Less can be more: Fine tuning the maternal brain

Dissociable intrinsic connectivity networks for salience processing and executive control

Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426 · see citing works

The reward circuit: linking primate anatomy and human imaging

Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718 · see citing works

Physiology of Microglia

Kettenmann, H., Hanisch, U.-K., Noda, M., & Verkhratsky, A. (2011) · Physiological Reviews · doi:10.1152/physrev.00011.2010 · Cited by 3,547 · see citing works

Complement and microglia mediate early synapse loss in Alzheimer mouse models

Hong, S., Beja-Glasser, V. F., Nfonoyim, B. M., Frouin, A., Li, S., Ramakrishnan, S., Merry, K. M., Shi, Q., Rosenthal, A., Barres, B. A., et al. (2016) · Science · doi:10.1126/science.aad8373 · Cited by 3,343 · see citing works

Cellular Scaling Rules for the Brains of Marsupials: Not as “Primitive” as Expected

Santos, S. E. D., Porfírio, J., Cunha, F., Manger, P. R., Tavares, W. C., Pessôa, L. M., Raghanti, M. A., Sherwood, C. C., & Herculano‐Houzel, S. (2017) · Brain Behavior and Evolution · doi:10.1159/000452856 · Cited by 2,651 · see citing works

Meta-analytic evidence for common and distinct neural networks associated with directly experienced pain and empathy for pain

Lamm, C., Decety, J., & Singer, T. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.014 · Cited by 2,016 · see citing works

Pleasure Systems in the Brain

Berridge, K. C., & Kringelbach, M. L. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.018 · Cited by 1,730 · see citing works

Fractionating theory of mind: a meta-analysis of functional brain imaging studies

Schurz, M., Radua, J., Aichhorn, M., Richlan, F., & Perner, J. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.01.009 · Cited by 1,656 · see citing works

The neural correlates of maternal and romantic love

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

Knobil and Neill's Physiology of Reproduction

(2015) · Elsevier eBooks · doi:10.1016/c2011-1-07288-0 · Cited by 1,276 · see citing works

The neuroscience of empathy: Progress, pitfalls and promise

Zaki, J., & Ochsner, K. N. (2012) · Nature Neuroscience · doi:10.1038/nn.3085 · Cited by 1,231 · see citing works

Energy limitation as a selective pressure on the evolution of sensory systems

Niven, J. E., & Laughlin, S. B. (2008) · Journal of Experimental Biology · doi:10.1242/jeb.017574 · Cited by 1,056 · see citing works

Estrogen Actions Throughout the Brain

McEwen, B. (2002) · Recent Progress in Hormone Research · doi:10.1210/rp.57.1.357 · Cited by 915 · 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

Oxytocin enables maternal behaviour by balancing cortical inhibition

Marlin, B. J., Mitre, M., D’amour, J. A., Chao, M. V., & Froemke, R. C. (2015) · Nature · doi:10.1038/nature14402 · Cited by 744 · see citing works

The glia/neuron ratio: How it varies uniformly across brain structures and species and what that means for brain physiology and evolution

Herculano‐Houzel, S. (2014) · Glia · doi:10.1002/glia.22683 · Cited by 731 · 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

Neurotransmitter receptors on microglia

Pocock, J. M., & Kettenmann, H. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.07.007 · Cited by 650 · see citing works

Neuroimmune mechanisms of depression

Hodes, G. E., Kana, V., Menard, C., Merad, M., & Russo, S. J. (2015) · Nature Neuroscience · doi:10.1038/nn.4113 · Cited by 585 · see citing works

Deconstructing and reconstructing theory of mind

Schaafsma, S. M., Pfaff, D. W., Spunt, R. P., & Adolphs, R. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.11.007 · Cited by 498 · see citing works

Mothers' neural activation in response to pictures of their children and other children

Leibenluft, E., Gobbini, M. I., Harrison, T., & Haxby, J. V. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.05.017 · Cited by 493 · see citing works

Microglia and Beyond: Innate Immune Cells As Regulators of Brain Development and Behavioral Function

Lenz, K. M., & Nelson, L. H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00698 · Cited by 491 · see citing works

Emotion regulation in parenthood

Rutherford, H. J. V., Wallace, N. S., Laurent, H. K., & Mayes, L. C. (2015) · Developmental Review · doi:10.1016/j.dr.2014.12.008 · Cited by 485 · see citing works

Estrogen Prevents the Lipopolysaccharide-Induced Inflammatory Response in Microglia

Vegeto, E., Bonincontro, C., Pollio, G., Sala, A., Viappiani, S., Nardi, F., Brusadelli, A., Viviani, B., Ciana, P., & Maggi, A. C. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-06-01809.2001 · Cited by 475 · see citing works

Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity

Sorg, B. A., Berretta, S., Blacktop, J. M., Fawcett, J. W., Kitagawa, H., Kwok, J. C. F., & Miquel, M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2351-16.2016 · Cited by 454 · 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

Regulation of adult neurogenesis by stress, sleep disruption, exercise and inflammation: Implications for depression and antidepressant action☆

Lucassen, P. J., Meerlo, P., Naylor, A. S., van Dam, A. M., Dayer, A. G., Fuchs, E., Oomen, C. A., & Czéh, B. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2009.08.003 · Cited by 449 · see citing works

The plasticity of human maternal brain: Longitudinal changes in brain anatomy during the early postpartum period

Kim, P., Leckman, J. F., Mayes, L. C., Feldman, R., Wang, X., & Swain, J. E. (2010) · Behavioral Neuroscience · doi:10.1037/a0020884 · Cited by 440 · see citing works

The adaptive human parental brain: implications for children's social development

Feldman, R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.04.004 · Cited by 419 · see citing works

Steroid hormone receptor expression and function in microglia

Sierra, A., Gottfried‐Blackmore, A., Milner, T. A., McEwen, B. S., & Bulloch, K. (2008) · Glia · doi:10.1002/glia.20644 · Cited by 405 · see citing works

Seasonal plasticity in the adult brain

Tramontin, A. D., & Brenowitz, E. A. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01558-7 · Cited by 376 · see citing works

Antiinflammatory Effects of Estrogen on Microglial Activation

Bruce‐Keller, A. J., Keeling, J. L., Keller, J. N., Huang, F. F., Camondola, S., & Mattson, M. P. (2000) · Endocrinology · doi:10.1210/endo.141.10.7693 · Cited by 374 · see citing works

Oxytocin improves long-lasting spatial memory during motherhood through MAP kinase cascade

Tomizawa, K., Iga, N., Lü, Y.-F., Moriwaki, A., Matsushita, M., Li, S., Miyamoto, O., Itano, T., & Matsui, H. (2003) · Nature Neuroscience · doi:10.1038/nn1023 · Cited by 372 · see citing works

A potential role for thalamocingulate circuitry in human maternal behavior

Lorberbaum, J. P., Newman, J. D., Horwitz, A. R., Dubno, J. R., Lydiard, R. B., Hamner, M. B., Bohning, D. E., & George, M. S. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01284-7 · Cited by 359 · see citing works

The Functional Neuroanatomy of Maternal Love: Mother’s Response to Infant’s Attachment Behaviors

Noriuchi, M., Kikuchi, Y., & Senoo, A. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.05.018 · Cited by 334 · see citing works

Pituitary gland growth during normal pregnancy: An in Vivo study using magnetic resonance imaging

GONZALEZ, J., Elizondo, G., Saldivar, D., Náñez-Terreros, H., Todd, L. E., & Villarreal, J. Z. (1988) · The American Journal of Medicine · doi:10.1016/s0002-9343(88)80346-2 · Cited by 330 · see citing works

Effects of steroid hormones on neurogenesis in the hippocampus of the adult female rodent during the estrous cycle, pregnancy, lactation and aging

Pawluski, J. L., Brummelte, S., Barha, C. K., Crozier, T. M., & Galea, L. A. M. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.03.007 · Cited by 306 · 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

Effects of Estrogen and Progesterone on Serum and Pituitary Prolactin Levels in Ovariectomized Rats

Chen, C. L., & Meites, J. (1970) · Endocrinology · doi:10.1210/endo-86-3-503 · Cited by 293 · see citing works

Sex and seasonal changes in the rate of cell proliferation in the dentate gyrus of adult wild meadow voles

Galea, L. A. M., & McEwen, B. S. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00345-5 · Cited by 276 · see citing works

Perinatal depression—The fourth inflammatory morbidity of pregnancy?

