ArticleHuman heredity2011
Causal models for investigating complex genetic disease: II. what causal models can tell us about penetrance for additive, heterogeneity, and multiplicative two-locus models.
Article in Human heredity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- The Causal Pivot: A structural approach to genetic heterogeneity and variant discovery in complex diseases.American journal of human genetics · 2025Article
- Sufficient component cause simulations: an underutilized epidemiologic teaching tool.Frontiers in epidemiology · 2023Article
- Genetic heterogeneity: Challenges, impacts, and methods through an associative lens.Genetic epidemiology · 2022Review
- Rare high-impact disease variants: properties and identifications.Genetics research · 2016Article
- Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory.Frontiers in genetics · 2016Article
- Article
- Digenic inheritance in medical genetics.Journal of medical genetics · 2013Review
- Assessing causal mechanistic interactions: a peril ratio index of synergy based on multiplicativity.PloS one · 2013Article
- Causal models for investigating complex disease: I. A primer.Human heredity · 2011Article
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3 authors.
Funding
Abstract
BACKGROUND/
aimsStatistical geneticists commonly use certain two-locus penetrance models because these models are familiar and mathematically tractable. We investigate whether and under what circumstances these two-locus penetrance models correspond to models of causation.
methodsWe describe a sufficient component cause model for a hypothetical disease with two genetic causes. We then use the potential outcomes framework to determine the expected two-locus penetrances from this causal model and contrast them with commonly used two-locus penetrance models (additive, heterogeneity, and multiplicative penetrance models, as formulated by Risch [Am J Hum Genet 1990;46:222-228]).
resultsConventional additive and multiplicative models can correspond to any two-locus causal model only when certain very specific algebraic relationships hold. The heterogeneity model corresponds to a two-locus causal model only if the model stipulates that no disease cases are caused by the combined presence of the causal genotypes at both loci (i.e. only when there is no causal gene-gene interaction). Hence the heterogeneity model provides a valid test of the null hypothesis of no gene-gene interaction, whereas the additive and multiplicative models do not.
conclusionWe suggest that causal principles should provide the basis for statistical modeling in genetics.
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