucocorticoid Effects on Memory Retrieval Require Concurrent Noradrenergic Activity in the Hippocampus and Basolateral Amygdala

Roozendaal, B., Hahn, E. L., Nathan, S. V., de Quervain, D. J.-F., & McGaugh, J. L. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.2574-04.2004 · Cited by 301 · see citing works

Abnormal activation of the social brain during face perception in autism

Hadjikhani, N. K., Joseph, R. M., Snyder, J., & Tager-Flusberg, H. B. (2006) · Human Brain Mapping · doi:10.1002/hbm.20283 · Cited by 300 · see citing works

Abolition of male sexual behaviors in mice lacking estrogen receptors α and β (αβERKO)

Ogawa, S., Chester, A. E., Hewitt, S. C., Walker, V. R., Gustafsson, J.-Α., Smithies, O., Korach, K. S., & Pfaff, D. W. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250473597 · Cited by 293 · see citing works

Modifications of Testosterone-Dependent Behaviors by Estrogen Receptor-α Gene Disruption in Male Mice1

Ogawa, S., Washburn, T. F., Taylor, J. A., Lubahn, D. B., Korach, K. S., & Pfaff, D. W. (1998) · Endocrinology · doi:10.1210/endo.139.12.6358 · Cited by 290 · see citing works

High vs Low Anxiety-Related Behavior Rats: An Animal Model of Extremes in Trait Anxiety

Landgraf, R., & Wigger, A. (2002) · Behavior Genetics · doi:10.1023/a:1020258104318 · Cited by 274 · 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

Memory-influencing intra-basolateral amygdala drug infusions modulate expression of Arc protein in the hippocampus

McIntyre, C. K., Miyashita, T., Setlow, B., Marjon, K. D., Steward, O., Guzowski, J. F., & McGaugh, J. L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504436102 · Cited by 252 · see citing works

The Endomorphin System and Its Evolving Neurophysiological Role

Fichna, J., Janecka, A. E., Costentin, J., & do-Rego, J.-C. (2007) · Pharmacological Reviews · doi:10.1124/pr.59.1.3 · Cited by 249 · see citing works

CHEMICAL COMMUNICATION IN RODENTS: FROM PHEROMONES TO INDIVIDUAL RECOGNITION

Johnston, R. E. (2003) · Journal of Mammalogy · doi:10.1644/ble-010 · Cited by 249 · see citing works

Serotonin transporter polymorphism related to amygdala excitability and symptom severity in patients with social phobia

Furmark, T., Tillfors, M., Garpenstrand, H., Marteinsdóttir, Í., Långström, B., Oreland, L., & Fredrikson, M. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.02.070 · Cited by 234 · see citing works

Topical Review: Fetal Testosterone and Sex Differences in Typical Social Development and in Autism

Knickmeyer, R. C., & Baron-Cohen, S. (2006) · Journal of Child Neurology · doi:10.1177/08830738060210101601 · Cited by 230 · see citing works

Nitric oxide synthase-containing neurons in the human hypothalamus: reduced number of immunoreactive cells in the paraventricular nucleus of depressive patients and schizophrenics

Bernstein, H., Stanarius, A., Baumann, B., Henning, H. J., Krell, D., Dános, P., Falkai, P., & Bogerts, B. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00461-2 · Cited by 223 · see citing works

Amygdala damage impairs eye contact during conversations with real people

Spezio, M. L., Huang, P.-Y. S., Castelli, F., & Adolphs, R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3789-06.2007 · Cited by 213 · see citing works

Low doses of oxytocin facilitate social recognition in rats

Popik, P., Vetulani, J., & van Ree, J. M. (1992) · Psychopharmacology · doi:10.1007/bf02253591 · Cited by 212 · see citing works

Social‐cognition and the broad autism phenotype: identifying genetically meaningful phenotypes

Losh, M. C., & Piven, J. (2006) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2006.01594.x · Cited by 209 · see citing works

Estrogen receptor α is essential for induction of oxytocin receptor by estrogen

Young, L. J., Wang, Z., Donaldson, R., & Rissman, E. F. (1998) · Neuroreport · doi:10.1097/00001756-199803300-00031 · Cited by 198 · see citing works

Sex differences and developmental effects of oxytocin on aggression and social behavior in prairie voles (Microtus ochrogaster)

Bales, K. L., & Carter, C. S. (2003) · Hormones and Behavior · doi:10.1016/s0018-506x(03)00154-5 · Cited by 195 · see citing works

Sexually Dimorphic Synaptic Organization of the Medial Amygdala

Cooke, B. M., & Woolley, C. S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2919-05.2005 · Cited by 194 · see citing works

Brain Arousal and Information Theory

Pfaff, D. W. (2006) · Harvard University Press eBooks · doi:10.4159/9780674042100 · Cited by 185 · 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

Involvement of estrogen receptor α, β and oxytocin in social discrimination: a detailed behavioral analysis with knockout female mice

Choleris, E., Ogawa, S., Kavaliers, M., Gustafsson, J.-Α., Korach, K. S., Muglia, L. J., & Pfaff, D. W. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00203.x · Cited by 173 · see citing works

Tracking the Fear Engram: The Lateral Amygdala Is an Essential Locus of Fear Memory Storage

Schafe, G. E., Doyère, V., & LeDoux, J. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3307-05.2005 · Cited by 161 · see citing works

Localization of oxytocin receptor messenger ribonucleic acid in the rat brain.

Yoshimura, R., Kiyama, H., Kimura, T., Araki, T., Maeno, H., Tanizawa, O., & Tohyama, M. (1993) · Endocrinology · doi:10.1210/endo.133.3.8396014 · Cited by 161 · see citing works

Female oxytocin gene-knockout mice, in a semi-natural environment, display exaggerated aggressive behavior

Ragnauth, A. K., Devidze, N., Moy, V., Finley, K., Goodwillie, A., Kow, L. ‐., Muglia, L. J., & Pfaff, D. W. (2005) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2005.00118.x · Cited by 160 · see citing works

Oxytocin, But Not Oxytocin Receptor, is Regulated by Oestrogen Receptor β in the Female Mouse Hypothalamus

Patisaul, H. B., Scordalakes, E. M., Young, L. J., & Rissman, E. F. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01061.x · Cited by 160 · see citing works

Genotype/Age Interactions on Aggressive Behavior in Gonadally Intact Estrogen Receptor β Knockout (βERKO) Male Mice

Nomura, M. J., Durbak, L., Chan, J. S. W., Smithies, O., Gustafsson, J.-Å., Korach, K. S., Pfaff, D. W., & Ogawa, S. (2002) · Hormones and Behavior · doi:10.1006/hbeh.2002.1773 · Cited by 158 · see citing works

Oxytocin as a possible mediator of SSRI-induced antidepressant effects

Uvnäs-Moberg, K., Björkstrand, E., Hillegaart, V., & Ahlenius, S. (1999) · Psychopharmacology · doi:10.1007/s002130050867 · Cited by 149 · see citing works

An oxytocin antagonist infused into the central nucleus of the amygdala increases maternal aggressive behavior

Lubin, D. A., Elliot, J. C., Black, M. C., & Johns, J. M. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.2.195 · Cited by 145 · see citing works

Reversal of Sex Roles in Genetic Female Mice by Disruption of Estrogen Receptor Gene

Ogawa, S., Taylor, J. A., Lubahn, D. B., Korach, K. S., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000127154 · Cited by 145 · see citing works

Testosterone Reduces Conscious Detection of Signals Serving Social Correction

van Honk, J., & Schutter, D. J. L. G. (2007) · Psychological Science · doi:10.1111/j.1467-9280.2007.01955.x · Cited by 142 · see citing works

Hypothalamic Paraventricular Nucleus Modulates Maternal Aggression in Rats: Effects of Ibotenic Acid Lesion and Oxytocin Antisense

Giovenardi, M., Padoin, M. J., Cadore, L. P., & Lucion, A. B. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(97)00434-4 · Cited by 135 · see citing works

Effects of estrogen on oxytocin receptor messenger ribonucleic acid expression in the uterus, pituitary, and forebrain of the female rat

Quiñones-Jenab, V., Jenab, S., Ogawa, S., Adan, R. A. M., Burbach, P. H., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000127160 · Cited by 134 · see citing works

Neuroendocrine Responses to Stress in Mice: Hyporesponsiveness in Pregnancy and Parturition

Douglas, A. J., Brunton, P. J., Bosch, O. J., Russell, J. A., & Neumann, I. D. (2003) · Endocrinology · doi:10.1210/en.2003-0461 · Cited by 134 · see citing works

Olfactory-mediated parasite recognition and avoidance: linking genes to behavior.

Kavaliers, M., Choleris, E., Ågmo, A., & Pfaff, D. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.03.005 · Cited by 128 · see citing works

Born to be anxious: neuroendocrine and genetic correlates of trait anxiety in HAB rats

Landgraf, R., & Wigger, A. (2003) · Stress · doi:10.1080/1025389031000104193 · Cited by 122 · see citing works

Oxytocin modulates psychotomimetic-induced deficits in sensorimotor gating

Feifel, D., & Reza, T. L. (1999) · Psychopharmacology · doi:10.1007/s002130050811 · Cited by 121 · see citing works

Topography of the oxytocin receptor system in rat brain: an autoradiographical study with a selective radioiodinated oxytocin antagonist.

Elands, J., Beetsma, A. L., Barberis, C., & de Kloet, E. R. (1988) · PubMed · Cited by 121 · see citing works

Noradrenergic regulation of parvocellular neurons in the rat hypothalamic paraventricular nucleus

Daftary, S. S., Boudaba, C., & Tasker, J. G. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00003-8 · Cited by 119 · see citing works

Oxytocin inhibits infanticide in female house mice (Mus domesticus)

McCarthy, M. J. (1990) · Hormones and Behavior · doi:10.1016/0018-506x(90)90015-p · Cited by 119 · see citing works

Neurobiological Correlates of Autism: A Review of Recent Research

Penn, H. E. (2006) · Child Neuropsychology · doi:10.1080/09297040500253546 · Cited by 117 · see citing works

Genetic contributions to generalized arousal of brain and behavior

Garey, J. D., Goodwillie, A., Fröhlich, J., Morgan, M. A., Gustafsson, J.-Α., Smithies, O., Korach, K. S., Ogawa, S., & Pfaff, D. W. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1633773100 · Cited by 109 · see citing works

Are patients with social developmental disorders prosopagnosic? Perceptual heterogeneity in the Asperger and socio-emotional processing disorders

Barton, J. J. S. (2004) · Brain · doi:10.1093/brain/awh194 · Cited by 109 · see citing works

ERβ-selective SERMs produce mnemonic-enhancing effects in the inhibitory avoidance and water maze tasks

RHODES, M., & Frye, C. A. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.10.003 · Cited by 106 · see citing works

Gene targeting approaches to neuroendocrinology: oxytocin, maternal behavior, and affiliation

Young, L. J., Winslow, J. T., Wang, Z., Gingrich, B., Guo, Q., Matzuk, M. M., & Insel, T. R. (1997) · Hormones and Behavior · doi:10.1006/hbeh.1997.1377 · Cited by 105 · see citing works

Neurohypophyseal peptides and social recognition in rats

Popik, P., & van Ree, J. M. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61585-x · Cited by 104 · see citing works

The role of endogenous opioids in neurohypophysial and hypothalamo-pituitary-adrenal axis hormone secretory responses to stress in pregnant rats

Douglas, A., Johnstone, H., Wigger, A., Landgraf, R., Russell, J., & Neumann, I. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1580285 · Cited by 102 · see citing works

Estrogen excites oxytocinergic, but not vasopressinergic cells in the paraventricular nucleus of female rat hypothalamus

Akaishi, T., & Sakuma, Y. (1985) · Brain Research · doi:10.1016/0006-8993(85)90481-0 · Cited by 99 · see citing works

Oxytocin receptor mRNA expression in the ventromedial hypothalamus during the estrous cycle

Bale, T., Dorsa, D. M., & Johnston, C. I. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05058.1995 · Cited by 98 · see citing works

Estrogen Receptor α Influences Socially Motivated Behaviors

Imwalle, D. B., Scordalakes, E. M., & Rissman, E. F. (2002) · Hormones and Behavior · doi:10.1006/hbeh.2002.1837 · Cited by 95 · see citing works

Oxytocin-induced excitation of neurones in the rat central and medial amygdaloid nuclei

Terenzi, M. G., & Ingram, C. D. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.004 · Cited by 91 · see citing works

Brief Exposure to Female Odors “Emboldens” Male Mice by Reducing Predator-Induced Behavioral and Hormonal Responses

Kavaliers, M., Choleris, E., & Colwell, D. D. (2001) · Hormones and Behavior · doi:10.1006/hbeh.2001.1714 · Cited by 89 · see citing works

Arousal Regulation, Emotional Flexibility, Medial Amygdala Function, and the Impact of Early Experience: Comments on the Paper of Lewis <i>et al.</i>

MAYES, L. C. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1376.018 · Cited by 79 · see citing works

Opposite action of oxytocin and its peptide antagonists on social memory in rats

Popik, P., & Vetulani, J. (1991) · Neuropeptides · doi:10.1016/0143-4179(91)90159-g · Cited by 77 · see citing works

Differential Effects of Estrogen Receptor Alpha and Beta Specific Agonists on Social Learning of Food Preferences in Female Mice

Clipperton‐Allen, A. E., Spinato, J. M., Chernets, C., Pfaff, D. W., & Choleris, E. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301625 · Cited by 77 · see citing works

Noradrenergic Inputs to the Bed Nucleus of the Stria Terminalis and Paraventricular Nucleus of the Hypothalamus Underlie Hypothalamic–Pituitary–Adrenal Axis But Not Hypophagic or Conditioned Avoidance Responses to Systemic Yohimbine

Banihashemi, L., & Rinaman, L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3561-06.2006 · Cited by 77 · see citing works

Vasopressin/oxytocin and aggression

Ferris, C. F. (2005) · Novartis Foundation symposium · doi:10.1002/0470010703.ch13 · Cited by 76 · see citing works

Functional Genomics of Social Recognition

Choleris, E., Kavaliers, M., & Pfaff, D. W. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.0953-8194.2004.01178.x · Cited by 75 · see citing works

Involvement of Opioid Receptors in Oxytocin-Induced Antinociception in the Nucleus Accumbens of Rats

Gu, X., & Yu, L. (2006) · Journal of Pain · doi:10.1016/j.jpain.2006.07.001 · Cited by 73 · see citing works

Morphometric evaluation of neurophysin-immunoreactivity in the human brain: pronounced inter-individual variability and evidence for altered staining patterns in schizophrenia.

Jk, M., Berger, K., & Mv, S. (1993) · PubMed · Cited by 64 · see citing works

Lower Incidence and Increased Male: Female Ratio in Schizophrenia

Nicole, L., LESAGE, A. D., & Lalonde, P. (1992) · The British Journal of Psychiatry · doi:10.1192/bjp.161.4.556 · Cited by 61 · see citing works

Genetic Influences on Aggressive Behaviors and Arousability in Animals

Ogawa, S., Choleris, E., & Pfaff, D. W. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1330.016 · Cited by 59 · see citing works

Site‐specific estrogen and progestin regulation of orphanin FQ/nociceptin and nociceptin opioid receptor mRNA expression in the female rat limbic hypothalamic system

Sinchak, K., Romeo, H. E., & Micevych, P. E. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20949 · Cited by 50 · see citing works

Hormonal regulation of agonistic and affiliative behavior in female mongolian gerbils (Meriones unguiculatus)

Razzoli, M., Cushing, B. S., Carter, C. S., & Valsecchi, P. (2003) · Hormones and Behavior · doi:10.1016/s0018-506x(03)00064-3 · Cited by 47 · see citing works

Staring fear in the face

Vuilleumier, P. O. (2005) · Nature · doi:10.1038/433022a · Cited by 46 · see citing works

Facilitation and attenuation of social recognition in rats by different oxytocin-related peptides

Popik, P., Vetulani, J., & Van Ree, J. M. (1996) · European Journal of Pharmacology · doi:10.1016/0014-2999(96)00215-4 · Cited by 42 · see citing works

Pituitary Portal Plasma Levels of Oxytocin during the Estrous Cycle, Lactation, and Hyperprolactinemia

Sarkar, D. K., Frautschy, S. A., & Mitsugi, N. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb34370.x · Cited by 35 · see citing works

Social transmission of flavored tea preferences: Facilitation by a vasopressin analog and oxytocin

Popik, P., & van Ree, J. M. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)91173-k · Cited by 34 · see citing works

Ovarian and circulating levels of oxytocin and arginine vasopressin during the estrous cycle in the rat

Ho, M., & Lee, J.-N. (1992) · European Journal of Endocrinology · doi:10.1530/acta.0.1260530 · Cited by 28 · see citing works

Noradrenergic axon terminals contact gastric preautonomic neurons in the paraventricular nucleus of the hypothalamus in rats

Balcita‐Pedicino, J. J., & Rinaman, L. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21267 · Cited by 23 · see citing works

Estrogen receptors alpha and beta mediate different aspects of the facilitatory effects of female cues on male risk taking.

Kavaliers, M., Devidze, N., Choleris, E., Fudge, M. A., Gustafsson, J., Korach, K., Pfaff, D., & Ogawa, S. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.02.003 · Cited by 23 · see citing works

Genetik autistischer Störungen

Freitag, C. M. (2008) · Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie · doi:10.1024/1422-4917.36.1.7 · Cited by 17 · see citing works

The effects of opioids, local anaesthetics and adjuvants on isolated pregnant rat uterine muscles

Nacıtarhan, C., Şadan, G., Kayacan, N., et al. (2007) · Methods and Findings in Experimental and Clinical Pharmacology · doi:10.1358/mf.2007.29.4.1106410 · Cited by 12 · see citing works

Opioid modulation of socially transmitted and spontaneous food preferences in female mice

Moles, A., Valsecchi, P., & Cooper, S. J. (1999) · Behavioural Processes · doi:10.1016/s0376-6357(98)00031-x · Cited by 8 · see citing works

The role of norepinephrine and nitric oxide in activities of rat arginine vasopressin neurons in response to immune challenge

Xu, S., Guo, S., Jiang, X., et al. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.04.033 · Cited by 8 · see citing works

Confocal imaging of acute hypothalamic slices maintained in vitro reveals rapid noradrenergic recruitment of p44/42 MAP kinases in CRH neurons of the hypothalamic paraventricular nucleus (PVH): Comparison with central injection studies

Khan, A. M., Ponzio, T. A., Hatton, G. I., et al. (2006) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2006.03.229 · Cited by 2 · see citing works

Functional neuroimaging studies of reading and reading disability (developmental dyslexia)

(2000) · doi:10.1002/1098-2779(2000)6:3

Untitled work

(1997) · doi:10.1002/(sici)1096-9861(19971201)388:4

The oxytocin receptor: from intracellular signaling to behavior

Jurek, B., & Neumann, I. D. (2018) · Physiological Reviews · doi:10.1152/physrev.00031.2017 · Cited by 999 · 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

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 · see citing works

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 · see citing works

Acute effects of steroid hormones and neuropeptides on human social-emotional behavior: A review of single administration studies

Bos, P. A., Panksepp, J., Bluthé, R.-M., & Honk, J. V. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2011.01.002 · Cited by 429 · 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

Oxytocin and social motivation

Gordon, I., Martin, C., Feldman, R., & Leckman, J. F. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.07.007 · Cited by 211 · see citing works

Neuroendocrinology of social information processing in rats and mice

Choleris, E., Clipperton-Allen, A. E., Phan, A., & Kavaliers, M. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.003 · Cited by 205 · see citing works

Helping oxytocin deliver: considerations in the development of oxytocin-based therapeutics for brain disorders

MacDonald, K., & Feifel, D. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00035 · Cited by 181 · see citing works

Consequences of Early Experiences and Exposure to Oxytocin and Vasopressin Are Sexually Dimorphic

Carter, C. S., Boone, E. M., Pournajafi-Nazarloo, H., & Bales, K. L. (2009) · Developmental Neuroscience · doi:10.1159/000216544 · Cited by 176 · 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

Social allostasis: anticipatory regulation of the internal milieu

Schulkin, J. (2011) · Frontiers in Evolutionary Neuroscience · doi:10.3389/fnevo.2010.00111 · Cited by 157 · see citing works

Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior

Dai, L., Carter, C. S., Ying, J., Bellugi, U., Pournajafi-Nazarloo, H., & Korenberg, J. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038513 · Cited by 119 · 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

Oxytocin facilitates social approach behavior in women

Preckel, K., Scheele, D., Kendrick, K. M., Maier, W., & Hurlemann, R. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00191 · Cited by 111 · see citing works

Oxytocin in the prelimbic medial prefrontal cortex reduces anxiety-like behavior in female and male rats

Sabihi, S., Durosko, N. E., Dong, S. M., & Leuner, B. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.03.009 · Cited by 106 · see citing works

Testosterone administration modulates neural responses to crying infants in young females

Bos, P. A., Hermans, E. J., Montoya, E. R., Ramsey, N. F., & van Honk, J. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.09.013 · Cited by 99 · see citing works

Oxytocin and social cognition in rhesus macaques: Implications for understanding and treating human psychopathology

Chang, S. W. C., & Platt, M. L. (2014) · Brain Research · doi:10.1016/j.brainres.2013.11.006 · Cited by 71 · see citing works

Endocrine Disruption of Vasopressin Systems and Related Behaviors

Patisaul, H. B. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00134 · Cited by 54 · see citing works

Challenging the challenge hypothesis on testosterone in fathers: Limited meta-analytic support

Meijer, W. M., van IJzendoorn, M. H., & Bakermans - Kranenburg, M. J. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104435 · Cited by 49 · see citing works

Opposite effects of oxytocin and vasopressin on the emotional expression of the fear response

VIVIANI, D., & STOOP, R. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(08)00418-4 · Cited by 96 · see citing works

Amygdala, Neuropeptides, and Fear Behavior

(2005) · Science s STKE · doi:10.1126/stke.2792005tw133

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

Immunocytochemical localization of substance P receptor in hypothalamic oxytocin-containing neurons of C57 mice

Liu, H.-L., Cao, R. Y., Jin, L., & Chen, L.-W. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03146-3 · Cited by 12 · see citing works

Oxytocin, But Not Oxytocin Receptor, is Regulated by Oestrogen Receptor β in the Female Mouse Hypothalamus

Patisaul, H. B., Scordalakes, E. M., Young, L. J., & Rissman, E. F. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01061.x · Cited by 160 · see citing works