B. Todd Webb

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Using genetic drug-target networks to develop new drug hypotheses for major depressive disorder

Unpacking genetic risk pathways for college student alcohol consumption: The mediating role of impulsivity

A gene co-expression network-based analysis of multiple brain tissues reveals novel genes and molecular pathways underlying major depression

Genetic correlations of psychiatric traits with body composition and glycemic traits are sex- and age-dependent

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

The role of polygenic risk score gene-set analysis in the context of the omnigenic model of schizophrenia

A validation of the diathesis-stress model for depression in Generation Scotland

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

A polygenic resilience score moderates the genetic risk for schizophrenia

Investigating the causal relationship between neuroticism and depression via Mendelian randomization

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

Assessment of bidirectional relationships between physical activity and depression among adults: A 2-sample Mendelian randomization study

Genes, roommates, and residence halls: A multidimensional study of the role of peer drinking on college students' alcohol use

Long-Chain omega-3 Levels Are Associated With Increased Alcohol Sensitivity in a Population-Based Sample of Adolescents

Identification of common genetic risk variants for autism spectrum disorder

Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricans