Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
DG Hernandez, X Reed… - Journal of …, 2016 - Wiley Online Library
Parkinson's disease is a common, progressive neurodegenerative disorder, affecting 3% of
those older than 75 years of age. Clinically, Parkinson's disease (PD) is associated with …
those older than 75 years of age. Clinically, Parkinson's disease (PD) is associated with …
[HTML][HTML] Common disease is more complex than implied by the core gene omnigenic model
The evidence that most adult-onset common diseases have a polygenic genetic architecture
fully consistent with robust biological systems supported by multiple back-up mechanisms is …
fully consistent with robust biological systems supported by multiple back-up mechanisms is …
Integrative approaches for large-scale transcriptome-wide association studies
Many genetic variants influence complex traits by modulating gene expression, thus altering
the abundance of one or multiple proteins. Here we introduce a powerful strategy that …
the abundance of one or multiple proteins. Here we introduce a powerful strategy that …
Rare and common variants: twenty arguments
G Gibson - Nature Reviews Genetics, 2012 - nature.com
Genome-wide association studies have greatly improved our understanding of the genetic
basis of disease risk. The fact that they tend not to identify more than a fraction of the specific …
basis of disease risk. The fact that they tend not to identify more than a fraction of the specific …
Next-generation phenoty**: requirements and strategies for enhancing our understanding of genotype–phenotype relationships and its relevance to crop …
More accurate and precise phenoty** strategies are necessary to empower high-
resolution linkage map** and genome-wide association studies and for training genomic …
resolution linkage map** and genome-wide association studies and for training genomic …
Finding the missing heritability of complex diseases
Genome-wide association studies have identified hundreds of genetic variants associated
with complex human diseases and traits, and have provided valuable insights into their …
with complex human diseases and traits, and have provided valuable insights into their …
Improved heritability estimation from genome-wide SNPs
Estimation of narrow-sense heritability, h 2, from genome-wide SNPs genotyped in
unrelated individuals has recently attracted interest and offers several advantages over …
unrelated individuals has recently attracted interest and offers several advantages over …
The genetics of asthma and allergic disease: a 21st century perspective
Asthma and allergy are common conditions with complex etiologies involving both genetic
and environmental contributions. Recent genome‐wide association studies (GWAS) and …
and environmental contributions. Recent genome‐wide association studies (GWAS) and …
Uncovering the roles of rare variants in common disease through whole-genome sequencing
Although genome-wide association (GWA) studies for common variants have thus far
succeeded in explaining only a modest fraction of the genetic components of human …
succeeded in explaining only a modest fraction of the genetic components of human …
Genetic heterogeneity in human disease
Strong evidence suggests that rare mutations of severe effect are responsible for a
substantial portion of complex human disease. Evolutionary forces generate vast genetic …
substantial portion of complex human disease. Evolutionary forces generate vast genetic …