Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Esben Agerbo
  • Preben Bo Mortensen
  • Wiuf, Carsten
  • Michael S Pedersen
  • John McGrath
  • Mads Vilhelm Hollegaard
  • Bent Nørgaard-Pedersen
  • David M Hougaard
  • Ole Mors
  • Carsten B Pedersen
Epidemiological studies indicate that having any family member with schizophrenia increases the risk of schizophrenia in the probands. However, genome-wide association studies (GWAS) have accounted for little of this variation. The aim of this study was to use a population-based sample to explore the influence of single-nucleotide polymorphisms (SNPs) on the excess schizophrenia risk in offspring of parents with a psychotic, bipolar affective or other psychiatric disorder.
OriginalsprogEngelsk
TidsskriftSchizophrenia Research
Vol/bind134
Udgave nummer2-3
Sider (fra-til)246-252
Antal sider7
ISSN0920-9964
DOI
StatusUdgivet - 2012

ID: 40763541