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SU25USING POLYGENIC RISK SCORE APPROACHES TO INVESTIGATE THE COMMON-VARIANT GENETIC ARCHITECTURE OF COGNITION IN SCHIZOPHRENIA.
- Source :
-
European Neuropsychopharmacology . 2019 Supplement4, Vol. 29, pS1281-S1281. 1p. - Publication Year :
- 2019
-
Abstract
- Highlights from the article: Identification of association-enriched gene-sets in each training set was derived from 134 central nervous system (CNS)-related gene-sets shown to capture the excess burden in schizophrenia for copy number variants [6]. The FMRP targets [1] gene-set preferentially captured variance in cognition in schizophrenia over other previously associated schizophrenia gene-sets when the GWAS of IQ was used to define risk alleles. One important observation was in marked contrast to genome wide polygenic risk score analyses, many gene-set polygenic risk scores capture maximal variance when risk alleles are defined at the genome wide significant threshold.
- Subjects :
- *22Q11 deletion syndrome
*SCHIZOPHRENIA
*COGNITION
*DNA copy number variations
Subjects
Details
- Language :
- English
- ISSN :
- 0924977X
- Volume :
- 29
- Database :
- Academic Search Index
- Journal :
- European Neuropsychopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 137723919
- Full Text :
- https://doi.org/10.1016/j.euroneuro.2018.08.389