Peter Holmans

De novo mutations in schizophrenia implicate synaptic networks

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

There is increasing evidence that genome-wide association (GWA) studies represent a powerful approach to the identification of genes involved in common human diseases. We descri...

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Abstract Imputing genotypes from reference panels created by whole-genome sequencing (WGS) provides a cost-effective strategy for augmenting the single-nucleotide polymorphism (...

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Biological insights from 108 schizophrenia-associated genetic loci

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Common variants on chromosome 6p22.1 are associated with schizophrenia

Identification of loci associated with schizophrenia by genome-wide association and follow-up

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC