© The Author(s) 2015. This article is published with open access at Springerlink.com Abstract The multiplex-case and control design in which multiple cases are sampled from the same family is considered. In such studies phenotype information of the un-genotyped relatives might be available.We intend to use additional family information when performing genetic association tests. A score test is revisited to provide a flexi-ble framework to accommodate various genetic models and to improve power of the association test by adding available family information. The proposed test accounts for correlations induced by multiple cases from the same pedigree, directly deals with X-linked SNPs in mixed-sex-related samples, and incorporates additional p...
Linkage mapping of complex diseases is often followed by association studies between phenotypes and ...
Thesis (Master's)--University of Washington, 2015Pleiotropy is a commonly observed phenomenon in hum...
BACKGROUND: The interest of the scientific community in investigating the impact of rare variants on...
We consider the problem of genomewide association testing of a binary trait when some sampled indivi...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Complex disorders are typically characterized by multiple phenotypes. Analyzing these phenotypes joi...
Association studies test for genetic variation influencing disease risk. We explore here the applica...
Abstract Background In human case-control association studies, one of the chi-square tests typically...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Genome-wide association studies become increasingly popular and important for detecting genetic asso...
Assumptions regarding the true underlying genetic model, or mode of inheritance, are necessary when ...
For complex diseases, we often sample and genotype affected sibships to map the disease of interest ...
Traditional case-control studies provide a powerful and efficient method for evaluation of associati...
We use likelihood-based score statistics to test for association between a disease and a diallelic p...
Linkage mapping of complex diseases is often followed by association studies between phenotypes and ...
Thesis (Master's)--University of Washington, 2015Pleiotropy is a commonly observed phenomenon in hum...
BACKGROUND: The interest of the scientific community in investigating the impact of rare variants on...
We consider the problem of genomewide association testing of a binary trait when some sampled indivi...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Complex disorders are typically characterized by multiple phenotypes. Analyzing these phenotypes joi...
Association studies test for genetic variation influencing disease risk. We explore here the applica...
Abstract Background In human case-control association studies, one of the chi-square tests typically...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Genome-wide association studies become increasingly popular and important for detecting genetic asso...
Assumptions regarding the true underlying genetic model, or mode of inheritance, are necessary when ...
For complex diseases, we often sample and genotype affected sibships to map the disease of interest ...
Traditional case-control studies provide a powerful and efficient method for evaluation of associati...
We use likelihood-based score statistics to test for association between a disease and a diallelic p...
Linkage mapping of complex diseases is often followed by association studies between phenotypes and ...
Thesis (Master's)--University of Washington, 2015Pleiotropy is a commonly observed phenomenon in hum...
BACKGROUND: The interest of the scientific community in investigating the impact of rare variants on...