ArticleHuman heredity2009
Detection of parent-of-origin effects based on complete and incomplete nuclear families with multiple affected children.
Article in Human heredity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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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.
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Who cites it
9 citing papers in PubMed.
- A powerful parent-of-origin effects test for qualitative traits on X chromosome in general pedigrees.BMC bioinformatics · 2018Article
- Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data.Journal of human genetics · 2014Article
- Detection of parent-of-origin effects for quantitative traits using general pedigree data.Journal of genetics · 2014Article
- Detection of imprinting effects for hypertension based on general pedigrees utilizing all affected and unaffected individuals.BMC proceedings · 2014Article
- Joint detection of association, imprinting and maternal effects using all children and their parents.European journal of human genetics : EJHG · 2013Article
- A powerful approach for association analysis incorporating imprinting effects.Bioinformatics (Oxford, England) · 2011Article
- Detection of parent-of-origin effects for quantitative traits in complete and incomplete nuclear families with multiple children.American journal of epidemiology · 2011Article
- Detection of parent-of-origin effects using general pedigree data.Genetic epidemiology · 2010Article
- Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers.Human heredity · 2009Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Parent-of-origin effects are important in studying genetic traits. More than 1% of all mammalian genes are believed to show parent-of-origin effects. Some statistical methods may be ineffective or fail to detect linkage or association for a gene with parent-of-origin effects. Based on case-parents trios, the parental-asymmetry test (PAT) is simple and powerful in detecting parent-of-origin effects. However, it is common in practice to collect nuclear families with both parents as well as nuclear families with only one parent. In this paper, when only one parent is available for each family with an arbitrary number of affected children, we firstly develop a new test statistic 1-PAT to test for parent-of-origin effects in the presence of association between an allele at the marker locus under study and a disease gene. Then we extend the PAT to accommodate complete nuclear families each with one or more affected children. Combining families with both parents and families with only one parent, the C-PAT is proposed to detect parent-of-origin effects. The validity of the test statistics is verified by simulation in various scenarios of parameter values. A power study shows that using the additional information from incomplete nuclear families in the analysis greatly improves the power of the tests, compared to that based on only complete nuclear families. Also, utilizing all affected children in each family, the proposed tests have a higher power than when only one affected child from each family is selected. Additional power comparison also demonstrates that the C-PAT is more powerful than a number of other tests for detecting parent-of-origin effects.
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