• Exemption from the institutional review board was obtained • 1.5 million free text PSL diagnoses from 327,000 patients from our clinical data repository were obtained • Common free text abbreviations and synonyms were mapped to the same concept (e.g. T1DM, Type 1 diabetes mellitus, Type I diabetes) • Data were then loaded into the locally developed Molecular Concept Map (MCM) application and interesting associations were explored » Originally designed to find significant associations of co-expressed gene signatures » Performs pair-wise association analyses of all signatures » We considered each patient to be a "signature " and their problems to be the associated "expressed genes" » An all-versus-all analysis was perfo...
Coronary artery disease (CAD) is a leading cause of morbidity and mortality worldwide. Although 58 g...
Coronary artery disease (CAD) is the commonest cause of death. Here, we report an association analys...
Background - Modern genotyping platforms permit a systematic search for inherited components of comp...
Background Coronary artery disease (CAD) is the leading cause of mortality worldwide. We aimed to sc...
Abstract Coronary artery disease (CAD) genome-wide association studies typically focus on single nuc...
Abstract Background This study investigated the pathways and genes involved in coronary artery disea...
The majority of the heritability of coronary artery disease (CAD) remains unexplained, despite recen...
The majority of the heritability of coronary artery disease (CAD) remains unexplained, despite recen...
Inference of co-expression network and identification of disease-related modules and gene sets can h...
BackgroundCoronary artery disease (CAD) is a main cause leading to increasing mortality of cardiovas...
Coronary artery disease (CAD) is the commonest cause of death. Here, we report an association analys...
peer reviewedOBJECTIVE: Genome-wide association studies have to date identified 159 significant and ...
ObjectiveRecent genome-wide association studies of coronary artery disease (CAD) have revealed 58 ge...
Coronary artery disease (CAD) is a complex disease driven by myriad interactions of genetics and env...
Objective Recent genome-wide association studies of coronary artery disease (CAD) have revealed 58 g...
Coronary artery disease (CAD) is a leading cause of morbidity and mortality worldwide. Although 58 g...
Coronary artery disease (CAD) is the commonest cause of death. Here, we report an association analys...
Background - Modern genotyping platforms permit a systematic search for inherited components of comp...
Background Coronary artery disease (CAD) is the leading cause of mortality worldwide. We aimed to sc...
Abstract Coronary artery disease (CAD) genome-wide association studies typically focus on single nuc...
Abstract Background This study investigated the pathways and genes involved in coronary artery disea...
The majority of the heritability of coronary artery disease (CAD) remains unexplained, despite recen...
The majority of the heritability of coronary artery disease (CAD) remains unexplained, despite recen...
Inference of co-expression network and identification of disease-related modules and gene sets can h...
BackgroundCoronary artery disease (CAD) is a main cause leading to increasing mortality of cardiovas...
Coronary artery disease (CAD) is the commonest cause of death. Here, we report an association analys...
peer reviewedOBJECTIVE: Genome-wide association studies have to date identified 159 significant and ...
ObjectiveRecent genome-wide association studies of coronary artery disease (CAD) have revealed 58 ge...
Coronary artery disease (CAD) is a complex disease driven by myriad interactions of genetics and env...
Objective Recent genome-wide association studies of coronary artery disease (CAD) have revealed 58 g...
Coronary artery disease (CAD) is a leading cause of morbidity and mortality worldwide. Although 58 g...
Coronary artery disease (CAD) is the commonest cause of death. Here, we report an association analys...
Background - Modern genotyping platforms permit a systematic search for inherited components of comp...