Influences of maternal and paternal PTSD on epigenetic regulation of the glucocorticoid receptor gene in Holocaust survivor offspring
Open accessAbstract
OBJECTIVE: Differential effects of maternal and paternal posttraumatic stress disorder (PTSD) have been observed in adult offspring of Holocaust survivors in both glucocorticoid receptor sensitivity and vulnerability to psychiatric disorder. The authors examined the relative influences of maternal and paternal PTSD on DNA methylation of the exon 1F promoter of the glucocorticoid receptor (GR-1F) gene (NR3C1) in peripheral blood mononuclear cells and its relationship to glucocorticoid receptor sensitivity in Holocaust offspring. METHOD: Adult offspring with at least one Holocaust survivor parent (N=80) and demographically similar participants without parental Holocaust exposure or parental PTSD (N=15) completed clinical interviews, self-report measures, and biological procedures. Blood samples were collected for analysis of GR-1F promoter methylation and of cortisol levels in response to low-dose dexamethasone, and two-way analysis of covariance was performed using maternal and paternal PTSD as main effects. Hierarchical clustering analysis was used to permit visualization of maternal compared with paternal PTSD effects on clinical variables and GR-1F promoter methylation. RESULTS: A significant interaction demonstrated that in the absence of maternal PTSD, offspring with paternal PTSD showed higher GR-1F promoter methylation, whereas offspring with both maternal and paternal PTSD showed lower methylation. Lower GR-1F promoter methylation was significantly associated with greater postdexamethasone cortisol suppression. The clustering analysis revealed that maternal and paternal PTSD effects were differentially associated with clinical indicators and GR-1F promoter methylation. CONCLUSIONS: This is the first study to demonstrate alterations of GR-1F promoter methylation in relation to parental PTSD and neuroendocrine outcomes. The moderation of paternal PTSD effects by maternal PTSD suggests different mechanisms for the intergenerational transmission of trauma-related vulnerabilities.
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Of the studies investigating NR3C1, four out of six reported higher DNA methylation in offspring after trauma exposure.
“Of the studies investigating specifically NR3C1, four out of six reported higher DNA methylation in offspring after trauma exposure [86,91,95,98]”
From Biological Embedding of Early-Life Adversity and a Scoping Review of the Evidence for Intergenerational Epigenetic Transmission of Stress and Trauma in Humans (2023) · cites this paper as [95]
The Results (page not provided) report higher NR3C1 promoter methylation in Holocaust survivor offspring with paternal PTSD only when maternal PTSD was absent. Offspring with both maternal and paternal PTSD showed lower methylation, so this paper does not support an unqualified increase after parental trauma or PTSD. As one of four citations, it need not independently establish the four-out-of-six count. (LLM, conf=0.85)
Experimental — accuracy not yet measuredStudies of Holocaust survivors and their offspring demonstrate differential DNA methylation of key HPA-axis genes, including NR3C1 and FKBP5, corresponding with variation in glucocorticoid receptor sensitivity and cortisol feedback regulation.
“Studies of Holocaust survivors and their offspring demonstrate differential DNA methylation of key HPA-axis genes, including NR3C1 and FKBP5, corresponding with variation in glucocorticoid receptor sensitivity and cortisol feedback regulation (82, 83).”
From Epigenetic changes associated with multi-generational trauma: characterization, mechanisms, and therapeutics (2026) · cites this paper as [82]
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredFunctional alterations in cortisol metabolism, including reduced cortisol excretion in survivors and increased activity of cortisol-inactivating enzymes in offspring, have been described.
“Functional alterations in cortisol metabolism, including reduced cortisol excretion in survivors and increased activity of cortisol-inactivating enzymes in offspring, have also been described (82, 85).”
From Epigenetic changes associated with multi-generational trauma: characterization, mechanisms, and therapeutics (2026) · cites this paper as [82]
The Introduction reports altered 24-hour urinary cortisol excretion in offspring, with lower excretion associated with maternal PTSD and higher excretion with paternal PTSD alone. It does not report reduced excretion in survivors or increased activity of cortisol-inactivating enzymes in offspring; searches for those terms found no supporting passage. Page numbers were not available in our copy. (LLM, conf=0.82)
Experimental — accuracy not yet measuredAcross multiple trauma contexts, altered methylation of NR3C1 has been reported, including genocide exposure, childhood maltreatment, and natural disasters.
“Across multiple trauma contexts, altered methylation of NR3C1 has been reported, including genocide exposure, childhood maltreatment, and natural disasters (10, 82, 88, 89).”
From Epigenetic changes associated with multi-generational trauma: characterization, mechanisms, and therapeutics (2026) · cites this paper as [82]
The Discussion reports altered NR3C1 GR-1F promoter methylation in Holocaust survivors’ offspring in relation to parental PTSD, and the Introduction reports associations with childhood abuse. The study does not establish altered methylation in people directly exposed to the Holocaust; it examines their offspring. The passages reviewed also do not address natural disasters. (LLM, conf=0.82)
Experimental — accuracy not yet measuredThe majority of studies looked at only maternal transmission, four considered both maternal and paternal, and two focused only on fathers.
“The majority of the studies looked at only maternal transmission, but four considered both maternal and paternal [83,94,95,102], and two focused only on fathers [97,104].”
There were six studies of trauma or PTSD following war, including two studies of Holocaust survivors, two on the Rwandan genocide, one from the Kosovo War, and one of Vietnam veterans.
“There were six studies of trauma or PTSD following war, including two studies of Holocaust survivors [83,94,95], two studies on the Rwandan genocide [90,91], and one each from the Kosovo War [96] and Vietnam veterans [97].”
Across survivor populations and their descendants, research suggests coordinated involvement of stress-response regulation, neurodevelopmental signaling, and behavioral adaptation.
“Across survivor populations and their descendants, research suggests coordinated involvement of stress-response regulation, neurodevelopmental signaling, and behavioral adaptation (7, 82–100).”
From Epigenetic changes associated with multi-generational trauma: characterization, mechanisms, and therapeutics (2026) · cites this paper as [82]
Paternal PTSD in the absence of maternal PTSD is associated with increased methylation of NR3C1 in offspring, whereas combined maternal and paternal PTSD is associated with decreased methylation.
“Divergent patterns have been observed depending on parental PTSD status, with paternal PTSD in the absence of maternal PTSD associated with increased methylation of NR3C1 in offspring, whereas combined maternal and paternal PTSD has been associated with decreased methylation (82).”
From Epigenetic changes associated with multi-generational trauma: characterization, mechanisms, and therapeutics (2026) · cites this paper as [82]
Many investigations focus on historically defined trauma-exposed populations, including Holocaust survivors, Rwandan genocide survivors, and Alaska Native communities.
“Many investigations focus on historically defined trauma-exposed populations, including Holocaust survivors, Rwandan genocide survivors, and Alaska Native communities (8, 82, 98).”
From Epigenetic changes associated with multi-generational trauma: characterization, mechanisms, and therapeutics (2026) · cites this paper as [82]
Differential methylation of the glucocorticoid receptor gene associated with maternal behavior has been observed in F1 rodents at Nr3c1 exon 1 7 promoter and in human offspring with parental PTSD at the ortholog NR3C1 exon 1 F promoter.
“Differential methylation of the glucocorticoid receptor (GR) gene associated with maternal behavior has been observed in F1 in rodents at Nr3c1 exon 1 7 promoter (16) and in human offspring with parental PTSD at the ortholog NR3C1 exon 1 F promoter (24).”
From Holocaust Exposure Induced Intergenerational Effects on FKBP5 Methylation (2016) · cites this paper as [24]
Lower GR 1F promoter methylation was significantly associated with greater GR sensitivity, as indicated by greater post-dexamethasone cortisol suppression.
“Lower GR 1F promoter methylation was significantly associated with greater GR sensitivity, as indicated by greater post-dexamethasone cortisol suppression.”
From Intergenerational transmission of trauma effects: putative role of epigenetic mechanisms (2018) · cites this paper as [126]
Results indicated a significant interaction of maternal and paternal PTSD on GR gene methylation.
“In parallel with the neuroendocrine observations, the results of these analyses indicated a significant interaction of maternal and paternal PTSD on GR gene methylation 126 .”
From Intergenerational transmission of trauma effects: putative role of epigenetic mechanisms (2018) · cites this paper as [126]
Maternal and paternal PTSD predicted different psychiatric and biological outcomes in offspring.
“This possibility is consistent with clinical, neuroendocrine and epigenetic findings, in which maternal and paternal PTSD predicted different psychiatric and biological outcomes in offspring 28,126 .”
From Intergenerational transmission of trauma effects: putative role of epigenetic mechanisms (2018) · cites this paper as [126]
In the absence of maternal PTSD, offspring with paternal PTSD showed higher GR promoter methylation, whereas offspring with both maternal and paternal PTSD showed lower methylation of this promoter region.
“The interaction demonstrated that, in the absence of maternal PTSD, offspring with paternal PTSD showed higher GR promoter methylation, whereas offspring with both maternal and paternal PTSD showed lower methylation of this promoter region.”
From Intergenerational transmission of trauma effects: putative role of epigenetic mechanisms (2018) · cites this paper as [126]
Variation in the methylation of the exon 1F GR promoter associated with PTSD symptoms and predicted treatment outcome.
“We recently addressed this issue in PTSD patients and provide evidence suggesting that variation in the methylation of the exon 1F GR promoter associated with PTSD symptoms and predicted treatment outcome.135-137”
From Early life adversity and the epigenetic programming of hypothalamic-pituitary-adrenal function (2014) · cites this paper as [136]
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Cites
Development and validation of a brief screening version of the Childhood Trauma Questionnaire
Bernstein, D. P., Stein, J. A., Newcomb, M. D., Walker, E., Pogge, D., Ahluvalia, T., Stokes, J., Handelsman, L., Medrano, M., Desmond, D., et al. (2003) · Child Abuse & Neglect · doi:10.1016/s0145-2134(02)00541-0 · Cited by 6,419 · see citing works
Epigenetic programming by maternal behavior
Weaver, I. C. G., Cervoni, N., Champagne, F. A., D'Alessio, A. C., Sharma, S., Seckl, J. R., Dymov, S., Szyf, M., & Meaney, M. J. (2004) · Nature Neuroscience · doi:10.1038/nn1276 · Cited by 6,177 · see citing works
Self-citationDevelopment, reliability, and validity of a dissociation scale
BERNSTEIN, E. M., & PUTNAM, F. W. (1986) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-198612000-00004 · Cited by 3,793 · cited 4× · see citing works
“To assess relevant psychiatric symptoms and early-life experiences, participants also completed measures such as the Beck Depression Inventory (19), the Spielberger State-Trait Anxiety Inventory (20), the Dissociative Experiences Scale (21), the Relationship Scales Questionnaire (22), and the Childhood Trauma Question…”
MethodInfluentialEpigenetic differences arise during the lifetime of monozygotic twins
Fraga, M. F., Ballestar, E., Paz, M. F., Ropero, S., Setien, F., Ballestar, M. L., Heine-Suñer, D., Cigudosa, J. C., Urioste, M., Benitez, J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500398102 · Cited by 3,602 · see citing works
Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse
McGowan, P. O., Sasaki, A., D'Alessio, A. C., Dymov, S., Labonté, B., Szyf, M., Turecki, G., & Meaney, M. J. (2009) · Nature Neuroscience · doi:10.1038/nn.2270 · Cited by 3,531 · see citing works
Self-citationHeim, C. (2000) · JAMA · doi:10.1001/jama.284.5.592 · Cited by 1,968 · see citing works
Models of the self and other: Fundamental dimensions underlying measures of adult attachment.
Griffin, D. W., & Bartholomew, K. (1994) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.67.3.430 · Cited by 1,874 · see citing works
Oberlander, T. F., Weinberg, J., Papsdorf, M., Grunau, R., Misri, S., & Devlin, A. M. (2008) · Epigenetics · doi:10.4161/epi.3.2.6034 · Cited by 1,432 · see citing works
Glucocorticoid receptors in major depression: relevance to pathophysiology and treatment
Pariante, C. M., & Miller, A. H. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(00)01088-x · Cited by 1,147 · see citing works
Post-Traumatic Stress Disorder
Yehuda, R. (2002) · New England Journal of Medicine · doi:10.1056/nejmra012941 · Cited by 1,134 · see citing works
Self-citationEpigenetic transmission of the impact of early stress across generations
Franklin, T. B., Russig, H., Weiss, I. C., Gräff, J., Linder, N., Michalon, A., Vizi, S., & Mansuy, I. M. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.05.036 · Cited by 1,125 · cited 1× · see citing works
“However, studies with rodents demonstrate that preconception paternal stress can influence behavior and biology in progeny through epigenetic changes in sperm (37), such that germ-line transmission of epigenetic marks associated with PTSD risk is possible.”
BackgroundYehuda, R., Engel, S. M., Brand, S. R., Seckl, J., Marcus, S. M., & Berkowitz, G. S. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2005-0550 · Cited by 711 · see citing works
Self-citationChampagne, D. L., Bagot, R. C., van Hasselt, F., Ramakers, G., Meaney, M. J., de Kloet, E. R., Joels, M., & Krugers, H. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0526-08.2008 · Cited by 661 · see citing works
Self-citationPerroud, N., Paoloni-Giacobino, A., Prada, P., Olié, E., Salzmann, A., Nicastro, R., Guillaume, S., Mouthon, D., Stouder, C., Dieben, K., et al. (2011) · Translational Psychiatry · doi:10.1038/tp.2011.60 · Cited by 516 · see citing works
Radtke, K. M., Ruf, M., Gunter, H. M., Dohrmann, K., Schauer, M., Meyer, A., & Elbert, T. (2011) · Translational Psychiatry · doi:10.1038/tp.2011.21 · Cited by 511 · cited 1× · see citing works
“Additionally, variations in the methylation status of the GR-1F promoter can occur in association with pre- as well as postnatal exposures (10, 11, 38, 39).”
BackgroundChampagne, F. A., & Meaney, M. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.016 · Cited by 510 · see citing works
Self-citationTyrka, A. R., Price, L. H., Marsit, C., Walters, O. C., & Carpenter, L. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030148 · Cited by 486 · see citing works
Factors underlying variable DNA methylation in a human community cohort
Lam, L. L., Emberly, E., Fraser, H. B., Neumann, S. M., Chen, E., Miller, G. E., & Kobor, M. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121249109 · Cited by 476 · see citing works
Epigenetics and the origins of paternal effects
Curley, J. P., Rahia Mashoodh, A., & Champagne, F. A. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.06.018 · Cited by 415 · see citing works
Ivy, A. S., Brunson, K. L., Sandman, C., & Baram, T. Z. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.019 · Cited by 407 · see citing works
Yehuda, R., Daskalakis, N. P., Desarnaud, F., Makotkine, I., Lehrner, A. L., Koch, E., Flory, J. D., Buxbaum, J. D., Meaney, M. J., & Bierer, L. M. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00118 · Cited by 358 · see citing works
Self-citationVulnerability to Posttraumatic Stress Disorder in Adult Offspring of Holocaust Survivors
Yehuda, R., Schmeidler, J., Wainberg, M., Binder-Brynes, K., & Duvdevani, T. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.9.1163 · Cited by 327 · see citing works
Self-citationYehuda, R., Bell, A., Bierer, L. M., & Schmeidler, J. (2008) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2008.01.002 · Cited by 326 · see citing works
Self-citationTransgenerational transmission of cortisol and PTSD risk
Yehuda, R., & Bierer, L. M. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)67009-5 · Cited by 306 · see citing works
Self-citationYehuda, R., Flory, J. D., Bierer, L. M., Henn-Haase, C., Lehrner, A., Desarnaud, F., Makotkine, I., Daskalakis, N. P., Marmar, C. R., & Meaney, M. J. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.02.006 · Cited by 293 · see citing works
Self-citationMinireview: Stress-related psychiatric disorders with low cortisol levels: A metabolic hypothesis
Yehuda, R., & Seckl, J. (2011) · Endocrinology · doi:10.1210/en.2011-1218 · Cited by 276 · see citing works
Self-citationToyokawa, S., Uddin, M., Koenen, K. C., & Galea, S. (2011) · Social Science & Medicine · doi:10.1016/j.socscimed.2011.09.036 · Cited by 219 · see citing works
A systematic investigation of depression
Beck, A. T. (1961) · Comprehensive Psychiatry · doi:10.1016/s0010-440x(61)80020-5 · Cited by 211 · see citing works
Yehuda, R., Teicher, M. H., Seckl, J. R., Grossman, R. A., Morris, A., & Bierer, L. M. (2007) · Archives of General Psychiatry · doi:10.1001/archpsyc.64.9.1040 · Cited by 195 · see citing works
Self-citationvan Zuiden, M., Geuze, E., Willemen, H. L. D. M., Vermetten, E., Maas, M., Heijnen, C. J., & Kavelaars, A. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.10050706 · Cited by 190 · see citing works
Maternal PTSD associates with greater glucocorticoid sensitivity in offspring of Holocaust survivors
Lehrner, A., Bierer, L. M., Passarelli, V., Pratchett, L. C., Flory, J. D., Bader, H. N., Harris, I. R., Bedi, A., Daskalakis, N. P., Makotkine, I., et al. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.11.019 · Cited by 160 · see citing works
Self-citationStructured Clinical Interview for DSM-IV (SCID)
Glasofer, D. R., Brown, A. J., & Riegel, M. (2017) · Springer eBooks · doi:10.1007/978-981-287-104-6_80 · Cited by 150 · see citing works
Palosaari, E. J., Punamäki, R., Qouta, S., & Diab, M. (2013) · Child Abuse & Neglect · doi:10.1016/j.chiabu.2013.04.006 · Cited by 96 · see citing works
Yehuda, R., Blair, W., Labinsky, E., & Bierer, L. M. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.1.163 · Cited by 89 · see citing works
Self-citationMaternal Exposure to the Holocaust and Health Complaints in Offspring
Flory, J. D., Bierer, L. M., & Yehuda, R. (2011) · Disease Markers · doi:10.1155/2011/250470 · Cited by 67 · see citing works
Self-citationField, N. P., Om, C., Kim, T., & Vorn, S. (2011) · Attachment & Human Development · doi:10.1080/14616734.2011.609015 · Cited by 52 · see citing works
Marceau, K., Ram, N., Neiderhiser, J. M., Laurent, H. K., Shaw, D. S., Fisher, P., Natsuaki, M. N., & Leve, L. D. (2013) · Stress · doi:10.3109/10253890.2013.825766 · Cited by 25 · see citing works
Are adult offspring reliable informants about parental PTSD? A validation study
YEHUDA, R., LABINSKY, E., TISCHLER, L., BRAND, S. R., LAVIN, Y., BLAIR, W., BIERER, L. M., GOODMAN, R. Z., & GROSSMAN, R. A. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1364.047 · Cited by 22 · see citing works
Self-citationChildhood maltreatment in adult offspring of Portuguese war veterans with and without PTSD
Dias, A., Sales, L., Cardoso, R. M., & Kleber, R. J. (2014) · European Journal of Psychotraumatology · doi:10.3402/ejpt.v5.20198 · Cited by 15 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [20]Spielberger CD The state-trait anxiety inventory (S T A I): test manual for Form X 1968 Consulting Psychologists Press Palo Alto
Cited by
Sorted by citations
Post-traumatic stress disorder.
Yehuda, R., Hoge, C. W., McFarlane, A. C., Vermetten, E., Lanius, R. A., Nievergelt, C. M., Hobfoll, S. E., Koenen, K. C., Neylan, T. C., & Hyman, S. E. (2015) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2015.57 · Cited by 870 · see citing works
Self-citationTurecki, G., & Meaney, M. J. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.11.022 · Cited by 796 · see citing works
Self-citationHolocaust Exposure Induced Intergenerational Effects on FKBP5 Methylation
Yehuda, R., Daskalakis, N. P., Bierer, L. M., Bader, H. N., Klengel, T., Holsboer, F., & Binder, E. B. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.08.005 · Cited by 782 · see citing works
Self-citationTransgenerational epigenetic programming via sperm microRNA recapitulates effects of paternal stress
Rodgers, A. B., Morgan, C. P., Leu, N. A., & Bale, T. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508347112 · Cited by 751 · see citing works
Intergenerational transmission of trauma effects: putative role of epigenetic mechanisms
Yehuda, R., & Lehrner, A. (2018) · World Psychiatry · doi:10.1002/wps.20568 · Cited by 730 · see citing works
Self-citationPathogenesis of depression: Insights from human and rodent studies
Ménard, C., Hodes, G. E., & Russo, S. J. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.05.053 · Cited by 593 · see citing works
Intergenerational Transmission of Stress in Humans
Bowers, M. E., & Yehuda, R. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.247 · Cited by 564 · see citing works
Self-citationTransformative Service Research
Anderson, L., & Ostrom, A. L. (2015) · Journal of Service Research · doi:10.1177/1094670515591316 · Cited by 485 · see citing works
The Role of the Epididymis and the Contribution of Epididymosomes to Mammalian Reproduction
James, E. R., Carrell, D. T., Aston, K. I., Jenkins, T. G., Yeste, M., & Salas‐Huetos, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155377 · Cited by 334 · see citing works
DNA Methylation Biomarkers: Cancer and Beyond
Mikeska, T., & Craig, J. M. (2014) · Genes · doi:10.3390/genes5030821 · Cited by 287 · see citing works
Prenatal Stress, Glucocorticoids, and Developmental Programming of the Stress Response
McGowan, P. O., & Matthews, S. G. (2017) · Endocrinology · doi:10.1210/en.2017-00896 · Cited by 265 · see citing works
The hypothalamic-pituitary-adrenal axis in PTSD: Pathophysiology and treatment interventions
Dunlop, B. W., & Wong, A. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.10.010 · Cited by 245 · see citing works
Parental Advisory: Maternal and Paternal Stress Can Impact Offspring Neurodevelopment
Chan, J. C., Nugent, B. M., & Bale, T. L. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.10.005 · Cited by 241 · see citing works
Palma-Gudiel, H., Córdova-Palomera, A., Eixarch, E., Deuschle, M., & Fañanás, L. (2015) · Epigenetics · doi:10.1080/15592294.2015.1088630 · Cited by 240 · see citing works
Early life adversity and the epigenetic programming of hypothalamic-pituitary-adrenal function
Anacker, C., O'Donnell, K. J., & Meaney, M. J. (2014) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2014.16.3/canacker · Cited by 237 · see citing works
Self-citationBryant, R. A., Edwards, B., Creamer, M., O'Donnell, M., Forbes, D., Felmingham, K. L., Silove, D., Steel, Z., Nickerson, A., McFarlane, A. C., et al. (2018) · The Lancet Public Health · doi:10.1016/s2468-2667(18)30051-3 · Cited by 200 · see citing works
Adult Hippocampal Neurogenesis, Fear Generalization, and Stress
Besnard, A., & Sahay, A. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.167 · Cited by 226 · see citing works
Chan, J. C., Morgan, C. P., Leu, N. A., Shetty, A. C., Cissé, Y. M., Nugent, B. M., Morrison, K. E., Jašarević, E., Huang, W., Kanyuch, N., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15305-w · Cited by 222 · see citing works
Epigenetics of posttraumatic stress disorder: current evidence, challenges, and future directions
Zannas, A. S., Provençal, N., & Binder, E. B. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.04.003 · Cited by 218 · see citing works
Parental Adverse Childhood Experiences and Offspring Development at 2 Years of Age
Folger, A. T., Eismann, E. A., Stephenson, N. B., Shapiro, R. A., Macaluso, M., Brownrigg, M. E., & Gillespie, R. J. (2018) · PEDIATRICS · doi:10.1542/peds.2017-2826 · Cited by 212 · see citing works
Dashorst, P., Mooren, T. M., Kleber, R. J., de Jong, P. J., & Huntjens, R. J. C. (2019) · European Journal of Psychotraumatology · doi:10.1080/20008198.2019.1654065 · Cited by 207 · 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
Ross, D. A., Arbuckle, M. R., Travis, M. J., Dwyer, J. B., van Schalkwyk, G. I., & Ressler, K. J. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.3325 · Cited by 165 · see citing works
Conching, A., & Thayer, Z. M. (2019) · Social Science & Medicine · doi:10.1016/j.socscimed.2019.04.001 · Cited by 162 · see citing works
Maternal PTSD associates with greater glucocorticoid sensitivity in offspring of Holocaust survivors
Lehrner, A., Bierer, L. M., Passarelli, V., Pratchett, L. C., Flory, J. D., Bader, H. N., Harris, I. R., Bedi, A., Daskalakis, N. P., Makotkine, I., et al. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.11.019 · Cited by 160 · see citing works
Self-citationDevelopment and the epigenome: the ‘synapse’ of gene–environment interplay
Boyce, W. T., & Kobor, M. S. (2014) · Developmental Science · doi:10.1111/desc.12282 · Cited by 152 · see citing works
The Trauma Lens of Police Violence against Racial and Ethnic Minorities
Bryant‐Davis, T., Adams, T., Alejandre, A., & Gray, A. A. (2017) · Journal of Social Issues · doi:10.1111/josi.12251 · Cited by 150 · see citing works
The preconception environment and sperm epigenetics
Marcho, C., Oluwayiose, O. A., & Pilsner, J. R. (2020) · Andrology · doi:10.1111/andr.12753 · Cited by 147 · see citing works
The epigenetic impacts of social stress: how does social adversity become biologically embedded?
Cunliffe, V. T. (2016) · Epigenomics · doi:10.2217/epi-2016-0075 · Cited by 141 · see citing works
Dierkhising, C. B., Ford, J. D., Branson, C. E., Grasso, D. J., & Lee, R. (2018) · Child Abuse & Neglect · doi:10.1016/j.chiabu.2018.07.022 · Cited by 141 · see citing works
Scorza, P., Duarte, C. S., Hipwell, A. E., Posner, J. E., Ortin‐Peralta, A., CANINO, G. J., Monk, C. E., & Outcomes, P. C. F. E. I. O. C. H. (2018) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12877 · Cited by 135 · see citing works
Epigenetic programming of the neuroendocrine stress response by adult life stress
Dirven, B. C. J., Homberg, J. R., Kozicz, T., & Henckens, M. J. A. G. (2017) · Journal of Molecular Endocrinology · doi:10.1530/jme-17-0019 · Cited by 134 · see citing works
Trauma across generations and paths to adaptation and resilience
Lehrner, A., & Yehuda, R. (2018) · Psychological Trauma: Theory, Research, Practice, and Policy · doi:10.1037/tra0000302 · Cited by 129 · see citing works
Self-citationRadtke, K. M., Schauer, M., Gunter, H. M., Ruf-Leuschner, M., Sill, J., Meyer, A., & Elbert, T. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.63 · Cited by 128 · see citing works
Cultural trauma and epigenetic inheritance
Lehrner, A. L., & Yehuda, R. (2018) · Development and Psychopathology · doi:10.1017/s0954579418001153 · Cited by 128 · see citing works
Self-citationCowan, C. S. M., Callaghan, B. L., Kan, J. M., & Richardson, R. (2015) · Genes Brain & Behavior · doi:10.1111/gbb.12263 · Cited by 127 · see citing works
Epigenetic mechanisms underlying learning and the inheritance of learned behaviors
Dias, B. G., Maddox, S. A., Klengel, T., & Ressler, K. J. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.12.003 · Cited by 125 · see citing works
Braun, J. M., Messerlian, C., & Hauser, R. B. (2017) · Current Epidemiology Reports · doi:10.1007/s40471-017-0098-8 · Cited by 125 · see citing works
Daskalakis, N. P., Cohen, H., Cai, G., Buxbaum, J. D., & Yehuda, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1401660111 · Cited by 124 · see citing works
Self-citationBush, N. R., Wakschlag, L. S., LeWinn, K. Z., Hertz‐Picciotto, I., Nozadi, S. S., Pieper, S., Lewis, J. L., Biezonski, D. K., Blair, C., Deardorff, J., et al. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00547 · Cited by 123 · see citing works
Watkeys, O. J., Kremerskothen, K., Quidé, Y., Fullerton, J. M., & Green, M. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.08.017 · Cited by 123 · see citing works
Jablonka, E. (2016) · The Sociological Review Monographs · doi:10.1002/2059-7932.12012 · Cited by 122 · see citing works
Yeshurun, S., & Hannan, A. J. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0039-z · Cited by 121 · see citing works
Models of Intergenerational and Transgenerational Transmission of Risk for Psychopathology in Mice
Klengel, T., Dias, B. G., & Ressler, K. J. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.249 · Cited by 118 · see citing works
Bockmühl, Y., Patchev, A. V., Madejska, A., Hoffmann, A., Sousa, J. C., Sousa, N., Holsboer, F., Almeida, O. F. X., & Spengler, D. (2015) · Epigenetics · doi:10.1080/15592294.2015.1017199 · Cited by 117 · see citing works
Traumatic stress and human DNA methylation: A critical review
Vinkers, C. H., Kalafateli, A. L., Rutten, B. P., Kas, M. J., Kaminsky, Z., Turner, J. D., & Boks, M. P. (2015) · Epigenomics · doi:10.2217/epi.15.11 · Cited by 112 · see citing works
Griffiths, B. B., & Hunter, R. G. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.041 · Cited by 111 · see citing works
Abbott, P. W., Gumusoglu, S. B., Bittle, J., Beversdorf, D. Q., & Stevens, H. E. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.01.019 · Cited by 109 · see citing works
Daskalakis, N. P., & Yehuda, R. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00369 · Cited by 108 · see citing works
Self-citationDaskalakis, N. P., Cohen, H., Nievergelt, C. M., Baker, D. G., Buxbaum, J. D., Russo, S. J., & Yehuda, R. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.07.024 · Cited by 105 · see citing works
Self-citationGlucocorticoids and Hippocampal Structure and Function in PTSD
Szeszko, P. R., Lehrner, A. L., & Yehuda, R. (2018) · Harvard Review of Psychiatry · doi:10.1097/hrp.0000000000000188 · Cited by 105 · see citing works
Self-citationImpact of Parental Exposure on Offspring Health in Humans
Jawaid, A., Jehle, K.-L., & Mansuy, I. M. (2020) · Trends in Genetics · doi:10.1016/j.tig.2020.10.006 · Cited by 103 · see citing works
Liu, P. Z., & Nusslock, R. (2017) · Current Genomics · doi:10.2174/1389202919666171228164350 · Cited by 102 · see citing works
Multigenerational legacies of trauma: Modeling the what and how of transmission.
Danieli, Y., Norris, F. H., & Engdahl, B. E. (2016) · American Journal of Orthopsychiatry · doi:10.1037/ort0000145 · Cited by 101 · see citing works
Early-life adversity and long-term neurobehavioral outcomes: epigenome as a bridge?
Vaiserman, A. M., & Koliada, A. K. (2017) · Human Genomics · doi:10.1186/s40246-017-0129-z · Cited by 96 · see citing works
A review of epigenetic contributions to post-traumatic stress disorder
Howie, J. H., Rijal, C. M., & Ressler, K. J. (2019) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2019.21.4/kressler · Cited by 95 · see citing works
Rodgers, A. B., & Bale, T. L. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.03.018 · Cited by 91 · see citing works
Matheson, K., Seymour, A. M., Landry, J., Ventura, K., Arsenault, E., & Anisman, H. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19116455 · Cited by 88 · see citing works
Intergenerational Effects of Maternal Holocaust Exposure on <i>FKBP5</i> Methylation
Bierer, L. M., Bader, H. N., Daskalakis, N. P., Lehrner, A., Provençal, N., Wiechmann, T., Klengel, T., Makotkine, I., Binder, E. B., & Yehuda, R. (2020) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2019.19060618 · Cited by 86 · see citing works
Self-citationGenetics of glucocorticoid regulation and posttraumatic stress disorder -what do we know?
Castro-Vale, I., van Rossum, E. F. C., Machado, J. C., Mota-Cardoso, R., & Carvalho, D. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.02.005 · Cited by 85 · see citing works
Programming the Brain and Behaviour by Early‐Life Stress: A Focus on Neuroactive Steroids
Brunton, P. J. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12265 · Cited by 85 · see citing works
Matosin, N., Cruceanu, C., & Binder, E. B. (2017) · Chronic Stress · doi:10.1177/2470547017710764 · Cited by 84 · see citing works
Nutrition and its role in epigenetic inheritance of obesity and diabetes across generations
Kaspar, D., Hastreiter, S., Irmler, M., de Angelis, M. H., & Beckers, J. (2020) · Mammalian Genome · doi:10.1007/s00335-020-09839-z · Cited by 81 · see citing works
Schechter, D. S., Moser, D. A., Paoloni‐Giacobino, A., Stenz, L., Gex‐Fabry, M., Aue, T., Adouan, W., Cordero, M. I., Suardi, F., Manini, A., et al. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.00690 · Cited by 81 · see citing works
Early origins of mental disorder - risk factors in the perinatal and infant period
Newman, L. K., Judd, F. K., Olsson, C. A., Castle, D. J., Bousman, C., Sheehan, P. M., Pantelis, C., Craig, J. M., Komiti, A., & Everall, I. (2016) · BMC Psychiatry · doi:10.1186/s12888-016-0982-7 · Cited by 80 · see citing works
Karanikas, E., Daskalakis, N. P., & Agorastos, A. (2021) · Brain Sciences · doi:10.3390/brainsci11060723 · Cited by 78 · see citing works
Self-citationMisiak, B., Szmida, E., Karpiński, P., Loska, O., Sąsiadek, M. M., & Frydecka, D. (2015) · Epigenomics · doi:10.2217/epi.15.68 · Cited by 77 · see citing works
Developmental programming of the HPA axis and related behaviours: epigenetic mechanisms
Matthews, S. G., & McGowan, P. O. (2019) · Journal of Endocrinology · doi:10.1530/joe-19-0057 · Cited by 77 · see citing works
Race in an epigenetic time: thinking biology in the plural
Meloni, M. (2017) · British Journal of Sociology · doi:10.1111/1468-4446.12248 · Cited by 76 · see citing works
Morgan, C. P., Chan, J. C., & Bale, T. L. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.09.007 · Cited by 75 · see citing works
Post, R. M. (2016) · Bipolar Disorders · doi:10.1111/bdi.12401 · Cited by 73 · see citing works
Epigenetics and the glucocorticoid receptor: A review of the implications in depression
Farrell, C. M., & O’Keane, V. (2016) · Psychiatry Research · doi:10.1016/j.psychres.2016.06.022 · Cited by 72 · see citing works
Brewerton, T. D. (2022) · Journal of Eating Disorders · doi:10.1186/s40337-022-00696-6 · Cited by 71 · see citing works
Bhushan, D., Kotz, K. J., McCall, J., Wirtz, S., Gilgoff, R., Dube, S. R., Powers, C., Olson-Morgan, J., Galeste, M., Patterson, K., et al. (2020) · doi:10.48019/peam8812 · Cited by 71 · see citing works
How are social determinants of health integrated into epigenetic research? A systematic review
Evans, L. A., Engelman, M., Mikulas, A., & Malecki, K. M. C. (2021) · Social Science & Medicine · doi:10.1016/j.socscimed.2021.113738 · Cited by 70 · see citing works
Mehta, D., Miller, O., Bruenig, D., David, G., & Shakespeare‐Finch, J. (2020) · Journal of Traumatic Stress · doi:10.1002/jts.22472 · Cited by 66 · see citing works
Maternal sensitivity and the empathic brain: Influences of early life maltreatment
Mielke, E. L., Neukel, C., Bertsch, K., Reck, C., Möhler, E., & Herpertz, S. C. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2016.02.013 · Cited by 64 · see citing works
O’Donnell, K. J., Chen, L., MacIsaac, J. L., McEwen, L. M., Nguyen, T. T. T., Beckmann, K., Zhu, Y., Chen, L. R., Jeanne Brooks-gunn, B., Goldman, D. A., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-017-0063-9 · Cited by 63 · see citing works
Self-citationBlaze, J., & Roth, T. L. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.04.004 · Cited by 62 · see citing works
Yeshurun, S., Short, A. K., Bredy, T. W., Pang, T. Y., & Hannan, A. J. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.11.013 · Cited by 60 · see citing works
Epigenetic alterations associated with war trauma and childhood maltreatment
Ramo‐Fernández, L., Schneider, A., Wilker, S., & Kolassa, I. (2015) · Behavioral Sciences & the Law · doi:10.1002/bsl.2200 · Cited by 59 · see citing works
Addressing mental health in patients and providers during the COVID-19 pandemic
Werner, E. A., Aloisio, C. E., Butler, A. D., D’Antonio, K., Kenny, J. M., Mitchell, A., Ona, S., & Monk, C. E. (2020) · Seminars in Perinatology · doi:10.1016/j.semperi.2020.151279 · Cited by 59 · see citing works
Prenatal programming of stress responsiveness and behaviours: Progress and perspectives
Hamada, H., & Matthews, S. G. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12674 · Cited by 58 · see citing works
Discrimination Exposure and DNA Methylation of Stress-Related Genes in Latina Mothers
Junior, H. P. D. O. S., Nephew, B. C., Bhattacharya, A., Tan, X. M., Smith, L., Alyamani, R. A. S., Martin, E. M., Perreira, K. M., Fry, R. C., & Murgatroyd, C. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.08.014 · Cited by 58 · see citing works
Zhou, A., & Ryan, J. (2023) · Genes · doi:10.3390/genes14081639 · Cited by 57 · see citing works
“Yehuda, 2014 [95] 80 adult offspring (conceived after trauma) and 15 matched controls.”
BackgroundInfluentialWhole-genome DNA methylation status associated with clinical PTSD measures of OIF/OEF veterans
Hammamieh, R., Chakraborty, N., Gautam, A., Muhie, S., Yang, R., Donohue, D., Kumar, R., Daigle, B. J., Zhang, Y., Amara, D. A., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.129 · Cited by 57 · see citing works
Self-citationBelsky, J., & Shalev, I. (2016) · Development and Psychopathology · doi:10.1017/s0954579416000900 · Cited by 56 · see citing works
Zaidan, H., & Gaisler‐Salomon, I. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.04.013 · Cited by 54 · see citing works
Sex‐specific plasticity across generations I: Maternal and paternal effects on sons and daughters
Hellmann, J. K., Bukhari, S. A., Deno, J., & Bell, A. M. (2020) · Journal of Animal Ecology · doi:10.1111/1365-2656.13364 · Cited by 54 · see citing works
Epigenetic perpetuation of the impact of early life stress on behavior
Janusek, L. W., Tell, D., & Mathews, H. L. (2019) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2019.01.004 · Cited by 53 · see citing works
Meta-analysis reveals glucocorticoid levels reflect variation in metabolic rate, not ‘stress’
Jimeno, B., & Verhulst, S. (2023) · eLife · doi:10.7554/elife.88205 · Cited by 52 · see citing works
Hjort, L., Rushiti, F., Wang, S.-J., Fransquet, P., P Krasniqi, S., I Çarkaxhiu, S., Arifaj, D., Xhemaili, V. D., Salihu, M., A Leku, N., et al. (2021) · Epigenomics · doi:10.2217/epi-2021-0015 · Cited by 51 · see citing works
Stenson, A. F., van Rooij, S. J. H., Carter, S. E., Powers, A. D., & Jovanović, T. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113017 · Cited by 51 · see citing works
Epigenetic regulation of brain development, plasticity, and response to early-life stress
Peña, C. J. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02179-z · Cited by 51 · see citing works
The Intergenerational Effects of Early Adversity
Galler, J. R., & Rabinowitz, D. G. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-800977-2.00007-3 · Cited by 51 · see citing works
The public reception of putative epigenetic mechanisms in the transgenerational effects of trauma
Yehuda, R., Lehrner, A. L., & Bierer, L. M. (2018) · Current Zoology · doi:10.1093/eep/dvy018 · Cited by 51 · see citing works
Self-citationTransgenerational inheritance of ethanol preference is caused by maternal NPF repression
Bozler, J., Kacsoh, B., & Bosco, G. (2019) · bioRxiv · doi:10.7554/elife.45391 · Cited by 41 · see citing works
Maternal Interpersonal Trauma and Child Social‐Emotional Development: An Intergenerational Effect
Folger, A. T., Putnam, K. T., Putnam, F. W., Peugh, J., Eismann, E. A., Sa, T., Shapiro, R. A., Ginkel, J. B. V., & Ammerman, R. T. (2017) · Paediatric and Perinatal Epidemiology · doi:10.1111/ppe.12341 · Cited by 49 · see citing works
Gumpp, A. M., Boeck, C., Behnke, A., Bach, A. M., Ramo‐Fernández, L., Welz, T., Gündel, H., Kolassa, I., & Karabatsiakis, A. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005885117 · Cited by 49 · see citing works
Tambelli, R., Cimino, S., Cerniglia, L., & Ballarotto, G. (2015) · Scientific Reports · doi:10.1038/srep13984 · Cited by 48 · see citing works
- Authors
- Yehuda, R., Daskalakis, N. P., Lehrner, A., Desarnaud, F., Bader, H. N., Makotkine, I., Flory, J. D., Bierer, L. M., & Meaney, M. J.
- Affiliations
- Agency for Science, Technology and Research (SG)
- From the James J. Peters Veterans Affairs Medical Center, Bronx, N.Y.; Departments of Psychiatry and Neuroscience, Icahn School of Medicine at Mount Sinai, New York; the Ludmer Centre for Neuroinformatics and Mental Health, Douglas Mental Health University Institute, McGill University, Montreal; and the Agency for Science, Technology, and Research, Singapore Institute for Clinical Sciences, Singapore.
- Corresponding author
- Yehuda, Rachel
- ORCID
- Venue
- American Journal of Psychiatry
- Published
- 2014-08
- Volume
- 171
- Issue
- 8
- Pages
- 872-880
- ISSN
- 0002-953X (ISSN-L)
- 1535-7228
- PMC
- PMC4127390
- OpenAlex
- W2137209519
- Cited by
- 514
- References
- 37
- Citations by year
- 2026: 16 · 2025: 46 · 2024: 37 · 2023: 38 · 2022: 36 · 2021: 42 · 2020: 75 · 2019: 34 · 2018: 45 · 2017: 46 · 2016: 38 · 2015: 44 · 2014: 14 · 2013: 1
- FWCI
- 55.87
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- American Journal of Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (UL1TR000067)
- National Institute of Mental Health (RC1MH088101)
- National Center for Research Resources (M01RR000071)
- National Center for Advancing Translational Sciences
- Topics
- Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- post-traumatic stress disorder, Holocaust survivors, glucocorticoid receptor, NR3C1, DNA methylation, intergenerational trauma, maternal PTSD, cortisol suppression, dexamethasone, glucocorticoid receptor sensitivity, neuroendocrine function
- MeSH terms
- Dexamethasone, Fathers, Female, Humans, Hydrocortisone, Leukocytes, Mononuclear, Male, Middle Aged, Mothers, Pituitary-Adrenal Function Tests, Promoter Regions, Genetic, Receptors, Glucocorticoid, Stress Disorders, Post-Traumatic, Case-Control Studies, Child of Impaired Parents, Survivors, Holocaust, DNA Methylation, Adult Children, Heredity, Epigenesis, Genetic
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