Glucocorticoid exposure during hippocampal neurogenesis primes future stress response by inducing changes in DNA methylation

Effects of stress throughout the lifespan on the brain, behaviour and cognition

Lupien, S. J., McEwen, B. S., Gunnar, M. R., & Heim, C. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2639 · Cited by 6,256

ChromHMM: automating chromatin-state discovery and characterization

Ernst, J., & Kellis, M. (2012) · Nature Methods · doi:10.1038/nmeth.1906 · Cited by 2,457

Spatio-temporal transcriptome of the human brain

Kang, H. J., Kawasawa, Y. I., Cheng, F., Zhu, Y., Xu, X., Li, M., Sousa, A. M. M., Pletikos, M., Meyer, K. A., Sedmak, G., et al. (2011) · Nature · doi:10.1038/nature10523 · Cited by 2,084

Biological sensitivity to context: I. An evolutionary-developmental theory of the origins and functions of stress reactivity

BOYCE, W. T., & ELLIS, B. J. (2005) · Development and Psychopathology · doi:10.1017/s0954579405050145 · Cited by 2,078

Fetal Origins of Mental Health: The Developmental Origins of Health and Disease Hypothesis

O’Donnell, K. J., & Meaney, M. J. (2017) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2016.16020138 · Cited by 608

Glucocorticoid excess and the developmental origins of disease: Two decades of testing the hypothesis – 2012 Curt Richter Award Winner

Reynolds, R. M. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.08.012 · Cited by 497

Prenatal stress diminishes neurogenesis in the dentate gyrus of juvenile rhesus monkeys

Coe, C. L., Kramer, M., Czéh, B., Gould, E., Reeves, A. J., Kirschbaum, C., & Fuchs, E. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00698-x · Cited by 477

Impact of Maternal Stress, Depression and Anxiety on Fetal Neurobehavioral Development

KINSELLA, M. T., & MONK, C. (2009) · Clinical Obstetrics & Gynecology · doi:10.1097/grf.0b013e3181b52df1 · Cited by 422

Glucocorticoid-Related Molecular Signaling Pathways Regulating Hippocampal Neurogenesis

Anacker, C., Cattaneo, A., Luoni, A., Musaelyan, K., Zunszain, P. A., Milanesi, E., Rybka, J., Berry, A., Cirulli, F., Thuret, S., et al. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.253 · Cited by 331

Role for the kinase SGK1 in stress, depression, and glucocorticoid effects on hippocampal neurogenesis

Anacker, C., Cattaneo, A., Musaelyan, K., Zunszain, P. A., Horowitz, M., Molteni, R., Luoni, A., Calabrese, F., Tansey, K., Gennarelli, M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300886110 · Cited by 319

Naturalistic Stress Hormone Levels Drive Cumulative Epigenomic Changes along the Cellular Lifespan

Zannas, A. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168778 · Cited by 9

DNA methylation signatures in human neonatal blood following maternal antenatal corticosteroid treatment

Kim, B., Sasaki, A., Murphy, K. E., & Matthews, S. G. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01902-4 · Cited by 11

No long-term effects of antenatal synthetic glucocorticoid exposure on epigenetic regulation of stress-related genes

Müller, S., Moser, D., Frach, L., Wimberger, P., Nitzsche, K. I., Li, S., Kirschbaum, C., & Alexander, N. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01828-x · Cited by 9

Late gestational exposure to dexamethasone and fetal programming of abnormal behavior in Wistar Kyoto rats

Lalonde, C., Grandbois, J., Khurana, S., Murray, A., Tharmalingam, S., & Tai, T. C. (2021) · Brain and Behavior · doi:10.1002/brb3.2049 · Cited by 10

Brain Transcriptome Responses to Dexamethasone Depending on Dose and Sex Reveal Factors Contributing to Sex-Specific Vulnerability to Stress-Induced Disorders

Muráni, E., Trakooljul, N., Hadlich, F., Ponsuksili, S., & Wimmers, K. (2021) · Neuroendocrinology · doi:10.1159/000516500 · Cited by 10

In vitro modeling of glucocorticoid mechanisms in stress-related mental disorders: Current challenges and future perspectives

Bassil, K. C., de Nijs, L., Rutten, B. P. F., van den Hove, D., & Kenis, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1046357 · Cited by 10

Cholic acid exposure during late pregnancy causes placental dysfunction and fetal growth restriction by reactive oxygen species‐mediated activation of placental GCN2 / eIF2α pathway

Lin, S., Ye, M., Fu, Q., Pan, C., Liu, Y., Zheng, L., Hong, Q., & Chen, Y. (2023) · The FASEB Journal · doi:10.1096/fj.202202126r · Cited by 10

Multiomics Analysis of the Molecular Response to Glucocorticoids: Insights Into Shared Genetic Risk From Psychiatric to Medical Disorders

Arloth, J., Hryhorzhevska, A., & Binder, E. B. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.10.004 · Cited by 9

Leveraging DNA methylation to predict treatment response in major depressive disorder: A critical review

Dahrendorff, J., Currier, G. W., & Uddin, M. (2024) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32985 · Cited by 9

Early prenatal but not postnatal glucocorticoid exposure is associated with enhanced HPA axis activity into adulthood in a wild primate

Anzà, S., Heistermann, M., Ostner, J., & Schülke, O. (2025) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2024.2418 · Cited by 8

Molecular insights into trauma: A framework of epigenetic pathways to resilience through intervention

Merrill, S. M., Konwar, C., Fraihat, Z., Parent, J. M., & Dajani, R. B. (2024) · Med · doi:10.1016/j.medj.2024.11.013 · Cited by 10

Common mechanisms cannot explain time- and dose-dependent DNA methylation changes in earthworms exposed to cadmium

Aigner, G. P., Pittl, V., Fiechtner, B., Egger, B., Šrut, M., & Höckner, M. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.151468 · Cited by 8

The role of preconditioning in the development of resilience: Mechanistic insights

Holcombe, J., & Weavers, H. (2022) · Current Opinion in Toxicology · doi:10.1016/j.cotox.2022.02.011 · Cited by 8

FKBP5 intron 7 methylation is associated with higher anxiety proneness and smaller right thalamus volume in adolescents

Womersley, J. S., Roeh, S., Martin, L. I., Ahmed-Leitao, F., Sauer, S., Rex‐Haffner, M., Hemmings, S. M. J., Binder, E. B., & Seedat, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02577-9 · Cited by 8

DNA methylation-environment interactions in the human genome

Johnston, R. A., Aracena, K. A., Barreiro, L. B., Lea, A. J., & Tung, J. (2023) · eLife · doi:10.7554/elife.89371 · Cited by 8

Cell-type specific impact of glucocorticoid receptor activation on the developing brainPreprint

Cruceanu, C., Dony, L., Krontira, A. C., Fischer, D. S., Roeh, S., Giaimo, R. D., Kyrousi, C., Arloth, J., Czamara, D., Martinelli, S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.09.897868 · Cited by 8

Biomarkers of aging through the life course: a recent literature update

Gaylord, A., Cohen, A. A., & Kupsco, A. J. (2023) · Current Opinion in Epidemiology and Public Health · doi:10.1097/pxh.0000000000000018 · Cited by 7

Prenatal programming of child neurocognitive abilities and maternal mental health

Tuovinen, S., Lahti‐Pulkkinen, M., Rantalainen, V., Kajantie, E., & Räikkönen, K. (2020) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2020.09.001 · Cited by 10

Novel Functional Genomics Approaches Bridging Neuroscience and Psychiatry

Restrepo-Lozano, J. M., Flores, C., & Silveira, P. P. (2022) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2022.07.005 · Cited by 7

Pro-aging effects of chronic glucocorticoid signaling

Lambertucci, F., Castinetti, F., Martins, I., López-Otı́n, C., & Kroemer, G. (2026) · Cell Metabolism · doi:10.1016/j.cmet.2026.05.002 · Cited by 8

The Unhealthy Relationship Between Stress and Poverty

Breitenbach, M., Kapferer, E., & Sedmak, C. (2021) · Springer eBooks · doi:10.1007/978-3-030-77738-8_8 · Cited by 6

Human myeloid progenitor glucocorticoid receptor activation causes genomic instability, type 1 IFN ‐ response pathway activation and senescence in differentiated microglia; an early life stress model

Wei, J., Arber, C., Wray, S., Hardy, J., Piers, T. M., & Pocock, J. M. (2022) · Glia · doi:10.1002/glia.24325 · Cited by 6

Epigenetic associations in HPA axis genes related to bronchopulmonary dysplasia and antenatal steroids

