Mendelian randomization (MR) studies typically assess the pathogenic relevance of environmental exposures or disease biomarkers, using genetic variants that instrument these exposures. The approach is gaining popularity-our systematic review reveals a greater than 10-fold increase in MR studies published between 2004 and 2015. When the MR paradigm was first proposed, few biomarker- or exposure-related genetic variants were known, most having been identified by candidate gene studies. However, genome-wide association studies (GWAS) are now providing a rich source of potential instruments for MR analysis. Many early reviews covering the concept, applications and analytical aspects of the MR technique preceded the surge in GWAS, and thus the q...
With the advent of very large scale genome‐wide association studies (GWASs), the promise of Mendelia...
Mendelian randomization uses genetic variants to make causal inferences about the effect of a risk f...
Importance: Mendelian randomization (MR) studies use genetic variation associated with modifiable ex...
Mendelian randomization (MR) studies typically assess the pathogenic relevance of environmental expo...
Mendelian randomization (MR) is a technique that seeks to establish causation between an exposure an...
Mendelian randomisation is an accessible and valuable epidemiological approach to provide insight in...
A study examining blood lipid traits takes epigenomics approaches to the next level by using careful...
Importance Mendelian randomization (MR) studies use genetic variation associated with modifiable ...
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex...
Mendelian randomization (MR) uses genetic variants as instrumental variables to infer whether a risk...
The number of Mendelian randomization (MR) analyses including large numbers of genetic variants is r...
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex...
Abstract A study examining blood lipid traits takes epigenomics approaches to the next...
Mendelian randomization (MR) is an epidemiological technique that uses genetic variants to distingui...
Mendelian randomisation uses genetic variation as a natural experiment to investigate the causal rel...
With the advent of very large scale genome‐wide association studies (GWASs), the promise of Mendelia...
Mendelian randomization uses genetic variants to make causal inferences about the effect of a risk f...
Importance: Mendelian randomization (MR) studies use genetic variation associated with modifiable ex...
Mendelian randomization (MR) studies typically assess the pathogenic relevance of environmental expo...
Mendelian randomization (MR) is a technique that seeks to establish causation between an exposure an...
Mendelian randomisation is an accessible and valuable epidemiological approach to provide insight in...
A study examining blood lipid traits takes epigenomics approaches to the next level by using careful...
Importance Mendelian randomization (MR) studies use genetic variation associated with modifiable ...
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex...
Mendelian randomization (MR) uses genetic variants as instrumental variables to infer whether a risk...
The number of Mendelian randomization (MR) analyses including large numbers of genetic variants is r...
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex...
Abstract A study examining blood lipid traits takes epigenomics approaches to the next...
Mendelian randomization (MR) is an epidemiological technique that uses genetic variants to distingui...
Mendelian randomisation uses genetic variation as a natural experiment to investigate the causal rel...
With the advent of very large scale genome‐wide association studies (GWASs), the promise of Mendelia...
Mendelian randomization uses genetic variants to make causal inferences about the effect of a risk f...
Importance: Mendelian randomization (MR) studies use genetic variation associated with modifiable ex...