-Gottesman (1991): family study on the risk of developing SCZ. Monozygotic twins = 48% likely to both have SCZ; dizygotic twins = 17% likely to both have SCZ; 2nd degree relatives = 4% likely to both have SCZ; general population = 1% likely to both have SCZ. Higher concordance rates when genetics are more similar.
genetic basis of schizophrenia (polygenic & aetiologically heterogenous)
-there are candidate genes involved in SCZ, mostly genes that code for dopamine
-SCZ is polygenic (more than one gene)
-aetiologically heterogenous: there are different combinations of genes that cause SCZ
-Ripke et al (2014): meta-analysis of studies into genomes. Found 108 gene variations associated with the risk of SCZ. Shows it is polygenic & aetiologically heterogenous
-supporting research: Tienari et al (2004): 19k adoptive children, bio mother = SCZ. These children have an increased risk of SCZ even if they grew up in a different environment. D: large sample, increases generalisability. Increases the validity of genetic explanation.
-research found higher concordance rates in MZ than DZ. increases the validity.
Weakness(es):
-contradictory evidence: evidence to say that SCZ is caused by more than genes e.g., smoking THC-rich cannabis throughout teenage years. Decreases the validity, is reductionist.
-alternative explanation: childhood trauma. 67% of people with SCZ reported having childhood trauma. Genetic explanation is reductionist as only considers genes.