Area of research
Genetics · Neurology
Research interest
Research interests include Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders, Genetic Mapping and Diversity in Plants and Animals, and Parkinson's Disease Mechanisms and Treatments.
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals
Bi-allelic LAMP3 Variants in Three Children With Interstitial Lung Disease: Evidence of a Novel Disease-gene Association
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice
The genetic legacy of African Americans from Catoctin Furnace
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
Genetic determinants of daytime napping and effects on cardiometabolic health
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
Genetic analyses identify widespread sex-differential participation bias
Resource profile and user guide of the Polygenic Index Repository
Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry
Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease
Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms