Evidence map›Paper›PMID 23572026›Full record

ArticleEuropean journal of human genetics : EJHG2013

A unifying framework for robust association testing, estimation, and genetic model selection using the generalized linear model.

Christina Loley, Inke R König, Ludwig Hothorn, Andreas Ziegler

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Association ofMolecular genetics and metabolism reports · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Decomposing Pearson's χAnnals of human genetics · 2018
    Article
  7. Article
  8. Article
  9. Article
  10. 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

4 authors.

Christina Loley1] Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Germany [2] Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Inke R König
Ludwig Hothorn
Andreas Ziegler

Funding

Malaria: Functional Genomics to Biology to MedicineR13AI068319 · NIAID · KEYSTONE SYMPOSIA · PI WIRTH, DYANN F · 2006 to 2006
$11k
Medical Research Council G1001799NIAID NIH HHS R13 AI068319Wellcome Trust 076113Wellcome Trust 077383Wellcome Trust WT095219MA
6 · The paper itself

Abstract

The analysis of genome-wide genetic association studies generally starts with univariate statistical tests of each single-nucleotide polymorphism. The standard approach is the Cochran-Armitage trend test or its logistic regression equivalent although this approach can lose considerable power if the underlying genetic model is not additive. An alternative is the MAX test, which is robust against the three basic modes of inheritance. Here, the asymptotic distribution of the MAX test is derived using the generalized linear model together with the Delta method and multiple contrasts. The approach is applicable to binary, quantitative, and survival traits. It may be used for unrelated individuals, family-based studies, and matched pairs. The approach provides point and interval effect estimates and allows selecting the most plausible genetic model using the minimum P-value. R code is provided. A Monte-Carlo simulation study shows that the asymptotic MAX test framework meets type I error levels well, has good power, and good model selection properties for minor allele frequencies ≥0.3. Pearson's χ(2)-test is superior for lower minor allele frequencies with low frequencies for the rare homozygous genotype. In these cases, the model selection procedure should be used with caution. The use of the MAX test is illustrated by reanalyzing findings from seven genome-wide association studies including case-control, matched pairs, and quantitative trait data.

Indexed as

Linear ModelsModels, GeneticCase-Control StudiesComputer SimulationGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLogistic ModelsPolymorphism, Single Nucleotide

Identifiers

PMID23572026
PMCPMC3820468

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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.