Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities

Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors

Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population

Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity

Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity

Stepwise iterative maximum likelihood clustering approach

Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma

Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid Arthritis

Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Genetic characteristics of inflammatory bowel disease in a Japanese population

ABCB1 polymorphism is associated with atorvastatin-induced liver injury in Japanese population

Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk

High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry

Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women

Variants near the HLA complex group 22 gene (HCG22) confer increased susceptibility to late-onset asthma in Japanese populations

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population

A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN