The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population

Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility

Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers

PADI4 polymorphism predisposes male smokers to rheumatoid arthritis

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population

Genome-wide association study identifies HLA-A*3101 allele as a genetic risk factor for carbamazepine-induced cutaneous adverse drug reactions in Japanese population

Genome-wide association study of epirubicin-induced leukopenia in Japanese patients

Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus

Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population

Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population

Identification of independent risk loci for Graves’ disease within the MHC in the Japanese population

Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population

New gene functions in megakaryopoiesis and platelet formation

Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians

Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk

Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes

PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data

Common variation in GPC5 is associated with acquired nephrotic syndrome

Variants of C-C motif chemokine 22 (CCL22) are associated with susceptibility to atopic dermatitis: case-control studies

A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids

Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility

Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma