The maternal brain: an organ with peripartal plasticity

Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants

Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., et al. (2003) · Science · doi:10.1126/science.1083328 · Cited by 4,321 · see citing works

Astrocytes, from brain glue to communication elements: the revolution continues

Volterra, A., & Meldolesi, J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1722 · Cited by 1,763 · see citing works

The role of medial prefrontal cortex in memory and decision making

Euston, D. R., Gruber, A. J., & McNaughton, B. L. (2012) · Neuron · doi:10.1016/j.neuron.2012.12.002 · Cited by 1,541 · see citing works

Immune modulation of learning, memory, neural plasticity and neurogenesis

Yirmiya, R., & Goshen, I. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2010.10.015 · Cited by 1,483 · see citing works

Adult hippocampal neurogenesis buffers stress responses and depressive behaviour

Snyder, J. S., Soumier, A., Brewer, M., Pickel, J., & Cameron, H. A. (2011) · Nature · doi:10.1038/nature10287 · Cited by 1,473 · see citing works

Adult neurogenesis and functional plasticity in neuronal circuits

Lledo, P., Alonso, M., & Grubb, M. S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1867 · Cited by 1,364 · see citing works

Implantation and the placenta: key pieces of the development puzzle

Cross, J. C., Werb, Z., & Fisher, S. J. (1994) · Science · doi:10.1126/science.7985020 · Cited by 1,350 · see citing works

Pathogenesis and genetics of pre-eclampsia

Roberts, J., & Cooper, D. (2001) · The Lancet · doi:10.1016/s0140-6736(00)03577-7 · Cited by 1,279 · see citing works

Natural killer cells and pregnancy

Moffett-King, A. (2002) · Nature Reviews Immunology · doi:10.1038/nri886 · Cited by 1,235 · see citing works

The course of anxiety and depression through pregnancy and the postpartum in a community sample

Heron, J., O'Connor, T. G., Evans, J., Golding, J., & Glover, V. (2004) · Journal of Affective Disorders · doi:10.1016/j.jad.2003.08.004 · Cited by 1,151 · see citing works

Diagnosis and Management of Gestational Hypertension and Preeclampsia

Sibai, B. M. (2003) · Obstetrics and Gynecology · doi:10.1016/s0029-7844(03)00475-7 · Cited by 1,149 · see citing works

Epidemiology of Puerperal Psychoses

Kendell, R. E., Chalmers, J. C., & Platz, C. (1987) · British Journal of Psychiatry · doi:10.1192/bjp.150.5.662 · Cited by 1,119 · see citing works

Placenta growth factor. Potentiation of vascular endothelial growth factor bioactivity, in vitro and in vivo, and high affinity binding to Flt-1 but not to Flk-1/KDR.

Park, J. E., Chen, H. H., Winer, J., Houck, K. A., & Ferrara, N. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47298-5 · Cited by 1,112 · see citing works

Naturally occurring fluctuation in dendritic spine density on adult hippocampal pyramidal neurons

Woolley, C., Gould, E., Frankfurt, M., & McEwen, B. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-12-04035.1990 · Cited by 1,107 · see citing works

Stress-induced changes in cerebral metabolites, hippocampal volume, and cell proliferation are prevented by antidepressant treatment with tianeptine

Czéh, B., Michaelis, T., Watanabe, T., Frahm, J., de Biurrun, G., van Kampen, M., Bartolomucci, A., & Fuchs, E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211427898 · Cited by 1,090 · see citing works

Adult neurogenesis: from precursors to network and physiology

Abrous, D. N., Koehl, M., & Le Moal, M. (2005) · Physiological Reviews · doi:10.1152/physrev.00055.2003 · Cited by 971 · see citing works

Stress-Induced Alterations in Prefrontal Cortical Dendritic Morphology Predict Selective Impairments in Perceptual Attentional Set-Shifting

Liston, C., Miller, M. M., Goldwater, D. S., Radley, J. J., Rocher, A. B., Hof, P. R., Morrison, J. H., & McEwen, B. S. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1184-06.2006 · Cited by 968 · see citing works

LYSOSOME FUNCTION IN THE REGULATION OF THE SECRETORY PROCESS IN CELLS OF THE ANTERIOR PITUITARY GLAND

Smith, R. E., & Farquhar, M. G. (1966) · The Journal of Cell Biology · doi:10.1083/jcb.31.2.319 · Cited by 957 · see citing works

Stress-induced atrophy of apical dendrites of hippocampal CA3c neurons: Involvement of glucocorticoid secretion and excitatory amino acid receptors

Magarin˜os, A. M., & McEwen, B. S. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00259-l · Cited by 863 · see citing works

Repeated Stress Induces Dendritic Spine Loss in the Rat Medial Prefrontal Cortex

Radley, J. J., Rocher, A. B., Miller, M., Janssen, W. G. M., Liston, C., Hof, P. R., McEwen, B. S., & Morrison, J. H. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhi104 · Cited by 820 · see citing works

Electrophysiology of hypothalamic magnocellular neurones secreting oxytocin and vasopressin

Poulain, D. A., & Wakerley, J. B. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90044-6 · Cited by 813 · see citing works

Core Conductor Theory and Cable Properties of Neurons

Rall, W. (1977) · Comprehensive physiology · doi:10.1002/cphy.cp010103 · Cited by 783 · see citing works

Brain oxytocin: A key regulator of emotional and social behaviours in both females and males

Neumann, I. D. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01726.x · Cited by 743 · see citing works

Pregnancy-Stimulated Neurogenesis in the Adult Female Forebrain Mediated by Prolactin

Shingo, T., Gregg, C., Enwere, E. K., Fujikawa, H., Hassam, R., Geary, C. L., Cross, J. C., & Weiss, S. (2003) · Science · doi:10.1126/science.1076647 · Cited by 711 · 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

CELL ADHESION MOLECULES: Implications for a Molecular Histology

Edelman, G. M., & Crossin, K. L. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.60.070191.001103 · Cited by 705 · see citing works

Maternal Care Associated with Methylation of the Estrogen Receptor-α1b Promoter and Estrogen Receptor-α Expression in the Medial Preoptic Area of Female Offspring

Champagne, F. A., Weaver, I. C. G., Diorio, J., Dymov, S., Szyf, M., & Meaney, M. J. (2006) · Endocrinology · doi:10.1210/en.2005-1119 · Cited by 675 · see citing works

Repeated restraint stress suppresses neurogenesis and induces biphasic PSA‐NCAM expression in the adult rat dentate gyrus

Pham, K., Nacher, J., Hof, P. R., & McEwen, B. S. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02513.x · Cited by 657 · see citing works

BrdU immunohistochemistry for studying adult neurogenesis: paradigms, pitfalls, limitations, and validation

Taupin, P. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.08.002 · Cited by 645 · see citing works

Prospective study of postpartum depression: Prevalence, course, and predictive factors.

O’Hara, M. W., Neunaber, D. J., & Zekoski, E. M. (1984) · Journal of Abnormal Psychology · doi:10.1037//0021-843x.93.2.158 · Cited by 632 · see citing works

Inhibition of neurogenesis interferes with hippocampus‐dependent memory function

Winocur, G., Wojtowicz, J. M., Sekeres, M. J., Snyder, J. S., & Wang, S. Z. (2006) · Hippocampus · doi:10.1002/hipo.20163 · Cited by 580 · see citing works

Adult hippocampal neurogenesis is involved in anxiety-related behaviors

Revest, J.-M., Dupret, D., Koehl, M., Funk-Reiter, C., Grosjean, N., Piazza, P.-V., & Abrous, D. N. (2009) · Molecular Psychiatry · doi:10.1038/mp.2009.15 · Cited by 549 · see citing works

Polysialic acid in the vertebrate nervous system: a promoter of plasticity in cell-cell interactions

Rutishauser, U. S. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10041-2 · Cited by 515 · see citing works

Blood vessels and nerves: common signals, pathways and diseases

Carmeliet, P. (2003) · Nature Reviews Genetics · doi:10.1038/nrg1158 · Cited by 513 · see citing works

Stress During Gestation Alters Postpartum Maternal Care and the Development of the Offspring in a Rodent Model

Champagne, F. A., & Meaney, M. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.016 · Cited by 510 · see citing works

Angiogenesis and vasculogenesis in pregnancy

Zygmunt, M., Herr, F., Münstedt, K., Lang, U., & Liang, O. D. (2003) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/s0301-2115(03)00168-4 · Cited by 473 · see citing works

Prevalence of depressive symptoms in late pregnancy and postpartum

Josefsson, A., Berg, G., Nordin, C., & Sydsjö, G. (2001) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1034/j.1600-0412.2001.080003251.x · Cited by 461 · 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

Structural Plasticity and Hippocampal Function

Leuner, B., & Gould, E. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100359 · Cited by 452 · see citing works

Prospective study of postpartum depression: Prevalence, course, and predictive factors.

