Expressive

rs10078807 - NIHCOLE - RNU6-334P

Magnitude 2.0 · 2 studies on file

Reported associations

  • Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders. - Progress in neuro-psychopharmacology & biological psychiatry (2022) · Mei L, Gao Y, Chen M, Zhang X, Yue W, Zhang D, Yu H · PubMed 34634379

    Major depressive disorders (MDDs) and anxiety and stress-related disorders (ASRDs) have overlapping symptoms and high rates of comorbidity. However, the underlying mechanisms remain largely unknown. Here, we aimed to examine whether MDD and ASRD share genetic risk factors utilizing recent large-scale genome-wide association studies (GWASs). To examine the genetic overlap between MDD and ASRD, we applied genetic correlation analysis to analyze GWAS summary statistics for MDD (16,823 cases and 25,632 controls) and ASRD (12,665 cases and 19,225 controls). We found positive and significant genetic correlations between MDD and ASRD (GNOVA: rho = 0.59, se = 0.01, P = 5.32 × 10 ). Our latent causal variable (LCV) analysis indicated the genetic correlation result from pleiotropic effects

  • Multi-trait analysis for genome-wide association study of five psychiatric disorders - Unknown journal (n.d.) · Unknown authors · PubMed 32606422

    ABSTRACT: We conducted a cross-trait meta-analysis of genome-wide association study on schizophrenia (SCZ) (n = 65,967), bipolar disorder (BD) (n = 41,653), autism spectrum disorder (ASD) (n = 46,350), attention deficit hyperactivity disorder (ADHD) (n = 55,374), and depression (DEP) (n = 688,809). After the meta-analysis, the number of genomic loci increased from 14 to 19 in ADHD, from 3 to 10 in ASD, from 45 to 57 in DEP, from 8 to 54 in BD, and from 64 to 87 in SCZ. We observed significant enrichment of overlapping genes among different disorders and identified a panel of cross-disorder genes. A total of seven genes were found being commonly associated with four out of five psychiatric conditions, namely GABBR1, GLT8D1, HIST1H1B, HIST1H2BN, HIST1H4L, KCNB1, and DCC.

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