Elizabeth C. Corfield

This study conducts a GWAS meta-analysis of stuttering, identifying genetic links with speech disorders and highlighting shared genetic architecture across different ascertainment methods.

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 introduces JODIE, a model to estimate direct, indirect, and parent-of-origin genetic effects on height, BMI, and educational attainment using family trios from two biobanks.

This study identifies six genome-wide significant risk loci for tic disorders and links genetic risk to specific brain cell types and circuits.

This paper identifies 58 genome-wide significant loci for major anxiety disorders using a large meta-analysis and highlights GABAergic signaling as a potential mechanism.

This study uses genome-wide meta-regression to analyze social behavior across different contexts, ages, and reporters, identifying six genetic loci and showing modest heritability.

This study conducts a genome-wide association analysis of generalised anxiety symptom severity, identifying 80 significant variants and showing genetic correlations with other mental and physical health traits.

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

The paper develops a polygenic score for dizygotic twinning, showing it explains 1.6% of liability variance and is linked to fertility outcomes and genetic correlations with related conditions.

This study identifies 1,257 genetic variants associated with human personality traits using large-scale GWAS and finds widespread genetic correlations with behaviors and life outcomes.

This study performs the first GWAS on a latent partner choice index using 206,617 individuals, identifying genetic correlates and solutions to reduce assortative mating biases in genetic studies.

The paper examines genetic and phenotypic heterogeneity in early neurodevelopmental traits using data from the Norwegian Mother, Father, and Child Cohort Study, identifying 11 latent factors and trait-specific genetic correlations with autism, ADHD, and schizophrenia.

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 shows genetic similarity between relatives can indicate assortative mating, finding evidence in nine traits and increased genetic variance in offspring for six of them.

This study identifies a genome-wide significant variant for OC traits and shows shared genetic risk between OC traits and OCD.

The paper validates the SWAN Scale as a tool for ADHD trait-based genetic research, showing it predicts ADHD diagnoses and is linked to ADHD polygenic risk.

The paper investigates the factor structure and heritability of obsessive-compulsive traits in children and adolescents using the TOCS, identifying six dimensions and estimating heritability ranges.