<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Katrinli S</submitter><funding>BLRD VA</funding><funding>NCATS NIH HHS</funding><funding>NICHD NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>NIOSH CDC HHS</funding><funding>CSRD VA</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>The occurrence of post-traumatic stress disorder (PTSD) following a traumatic event is associated with biological differences that can represent the susceptibility to PTSD, the impact of trauma, or the sequelae of PTSD itself. These effects include differences in DNA methylation (DNAm), an important form of epigenetic gene regulation, at multiple CpG loci across the genome. Moreover, these effects can be shared or specific to both central and peripheral tissues. Here, we aim to identify blood DNAm differences associated with PTSD and characterize the underlying biological mechanisms by examining the extent to which they mirror associations across multiple brain regions.&lt;h4>Methods&lt;/h4>As the Psychiatric Genomics Consortium (PGC) PTSD Epigenetics Workgroup, we conducted t</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2024.07.15.24310422</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11275670</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Epigenome-wide association studies identify novel DNA methylation sites associated with PTSD: A meta-analysis of 23 military and civilian cohorts.</pubmed_title><pmcid>PMC11275670</pmcid><funding_grant_id>R01 MD011728</funding_grant_id><funding_grant_id>IK2 CX000525</funding_grant_id><funding_grant_id>UL1 TR000433</funding_grant_id><funding_grant_id>U01 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AG051877</funding_grant_id><funding_grant_id>DP1 DA058737</funding_grant_id><funding_grant_id>R01 MH093500</funding_grant_id><funding_grant_id>R15 MH099521</funding_grant_id><funding_grant_id>R01 MH106595</funding_grant_id><funding_grant_id>K12 HD085850</funding_grant_id><funding_grant_id>U01 MH115485</funding_grant_id><pubmed_authors>Wani AH</pubmed_authors><pubmed_authors>Galea S</pubmed_authors><pubmed_authors>Luft BJ</pubmed_authors><pubmed_authors>Mehta D</pubmed_authors><pubmed_authors>Marx CE</pubmed_authors><pubmed_authors>Kimbrel NA</pubmed_authors><pubmed_authors>Milberg W</pubmed_authors><pubmed_authors>Nievergelt CM</pubmed_authors><pubmed_authors>Avetyan D</pubmed_authors><pubmed_authors>Wildman DE</pubmed_authors><pubmed_authors>Chen CY</pubmed_authors><pubmed_authors>Nunez-Rios DL</pubmed_authors><pubmed_authors>Fatumo S</pubmed_authors><pubmed_authors>Linnstaedt SD</pubmed_authors><pubmed_authors>Mutesa L</pubmed_authors><pubmed_authors>Logue MW</pubmed_authors><pubmed_authors>Geuze E</pubmed_authors><pubmed_authors>Vinkers CH</pubmed_authors><pubmed_authors>Orcutt HK</pubmed_authors><pubmed_authors>Rauch SAM</pubmed_authors><pubmed_authors>Daskalakis NP</pubmed_authors><pubmed_authors>Fortier C</pubmed_authors><pubmed_authors>Garrett ME</pubmed_authors><pubmed_authors>Vermetten E</pubmed_authors><pubmed_authors>Maihofer AX</pubmed_authors><pubmed_authors>Qin XJ</pubmed_authors><pubmed_authors>Beckham JC</pubmed_authors><pubmed_authors>Brick LA</pubmed_authors><pubmed_authors>Dalvie S</pubmed_authors><pubmed_authors>Mutabaruka J</pubmed_authors><pubmed_authors>Uwineza A</pubmed_authors><pubmed_authors>Hayes JP</pubmed_authors><pubmed_authors>Ware EB</pubmed_authors><pubmed_authors>Lori A</pubmed_authors><pubmed_authors>Rutten BPF</pubmed_authors><pubmed_authors>Hemmings SM</pubmed_authors><pubmed_authors>Ursano RJ</pubmed_authors><pubmed_authors>Ashley-Koch AE</pubmed_authors><pubmed_authors>Champagne FA</pubmed_authors><pubmed_authors>Ratanatharathorn A</pubmed_authors><pubmed_authors>Luykx JJ</pubmed_authors><pubmed_authors>Stein MB</pubmed_authors><pubmed_authors>Verfaellie MH</pubmed_authors><pubmed_authors>Michael A Hauser</pubmed_authors><pubmed_authors>Nemeroff CB</pubmed_authors><pubmed_authors>Baker DG</pubmed_authors><pubmed_authors>Grant G</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Bromet E</pubmed_authors><pubmed_authors>Smith AK</pubmed_authors><pubmed_authors>Ressler KJ</pubmed_authors><pubmed_authors>Toikumo S</pubmed_authors><pubmed_authors>Aiello AE</pubmed_authors><pubmed_authors>Boks MP</pubmed_authors><pubmed_authors>Kessler RC</pubmed_authors><pubmed_authors>McLean SA</pubmed_authors><pubmed_authors>Koenen KC</pubmed_authors><pubmed_authors>Risbrough VB</pubmed_authors><pubmed_authors>Wolf EJ</pubmed_authors><pubmed_authors>Koen N</pubmed_authors><pubmed_authors>Kuan PF</pubmed_authors><pubmed_authors>PGC-PTSD Epigenetics Workgroup, PsychENCODE PTSD Brainomics Project, Traumatic Stress Brain Research Group</pubmed_authors><pubmed_authors>Miller MW</pubmed_authors><pubmed_authors>Huber BR</pubmed_authors><pubmed_authors>Mufford MS</pubmed_authors><pubmed_authors>Young RM</pubmed_authors><pubmed_authors>Kleinman JE</pubmed_authors><pubmed_authors>King AP</pubmed_authors><pubmed_authors>Katrinli S</pubmed_authors><pubmed_authors>Seedat S</pubmed_authors><pubmed_authors>Jajoo A</pubmed_authors><pubmed_authors>Liberzon I</pubmed_authors><pubmed_authors>Musanabaganwa C</pubmed_authors><pubmed_authors>Dennis MF</pubmed_authors><pubmed_authors>Uddin M</pubmed_authors><pubmed_authors>Jansen S</pubmed_authors><pubmed_authors>Stein DJ</pubmed_authors><pubmed_authors>Montalvo-Ortiz J</pubmed_authors><pubmed_authors>Zannas AS</pubmed_authors><pubmed_authors>Nugent NR</pubmed_authors><pubmed_authors>Rutembesa E</pubmed_authors><pubmed_authors>van den Heuvel LL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Epigenome-wide association studies identify novel DNA methylation sites associated with PTSD: A meta-analysis of 23 military and civilian cohorts.</name><description>&lt;h4>Background&lt;/h4>The occurrence of post-traumatic stress disorder (PTSD) following a traumatic event is associated with biological differences that can represent the susceptibility to PTSD, the impact of trauma, or the sequelae of PTSD itself. These effects include differences in DNA methylation (DNAm), an important form of epigenetic gene regulation, at multiple CpG loci across the genome. Moreover, these effects can be shared or specific to both central and peripheral tissues. Here, we aim to identify blood DNAm differences associated with PTSD and characterize the underlying biological mechanisms by examining the extent to which they mirror associations across multiple brain regions.&lt;h4>Methods&lt;/h4>As the Psychiatric Genomics Consortium (PGC) PTSD Epigenetics Workgroup, we conducted t</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-04T20:27:17.852Z</modification><creation>2025-04-04T20:27:17.852Z</creation></dates><accession>S-EPMC11275670</accession><cross_references><pubmed>39072012</pubmed><doi>10.1101/2024.07.15.24310422</doi></cross_references></HashMap>