Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Genetic Mapping and Diversity in Plants and Animals, and Dermatology and Skin Diseases.
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function
Genome-wide association meta-analysis identifies 29 new acne susceptibility loci
Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Meta-analyses identify DNA methylation associated with kidney function and damage
Identical twins carry a persistent epigenetic signature of early genome programming
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
A reference panel of 64,976 haplotypes for genotype imputation
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
The UK10K project identifies rare variants in health and disease
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants
Whole-genome sequence-based analysis of thyroid function
Differential methylation of the TRPA1 promoter in pain sensitivity
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements
Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics
Mapping cis- and trans-regulatory effects across multiple tissues in twins
Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes