Lack of association between variations of PDE4D and ischemic stroke in the Japanese population

Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients

A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians

Estimation of the warfarin dose with clinical and pharmacogenetic data

CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection

Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk

Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation

Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression

Targeted serum glycoproteomics for the discovery of lung cancer-associated glycosylation disorders using lectin-coupled ProteinChip arrays

Effects of structural variations of APOBEC3A and APOBEC3B genes in chronic hepatitis B virus infection

Serum levels of nicotinamide N-methyltransferase in patients with lung cancer

Identification of nectin-4 oncoprotein as a diagnostic and therapeutic target for lung cancer

A single nucleotide polymorphism in the IRF5 promoter region is associated with susceptibility to rheumatoid arthritis in the Japanese population

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’s disease

Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individuals

Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1

Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis