Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium

Second-generation PLINK: rising to the challenge of larger and richer datasets

(2015) Christopher C Chang et al.   GigaScience

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

(2014) Stéphanie Debette et al.   NATURE GENETICS

Integrative Genomics Reveals Novel Molecular Pathways and Gene Networks for Coronary Artery Disease

(2014) Ville-Petteri Mäkinen et al.   PLoS Genetics

Functional Genomics of the 9p21.3 Locus for Atherosclerosis: Clarity or Confusion?

(2014) Hsiao-Huei Chen et al.   Current Cardiology Reports

ADAMTS7 Cleavage and Vascular Smooth Muscle Cell Migration Is Affected by a Coronary-Artery-Disease-Associated Variant

(2013) Xiangyuan Pu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mendel: the Swiss army knife of genetic analysis programs

(2013) Kenneth Lange et al.   BIOINFORMATICS

Resequencing and Clinical Associations of the 9p21.3 Region

(2013) Andrew D. Johnson et al.   CIRCULATION

Trans-ethnic fine mapping identifies a novel independent locus at the 3′ end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population

(2013) Jane Z. Kuo et al.   DIABETOLOGIA

Genome-wide association study in a Chinese population with diabetic retinopathy

(2013) Wayne H.-H. Sheu et al.   HUMAN MOLECULAR GENETICS

Identification of CAD candidate genes in GWAS loci and their expression in vascular cells

(2013) Ayca Erbilgin et al.   JOURNAL OF LIPID RESEARCH

Shorter GT repeats in the heme oxygenase-1 gene promoter are associated with a lower severity score in coronary artery disease

(2013) Kae-Woei Liang et al.   Journal of the Chinese Medical Association

Next-Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data

(2013) Kenneth Lange et al.   Annual Review of Statistics and Its Application

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency

(2012) R. Lemmens et al.   HUMAN MOLECULAR GENETICS

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Large-scale association analysis identifies new risk loci for coronary artery disease

(2012) Panos Deloukas et al.   NATURE GENETICS

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease

(2012) Xiangfeng Lu et al.   NATURE GENETICS

The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

(2012) Benjamin F. Voight et al.   PLoS Genetics

Depletion of the novel protein PHACTR-1 from human endothelial cells abolishes tube formation and induces cell death receptor apoptosis

(2011) Rafika Jarray et al.   BIOCHIMIE

Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort

(2011) Yi-Cheng Chang et al.   CLINICAL ENDOCRINOLOGY

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

(2011) Heribert Schunkert et al.   NATURE GENETICS

LocusZoom: regional visualization of genome-wide association scan results

(2010) R. J. Pruim et al.   BIOINFORMATICS

Genetic variants of human urea transporter-2 are associated with metabolic syndrome in Asian population

(2010) Hui-Ju Tsai et al.   CLINICA CHIMICA ACTA

Genome-wide association analysis by lasso penalized logistic regression

(2009) Tong Tong Wu et al.   BIOINFORMATICS

Common PCSK1 Haplotypes Are Associated With Obesity in the Chinese Population

(2009) Yi-Cheng Chang et al.   Obesity