Hormones, Brain and Behavior

Sex bias in neuroscience and biomedical research

Beery, A. K., & Zucker, I. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.07.002 · Cited by 1,763

The Adaptive Calibration Model of stress responsivity

Del Giudice, M., Ellis, B. J., & Shirtcliff, E. A. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.11.007 · Cited by 1,373

The Darwinian concept of stress: benefits of allostasis and costs of allostatic load and the trade-offs in health and disease

Korte, S. M., Koolhaas, J. M., Wingfield, J. C., & McEwen, B. S. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.08.009 · Cited by 1,097

Pubertal hormones organize the adolescent brain and behavior

Sisk, C. L., & Zehr, J. L. (2005) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2005.10.003 · Cited by 1,082

Estradiol and the Developing Brain

McCARTHY, M. M. (2008) · Physiological Reviews · doi:10.1152/physrev.00010.2007 · Cited by 885

Biosocial construction of sex differences and similarities in behavior

Wood, W., & Eagly, A. H. (2012) · Advances in experimental social psychology · doi:10.1016/b978-0-12-394281-4.00002-7 · Cited by 770

The evolutionary basis of risky adolescent behavior: Implications for science, policy, and practice.

Ellis, B. J., Del Giudice, M., Dishion, T. J., Figueredo, A. J., Gray, P., Griskevicius, V., Hawley, P. H., Jacobs, W. J., James, J., Volk, A. A., et al. (2012) · Developmental Psychology · doi:10.1037/a0026220 · Cited by 745

Reframing sexual differentiation of the brain

McCarthy, M. M., & Arnold, A. P. (2011) · Nature Neuroscience · doi:10.1038/nn.2834 · Cited by 728

Sex Differences in the Brain: The Not So Inconvenient Truth

McCarthy, M. M., Arnold, A. P., Ball, G. F., Blaustein, J. D., & De Vries, G. J. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5372-11.2012 · Cited by 724

Chronic stress and comfort foods: Self-medication and abdominal obesity

Dallman, M. F., Pecoraro, N. C., & la Fleur, S. E. (2005) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2004.11.004 · Cited by 656

The organizational–activational hypothesis as the foundation for a unified theory of sexual differentiation of all mammalian tissues

Arnold, A. P. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.03.011 · Cited by 625

Oxytocin is associated with human trustworthiness

ZAK, P., KURZBAN, R., & MATZNER, W. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.07.009 · Cited by 595

Back to the future: The organizational-activational hypothesis adapted to puberty and adolescence

Schulz, K. M., Molenda-Figueira, H. A., & Sisk, C. L. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.03.010 · Cited by 587

What does the “four core genotypes” mouse model tell us about sex differences in the brain and other tissues?

Arnold, A. P., & Chen, X. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2008.11.001 · Cited by 587

Early experience in humans is associated with changes in neuropeptides critical for regulating social behavior

Fries, A. B. W., Ziegler, T. E., Kurian, J. R., Jacoris, S., & Pollak, S. D. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504767102 · Cited by 570

Lethargus is a Caenorhabditis elegans sleep-like state

Raizen, D. M., Zimmerman, J. E., Maycock, M. H., Ta, U. D., You, Y.-J., Sundaram, M. V., & Pack, A. I. (2008) · Nature · doi:10.1038/nature06535 · Cited by 536

Minireview: sex differences in adult and developing brains: compensation, compensation, compensation

De Vries, G. J. (2004) · Endocrinology · doi:10.1210/en.2003-1504 · Cited by 486

Psychobiological allostasis: resistance, resilience and vulnerability

Karatsoreos, I. N., & McEwen, B. S. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.10.005 · Cited by 458

Dopamine and serotonin: influences on male sexual behavior

Hull, E. M., Muschamp, J. W., & Sato, S. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.08.018 · Cited by 465

Brain Oxytocin Correlates with Maternal Aggression: link to Anxiety

Bosch, O. J., Meddle, S. L., Beiderbeck, D. I., Douglas, A. J., & Neumann, I. D. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1342-05.2005 · Cited by 439

Sex differences in oxytocin and vasopressin: Implications for autism spectrum disorders?

