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Prospective association of maternal psychosocial stress in pregnancy with newborn hippocampal volume and implications for infant social-emotional development
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“No effects were found in the amygdala.”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [49]
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“In one study, greater maternal perceived stress during pregnancy was associated with smaller left, but not right, hippocampus volumes in infants shortly after birth.49”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [49]
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“For example, the link between prenatal maternal perceived stress and socioemotional scores on the Bayley Scales of Infant and Toddler, 3rd edition at ages 6 and 12 months was mediated by left hippocampus volume.49”
From Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development (2024) · cites this paper as [49]
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Yushkevich, P. A., Piven, J., Hazlett, H. C., Smith, R. G., Ho, S., Gee, J. C., & Gerig, G. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.015 · Cited by 8,868
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · cited 2×
“ation and learning, including fear and reward learning, as well as the processing of salience and novelty (Fareri and Tottenham, 2016; Lindquist et al., 2012).”
BackgroundHippocampal volume and depression: a meta-analysis of MRI studies
Videbech, P., & Ravnkilde, B. (2004) · American Journal of Psychiatry · doi:10.1176/appi.ajp.161.11.1957 · Cited by 1,590
Lemaire, V., Koehl, M., Le Moal, M., & Abrous, D. N. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.20.11032 · Cited by 1,044 · cited 2×
“In rodents and non-human primates, prenatal stress induces a global (i.e., not regionally-specific) decrease in HCV and inhibits local postnatal neurogenesis in regions including the dentate gyrus (Coe et al., 2003; Kawamura et al., 2006; Lemaire et al., 2000; Szuran et al., 1994).”
BackgroundBurt, K. B., Obradović, J., Long, J. D., & Masten, A. S. (2008) · Child Development · doi:10.1111/j.1467-8624.2007.01130.x · Cited by 383 · cited 2×
“…size with emotion regulation and empathic responding (Barch et al., 2019; Stern et al., 2019), and, as noted earlier, HCV-related social-emotional competence in childhood represents a key prognosticator of subsequent mental health and well-being (Bornstein et al., 2010; Burt et al., 2008).”
BackgroundPruessner, J. C., Dedovic, K., Pruessner, M., Lord, C., Buss, C., Collins, L., Dagher, A., & Lupien, S. J. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.02.016 · Cited by 333
Entringer, S., Buss, C., & Wadhwa, P. D. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.08.019 · Cited by 324
Self-citationProspective reports of chronic life stress predict decreased grey matter volume in the hippocampus
Gianaros, P. J., Jennings, J. R., Sheu, L. K., Greer, P. J., Kuller, L. H., & Matthews, K. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.10.045 · Cited by 324
Graham, A. M., Rasmussen, J. M., Rudolph, M. D., Heim, C. M., Gilmore, J. H., Styner, M., Potkin, S. G., Entringer, S., Wadhwa, P. D., Fair, D. A., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.05.027 · Cited by 282
Self-citationLocalization of glucocorticoid receptor mRNA in the male rat brain by in situ hybridization
Aronsson, M., Fuxe, K., Dong, Y., Agnati, L. F., Okret, S., & Gustafsson, J. A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.23.9331 · Cited by 261
Prenatal maternal depression associates with microstructure of right amygdala in neonates at birth.
Rifkin-Graboi, A., Bai, J., Chen, H., Hameed, W. B., Sim, L. W., Tint, M. T., Leutscher-Broekman, B., Chong, Y.-S., Gluckman, P. D., Fortier, M. V., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.06.019 · Cited by 258
Lebel, C., Walton, M., Letourneau, N., Giesbrecht, G. F., Kaplan, B. J., & Dewey, D. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.12.004 · Cited by 237
Wu, Y., Lu, Y.-C., Jacobs, M., Pradhan, S., Kapse, K., Zhao, L., Niforatos-Andescavage, N., Vezina, G., du Plessis, A. J., & Limperopoulos, C. (2020) · JAMA Network Open · doi:10.1001/jamanetworkopen.2019.19940 · Cited by 218
Graham, A. M., Rasmussen, J. M., Entringer, S., Ben Ward, E., Rudolph, M. D., Gilmore, J. H., Styner, M., Wadhwa, P. D., Fair, D. A., & Buss, C. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.06.023 · Cited by 203
Self-citationWen, D. J., Poh, J. S., Ni, S. N., Chong, Y.-S., Chen, H., Kwek, K., Shek, L. P., Gluckman, P. D., Fortier, M. V., Meaney, M. J., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.74 · Cited by 186
Milham, M. P., Nugent, A. C., Drevets, W. C., Dickstein, D. S., Leibenluft, E., Ernst, M., Charney, D., & Pine, D. S. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.01.038 · Cited by 186
Differential effects of prenatal stress on the morphological maturation of hippocampal neurons
Fujioka, A., Fujioka, T., Ishida, Y., Maekawa, T., & Nakamura, S. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.04.046 · Cited by 165
Reduced amygdalar and hippocampal size in adults with generalized social phobia
Irle, E., Ruhleder, M., Lange, C., Seidler-Brandler, U., Salzer, S., Dechent, P., Weniger, G., Leibing, E., & Leichsenring, F. (2010) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.090041 · Cited by 148
Glucocorticoid receptor protein expression in human hippocampus; stability with age
Wang, Q., Van Heerikhuize, J., Aronica, E., Kawata, M., Seress, L., Joels, M., Swaab, D. F., & Lucassen, P. J. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.11.019 · Cited by 144
Dean, D. C., Planalp, E. M., Wooten, W., Kecskemeti, S. R., Adluru, N., Schmidt, C. K., Frye, C., Birn, R. M., Burghy, C. A., Schmidt, N. L., et al. (2018) · JAMA Pediatrics · doi:10.1001/jamapediatrics.2018.2132 · Cited by 138
Self-citationLateral amygdaloid nucleus expansion in adult rats is associated with exposure to prenatal stress
Salm, A. K., Pavelko, M., Krouse, E. M., Webster, W., Kraszpulski, M., & Birkle, D. L. (2004) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.11.005 · Cited by 125
Association of Prenatal Maternal Anxiety With Fetal Regional Brain Connectivity
De Asis-Cruz, J., Krishnamurthy, D., Zhao, L., Kapse, K., Vezina, G., Andescavage, N., Quistorff, J., Lopez, C., & Limperopoulos, C. (2020) · JAMA Network Open · doi:10.1001/jamanetworkopen.2020.22349 · Cited by 81
Scheinost, D., Spann, M. N., McDonough, L., Peterson, B. S., & Monk, C. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0677-0 · Cited by 73
Prenatal Stress, Mood, and Gray Matter Volume in Young Adulthood
Marečková, K., Klasnja, A., Bencurova, P., Andrýsková, L., Brázdil, M., & Paus, T. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy030 · Cited by 52
Research works printed but not linked: 74
- Acosta, 2019, Maternal pregnancy-related anxiety is associated with sexually dimorphic alterations in amygdala volume in 4-year-old children, Front. Behav. Neurosci., 13, 10.3389/fnbeh.2019.00175 · DOI · Paper page
- Arnold, 1996, Human fetal hippocampal development: I. Cytoarchitecture, myeloarchitecture, and neuronal morphologic features, J. Comp. Neurol., 367, 274, 10.1002/(SICI)1096-9861(19960401)367:2<274::AID-CNE9>3.0.CO;2-2 · DOI
- Badihian, 2019, Transcriptional and epigenetic changes of brain derived neurotrophic factor following prenatal stress: a systematic review of animal studies, Neurosci. Biobehav. Rev.
- Barch, 2019, Early childhood depression, emotion regulation, episodic memory and hippocampal development, J. Abnorm. Psychol., 128, 81, 10.1037/abn0000392 · DOI
- Barros, 2006, Astrocyte–neuron vulnerability to prenatal stress in the adult rat brain, J. Neurosci. Res., 83, 787, 10.1002/jnr.20758 · DOI
- Blumenthal, 2002, Motion artifact in magnetic resonance imaging: implications for automated analysis, Neuroimage, 16, 89, 10.1006/nimg.2002.1076 · DOI
- Bornstein, 2010, Social competence, externalizing, and internalizing behavioral adjustment from early childhood through early adolescence: developmental cascades, Dev. Psychopathol., 22, 717, 10.1017/S0954579410000416 · DOI
- Buss, 2012, Maternal cortisol over the course of pregnancy and subsequent child amygdala and hippocampus volumes and affective problems, Proc. Natl. Acad. Sci. Unit. States Am., 109, E1312, 10.1073/pnas.1201295109 · DOI · Paper page
- Buss, 2012, Fetal programming of brain development: intrauterine stress and susceptibility to psychopathology, Sci. Signal., 5
- Buss, 2007, Maternal care modulates the relationship between prenatal risk and hippocampal volume in women but not in men, J. Neurosci., 27, 2592, 10.1523/JNEUROSCI.3252-06.2007 · DOI · Paper page
- Calcia, 2016, Stress and neuroinflammation: a systematic review of the effects of stress on microglia and the implications for mental illness, Psychopharmacology (Berl.), 233, 1637, 10.1007/s00213-016-4218-9 · DOI
- Charil, 2010, Prenatal stress and brain development, Brain Res. Rev., 65, 56, 10.1016/j.brainresrev.2010.06.002 · DOI
- Cherel, 2015, Automatic tissue segmentation of neonate brain MR images with subject-specific atlases, Proc. SPIE-Int. Soc. Opt. Eng., 9413
- Coe, 2003, Prenatal stress diminishes neurogenesis in the dentate gyrus of juvenile Rhesus monkeys, Biol. Psychiatr., 54, 1025, 10.1016/S0006-3223(03)00698-X · DOI · Paper page
- Cohen, 1983, A global measure of perceived stress, J. Health Soc. Behav., 24, 385, 10.2307/2136404 · DOI · Paper page
- Coussons-Read, 2007, Psychosocial stress increases inflammatory markers and alters cytokine production across pregnancy, Brain Behav. Immun., 21, 343, 10.1016/j.bbi.2006.08.006 · DOI · Paper page
- Davis, 2020, Prenatal maternal stress, child cortical thickness, and adolescent depressive symptoms, Child Dev., 91, e432, 10.1111/cdev.13252 · DOI · Paper page
- Dickerson, 2004, Acute stressors and cortisol responses: a theoretical integration and synthesis of laboratory research, Psychol. Bull., 130, 355, 10.1037/0033-2909.130.3.355 · DOI · Paper page
- Donnici, 2021, Prenatal and postnatal maternal anxiety and amygdala structure and function in young children, Sci. Rep., 11, 4019, 10.1038/s41598-021-83249-2 · DOI · Paper page
- Fareri, 2016, Effects of early life stress on amygdala and striatal development, Dev. Cogn. Neurosci., 19, 233, 10.1016/j.dcn.2016.04.005 · DOI
- Favaro, 2015, Neural correlates of prenatal stress in young women, Psychol. Med., 45, 2533, 10.1017/S003329171500046X · DOI · Paper page
- Ge, 2015, Development of the human fetal hippocampal formation during early second trimester, Neuroimage, 119, 33, 10.1016/j.neuroimage.2015.06.055 · DOI
- Gilmore, 2007, Regional gray matter growth, sexual dimorphism, and cerebral asymmetry in the neonatal brain, J. Neurosci., 27, 1255, 10.1523/JNEUROSCI.3339-06.2007 · DOI · Paper page
- Halligan, 2013, The longitudinal development of emotion regulation capacities in children at risk for externalizing disorders, Dev. Psychopathol., 25, 391, 10.1017/S0954579412001137 · DOI
- Hamilton, 2008, Amygdala volume in major depressive disorder: a meta-analysis of magnetic resonance imaging studies, Mol. Psychiatr., 13, 993, 10.1038/mp.2008.57 · DOI
- Harville, 2009, Stress questionnaires and stress biomarkers during pregnancy, J. Womens Health, 18, 1425, 10.1089/jwh.2008.1102 · DOI
- Hayashi, 1998, Maternal stress induces synaptic loss and developmental disabilities of offspring, Int. J. Dev. Neurosci., 16, 209, 10.1016/S0736-5748(98)00028-8 · DOI · Paper page
- Herman, 2005, Limbic system mechanisms of stress regulation: hypothalamo-pituitary-adrenocortical axis, Prog. Neuro-Psychopharmacol. Biol. Psychiatry, 29, 1201, 10.1016/j.pnpbp.2005.08.006 · DOI · Paper page
- Himes, 2011, Plasma corticotropin-releasing hormone and cortisol concentrations and perceived stress among pregnant women with preterm and term birth, Am. J. Perinatol., 28, 443, 10.1055/s-0030-1270119 · DOI
- Hou, 2013, Hippocampal asymmetry: differences in structures and functions, Neurochem. Res., 38, 453, 10.1007/s11064-012-0954-3 · DOI
- Immordino-Yang, 2013, Hippocampal contributions to the processing of social emotions, Hum. Brain Mapp., 34, 945, 10.1002/hbm.21485 · DOI
- Jacob, 2011, Fetal hippocampal development: analysis by magnetic resonance imaging volumetry, Pediatr. Res., 69, 425, 10.1203/PDR.0b013e318211dd7f · DOI
- Jia, 2010, Prenatal stress causes dendritic atrophy of pyramidal neurons in hippocampal CA3 region by glutamate in offspring rats, Dev. Neurobiol., 70, 114, 10.1002/dneu.20766 · DOI
- Kalra, 2007, The relationship between stress and hair cortisol in healthy pregnant women, Clin. Invest. Med. E103–E107, 10.25011/cim.v30i2.986 · DOI
- Kawamura, 2006, Prenatal stress suppresses cell proliferation in the early developing brain, Neuroreport, 17, 1515, 10.1097/01.wnr.0000236849.53682.6d · DOI
- Kendig, 2017, Consensus bundle on maternal mental health: perinatal depression and anxiety, Obstet. Gynecol., 129, 422, 10.1097/AOG.0000000000001902 · DOI
- Kier, 1997, Embryology of the human fetal hippocampus: MR imaging, anatomy, and histology, AJNR Am. J. Neuroradiol., 18, 525
- Kraszpulski, 2006, Prenatal stress affects the developmental trajectory of the rat amygdala, Stress, 9, 85, 10.1080/10253890600798109 · DOI · Paper page
- Lautarescu, 2020, Maternal prenatal stress is associated with altered uncinate fasciculus microstructure in premature neonates, Biol. Psychiatry, Stress Mechanisms and Fear Memories, 87, 559
- Lazarides, 2020, Psychological stress and cortisol during pregnancy: an ecological momentary assessment (EMA)-Based within- and between-person analysis, Psychoneuroendocrinology, 121, 104848, 10.1016/j.psyneuen.2020.104848 · DOI
- Lehtola, 2020, Newborn amygdalar volumes are associated with maternal prenatal psychological distress in a sex-dependent way, NeuroImage Clin, 28, 102380, 10.1016/j.nicl.2020.102380 · DOI · Paper page
- Levine, 2016, Prenatal stress and hemodynamics in pregnancy: a systematic review, Arch. Womens Ment. Health, 19, 721, 10.1007/s00737-016-0645-1 · DOI
- Lupien, 2007, Hippocampal volume is as variable in young as in older adults: implications for the notion of hippocampal atrophy in humans, Neuroimage, 34, 479, 10.1016/j.neuroimage.2006.09.041 · DOI · Paper page
- Lupien, 2018, The effects of chronic stress on the human brain: from neurotoxicity, to vulnerability, to opportunity, Front. Neuroendocrinol., Stress and the Brain, 49, 91, 10.1016/j.yfrne.2018.02.001 · DOI
- Madigan, 2018, A meta-analysis of maternal prenatal depression and anxiety on child socioemotional development, J. Am. Acad. Child Adolesc. Psychiatry, 57, 645, 10.1016/j.jaac.2018.06.012 · DOI
- Maltbie, 2012, Asymmetric bias in user guided segmentations of brain structures, Neuroimage, 59, 1315, 10.1016/j.neuroimage.2011.08.025 · DOI
- Marečková, 2018, Perinatal stress and human hippocampal volume: findings from typically developing young adults, Sci. Rep., 8, 4696, 10.1038/s41598-018-23046-6 · DOI
- Martínez-Téllez, 2009, Prenatal stress alters spine density and dendritic length of nucleus accumbens and hippocampus neurons in rat offspring, Synapse, 63, 794, 10.1002/syn.20664 · DOI
- McEwen, 1992, The vulnerability of the hippocampus to protective and destructive effects of glucocorticoids in relation to stress, Br. J. Psychiatr. Suppl., 18, 10.1192/S0007125000296645 · DOI
- McQuaid, 2019, Altered cortical structure and psychiatric symptom risk in adolescents exposed to maternal stress in utero: a retrospective investigation, Behav. Brain Res., 375, 112145, 10.1016/j.bbr.2019.112145 · DOI
- Merz, 2018, Socioeconomic status, amygdala volume, and internalizing symptoms in children and adolescents, J. Clin. Child Adolesc. Psychol., 47, 312, 10.1080/15374416.2017.1326122 · DOI
- Müller, 2006, The amygdaloid complex and the medial and lateral ventricular eminences in staged human embryos, J. Anat., 208, 547, 10.1111/j.1469-7580.2006.00553.x · DOI
- Neveu, 1998, Asymmetrical distribution of hippocampal mineralocorticoid receptors depends on lateralization in mice, Neuroimmunomodulation, 5, 16, 10.1159/000026322 · DOI
- Nolvi, 2021, Neonatal amygdala volumes and the development of self-regulation from early infancy to toddlerhood, Neuropsychology, 35, 285, 10.1037/neu0000724 · DOI
- O'Brien, 1981, Assessment of gestational age in the second trimester by real-time ultrasound measurement of the femur length, Am. J. Obstet. Gynecol., 139, 540, 10.1016/0002-9378(81)90514-7 · DOI
- Ong, 2019, Neonatal amygdalae and hippocampi are influenced by genotype and prenatal environment, and reflected in the neonatal DNA methylome, Gene Brain Behav., 18, 10.1111/gbb.12576 · DOI · Paper page
- Qiu, 2015, Prenatal maternal depression alters amygdala functional connectivity in 6-month-old infants, Transl. Psychiatry, 5, e508, 10.1038/tp.2015.3 · DOI · Paper page
- Qiu, 2013, Maternal anxiety and infants' hippocampal development: timing matters, Transl. Psychiatry, 3, e306, 10.1038/tp.2013.79 · DOI · Paper page
- Rasmussen, 2019, Maternal Interleukin-6 concentration during pregnancy is associated with variation in frontolimbic white matter and cognitive development in early life, Neuroimage, 185, 825, 10.1016/j.neuroimage.2018.04.020 · DOI
- Rasmussen, 2017, A novel maturation index based on neonatal diffusion tensor imaging reflects typical perinatal white matter development in humans, Int. J. Dev. Neurosci. Off. J. Int. Soc. Dev. Neurosci., 56, 42, 10.1016/j.ijdevneu.2016.12.004 · DOI
- Robinson, 2016, Functional connectivity of the left and right hippocampi: evidence for functional lateralization along the long-axis using meta-analytic approaches and ultra-high field functional neuroimaging, Neuroimage, 135, 64, 10.1016/j.neuroimage.2016.04.022 · DOI
- Rogers, 2012, Regional cerebral development at term relates to school-age social-emotional development in very preterm children, J. Am. Acad. Child Adolesc. Psychiatry, 51, 181, 10.1016/j.jaac.2011.11.009 · DOI
- Rosso, 2005, Amygdala and hippocampus volumes in pediatric major depression, Biol. Psychiatr., 57, 21, 10.1016/j.biopsych.2004.10.027 · DOI