Hodge, K. M., Zhabotynsky, V., Burt, A., Carter, B. S., Fry, R. C., Helderman, J., Hofheimer, J. A., McGowan, E. C., Neal, C. R., Pastyrnak, S. L., et al. (2024) · Pediatric Research · doi:10.1038/s41390-024-03116-4 · Cited by 6

The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction

Jiao, Y., Shi, C., & Sun, Y. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1234817 · Cited by 5

Exploring transcriptional and post-transcriptional epigenetic regulation of crf and 11βhsd2 in rainbow trout brain during chronic social stress

Best, C., Mennigen, J. A., & Gilmour, K. M. (2023) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2023.111557 · Cited by 5

Epigenetic associations with neonatal age in infants born very preterm, particularly among genes involved in neurodevelopment

Hodge, K. M., Burt, A., Camerota, M., Carter, B. S., Check, J. F., Conneely, K. N., Helderman, J., Hofheimer, J. A., Hüls, A., McGowan, E. C., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-68071-w · Cited by 5

Positive maternal mental health during pregnancy and psychiatric problems in children from early childhood to late childhood

Lähdepuro, A., Lahti‐Pulkkinen, M., Girchenko, P. V., Villa, P., Heinonen, K., Lahti, J. M. T., Pyhälä, R., Laivuori, H. M., Kajantie, E., & Räikkönen, K. (2023) · Development and Psychopathology · doi:10.1017/s0954579423001244 · Cited by 6

Timing of antenatal corticosteroid exposure and its association with childhood mental disorders in early- and full-term births: A population-based cohort study

Ho, F.-C., Chung, H., Yu, C., Huang, C.-Y., & Liang, F. (2025) · European Journal of Pediatrics · doi:10.1007/s00431-025-05994-0 · Cited by 6

A polyepigenetic glucocorticoid exposure score and HPA axis-related DNA methylation are associated with gestational epigenetic aging

Appleton, A. A. (2025) · Epigenetics · doi:10.1080/15592294.2025.2471129 · Cited by 5

Epigenetic alterations associated with dexamethasone sodium phosphate through DNMT and TET in RPE cells.

Liu, W., Mohan, S. P., Nareshkumar, R. N., Jaganathan, S. S., Wen, Y., Ramasubramanyan, S., & Irudayaraj, J. (2021) · PubMed Central · Cited by 5

Epigenetics of Stress in Farmed Fish

Guinand, B., & Σαμαράς, Α. (2023) · Wiley eBooks · doi:10.1002/9781119821946.ch12 · Cited by 5

Molecular integrators of stress and aging: the example of FKBP5

Zannas, A. S. (2023) · Acta Neuropathologica · doi:10.1007/s00401-023-02572-2 · Cited by 6

Absence of Depressive and Anxious Behavior with Genetic Dysregulation in Adult C57Bl/6J Mice after Prenatal Exposure to Ionizing Radiation

Lalonde, C., Sreetharan, S., Murray, A., Stoa, L., Cybulski, M. E., Kennedy, A. E., Landry, N., Stillar, A., Khurana, S., Tharmalingam, S., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24108466 · Cited by 5

DNA methylation variation after a parenting program for child conduct problems: Findings from a randomized controlled trial

Creasey, N., Leijten, P. H. O., Tollenaar, M. S., Boks, M. P., & Overbeek, G. J. (2024) · Child Development · doi:10.1111/cdev.14090 · Cited by 4

Prenatal exposures and cell type proportions are main drivers of FKBP5 DNA methylation in maltreated and non-maltreated children

Karlbauer, V. N., Martins, J., Rex‐Haffner, M., Sauer, S., Roeh, S., Dittrich, K., Dörr, P., Klawitter, H., Entringer, S., Buß, C., et al. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100687 · Cited by 5

Prenatal corticosteroid use and offspring neurological outcomes

Yan, Y., Wang, J., & Lei, X. (2025) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2025.107564 · Cited by 3

Prenatal stress, epigenetically-assessed glucocorticoid exposure at birth, and child psychiatric symptoms: A prospective, multi-cohort study

Creasey, N., Schuurmans, I. K., Tsotsi, S., Defina, S., Baltramonaityte, V., Felix, J. F., Neumann, A., Page, C. M., Tollenaar, M. S., Bekkhus, M., et al. (2025) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2025.107388 · Cited by 3

How Many Are Too Much? Clinical and Epidemiological Considerations for the Era of Poly–Pre- and Postnatal Exposures Relevant for the Developing Brain

Buß, C., & Genuneit, J. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.06.025 · Cited by 3

Legacies of salient environmental experiences—insights from chemosensation

Dias, B. G. (2024) · Chemical Senses · doi:10.1093/chemse/bjae002 · Cited by 2

Dissecting the Long-Term Effect of Stress Early in Life on FKBP5: The Role of miR-20b-5p and miR-29c-3p

Cattane, N., Benedetto, M. G. D., D’Aprile, I., Riva, M. A., & Cattaneo, A. (2024) · Biomolecules · doi:10.3390/biom14030371 · Cited by 3

Dissecting the networks underlying diverse brain disorders after prenatal glucocorticoid overexposure

Zheng, B., Zheng, Y., Hu, W., & Chen, Z. (2024) · Archives of Toxicology · doi:10.1007/s00204-024-03733-2 · Cited by 3

Convergent Functional Genomics approach to prioritize molecular targets of risk in early life stress-related psychiatric disorders

Cattaneo, A., Cattane, N., Scassellati, C., D’Aprile, I., Riva, M. A., & Pariante, C. M. (2020) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2020.100120 · Cited by 3

Lifelong molecular consequences of high Glucocorticoids exposure during developmentPreprint

Choi, M., Cook, A., Mungikar, K., Eachus, H., Tochwin, A., Linke, M., Gerber, S., & Ryu, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.13.528363 · Cited by 3

Exposure to elevated glucocorticoid during development primes altered transcriptional responses to acute stress in adulthood

Choi, M., Cook, A., Mungikar, K., Eachus, H., Tochwin, A., Linke, M., Gerber, S., & Ryu, S. (2024) · iScience · doi:10.1016/j.isci.2024.110160 · Cited by 5

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

Sex-dependent biobehavioural responses to transgenerational maternal stress: evidence of stress resilience and vulnerability in the F3 generation

Faraji, J., Schatz, N. A., King, S. E., Soltanpour, N., & Metz, G. A. S. (2025) · Current Zoology · doi:10.1093/eep/dvaf031 · Cited by 2

Child and adolescent internalizing and externalizing traits, and epigenetic summary scores: A scoping review

Ware, E. B., Goode, J. A., Hornish, U. N., McNulty, D. P., Karadimas, T., Acedo, G. R., Birchmier, J., Histed, A., Hsu, R., Jones, N., et al. (2025) · Biological Psychology · doi:10.1016/j.biopsycho.2025.109164 · Cited by 3

Stress-induced epigenome changes as a risk factor in the onset of mental disorders

Shkarina, L., Дмитриевич, Б. К., Станиславович, Д. С., Primak, A. L., Tkachuk, V., Chaika, Y. A., Neyfeld, E. A., & Karagyaur, M. N. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1764368 · Cited by 2

Association Between Age-Dependent DNA Methylation Changes at FKBP5 Enhancer Sites and Increased Cortical Gene Expression in Schizophrenia

Edmond, K. Z., Kaul, D., Yusupov, N., Ködel, M., Sauer, S., Fröhlich, A. S., Kentro, J. A., Ran, T. A. O., Kleinman, J. E., Weinberger, D. R., et al. (2026) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20250473 · Cited by 2

The science of flourishing in child and adolescent development: description, explanation and implications for prevention and promotion

Dorjee, D., & Roeser, R. W. (2022) · UNESCO MGIEP eBooks · doi:10.56383/horu5152 · Cited by 2

Sex differences in fetal programming: Antenatal origins of health and disease (AOHD)

Glezerman, M. (2023) · Principles of Gender-Specific Medicine · doi:10.1016/b978-0-323-88534-8.00004-3 · Cited by 2

Glucocorticoid-Dependent Retinal Degeneration and Vision Impairment in Mice Susceptible to Prenatal Stress-Induced Behavioral Abnormalities

Ryu, M.-O., Jung, J.-Y., Suh, H. N., Lee, C.-Y., Kim, M. K., Oh, J. Y., Song, W., Ahn, C., Yang, Y., & Choi, G. E. (2024) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-024-01525-x · Cited by 2

Glucocorticoid exposure-induced alterations in epigenetic age from human preterm infants and human lung fibroblasts and hippocampal neuronal cells

Wu, X., Lu, C., Deng, Z., Xiao, W., Ni, H., & Zhao, C. (2025) · Clinical Epigenetics · doi:10.1186/s13148-025-01837-9 · Cited by 3

Gestational glucocorticoid exposure impaired endothelial nitric oxide synthesis via downregulating IP3 receptor 3 expression in male offspring vessels

Lei, J., Deng, F., Qiu, J., Zhao, C., Zhang, M., & Gao, Q. (2025) · Journal of Hypertension · doi:10.1097/hjh.0000000000004067 · Cited by 2

Epigenetic effects of endogenous and exogenous glucocorticosteroids during pregnancy on the offspring: a systematic-narrative review

Kanouta, F., Karampitsakos, Τ., Memi, E., Vrachnis, N., Μacut, D., & Mastorakos, G. P. (2025) · HORMONES · doi:10.1007/s42000-025-00671-1 · Cited by 2

Adversity across time: Do sensitive periods across the life span determine adversity-induced epigenetic changes?

Halldorsdottir, T., Valdimarsdottir, H. B., & Valdimarsdóttir, U. A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823039-8.00007-1 · Cited by 2

Exploring the relationship between methylation of the cortisol receptor genes and brain and cognitive outcomes in individuals with elevated amyloid-βPreprint

Porter, T., Armstrong, A. M., Milicic, L., Vacher, M. A., Fernandez, S., O’Brien, E. K., Doré, V., Bourgeat, P., Shishegar, R., Xia, Y., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-7540786/v1 · Cited by 2

Toward Understanding and Halting Legacies of Trauma

Taylor, W., Korobkova, L., Bhinderwala, N., & Dias, B. G. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.02.010 · Cited by 1

Corticosteroid‐regulated gene transcription in SH ‐ SY5Y ‐derived neurons: Insights into the mineralocorticoid and glucocorticoid receptor‐mediated response

Lugenbühl, J. F., Snijders, C., Pernia, C. D., Estruch, M. S., Kenis, G., & Daskalakis, N. P. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70021 · Cited by 1

Epigenetic Modulation by Vitamin C and in Prenatal Depression: Implications for Offspring Health

Xu, J.-S., Li, Y., & Wei, L.-Q. (2026) · Current Medical Science · doi:10.1007/s11596-026-00163-2 · Cited by 1

Glucocorticoid Signaling in PSC-Derived Neural Systems to Elucidate Mechanisms of Stress-Induced Psychiatric Vulnerability

Molin, E. A. D., Kaster, M. P., & Nascimento, J. M. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06041-1 · Cited by 2

Die frühe Entwicklung zur Aufmerksamkeit ...

Oberle, A., & Oberle, C. (2023) · Pädiatrie · doi:10.1007/s15014-023-4930-y · Cited by 1

The association between depression and the cortisol awakening response is moderated by loneliness in men from a non-clinical sample

Stańczykiewicz, B., Bogudzińska, B., Kowalski, K., & Misiak, B. (2023) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2023.106924 · Cited by 1

Associations of psychiatric disease and aging on FKBP5 expression converge on cortical supragranular neuronsPreprint

Matosin, N., Arloth, J., Czamara, D., Edmond, K. Z., Maitra, M., Fröhlich, A. S., Martinelli, S., Kaul, D., Bartlett, R., Curry, A. R., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.27.428487 · Cited by 1

Modeling gene x environment interactions in PTSD using glucocorticoid-induced transcriptomics in human neuronsPreprint

Breen, M. S., Rusielewicz, T., Bader, H. N., Seah, C., Xu, C., Hunter, C. J., McCarthy, B., Chattopadhyay, M., Désarnaud, F., Makotkine, I., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.01.433391 · Cited by 1

DNA methylation-environment interactions in the human genomePreprint

Johnston, R. A., Aracena, K. A., Barreiro, L. B., Lea, A. J., & Tung, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.19.541437 · Cited by 1

Epigenetic Signatures Reveal Biological Embedding of the Early-Life Environment Two Decades after Exposure to AdversityPreprint

Mposhi, A., Buchanan, M., Mériaux, S. B., Cléac’h, J. L., Elwenspoek, M. M. C., Leenen, F. A. D., Muller, C. P., Vögele, C., & Turner, J. D. (2026) · medRxiv · doi:10.64898/2026.01.28.26345020 · Cited by 1

Role of Non-Coding Regulatory Elements in the Control of GR-Dependent Gene Expression

Borczyk, M., Zięba, M., Korostyński, M., & Piechota, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084258 · Cited by 2

Experience and the genome: the role of epigenetics

Szyf, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90752-1.00001-8 · Cited by 1

Behavioral medical epigenetics

Cox, O., & Lee, R. S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823928-5.00017-7

Genes, Environment and Their Interaction in the Vulnerability or Resilience to Stress-Related Psychiatric Disorders: Where Are We Now?

Cattane, N. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819641-0.00082-7

Naturalistic Glucocorticoid Receptor Activation Programs Key Cell Phenotypes and Functional Epigenomic Patterns in Human FibroblastsPreprint

Leung, C. S., Kosyk, O., Welter, E. M., Dietrich, N., Archer, T., & Zannas, A. S. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4077247

Embryo as Person: As in the Womb, So in the World

Life, B. Y., & Menzam-Sills, C. (2023) · doi:10.24946/ijpls/202312305

Maternal anxiety during pregnancy and the lack of fetal DNA methylation in cord blood

Lahti, J. M. T. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823937-7.00001-8

Die ungesunde Beziehung zwischen Stress und Armut

Breitenbach, M., Kapferer, E., & Sedmak, C. (2023) · Springer eBooks · doi:10.1007/978-3-031-23697-6_8

DNA methylation-environment interactions in the human genomePreprint

Johnston, R. A., Aracena, K. A., Barreiro, L. B., Lea, A. J., & Tung, J. (2023) · eLife · doi:10.7554/elife.89371.1

3 Biologische Einbettung von traumatischen Erfahrungen in der Kindheit: Relevanz von früher Intervention zur Verhinderung von Langzeitfolgen

Heim, C. C. (2023) · Vandenhoeck & Ruprecht eBooks · doi:10.13109/9783666408687.39

Reviewer #2 (Public Review): DNA methylation-environment interactions in the human genome

(2024) · eLife · doi:10.7554/elife.89371.2.sa0

DNA methylation-environment interactions in the human genomePreprint

Johnston, R. A., Aracena, K. A., Barreiro, L. B., Lea, A. J., & Tung, J. (2024) · eLife · doi:10.7554/elife.89371.2

Additional file 6 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780889

Additional file 7 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780895

Additional file 12 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780862

Additional file 10 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780853

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 2 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780874

Additional file 3 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780877

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 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 13 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780865

Additional file 4 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780880

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

Additional file 8 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780898

Additional file 5 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780883

Additional file 9 of Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus

Soliai, M. M., Kato, A., Helling, B. A., Stanhope, C. T., Norton, J. E., Naughton, K. A., Klinger, A. I., Thompson, E. E., Clay, S. M., Kim, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16780901

Epigenetic Processes as Mediators of the Impact of the Social Environment

Szyf, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-59286-7_6

Hypothetical involvement of stress hormones-induced reprograming of adult stem/progenitor cells in tumorigenesis

Kanczkowski, W., Sue, M., Wlodarczyk, A., & Chrousos, G. P. (2024) · Exploration of Endocrine and Metabolic Diseases · doi:10.37349/eemd.2024.00012 · Cited by 2

Personalized epigenetics and neurological disorders

Dahiya, B., Iyer, M., Michel, T. M., & Vellingiri, B. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23802-4.00011-9

Glucocorticoid Exposure During Hippocampal Neurogenesis Primes Future Stress Response by Inducing Changes in DNA Methylation: Glucocorticoids induce DNAm changes during neurogenesis

Provençal, N., Arloth, J., Cattaneo, A., Anacker, C., Cattane, N., Wiechmann, T., Röh, S., Ködel, M., Klengel, T., Czamara, D., et al. (2019) · Research Portal (King's College London)

Long-term effects of antenatal synthetic glucocorticoids on epigenetic regulation of stress-associated genesPreprint

Müller, S., Moser, D., Frach, L., Wimberger, P., Nitzsche, K. I., Li, S.-C., Kirschbaum, C., & Alexander, N. (2021) · doi:10.17605/osf.io/akdtv

No long-term effects of antenatal synthetic glucocorticoid exposure on epigenetic regulation of stress-related genes

Müller, S., Moser, D., Frach, L., Wimberger, P., Nitzsche, K. I., Li, S., Kirschbaum, C., & Alexander, N. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01828-x · Cited by 9

DNA methylome signatures of prenatal exposure to synthetic glucocorticoids in hippocampus and peripheral whole blood of female guinea pigs in early life

Sasaki, A., Eng, M. E., Lee, A. H., Kostaki, A., & Matthews, S. G. (2021) · Translational Psychiatry · doi:10.1038/s41398-020-01186-6 · Cited by 13

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