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Nonrandom sampling in genetic epidemiology: maximum likelihood methods for multifactorial analysis of quantitative data ascertained through truncation.

作者信息

Rao D C, Wette R

机构信息

Division of Biostatistics, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Genet Epidemiol. 1987;4(5):357-76. doi: 10.1002/gepi.1370040505.

DOI:10.1002/gepi.1370040505
PMID:3319764
Abstract

Three types of nonrandom sampling of family data are described, and appropriate maximum likelihood methods are proposed for each. The three types arise depending on whether the selection of probands, based on truncation, is applied directly to the phenotypic distribution, to the distribution of a correlated trait, or to the liability distribution of an associated disease. Family data ascertained through random and nonrandom sampling can be analyzed together in a unified approach. Results of a Monte Carlo study are presented that demonstrate the utility of the proposed methods. In particular, likelihood ratio tests of null hypotheses are shown to be distributed as chi-square, even in samples as small as 50 families (with variable sibship size).

摘要

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引用本文的文献

1
Multifactorial analysis of family data ascertained through truncation: a comparative evaluation of two methods of statistical inference.通过截断确定的家庭数据的多因素分析:两种统计推断方法的比较评估。
Am J Hum Genet. 1988 Mar;42(3):506-15.
2
Correcting for single ascertainment by truncation for a quantitative trait.针对数量性状通过截断法校正单一确定情况。
Am J Hum Genet. 1988 Nov;43(5):705-8.
3
Analyzing the relationship between age at onset and risk to relatives.分析发病年龄与亲属患病风险之间的关系。
Am J Hum Genet. 1989 Aug;45(2):226-39.