paperKB
coga / coga-kb
Help
Sign in

Chunk #3 — Introduction

Source
Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.
Embedded
yes

Text

number variants in schizophrenia13,14,15 and an excess of de novo CNV events16 in that disorder have raised the possibility of a significant contribution from rare events, some of apparently high penetrance. Whilst it is not yet clear whether the contribution from CNVs is small or substantial, these findings can be interpreted as supporting the hypothesis that common variation may be less important than has generally been assumed.