<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Moccia C</submitter><funding>Italian Ministry for Education, University and Research</funding><funding>Horizon 2020</funding><funding>Compagnia di San Paolo</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Low birthweight has been repeatedly associated with long-term adverse health outcomes and many non-communicable diseases. Our aim was to look-up cord blood birthweight-associated CpG sites identified by the PACE Consortium in infant saliva, and to explore saliva-specific DNA methylation signatures of birthweight.&lt;h4>Methods&lt;/h4>DNA methylation was assessed using Infinium HumanMethylation450K array in 135 saliva samples collected from children of the NINFEA birth cohort at an average age of 10.8 (range 7-17) months. The association analyses between birthweight and DNA methylation variations were carried out using robust linear regression models both in the exploratory EWAS analyses and in the look-up of the PACE findings in infant saliva.&lt;h4>Results&lt;/h4>None of the cord b</pubmed_abstract><journal>Clinical epigenetics</journal><pagination>57</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7980592</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Birthweight DNA methylation signatures in infant saliva.</pubmed_title><pmcid>PMC7980592</pmcid><pubmed_authors>Trevisan M</pubmed_authors><pubmed_authors>Richiardi L</pubmed_authors><pubmed_authors>Polidoro S</pubmed_authors><pubmed_authors>Popovic M</pubmed_authors><pubmed_authors>Rusconi F</pubmed_authors><pubmed_authors>Isaevska E</pubmed_authors><pubmed_authors>Fiano V</pubmed_authors><pubmed_authors>Moccia C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Birthweight DNA methylation signatures in infant saliva.</name><description>&lt;h4>Background&lt;/h4>Low birthweight has been repeatedly associated with long-term adverse health outcomes and many non-communicable diseases. Our aim was to look-up cord blood birthweight-associated CpG sites identified by the PACE Consortium in infant saliva, and to explore saliva-specific DNA methylation signatures of birthweight.&lt;h4>Methods&lt;/h4>DNA methylation was assessed using Infinium HumanMethylation450K array in 135 saliva samples collected from children of the NINFEA birth cohort at an average age of 10.8 (range 7-17) months. The association analyses between birthweight and DNA methylation variations were carried out using robust linear regression models both in the exploratory EWAS analyses and in the look-up of the PACE findings in infant saliva.&lt;h4>Results&lt;/h4>None of the cord b</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-20T02:29:04.596Z</modification><creation>2025-04-20T02:29:04.596Z</creation></dates><accession>S-EPMC7980592</accession><cross_references><pubmed>33741061</pubmed><doi>10.1186/s13148-021-01053-1</doi></cross_references></HashMap>