Evidence map›Paper›PMID 20203526›Full record

ArticleHuman heredity2010

Using both cases and controls for testing hardy-weinberg proportions in a genetic association study.

Jian Wang, Sanjay Shete

Abstract readEvaluation Study
In one paragraph

Article in Human heredity, 2010. 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

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

10 citing papers in PubMed.

  1. Article
  2. Glucocorticoid receptor (NR3C1) genetic polymorphisms and the outcomes of sudden sensorineural hearing loss.Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale · 2023
    Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. A Pilot Study of the AssociationIn vivo (Athens, Greece)
    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

2 authors.

Jian WangDepartment of Epidemiology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Sanjay Shete

Funding

Genome Wide Association Study of Head and Neck CancerR01CA131324 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHETE, SANJAY · 2009 to 2013
$2.8M
NCI NIH HHS 1R01CA131324NCI NIH HHS R01 CA131324
6 · The paper itself

Abstract

objectivesAssessment of the Hardy-Weinberg proportion (HWP) in controls has been widely used as a quality control measure in case-control association studies. However, when the disease being studied is common, controls might not represent the general population, which could result in inaccurate HWP test results. Such results could lead investigators to discard important single-nucleotide polymorphisms (SNPs) that could potentially be causal. In this paper, we showed the inappropriateness of the HWP test in controls and proposed a mixture HWP (mHWP) exact test using a mixture sample that mimics the general population.

methodsThe mHWP exact test estimates HWP in a mixture sample that is a combination of both cases and controls proportional to the prevalence of disease. We implemented a re-sampling procedure to construct mixture samples and then obtained the empirical p value of HWP in the general population. Simulation studies were performed to investigate the performance of the proposed mHWP exact test. The method was also applied to a genetic association study of obesity.

resultsThe results showed that the mHWP exact test is more likely than either the traditional HWP method in controls or the likelihood-based approach to keep causal SNPs for further analysis when the disease is more common.

conclusionThe mHWP exact test using a mixture sample is a better HWP test for case-control genetic association studies than the traditional HWP in controls or the likelihood-based approach, and it will improve our ability to keep causal SNPs in the case-control genetic association studies.

Indexed as

Models, StatisticalAdolescentAdultCase-Control StudiesChildChild, PreschoolComputer SimulationDiabetes Mellitus, Type 2Gene FrequencyGenetics, PopulationGenome-Wide Association StudyGenotypeHumansInfantInfant, NewbornMiddle Aged

Identifiers

PMID20203526
PMCPMC2918648

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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.