Per Minor Magnus

The paper describes the MoBaPsychGen pipeline for quality controlling and imputing genotyping data from the MoBa cohort, identifying extensive family relationships across 207,569 individuals.

The paper investigates how nulliparity affects maternal genetic effects on gestational duration and birth weight using GWAS data from a large cohort.

This study identifies a genome-wide association for neonatal jaundice, revealing distinct genetic pathways compared to adult bilirubin metabolism.

This study identifies genetic variants associated with income and shows they correlate with health outcomes and educational attainment.

This study identifies 40 genetic loci associated with placental weight using GWAS in 179,025 children and parents, revealing shared and distinct genetic influences with fetal growth.

The paper identifies five genetic loci associated with postpartum hemorrhage through a meta-analysis and links them to progesterone receptor binding sites and related traits.

This study identifies genetic loci associated with gestational duration and preterm delivery, showing maternal and fetal genetic effects and antagonistic pleiotropy with birth weight.

This study investigates DNA methylation differences on the X chromosome in ART-conceived versus naturally-conceived newborns, finding sex-specific methylation changes linked to neurodevelopmental processes.

This study identifies 46 BMI loci in children aged 0-8 years, revealing age-specific effects and pathways linked to Mendelian obesity.

This study conducts a genome-wide association meta-analysis of childhood aggression across multiple raters, instruments, and ages, identifying genetic correlations with various traits but no genome-wide significant SNPs.

The paper introduces Trio-GCTA, a model to separate direct and indirect genetic effects in parent-offspring trios, applied to four phenotypes using real data.

This study uses genomic analysis of parent-offspring trios to estimate the genetic nurture effect on child anxiety and depression symptoms at age 8, finding significant influence on depression but not anxiety.

This study identifies five BMI-associated loci across 12 time points in children, highlighting transient effects of common genetic variation in the leptin signaling pathway during infancy.

This study identifies 99 genes associated with autism spectrum disorder through large-scale exome sequencing, showing differences in mutation frequencies between ASD and severe neurodevelopmental delay groups.

This study investigates the genetic contributions to gestational weight gain, finding that maternal common variants explain about 20% of variability, while fetal variants have a minor role.