Several family-based approaches have been previously proposed to enhance the power for testing genetic association when the traits are measured longitudinally or repeatedly. In this paper, we show that some of these FBAT approaches can be easily extended to accommodate incomplete data and remain unbiased tests. We also show that because of the nature of FBAT approaches, we can impute the missing phenotypes without biasing our tests and achieve higher power. We propose two imputation techniques based on E-M algorithm and the conditional mean model, respectively. Through simulation studies, these two imputation techniques are shown to have correct false positive rate and generally achieve higher power than complete case analysis or simple mean-imputation. Application of these approaches for testing an association between Body Mass Index and a previously reported candidate SNP confirms our results. Copyright (C) 2009 S. Karger AG, Basel
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Columbia Univ, Dept Biostat, New York, NY 10032 USAColumbia Univ, Dept Biostat, New York, NY 10032 USA
Ionita-Laza, Iuliana
Lee, Seunggeun
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Harvard Univ, Dept Biostat, Boston, MA 02115 USAColumbia Univ, Dept Biostat, New York, NY 10032 USA
Lee, Seunggeun
Makarov, Vladimir
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Columbia Univ, Dept Biostat, New York, NY 10032 USAColumbia Univ, Dept Biostat, New York, NY 10032 USA
Makarov, Vladimir
Buxbaum, Joseph D.
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Mt Sinai Sch Med, Seaver Autism Ctr Res & Treatment, New York, NY USA
Mt Sinai Sch Med, Dept Psychiat, New York, NY USA
Mt Sinai Sch Med, Dept Genet, New York, NY USA
Mt Sinai Sch Med, Dept Genom Sci, New York, NY USAColumbia Univ, Dept Biostat, New York, NY 10032 USA
Buxbaum, Joseph D.
Lin, Xihong
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Harvard Univ, Dept Biostat, Boston, MA 02115 USAColumbia Univ, Dept Biostat, New York, NY 10032 USA