Expressive

rs117780815 - NKAIN2

Magnitude 2.2 · 2 studies on file

Reported associations

  • Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders - Unknown journal (n.d.) · Unknown authors · PubMed 34099189

    ABSTRACT: BACKGROUND: Sex differences in incidence and/or presentation of schizophrenia (SCZ), major depressive disorder (MDD), and bipolar disorder (BIP) are pervasive. Previous evidence for shared genetic risk and sex differences in brain abnormalities across disorders suggest possible shared sex-dependent genetic risk. METHODS: We conducted the largest to date genome-wide genotype-by-sex (GxS) interaction of risk for these disorders, using 85,735 cases (33,403 SCZ, 19,924 BIP, 32,408 MDD) and 109,946 controls from the Psychiatric Genomics Consortium (PGC) and iPSYCH. RESULTS: Across disorders, genome-wide significant SNP-by-sex interaction was detected for a locus encompassing NKAIN2 (rs117780815; p=3.2×10−8), that interacts with sodium/potassium-transporting ATPase enzymes impli

  • Genome Wide Association Study of the Rate of Cognitive Decline in Alzheimer's Disease - Unknown journal (n.d.) · Unknown authors · PubMed 23535033

    ABSTRACT: Background Substantial inter-individual variability exists in the disease trajectories of Alzheimer's disease (AD) patients. Some decline rapidly while others decline slowly and there are no known explanations for this variability. We describe the first genome wide association study to examine rate of cognitive decline in a sample of AD patients with longitudinal measures of cognition. Methods The discovery sample was 303 AD cases recruited in the AD Neuroimaging Initiative and the replication sample was 323 AD cases from the Religious Orders Study and Rush Memory and Aging Project. In the discovery sample, Alzheimer's Disease Assessment Scale-cognitive subscale responses were tested for association with genome-wide SNP data using linear regression. We tested the 65 most sign

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