Journal of Human Genetics

A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene

Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes

Association of the T-cell regulatory gene CTLA4 with Graves' disease and autoimmune thyroid disease in the Japanese

Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss

Association of polymorphisms of paraoxonase 1 and 2 genes, alone or in combination, with bone mineral density in community-dwelling Japanese

Association of over-expressed TFDP1 with progression of hepatocellular carcinomas

Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women

Association of common missense changes in ELAC2 (HPC2) with prostate cancer in a Japanese case-control series

Association of a polymorphism of the dopamine receptor D4 gene with bone mineral density in Japanese men

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

Are fetal cells in maternal plasma really there? We think they are

Allele frequencies of single nucleotide polymorphisms (SNPs) in 40 candidate genes for gene-environment studies on cancer: data from population-based Japanese random samples