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Functional impact of global rare copy number variation in autism spectrum disorders
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma.
Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism.
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
