ArticleStatistics and its interface2010
Within-Cluster Resampling for Analysis of Family Data: Ready for Prime-Time?
Article in Statistics and its interface, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed.
- Antipsychotic prescribing in youths: a French community-based study from 2006 to 2013.European child & adolescent psychiatry · 2015Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Hoffman et al. [1] proposed an elegant resampling method for analyzing clustered binary data. The focus of their paper was to perform association tests on clustered binary data using within-cluster-resampling (WCR) method. Follmann et al. [2] extended Hoffman et al.'s procedure more generally with applicability to angular data, combining of p-values, testing of vectors of parameters, and Bayesian inference. Follmann et al. [2] termed their procedure multiple outputation because all "excess" data within each cluster is thrown out multiple times. Herein, we refer to this procedure as WCR-MO. For any statistical test to be useful for a particular design, it must be robust, have adequate power, and be easy to implement and flexible. WCR-MO can be easily extended to continuous data and is a computationally intensive but simple and highly flexible method. Considering family as a cluster, one can apply WCR to familial data in genetic studies. Using simulations, we evaluated WCR-MO's robustness for analysis of a continuous trait in terms of type I error rates in genetic research. WCR-MO performed well at the 5% α-level. However, it provided inflated type I error rates for α-levels less than 5% implying the procedure is liberal and may not be ready for application to genetic studies where α levels used are typically much less than 0.05.
Identifiers
What OpenQuestion holds
Registered trials
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.