Literature DB >> 20436936

A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes.

Michael P Epstein1, Jessica E Hunter, Emily G Allen, Stephanie L Sherman, Xihong Lin, Michael Boehnke.   

Abstract

Variance-component methods are popular and flexible analytic tools for elucidating the genetic mechanisms of complex quantitative traits from pedigree data. However, variance-component methods typically assume that the trait of interest follows a multivariate normal distribution within a pedigree. Studies have shown that violation of this normality assumption can lead to biased parameter estimates and inflations in type-I error. This limits the application of variance-component methods to more general trait outcomes, whether continuous or categorical in nature. In this paper, we develop and apply a general variance-component framework for pedigree analysis of continuous and categorical outcomes. We develop appropriate models using generalized-linear mixed model theory and fit such models using approximate maximum-likelihood procedures. Using our proposed method, we demonstrate that one can perform variance-component pedigree analysis on outcomes that follow any exponential-family distribution. Additionally, we also show how one can modify the method to perform pedigree analysis of ordinal outcomes. We also discuss extensions of our variance-component framework to accommodate pedigrees ascertained based on trait outcome. We demonstrate the feasibility of our method using both simulated data and data from a genetic study of ovarian insufficiency.

Entities:  

Year:  2009        PMID: 20436936      PMCID: PMC2860148          DOI: 10.1007/s12561-009-9010-5

Source DB:  PubMed          Journal:  Stat Biosci        ISSN: 1867-1764


  35 in total

1.  A general test of association for quantitative traits in nuclear families.

Authors:  G R Abecasis; L R Cardon; W O Cookson
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Ascertainment adjustment: where does it take us?

Authors:  P R Burton; L J Palmer; K Jacobs; K J Keen; J M Olson; R C Elston
Journal:  Am J Hum Genet       Date:  2000-11-14       Impact factor: 11.025

3.  Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs.

Authors:  P C Sham; S Purcell
Journal:  Am J Hum Genet       Date:  2001-05-14       Impact factor: 11.025

4.  Ascertainment adjustment in complex diseases.

Authors:  David V Glidden; Kung-Yee Liang
Journal:  Genet Epidemiol       Date:  2002-10       Impact factor: 2.135

5.  Random-effects Cox proportional hazards model: general variance components methods for time-to-event data.

Authors:  V Shane Pankratz; Mariza de Andrade; Terry M Therneau
Journal:  Genet Epidemiol       Date:  2005-02       Impact factor: 2.135

6.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

7.  Association of FMR1 repeat size with ovarian dysfunction.

Authors:  A K Sullivan; M Marcus; M P Epstein; E G Allen; A E Anido; J J Paquin; M Yadav-Shah; S L Sherman
Journal:  Hum Reprod       Date:  2004-12-17       Impact factor: 6.918

8.  Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

Authors:  Jessica Ezzell Hunter; Michael P Epstein; Stuart W Tinker; Krista H Charen; Stephanie L Sherman
Journal:  Genet Epidemiol       Date:  2008-09       Impact factor: 2.135

9.  Examination of reproductive aging milestones among women who carry the FMR1 premutation.

Authors:  E G Allen; A K Sullivan; M Marcus; C Small; C Dominguez; M P Epstein; K Charen; W He; K C Taylor; S L Sherman
Journal:  Hum Reprod       Date:  2007-06-22       Impact factor: 6.918

10.  Fragile X syndrome: diagnostic and carrier testing.

Authors:  Stephanie Sherman; Beth A Pletcher; Deborah A Driscoll
Journal:  Genet Med       Date:  2005-10       Impact factor: 8.822

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