Substantial advances have been made in identifying common genetic variants influencing cardiometabolic traits and disease outcomes through genome wide association studies. Nevertheless, gaps in knowledge remain and new questions have arisen regarding the population relevance, mechanisms, and applications for healthcare. Using a new high-resolution custom single nucleotide polymorphism (SNP) array (Metabochip) incorporating dense coverage of genomic regions linked to cardiometabolic disease, the University College-London School-Edinburgh-Bristol (UCLEB) consortium of highly-phenotyped population-based prospective studies, aims to: (1) fine map functionally relevant SNPs; (2) precisely estimate individual absolute and population attributable ...
Cardiovascular disease is a major health concern affecting over 80,000,000 people in the U.S. alone....
Background and aims: Cardiometabolic disorders (CMD) arise from a constellation of features such as ...
Linkage studies and genome-wide linkage analyses, which use polymorphic DNA markers throughout the g...
Substantial advances have been made in identifying common genetic variants influencing cardiometabol...
Substantial advances have been made in identifying common genetic variants influencing cardiometabol...
Substantial advances have been made in identifying common genetic variants influencing cardiometabol...
A set of tabular datasets and documents produced by the UCL-LSHTM-Edinburgh-Bristol (UCLEB) Consorti...
Genome-wide association studies (GWAS) have identified more than 1500 disease-associated single nucl...
Continuous updating of the genotyping technology has led to improvement of genetic study design. The...
Genetic research made a remarkable progress in the past 20 years, with the Human Genome Project, whi...
Large-scale whole-genome sequence data sets offer novel opportunities to identify genetic variation ...
Cardiometabolic diseases represent a common complex disorder with a strong genetic component. Curren...
BackgroundAlthough largely preventable, cardiovascular diseases (CVDs) are the biggest cause of deat...
A wealth of genetic associations for cardiovascular and metabolic phenotypes in humans has been accu...
Longitudinal, well phenotyped, population-based cohort studies offer unique research opportunities i...
Cardiovascular disease is a major health concern affecting over 80,000,000 people in the U.S. alone....
Background and aims: Cardiometabolic disorders (CMD) arise from a constellation of features such as ...
Linkage studies and genome-wide linkage analyses, which use polymorphic DNA markers throughout the g...
Substantial advances have been made in identifying common genetic variants influencing cardiometabol...
Substantial advances have been made in identifying common genetic variants influencing cardiometabol...
Substantial advances have been made in identifying common genetic variants influencing cardiometabol...
A set of tabular datasets and documents produced by the UCL-LSHTM-Edinburgh-Bristol (UCLEB) Consorti...
Genome-wide association studies (GWAS) have identified more than 1500 disease-associated single nucl...
Continuous updating of the genotyping technology has led to improvement of genetic study design. The...
Genetic research made a remarkable progress in the past 20 years, with the Human Genome Project, whi...
Large-scale whole-genome sequence data sets offer novel opportunities to identify genetic variation ...
Cardiometabolic diseases represent a common complex disorder with a strong genetic component. Curren...
BackgroundAlthough largely preventable, cardiovascular diseases (CVDs) are the biggest cause of deat...
A wealth of genetic associations for cardiovascular and metabolic phenotypes in humans has been accu...
Longitudinal, well phenotyped, population-based cohort studies offer unique research opportunities i...
Cardiovascular disease is a major health concern affecting over 80,000,000 people in the U.S. alone....
Background and aims: Cardiometabolic disorders (CMD) arise from a constellation of features such as ...
Linkage studies and genome-wide linkage analyses, which use polymorphic DNA markers throughout the g...