Osborne, L. M., & Monk, C. E. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.03.019 · Cited by 261 · see citing works

Beyond the Hippocampus and the SVZ: Adult Neurogenesis Throughout the Brain

Jurkowski, M. P., Bettio, L. E. B., Woo, E. K., Patten, A. R., Yau, S., & Gil‐Mohapel, J. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.576444 · Cited by 255 · see citing works

Where is Cingulate Cortex? A Cross-Species View

van Heukelum, S., Mars, R. B., Guthrie, M., Buitelaar, J. K., Beckmann, C. F., Tiesinga, P. H. E., Vogt, B. A., Glennon, J. C., & Havenith, M. N. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.03.007 · Cited by 248 · see citing works

A lifetime of neurogenesis in the olfactory system

Brann, J. H., & Firestein, S. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00182 · Cited by 238 · 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

Elevated ethnocentrism in the first trimester of pregnancy

Navarrete, C. D., Fessler, D. M. T., & Eng, S. J. (2007) · Evolution and Human Behavior · doi:10.1016/j.evolhumbehav.2006.06.002 · 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

Menstrual cycle, pregnancy and oral contraceptive use alter attraction to apparent health in faces

Jones, B. C., Perrett, D. I., Little, A. C., Boothroyd, L. G., Cornwell, R. E., Feinberg, D. R., Tiddeman, B., Whiten, S., Pitman, R. M., Hillier, S. G., et al. (2005) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2004.2962 · Cited by 229 · 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

Parenting begets parenting: A neurobiological perspective on early adversity and the transmission of parenting styles across generations

Lomanowska, A. M., Boivin, M., Hertzman, C., & Fleming, A. S. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2015.09.029 · Cited by 224 · 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

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

Sex steroids and brain structure in pubertal boys and girls: a mini-review of neuroimaging studies

Peper, J. S., Pol, H. E. H., Crone, E. A., & van Honk, J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.02.014 · Cited by 204 · 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

Parental Care: Evolution, Mechanisms, and Adaptive Significance

(1996) · Advances in the study of behavior · doi:10.1016/s0065-3454(08)x6027-9 · Cited by 185 · see citing works

Dopamine in the medial amygdala network mediates human bonding

Atzil, S., Touroutoglou, A., Rudy, T., Salcedo, S., Feldman, R., Hooker, J. M., Dickerson, B. C., Catana, C., & Barrett, L. F. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1612233114 · Cited by 182 · see citing works

Somatosensation and Maternal Care in Norway Rats

Stern, J. M. (1996) · Advances in the study of behavior · doi:10.1016/s0065-3454(08)60335-6 · Cited by 181 · see citing works

The neural correlates of maternal sensitivity: an fMRI study

Musser, E. D., Kaiser-Laurent, H., & Ablow, J. C. (2012) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2012.04.003 · Cited by 177 · 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

Neural basis of maternal communication and emotional expression processing during infant preverbal stage

Lenzi, D., Trentini, C., Pantano, P., Macaluso, E., Iacoboni, M., Lenzi, G. L., & Ammaniti, M. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn153 · Cited by 174 · 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

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

The neural mechanisms and consequences of paternal caregiving

Feldman, R., Braun, K., & Champagne, F. A. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0124-6 · Cited by 168 · see citing works

Alterations of the cortical representation of the rat ventrum induced by nursing behavior

Xerri, C., Stern, J. M., & Merzenich, M. M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01710.1994 · Cited by 167 · see citing works

Neuron–Microglia Interactions in Mental Health Disorders: “For Better, and For Worse”

Wohleb, E. S. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00544 · Cited by 164 · see citing works

Neural plasticity in fathers of human infants

Kim, P., Rigo, P., Mayes, L. C., Feldman, R., Leckman, J. F., & Swain, J. E. (2014) · Social Neuroscience · doi:10.1080/17470919.2014.933713 · 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

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

Parenting and plasticity

Leuner, B., Glasper, E. R., & Gould, E. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.07.003 · Cited by 159 · see citing works

Immune activation in the early puerperium is related to postpartum anxiety and depressive symptoms

Maes, M. H. J., Lin, A.-H., Ombelet, W. U. A. M., Stevens, K., Kenis, G., Jongh, R. F. D., Cox, J., & Bosmans, E. (2000) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(99)00043-8 · Cited by 155 · 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

Shaping of the Female Human Brain by Sex Hormones: A Review

Rehbein, E., Hornung, J., Poromaa, I. S., & Derntl, B. (2020) · Neuroendocrinology · doi:10.1159/000507083 · Cited by 152 · 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

Perceived quality of maternal care in childhood and structure and function of mothers' brain

Kim, P., Leckman, J. F., Mayes, L. C., Newman, M., Feldman, R., & Swain, J. E. (2009) · Developmental Science · doi:10.1111/j.1467-7687.2009.00923.x · Cited by 149 · see citing works

Investigating the association between parental reflective functioning and distress tolerance in motherhood.

Rutherford, H. J. V., Booth, C. R., Luyten, P., Bridgett, D. J., & Mayes, L. C. (2015) · Infant Behavior and Development · doi:10.1016/j.infbeh.2015.04.005 · Cited by 149 · see citing works

The HPA Axis During the Perinatal Period: Implications for Perinatal Depression

Dickens, M. J., & Pawluski, J. L. (2018) · Endocrinology · doi:10.1210/en.2018-00677 · Cited by 148 · see citing works

Maternal Experience Produces Long-Lasting Behavioral Modifications in the Rat.

Love, G., Torrey, N., McNamara, I. M., Morgan, M. D., Banks, M., Hester, N. W., Glasper, E. R., DeVries, A. C., Kinsley, C. H., & Lambert, K. G. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.1084 · Cited by 142 · see citing works

Estrogen and brain inflammation: Effects on microglial expression of MHC, costimulatory molecules and cytokines

Dimayuga, F. O., Reed, J. L., Carnero, G. A., Wang, C., Dimayuga, E. R., Smith, V. D., Perger, A., Wilson, M. E., Keller, J. N., & Bruce‐Keller, A. J. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2004.12.016 · Cited by 142 · 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

Anti-Inflammatory Effects of Progesterone in Lipopolysaccharide-Stimulated BV-2 Microglia

Lei, B., Mace, B. E., Dawson, H. N., Warner, D. S., Laskowitz, D. T., & James, M. L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0103969 · Cited by 140 · see citing works

Emotional sensitivity for motherhood: Late pregnancy is associated with enhanced accuracy to encode emotional faces

Pearson, R. M., Lightman, S. L., & Evans, J. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.09.013 · Cited by 136 · see citing works

The development of maternal responsiveness in the rat.

Rosenblatt, J. S. (1969) · American Journal of Orthopsychiatry · doi:10.1111/j.1939-0025.1969.tb00619.x · Cited by 136 · see citing works

Excitability Changes Related to GABAAReceptor Plasticity during Pregnancy

Maguire, J. L., Ferando, I., Simonsen, C., & Módy, I. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2162-09.2009 · Cited by 134 · 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

Auditory Cortical Detection and Discrimination Correlates with Communicative Significance

Liu, R. C., & Schreiner, C. E. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050173 · Cited by 130 · see citing works

Intracerebral oxytocin is important for the onset of maternal behavior in inexperienced ewes delivered under peridural anesthesia.

Lévy, F., Kendrick, K. M., Keverne, E. B., Piketty, V., & al, E. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.2.427 · 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

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

Male pheromones initiate prolactin-induced neurogenesis and advance maternal behavior in female mice

Larsen, C. M., Kokay, I. C., & Grattan, D. R. (2008) · Hormones and Behavior · doi:10.1016/j.yhbeh.2007.11.020 · Cited by 121 · see citing works

Neurotransmitters and Microglial-Mediated Neuroinflammation

Lee, M. (2013) · Current Protein and Peptide Science · doi:10.2174/1389203711314010005 · Cited by 120 · see citing works

The maternal brain: an organ with peripartal plasticity

Hillerer, K. M., Jacobs, V. R., Fischer, T., & Aigner, L. (2014) · Neural Plasticity · doi:10.1155/2014/574159 · Cited by 120 · see citing works

Hippocampal lesions disrupt maternal, not sexual, behavior in the albino rat.

Kimble, D. P., Rogers, L., & Hendrickson, C. W. (1967) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0024605 · Cited by 119 · see citing works

CSF and plasma cytokines at delivery and postpartum mood disturbances

Boufidou, F., Lambrinoudaki, I., Argeitis, J., Zervas, I. M., Pliatsika, P., Leonardou, A. A., Petropoulos, G., Hassiakos, D., Papadias, K., & Nikolaou, C. (2008) · Journal of Affective Disorders · doi:10.1016/j.jad.2008.07.008 · Cited by 118 · see citing works

Cognitive Reorganization during Pregnancy and the Postpartum Period: An Evolutionary Perspective

Anderson, M. V., & Rutherford, M. D. (2012) · Evolutionary Psychology · doi:10.1177/147470491201000402 · 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

Innate and plastic mechanisms for maternal behaviour in auditory cortex

Schiavo, J. K., Valtcheva, S., Bair-Marshall, C. J., Song, S. C., Martin, K. A., & Froemke, R. C. (2020) · Nature · doi:10.1038/s41586-020-2807-6 · Cited by 113 · see citing works

Bidirectional psychoneuroimmune interactions in the early postpartum period influence risk of postpartum depression

Corwin, E. J., PAJER, K. A., Paul, S., Lowe, N. K., Weber, M., & McCarthy, D. O. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.04.012 · Cited by 112 · 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

Improved cortical entrainment to infant communication calls in mothers compared with virgin mice

Liu, R. C., Linden, J. F., & Schreiner, C. E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04840.x · 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

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

Serotonin and Sleep: Molecular, Functional and Clinical Aspects

Monti, J. M., Pandi-Perumal, S. R., Jacobs, B. L., & Nutt, D. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8561-3 · Cited by 107 · see citing works

Becoming a mother entails anatomical changes in the ventral striatum of the human brain that facilitate its responsiveness to offspring cues

Hoekzema, E. A., Tamnes, C. K., Berns, P., Barba‐Müller, E., Pozzobon, C., Picado, M., Lucco, F., Martínez‐Garcia, M., Desco, M., Ballesteros, A., et al. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104507 · 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

Mother to infant or infant to mother? Reciprocal regulation of responsiveness to stress in rodents and the implications for humans

Walker, C., Deschamps, S., Proulx, K., Tu, M. T., Salzman, C., Woodside, B. C., LUPIEN, S. J., Gallo‐Payet, N., & Richard, D. (2004) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0436 · Cited by 99 · see citing works

The Temporal Association Cortex Plays a Key Role in Auditory-Driven Maternal Plasticity

Tasaka, G., Feigin, L., Maor, I., Groysman, M., DeNardo, L. A., Schiavo, J. K., Froemke, R. C., Luo, L., & Mizrahi, A. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.004 · Cited by 98 · see citing works

Number of children is associated with neuropathology of Alzheimer's disease in women

Beeri, M. S., Rapp, M. A., Schmeidler, J., Reichenberg, A., Purohit, D. P., Perl, D. P., Grossman, H. T., Prohovnik, I., Haroutunian, V. H., & Silverman, J. M. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.11.011 · Cited by 96 · see citing works

Early and late effects of maternal experience on hippocampal neurogenesis, microglia, and the circulating cytokine milieu

Eid, R. S., Chaiton, J. A., Lieblich, S. E., Bodnar, T. S., Weinberg, J., & Galea, L. A. M. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.01.021 · Cited by 95 · see citing works

Pregnancy and adolescence entail similar neuroanatomical adaptations: a comparative analysis of cerebral morphometric changes

Carmona, S., Martínez‐García, M., Paternina‐Die, M., Barba‐Müller, E., Wierenga, L. M., Alemán‐Gómez, Y., Pretus, C., Marcos‐Vidal, L., Beumala, L., Cortizo, R., et al. (2019) · Human Brain Mapping · doi:10.1002/hbm.24513 · Cited by 95 · see citing works

Motherhood alters the cellular response to estrogens in the hippocampus later in life

Barha, C. K., & Galea, L. A. M. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.12.004 · 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

Baby stimuli and the parent brain: functional neuroimaging of the neural substrates of parent-infant attachment.

Swain, J. E. (2008) · Europe PMC (PubMed Central) · Cited by 89 · 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

Do Pregnancy-Induced Brain Changes Reverse? The Brain of a Mother Six Years after Parturition

Martínez‐Garcia, M., Paternina-Die, M., Barba‐Müller, E., de Blas, D. M., Beumala, L., Cortizo, R., Pozzobon, C., Vidal, L. M., Fernández‐Pena, A., Picado, M., et al. (2021) · Brain Sciences · doi:10.3390/brainsci11020168 · Cited by 86 · see citing works

The Best Laid Plans: Computational Principles of Anterior Cingulate Cortex

Holroyd, C. B., & Verguts, T. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.01.008 · Cited by 84 · see citing works

Blood mononuclear cell gene expression signature of postpartum depression

Segman, R. H., Goltser‐Dubner, T., Weiner, I., Canetti, L., Galili‐Weisstub, E., Milwidsky, A., Pablov, V., Friedman, N., & Hochner‐Celnikier, D. (2009) · Molecular Psychiatry · doi:10.1038/mp.2009.65 · Cited by 83 · see citing works

Reproductive experience alters corticosterone and CBG levels in the rat dam

Pawluski, J. L., Charlier, T. D., Lieblich, S. E., Hammond, G. L., & Galea, L. A. M. (2008) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.09.004 · Cited by 83 · see citing works

Neurofunctional maps of the ‘maternal brain’ and the effects of oxytocin: a multimodal voxel-based meta-analysis

Rocchetti, M., Radua, J., Paloyelis, Y., Xenaki, L., Frascarelli, M., Caverzasi, E., Politi, P., & Fusar‐Poli, P. (2014) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12185 · Cited by 83 · see citing works

Pup exposure facilitates retrieving behavior via the oxytocin neural system in female mice

Okabe, S., Tsuneoka, Y., Takahashi, A., Ooyama, R., Watarai, A., Maeda, S., Honda, Y., Nagasawa, M., Mogi, K., Nishimori, K., et al. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.01.036 · Cited by 82 · see citing works

Plasticity during Motherhood: Changes in Excitatory and Inhibitory Layer 2/3 Neurons in Auditory Cortex

Cohen, L., & Mizrahi, A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1786-14.2015 · Cited by 82 · see citing works

The missing link: Mothers’ neural response to infant cry related to infant attachment behaviors

Laurent, H. K., & Ablow, J. C. (2012) · Infant Behavior and Development · doi:10.1016/j.infbeh.2012.07.007 · Cited by 82 · see citing works

Parity modifies the effects of fluoxetine and corticosterone on behavior, stress reactivity, and hippocampal neurogenesis

Workman, J. L., Gobinath, A. R., Kitay, N. F., Chow, C., Brummelte, S., & Galea, L. A. M. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.11.027 · Cited by 82 · 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

Topographic organization and chemoarchitecture of the dorsal raphe nucleus and the median raphe nucleus

Lowry, C. A., Evans, A. K., Gasser, P. J., Hale, M. W., Staub, D. R., & Shekhar, A. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8561-3_2 · Cited by 75 · see citing works

Plasticity in the maternal circuit: Effects of experience and partum condition on brain astroctye number in female rats.

Featherstone, R. E., Fleming, A. S., & Ivy, G. O. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.1.158 · Cited by 74 · see citing works

Plasticity of the Parental Brain: A Case for Neurogenesis

Lévy, F., Gheusi, G., & Keller, M. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02203.x · Cited by 74 · see citing works

Exteroceptive stimulation of maternal behavior in the naive rat

Herrenkohl, L. R., & Rosenberg, P. A. (1972) · Physiology & Behavior · doi:10.1016/0031-9384(72)90080-7 · Cited by 72 · see citing works

Somatosensory maps

Harding-Forrester, S., & Feldman, D. E. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00004-8 · Cited by 72 · see citing works

Parity is associated with cognitive function and brain age in both females and males

Ning, K., Zhao, L., Franklin, M., Matloff, W. J., Batta, I., Arzouni, N., Sun, F., & Toga, A. W. (2020) · Scientific Reports · doi:10.1038/s41598-020-63014-7 · Cited by 71 · 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

From baby brain to mommy brain: Widespread gray matter gain after giving birth

Eileen Luders, A., Kurth, F., Gingnell, M., Engman, J., Yong, E., Poromaa, I. S., & Christian Gaser, B. (2020) · Cortex · doi:10.1016/j.cortex.2019.12.029 · Cited by 69 · see citing works

Neural correlates of hypothalamic–pituitary–adrenal regulation of mothers with their infants

Laurent, H. K., Stevens, A., & Ablow, J. C. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.06.011 · Cited by 67 · see citing works

Paternal experience suppresses adult neurogenesis without altering hippocampal function in <i>Peromyscus californicus</i>

Glasper, E. R., Kozorovitskiy, Y., Pavlic, A., & Gould, E. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22628 · Cited by 66 · see citing works

Stress and the pregnant female: Impact on hippocampal cell proliferation, but not affective-like behaviors

Pawluski, J. L., van den Hove, D., Rayen, I., Prickaerts, J., & Steinbusch, H. W. M. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.02.012 · Cited by 66 · see citing works

An examination of changes in maternal neuroimmune function during pregnancy and the postpartum period

Sherer, M., Posillico, C. K., & Schwarz, J. (2017) · Brain, behavior, and immunity · doi:10.1016/j.bbi.2017.06.016 · Cited by 66 · see citing works

Evidence for cell proliferation in the sheep brain and its down-regulation by parturition and interactions with the young

Brus, M., Meurisse, M., Franceschini, I., Keller, M., & Lévy, F. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.07.006 · Cited by 65 · see citing works

An investigation into the effects of antenatal stressors on the postpartum neuroimmune profile and depressive-like behaviors

Posillico, C. K., & Schwarz, J. M. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.11.011 · Cited by 65 · see citing works

Dendritic morphology in the striatum and hypothalamus differentially exhibits experience-dependent changes in response to maternal care and early social isolation

Shams, S., Pawluski, J. L., Chatterjee‐Chakraborty, M., Oatley, H., Mastroianni, A., & Fleming, A. S. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.048 · Cited by 64 · see citing works

Enhanced Synaptic Integration of Adult-Born Neurons in the Olfactory Bulb of Lactating Mothers

Kopel, H., Schechtman, E., Groysman, M., & Mizrahi, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6354-11.2012 · Cited by 64 · 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

Pup exposure elicits hippocampal cell proliferation in the prairie vole

Ruscio, M. G., Sweeny, T. D., Hazelton, J. L., Suppatkul, P., Boothe, E., & Carter, C. S. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.08.028 · Cited by 62 · see citing works

Cocaine alters dendritic spine density in cortical and subcortical brain regions of the postpartum and virgin female rat

Frankfurt, M., Salas-Ramirez, K. Y., Friedman, E., & Luine, V. N. (2011) · Synapse · doi:10.1002/syn.20918 · Cited by 61 · 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

Relationship between parenthood and cortical thickness in late adulthood

Orchard, E. R., Ward, P. G. D., Sforazzini, F., Storey, E., Egan, G. F., & Jamadar, S. D. (2020) · PLoS ONE · doi:10.1371/journal.pone.0236031 · Cited by 59 · see citing works

Pregnancy Decreases Oestrogen Receptor α Expression and Pyknosis, but not Cell Proliferation or Survival, in the Hippocampus

Pawluski, J. L., Barakauskas, V., & Galea, L. A. M. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.01960.x · Cited by 57 · see citing works

Emotion Reactivity Is Increased 4-6 Weeks Postpartum in Healthy Women: A Longitudinal fMRI Study

Gingnell, M., Bannbers, E., Moes, H. R., Engman, J., Sylvén, S. M., Skalkidou, A., Kask, K., Wikström, J., & Poromaa, I. S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128964 · Cited by 57 · see citing works

More than just mothers: The neurobiological and neuroendocrine underpinnings of allomaternal caregiving

Glasper, E. R., Kenkel, W. M., Bick, J. R., & Rilling, J. K. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.02.005 · Cited by 54 · see citing works

The main and accessory olfactory systems of female mice are activated differentially by dominant versus subordinate male urinary odors

Veyrac, A., Wang, G., Baum, M. J., & Bakker, J. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.035 · Cited by 52 · see citing works

Functional neurogenesis over the years

Snyder, J. S., & Drew, M. R. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112470 · Cited by 52 · see citing works

Brain orchestration of pregnancy and maternal behavior in mice: A longitudinal morphometric study

Barrière, D. A., Ella, A., Szeremeta, F., Adriaensen, H., Même, W., Chaillou, É., Migaud, M., Même, S., Lévy, F., & Keller, M. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117776 · Cited by 52 · see citing works

Duration of motherhood has incremental effects on mothers’ neural processing of infant vocal cues: a neuroimaging study of women

Parsons, C. E., Young, K. S., Petersen, M. V., Jegindoe Elmholdt, E.-M., Vuust, P., Stein, A., & Kringelbach, M. L. (2017) · Scientific Reports · doi:10.1038/s41598-017-01776-3 · Cited by 52 · see citing works

Effects of fimbria lesions on maternal behavior in the rat☆

Terlecki, L. J., & Sainsbury, R. (1978) · Physiology & Behavior · doi:10.1016/0031-9384(78)90281-0 · Cited by 51 · see citing works

Effects of stress early in gestation on hippocampal neurogenesis and glucocorticoid receptor density in pregnant rats

Pawluski, J. L., Császár, E., Savage, E., Martínez-Claros, M., Steinbusch, H. W. M., & van den Hove, D. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.048 · Cited by 51 · see citing works

Pregnancy or stress decrease complexity of CA3 pyramidal neurons in the hippocampus of adult female rats

Pawluski, J. L., Valença, A., Santos, A. I., Costa-Nunes, J. P., Steinbusch, H. W. M., & Strekalova, T. V. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.059 · Cited by 51 · see citing works

Lactation‐induced reduction in hippocampal neurogenesis is reversed by repeated stress exposure

Hillerer, K. M., Neumann, I. D., Couillard‐Després, S., Aigner, L., & Slattery, D. A. (2014) · Hippocampus · doi:10.1002/hipo.22258 · Cited by 50 · see citing works

Reversible plasticity in brain size, behaviour and physiology characterizes caste transitions in a socially flexible ant ( Harpegnathos saltator )

Penick, C. A., Ghaninia, M., Haight, K. L., Opachaloemphan, C., Yan, H., Reinberg, D., & Liebig, J. (2021) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2021.0141 · Cited by 50 · see citing works

The maternal brain: Neural responses to infants in mothers with and without mood disorder

Bjertrup, A. J., Friis, N. K., & Miskowiak, K. W. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.011 · Cited by 49 · see citing works

Experience-dependent cell survival in the maternal rat brain.

Akbari, E. M., Chatterjee, D., Lévy, F., & Fleming, A. S. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.5.1001 · Cited by 49 · see citing works

Olfactory Bulb Cells Generated in Adult Male Golden Hamsters Are Specifically Activated by Exposure to Estrous Females

Huang, L., & Bittman, E. L. (2002) · Hormones and Behavior · doi:10.1006/hbeh.2002.1767 · Cited by 48 · see citing works

Selective attention to fearful faces during pregnancy

Roos, A., Löchner, C., Kidd, M., van Honk, J., Vythilingum, B., & Stein, D. J. (2011) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2011.11.012 · Cited by 48 · see citing works

Mothering revisited: A role for cortisol?

Almanza-Sepúlveda, M. L., Fleming, A. S., & Jonas, W. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104679 · Cited by 48 · 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

A role for maternal physiological state in preserving auditory cortical plasticity for salient infant calls

Lin, F. G., Galindo-Leon, E. E., Ivanova, T. N., Mappus, R. C., & Liu, R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.020 · Cited by 45 · see citing works

Offspring-exposure reduces depressive-like behaviour in the parturient female rat

Pawluski, J. L., Lieblich, S. E., & Galea, L. A. M. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.08.001 · Cited by 45 · see citing works

Effects of maternal behavior induction and pup exposure on neurogenesis in adult, virgin female rats

Furuta, M., & Bridges, R. S. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.08.011 · Cited by 44 · see citing works

Neural pathways of maternal responding: systematic review and meta-analysis

Paul, S., Austin, J., Elliott, R., Ellison-Wright, I., Wan, M. W., Drake, R., Downey, D., Elmadih, A., Mukherjee, I., Heaney, L., et al. (2018) · Archives of Women s Mental Health · doi:10.1007/s00737-018-0878-2 · Cited by 43 · see citing works

Maternal brain resting‐state connectivity in the postpartum period

Dufford, A. J., Erhart, A., & Kim, P. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12737 · Cited by 43 · see citing works

Behavioral and neural correlates of cognitive–affective function during late pregnancy: An Event-Related Potentials Study

Raz, S. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.03.021 · Cited by 42 · see citing works

Nursing-Induced Somatosensory Cortex Plasticity: Temporally Decoupled Changes in Neuronal Receptive Field Properties Are Accompanied by Modifications in Activity-Dependent Protein Expression

Rosselet, C., Zennou-Azogui, Y., & Xerri, C. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3253-06.2006 · Cited by 42 · see citing works

Behavioral Relevance Helps Untangle Natural Vocal Categories in a Specific Subset of Core Auditory Cortical Pyramidal Neurons

Shepard, K. N., Lin, F. G., Zhao, C. L., Chong, K. K., & Liu, R. C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3803-14.2015 · Cited by 41 · see citing works

The Parental Brain: Mechanisms, Development, and Evolution

Numan, M. (2020) · Cited by 41 · see citing works

Postpartal Neural Plasticity of the Maternal Brain: Early Renormalization of Pregnancy-Related Decreases?

Lisofsky, N., Gallinat, J., Lindenberger, U., & Kühn, S. (2019) · Neurosignals · doi:10.33594/000000105 · Cited by 39 · 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

Plasticity in the olfactory bulb of the maternal mouse is prevented by gestational stress

Belnoue, L., Malvaut, S., Ladevèze, E., Abrous, D. N., & Koehl, M. (2016) · Scientific Reports · doi:10.1038/srep37615 · Cited by 37 · see citing works

Maternal experience and adult neurogenesis in mammals: Implications for maternal care, cognition, and mental health

Medina, J., & Workman, J. L. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24311 · Cited by 37 · see citing works

Mother-offspring interaction and pup development in genetically deaf mice

D'Amato, F. R., & Populin, R. (1987) · Behavior Genetics · doi:10.1007/bf01073113 · Cited by 34 · see citing works

Adult hypothalamic neurogenesis and sleep–wake dysfunction in aging

Kostin, A., Alam, A., McGinty, D., & Alam, M. N. (2020) · SLEEP · doi:10.1093/sleep/zsaa173 · Cited by 33 · see citing works

Motherhood and infant contact regulate neuroplasticity in the serotonergic midbrain dorsal raphe

Holschbach, M., & Lonstein, J. S. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.10.023 · Cited by 31 · see citing works

Disrupted Spontaneous Neural Activity Related to Cognitive Impairment in Postpartum Women

Zheng, J.-X., Chen, Y., Chen, H., Jiang, L., Bo, F., Feng, Y., Tang, W., Yin, X., & Gu, J. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.00624 · Cited by 31 · see citing works

Magnetic resonance spectroscopy in pre-eclampsia: evidence of cerebral ischaemia

Rutherford, J. M., Moody, A. R., Crawshaw, S., & Rubin, P. C. (2003) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1046/j.1471-0528.2003.00416.x · Cited by 31 · see citing works

Effects of pregnancy and differential environments on rat cerebral cortical depth

Hamilton, W. L., Diamond, M. C., Johnson, R. E., & Ingham, C. A. (1977) · Behavioral Biology · doi:10.1016/s0091-6773(77)91674-1 · Cited by 31 · see citing works

Bromodeoxyuridine infused into the cerebral ventricle of adult mice labels nigral neurons under physiological conditions—A method to detect newborn nerve cells in regions with a low rate of neurogenesis

Zhao, M., & Lang, A. M. J. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.08.007 · Cited by 29 · see citing works

Interactions with the young down-regulate adult olfactory neurogenesis and enhance the maturation of olfactory neuroblasts in sheep mothers

Brus, M., Meurisse, M., Keller, M., & Lévy, F. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00053 · Cited by 26 · see citing works

Optimizing brain performance: Identifying mechanisms of adaptive neurobiological plasticity

Lambert, K. G., Eisch, A. J., Galea, L. A. M., Kempermann, G., & Merzenich, M. M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.033 · Cited by 26 · see citing works

Effect of sertraline on central serotonin and hippocampal plasticity in pregnant and non-pregnant rats

Pawluski, J. L., Paravatou, R., Even, A., Cobraiville, G., Fillet, M., Kokras, N., Dalla, C., & Charlier, T. D. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.107950 · Cited by 26 · see citing works

Serotonin-specific lesions of the dorsal raphe disrupt maternal aggression and caregiving in postpartum rats

Holschbach, M., Vitale, E. M., & Lonstein, J. S. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.04.008 · Cited by 25 · see citing works

Differential effects of reproductive and hormonal state on basic fibroblast growth factor and glial fibrillary acid protein immunoreactivity in the hypothalamus and cingulate cortex of female rats

Salmaso, N., Popeski, N., Peronace, L., & Woodside, B. C. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.038 · Cited by 25 · see citing works

Disruption of adult olfactory neurogenesis induces deficits in maternal behavior in sheep

Corona, R., Meurisse, M., Cornilleau, F., Moussu, C., Keller, M., & Lévy, F. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.02.043 · Cited by 24 · see citing works

The Application of Connectome-Based Predictive Modeling to the Maternal Brain: Implications for Mother-Infant Bonding.

Rutherford, H., Potenza, M., Mayes, L., & Scheinost, D. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz185 · Cited by 24 · see citing works

The brain oxytocin and corticotropin-releasing factor systems in grieving mothers: What we know and what we need to learn

Demarchi, L., Pawluski, J. L., & Bosch, O. J. (2021) · Peptides · doi:10.1016/j.peptides.2021.170593 · Cited by 24 · see citing works

Lateralized Expression of Cortical Perineuronal Nets during Maternal Experience is Dependent on MECP2

Lau, B. Y. B., Layo-Carris, D. E., Emery, B. A., Everett, M., Kumar, A., Stevenson, P. K., Reynolds, K. G., Cherosky, A., Bowyer, S.-A. H., Roth, S., et al. (2020) · eNeuro · doi:10.1523/eneuro.0500-19.2020 · Cited by 24 · see citing works

Upregulation of astrocytic basic fibroblast growth factor in the cingulate cortex of lactating rats: Time course and role of suckling stimulation

Salmaso, N., & Woodside, B. C. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.05.006 · Cited by 23 · see citing works

Fluctuations in astrocytic basic fibroblast growth factor in the cingulate cortex of cycling, ovariectomized and postpartum animals

Salmaso, N., & Woodside, B. C. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.063 · Cited by 22 · see citing works

High nursing demand reduces depression-like behavior despite increasing glucocorticoid concentrations and reducing hippocampal neurogenesis in late postpartum rats

Guzman, R. M. D., Saulsbery, A. I., & Workman, J. L. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.07.012 · Cited by 21 · see citing works

Brain Structural Plasticity Associated with Maternal Caregiving in Mothers: A Voxel- and Surface-Based Morphometry Study

Zhang, K., Wang, M., Zhang, J., Du, X., & Chen, Z. (2019) · Neurodegenerative Diseases · doi:10.1159/000506258 · Cited by 20 · see citing works

Frontal circuit specialisations for decision making

Hunt, L. T. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15236 · Cited by 20 · see citing works

Oxytocin receptors in the midbrain dorsal raphe are essential for postpartum maternal social and affective behaviors

Grieb, Z. A., Ford, E. G., Yagan, M., Lau, B. Y. B., Manfredsson, F. P., Krishnan, K., & Lonstein, J. S. (2021) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2021.105332 · Cited by 20 · see citing works

Parity and neural responses to social and non-social stimuli in pregnancy

Rutherford, H. J. V., Maupin, A. N., & Mayes, L. C. (2018) · Social Neuroscience · doi:10.1080/17470919.2018.1518833 · Cited by 19 · see citing works

Neuroanatomical changes observed over the course of a human pregnancy

Pritschet, L., Taylor, C. M., Cossio, D. M., Faskowitz, J., Santander, T., Handwerker, D. A., Grotzinger, H., Layher, E., Chrastil, E. R., & Jacobs, E. G. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01741-0 · Cited by 178 · see citing works

Matrescence: lifetime impact of motherhood on cognition and the brain

Orchard, E. R., Rutherford, H. J. V., Holmes, A. J., & Jamadar, S. D. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2022.12.002 · Cited by 120 · see citing works

The transition to motherhood: linking hormones, brain and behaviour

Servin-Barthet, C., Martínez‐Garcia, M., Pretus, C., Paternina-Die, M., Soler, A., Khymenets, O., Pozo, Ó. J., Leuner, B., Vilarroya, Ó., & Carmona, S. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00733-6 · Cited by 105 · see citing works

Mapping the effects of pregnancy on resting state brain activity, white matter microstructure, neural metabolite concentrations and grey matter architecture

Hoekzema, E. A., van Steenbergen, H., Straathof, M., Beekmans, A., Freund, I. M., Pouwels, P. J. W., & Crone, E. A. (2022) · Nature Communications · doi:10.1038/s41467-022-33884-8 · Cited by 103 · 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

First-time fathers show longitudinal gray matter cortical volume reductions: evidence from two international samples

Martínez‐Garcia, M., Paternina-Die, M., Cárdenas, S. I., Vilarroya, Ó., Desco, M., Carmona, S., & Saxbe, D. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac333 · Cited by 45 · see citing works

Transmission of the adverse consequences of childhood maltreatment across generations: Focus on gestational biology

Moog, N. K., Heim, C. C., Entringer, S., Simhan, H. N., Wadhwa, P. D., & Buß, C. (2022) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2022.173372 · Cited by 43 · see citing works

A critical need for the concept of matrescence in perinatal psychiatry

Athan, A. M. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1364845 · Cited by 32 · see citing works

It’s time to rebrand “Mommy brain”

McCormack, C., Callaghan, B. L., & Pawluski, J. L. (2023) · JAMA Neurology · doi:10.1001/jamaneurol.2022.5180 · Cited by 30 · see citing works

Understanding the maternal brain in the context of the mental load of motherhood

Callaghan, B. L., McCormack, C. A., Kim, P., & Pawluski, J. L. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00268-4 · Cited by 25 · see citing works

Steroid hormones: risk and resilience in women’s Alzheimer disease

Calvo, N., & Einstein, G. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1159435 · Cited by 26 · see citing works

Prenatal prolactin predicts postnatal parenting attitudes and brain structure remodeling in first-time fathers

Aviv, E. C., Cárdenas, S. I., León, G. A., Waizman, Y. H., Gonzales, C. W., Flores, G., Martínez‐Garcia, M., & Saxbe, D. (2023) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2023.106332 · Cited by 20 · see citing works

Cellular and molecular signatures of motherhood in the adult and ageing rat brain

Duarte‐Guterman, P., Richard, J. E., Lieblich, S. E., Eid, R. S., Lamers, Y., & Galea, L. A. M. (2023) · Open Biology · doi:10.1098/rsob.230217 · Cited by 21 · 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

Recalibration of the stress response system over adult development: Is there a perinatal recalibration period?

Howland, M. A. (2023) · Development and Psychopathology · doi:10.1017/s0954579423000998 · Cited by 19 · see citing works

Changes in left hippocampal volume in first-time fathers: Associations with oxytocin, testosterone, and adaptation to parenthood.

Saxbe, D., Martínez-García, M., Cardenas, S. I., Waizman, Y. H., & Carmona, S. (2023) · Journal of neuroendocrinology · doi:10.1111/jne.13270 · Cited by 16 · see citing works

Gestational stress and perinatal SSRIs differentially impact the maternal and neonatal microbiome‐gut‐brain axis

Pawluski, J. L., Murail, P., Grudet, F., Bys, L., Golubeva, A. V., Bastiaanssen, T. F. S., Oberlander, T. F., Cryan, J. F., O’Mahony, S. M., & Charlier, T. D. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13261 · Cited by 17 · see citing works

Inhibition of the medial amygdala disrupts escalated aggression in lactating female mice after repeated exposure to male intruders

Abellán‐Álvaro, M., Martínez‐Garciá, F., Lanuza, E., & Agustín‐Pavón, C. (2022) · Communications Biology · doi:10.1038/s42003-022-03928-2 · Cited by 15 · see citing works

The parental brain, perinatal mental illness, and treatment: A review of key structural and functional changes

Pawluski, J. L. (2024) · Seminars in Perinatology · doi:10.1016/j.semperi.2024.151951 · Cited by 14 · see citing works

Pair-bonding and social experience modulate new neurons survival in adult male and female prairie voles (Microtus ochrogaster)

Castro, A. E., Domínguez‐Ordóñez, R., Young, L. J., Camacho, F., Ávila‐González, D., Paredes, R. G., Díaz, N. F., & Portillo, W. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.987229 · Cited by 14 · see citing works

Improving maternal well-being: a matrescence education pilot study for new mothers

Trinko, V., Sarewitz, J., & Athan, A. M. (2025) · Maternal Health Neonatology and Perinatology · doi:10.1186/s40748-025-00203-0 · Cited by 19 · see citing works

Pregnancy history and estradiol influence spatial memory, hippocampal plasticity, and inflammation in middle-aged rats

Puri, T. A., Lieblich, S. E., Ibrahim, M., & Galea, L. A. M. (2024) · Hormones and Behavior · doi:10.1016/j.yhbeh.2024.105616 · Cited by 13 · see citing works

Beyond sex and gender differences: The case for women's health research

Galea, L. A. M., Lee, B. H., de leon, R. G., Rajah, M. N., & Einstein, G. (2023) · Principles of Gender-Specific Medicine · doi:10.1016/b978-0-323-88534-8.00045-6 · Cited by 11 · see citing works

Neurosteroids: a lifelong impact on brain health

Walton, N. L., & Maguire, J. L. (2025) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2025.1644615 · Cited by 11 · see citing works

The mother–child interface: A neurobiological metamorphosis

Cainelli, E., Vedovelli, L., & Bisiacchi, P. S. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.10.027 · Cited by 11 · see citing works

Interoception in pregnancy: Implications for peripartum depression

Savoca, P. W., Glynn, L. M., Fox, M. M., Richards, M., & Callaghan, B. L. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105874 · Cited by 11 · see citing works

Parental status and markers of brain and cellular age: A 3D convolutional network and classification study

de Lange, A. G., Leonardsen, E. H., Barth, C., Schindler, L. S., Crestol, A., Holm, M. C., Subramaniapillai, S., Hill, D., Alnæs, D., & Westlye, L. T. (2024) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2024.107040 · Cited by 9 · see citing works

Re‐wiring of the bonded brain: Gene expression among pair bonded female prairie voles changes as they transition to motherhood

Forero, S. A., Liu, S., Shetty, N., & Ophir, A. G. (2024) · Genes Brain & Behavior · doi:10.1111/gbb.12906 · Cited by 9 · 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

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

Maternal History of Childhood Maltreatment and Brain Responses to Infant Cues Across the Postpartum Period

Bublitz, M. H., Swain, J. E., Lustig, S., Barthelemy, C., DeYoung, L. L. A., & Dickstein, D. P. (2022) · Child Maltreatment · doi:10.1177/10775595221128952 · Cited by 6 · see citing works

Dissociable role of the basolateral complex of the amygdala in the acquisition and extinction of conditioned fear following reproductive experience in female rats

Kershaw, K. A., Pestana, J. E., Brooke, M., Cardona, L. S., & Graham, B. M. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107863 · Cited by 6 · see citing works

Event-related potentials and behavioral correlates of emotional recognition memory in late pregnancy

Raz, S. (2024) · Archives of Women's Mental Health · doi:10.1007/s00737-024-01503-8 · Cited by 5 · see citing works

The effects of a second pregnancy on women’s brain structure and function

Straathof, M., Halmans, S., Pouwels, P. J. W., Crone, E. A., & Hoekzema, E. A. (2026) · Nature Communications · doi:10.1038/s41467-026-69370-8 · Cited by 9 · see citing works

Psilocybin during the postpartum period induces long-lasting adverse effects in both mothers and offspring

Hatzipantelis, C. J., Liu, M., Love, A., Leventhal, S. J., Maera, H., Viswanathan, S., Avetisyan, E., Belinsky, L., Rangel, M. M., Jain, N. J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64371-5 · Cited by 5 · see citing works

Executive functioning in matrescence and implications for perinatal depression

Ghadimi, T. R., & McCormack, C. A. (2025) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2025.1663017 · Cited by 5 · see citing works

GABAergic Neuroactive Steroids and Network States: Relevance to Peripartum Depression

Maguire, J. L., Antonoudiou, P., & Deligiannidis, K. M. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.09.019 · Cited by 4 · see citing works

Enduring maternal brain changes and their role in mediating motherhood’s impact on well-being

Rotondi, V., Allegra, M., Kashyap, R., Barban, N., Sironi, M., & Reverberi, C. (2024) · Scientific Reports · doi:10.1038/s41598-024-67316-y · Cited by 4 · see citing works

Redefining the mom brain narrative: Adaptive cognitive enhancements during the perinatal period

Ettinger, S., & Geller, P. A. (2025) · Journal of Health Psychology · doi:10.1177/13591053251329667 · Cited by 3 · see citing works

Plasticity of the parental brain

Husain, B. F. A., & Kohl, J. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103129 · Cited by 3 · see citing works

What can challenging reproductive contexts tell us about the rat’s maternal behavior?

Agrati, D., & Uriarte, N. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1239681 · Cited by 3 · 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

Pregnancy, Menopause, and Other Hormonal Factors

Combs, J. L., Netherton, E., & Combs, H. L. (2025) · Springer eBooks · doi:10.1007/978-3-031-87228-0_11 · Cited by 3 · see citing works

Motherhood and drinking: The relative importance of mental health and psychosocial factors on maternal alcohol misuse during the postpartum period

Prior, K., Piggott, M., Hunt, S., Vanstone, V., McCormack, C. A., Newton, N. C., Teesson, M., Birrell, L., Kershaw, S., Thornton, L. K., et al. (2024) · Journal of Studies on Alcohol and Drugs · doi:10.15288/jsad.23-00391 · Cited by 3 · see citing works

Dynamic brain plasticity during the transition to motherhood

Halmans, S., Straathof, M., & Hoekzema, E. A. (2024) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2024.10.011 · Cited by 2 · see citing works

Maternal brain plasticity, physiology and exercise science: A scoping narrative review

Barrett, C. M. E., Zeidy, Z., Farrell, A., Cahill, L. S., & Wadden, K. P. (2025) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2025.101185 · Cited by 2 · see citing works

Puberty, pregnancy, and menopause show shared and distinct structural changes across the lifespan

Hof, S. R. V. ’., Bos, M. G. N., Straathof, M., Crone, E. A., & Hoekzema, E. A. (2026) · Nature Communications · doi:10.1038/s41467-026-76755-2 · Cited by 2 · see citing works

Roadmap for maternal behavior research in domestic dogs: lessons from decades of laboratory rodent work

Li, M. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1394201 · Cited by 2 · see citing works

Longitudinal neuroanatomical increases from early to one-year postpartum

Dufford, A. J., Patterson, G., & Kim, P. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02852-x · Cited by 2 · 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

Letter to the Editor: Does fetal movement shape the maternal brain?

Ayala, K., Voegtline, K., & Rutherford, H. J. V. (2024) · Developmental Psychobiology · doi:10.1002/dev.22467 · Cited by 2 · see citing works

Improving maternal bonding through Real-time fMRI Neurofeedback in Mothers with Postpartum Bonding ProblemsPreprint

Zietlow, A., Brenner, I., Krauch, M., Gerchen, M. F., Schmitgen, M. M., Kirsch, P., Ditzen, B., & Eckstein, M. (2026) · Research Square · doi:10.21203/rs.3.rs-8166275/v1 · Cited by 2 · see citing works

Affective cognition in response to infant stimuli in pregnant compared with non-pregnant women

Bjertrup, A. J., Jahn, F. S., Hansen, L. S., & Miskowiak, K. W. (2024) · Women & Health · doi:10.1080/03630242.2024.2349562 · Cited by 1 · see citing works

Natural variations in maternal behavior shape anxiety and hippocampal neurogenesis in offspring

Grieco, F., van Gelderen, P., Ali, M., Larrieu, T., & Toni, N. (2026) · Life Science Alliance · doi:10.26508/lsa.202503419 · Cited by 3 · see citing works

Integrative perspective on the maternal gut-brain-breast axis: Linking dietary polyphenols, mental health, and human milk composition

