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Updated: Jul 16, 2025

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease
Published on: January 7, 2014
Extensions of the causal framework to Mendelian randomisation and gene-environment interaction
Claire M A Haworth1, Robyn E Wootton1,2
1School of Psychological Science, University of Bristol, Bristol, UK claire.haworth@bristol.ac.ukhttps://www.bristol.ac.uk/people/person/Claire-Haworth-04ed5882-f1f6-4fb5-8960-5581b0cc8bc4/ robyn.wootton@bristol.ac.uk.
Abstract:
In our commentary we ask whether we should ultimately endeavour to find the deep causes of behaviours? Then we discuss two extensions of the proposed framework: (1) Mendelian randomisation and (2) hypothesis-free gene-environment interaction (leveraging heterogeneity in genetic associations). These complementary methods help move us towards second-generation causal knowledge, ultimately understanding mechanistic pathways and identifying more effective intervention targets.
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