Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Genetics and Neurodevelopmental Disorders, and Genomic variations and chromosomal abnormalities.
Robust inference and widespread genetic correlates from a large-scale genetic association study of human personality
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Cluster Headache Genomewide Association Study and Meta‐Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor
A causal effects of gut microbiota in the development of migraine
Genetic variants associated with syncope implicate neural and autonomic processes
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond
Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
Integration of evidence across human and model organism studies: A meeting report
A large-scale genome-wide association study meta-analysis of cannabis use disorder
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression
The nature of nurture: Effects of parental genotypes
Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence
Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence