Area of research
Genetics · Neurology
Research interest
Research focused on Genome-wide association study and Phenome, with related work in Disease, Genetic association, Mendelian randomization. Notable publications include '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', and 'Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation'.
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals
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
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
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation
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