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Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
Biography:
Nakamura M, et al.: Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in Japanese. Am. J. Hum. Genet . 91: 721-728, 2012kamoto K, To Common variation in GPC5 is associated with acquired nephrotic syndrome. Nat. Genet. 43: 459-463, 2011. Transcriptional regulation of endochondral ossification by HIF-2alpha during skeletal growth and osteoarthritis development. Nat. Med. 16: 678-686, 201HUGO Pan-Asian SNP Consortium: Mapping human genetic diversity in Asia. Science 326: 1541-1545, 2009.anaka Y, et al.: Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. Nat. Genet. 41: 1105-1109, 2009.
Subjects of specialization: allele-specific gene silencing, amyloid precursor protein, Swedish mutation, London mutation, reporter allele
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