Although recent genome-wide studies have provided valuable insights into the genetic basis of human disease, they have explained relatively little of the heritability of most complex traits, and the variants identified through these studies have small effect sizes. This has led to the important and hotly debated issue of where the 'missing heritability' of complex diseases might be found. Here, seven leading geneticists offer their opinion about where this heritability is likely to lie, what this could tell us about the underlying genetic architecture of common diseases and how this could inform research strategies for uncovering genetic risk factors
A central goal of genetics is to understand the links between genetic variation and disease. Intuiti...
Despite the recent explosive rise in number of genetic markers for complex disease traits identified...
Identification of common-variant associations for many common disorders has been highly effective, b...
Genome-wide association studies have identified hundreds of genetic variants associated with complex...
Many challenges related to understanding the mystery of missing heritability and discovering the var...
Diseases of complex origin have a component of quantitative genetics that contributes to their susce...
This article critiques the “missing heritability ” position, which calls for greater efforts and fun...
Recently, an increasing number of susceptibility variants have been identified for complex diseases....
Much of the literature on genome-wide association studies (GWAS) is based on the premise that an imp...
A plethora of genetic association analyses have identified several genetic risk loci. Technological ...
The heritability (h2) of a disease is the proportion of phenotypic variance that is due to genetics....
Abstract: During the initial stages of the genome revolution human genetics was hugely successful in...
In the past decade, rapid advances in genomic technologies have dramatically changed the genetic stu...
Diseases of complex origin have a component of quantitative genetics that contributes to their susce...
Much of the literature on genome-wide association studies (GWAS) is based on the premise that an imp...
A central goal of genetics is to understand the links between genetic variation and disease. Intuiti...
Despite the recent explosive rise in number of genetic markers for complex disease traits identified...
Identification of common-variant associations for many common disorders has been highly effective, b...
Genome-wide association studies have identified hundreds of genetic variants associated with complex...
Many challenges related to understanding the mystery of missing heritability and discovering the var...
Diseases of complex origin have a component of quantitative genetics that contributes to their susce...
This article critiques the “missing heritability ” position, which calls for greater efforts and fun...
Recently, an increasing number of susceptibility variants have been identified for complex diseases....
Much of the literature on genome-wide association studies (GWAS) is based on the premise that an imp...
A plethora of genetic association analyses have identified several genetic risk loci. Technological ...
The heritability (h2) of a disease is the proportion of phenotypic variance that is due to genetics....
Abstract: During the initial stages of the genome revolution human genetics was hugely successful in...
In the past decade, rapid advances in genomic technologies have dramatically changed the genetic stu...
Diseases of complex origin have a component of quantitative genetics that contributes to their susce...
Much of the literature on genome-wide association studies (GWAS) is based on the premise that an imp...
A central goal of genetics is to understand the links between genetic variation and disease. Intuiti...
Despite the recent explosive rise in number of genetic markers for complex disease traits identified...
Identification of common-variant associations for many common disorders has been highly effective, b...