Distress During Pregnancy: Epigenetic Regulation of Placenta Glucocorticoid-Related Genes and Fetal Neurobehavior

A Global Measure of Perceived Stress

Cohen, S., Kamarck, T., & Mermelstein, R. (1983) · Journal of Health and Social Behavior · doi:10.2307/2136404 · Cited by 32,807

The assessment of anxiety states by rating

HAMILTON, M. (1959) · British Journal of Medical Psychology · doi:10.1111/j.2044-8341.1959.tb00467.x · Cited by 11,455

Untitled work

Wilamowska (2010) · doi:10.1001/archpsyc.1988.01800320058007 · Cited by 2,115

The role of FKBP5, a co-chaperone of the glucocorticoid receptor in the pathogenesis and therapy of affective and anxiety disorders

Binder, E. B. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.05.021 · Cited by 968

Early Life Programming and Neurodevelopmental Disorders

Bale, T. L., Baram, T. Z., Brown, A. S., Goldstein, J. M., Insel, T. R., McCarthy, M. M., Nemeroff, C. B., Reyes, T. M., Simerly, R. B., Susser, E. S., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.05.028 · Cited by 961

Glucocorticoids and fetal programming part 1: outcomes

Moisiadis, V. G., & Matthews, S. G. (2014) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2014.73 · Cited by 586

Epigenetic and transgenerational reprogramming of brain development

Bale, T. L. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3818 · Cited by 505

Maternal prenatal anxiety and downregulation of placental 11β-HSD2

O’Donnell, K. J., Bugge Jensen, A., Freeman, L., Khalife, N., O’Connor, T. G., & Glover, V. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.09.014 · Cited by 449

Prenatal Stress and Its Effects on the Fetus and the Child: Possible Underlying Biological Mechanisms

Glover, V. A. S. (2014) · Advances in neurobiology · doi:10.1007/978-1-4939-1372-5_13 · Cited by 422

Epigenetic Effects of Prenatal Stress on 11β-Hydroxysteroid Dehydrogenase-2 in the Placenta and Fetal Brain

Peña, C. J., Monk, C. E., & Champagne, F. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039791 · Cited by 377

Visual Development

Maurer, D. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.006 · Cited by 3

Epigenetic Effects of Prenatal Stress

Mueller, I., Shakiba, N., Brown, M. A., Crowel, S. E., & Conradt, E. D. (2021) · Springer eBooks · doi:10.1007/978-3-030-60159-1_5 · Cited by 4

Infant Learning in the Digital Age

Rusnak, S. N., & Barr, R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.016 · Cited by 3

Maternal-fetal Stress and Dna Methylation Signatures in Neonatal Saliva: an Epigenome-wide Association Study.Preprint

Sharma, R., Frasch, M. G., Zelgert, C., Zimmermann, P., Fabre, B. R., Wilson, R., Waldenberger, M., MacDonald, J. W., Bammler, T. K., Lobmaier, S. M., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1348030/v1 · Cited by 3

Infant Memory

Hayne, H., & Herbert, J. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.012 · Cited by 1

Advance in the mechanisms underlying prenatal stress-induced depressive-like behavior in offspring

Xu, K., Song, D., Li, H., Lu, Y., & Zhu, Z. (2025) · Brain Behavior and Immunity Integrative · doi:10.1016/j.bbii.2025.100108 · Cited by 2

Dual Mechanisms of Chronic Stress in Recurrent Pregnancy Loss: Progesterone Deficiency and Inflammatory Amplification

Lu, J., Yang, X., Liu, C., Wang, W., Wei, X., Xu, J., & Wang, F. (2025) · Comprehensive physiology · doi:10.1002/cph4.70063 · Cited by 2

Health disturbances stemming from overcrowding and inadequate housing among indigenous peoples within Canada

Anisman, H., Bombay, A., & Matheson, K. (2025) · Frontiers in Environmental Health · doi:10.3389/fenvh.2025.1720326 · Cited by 4

Early Life Stress and Adversity in Children: Neuroendocrine Mechanisms, Epigenetic Regulation, and Lifespan Developmental Outcomes—A Narrative Review

Pipelias, P., Kanaka‐Gantenbein, C., & Pervanidou, P. (2026) · Children · doi:10.3390/children13060802 · Cited by 4

Epigenetic modifications in the human placenta

Robinson, W. P., Peñaherrera, M. S., Konwar, C., Yuan, V., & Wilson, S. L. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91380-5.00031-9 · Cited by 2

Stress and DNA Methylation of Blood Leukocytes among Pregnant Latina Women

Barcelona, V., Abuaish, S., Lee, S., Harkins, S., Butler, A. D., Tycko, B., Baccarelli, A., Walsh, K., & Monk, C. E. (2023) · Epigenomes · doi:10.3390/epigenomes7040027 · Cited by 3

Placental DNA methylation key topics: Sex- and cell-type specificity, mediation, multi-omics, and biomarker discovery

Cohen, N. J., Lesseur, C., Cardenas, A., Ward-Caviness, C. K., Spring, A. C., Rager, J. E., Fry, R. C., & Eaves, L. A. (2025) · Epigenomics · doi:10.1080/17501911.2025.2533115 · Cited by 2

Examining cross-lag associations between perceived stress and hair cortisol from pregnancy to 15 months postpartum

Khoury, J. E., Jambon, M. M., González, A., & Atkinson, L. R. (2025) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2025.107556 · Cited by 2

Placenta and Cord Blood as Source of Immune Markers of Offspring Neurodevelopment and Psychopathology

Silva, A. C. S. E., Moreira, J. M., & Magalhães, R. C. (2020) · Progress in inflammation research · doi:10.1007/978-3-030-39335-9_14 · Cited by 2

Embodied Brain Model for Understanding Functional Neural Development of Fetuses and Infants

Yamada, Y., Kanazawa, H., & Kuniyoshi, Y. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.001 · Cited by 3

Prenatal Programming in the Fetus and Placenta

Scorza, P., Doyle, C., & Monk, C. E. (2021) · Springer eBooks · doi:10.1007/978-3-030-60159-1_4 · Cited by 2

Proceedings of the 2021 annual meeting of the Fetal Alcohol Spectrum Disorders Study Group

Mooney, S. M., Petrenko, C. L. M., Hamre, K. M., & Brigman, J. L. (2022) · Alcohol · doi:10.1016/j.alcohol.2022.04.006 · Cited by 2

ANSIEDADE PRÉ-NATAL E SEUS IMPACTOS NA PROGRAMAÇÃO FETAL

Gomes, G. F., Fukushima, A. R., & Nicoletti, M. A. (2022) · Revista Intertox de Toxicologia Risco Ambiental e Sociedade · doi:10.22280/revintervol15ed2.512 · Cited by 2

The Effects of Maternal Prenatal Stress on Fetal and Child Development

Glover, V. A. S. (2021) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190674687.013.7 · Cited by 2

What Are the Transgenerational Consequences of Maternal Childhood Adversity and Maternal Stress During Pregnancy?

Leckman, J. F. (2017) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2017.09.421 · Cited by 2

The Development of Touch Perception and Body Representation

Bremner, A. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.009 · Cited by 3

Infant Development and Stigma

Wittenberg, J. P. (2023) · Springer eBooks · doi:10.1007/978-3-031-42502-8_6 · Cited by 1

Brain Training to Facilitate Labor and Birth: Impact of a Mobile Health Application

Hock, A., Donegan, T., Macedo, L. G., Pelino, S. D., & Dufour, S. P. (2024) · The Journal of Perinatal Education · doi:10.1891/jpe-2023-0033 · Cited by 1

Associations among prenatal stress, socioeconomic status, and infant epigenetic aging

Sperber, J. F., Hart, E. R., Troller‐Renfree, S. V., Watts, T. W., Miller, M., Bellatin, A., Meyer, J. S., Dettmer, A. M., Champagne, F. A., & Noble, K. G. (2025) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2025.107575 · Cited by 1

Pregnancy psychological distress: A concept analysis

Zhao, M., Han, J., Zhang, S., & Luo, T. (2025) · Midwifery · doi:10.1016/j.midw.2025.104626 · Cited by 1

Neuroplacentology of stress: Novel frontiers linking maternal mental health to offspring neurodevelopment

Cruceanu, C. (2025) · Neurobiology of Stress · doi:10.1016/j.ynstr.2025.100778 · Cited by 1

Glucocorticoid Receptor Signaling: Multilevel Organization, Roles in Fetal Development, and Postnatal Outcomes

Potapova, S., Isakov, Y., Tyulkova, E. I., & Vetrovoy, O. V. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062873 · Cited by 2

Infant Visual Attention

Amso, D., & Tummeltshammer, K. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.007 · Cited by 1

Early Knowledge About Space and Quantity

Newcombe, N. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.015 · Cited by 1

Stress-Mediated Regulation of the DNA Methylome

Dick, A. L. W., & Chen, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813156-5.00004-2 · Cited by 1

Traces of the Invisible World of Becoming – Epigenetics as a Molecular Correlate of Prenatal Psychology

Assmann, B. (2020) · Springer eBooks · doi:10.1007/978-3-030-41716-1_11 · Cited by 1

Maternal prenatal depression is associated with dysregulation over the first five years of life moderated by child polygenic risk for comorbid psychiatric problems

Babineau, V., Jolicoeur‐Martineau, A., Székely, E., Green, C. G., Sassi, R. B., Gaudreau, H., Levitan, R. D., Lydon, J. E., Steiner, M. S., O’Donnell, K. J., et al. (2023) · Developmental Psychobiology · doi:10.1002/dev.22395 · Cited by 1

Teaching Cognitive/Behavioral Neuroscience Through a DEI Lens

Opper, J. K. (2023) · Teaching of Psychology · doi:10.1177/00986283231183936 · Cited by 1

The epigenetics of anxiety

Richter, T. A., Baraty, L. J., & Hunter, R. G. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18516-8.00004-1 · Cited by 1

Reconstructing birth: women’s memory processes and recall of birth experience in the first year postpartum

Çalık, K. Y., & Durum, H. N. (2025) · Current Psychology · doi:10.1007/s12144-025-08087-1 · Cited by 1

Distinct maternal DNA methylation associations with gestational age at early and late-mid term pregnancy in a low- and middle-income country: evaluation of biological, genetic, and psychosocial contributors

Jude, M. S., Konwar, C., McQuaid, R. J., Ghani, F., Islam, N., Lalani, S. B., Merrill, S. M., Fatima, F., MacIsaac, J. L., Forcheh, N., et al. (2025) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-025-08037-6 · Cited by 1

Infant Word Learning and Emerging Syntax

Levine, D., Hirsh‐Pasek, K., & Golinkoff, R. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.023 · Cited by 2

Infants’ Perception of Auditory Patterns

Cirelli, L. K., & Trehub, S. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.008 · Cited by 1

The Mirror Neuron System and Social Cognition

Fox, N. A., Salo, V. C., Debnath, R., Morales, S., & Smith, E. G. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.018 · Cited by 1

Infant Categorization

Oakes, L. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.014 · Cited by 1

Invited Commentary: An Ingenious Approach to Examining the Relationship Between Maternal Stress and Offspring Health?

Keyes, K. M., & Susser, E. (2016) · American Journal of Epidemiology · doi:10.1093/aje/kww173 · Cited by 1

Maternal distress, DNA methylation, and fetal programming of stress physiology in Brazilian mother-infant pairsPreprint

Wiley, K. S., Camilo, C., Gouveia, G. R., Euclydes, V. L. V., Panter‐Brick, C., Matijasevich, A., Ferraro, A. A., Fracolli, L. A., Chiesa, A. M., Miguel, E. C., et al. (2022) · doi:10.31234/osf.io/6mfbe · Cited by 1

Associations between prenatal distress, mitochondrial health, and gestational age: findings from two pregnancy studies in the USA and TurkeyPreprint

Huang, Q., Shire, D., Hollis, F., Abuaish, S., Picard, M. A., Monk, C. E., Duman, E. A., & Trumpff, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.16.618719 · Cited by 1

Effects of Maternal stress on epigenetic markers on fetal tissues and neurodevelopment at various gestational ages: A Systematic reviewPreprint

Jassim, S., & Basheer, S. (2025) · medRxiv · doi:10.1101/2025.04.05.25325300 · Cited by 1

Discussione del lavoro di Mark Solms: "Fondamenta biologiche del genere. Un equilibrio delicato"

Mariotti, P. (2018) · PSICOANALISI · doi:10.3280/psi2018-001003

An Introduction to Women’s Mental Health

Ribeiro, J. D. A. M., da Silva, A. G., & Rennó, J. (2020) · Springer eBooks · doi:10.1007/978-3-030-29081-8_1

Investigating prenatal stress in a stem cell model of human neuronal development

Papst, L. (2019) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.25120

Infant Physical Growth

Lampl, M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.002

Infant Physical Knowledge

Hespos, S. J., & Anderson, E. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.013

