Evidence map›Paper›PMID 21912139›Full record

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.

Ann M Madsen, Ruth Ottman, Susan E Hodge

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Digenic inheritance in medical genetics.Journal of medical genetics · 2013
    Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ann M MadsenDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, USA.
Ruth Ottman
Susan E Hodge

Funding

The Epilepsy Phenome/ Genome Project (EPGP)U01NS053998 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOWENSTEIN, DANIEL H · 2007 to 2013
$26.4M
Genetic Epidemiology of Seizure Disorders In RochesterR01NS043472 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OTTMAN, RUTH · 2002 to 2006
$6.2M
GENETICS OF AD PARTIAL EPILEPSY WITH AUDITORY FEATURESR01NS036319 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OTTMAN, RUTH · 1997 to 2007
$3.7M
Whole-genome sequencing in multiplex epilepsy familiesRC2NS070344 · NINDS · DUKE UNIVERSITY · PI GOLDSTEIN, DAVID B., OTTMAN, RUTH · 2009 to 2010
$2.0M
Genetic Analysis: Psychiatric and Other Complex DiseasesT32MH065213 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WEISSMAN, MYRNA M · 2002 to 2011
$1.7M
PSYCHIATRIC GENETICS AND FAMILY STUDIES--ROBUST METHODSR01MH048858 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HODGE, SUSAN E. · 1992 to 2010
$1.5M
NIMH NIH HHS R01 MH048858NIMH NIH HHS R01-MH048858NIMH NIH HHS T32 MH065213NIMH NIH HHS T32-MH065213NINDS NIH HHS R01 NS036319NINDS NIH HHS R01 NS043472NINDS NIH HHS R01-NS043472NINDS NIH HHS R01-NS053998NINDS NIH HHS RC2 NS070344NINDS NIH HHS RC2-NS070344NINDS NIH HHS U01 NS053998
6 · The paper itself

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.

Indexed as

Data Interpretation, StatisticalModels, GeneticPenetranceGenetic Association StudiesGenetic Diseases, InbornHumansMolecular Epidemiology

Identifiers

PMID21912139
PMCPMC3190173

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.