Miranda, A. R., Barral, P. E., Serra, S. V., & Soria, E. A. (2026) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2026.110334 · Cited by 1 · see citing works

The Maternal Brain in Context: Systemic Physiological Changes Across Pregnancy

Grotzinger, H., Martínez‐Garcia, M., Miller, E. C., Stelzer, I. A., Collado, M. C., & Jacobs, E. G. (2026) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-102124-043515 · Cited by 1 · see citing works

Le cerveau parental : structure, fonction et synchronisation intercérébrale parent-enfant

Pawluski, J. L., & Vrtička, P. (2024) · Spirale · doi:10.3917/spi.107.0127 · Cited by 1 · see citing works

Pregnancy restructures the brain to prepare for childbirth and parenthood

McCormack, C. A., & Thomason, M. E. (2024) · Nature · doi:10.1038/d41586-024-03942-w · Cited by 1 · see citing works

Parent brain responses to child facial and vocal communication: What different methodologies reveal about parenting cognitions and practices as well as their moderation by parental status, gender, and culture as well as child characteristics

Bornstein, M. H., Gandjbakhche, A., Nguyen, T. K., & Esposito, G. (2025) · Neuroscience Research · doi:10.1016/j.neures.2025.104925 · Cited by 1 · see citing works

Natural variations in maternal behaviour shape trait anxiety and hippocampal neurogenesis in offspringPreprint

Grieco, F., van Gelderen, P., Larrieu, T., & Toni, N. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.28.615571 · Cited by 1 · see citing works

Anomalous cerebral morphology of pregnant women with cleft fetuses

Li, Z., Li, C., Liang, Y., Wang, K., Wang, L., Zhang, X., & Wu, Q. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.959710

Reproductive state matters when looking at the female brain and drug treatment effects

Dooper, M. (2022) · doi:10.55788/098ff967

Judith M. Stern

Lonstein, J. S. (2022) · Springer eBooks · doi:10.1007/978-3-031-12970-4_41

Brain structural and cognitive changes during pregnancy

Nasrallah, H. A. (2023) · Current Psychiatry · doi:10.12788/cp.0408

Current Trends

Roskam, I., Gross, J. J., & Mikolajczak, M. (2023) · Cambridge University Press eBooks · doi:10.1017/9781009304368.014

Neurobiology of Parenting and Implications for Emotion Regulation

Rutherford, H. J. V. (2023) · Cambridge University Press eBooks · doi:10.1017/9781009304368.017

Foetal Microchimerism and the Human Female Brain

Besser, M. (2024) · American Journal of Biomedical Science & Research · doi:10.34297/ajbsr.2024.21.002814

A common neural response to perceiving but not implicitly regulating infant and adult affect in postpartum mothers

Haigler, K., Finnegan, M. K., & Laurent, H. K. (2024) · Social Neuroscience · doi:10.1080/17470919.2024.2419650

Commentary on “Having two children might be best for women's mental health: Evidence from UK Biobank”

Brosch, K., Christensen, E. F., Wiersch, L., Hagen, D., Orchard, E. R., D'Anna‐Hernandez, K., Stolzenberg, D. S., & Dhamala, E. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.119687

Reproductive experience influences the effects of Lactocaseibacillus rhamnosus HN001 on gut microbiota and hippocampal plasticity in female rats

Pawluski, J. L., Kacimi, K., Zhang, C., Laetitia Guillot, D., Guidice, A. L., Charlier, T. D., & Lonstein, J. S. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70068

How FDA panelists casting doubt on antidepressant use during pregnancy could lead to devastating outcomes for mothers

PMH-C, N., & PhD, A. (2025) · doi:10.64628/aai.v6wy357cu

A Role for Fetal Movement in Shaping Maternal Neurodevelopment

Rutherford, H. J. V., Ayala, K., Falcioni, L., Eilbott, J., & Voegtline, K. (2025) · Developmental Psychobiology · doi:10.1002/dev.70073

Brain study identifies a cost of caregiving for new fathers

Saxbe, D. (2024) · doi:10.64628/aai.mnfxrddnd

Why do mood disturbances often occur in early postpartum? An integrative neurobiological and evolutionary perspective

Li, M. (2025) · Hormones and Behavior · doi:10.1016/j.yhbeh.2025.105857

Cell Type-Specific Remodelling of the Rat Hippocampus by Parity and AgePreprint

McGovern, A. J., Duarte‐Guterman, P., & Galea, L. A. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.17.676894

Santé mentale et cerveau maternel

Ayala, K., & Rutherford, H. J. V. (2025) · Sages-Femmes · doi:10.1016/j.sagf.2025.11.009

Das Erleben von Schwangerschaft und Geburt

Bolt, O. C., & Häne, A. (2026) · Springer eBooks · doi:10.1007/978-3-662-72027-1_2

Spatial mapping of cellular and molecular plasticity in the maternal and postpartum mouse brainPreprint

Arbabi, K., Ghazisaeidi, S., Kim, M., Kukreja, B., Feng, M. Y., Pogue, S., Hudson, H., Fafouti, M. E., Crouch, E. L., Galea, L. A. M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.03.697464

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Clephane, K., Lorenz, T. K., Calkins, F. C., Phillips, E. M., & Brock, R. L. (2026) · Evolutionary Psychological Science · doi:10.1007/s40806-025-00459-x

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Adam, N. (2022) · theses.fr (ABES) · doi:10.70675/f8535eb9z782dz40b8zb1d0z583132d3fd1b

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Lipschutz, R. S., Dahlgren, K., Santos, J., Chambers, K., McAfee, E., Abrams, C., Merrill, N. A., Brennan, P. A., Rilling, J. K., Michopoulos, V., et al. (2026) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2026.04.009

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Losse, E. M., Daneshnia, N., Dukart, J., Nehls, S., & Chechko, N. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-04104-4

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Cao, Y., Du, L., Zhang, S., Xu, L., Li, Q., Liu, J., Wang, W., (34472), D. W., Zhao, D., Cui, M., et al. (2026) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2026.111769

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Peng, W., & Rilling, J. K. (2026) · Human Brain Mapping · doi:10.1002/hbm.70591

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Breton, É., Tissink, E., Bon, G. M., van der Meer, D., Andreassen, O. A., & Kaufmann, T. (2026) · Biology of Sex Differences · doi:10.1186/s13293-026-00943-4

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Huang, M., Shi, D., Ni, J., Shi, Q., & Xu, R. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1867202

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Abuaish, S., Rutherford, H. J. V., Lonstein, J. S., & Pawluski, J. L. (2026) · Current Psychiatry Reports · doi:10.1007/s11920-026-01715-y

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Contelles-Marco, E., Sanchez-Palomares, P., Gómez-Sánchez, R. M., Chover‐Sierra, E., Navas-Echazarreta, N., Pozo‐Herce, P. D., Czapla, M., Juárez‐Vela, R., Martínez‐Sabater, A., & Martínez-Pascual, R. M. (2026) · Women · doi:10.3390/women6030056

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Thomas, E. B. K., Williams, M. A., Breheny, P. J., Miskolczi, A., & Demir‐Lira, Ö. E. (2026) · Journal of Neuroendocrinology · doi:10.1111/jne.70252

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Ayala, K., Niu, K., Murray, C. L., Voegtline, K., & Rutherford, H. J. V. (2026) · Journal of Neuroendocrinology · doi:10.1111/jne.70251

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Rilling, J. K. (2026) · doi:10.1002/9781394366156.ch2

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Hillerer, K. M., Jacobs, V. R., Fischer, T., & Aigner, L. (2014) · Neural Plasticity · doi:10.1155/2014/574159 · Cited by 120 · 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

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Tsuprykov, O., Hami, J., Freund, N., & Patzke, N. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.7303580

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