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

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

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

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

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

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

Estimation of the warfarin dose with clinical and pharmacogenetic data

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

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

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

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

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

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

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

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

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

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