Evidence map›Paper›PMID 23266418›Full record

ArticleBiostatistics (Oxford, England)2013

Incorporating parental information into family-based association tests.

Zhaoxia Yu, Daniel Gillen, Carey F Li, Michael Demetriou

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Zhaoxia YuDepartment of Statistics, University of California at Irvine, Irvine, CA 92697, USA. yu.zhaoxia@ics.uci.edu
Daniel Gillen
Carey F Li
Michael Demetriou

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
UC Irvine Alzheimer's Disease Research Center Induced Pluripotent Stem Cell CoreP50AG016573 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI LAFERLA, FRANK M · 2000 to 2019
$37.0M
Human Autoimmunity and Genetic Defects in N-GlycosylationR01AI082266 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI DEMETRIOU, MICHAEL · 2010 to 2013
$1.5M
Improving genotype call accuracyR01HG004960 · NHGRI · UNIVERSITY OF WASHINGTON · PI BROWNING, BRIAN LEE · 2009 to 2014
$1.4M
NCI NIH HHS P30 CA062203NCI NIH HHS P30CA062203NHGRI NIH HHS R01HG004960NIAID NIH HHS R01AI082266NIA NIH HHS P50 AG016573
6 · The paper itself

Abstract

Assumptions regarding the true underlying genetic model, or mode of inheritance, are necessary when quantifying genetic associations with disease phenotypes. Here we propose new methods to ascertain the underlying genetic model from parental data in family-based association studies. Specifically, for parental mating-type data, we propose a novel statistic to test whether the underlying genetic model is additive, dominant, or recessive; for parental genotype-phenotype data, we propose three strategies to determine the true mode of inheritance. We illustrate how to incorporate the information gleaned from these strategies into family-based association tests. Because family-based association tests are conducted conditional on parental genotypes, the type I error rate of these procedures is not inflated by the information learned from parental data. This result holds even if such information is weak or when the assumption of Hardy-Weinberg equilibrium is violated. Our simulations demonstrate that incorporating parental data into family-based association tests can improve power under common inheritance models. The application of our proposed methods to a candidate-gene study of type 1 diabetes successfully detects a recessive effect in MGAT5 that would otherwise be missed by conventional family-based association tests.

Indexed as

AlgorithmsBiostatisticsComputer SimulationDiabetes Mellitus, Type 1FamilyFemaleGene FrequencyGenes, RecessiveGenetic Association StudiesHumansLikelihood FunctionsMaleModels, GeneticModels, StatisticalN-AcetylglucosaminyltransferasesParentsalpha-1,6-mannosylglycoprotein beta 1,6-N-acetylglucosaminyltransferaseN-AcetylglucosaminyltransferasesCase–parentsDominantMode of inheritanceNuclear familiesRecessiveRobust

Identifiers

PMID23266418
PMCPMC3732025

What OpenQuestion holds

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Registered trials

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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.