David Davtian

The paper identifies shared epigenetic and genetic loci between generalized anxiety disorder and COVID-19, implicating neuroimmune pathways in their comorbidity.

This study identifies shared and disorder-specific genetic loci across internalizing disorders using a multivariate genome-wide association approach in diverse populations.

This study identifies genetic correlations and pleiotropy between neurodevelopmental disorders and hearing problems, suggesting shared biological mechanisms.

This paper identifies 90 genome-wide significant SNPs for suicidal behaviors in diverse populations, with 49 novel findings, and highlights genetic correlations with mental and physical health traits.

This study identifies 80 genome-wide significant associations for endometriosis and adenomyosis in 1.4 million women, uncovering novel loci and pathways involved in disease mechanisms.

The paper identifies shared genetic regulation across mRNA, proteins, and metabolites in blood, revealing networks and mediators of GWAS variants.

This study identifies XBP1 expression in pancreatic islets as a genetic factor associated with poor glycaemic control and increased T2DM risk in South and East Asians, particularly in young non-obese onset diabetes.

This study identifies genetic variants associated with glycaemic response to GLP-1 receptor agonists using observational and trial data, finding variants in GLP-1R and ARRB1 linked to HbA1c reduction.