Dual Language Exposure and Early Learning

Brito, N. H. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.024

Infant Speech Perception

Reh, R. K., & Werker, J. F. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.021

Development During Infancy in Children Later Diagnosed with Autism Spectrum Disorder

Falck‐Ytter, T., & Jones, E. J. H. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.005

Dynamic Epigenetic Impact of the Environment on the Developing Brain

Champagne, F. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.003

Combination Analysis of NR3C1, MTHFR and IGFBP3 Gene Polymorphisms and DNA Methylation With Steroid-induced Osteonecrosis of the Femoral Head Risk in Chinese Han PopulationPreprint

Huang, R., Zhan, Q., Hu, W., Yang, R., Cheng, N., & Han, Y. (2020) · Research Square · doi:10.21203/rs.3.rs-87796/v1

CLINICAL HISTORY OF A CHIMPANZEE CALF WITH EARLY SEPARATION FROM THE MOTHER: A LONGITUDINAL STUDY

Kuznetsova, T. G. (2021) · International Journal of Applied and Fundamental Research (Международный журнал прикладных и фундаментальных исследований) · doi:10.17513/mjpfi.13323

Preface

Lockman, J. J., & Tamis‐LeMonda, C. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.031

Stressors: Psychological and neurobiological processes

Anisman, H., & Kusnecov, A. W. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91904-3.00005-7

Perinatal Stress on Behavior and Neuroendocrine Functionality in the Offspring: Biological Substrates

Cattaneo, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819641-0.00166-3

Index

Lockman, J. J., & Tamis‐LeMonda, C. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.030

Prenatal environment and developmental trajectories: the intrauterine growth restriction

Lovato, I., Simonelli, A., Visentin, S., Priante, E., Baraldi, E., & Sacchi, C. (2022) · Minerva Pediatrics · doi:10.23736/s2724-5276.22.06949-x

Prenatal stress increases corticosterone levels in offspring by impairing placental glucocorticoid barrier functionPreprint

Liu, H., Wang, R., Zhu, J., Li, Y., Li, J., Yao, G. X., Ma, S., & Guan, S. (2023) · Research Square · doi:10.21203/rs.3.rs-3303973/v1

Additional file 3 of Prenatal social support in low-risk pregnancy shapes placental epigenome

Tesfaye, M., Wu, J., Biedrzycki, R. J., Grantz, K. L., Joseph, P. V., & Ayele, F. T. (2023) · Figshare · doi:10.6084/m9.figshare.22614749

Additional file 4 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456851

Additional file 12 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456818

Additional file 5 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456857

Additional file 6 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456872

Additional file 10 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456809

Additional file 2 of Prenatal social support in low-risk pregnancy shapes placental epigenome

Tesfaye, M., Wu, J., Biedrzycki, R. J., Grantz, K. L., Joseph, P. V., & Ayele, F. T. (2023) · Figshare · doi:10.6084/m9.figshare.22614746

Additional file 8 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456881

Additional file 11 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H. M., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456815

Epigenetics and Transmissible Diseases

Kamel, M. S., Davidson, J., Munds, R. A., Wang, J., Kaur, S., Kumar, V., & Verma, M. S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-28818-0.00013-6

Association between maternal depressive symptoms and hair cortisol concentration during pregnancy with corpus callosum integrity in newbornsPreprint

Wigley, I. L. C. M., Mustonen, P., Karlsson, L., Nolvi, S., Scheinin, N. M., Kortesluoma, S., Pastore, M., Tervahartiala, K., Coimbra, B., Rodrigues, A. J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.06.610927

Maternal and Fetal Conditions With Consequences for the Fetal Brain

du Plessis, A. J., & Volpe, J. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-10513-5.00011-5

Chapter 4. Epigenetics of Childhood Trauma and Resilience

(2023) · American Psychiatric Association Publishing eBooks · doi:10.1176/appi.books.9781615379828.lg04

Chapter 11. Stress in Pregnancy: Impacts on Mother and Child

Takács, L., Babineau, V., & Monk, C. E. (2021) · American Psychiatric Association Publishing eBooks · doi:10.1176/appi.books.9781615379545.lg11

Prenatal depression comorbid with diabetes or hypertension and the risk of adverse neonatal outcomes: A systematic review and meta-analysis

