Evidence map›Paper›PMID 18636528›Full record

ArticleGenetic epidemiology2009

Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.

Chao-Yu Guo, Kathryn L Lunetta, Anita L DeStefano, L Adrienne Cupples

Abstract read
In one paragraph

Article in Genetic epidemiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Chao-Yu GuoClinical Research Program, Children's Hospital Boston, Boston, Massachusetts 02115, USA. chao-yu.guo@childrens.harvard.edu
Kathryn L Lunetta
Anita L DeStefano
L Adrienne Cupples

Funding

THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
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NHLBI NIH HHS N01 HC025195NHLBI NIH HHS N01-HC-25195
6 · The paper itself

Abstract

In some genetic association studies, samples contain both parental and unrelated controls. Under such scenarios, instead of analyzing only trios using family-based association tests or only unrelated subjects using a case-control study design, Nagelkerke et al. ([2004] Eur. J. Hum. Genet. 12:964-970) and Epstein et al. ([2005] Am. J. Hum. Genet. 76:592-608) proposed methods that implemented a likelihood ratio test to combine the two different types of data. In this article, we put forward a more powerful and simplified strategy to combine trios with unrelated subjects based on the haplotype relative risk (HRR) (Falk and Rubinstein [1987] Ann. Hum. Genet. 51:227-233). The HRR compares parental marker alleles transmitted to an affected offspring to those not transmitted as a test for association, a strategy that is similar to a case-control study that compares allele frequencies in diseased cases to those of unrelated controls. We prove that affected offspring can be pooled with diseased cases and that parental controls can be treated as unrelated controls when the trios and unrelated subjects are randomly sampled from the same population. Therefore, unrelated subjects can be incorporated into the HRR intuitively and effortlessly. For trios without complete parental genotypes, we adopted the strategy proposed by (Guo et al. [2005a] BMC Genet. 6:S90; [2005b] Hum. Hered. 59: 125-135), which is more feasible than the one proposed by Weinberg ([1999] Am. J. Hum. Genet. 64:1186-1193). In addition, simulation results suggest that the combined haplotype relative risk is more powerful than Epstein et al.'s method regardless of the disease prevalence in a homogeneous population.

Indexed as

Case-Control StudiesFemaleGenome-Wide Association StudyHaplotypesHumansMaleModels, GeneticModels, StatisticalMolecular EpidemiologyRisk Factors

Identifiers

PMID18636528
PMCPMC2700841

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.