| Rapid effects of ovarian hormones in dorsal striatum and nucleus accumbens |
19 |
| Endocrine-disrupting chemicals: Effects on neuroendocrine systems and the neurobiology of social behavior |
19 |
| A plurality of molecular targets: The receptor ecosystem for bisphenol-A (BPA) |
19 |
| Exposure to polybrominated diphenyl ethers (PBDEs) and child behavior: Current findings and future directions |
17 |
| Opening the black box of endocrine disruption of brain development: Lessons from the characterization of Bisphenol A |
14 |
| Prenatal paracetamol exposure and child neurodevelopment: A review |
14 |
| Human social neuroendocrinology: Review of the rapid effects of testosterone |
14 |
| A gut feeling: Microbiome-brain-immune interactions modulate social and affective behaviors |
12 |
| Consequences of continuous social defeat stress on anxiety- and depressive-like behaviors and ethanol reward in mice |
12 |
| Women's preferences for men's beards show no relation to their ovarian cycle phase and sex hormone levels |
11 |
| Early life stress and cortisol: A meta-analysis |
11 |
| Mate choice, sexual selection, and endocrine-disrupting chemicals |
11 |
| Steroids and the brain: 50 years of research, conceptual shifts and the ascent of non-classical and membrane-initiated actions |
11 |
| Effects of systemic estradiol on fear extinction in female rats are dependent on interactions between dose, estrous phase, and endogenous estradiol levels |
10 |
| Applications for non-invasive thyroid hormone measurements in mammalian ecology, growth, and maintenance |
10 |
| Rapid effects of estrogens on short-term memory: Possible mechanisms |
10 |
| Is the membrane estrogen receptor, GPER a promiscuous receptor that modulates nuclear estrogen receptor-mediated functions in the brain? |
10 |
| Do women's preferences for masculine voices shift across the ovulatory cycle? |
10 |
| Testosterone, cortisol, and status-striving personality features: A review and empirical evaluation of the Dual Hormone hypothesis |
10 |
| The absence of maternal pineal melatonin rhythm during pregnancy and lactation impairs offspring physical growth, neurodevelopment, and behavior |
9 |
| Effects of experimental chronic traffic noise exposure on adult and nestling corticosterone levels, and nestling body condition in a free-living bird |
9 |
| Interactions between estrogen receptors and metabotropic glutamate receptors and their impact on drug addiction in females |
9 |
| Genetic and epigenetic regulatory mechanisms of the oxytocin receptor gene (OXTR) and the (clinical) implications for social behavior |
9 |
| Oxytocin receptor knockout prairie voles generated by CRISPR/Cas9 editing show reduced preference for social novelty and exaggerated repetitive behaviors |
9 |
| Are endocrine disrupting compounds environmental risk factors for autism spectrum disorder? |
9 |
| Sex differences in sleep and sleep loss-induced cognitive deficits: The influence of gonadal hormones |
8 |
| Concepts derived from the Challenge Hypothesis |
8 |
| Mothers are sensitive to men's beards as a potential cue of paternal investment |
8 |
| Rapid effects of estradiol on aggression depend on genotype in a species with an estrogen receptor polymorphism |
8 |
| Linking stress and immunity: Immunoglobulin A as a non-invasive physiological biomarker in animal welfare studies |
8 |
| Progesterone and women's anxiety across the menstrual cycle |
8 |
| Exploratory behavior is linked to stress physiology and social network centrality in free-living house finches (Haemorhous mexicanus) |
8 |
| The physiological significance of the circadian dynamics of the HPA axis: Interplay between circadian rhythms, allostasis and stress resilience |
7 |
| Mice exposed to bisphenol A exhibit depressive-like behavior with neurotransmitter and neuroactive steroid dysfunction |
7 |
| Saliva oxytocin measures do not reflect peripheral plasma concentrations after intranasal oxytocin administration in men |
7 |
| Diverse actions of estradiol on anorexigenic and orexigenic hypothalamic arcuate neurons |
7 |
| Fathers' cortisol and testosterone in the days around infants' births predict later paternal involvement |
7 |
| Nanoparticle encapsulation increases the brain penetrance and duration of action of intranasal oxytocin |
7 |
| Effects of the estrous cycle and ovarian hormones on cue-triggered motivation and intrinsic excitability of medium spiny neurons in the Nucleus Accumbens core of female rats |
7 |
| The effects of different rearing conditions on sexual maturation and maternal care in heterozygous mineralocorticoid receptor knockout mice |
7 |
| Phenotypic variation reveals sites of evolutionary constraint in the androgenic signaling pathway |
7 |
| Urinary oxytocin levels in relation to post-conflict affiliations in wild male chimpanzees (Pan troglodytes verus) |
7 |
| Sex differences in circuits activated by corticotropin releasing factor in rats |
6 |
| The cooperative sex: Sexual interactions among female bonobos are linked to increases in oxytocin, proximity and coalitions |
6 |
| Activation of androgen receptors protects intact male mice from memory impairments caused by aromatase inhibition |
6 |
| Prolactin and avian parental care: New insights and unanswered questions |
6 |
| Oxytocin blurs the self-other distinction implicitly but not explicitly |
6 |
| Rapid effects of 17 beta-estradiol on aggressive behavior in songbirds: Environmental and genetic influences |
6 |
| Rapid effects on memory consolidation and spine morphology by estradiol in female and male rodents |
6 |
| Average ovarian hormone levels, rather than daily values and their fluctuations, are related to facial preferences among women |
6 |
