Literature DB >> 8533778

The relative efficiency of the Hardy-Weinberg equilibrium-likelihood and the conditional on parental genotype-likelihood methods for candidate-gene association studies.

M Knapp1, G Wassmer, M P Baur.   

Abstract

Selecting a control group that is perfectly matched for ethnic ancestry with a group of affected individuals is a major problem in studying the association of a candidate gene with a disease. This problem can be avoided by a design that uses parental data in place of nonrelated controls. Schaid and Sommer presented two new methods for the statistical analysis using this approach: (1) a likelihood method (Hardy-Weinberg equilibrium [HWE] method), which rests on the assumption that HWE holds, and (2) a conditional likelihood method (conditional on parental genotype [CPG] method) appropriate when HWE is absent. Schaid and Sommer claimed that the CPG method can be more efficient than the HWE method, even when equilibrium holds. It can be shown, however that in the equilibrium situation the HWE method is always more efficient than the CPG method. For a dominant disease, the differences are slim. But for a recessive disease, the CPG method requires a much larger sample size to achieve a prescribed power than the HWE method. Additionally, we show how the relative risks for the various candidate-gene genotypes can be estimated without relying on iterative methods. For the CPG method, we represent an asymptotic power approximation that is sufficiently precise for planning the sample size of an association study.

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Year:  1995        PMID: 8533778      PMCID: PMC1801396     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  9 in total

1.  A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

Authors:  J D Terwilliger; J Ott
Journal:  Hum Hered       Date:  1992       Impact factor: 0.444

Review 2.  Delineation of genetic predisposition to multifactorial disease: a general approach on the threshold of feasibility.

Authors:  J L Sobell; L L Heston; S S Sommer
Journal:  Genomics       Date:  1992-01       Impact factor: 5.736

Review 3.  HLA disease associations: models for insulin dependent diabetes mellitus and the study of complex human genetic disorders.

Authors:  G Thomson
Journal:  Annu Rev Genet       Date:  1988       Impact factor: 16.830

4.  Genotype relative risks: methods for design and analysis of candidate-gene association studies.

Authors:  D J Schaid; S S Sommer
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

5.  The haplotype-relative-risk (HRR) method for analysis of association in nuclear families.

Authors:  M Knapp; S A Seuchter; M P Baur
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

Review 6.  Genetic dissection of complex traits.

Authors:  E S Lander; N J Schork
Journal:  Science       Date:  1994-09-30       Impact factor: 47.728

7.  Statistical properties of the haplotype relative risk.

Authors:  J Ott
Journal:  Genet Epidemiol       Date:  1989       Impact factor: 2.135

8.  Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations.

Authors:  C T Falk; P Rubinstein
Journal:  Ann Hum Genet       Date:  1987-07       Impact factor: 1.670

9.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

Authors:  R S Spielman; R E McGinnis; W J Ewens
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

  9 in total
  1 in total

Review 1.  A behavior-genetic approach to multiple chemical sensitivity.

Authors:  D B Newlin
Journal:  Environ Health Perspect       Date:  1997-03       Impact factor: 9.031

  1 in total

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