Abate, B. B., Dachew, B. A., Ayano, G., Betts, K. S., & Alati, R. (2025) · Annals of Epidemiology · doi:10.1016/j.annepidem.2025.10.002

Cortisol as a Mediator of Prenatal Distress and Difficult Infant Temperament: A Systematic Review and Meta‐Analysis Protocol

Sörensen, F., Fransson, E., Skalkidou, A., Krägeloh‐Mann, I., & Derntl, B. (2025) · Health Science Reports · doi:10.1002/hsr2.71309

Additional file 3 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456845

Additional file 1 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571244

Additional file 1 of Maternal–fetal stress and DNA methylation signatures in neonatal saliva: an epigenome-wide association study

Sharma, R., Frasch, M. G., Zelgert, C., Zimmermann, P., Fabre, B. R., Wilson, R., Waldenberger, M., MacDonald, J. W., Bammler, T. K., Lobmaier, S. M., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20317568

Additional file 6 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571259

Additional file 7 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571262

Additional file 11 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571274

Additional file 1 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456836

Additional file 4 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571253

Additional file 1 of Prenatal social support in low-risk pregnancy shapes placental epigenome

Tesfaye, M., Wu, J., Biedrzycki, R. J., Grantz, K. L., Joseph, P. V., & Ayele, F. T. (2023) · Figshare · doi:10.6084/m9.figshare.22614743

Additional file 13 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456821

Additional file 1 of Associations of prenatal maternal depressive symptoms with cord blood glucocorticoids and child hair cortisol levels in the project viva and the generation R cohorts: a prospective cohort study

Cohen, N. J., Defina, S., Rifas-Shiman, S. L., Faleschini, S., Kirby, R. S., Chen, H., Wilson, R., Fryer, K. E., Marroun, H. E., Cecil, C. A. M., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24454969

Additional file 5 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571256

Additional file 7 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456875

Additional file 9 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456884

Additional file 2 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571247

Additional file 9 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571268

Additional file 15 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456830

Additional file 14 of Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

Czamara, D., Dieckmann, L., Röh, S., Kraemer, S., Rancourt, R. C., Sammallahti, S., Kajantie, E., Laivuori, H., Eriksson, J. G., Räikkönen, K., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16456827

Additional file 4 of Prenatal social support in low-risk pregnancy shapes placental epigenome

Tesfaye, M., Wu, J., Biedrzycki, R. J., Grantz, K. L., Joseph, P. V., & Ayele, F. T. (2023) · Figshare · doi:10.6084/m9.figshare.22614752

Additional file 8 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571265

Additional file 3 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571250

Additional file 10 of Transcriptomic profiling of the developing brain revealed cell-type and brain-region specificity in a mouse model of prenatal stress

Dong, Y., Weng, J., Zhu, Y., Sun, D., He, W., Chen, Q., Cheng, J., Zhu, Y., & Jiang, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26571271

2.3 Using Epigenetics to Understand How Distress During Pregnancy Impacts Fetal Behavioral Outcomes

Monk, C. E. (2016) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2016.07.016

Placental epigenetic signatures of maternal distress in glucocorticoid-related genes and newborn outcomes: A study of Spanish primiparous women

Castro-Quintas, Á., Palma‐Gudiel, H., Eixarch, E., Martín-González, N. S., Röh, S., Sauer, S., Rex‐Haffner, M., Garcia, J. L. M., de la Fuente-Tomás, L., Crispi, F., et al. (2024) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2024.10.001 · Cited by 18

Maternal distress in late pregnancy alters obstetric outcomes and the expression of genes important for placental glucocorticoid signalling

Togher, K. L., Treacy, E., O’Keeffe, G. W., & Kenny, L. C. (2017) · Psychiatry Research · doi:10.1016/j.psychres.2017.05.013 · Cited by 44

Differential impact of prenatal PTSD symptoms and preconception trauma exposure on placental NR3C1 and FKBP5 methylation

Stroud, L. R., Jao, N. C., Ward, L. G., Lee, S. Y., & Marsit, C. J. (2024) · Stress · doi:10.1080/10253890.2024.2321595 · Cited by 9

Impact of Depression and Stress on Placental DNA Methylation in Ethnically Diverse Pregnant Women

Tesfaye, M., Chatterjee, S., Zeng, X., Joseph, P. V., & Ayele, F. T. (2021) · Epigenomics · doi:10.2217/epi-2021-0192 · Cited by 27