Dai Osabe

Identification of a Novel Splice Site Mutation of the<i>CSPG2</i>Gene in a Japanese Family with Wagner Syndrome

Tatsuro Miyamoto, Hiroshi Inoue, Yukiko Sakamoto et al. · Investigative Ophthalmology & Visual Science · 2005 · 82 citations

Familial juvenile hyperuricemic nephropathy: Detection of mutations in the uromodulin gene in five Japanese families

Eiji Kudo, Naoyuki Kamatani, Osamu Tezuka et al. · Kidney International · 2004 · 64 citations

Glomerulonephritis, Urology, Renal Function +12

Association of single-nucleotide polymorphisms in the suppressor of cytokine signaling 2 (SOCS2) gene with type 2 diabetes in the Japanese

Hitoshi Kato, Kyoko Nomura, Dai Osabe et al. · Genomics · 2006 · 42 citations

Metabolic Syndrome, Single-nucleotide Polymorphisms, Genetic Determinant +12

Genetic association between the <i>PRKCH</i> gene encoding protein kinase Cη isozyme and rheumatoid arthritis in the Japanese population

Yoichiro Takata, Daisuke Hamada, Katsutoshi Miyatake et al. · Arthritis & Rheumatism · 2006 · 39 citations

Association study on chromosome 20q11.21-13.13 locus and its contribution to type 2 diabetes susceptibility in Japanese

Toshihito Tanahashi, Dai Osabe, Kyoko Nomura et al. · Human Genetics · 2006 · 19 citations

Genome-wide Association Study, Metabolic Syndrome, Chromosome 20Q11.21-13.13 Locus +12