ArticleStatistics in medicine2011
Flexible estimation of covariance function by penalized spline with application to longitudinal family data.
Article in Statistics in medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- FSEM: Functional Structural Equation Models for Twin Functional Data.Journal of the American Statistical Association · 2019Article
- Semiparametric variance components models for genetic studies with longitudinal phenotypes.Biostatistics (Oxford, England) · 2012Article
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1 author.
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Abstract
Longitudinal data are routinely collected in biomedical research studies. A natural model describing longitudinal data decomposes an individual's outcome as the sum of a population mean function and random subject-specific deviations. When parametric assumptions are too restrictive, methods modeling the population mean function and the random subject-specific functions nonparametrically are in demand. In some applications, it is desirable to estimate a covariance function of random subject-specific deviations. In this work, flexible yet computationally efficient methods are developed for a general class of semiparametric mixed effects models, where the functional forms of the population mean and the subject-specific curves are unspecified. We estimate nonparametric components of the model by penalized spline (P-spline, Biometrics 2001; 57:253-259), and reparameterize the random curve covariance function by a modified Cholesky decomposition (Biometrics 2002; 58:121-128) which allows for unconstrained estimation of a positive-semidefinite matrix. To provide smooth estimates, we penalize roughness of fitted curves and derive closed-form solutions in the maximization step of an EM algorithm. In addition, we present models and methods for longitudinal family data where subjects in a family are correlated and we decompose the covariance function into a subject-level source and observation-level source. We apply these methods to the multi-level Framingham Heart Study data to estimate age-specific heritability of systolic blood pressure nonparametrically.
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