Rosa H. Mulder

This study integrates prenatal exposures and genetics to predict DNA methylation at birth, finding that the exposome explains additional variation beyond genetic factors.

The paper investigates genetic variants and oral contraceptive use interactions on depression risk in the UK Biobank, finding no genome-wide significant interactions.

This study conducts an epigenome-wide association study (EWAS) meta-analysis of wellbeing using DNA methylation data, finding no significant methylation sites but suggesting the need for larger studies.

The paper identifies age-dependent methylation quantitative trait loci (longitudinal mQTLs) across the lifespan using blood DNAm data from two cohorts, finding consistent genotype-by-age effects and associations with multiple phenotypes.

This study identifies cell type-specific DNA methylation associations with childhood ADHD symptoms using deconvolution and sequencing-based methylation data from peripheral and cord blood.

The paper characterizes the developmental trajectories of adult epigenetic clock sites using longitudinal cohort data, finding divergent patterns, early individual variation, and enrichment for genetic and prenatal environmental factors.

This study uses longitudinal meta-regression to examine how DNA methylation effects on child health outcomes vary by timing, finding larger effects in childhood but noisier associations and time-specific signals.

This study identifies regional DNA methylation associations with early childhood appetitive traits using epigenome-wide analysis of cord blood samples.

This study examines DNA methylation at birth and its association with childhood cognitive skills, finding weak single CpG site associations and one region near DUSP22 linked to non-verbal cognition.

The paper analyzes DNA methylation changes across birth to late adolescence in two cohorts, finding widespread nonlinear changes and sex-specific patterns.

This paper identifies DNA methylation sites associated with aggression through a meta-analysis of epigenome-wide studies across different age groups and tissues.