O’Hara, M. W., Neunaber, D. J., & Zekoski, E. M. (1984) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.93.2.158 · Cited by 452 · see citing works

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 · see citing works

The expectant brain: adapting for motherhood

Brunton, P. J., & Russell, J. A. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2280 · Cited by 407 · 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

Effects of suckling on hypothalamic-pituitary-adrenal axis responses to psychosocial stress in postpartum lactating women

Heinrichs, M., Meinlschmidt, G., Neumann, I., Wagner, S., Kirschbaum, C., Ehlert, U., & Hellhammer, D. H. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.10.7919 · Cited by 386 · see citing works

Suppression of hypothalmic-pituitary-adrenal axis responses to stress in lactating women

Altemus, M. M., Deuster, P. A., Galliven, E., Carter, C. S., & Gold, P. W. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.10.7559880 · Cited by 383 · see citing works

Exposure to fox odor inhibits cell proliferation in the hippocampus of adult rats via an adrenal hormone‐dependent mechanism

Tanapat, P., Hastings, N. B., Rydel, T. A., Galea, L. A. M., & Gould, E. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1297 · Cited by 376 · see citing works

Chronic psychosocial stress and concomitant repetitive transcranial magnetic stimulation: effects on stress hormone levels and adult hippocampal neurogenesis

Czéh, B., Welt, T., Fischer, A., Erhardt, A., Schmitt, W. B., Müller, M. B., Toschi, N., Fuchs, E., & Keck, M. E. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01457-9 · Cited by 370 · see citing works

Direct Stimulation of Adult Neural Stem Cells In Vitro and Neurogenesis In Vivo by Vascular Endothelial Growth Factor

Schänzer, A., Wachs, F., Wilhelm, D., Acker, T., Cooper‐Kuhn, C. M., Beck, H., Winkler, J., Aigner, L., Plate, K. H., & Kuhn, H. G. (2004) · Brain Pathology · doi:10.1111/j.1750-3639.2004.tb00060.x · Cited by 366 · see citing works

Attenuated neuroendocrine responses to emotional and physical stressors in pregnant rats involve adenohypophysial changes

Neumann, I. D., Johnstone, H. A., Hatzinger, M., Liebsch, G., Shipston, M. J., Russell, J. A., Landgraf, R., & Douglas, A. J. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.289br.x · Cited by 365 · see citing works

Motivational systems and the neural circuitry of maternal behavior in the rat

Numan, M. (2007) · Developmental Psychobiology · doi:10.1002/dev.20198 · Cited by 358 · see citing works

Severe Maternal Morbidity Associated with Hypertensive Disorders in Pregnancy in the United States

Zhang, J., Meikle, S., & Trumble, A. C. (2003) · Hypertension in Pregnancy · doi:10.1081/prg-120021066 · Cited by 351 · see citing works

Plasma oxytocin concentration during pregnancy is associated with development of postpartum depression

Skrundz, M., Bolten, M., Nast, I., Hellhammer, D. H., & Meinlschmidt, G. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.74 · Cited by 349 · see citing works

Pilot Study of Extracorporeal Removal of Soluble Fms-Like Tyrosine Kinase 1 in Preeclampsia

Thadhani, R., Kisner, T., Hagmann, H., Boßung, V., Noack, S., Schaarschmidt, W., Jank, A., Kribs, A., Cornely, O. A., Kreyssig, C., et al. (2011) · Circulation · doi:10.1161/circulationaha.111.034793 · Cited by 347 · see citing works

Depression and anxiety during pregnancy and six months postpartum: a follow‐up study

Andersson, L., Poromaa, I. S., Wulff, M., Åström, M., & Bixo, M. (2006) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1080/00016340600697652 · Cited by 338 · see citing works

Cytokines of the Placenta and Extra-placental Membranes: Roles and Regulation During Human Pregnancy and Parturition

Bowen, J. M., Chamley, L., Keelan, J. A., & Mitchell, M. D. (2002) · Placenta · doi:10.1053/plac.2001.0782 · Cited by 336 · see citing works

Local origins of some GABAergic projections to the paraventricular and supraoptic nuclei of the hypothalamus in the rat

Roland, B. L., & Sawchenko, P. E. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903320109 · Cited by 334 · see citing works

NEURAL MECHANISMS OF MAMMALIAN OLFACTORY LEARNING

Brennan, P., & Keverne, E. B. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00069-x · Cited by 334 · see citing works

Physiological Mapping of Local Inhibitory Inputs to the Hypothalamic Paraventricular Nucleus

Boudaba, C., Szabó, K., & Tasker, J. G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-22-07151.1996 · Cited by 333 · 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

Polysialic acid in the vertebrate nervous system: a promoter of plasticity in cell-cell interactions

Rutishauser, U. S. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10041-2 · Cited by 325 · see citing works

Mechanisms of Disease: pre-eclampsia

Noris, M., Perico, N., & Remuzzi, G. (2005) · Nature Reviews Nephrology · doi:10.1038/ncpneph0035 · Cited by 319 · see citing works

Molecular mechanisms of preeclampsia

Mutter, W. P., & Karumanchi, S. A. (2007) · Microvascular Research · doi:10.1016/j.mvr.2007.04.009 · Cited by 314 · see citing works

Neural control of maternal behaviour and olfactory recognition of offspring

Kendrick, K. M., Da Costa, A. P. C., Broad, K. D., Ohkura, S., Guevara, R., Lévy, F., & Keverne, E. B. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00218-9 · Cited by 311 · see citing works

Chronic high corticosterone reduces neurogenesis in the dentate gyrus of adult male and female rats

Brummelte, S., & Galea, L. A. M. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.023 · Cited by 309 · see citing works

Consequences of Neural Cell Adhesion Molecule Deficiency on Cell Migration in the Rostral Migratory Stream of the Mouse

Chazal, G., Durbec, P. L., Jankovski, A., Rougon, G. N., & Cremer, H. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-04-01446.2000 · Cited by 304 · see citing works

Inhibition of post-partum maternal behaviour in the rat by injecting an oxytocin antagonist into the cerebral ventricles

van Leengoed, E., Kerker, E., & Swanson, H. H. (1987) · Journal of Endocrinology · doi:10.1677/joe.0.1120275 · Cited by 300 · see citing works

Adaptive Responses of the Maternal Hypothalamic‐Pituitary‐Adrenal Axis during Pregnancy and Lactation

Brunton, P. J., Russell, J. A., & Douglas, A. J. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01735.x · Cited by 298 · see citing works

Motherhood improves learning and memory

Kinsley, C. H., Madonia, L., Gifford, G. W., Tureski, K., Griffin, G. R., Lowry, C., Williams, J., Collins, J., McLearie, H., & Lambert, K. G. (1999) · Nature · doi:10.1038/45957 · Cited by 297 · see citing works

Natural Variations in Maternal Care Are Associated with Estrogen Receptor α Expression and Estrogen Sensitivity in the Medial Preoptic Area

Champagne, F. A., Weaver, I. C. G., Diorio, J. C., Sharma, S., & Meaney, M. J. (2003) · Endocrinology · doi:10.1210/en.2003-0564 · Cited by 295 · see citing works

No stress please! Mechanisms of stress hyporesponsiveness of the maternal brain

Slattery, D. A., & Neumann, I. D. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.145896 · Cited by 293 · see citing works

The Pituitary Gland in Pregnancy: A Clinicopathologic and Immunohistochemical Study of 69 Cases

Scheithauer, B. W., Sano, T., Kovács, K., Young, W. F., Ryan, N., & Randall, R. V. (1990) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)60946-x · Cited by 278 · see citing works

How immune mechanisms are affected by pregnancy

Luppi, P. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00331-1 · Cited by 269 · see citing works

Anxiolytic and Anti-Stress Effects of Brain Prolactin: Improved Efficacy of Antisense Targeting of the Prolactin Receptor by Molecular Modeling

Torner, L., Toschi, N., Pohlinger, A., Landgraf, R., & Neumann, I. D. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-09-03207.2001 · Cited by 266 · see citing works

Placenta Growth Factor

Persico, M. G. (2001) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4612-0213-4_16 · Cited by 259 · see citing works

Trophoblast pseudo-vasculogenesis: faking it with endothelial adhesion receptors

Damsky, C. H., & Fisher, S. J. (1998) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(98)80043-4 · Cited by 248 · see citing works

Vasculogenesis and angiogenesis in the early human placenta

Demir, R., Seval, Y., & Huppertz, B. (2007) · Acta Histochemica · doi:10.1016/j.acthis.2007.02.008 · Cited by 241 · see citing works

Integrative Functions of Lactational Hormones in Social Behavior and Stress Managementa

Carter, C. S., & Altemus, M. M. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb51918.x · Cited by 241 · see citing works

Sex, Hormones and Neurogenesis in the Hippocampus: Hormonal Modulation of Neurogenesis and Potential Functional Implications

Galea, L. A. M., Wainwright, S. R., Roes, M., Duarte‐Guterman, P., Chow, C., & Hamson, D. K. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12070 · Cited by 238 · see citing works

Oxytocin stimulates adult neurogenesis even under conditions of stress and elevated glucocorticoids

Leuner, B., Caponiti, J., & Gould, E. (2011) · Hippocampus · doi:10.1002/hipo.20947 · Cited by 237 · see citing works

ORIGIN AND FATE OF SECRETORY GRANULES IN CELLS OF THE ANTERIOR PITUITARY GLAND*

Farquhar, M. G. (1961) · Transactions of the New York Academy of Sciences · doi:10.1111/j.2164-0947.1961.tb01361.x · Cited by 237 · 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

Motherhood and the hormones of pregnancy modify concentrations of hippocampal neuronal dendritic spines

Kinsley, C. H., Trainer, R., Stafisso-Sandoz, G., Quadros, P. S., Keyser‐Marcus, L., Hearon, C., Meyer, E. A. A., Hester, N. W., Morgan, M. D., & Kozub, F. J. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.05.017 · Cited by 233 · see citing works

Change in brain size during and after pregnancy: study in healthy women and women with preeclampsia.

Oatridge, A., Holdcroft, A., Saeed, N., Hajnal, J. V., Puri, B. K., Fusi, L., & Bydder, G. M. (2002) · PubMed Central · Cited by 232 · see citing works

Pregnancy, the postpartum, and steroid hormones: effects on cognition and mood

Buckwalter, J. G., Stanczyk, F. Z., McCleary, C. A., Bluestein, B. W., Buckwalter, D. K., Rankin, K. P., Chang, L., & Goodwin, T. M. (1999) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(98)00044-4 · Cited by 227 · see citing works

Serotonin mediates oestrogen stimulation of cell proliferation in the adult dentate gyrus

Banasr, M., Héry, M., Brezun, J. M., & Daszuta, A. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01763.x · Cited by 226 · see citing works

Increased hypothalamic expression of prolactin in lactation: involvement in behavioural and neuroendocrine stress responses

Torner, L., Toschi, N., Nava, G., Clapp, C., & Neumann, I. D. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.01965.x · Cited by 221 · see citing works

Size and shape of the pituitary gland during pregnancy and post partum: measurement with MR imaging.

Elster, A. D., Sanders, T. G., Vines, F. S., & Chen, M. Y. (1991) · Radiology · doi:10.1148/radiology.181.2.1924800 · Cited by 220 · see citing works

Expression of polysialylated neural cell adhesion molecule by proliferating cells in the subependymal layer of the adult rat, in its rostral extension and in the olfactory bulb

Bonfanti, L., & Theodosis, D. T. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90333-6 · Cited by 215 · see citing works

Adult-Born and Preexisting Olfactory Granule Neurons Undergo Distinct Experience-Dependent Modifications of their Olfactory ResponsesIn Vivo

Magavi, S. S. P., Mitchell, B. D., Szentirmai, O., Carter, B. S., & Macklis, J. D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2250-05.2005 · Cited by 215 · see citing works

Pituitary-Adrenal Responsiveness during Lactation in Rats

Stern, J. M., Goldman, L., & Levine, S. (2008) · Neuroendocrinology · doi:10.1159/000122167 · Cited by 214 · see citing works

Oxytocin induces morphological plasticity in the adult hypothalamo-neurohypophysial system

Theodosis, D. T., Montagnese, C. M., Rodriguez, F., Vincent, J., & Poulain, D. A. (1986) · Nature · doi:10.1038/322738a0 · Cited by 211 · see citing works

Olfactory Bulb Removal Eliminates Maternal Behavior in the Mouse

Gandelman, R. J., ZARROW, M. X., Denenberg, V. H., & Myers, M. D. (1971) · Science · doi:10.1126/science.171.3967.210 · Cited by 209 · see citing works

Reproductive experience alters hippocampal neurogenesis during the postpartum period in the dam

Pawluski, J. L., & Galea, L. A. M. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.031 · Cited by 209 · see citing works

Experience induces structural and biochemical changes in the adult primate brain

Kozorovitskiy, Y., Gross, C. G., Kopil, C., Battaglia, L., McBreen, M., Stranahan, A. M., & Gould, E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508817102 · Cited by 202 · see citing works

Paternal recognition of adult offspring mediated by newly generated CNS neurons

Mak, G. K., & Weiss, S. (2010) · Nature Neuroscience · doi:10.1038/nn.2550 · Cited by 201 · see citing works

Pregnant women become insensitive to cold stress

Kammerer, M. H., Adams, D., von Castelberg, B., & Glover, V. A. S. (2002) · BMC Pregnancy and Childbirth · doi:10.1186/1471-2393-2-8 · Cited by 201 · see citing works

Prolactin-Induced Mitogenesis in the Subventricular Zone of the Maternal Brain during Early Pregnancy Is Essential for Normal Postpartum Behavioral Responses in the Mother

Larsen, C. M., & Grattan, D. R. (2010) · Endocrinology · doi:10.1210/en.2009-1385 · Cited by 201 · see citing works

Continuous neurogenesis in the adult forebrain is required for innate olfactory responses

Sakamoto, M., Imayoshi, I., Ohtsuka, T., Yamaguchi, M., Mori, K., & Kageyama, R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018782108 · 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

Evidence for structural plasticity in the supraoptic nucleus of the rat hypothalamus in relation to gestation and lactation

Theodosis, D. T., & Poulain, D. A. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90222-7 · Cited by 191 · see citing works

Selection, evolution of behavior and animal models in behavioral neuroscience

Parmigiani, S., Palanza, P., Rodgers, J., & Ferrari, P. F. (1999) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00029-9 · Cited by 188 · see citing works

Chapter 1 Brain preparations for maternity — adaptive changes in behavioral and neuroendocrine systems during pregnancy and lactation. An overview

Russell, J. A., Douglas, A. J., & Ingram, C. D. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33002-9 · Cited by 187 · see citing works

Maternal Serum sFlt1 Concentration Is an Early and Reliable Predictive Marker of Preeclampsia

Hertig, A., Berkane, N. B., Lefèvre, G., Toumi, K., Marti, H., Capeau, J., Uzan, S., & Rondeau, É. (2004) · Clinical Chemistry · doi:10.1373/clinchem.2004.036715 · Cited by 186 · see citing works

Lactation Inhibits Stress-Mediated Secretion of Corticosterone and Oxytocin and Hypothalamic Accumulation of Corticotropin-Releasing Factor and Enkephalin Messenger Ribonucleic Acids

Lightman, S. L., & Young, W. S. (1989) · Endocrinology · doi:10.1210/endo-124-5-2358 · Cited by 184 · see citing works

Cell Surface Expression of Polysialic Acid on NCAM Is a Prerequisite for Activity-Dependent Morphological Neuronal and Glial Plasticity

Theodosis, D. T., Bonhomme, R., Vitiello, S., Rougon, G. N., & Poulain, D. A. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10228.1999 · Cited by 183 · see citing works

A new chapter in the field of memory: adult hippocampal neurogenesis

Koehl, M., & Abrous, D. N. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07609.x · Cited by 183 · see citing works

Structural plasticity in the hypothalamic supraoptic nucleus at lactation affects oxytocin-, but not vasopressin-secreting neurones

Theodosis, D. T., Chapman, D. B., Montagnese, C. M., Poulain, D. A., & Morris, J. F. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90038-2 · Cited by 177 · see citing works

Possible morphological bases for synchronisation of neuronal firing in the rat supraoptic nucleus during lactation

Theodosis, D. T., Poulain, D. A., & Vincent, J. D. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90173-1 · Cited by 176 · see citing works

Maternal experience inhibits the production of immature neurons in the hippocampus during the postpartum period through elevations in adrenal steroids

Leuner, B., Mirescu, C., Noiman, L., & Gould, E. (2007) · Hippocampus · doi:10.1002/hipo.20278 · Cited by 174 · see citing works

Mother–infant interactions in free-ranging rhesus macaques: Relationships between physiological and behavioral variables

Maestripieri, D., Hoffman, C. L., Anderson, G. M., Carter, C. S., & Higley, J. D. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.12.016 · Cited by 174 · see citing works

Pituitary dimensions and volume measurements in pregnancy and post partum

Dinç, H., Esen, F., Demırcı, A., Sari, A., & Gümele, H. R. (1998) · Acta Radiologica · doi:10.1080/02841859809172152 · Cited by 172 · see citing works

Hippocampal morphology is differentially affected by reproductive experience in the mother

Pawluski, J. L., & Galea, L. A. M. (2005) · Journal of Neurobiology · doi:10.1002/neu.20194 · Cited by 172 · see citing works

Chapter 8 Peripartum plasticity within the hypothalamo-pituitary-adrenal axis

Lightman, S. L., Windle, R. J., Wood, S. A., Kershaw, Y. M., Shanks, N. M., & Ingram, C. D. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33009-1 · Cited by 171 · see citing works

Priming and remodelling of human placental bed spiral arteries during pregnancy – A Review

Lyall, F. (2005) · Placenta · doi:10.1016/j.placenta.2005.02.010 · Cited by 171 · see citing works

The fetal vascularisation of term human placental villi

Kaufmann, P., Bruns, U., Leiser, R., Luckhardt, M., & Winterhager, E. (1985) · Anatomy and Embryology · doi:10.1007/bf00316301 · Cited by 170 · see citing works

Chapter 10 Alterations in behavioral and neuroendocrine stress coping strategies in pregnant, parturient and lactating rats

Neumann, I. D. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33011-x · Cited by 169 · see citing works

Changes in anxiety and cognition due to reproductive experience: A review of data from rodent and human mothers

Macbeth, A. H., & Luine, V. N. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.08.011 · Cited by 169 · see citing works

Regional Changes in Brain Oxytocin Receptors Post‐Partum: Time‐Course and Relationship to Maternal Behaviour

Insel, T. R. (1990) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1990.tb00445.x · Cited by 164 · see citing works

Neurobiology of the Parental Brain

(2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374285-8.x0001-7 · Cited by 161 · see citing works

Stimuli and consequences of dendritic release of oxytocin within the brain

Neumann, I. D. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351252 · Cited by 161 · see citing works

Reduced fearfulness in the lactating rat

Hȧrd, E., & HANSEN, S. (1985) · Physiology & Behavior · doi:10.1016/0031-9384(85)90155-6 · Cited by 161 · see citing works

Dissociation Between Behavioral and Hormonal Responses to the Forced Swim Stress in Lactating Rats

Walker, C., Trottier, G., Rochford, J. M., & Lavallée, D. (1995) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1995.tb00799.x · Cited by 159 · see citing works

Maternal stress and high-fat diet effect on maternal behavior, milk composition, and pup ingestive behavior

Purcell, R. H., Sun, B., Pass, L. L., Power, M. L., Moran, T. H., & Tamashiro, K. L. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.05.012 · Cited by 158 · see citing works

Motherhood mitigates aging-related decrements in learning and memory and positively affects brain aging in the rat

Gatewood, J. D., Morgan, M. D., Eaton, M., McNamara, I. M., Stevens, L. F., Macbeth, A. H., Meyer, E. A. A., Lomas, L. M., Kozub, F. J., Lambert, K. G., et al. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.03.016 · Cited by 155 · see citing works

Maternal nurturing is dependent on her innate anxiety: The behavioral roles of brain oxytocin and vasopressin

Bosch, O. J. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.11.012 · Cited by 153 · see citing works

Central Lactogenic Regulation of Maternal Behavior in Rats: Steroid Dependence, Hormone Specificity, and Behavioral Potencies of Rat Prolactin and Rat Placental Lactogen I

Bridges, R. S., Robertson, M. C., Shiu, R. P. C., Sturgis, J. D., Henriquez, B. M., & Mann, P. E. (1997) · Endocrinology · doi:10.1210/endo.138.2.4921 · Cited by 153 · see citing works

Reproductive experience differentially affects spatial reference and working memory performance in the mother

Pawluski, J. L., Walker, S. K., & Galea, L. A. M. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.05.016 · Cited by 150 · see citing works

Corticotropin-Releasing Factor Inhibits Maternal Aggression in Mice.

Gammie, S. C., Negrón, A., Newman, S. M., & Rhodes, J. S. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.4.805 · Cited by 145 · see citing works

Chapter 11 The actions of prolactin in the brain during pregnancy and lactation

Grattan, D. R. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33012-1 · Cited by 144 · see citing works

Human cytotrophoblasts promote endothelial survival and vascular remodeling through secretion of Ang2, PlGF, and VEGF-C

Zhou, Y., Bellingard, V., Feng, K.-T., McMaster, M., & Fisher, S. J. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00449-4 · Cited by 143 · see citing works

Spatial Working Memory and Hippocampal Size across Pregnancy in Rats

Galea, L. A. M., Ormerod, B. K., Sampath, S., Kostaras, X., Wilkie, D. M., & Phelps, M. T. (2000) · Hormones and Behavior · doi:10.1006/hbeh.1999.1560 · Cited by 140 · see citing works

Plasticity in the maternal circuit: Effects of maternal experience on Fos-Lir in hypothalamic, limbic, and cortical structures in the postpartum rat.

Fleming, A. S., & Korsmit, M. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.3.567 · Cited by 136 · see citing works

Brain plasticity and ion channels

Debanne, D., Daoudal, G., Sourdet, V., & Russier, M. (2003) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2004.01.004 · Cited by 134 · see citing works

Vasopressin released within the central amygdala promotes maternal aggression

Bosch, O. J., & Neumann, I. D. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07115.x · Cited by 134 · see citing works

The number of pregnancies is a risk factor for Alzheimer's disease

Colucci, M. E. W., Cammarata, S., Assini, A., Croce, R., Clerici, F., Novello, C., Mazzella, L., Dagnino, N., Mariani, C., & Tanganelli, P. (2006) · European Journal of Neurology · doi:10.1111/j.1468-1331.2006.01520.x · Cited by 134 · see citing works

Maternal Behaviour is Associated with Vasopressin Release in the Medial Preoptic Area and Bed Nucleus of the Stria Terminalis in the Rat

Bosch, O. J., Pförtsch, J., Beiderbeck, D. I., Landgraf, R., & Neumann, I. D. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.01984.x · Cited by 130 · see citing works

Reorganization of the Dendritic Trees of Oxytocin and Vasopressin Neurons of the Rat Supraoptic Nucleus during Lactation

Stern, J. E., & Armstrong, W. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-03-00841.1998 · Cited by 130 · see citing works

Adrenal steroid receptor immunoreactivity in cells born in the adult rat dentate gyrus

Cameron, H. A., Woolley, C. S., & Gould, E. (1993) · Brain Research · doi:10.1016/0006-8993(93)90524-q · Cited by 129 · see citing works

Early motherhood in rats is associated with a modification of hippocampal function

Darnaudéry, M., Perez-Martin, M., Del Favero, F., Gomez-Roldan, C., Garcia-Segura, L. M., & Maccari, S. (2007) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2007.05.012 · Cited by 128 · see citing works

Osmotic stimulation causes structural plasticity of neurone-glia relationships of the oxytocin but not vasopressin secreting neurones in the hypothalamic supraoptic nucleus

Chapman, D. B., Theodosis, D. T., Montagnese, C. M., Poulain, D. A., & Morris, J. F. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90039-4 · Cited by 127 · see citing works

First reproductive experience persistently affects spatial reference and working memory in the mother and these effects are not due to pregnancy or ‘mothering’ alone

Pawluski, J. L., Vanderbyl, B. L., Ragan, K., & Galea, L. A. M. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.08.017 · Cited by 127 · see citing works

Synaptic plasticity in the rat supraoptic nucleus during lactation involves GABA innervation and oxytocin neurons: a quantitative immunocytochemical analysis

Gies, U., & Theodosis, D. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-05-02861.1994 · Cited by 125 · see citing works

Estrous cycle, pregnancy, and parity enhance performance of rats in object recognition or object placement tasks

Paris, J. J., & Frye, C. A. (2008) · Reproduction · doi:10.1530/rep-07-0512 · Cited by 124 · see citing works

Exposure to Chronic Pregnancy Stress Reverses Peripartum-Associated Adaptations: Implications for Postpartum Anxiety and Mood Disorders

Hillerer, K. M., Reber, S. O., Neumann, I. D., & Slattery, D. A. (2011) · Endocrinology · doi:10.1210/en.2011-1091 · Cited by 122 · see citing works

Memory loss during pregnancy

Sharp, K., Brindle, P. M., Brown, M. W., & TURNER, G. M. (1993) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1993.tb15232.x · Cited by 121 · see citing works

Giving birth to a new brain: hormone exposures of pregnancy influence human memory

Glynn, L. M. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2010.01.015 · Cited by 121 · see citing works

Regular exercise cures depression-like behavior via VEGF-Flk-1 signaling in chronically stressed mice

Kiuchi, T., Lee, H., & Mikami, T. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.01.023 · Cited by 116 · see citing works

Alterations of medial preoptic area neurons following pregnancy and pregnancy-like steroidal treatment in the rat

Keyser‐Marcus, L., Stafisso-Sandoz, G., Gerecke, K. M., Jasnow, A. M., Nightingale, L., Lambert, K. G., Gatewood, J. D., & Kinsley, C. H. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00554-8 · Cited by 115 · see citing works

Prolactin cells in the human pituitary. A quantitative immunocytochemical analysis.

Asa, S. L., Penz, G., Kovács, K., & EZRIN, C. (1982) · PubMed · Cited by 114 · see citing works

Disruption of Adult Neurogenesis in the Olfactory Bulb Affects Social Interaction but not Maternal Behavior

Feierstein, C. E., Lazarini, F., Wagner, S., Gabellec, M., de Chaumont, F., Olivo‐Marín, J., Boussin, F. D., Lledo, P., & Gheusi, G. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00176 · Cited by 112 · see citing works

Gestation-induced cell proliferation in the rat brain

Furuta, M., & Bridges, R. S. (2005) · Developmental Brain Research · doi:10.1016/j.devbrainres.2005.01.008 · Cited by 111 · see citing works

Cognition in pregnancy and the first year post‐partum

Crawley, R. A., Dennison, K., & Carter, C. (2003) · Psychology and Psychotherapy Theory Research and Practice · doi:10.1348/14760830260569265 · Cited by 111 · see citing works

Plasticity in the maternal circuit: Effects of maternal experience on Fos-Lir in hypothalamic, limbic, and cortical structures in the postpartum rat.

Fleming, A. S., & Korsmit, M. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.3.567 · Cited by 111 · see citing works

Decrease and Senescence of Endothelial Progenitor Cells in Patients with Preeclampsia

Sugawara, J., Mitsui‐Saito, M., Hayashi, C., Hoshiai, T., Senoo, M., Chisaka, H., Yaegashi, N., & Okamura, K. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2005-0532 · Cited by 110 · see citing works

Immunologic Characteristics of Preeclampsia, a Comprehensive Review

Ahn, H.-K., Park, J.-C., Gilman‐Sachs, A., & Kwak-Kim, J. Y.-H. (2010) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2010.00913.x · Cited by 107 · see citing works

Changes in the intensity of maternal aggression and central oxytocin and vasopressin V1a receptors across the peripartum period in the rat

Caughey, S. D., Klampfl, S. M., Bishop, V. R., Pfoertsch, J., Neumann, I. D., Bosch, O. J., & Meddle, S. L. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02224.x · Cited by 107 · see citing works

Dendritic Growth in Medial Prefrontal Cortex and Cognitive Flexibility Are Enhanced during the Postpartum Period

Leuner, B., & Gould, E. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3388-10.2010 · Cited by 105 · see citing works

Perceptual Attentional Set-Shifting Is Impaired in Rats with Neurotoxic Lesions of Posterior Parietal Cortex

Fox, M. T., Barense, M. D., & Baxter, M. G. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00676.2003 · Cited by 104 · see citing works

Differences in cognitive performance during pregnancy and early motherhood

de Groot, R. H. M., Vuurman, E. F. P. M., Hornstra, G., & Jolles, J. (2006) · Psychological Medicine · doi:10.1017/s0033291706007380 · 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

Oxytocin receptor activity in the ventrocaudal periaqueductal gray modulates anxiety-related behavior in postpartum rats.

