Christal N. Davis

This study identifies shared genetic and neurobiological pathways between problematic alcohol use and anxiety disorders using genomic analyses.

This study identifies shared and distinct genetic factors underlying suicidality phenotypes using GWAS and structural equation modelling.

The paper examines how polygenic risk for suicide attempts interacts with alcohol use disorder and childhood adversity to influence suicide attempt risk.

The paper uses genetically imputed brain imaging phenotypes to find associations with psychiatric traits in a multi-ancestry cohort.

This study investigates genetic predictors of inpatient opioid exposure after knee or hip surgery using EHR and genotype data from 27,896 individuals across three ancestries, finding no genome-wide significant loci.

The paper investigates the genetic overlap between educational attainment and substance use traits, finding distinct genetic patterns for cognitive and non-cognitive components of education.

The paper investigates genetic and neural overlaps between alcohol use disorder and BMI, finding polygenic overlap despite minimal genetic correlation and identifying shared brain regions involved in executive function and reward.

This study identifies 343 genetic loci for chronic pain in 1.2 million individuals, revealing pleiotropy with psychiatric disorders and brain structures.

The paper integrates HiTOP and RDoC frameworks to identify shared and distinct biological mechanisms of externalizing and internalizing psychopathology using multi-omics approaches.

The paper uses genomic structural equation modeling to identify the genetic architecture of externalizing and internalizing psychopathology, finding a moderate genetic correlation and shared causal variants.

This paper combines transdiagnostic and disorder-level GWAS to enhance genetic risk profiles for psychiatric disorders in multi-ancestry samples, identifying novel SNPs and shared genetic variance.