CARTER, C. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.08.025 · Cited by 432

Endocrine disruptors and childhood social impairment

Miodovnik, A., Engel, S. M., Zhu, C., Ye, X., Soorya, L. V., Silva, M. J., Calafat, A. M., & Wolff, M. S. (2011) · NeuroToxicology · doi:10.1016/j.neuro.2010.12.009 · Cited by 423

Oxytocin and sexual behavior

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

Transgenerational epigenetic imprints on mate preference

Crews, D., Gore, A. C., Hsu, T. S., Dangleben, N. L., Spinetta, M., Schallert, T., Anway, M. D., & Skinner, M. K. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610410104 · Cited by 418

Pubertal hormones modulate the addition of new cells to sexually dimorphic brain regions

Ahmed, E. I., Zehr, J. L., Schulz, K. M., Lorenz, B. H., DonCarlos, L. L., & Sisk, C. L. (2008) · Nature Neuroscience · doi:10.1038/nn.2178 · Cited by 396

Gender development and the human brain

Hines, M. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113654 · Cited by 378

Developmental consequences of oxytocin

Carter, C. S. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00151-3 · Cited by 367

Sleep Deprivation and Circadian Disruption

McEwen, B. S., & Karatsoreos, I. N. (2015) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2014.11.007 · Cited by 338

Sexual orientation in women with classical or non-classical congenital adrenal hyperplasia as a function of degree of prenatal androgen excess

Meyer-Bahlburg, H. F. L., Dolezal, C., Baker, S. W., & New, M. I. (2008) · Archives of Sexual Behavior · doi:10.1007/s10508-007-9265-1 · Cited by 326

For better or worse? Coregulation of couples’ cortisol levels and mood states

Saxbe, D., & Repetti, R. L. (2010) · Journal of Personality and Social Psychology · doi:10.1037/a0016959 · Cited by 324

Hormonal influences on sexually differentiated behavior in nonhuman primates.

Wallen, K. (2005) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2005.02.001 · Cited by 305

Sex chromosome genes directly affect brain sexual differentiation

Carruth, L. L., Reisert, I., & Arnold, A. P. (2002) · Nature Neuroscience · doi:10.1038/nn922 · Cited by 298

Minireview: translational animal models of human menopause: challenges and emerging opportunities

Diaz Brinton, R. (2012) · Endocrinology · doi:10.1210/en.2012-1340 · Cited by 272

Dopamine, the medial preoptic area, and male sexual behavior

DOMINGUEZ, J., & HULL, E. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.006 · Cited by 277

Investigations of HPA function and the enduring consequences of stressors in adolescence in animal models

McCormick, C. M., Mathews, I. Z., Thomas, C., & Waters, P. (2010) · Brain and Cognition · doi:10.1016/j.bandc.2009.06.003 · Cited by 276

Social conflict models: Can they inform us about human psychopathology?

Huhman, K. L. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.06.022 · Cited by 243

Interplay of oxytocin, vasopressin, and sex hormones in the regulation of social recognition

Gabor, C. S., Phan, A., Clipperton-Allen, A. E., Kavaliers, M., & Choleris, E. (2012) · Behavioral Neuroscience · doi:10.1037/a0026464 · Cited by 221

Do you know the sex of your cells?

Shah, K., McCormack, C. E., & Bradbury, N. A. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00281.2013 · Cited by 219

Both oxytocin and vasopressin may influence alloparental behavior in male prairie voles

Bales, K. L., Kim, A. J., Lewis-Reese, A. D., & Sue Carter, C. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.01.004 · Cited by 217

Untitled work

Maier (2005) · doi:10.1016/j.neubiorev.2004.08.001 · Cited by 216

Genes, brains and mammalian social bonds

Curley, J. P., & Keverne, E. B. (2005) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2005.05.018 · Cited by 214

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

Mechanisms underlying epigenetic effects of early social experience: the role of neuropeptides and steroids

CUSHING, B., & KRAMER, K. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.04.001 · Cited by 209