- Rubin, 2014, The role of the hippocampus in flexible cognition and social behavior, Front. Hum. Neurosci., 8, 10.3389/fnhum.2014.00742 · DOI · Paper page
- Rudolph, 2018, Maternal IL-6 during pregnancy can be estimated from newborn brain connectivity and predicts future working memory in offspring, Nat. Neurosci., 21, 765, 10.1038/s41593-018-0128-y · DOI · Paper page
- Seth, 2016, Perinatal maternal depression and cortisol function in pregnancy and the postpartum period: a systematic literature review, BMC Pregnancy Childbirth, 16, 124, 10.1186/s12884-016-0915-y · DOI
- Skovgaard, 2008, Predictors (0–10 months) of psychopathology at age 1½ years – a general population study in the Copenhagen Child Cohort CCC 2000*, JCPP (J. Child Psychol. Psychiatry), 49, 553, 10.1111/j.1469-7610.2007.01860.x · DOI
- Stern, 2019, Empathic responding and hippocampal volume in young children, Dev. Psychol., 55, 1908, 10.1037/dev0000684 · DOI
- Szuran, 1994, Water maze performance and hippocampal weight of prenatally stressed rats, Behav. Brain Res., 65, 153, 10.1016/0166-4328(94)90100-7 · DOI
- Tamura, 2011, Prenatal stress inhibits neuronal maturation through downregulation of mineralocorticoid receptors, J. Neurosci., 31, 11505, 10.1523/JNEUROSCI.3447-10.2011 · DOI
- Tang, 2020, Infant behavioral inhibition predicts personality and social outcomes three decades later, Proc. Natl. Acad. Sci. Unit. States Am., 117, 9800, 10.1073/pnas.1917376117 · DOI
- Tuulari, 2020, Newborn left amygdala volume associates with attention disengagement from fearful faces at eight months, Dev. Cogn. Neurosci., 45, 10.1016/j.dcn.2020.100839 · DOI
- van den Heuvel, 2021, Maternal stress during pregnancy alters fetal cortico-cerebellar connectivity in utero and increases child sleep problems after birth, Sci. Rep., 11, 2228, 10.1038/s41598-021-81681-y · DOI · Paper page
- Wang, 2014, Multi-atlas segmentation of subcortical brain structures via the AutoSeg software pipeline, Front. Neuroinf., 8, 7, 10.3389/fninf.2014.00007 · DOI
Cited by
Wu, Y., De Asis-Cruz, J., & Limperopoulos, C. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02449-0 · Cited by 124
“Studies examining the effects of prenatal maternal stress exposure on brain development in the offspring have focused on newborns [14 – 19], children [20 – 27], adults [28 – 31], and more recently, fetuses [4, 32 – 35].”
BackgroundMaternal depressive symptoms, neonatal white matter, and toddler social-emotional development
Lautarescu, A., Bonthrone, A. F., Pietsch, M., Batalle, D., Cordero-Grande, L., Tournier, J.-D., Christiaens, D., Hajnal, J. V., Chew, A., Falconer, S., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02073-y · Cited by 29
Herzberg, M. P., & Smyser, C. D. (2024) · Pediatric Research · doi:10.1038/s41390-024-03345-7 · Cited by 22
Acosta, H., Kantojärvi, K., Tuulari, J. J., Lewis, J. D., Hashempour, N., Scheinin, N. M., Lehtola, S. J., Nolvi, S., Fonov, V. S., Collins, D. L., et al. (2024) · Development and Psychopathology · doi:10.1017/s0954579423000275 · Cited by 11
Self-citation
Metadata
- Authors
- Moog, N. K., Nolvi, S., Kleih, T. S., Styner, M., Gilmore, J. H., Rasmussen, J. M., Heim, C. M., Entringer, S., Wadhwa, P. D., & Buss, C.
- Venue
- Neurobiology of Stress
- Publisher
- Elsevier BV
- Published
- 2021-11
- Volume
- 15
- Pages
- 100368
- ISSN
- 2352-2895
- Cited by
- 65
- References
- 24
- Language
- en
- Licence
- Funders
- National Institutes of Health (UH3 OD-023349, R01 MH-105538, R01 HD-060628)
- Emil Aaltosen Säätiö
- Alexander von Humboldt-Stiftung
- ERC
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