ArticleBMC proceedings2011
Family- and population-based designs identify different rare causal variants.
Article in BMC proceedings, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00930280 (Genetic and Environmental Risk Factors for Hemorrhagic Stroke), which is not on this map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Genetic and Environmental Risk Factors for Hemorrhagic Stroke
Who cites it
1 citing paper in PubMed.
- Population-based and family-based designs to analyze rare variants in complex diseases.Genetic epidemiology · 2011Article
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Authors and funding
6 authors.
Funding
Abstract
Both family- and population-based samples are used to identify genetic variants associated with phenotypes. Each strategy has demonstrated advantages, but their ability to identify rare variants and genes containing rare variants is unclear. To compare these two study designs in the identification of rare causal variants, we applied various methods to the population- and family-based data simulated by the Genetic Analysis Workshop 17 with knowledge of the simulated model. Our results suggest that different variants can be identified by different study designs. Family-based and population-based study designs can be complementary in the identification of rare causal variants and should be considered in future studies.
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Registered trials
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