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 tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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.
Originalsprog | Engelsk |
---|---|
Tidsskrift | Schizophrenia Research |
Vol/bind | 134 |
Udgave nummer | 2-3 |
Sider (fra-til) | 246-252 |
Antal sider | 7 |
ISSN | 0920-9964 |
DOI | |
Status | Udgivet - 2012 |
ID: 40763541