Expressive

rs10865974 - PBRM1, GNL3

Magnitude 2.2 · 2 studies on file

Reported associations

  • Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning - Unknown journal (n.d.) · Unknown authors · PubMed 35974141

    ABSTRACT: Understanding the genomic basis of memory processes may help in combating neurodegenerative disorders. Hence, we examined the associations of common genetic variants with verbal short-term memory and verbal learning in adults without dementia or stroke (N = 53,637). We identified novel loci in the intronic region of CDH18, and at 13q21 and 3p21.1, as well as an expected signal in the APOE/APOC1/TOMM40 region. These results replicated in an independent sample. Functional and bioinformatic analyses supported many of these loci and further implicated POC1. We showed that polygenic score for verbal learning associated with brain activation in right parieto-occipital region during working memory task. Finally, we showed genetic correlations of these memory traits with several neur

  • Genome-wide association of mood-incongruent psychotic bipolar disorder - Unknown journal (n.d.) · Unknown authors · PubMed 23092984

    ABSTRACT: Mood-incongruent psychotic features (MICP) are familial symptoms of bipolar disorder (BP) that also occur in schizophrenia (SZ), and may represent manifestations of shared etiology between the major psychoses. In this study we have analyzed three large samples of BP with imputed genome-wide association data and have performed a meta-analysis of 2196 cases with MICP and 8148 controls. We found several regions with suggestive evidence of association (P<10-6), although no marker met genome-wide significance criteria. The top associations were on chromosomes: 6q14.2 within the PRSS35/SNAP91 gene complex (rs1171113, P=9.67 × 10-8); 3p22.2 downstream of TRANK/LBA1 (rs9834970, P=9.71 × 10-8); and 14q24.2 in an intron of NUMB (rs2333194, P=7.03 × 10-7). These associations were

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