Figueira, R. J., Peabody, M. F., & Lonstein, J. S. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.618 · Cited by 101 · see citing works

Expression of the long form of the prolactin receptor in magnocellular oxytocin neurons is associated with specific prolactin regulation of oxytocin neurons

Kokay, I. C., Bull, P. M., Davis, R. L., Ludwig, M., & Grattan, D. R. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00730.2005 · Cited by 101 · see citing works

Impaired maternal cognitive functioning after pregnancies complicated by severe pre‐eclampsia: a pilot case‐control study

Brussé, I. A., Duvekot, J. J., Jongerling, J., Steegers, E. A. P., & de Koning, I. (2008) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1080/00016340801915127 · Cited by 100 · see citing works

The Many Faces of Postpartum Depression

Beck, C. T., & Indman, P. (2005) · Journal of Obstetric, Gynecologic & Neonatal Nursing · doi:10.1177/0884217505279995 · Cited by 99 · see citing works

The Noradrenergic Innervation of Identified Hypothalamic Magnocellular Somata and its Contribution to Lactation‐Induced Synaptic Plasticity

Michaloudi, H. C., Majdoubi, M. E., Poulain, D. A., Papadopoulos, G. C., & Theodosis, D. T. (1997) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1997.00583.x · Cited by 99 · see citing works

Objective and subjective memory impairment in pregnancy

Brindle, P. M., Brown, M. W., Brown, J. L., Griffith, H. B., & TURNER, G. M. (1991) · Psychological Medicine · doi:10.1017/s0033291700022285 · Cited by 98 · see citing works

The Hypothalamic‐Pituitary‐Adrenal Axis Response to Endotoxin is Attenuated During Lactation

Shanks, Windle, Perks, Wood, Ingram, I., & Lightman, S. L. (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00400.x · Cited by 97 · see citing works

Hippocampus-dependent learning influences hippocampal neurogenesis

Epp, J. R., Chow, C., & Galea, L. A. M. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00057 · Cited by 95 · see citing works

Quantitative studies on the supraoptic nucleus in the rat. II. Afferent fiber connections

Z�borszky, L., L�r�nth, C., Makara, G. B., & Palkovits, M. (1975) · Experimental Brain Research · doi:10.1007/bf00237352 · Cited by 94 · see citing works

Role of neural guidance signals in blood vessel navigation

Autiero, M., Smet, F. D., CLAES, F., & Carmeliet, P. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.09.013 · Cited by 94 · see citing works

Prolactin Receptors in the Brain during Pregnancy and Lactation: Implications for Behavior

Grattan, D. R., Pi, X., Andrews, Z. B., Augustine, R. A., Kokay, I. C., Summerfield, M., Todd, B. J., & Bunn, S. J. (2001) · Hormones and Behavior · doi:10.1006/hbeh.2001.1698 · Cited by 93 · see citing works

Cognitive deficits in women after childbirth.

Eidelman, A. I., Hoffmann, N., & Kaitz, M. (1993) · PubMed · Cited by 92 · see citing works

Motherhood‐induced memory improvement persists across lifespan in rats but is abolished by a gestational stress

Lemaire, V., Billard, J., Dutar, P., George, O., Piazza, P. V., Epelbaum, J., Moal, M. L., & Mayo, W. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04870.x · Cited by 90 · see citing works

Effects of multiparity on recognition memory, monoaminergic neurotransmitters, and brain-derived neurotrophic factor (BDNF)

Macbeth, A. H., Scharfman, H. E., MacLusky, N. J., Gautreaux, C., & Luine, V. N. (2007) · Hormones and Behavior · doi:10.1016/j.yhbeh.2007.08.011 · Cited by 88 · see citing works

Structural plasticity in the rat supraoptic nucleus during gestation, post-partum lactation and suckling-induced pseudogestation and lactation

Montagnese, C. M., Poulain, D. A., Vincent, J. D., & Theodosis, D. T. (1987) · Journal of Endocrinology · doi:10.1677/joe.0.1150097 · Cited by 86 · see citing works

The Glutamatergic Innervation of Oxytocin‐ and Vasopressin‐secreting Neurons in the Rat Supraoptic Nucleus and its Contribution to Lactation‐induced Synaptic Plasticity

Majdoubi, M. E., Poulain, D. A., & Theodosis, D. T. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01600.x · Cited by 86 · see citing works

Lactation-induced plasticity in the supraoptic nucleus augments axodendritic and axosomatic GABAergic and glutamatergic synapses: an ultrastructural analysis using the disector method

Majdoubi, M. E., Poulain, D. A., & Theodosis, D. T. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00193-0 · Cited by 86 · see citing works

Increased expression of both short and long forms of prolactin receptor mRNA in hypothalamic nuclei of lactating rats

Pi, X., & Grattan, D. R. (1999) · Journal of Molecular Endocrinology · doi:10.1677/jme.0.0230013 · Cited by 85 · see citing works

Temporary peripartal impairment in memory and attention and its possible relation to oxytocin concentration

Silber, M., Almkvist, O., Larsson, B., & Uvnäs‐Moberg, K. (1990) · Life Sciences · doi:10.1016/0024-3205(90)90566-a · Cited by 83 · see citing works

From stress to postpartum mood and anxiety disorders: How chronic peripartum stress can impair maternal adaptations

Hillerer, K. M., Neumann, I. D., & Slattery, D. A. (2012) · Neuroendocrinology · doi:10.1159/000330445 · Cited by 82 · see citing works

Circulating Endothelial Progenitor Cells during Human Pregnancy

Sugawara, J., Mitsui‐Saito, M., Hoshiai, T., Hayashi, C., Kimura, Y., & Okamura, K. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-0541 · Cited by 79 · see citing works

Chapter 22 Pregnancy and postpartum: changes in cognition and mood

Buckwalter, J. G., Buckwalter, D. K., Bluestein, B. W., & Stanczyk, F. Z. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33023-6 · Cited by 78 · see citing works

Pup exposure differentially enhances foraging ability in primiparous and nulliparous rats

Lambert, K. G., Berry, A. E., Griffin, G. R., Amory, E., Madonia, L., Love, G., & Kinsley, C. H. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.03.012 · Cited by 77 · see citing works

Influence of Ovarian Steroids on the Ultrastructural Plasticity of the Adult Rat Supraoptic Nucleus Induced by Central Administration of Oxytocin

Montagnese, C. M., Poulain, D. A., & Theodosis, D. T. (1990) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1990.tb00855.x · Cited by 77 · see citing works

Reduced oxytocin response to osmotic stimulus and immobilization stress in lactating rats

Higuchi, T., Honda, K., Takano, S., & Negoro, H. (1988) · Journal of Endocrinology · doi:10.1677/joe.0.1160225 · Cited by 73 · see citing works

Anxiety and maternal aggression in house mice (Mus musculus): A look at interindividual variability.

Maestripieri, D., & D'Amato, F. R. (1991) · Journal of comparative psychology · doi:10.1037/0735-7036.105.3.295 · Cited by 73 · see citing works

Agomelatine reverses the decrease in hippocampal cell survival induced by chronic mild stress

Dagytė, G., Crescente, I., Postema, F., Seguin, L., Gabriel, C., Mocaër, E., den Boer, J. A., & Koolhaas, J. M. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.045 · Cited by 69 · see citing works

Decrease in hippocampal neurogenesis during pregnancy: a link to immunity

Rolls, A., Schori, H., London, A., & Schwartz, M. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002126 · Cited by 69 · see citing works

Aggression in the lactating rat: Effects of intruder age and test arena

Erskine, M. S., Denenberg, V. H., & Goldman, B. D. (1978) · Behavioral Biology · doi:10.1016/s0091-6773(78)91148-3 · Cited by 69 · see citing works

Neuropilin ligands in vascular and neuronal patterning

Fantin, A., Maden, C. H., & Ruhrberg, C. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371228 · Cited by 69 · see citing works

The fetal vascularisation of term human placental villi

Leiser, R., Luckhardt, M., Kaufmann, P., Winterhager, E., & Bruns, U. (1985) · Anatomy and Embryology · doi:10.1007/bf00707305 · Cited by 69 · see citing works

Central noradrenergic mechanisms underlying acute stress responses of the Hypothalamo-pituitary-adrenal axis: Adaptations through pregnancy and lactation

Douglas, A. J. (2005) · Stress · doi:10.1080/10253890500044380 · Cited by 68 · see citing works

Gonadal steroid regulation of oxytocin and oxytocin receptor gene expression.

Zingg, H., Rozen, F., Breton, C., Larcher, A., Neculcea, J., Chu, K., Russo, C., & Arslan, A. (1995) · PubMed · Cited by 67 · see citing works

Reduced Response of the Hypothalamo-Pituitary-Adrenal Axis toα 1-Agonist Stimulation during Lactation*

Windle, R. J., Brady, M. M., Kunanandam, T., Costa, A. P. C., Wilson, B. C., Harbuz, M. S., Lightman, S. L., & Ingram, C. D. (1997) · Endocrinology · doi:10.1210/endo.138.9.5405 · Cited by 67 · see citing works

Pregnant rats show enhanced spatial memory, decreased anxiety, and altered levels of monoaminergic neurotransmitters

Macbeth, A. H., Gautreaux, C., & Luine, V. N. (2008) · Brain Research · doi:10.1016/j.brainres.2008.09.006 · Cited by 67 · see citing works

Induction of rapid, activity‐dependent neuronal–glial remodelling in the adult rat hypothalamus in vitro

Langle, S. L., Poulain, D. A., & Theodosis, D. T. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02741.x · Cited by 67 · see citing works

Prescribing physical activity to prevent and manage gestational diabetes

Colberg, S. R. (2013) · World Journal of Diabetes · doi:10.4239/wjd.v4.i6.256 · Cited by 67 · see citing works

Estradiol receptor-α expression in hypothalamic and limbic regions of ewes is influenced by physiological state and maternal experience

Meurisse, M., Gonzalez, A., Delsol, G., Caba, M., Lévy, F., & Poindron, P. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.02.007 · Cited by 66 · see citing works

Regression of redundant lactotrophs in rat pituitary gland after cessation of lactation

Haggi, E. S., Torres, A. I., Maldonado, C. A., & Aoki, A. (1986) · Journal of Endocrinology · doi:10.1677/joe.0.1110367 · Cited by 66 · see citing works

Postpartum Corticosterone Administration Reduces Dendritic Complexity and Increases the Density of Mushroom Spines of Hippocampal CA 3 Arbours in Dams

Workman, J. L., Brummelte, S., & Galea, L. A. M. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2012.02380.x · Cited by 66 · see citing works

Pregnancy leads to long-lasting changes in human brain structure

Hoekzema, E., Barba-Müller, E., Pozzobon, C., Picado, M., Lucco, F., García-García, D., Soliva, J. C., Tobeña, A., Desco, M., Crone, E. A., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4458 · Cited by 788 · see citing works

Brain plasticity in pregnancy and the postpartum period: links to maternal caregiving and mental health

Barba‐Müller, E., Craddock, S., Carmona, S., & Hoekzema, E. A. (2018) · Archives of Women s Mental Health · doi:10.1007/s00737-018-0889-z · Cited by 240 · see citing works

Population-based neuroimaging reveals traces of childbirth in the maternal brain

de Lange, A. G., Kaufmann, T., van der Meer, D., Maglanoc, L. A., Alnæs, D., Moberget, T., Douaud, G., Andreassen, O. A., & Westlye, L. T. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910666116 · Cited by 160 · see citing works

Peripheral oxytocin and vasopressin: Biomarkers of psychiatric disorders? A comprehensive systematic review and preliminary meta-analysis

Rutigliano, G., Rocchetti, M., Paloyelis, Y., Gilleen, J., Sardella, A., Cappucciati, M., Palombini, E., Dell’Osso, L., Caverzasi, E., Politi, P., et al. (2016) · Psychiatry Research · doi:10.1016/j.psychres.2016.04.117 · Cited by 149 · see citing works

Neuroplasticity in the maternal hippocampus: Relation to cognition and effects of repeated stress

Pawluski, J. L., Lambert, K. G., & Kinsley, C. H. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.06.004 · Cited by 130 · see citing works

How maternal pre- and postnatal symptoms of depression and anxiety affect early mother-infant interaction?

Hakanen, H., Flykt, M. S., Sinervä, E., Nolvi, S., Kataja, E., Pelto, J., Karlsson, H., Karlsson, L., & Korja, R. (2019) · Journal of Affective Disorders · doi:10.1016/j.jad.2019.06.048 · Cited by 125 · see citing works

Oxytocin pathways in the intergenerational transmission of maternal early life stress

Töpfer, P., Heim, C. C., Entringer, S., Binder, E. B., Wadhwa, P. D., & Buß, C. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.12.026 · Cited by 114 · see citing works

Hormone-mediated neural remodeling orchestrates parenting onset during pregnancy

Ammari, R., Monaca, F., Cao, M., Nassar, E., Wai, P. T., Grosso, N. A. D., Lee, M., Borak, N., Schneider-Luftman, D., & Kohl, J. (2023) · Science · doi:10.1126/science.adi0576 · Cited by 114 · see citing works

Influence of sex and stress exposure across the lifespan on endophenotypes of depression: focus on behavior, glucocorticoids, and hippocampus

Gobinath, A. R., Mahmoud, R., & Galea, L. A. M. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00420 · Cited by 105 · see citing works

Human Maternal Brain Plasticity: Adaptation to Parenting

Kim, P. (2016) · New Directions for Child and Adolescent Development · doi:10.1002/cad.20168 · Cited by 102 · see citing works

Women's brain aging: Effects of sex‐hormone exposure, pregnancies, and genetic risk for Alzheimer's disease

de Lange, A. G., Barth, C., Kaufmann, T., Maximov, I. I., van der Meer, D., Agartz, I., & Westlye, L. T. (2020) · Human Brain Mapping · doi:10.1002/hbm.25180 · Cited by 101 · see citing works

Prenatal Stress and the Developing Brain: Postnatal Environments Promoting Resilience

Nolvi, S., Merz, E. C., Kataja, E., & Parsons, C. E. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.11.023 · Cited by 108 · see citing works

Less can be more: Fine tuning the maternal brain

Pawluski, J. L., Hoekzema, E., Leuner, B., & Lonstein, J. S. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.045 · Cited by 91 · see citing works

Women’s neuroplasticity during gestation, childbirth and postpartum

Paternina-Die, M., Martínez‐Garcia, M., de Blas, D. M., Noguero-Soler, I., Servin-Barthet, C., Pretus, C., Soler, A., Montoya, G. L., Desco, M., & Carmona, S. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01513-2 · Cited by 96 · see citing works

A survey of neuroimmune changes in pregnant and postpartum female rats

Haim, A., Julian, D. L., Albin-Brooks, C., Brothers, H. M., Lenz, K. M., & Leuner, B. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.09.026 · Cited by 82 · see citing works

The maternal brain: Region‐specific patterns of brain aging are traceable decades after childbirth

de Lange, A. G., Barth, C., Kaufmann, T., Anatürk, M., Suri, S., Ebmeier, K. P., & Westlye, L. T. (2020) · Human Brain Mapping · doi:10.1002/hbm.25152 · Cited by 86 · see citing works

How stress can influence brain adaptations to motherhood

Kim, P. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100875 · Cited by 73 · see citing works

Cortical thickness variation of the maternal brain in the first 6 months postpartum: associations with parental self-efficacy

Kim, P., Dufford, A. J., & Tribble, R. C. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1688-z · Cited by 63 · see citing works

Preeclampsia and the brain: neural control of cardiovascular changes during pregnancy and neurological outcomes of preeclampsia

Logue, O. C., George, E. M., & Bidwell, G. L. (2016) · Clinical Science · doi:10.1042/cs20160108 · Cited by 66 · see citing works

Non-pharmacological interventions for improving postpartum maternal sleep: A systematic review and meta-analysis

Owais, S., Chow, C. H. T., Furtado, M., Frey, B. N., & Lieshout, R. J. V. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2018.01.005 · Cited by 69 · see citing works

An Examination of Dynamic Gene Expression Changes in the Mouse Brain During Pregnancy and the Postpartum Period

Ray, S., Tzeng, R.-Y., DiCarlo, L. M., Bundy, J. L., Vied, C., Tyson, G., Nowakowski, R. S., & Arbeitman, M. N. (2015) · G3 Genes Genomes Genetics · doi:10.1534/g3.115.020982 · Cited by 63 · see citing works

Gestational hormone profiles predict human maternal behavior at 1-year postpartum

Glynn, L. M., Davis, E. P., Sandman, C. A., & Goldberg, W. A. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.07.002 · Cited by 62 · see citing works

The parental brain and behavior: A target for endocrine disruption

Keller, M., Vandenberg, L. N., & Charlier, T. D. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100765 · Cited by 62 · see citing works

Pregnancy, postpartum and parity: Resilience and vulnerability in brain health and disease

Deems, N. P., & Leuner, B. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100820 · Cited by 63 · see citing works

Towards an understanding of women’s brain aging: the immunology of pregnancy and menopause

Barth, C., & de Lange, A. G. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100850 · Cited by 59 · see citing works

Adaptations in reward-related behaviors and mesolimbic dopamine function during motherhood and the postpartum period

Rincón‐Cortés, M., & Grace, A. A. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100839 · Cited by 60 · see citing works

Sex Hormones Regulate Cytoskeletal Proteins Involved in Brain Plasticity

Hansberg-Pastor, V., González‐Arenas, A., Piña-Medina, A. G., & Camacho‐Arroyo, I. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00165 · Cited by 58 · see citing works

Inflammatory and neurodegenerative pathophysiology implicated in postpartum depression

Worthen, R. J., & Beurel, E. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105646 · Cited by 58 · see citing works

Mom doesn’t care: When increased brain CRF system activity leads to maternal neglect in rodents

Klampfl, S. M., & Bosch, O. J. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.01.001 · Cited by 51 · see citing works

Neurogenomic insights into paternal care and its relation to territorial aggression

Bukhari, S. A., Saul, M. C., James, N., Bensky, M. K., Stein, L. R., Trapp, R. M., & Bell, A. M. (2019) · Nature Communications · doi:10.1038/s41467-019-12212-7 · Cited by 50 · see citing works

Maternal care boosted by paternal imprinting in mammals

Creeth, H., McNamara, G. I., Tunster, S. J., Boqué-Sastre, R., Allen, B., Sumption, L. A., Eddy, J. B., Isles, A. R., & John, R. M. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2006599 · Cited by 49 · see citing works

Neuroimmunology of the female brain across the lifespan: Plasticity to psychopathology

Barrientos, R. M., Brunton, P. J., Lenz, K. M., Pyter, L. M., & Spencer, S. J. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.03.010 · Cited by 49 · see citing works

The maternal brain under stress: Consequences for adaptive peripartum plasticity and its potential functional implications

Slattery, D. A., & Hillerer, K. M. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.01.004 · Cited by 47 · see citing works

“Pregnancy Brain”: A Review of Cognitive Changes in Pregnancy and Postpartum

Brown, E., & Schaffir, J. (2019) · Obstetrical & Gynecological Survey · doi:10.1097/ogx.0000000000000655 · Cited by 47 · see citing works

Oxytocin-mediated social enrichment promotes longer telomeres and novelty seeking

Faraji, J., Karimi, M., Soltanpour, N., Moharrerie, A., Rouhzadeh, Z., Lotfi, H., Hosseini, S. A., Jafari, S. Y., Roudaki, S., Moeeini, R., et al. (2018) · eLife · doi:10.7554/elife.40262 · Cited by 45 · see citing works

The Role of Adiponectin during Pregnancy and Gestational Diabetes

Gruber, B. L. M., & Dolinsky, V. W. (2023) · Life · doi:10.3390/life13020301 · Cited by 40 · see citing works

Early life social stress and resting state functional connectivity in postpartum rat anterior cingulate circuits

