TY - JOUR T1 - Genomic analysis of family data reveals additional genetic effects on intelligence and personality JF - bioRxiv DO - 10.1101/106203 SP - 106203 AU - W. David Hill AU - Ruben C. Arslan AU - Charley Xia AU - Michelle Luciano AU - Carmen Amador AU - Pau Navarro AU - Caroline Hayward AU - Reka Nagy AU - David J. Porteous AU - Andrew M. McIntosh AU - Ian J. Deary AU - Chris S. Haley AU - Lars Penke Y1 - 2017/01/01 UR - http://biorxiv.org/content/early/2017/02/06/106203.abstract N2 - Pedigree-based analyses of intelligence have reported that genetic differences account for 50-80% of the phenotypic variation. For personality traits, these effects are smaller with 34-48% of the variance being explained by genetic differences. However, molecular genetic studies using unrelated individuals typically report a heritability estimate of around 30% for intelligence and between 0% and 15% for personality variables. Pedigree-based estimates and molecular genetic estimates may differ because current genotyping platforms are poor at tagging causal variants, variants with low minor allele frequency, copy number variants, and structural variants. Using ~20 000 individuals in the Generation Scotland family cohort genotyped for ~520 000 single nucleotide polymorphisms (SNPs), we exploit the high levels of linkage disequilibrium (LD) found in members of the same family to quantify the total effect of genetic variants that are not tagged in GWASs of unrelated individuals. In our models, genetic variants in low LD with genotyped SNPs explain over half of the genetic variance in intelligence, education, and neuroticism. By capturing these additional genetic effects our models closely approximate the heritability estimates from twin studies for intelligence and education, but not for neuroticism and extraversion. From an evolutionary genetic perspective, a substantial contribution of genetic variants that are not common within the population to individual differences in intelligence, education, and neuroticism is consistent with mutation-selection balance. ER -