Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons

The genetic architecture of type 2 diabetes

(2016) Christian Fuchsberger et al.   NATURE

Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction

(2016) Wei Yang et al.   PLoS Genetics

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

(2014) Ron Do et al.   NATURE

Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

(2012) Seunggeun Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

RARE CODING MUTATIONS AND RISK FOR EARLY-ONSET MYOCARDIAL INFARCTION: AN EXOME SEQUENCING STUDY OF >2,000 CASES AND CONTROLS

(2012) Nathan O. Stitziel   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

(2011) Christopher J. O'Donnell et al.   CIRCULATION

A novel mechanism for the transcriptional regulation of Wnt signaling in development

(2011) T. Vacik et al.   GENES & DEVELOPMENT

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

(2010) William McLaren et al.   BIOINFORMATICS

Association of Genetic Risk Variants With Expression of Proximal Genes Identifies Novel Susceptibility Genes for Cardiovascular Disease

(2010) Lasse Folkersen et al.   Circulation-Cardiovascular Genetics

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

COL4A1 Is Associated With Arterial Stiffness by Genome-Wide Association Scan

(2009) Kirill V. Tarasov et al.   Circulation-Cardiovascular Genetics

Wnt signaling in heart valve development and osteogenic gene induction

(2009) Christina M. Alfieri et al.   DEVELOPMENTAL BIOLOGY

TCF7L2 Polymorphism rs7903146 Is Associated with Coronary Artery Disease Severity and Mortality

(2009) André Gustavo P. Sousa et al.   PLoS One

Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

(2008) Bingshan Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS