| The reactive scope model — A new model integrating homeostasis, allostasis, and stress | 2009/03/01 | English | 695 |
| Gonadal Steroid Hormone Receptors and Sex Differences in the Hypothalamo-Pituitary-Adrenal Axis | 1994/12/01 | English | 587 |
| Glucocorticoids, prenatal stress and the programming of disease | 2011/03/01 | English | 549 |
| The vertebrate social behavior network: Evolutionary themes and variations | 2005/06/01 | English | 515 |
| Child maltreatment and the developing HPA axis | 2006/11/01 | English | 455 |
| Pregnancy and pregnancy-associated hormones alter immune responses and disease pathogenesis | 2012/08/01 | English | 429 |
| Neuropeptidergic regulation of affiliative behavior and social bonding in animals | 2006/11/01 | English | 414 |
| Oxytocin and social affiliation in humans | 2012/03/01 | English | 408 |
| Back to the future: The organizational–activational hypothesis adapted to puberty and adolescence | 2009/05/01 | English | 389 |
| The organizational–activational hypothesis as the foundation for a unified theory of sexual differentiation of all mammalian tissues | 2009/05/01 | English | 378 |
| A Proposed Test Battery and Constellations of Specific Behavioral Paradigms to Investigate the Behavioral Phenotypes of Transgenic and Knockout Mice | 1997/06/01 | English | 374 |
| What is in a name? Integrating homeostasis, allostasis and stress | 2010/02/01 | English | 348 |
| Neurotoxicity of Glucocorticoids in the Primate Brain | 1994/12/01 | English | 343 |
| Testosterone and cortisol jointly regulate dominance: Evidence for a dual-hormone hypothesis | 2010/11/01 | English | 343 |
| Masculinized Finger Length Patterns in Human Males and Females with Congenital Adrenal Hyperplasia | 2002/12/01 | English | 342 |
| Estradiol Enhances Learning and Memory in a Spatial Memory Task and Effects Levels of Monoaminergic Neurotransmitters | 1998/10/01 | English | 321 |
| Sexual behavior in male rodents | 2007/06/01 | English | 313 |
| Cellular Mechanisms of Social Attachment | 2001/09/01 | English | 308 |
| Rat RFamide-related peptide-3 stimulates GH secretion, inhibits LH secretion, and has variable effects on sex behavior in the adult male rat | 2007/01/01 | English | 299 |
| Modulating social behavior with oxytocin: How does it work? What does it mean? | 2012/03/01 | English | 294 |
| Postpartum depression: Etiology, treatment and consequences for maternal care | 2016/01/01 | English | 292 |
| Estradiol and cognitive function: Past, present and future | 2014/09/01 | English | 291 |
| Oxytocin is associated with human trustworthiness | 2005/12/01 | English | 287 |
| Lab and field experiments: Are they the same animal? | 2009/06/01 | English | 275 |
| Estrogen-Mediated Structural and Functional Synaptic Plasticity in the Female Rat Hippocampus | 1998/10/01 | English | 274 |
| Both oxytocin and vasopressin are mediators of maternal care and aggression in rodents: From central release to sites of action | 2012/03/01 | English | 271 |
| A critical review of the influence of oxytocin nasal spray on social cognition in humans: Evidence and future directions | 2012/03/01 | English | 268 |
| Epigenetics and the origins of paternal effects | 2011/03/01 | English | 261 |
| Analyzing corticosterone metabolites in fecal samples of mice: a noninvasive technique to monitor stress hormones | 2004/01/01 | English | 258 |
| Testosterone, Endurance, and Darwinian Fitness: Natural and Sexual Selection on the Physiological Bases of Alternative Male Behaviors in Side-Blotched Lizards | 2000/12/01 | English | 253 |