Foetal testosterone and autistic traits in 18 to 24-month-old children

Auyeung, B., Taylor, K., Hackett, G., & Baron-Cohen, S. (2010) · Molecular Autism · doi:10.1186/2040-2392-1-11 · Cited by 208

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

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

Membrane estradiol signaling in the brain

Micevych, P., & Dominguez, R. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.04.011 · Cited by 177

Behavior-specific changes in transcriptional modules lead to distinct and predictable neurogenomic states

Chandrasekaran, S., Ament, S. A., Eddy, J. A., Rodriguez-Zas, S. L., Schatz, B. R., Price, N. D., & Robinson, G. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114093108 · Cited by 176

Convergence of Sex Differences and the Neuroimmune System in Autism Spectrum Disorder

McCarthy, M. M., & Wright, C. L. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.10.004 · Cited by 158

Developmental exposure to oxytocin facilitates partner preferences in male prairie voles (Microtus ochrogaster)

Bales, K. L., & Carter, C. S. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.4.854 · Cited by 155

Why Endocrine Disrupting Chemicals (EDCs) Challenge Traditional Risk Assessment and How to Respond

Futran Fuhrman, V., Tal, A., & Arnon, S. (2015) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2014.12.012 · Cited by 152

Neonatal oxytocin manipulations have long-lasting, sexually dimorphic effects on vasopressin receptors

Bales, K. L., Plotsky, P. M., Young, L. J., Lim, M. M., Grotte, N., Ferrer, E., & Carter, C. S. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.09.009 · Cited by 150

Social attachment and aversion in human moral cognition

Moll, J., & Schulkin, J. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.12.001 · Cited by 141

Overlapping neurobiology of learned helplessness and conditioned defeat: Implications for PTSD and mood disorders

Hammack, S. E., Cooper, M. A., & Lezak, K. R. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.02.024 · Cited by 142

Estradiol Induces Hypothalamic Dendritic Spines by Enhancing Glutamate Release: A Mechanism for Organizational Sex Differences

Schwarz, J. M., Liang, S.-L., Thompson, S. M., & McCarthy, M. M. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.008 · Cited by 139

How it’s Made: Organisational Effects of Hormones on the Developing Brain

McCarthy, M. M. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.02021.x · Cited by 138

A psychobiological rationale for oxytocin in the treatment of posttraumatic stress disorder

Olff, M., Langeland, W., Witteveen, A., & Denys, D. (2010) · CNS Spectrums · doi:10.1017/s109285290000047x · Cited by 135

Organized for sex – steroid hormones and the developing hypothalamus

Lenz, K. M., & McCarthy, M. M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07511.x · Cited by 127

Genetic determinants of pubertal timing in the general population

Gajdos, Z. K. Z., Henderson, K. D., Hirschhorn, J. N., & Palmert, M. R. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.01.038 · Cited by 121

Social influences on the arginine vasotocin system are independent of gonads in a sex-changing fish

Semsar, K., & Godwin, J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04386.2003 · Cited by 111

Processing of body odor signals by the human brain

Pause, B. M. (2012) · Chemosensory Perception · doi:10.1007/s12078-011-9108-2 · Cited by 107

Bisphenol A interferes with synaptic remodeling

Hajszan, T., & Leranth, C. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.06.004 · Cited by 101

Minireview: the neuroendocrinology of the suprachiasmatic nucleus as a conductor of body time in mammals

Karatsoreos, I. N., & Silver, R. (2007) · Endocrinology · doi:10.1210/en.2007-1083 · Cited by 101

Effect of photoperiod on vasopressin-induced aggression in Syrian hamsters

Caldwell, H. K., & Albers, H. E. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.04.006 · Cited by 97

Early deprivation under specific conditions leads to reduced interest in reward in adulthood in Wistar rats

Rüedi-Bettschen, D., Pedersen, E.-M., Feldon, J., & Pryce, C. R. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.06.001 · Cited by 97

Estrogens and cognition: Friends or foes?

Korol, D. L., & Pisani, S. L. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.06.017 · Cited by 97

Androgens modulate structure and function of the suprachiasmatic nucleus brain clock

Karatsoreos, I. N., Butler, M. P., LeSauter, J., & Silver, R. (2011) · Endocrinology · doi:10.1210/en.2010-1398 · Cited by 97

Involvement of arginine vasopressin and V1b receptor in heroin withdrawal and heroin seeking precipitated by stress and by heroin

Zhou, Y., Leri, F., Cummins, E., Hoeschele, M., & Kreek, M. J. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301419 · Cited by 89

Repeated social stress and the development of agonistic behavior: individual differences in coping responses in male golden hamsters

Wommack, J. C., & Delville, Y. (2003) · Physiology & Behavior · doi:10.1016/j.physbeh.2003.08.002 · Cited by 89

Effects of Circadian Disruption on Mental and Physical Health

Karatsoreos, I. N. (2012) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-012-0252-0 · Cited by 85

Social environment regulates corticotropin releasing factor, corticosterone and vasopressin in juvenile prairie voles

Ruscio, M. G., Sweeny, T., Hazelton, J., Suppatkul, P., & Sue Carter, C. (2007) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.08.004 · Cited by 81

Effects of Intravenous Cocaine and Cigarette Smoking on Luteinizing Hormone, Testosterone, and Prolactin in Men

Mendelson, J. H., Sholar, M. B., Mutschler, N. H., Jaszyna-Gasior, M., Goletiani, N. V., Siegel, A. J., & Mello, N. K. (2003) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.103.052928 · Cited by 81

Oxytocin receptors in the nucleus accumbens shell are involved in the consolidation of maternal memory in postpartum rats

D'Cunha, T. M., King, S. J., Fleming, A. S., & Lévy, F. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.09.007 · Cited by 81

Behavior-related gene regulatory networks: A new level of organization in the brain

Sinha, S., Jones, B. M., Traniello, I. M., Bukhari, S. A., Halfon, M. S., Hofmann, H. A., Huang, S., Katz, P. S., Keagy, J., Lynch, V. J., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921625117 · Cited by 85

Role of V1a vasopressin receptors in the control of aggression in Syrian hamsters

Elliott Albers, H., Dean, A., Karom, M. C., Smith, D., & Huhman, K. L. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.081 · Cited by 78

Intraspecific variation in estrogen receptor alpha and the expression of male sociosexual behavior in two populations of prairie voles

Cushing, B. S., Razzoli, M., Murphy, A. Z., Epperson, P. M., Le, W.-W., & Hoffman, G. E. (2004) · Brain Research · doi:10.1016/j.brainres.2004.05.010 · Cited by 77

A role for homeostatic drive in the perpetuation of complex chronic illness: gulf War illness and chronic fatigue syndrome

Craddock, T. J. A., Fritsch, P., Rice, M. A., del Rosario, R. M., Miller, D. B., Fletcher, M. A., Klimas, N. G., & Broderick, G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084839 · Cited by 75

Dose-Dependent Effects of Androgens on the Circadian Timing System and Its Response to Light

Butler, M. P., Karatsoreos, I. N., LeSauter, J., & Silver, R. (2012) · Endocrinology · doi:10.1210/en.2011-1842 · Cited by 74

Roles of α- and β-estrogen receptors in mouse social recognition memory: Effects of gender and the estrous cycle

Sánchez-Andrade, G., & Kendrick, K. M. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.10.016 · Cited by 72

Oxytocin in the medial preoptic area facilitates male sexual behavior in the rat

Gil, M., Bhatt, R., Picotte, K. B., & Hull, E. M. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.12.012 · Cited by 70

Neurobiology of sociability

Caldwell, H. K. (2012) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4614-1704-0_12 · Cited by 58

Validation of a rodent model of episodic memory

Zhou, W., & Crystal, J. D. (2011) · Animal Cognition · doi:10.1007/s10071-010-0367-0 · Cited by 60

Effects of anabolic androgenic steroids on the development and expression of running wheel activity and circadian rhythms in male rats

McGinnis, M. Y., Lumia, A. R., Tetel, M. J., Molenda-Figueira, H. A., & Possidente, B. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.07.010 · Cited by 58

Increased aggressive behavior and decreased affiliative behavior in adult male monkeys after long-term consumption of diets rich in soy protein and isoflavones

Simon, N. G., Kaplan, J. R., Hu, S., Register, T. C., & Adams, M. R. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2003.12.005 · Cited by 56

Activation of 5-HT1A autoreceptors in the dorsal raphe nucleus reduces the behavioral consequences of social defeat

Cooper, M. A., McIntyre, K. E., & Huhman, K. L. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.06.009 · Cited by 52

Genome scan for cis-regulatory DNA motifs associated with social behavior in honey bees

Sinha, S., Ling, X., Whitfield, C. W., Zhai, C., & Robinson, G. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607448103 · Cited by 52

Seasonal variation of salivary testosterone in men, normally cycling women, and women using hormonal contraceptives

Stanton, S. J., Mullette-Gillman, O. A., & Huettel, S. A. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.07.009 · Cited by 48

The Role of VIP in Social Behavior: Neural Hotspots for the Modulation of Affiliation, Aggression, and Parental Care

Kingsbury, M. A., & Wilson, L. C. (2016) · Integrative and Comparative Biology · doi:10.1093/icb/icw122 · Cited by 48

Effects of neonatal oxytocin manipulations on male reproductive potential in prairie voles

BALES, K., ABDELNABI, M., CUSHING, B., OTTINGER, M., & CARTER, C. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.02.016 · Cited by 47

Fetal hormones and sexual differentiation

Sobel, V., Zhu, Y.-S., & Imperato-McGinley, J. (2004) · Obstetrics and Gynecology Clinics of North America · doi:10.1016/j.ogc.2004.08.005 · Cited by 44

Sex differences of microglia in the healthy brain from embryonic development to adulthood and across lifestyle influences

Bobotis, B. C., Braniff, O., Gargus, M., Akinluyi, E. T., Awogbindin, I. O., & Tremblay, M.-È. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.110752 · Cited by 40

Individual differences in offensive aggression in golden hamsters: A model of reactive and impulsive aggression?

Cervantes, M. C., & Delville, Y. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.09.034 · Cited by 40

Early embryonic administration of xenoestrogens alters vasotocin system and male sexual behavior of the Japanese quail

Panzica, G., Mura, E., Pessatti, M., & Viglietti-Panzica, C. (2005) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2005.02.010 · Cited by 38

Neonatal manipulation of oxytocin influences the partner preference in mandarin voles (Microtus mandarinus)

Jia, R., Tai, F., An, S., Broders, H., & Sun, R. (2008) · Neuropeptides · doi:10.1016/j.npep.2008.06.001 · Cited by 35

Oxytocin injected into the hippocampal ventral subiculum induces penile erection in male rats by increasing glutamatergic neurotransmission in the ventral tegmental area

Succu, S., Sanna, F., Argiolas, A., & Melis, M. R. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.03.026 · Cited by 35

Adult-Onset Hypothyroidism Enhances Fear Memory and Upregulates Mineralocorticoid and Glucocorticoid Receptors in the Amygdala

Montero-Pedrazuela, A., Fernández-Lamo, I., Alieva, M., Pereda-Pérez, I., Venero, C., & Guadaño-Ferraz, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026582 · Cited by 30

Intimate Relationships Then and Now: How Old Hormonal Processes are Influenced by Our Modern Psychology

Wardecker, B. M., Smith, L. K., Edelstein, R. S., & Loving, T. J. (2015) · Adaptive Human Behavior and Physiology · doi:10.1007/s40750-015-0021-9 · Cited by 21

A masculinized skeletomusculature is not necessary for male-typical patterns of food-protective movement

Field, E. F., Watson, N. V., Whishaw, I. Q., & Pellis, S. M. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.08.007 · Cited by 10

Sex Differences in Righting From Supine to Prone in Rats (Rattus norvegicus): A Masculinized Skeletomusculature Is Not Required.

Field, E. F., Martens, D. J., Watson, N. V., & Pellis, S. M. (2005) · Journal of Comparative Psychology · doi:10.1037/0735-7036.119.2.238 · Cited by 7