Abstract We apply a multiphase strategy for pedigree-based genetic analysis of systolic blood pressure data collected in a longitudinal study of large Mexican American pedigrees. In the first phase, we conduct variance-components linkage analysis to identify regions that may harbor quantitative trait loci. In the second phase, we carry out pedigree-based association analysis in a selected region with common and low-frequency variants from genome-wide association studies and whole genome sequencing data. Using sequencing data, we compare approaches to pedigree analysis in a 10 megabase candidate region on chromosome 3 harboring a gene previously identified by a consortium for blood pressure genome-wide association studies. We o...
Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci...
We applied a gene-based haplotype approach for the genome-wide association analysis on hypertension ...
1. Essential hypertension occurs in people with an underlying genetic predisposition who subject the...
Abstract We apply a multiphase strategy for pedigree-based genetic analysis of systoli...
Abstract We conduct pedigree-based linkage and association analyses of simulated systo...
Admixture mapping can be used to detect genetic association regions in admixed populations, such as ...
Although previous genome scans have searched for quantitative-trait loci (QTLs) influencing variatio...
Although previous genome scans have searched for quantitative-trait loci (QTLs) influencing variatio...
Abstract Systolic blood pressure (SBP) is an age-dependent complex trait for which bot...
Abstract Population-based identity by descent (IBD) mapping is a statistical method fo...
Abstract Background Blood pressure (BP) is a complex trait, with a heritability of 30 to 40%. Severa...
High blood pressure (BP) is a major risk factor for cardiovascular disease (CVD) and is more prevale...
The genetic variants associated with blood pressure identified so far explain only a small proportio...
Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci...
[[abstract]]Linkage analyses of complex, multifactorial traits and diseases, such as essential hyper...
Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci...
We applied a gene-based haplotype approach for the genome-wide association analysis on hypertension ...
1. Essential hypertension occurs in people with an underlying genetic predisposition who subject the...
Abstract We apply a multiphase strategy for pedigree-based genetic analysis of systoli...
Abstract We conduct pedigree-based linkage and association analyses of simulated systo...
Admixture mapping can be used to detect genetic association regions in admixed populations, such as ...
Although previous genome scans have searched for quantitative-trait loci (QTLs) influencing variatio...
Although previous genome scans have searched for quantitative-trait loci (QTLs) influencing variatio...
Abstract Systolic blood pressure (SBP) is an age-dependent complex trait for which bot...
Abstract Population-based identity by descent (IBD) mapping is a statistical method fo...
Abstract Background Blood pressure (BP) is a complex trait, with a heritability of 30 to 40%. Severa...
High blood pressure (BP) is a major risk factor for cardiovascular disease (CVD) and is more prevale...
The genetic variants associated with blood pressure identified so far explain only a small proportio...
Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci...
[[abstract]]Linkage analyses of complex, multifactorial traits and diseases, such as essential hyper...
Blood pressure (BP) is a major risk factor for cardiovascular disease and more than 200 genetic loci...
We applied a gene-based haplotype approach for the genome-wide association analysis on hypertension ...
1. Essential hypertension occurs in people with an underlying genetic predisposition who subject the...