Nephew, B. C., Febo, M., Huang, W., Colón-Pérez, L. M., Payne, L., Poirier, G. L., Greene, O., & King, J. A. (2018) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.12.089 · Cited by 38 · see citing works

Reorganization of perineuronal nets in the medial Preoptic Area during the reproductive cycle in female rats

Uriarte, N., Ferreño, M., Méndez, D., & Nogueira, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-62163-z · Cited by 39 · see citing works

Evidence for functional interactions between the placenta and brain in pregnant mice

Behura, S. K., Kelleher, A. M., & Spencer, T. E. (2018) · The FASEB Journal · doi:10.1096/fj.201802037r · Cited by 37 · see citing works

Perinatal depression: Heterogeneity of disease and in animal models

Qiu, W., Hodges, T. E., Clark, E. L., Blankers, S. A., & Galea, L. A. M. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100854 · Cited by 37 · see citing works

Beyond a means of exposure: a new view of the mother in toxicology research

Catanese, M. C., Suvorov, A., & Vandenberg, L. N. (2014) · Toxicology Research · doi:10.1039/c4tx00119b · Cited by 34 · see citing works

Loss of offspring Peg3 reduces neonatal ultrasonic vocalizations and increases maternal anxiety in wild-type mothers

McNamara, G. I., Creeth, H., Harrison, D. J., Tansey, K. E., Andrews, R., Isles, A. R., & John, R. M. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx412 · Cited by 31 · see citing works

Structural and Functional Plasticity in the Maternal Brain Circuitry

Pereira, M. (2016) · New Directions for Child and Adolescent Development · doi:10.1002/cad.20163 · Cited by 30 · see citing works

The oxytocinergic system in PTSD following traumatic childbirth: endogenous and exogenous oxytocin in the peripartum period

Witteveen, A. B., Stramrood, C. A. I., Henrichs, J., Flanagan, J. C., van Pampus, M. G., & Olff, M. (2019) · Archives of Women s Mental Health · doi:10.1007/s00737-019-00994-0 · Cited by 29 · see citing works

Programming of weight and obesity across the lifecourse by the maternal metabolic exposome: A systematic review

Strain, J., Spaans, F., Serhan, M., Davidge, S. T., & Connor, K. L. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.100986 · Cited by 29 · see citing works

The hypothalamo-pituitary-adrenal (HPA) axis in sheep is attenuated during lactation in response to psychosocial and predator stress

Ralph, C. R., & Tilbrook, A. J. (2015) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2015.11.003 · Cited by 27 · see citing works

Imprinted genes influencing the quality of maternal care

Creeth, H., McNamara, G. I., Isles, A. R., & John, R. M. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.12.003 · Cited by 27 · see citing works

The placental programming hypothesis: Placental endocrine insufficiency and the co-occurrence of low birth weight and maternal mood disorders

Creeth, H., & John, R. M. (2020) · Placenta · doi:10.1016/j.placenta.2020.03.011 · Cited by 26 · see citing works

Intergenerational Sex-Specific Transmission of Maternal Social Experience

Faraji, J., Karimi, M., Soltanpour, N., Rouhzadeh, Z., Roudaki, S., Hosseini, S. A., Jafari, S. Y., Abdollahi, A. A., Soltanpour, N., Moeeini, R., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-28729-8 · Cited by 25 · see citing works

Dysfunctions of brain oxytocin signaling: Implications for poor mothering

Sanson, A., & Bosch, O. J. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109049 · Cited by 20 · see citing works

Memory and affective changes during the antepartum: A narrative review and integrative hypothesis

Ouellette, S. J., & Hampson, E. (2018) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803395.2018.1485881 · Cited by 22 · see citing works

Long-term association of pregnancy and maternal brain structure: the Rotterdam Study

Aleknavičiūtė, J., Evans, T. E., Aribas, E., de Vries, M. W., Steegers, E. A. P., Ikram, M. A., Tiemeier, H. W., Kavousi, M., Vernooij, M. W., & Kushner, S. A. (2022) · European Journal of Epidemiology · doi:10.1007/s10654-021-00818-5 · Cited by 25 · see citing works

Pregnancy renders anatomical changes in hypothalamic substructures of the human brain that relate to aspects of maternal behavior

Spalek, K., Straathof, M., Koyuncu, L., Grydeland, H., van der Geest, A., Hof, S. R. V. ’., Crone, E. A., Barba‐Müller, E., Carmona, S., Denys, D. A. J. P., et al. (2024) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2024.107021 · Cited by 22 · see citing works

Changes in behavior and brain immediate early gene expression in male threespined sticklebacks as they become fathers

Kent, M., & Bell, A. M. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.11.002 · Cited by 20 · see citing works

Associations between maternal socioeconomic, psychosocial and seasonal factors, infant characteristics and human milk cortisol concentrations

Lindberg, M. E., Nolvi, S., Härkönen, J., Aatsinki, A., Karlsson, L., Karlsson, H., & Uusitupa, H. (2021) · American Journal of Human Biology · doi:10.1002/ajhb.23561 · Cited by 20 · see citing works

Animal models of postpartum depression revisited

Mir, F. R., Pollano, A., & Rivarola, M. A. (2021) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2021.105590 · Cited by 20 · see citing works

The Mother-Baby Bond: Role of Past and Current Relationships

Bianciardi, E., Ongaretto, F., Stefano, A. D., Siracusano, A., & Niolu, C. (2023) · Children · doi:10.3390/children10030421 · Cited by 24 · see citing works

The Organism as the Niche: Physiological States Crack the Code of Adult Neural Stem Cell Heterogeneity

Chaker, Z., Makarouni, E., & Doetsch, F. K. (2024) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-120320-040213 · Cited by 20 · see citing works

Sex hormones and proteins involved in brain plasticity

Camacho‐Arroyo, I., Piña-Medina, A. G., Bello‐Alvarez, C., & Zamora-Sánchez, C. J. (2020) · Vitamins and hormones · doi:10.1016/bs.vh.2020.04.002 · Cited by 21 · see citing works

The sleeper effect of perceived insufficient milk supply in US mothers

Whipps, M. D. M., & Demirci, J. R. (2020) · Public Health Nutrition · doi:10.1017/s1368980020001482 · Cited by 18 · see citing works

Why monkeys do not get multiple sclerosis (spontaneously)

Bove, R. M. (2018) · Evolution Medicine and Public Health · doi:10.1093/emph/eoy002 · Cited by 18 · see citing works

Differences in navigation performance and postpartal striatal volume associated with pregnancy in humans

Lisofsky, N., Wiener, J. M., de Condappa, O., Gallinat, J., Lindenberger, U., & Kühn, S. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.08.022 · Cited by 17 · see citing works

The Characterization of Sex Differences in Hypoglycemia-Induced Activation of HPA Axis on the Transcriptomic Level

Taheri, S., Karaca, Z., Rassoulzadegan, M., Mehmetbeyoğlu, E., Zararsız, G., Şener, E. F., Bayram, K. K., Tufan, E., Şahin, M. Ç., Maraşlı, M. K., et al. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01043-0 · Cited by 17 · see citing works

The Connection and Development of Unpredictability and Sensitivity in Maternal Care Across Early Childhood

Holmberg, E., Kataja, E., Davis, E. P., Pajulo, M., Nolvi, S., Hakanen, H., Karlsson, L., Karlsson, H., & Korja, R. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.803047 · Cited by 17 · see citing works

The insulin-like growth factor-1 system in the adult mammalian brain and its implications in central maternal adaptation

Dobolyi, Á., & Lékó, A. H. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.12.002 · Cited by 17 · see citing works

Gestational stress decreases postpartum mitochondrial respiration in the prefrontal cortex of female rats

Gorman‐Sandler, E., Robertson, B., Crawford, J., Wood, G., Ramesh, A., Arishe, O. O., Webb, R. C., & Hollis, F. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100563 · Cited by 16 · see citing works

Maternal Anxiety Symptoms and Self-Regulation Capacity Are Associated With the Unpredictability of Maternal Sensory Signals in Caregiving Behavior

Holmberg, E., Teppola, T., Pajulo, M., Davis, E. P., Nolvi, S., Kataja, E., Sinervä, E., Karlsson, L., Karlsson, H., & Korja, R. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.564158 · Cited by 13 · see citing works

Cerebrospinal fluid levels of tau and phospho-tau-181 proteins during pregnancy

Lederer, W., Alomar-Dominguez, C., Popovscaia, M., Putz, G., & Humpel, C. (2016) · Pregnancy Hypertension · doi:10.1016/j.preghy.2016.08.243 · Cited by 13 · see citing works

Mechanism of Progesterone Action in the Brain

Camacho‐Arroyo, I., Hansberg-Pastor, V., Vázquez-Martínez, E. R., & Cerbón, M. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803592-4.00053-5 · Cited by 14 · see citing works

Organophosphate ester flame retardants and plasticizers in house dust and mental health outcomes among Canadian mothers: A nested prospective cohort study in CHILD

Foster, S. A., Kile, M. L., Hystad, P., Diamond, M. L., Jantunen, L. M., Mandhane, P. J., Moraes, T. J., Navaranjan, G., Scott, J. A., Simons, E., et al. (2023) · Environmental Research · doi:10.1016/j.envres.2023.117451 · Cited by 12 · see citing works

Linking the reversal of gestational insulin resistance to postpartum depression

Abeysekera, M. V., Ni, D., Gilbert, L., Hibbert, E., & Nanan, R. K. H. (2024) · BMC Medicine · doi:10.1186/s12916-024-03659-7 · Cited by 12 · see citing works

Postpartum environmental challenges alter maternal responsiveness and offspring development

Scarola, S. J., Kent, M., Neal, S., Trejo, J. R. P., Bardi, M., & Lambert, K. G. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104761 · Cited by 11 · see citing works

Recent Neuroscience Advances in Human Parenting

Martínez‐Garcia, M., Cárdenas, S. I., Pawluski, J. L., Carmona, S., & Saxbe, D. (2022) · Advances in neurobiology · doi:10.1007/978-3-030-97762-7_8 · Cited by 9 · see citing works

Kind of blue – An evaluation of etiologies for prenatal versus postnatal depression symptoms

Samuelsen, K., Ystrøm, E., Gjerde, L. C., & Eilertsen, E. M. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.04.135 · Cited by 8 · see citing works

Upregulation of GH, but not IGF1, in the hippocampus of the lactating dam after kainic acid injury

Arellanes-Licea, E. D. C., Ávila-Mendoza, J., Ramírez-Martínez, E. C., Ramos, E., Uribe-González, N., Arámburo, C., Morales, T., & Luna, M. (2018) · Endocrine Connections · doi:10.1530/ec-17-0380 · Cited by 9 · see citing works

Walking for Cognitive Health: Previous Parity Moderates the Relationship Between Self-Reported Walking and Cognition

Barha, C. K., Best, J. R., Rosano, C., Yaffe, K. S., Catov, J. M., & Liu-Ambrose, T. Y. L. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac123 · Cited by 9 · see citing works

Cumulative estrogen exposure, APOE genotype, and women’s brain aging: A population-based neuroimaging studyPreprint

de Lange, A. G., Barth, C., Kaufmann, T., Maximov, I. I., van der Meer, D., Agartz, I., & Westlye, L. T. (2019) · MPG.PuRe (Max Planck Society) · Cited by 11 · see citing works

Sex and sex hormone differences in hippocampal neurogenesis and their relevance to Alzheimer’s disease

Lee, B. H., Puri, T. A., & Galea, L. A. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819344-0.00010-7 · Cited by 8 · see citing works

The glass ceiling: A biological phenomenon

Schulpen, T. W. J. (2017) · Medical Hypotheses · doi:10.1016/j.mehy.2017.07.002 · Cited by 8 · see citing works

Temporal changes in the cerebrospinal fluid allopregnanolone concentration and hypothalamic-pituitary-adrenal axis activity in sheep during pregnancy and early lactation

Misztal, T., Czauderna, M., Młotkowska, P., Misztal, A., & Marciniak, E. (2019) · Livestock Science · doi:10.1016/j.livsci.2019.103871 · Cited by 7 · see citing works

Impact of Chronic Prenatal Stress on Maternal Neuroendocrine Function and Embryo and Placenta Development During Early-to-Mid-Pregnancy in Mice

Gotlieb, N., Wilsterman, K., Finn, S. L., Browne, M. F., Bever, S. R., Ukena, K., Ukena, K., Bentley, G. E., & Kriegsfeld, L. J. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.886298 · Cited by 7 · see citing works

The Genomic Architecture of Pregnancy-Associated Plasticity in the Maternal Mouse Hippocampus

Celik, A., Somer, M., Kukreja, B., Wu, T., & Kalish, B. T. (2022) · eNeuro · doi:10.1523/eneuro.0117-22.2022 · Cited by 7 · see citing works

Mitochondrial might: powering the peripartum for risk and resilience

Gorman‐Sandler, E., Wood, G., Cloude, N., Frambes, N. I., Brennen, H., Robertson, B., & Hollis, F. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1286811 · Cited by 6 · see citing works

The landscape of long noncoding RNA expression in the goat brain

Varela-Martínez, E., Luigi‐Sierra, M. G., Guan, D., López‐Béjar, M., Casas‐Díaz, E., Olvera‐Maneu, S., Gardela, J., Palomo, M. J., Osuagwuh, U. I., Ohaneje, U. L., et al. (2024) · Journal of Dairy Science · doi:10.3168/jds.2023-23966 · Cited by 7 · see citing works

Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic?

Provenzi, L., Villa, M., Mambretti, F., Citterio, A., Grumi, S., Bertazzoli, E., Biasucci, G., Decembrino, L., Gardella, B., Giacchero, R., et al. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.950455 · Cited by 6 · see citing works

Maternal Experience Leads to Lasting Gene Expression Changes in Some Regions of the Mouse Brain

Arbeitman, M. N. (2019) · G3 Genes Genomes Genetics · doi:10.1534/g3.119.400249 · Cited by 6 · see citing works

Regulation of uterine genes during the peri‐implantation period, and its relationship to the maternal brain in gestating mice

Behura, S. K., Kelleher, A. M., & Spencer, T. E. (2020) · Molecular Reproduction and Development · doi:10.1002/mrd.23338 · Cited by 6 · see citing works

Sulfamethoxazole induces zinc changes at hippocampal mossy fiber synapses from pregnant rats

Corceiro, V. N., Bastos, F. C., Matias, C. M., Dionı́sio, J. C., Santos, R. M., Rosário, L. M., Quinta-Ferreira, R. M., & Quinta-Ferreira, M. E. (2018) · General Physiology and Biophysics · doi:10.4149/gpb_2017037 · Cited by 5 · see citing works

History of childbirths relates to region-specific brain aging patterns in middle and older-aged womenPreprint

de Lange, A. G., Barth, C., Kaufmann, T., Anatürk, M., Suri, S., Ebmeier, K. P., & Westlye, L. T. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.08.084616 · Cited by 5 · see citing works

Peripartum sertraline impacts maternal neurobehavioral and neurodegenerative mechanisms in pregnant and postpartum mice

Blaine, B., Kamal, M., Roberts, M., Schickling, B., Lauffer, M. C., Zhang, Y., Bertolli, A. X., Weber, M. A., Taylor, R., Nadeem, S., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03094-x · Cited by 4 · see citing works

Associations Between Parity and Cognition: Race/Ethnic Differences

Araujo-Menendez, C. E. E., Saelzler, U. G., Stickel, A. M., Sundermann, E. E., Banks, S. J., Paipilla, A., Barnes, M. L., & Panizzon, M. S. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-221210 · Cited by 4 · see citing works

Pregnancy-induced oxidative stress and inflammation are not associated with impaired maternal neuronal activity or memory function

Bradshaw, J. L., Wilson, E. N., Gardner, J. J., Mabry, S., Tucker, S. M., Rybalchenko, N., Vera, E., Goulopoulou, S., & Cunningham, R. L. (2024) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00026.2024 · Cited by 4 · see citing works

Adult neurogenesis and the microbiota-gut-brain axis in farm animals: underestimated and understudied parameters for improving welfare in livestock farming

Hillerer, K. M., & Gimsa, U. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1493605 · Cited by 4 · see citing works

Gender Inequality and Women Mental Health: Where Do We Stand?

Niolu, C., Bianciardi, E., & Siracusano, A. (2024) · Sustainable development goals series · doi:10.1007/978-3-031-70165-8_7 · Cited by 4 · see citing works

Estrogenic Regulation of Hippocampal Neurogenesis Throughout the Lifespan

Yagi, S., Eid, R. S., Qiu, W., Duarte‐Guterman, P., & Galea, L. A. M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190645908.003.0016 · Cited by 4 · see citing works

The Perinatal Microbiota-Gut-Brain Axis: Implications for Postpartum Depression

Armbruster, M., & Forsythe, P. (2025) · NeuroImmunoModulation · doi:10.1159/000543691 · Cited by 5 · see citing works

Regulation of the Hypothalamo-Pituitary-Adrenal Axis in Pregnancy and Lactation

Brunton, P. J., & Walker, C. (2024) · Masterclass in neuroendocrinology · doi:10.1007/978-3-031-51138-7_4 · Cited by 4 · see citing works

The density of doublecortin cells in the piriform cortex is affected by transition to adulthood but not first pregnancy in mice

Esteve-Pérez, R., Abellán‐Álvaro, M., Navarro-Moreno, C., Prina, M., Barneo‐Muñoz, M., Lanuza, E., Sánchez-Catalán, M. J., Martínez‐Garciá, F., Torres-Pérez, J. V., & Agustín‐Pavón, C. (2025) · Brain Structure and Function · doi:10.1007/s00429-025-02957-x · Cited by 2 · see citing works

Memory in pregnancy and post‐partum: Item specific and relational encoding processes in recall and recognition

Spataro, P., Saraulli, D., Oriolo, D., Costanzi, M., Zanetti, H., Cestari, V., & Rossi‐Arnaud, C. (2016) · Scandinavian Journal of Psychology · doi:10.1111/sjop.12293 · Cited by 2 · see citing works

Physiological Mechanisms in Pregnancy and Their Relevance to the Clinical Management of Perinatal Mental Illness

Unger, A., Rosenberg, N., Kautzky‐Willer, A., & Kautzky, A. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15124559 · Cited by 1 · see citing works

Review Article The Maternal Brain: An Organ with Peripartal Plasticity

Hillerer, K. M., Jacobs, V. R., Fischer, T., & Aigner, L. (2016)

Brain plasticity in pregnancy and the postpartum period: links to maternal caregiving and mental health

Barba‐Müller, E., Craddock, S., Carmona, S., & Hoekzema, E. A. (2018) · Archives of Women s Mental Health · doi:10.1007/s00737-018-0889-z · Cited by 240 · see citing works

The birth of new neurons in the maternal brain: Hormonal regulation and functional implications

Leuner, B., & Sabihi, S. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.02.004 · Cited by 110 · see citing works

Less can be more: Fine tuning the maternal brain

Pawluski, J. L., Hoekzema, E., Leuner, B., & Lonstein, J. S. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.045 · Cited by 91 · see citing works

The maternal brain under stress: Consequences for adaptive peripartum plasticity and its potential functional implications

Slattery, D. A., & Hillerer, K. M. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.01.004 · Cited by 47 · see citing works