Harriet Cullen

The paper recalculates CNV penetrance for intellectual disability, showing lower estimates due to methodological differences, and recommends phenotype-specific risk reporting.

This study shows that HTT CAG repeat length within the normal and intermediate range is associated with brain structure and neuropsychiatric risk, challenging the view of CAG repeats as purely categorical.

This study links ASD common genetic variants to regional brain volume differences in newborns, finding positive associations with frontal and fronto-temporal volumes and negative associations with parietal and parieto-occipital volumes.

This paper conducts a genome-wide association meta-analysis of age at onset of walking, identifying 11 loci and showing genetic correlations with ADHD, BMI, intelligence, and brain structure.

The paper investigates the role of common genetic variation in neonatal subcortical brain development by examining SNP associations and polygenic scores from adult studies.

The paper finds that genetic risk for neuropsychiatric diseases is linked to reduced deep grey matter volume in preterm infants, suggesting a mechanism for how early adversity interacts with genetic vulnerability.