We applied a gene-based haplotype approach for the genome-wide association analysis on hypertension using Genetic Analysis Workshop 18 data for unrelated individuals. Association of single-nucleotide polymorphisms and clinical outcome were first assessed and haplotypes were then constructed based on the gene information and the linkage disequilibrium plot. Extensive haplotype analysis was also conducted for the whole chromosome 3. We found 1 block from the ULK4 gene and 2 blocks from the LOC64690 gene that were significantly associated with hypertension. Background Hypertension is a major risk factor for many diseases, including stroke and heart failure. Various genetic studies have been done and a number of genes have been identi-fied as h...
Primary hypertension is widely believed to be a complex polygenic disorder with the manifestation in...
Essential hypertension is a multifactorial disorder and is the main risk factor for renal and cardio...
Following up genetic linkage studies to identify the underlying susceptibility gene(s) for complex d...
Abstract We applied a gene-based haplotype approach for the genome-wide association an...
Among the common complex diseases, hypertension has been particularly unlucky in the recent surge of...
1. Essential hypertension occurs in people with an underlying genetic predisposition who subject the...
Thesis (Ph.D.)--University of Rochester. School of Nursing. Dept. of Health Practice Research, 2016....
Background:Blood pressure may contribute to 50% of the global cardiovascular disease epidemic. By un...
In Genetic Analysis Workshop 18 data, we used a 3-stage approach to explore the benefits of pathway ...
[[abstract]]We conducted linkage analysis using the genome-wide association study data on chromosome...
Hypertension is caused by the interaction of environmental and genetic factors. The condition which ...
Genetic linkage and association methods have long been the most important tools for gene identificat...
Abstract—Over the past few years, it has been asserted that genome-wide association studies would op...
Genetic linkage and association methods have long been the most important tools for gene identificat...
<div><p>Hypertension is caused by the interaction of environmental and genetic factors. The conditio...
Primary hypertension is widely believed to be a complex polygenic disorder with the manifestation in...
Essential hypertension is a multifactorial disorder and is the main risk factor for renal and cardio...
Following up genetic linkage studies to identify the underlying susceptibility gene(s) for complex d...
Abstract We applied a gene-based haplotype approach for the genome-wide association an...
Among the common complex diseases, hypertension has been particularly unlucky in the recent surge of...
1. Essential hypertension occurs in people with an underlying genetic predisposition who subject the...
Thesis (Ph.D.)--University of Rochester. School of Nursing. Dept. of Health Practice Research, 2016....
Background:Blood pressure may contribute to 50% of the global cardiovascular disease epidemic. By un...
In Genetic Analysis Workshop 18 data, we used a 3-stage approach to explore the benefits of pathway ...
[[abstract]]We conducted linkage analysis using the genome-wide association study data on chromosome...
Hypertension is caused by the interaction of environmental and genetic factors. The condition which ...
Genetic linkage and association methods have long been the most important tools for gene identificat...
Abstract—Over the past few years, it has been asserted that genome-wide association studies would op...
Genetic linkage and association methods have long been the most important tools for gene identificat...
<div><p>Hypertension is caused by the interaction of environmental and genetic factors. The conditio...
Primary hypertension is widely believed to be a complex polygenic disorder with the manifestation in...
Essential hypertension is a multifactorial disorder and is the main risk factor for renal and cardio...
Following up genetic linkage studies to identify the underlying susceptibility gene(s) for complex d...