Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study - Nolte, Ilja M; van der Most, Peter J; Alizadeh, Behrooz Z; de Bakker, Paul IW; Boezen, H Marike; Bruinenberg, Marcel; Franke, Lude; van der Harst, Pim; Navis, Gerjan; Postma, Dirkje S; Rots, Marianne G; Stolk, Ronald P; et al. (European journal of human genetics : EJHG, 2017)
Keywords: Bioinformatics; Blood Cell Count; Blood Pressure - genetics; Clinical medicine; Diabetes; Disease; Epidemiology; Gene loci; Genes, Dominant; Genetic markers; Genetic Predisposition to Disease; Genetics; Genome-Wide Association Study - methods; Genome-Wide Association Study - standards; Genomes; Health risk assessment; Heart Rate - genetics; Heritability; Humans; Morbidity; Phenotype; Polymorphism, Single Nucleotide; Quantitative Trait, Heritable; Respiration - genetics; Single-nucleotide polymorphism; Studies; Netherlands