<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kotsakis Ruehlmann A</submitter><funding>Intramural NIH HHS</funding><funding>NICHD NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>Medical Research Council</funding><funding>NHLBI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>South African Medical Research Council</funding><funding>Wellcome Trust</funding><funding>Orionin Tutkimussäätiö</funding><funding>U.S. Department of Health &amp;amp; Human Services | National Institutes of Health</funding><pagination>5090-5100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12486153</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(12)</volume><pubmed_abstract>Prenatal maternal stressful life events are associated with adverse neurodevelopmental outcomes in offspring. Biological mechanisms underlying these associations are largely unknown, but DNA methylation likely plays a role. This meta-analysis included twelve non-overlapping cohorts from ten independent longitudinal studies (N = 5,496) within the international Pregnancy and Childhood Epigenetics consortium to examine maternal stressful life events during pregnancy and DNA methylation in cord blood. Children whose mothers reported higher levels of cumulative maternal stressful life events during pregnancy exhibited differential methylation of cg26579032 in ALKBH3. Stressor-specific domains of conflict with family/friends, abuse (physical, sexual, and emotional), and death of a close friend/r</pubmed_abstract><journal>Molecular psychiatry</journal><pubmed_title>Epigenome-wide meta-analysis of prenatal maternal stressful life events and newborn DNA methylation.</pubmed_title><pmcid>PMC12486153</pmcid><funding_grant_id>R01 ES020392</funding_grant_id><funding_grant_id>P01 ES011269</funding_grant_id><funding_grant_id>PS0ES006096</funding_grant_id><funding_grant_id>P30 ES019776</funding_grant_id><funding_grant_id>U01 NS047537</funding_grant_id><funding_grant_id>MR/S036520/1</funding_grant_id><funding_grant_id>R01 HD068437</funding_grant_id><funding_grant_id>R00 ES024116</funding_grant_id><funding_grant_id>217065/Z/19/Z</funding_grant_id><funding_grant_id>R01 HL114396</funding_grant_id><funding_grant_id>R01 HL095606</funding_grant_id><funding_grant_id>R21 HD085849</funding_grant_id><funding_grant_id>T32ES010957</funding_grant_id><funding_grant_id>MC_PC_15018</funding_grant_id><funding_grant_id>K12 HD051958</funding_grant_id><funding_grant_id>T32 ES010957</funding_grant_id><funding_grant_id>G9815508</funding_grant_id><funding_grant_id>R01 ES025531</funding_grant_id><funding_grant_id>R01 ES025574</funding_grant_id><funding_grant_id>R01 ES028089</funding_grant_id><funding_grant_id>MR/S009310/1</funding_grant_id><funding_grant_id>P30 ES023515</funding_grant_id><funding_grant_id>P30 ES006096</funding_grant_id><funding_grant_id>R24 ES028533</funding_grant_id><funding_grant_id>Z01 ES049019</funding_grant_id><funding_grant_id>MC_PC_19009</funding_grant_id><pubmed_authors>Mulder RH</pubmed_authors><pubmed_authors>Witt SH</pubmed_authors><pubmed_authors>Haberg SE</pubmed_authors><pubmed_authors>Wright R</pubmed_authors><pubmed_authors>Hoang TT</pubmed_authors><pubmed_authors>Zillich L</pubmed_authors><pubmed_authors>Send TS</pubmed_authors><pubmed_authors>Mancano G</pubmed_authors><pubmed_authors>Czamara D</pubmed_authors><pubmed_authors>Sammallahti S</pubmed_authors><pubmed_authors>Houtepen LC</pubmed_authors><pubmed_authors>Bakulski KM</pubmed_authors><pubmed_authors>Huls A</pubmed_authors><pubmed_authors>Sharp G</pubmed_authors><pubmed_authors>Streit F</pubmed_authors><pubmed_authors>Frank J</pubmed_authors><pubmed_authors>Koen N</pubmed_authors><pubmed_authors>Lahti J</pubmed_authors><pubmed_authors>Roder S</pubmed_authors><pubmed_authors>Schmidt RJ</pubmed_authors><pubmed_authors>Cecil CAM</pubmed_authors><pubmed_authors>Binder EB</pubmed_authors><pubmed_authors>Dou J</pubmed_authors><pubmed_authors>Colicino E</pubmed_authors><pubmed_authors>Zar HJ</pubmed_authors><pubmed_authors>Page CM</pubmed_authors><pubmed_authors>Cruceanu C</pubmed_authors><pubmed_authors>London SJ</pubmed_authors><pubmed_authors>Raikkonen K</pubmed_authors><pubmed_authors>Cortes Hidalgo AP</pubmed_authors><pubmed_authors>Campbell ML</pubmed_authors><pubmed_authors>Caramaschi D</pubmed_authors><pubmed_authors>Dieckmann L</pubmed_authors><pubmed_authors>Felix JF</pubmed_authors><pubmed_authors>Herberth G</pubmed_authors><pubmed_authors>Stein DJ</pubmed_authors><pubmed_authors>Zenclussen AC</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Brunst KJ</pubmed_authors><pubmed_authors>Tuhkanen J</pubmed_authors><pubmed_authors>Magnus MC</pubmed_authors><pubmed_authors>Kotsakis Ruehlmann A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Epigenome-wide meta-analysis of prenatal maternal stressful life events and newborn DNA methylation.</name><description>Prenatal maternal stressful life events are associated with adverse neurodevelopmental outcomes in offspring. Biological mechanisms underlying these associations are largely unknown, but DNA methylation likely plays a role. This meta-analysis included twelve non-overlapping cohorts from ten independent longitudinal studies (N = 5,496) within the international Pregnancy and Childhood Epigenetics consortium to examine maternal stressful life events during pregnancy and DNA methylation in cord blood. Children whose mothers reported higher levels of cumulative maternal stressful life events during pregnancy exhibited differential methylation of cg26579032 in ALKBH3. Stressor-specific domains of conflict with family/friends, abuse (physical, sexual, and emotional), and death of a close friend/r</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2026-06-04T01:40:16.286Z</modification><creation>2026-05-04T03:12:31.459Z</creation></dates><accession>S-EPMC12486153</accession><cross_references><pubmed>36899042</pubmed><doi>10.1038/s41380-023-02010-5</doi></cross_references></HashMap>