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Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia
