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High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population.
Cha PC, Mushiroda T, Takahashi A, Saito S, Shimomura H, Suzuki T, Kamatani N, Nakamura Y. Cha PC, et al. Among authors: nakamura y. J Hum Genet. 2007;52(10):856-864. doi: 10.1007/s10038-007-0183-9. Epub 2007 Sep 5. J Hum Genet. 2007. PMID: 17786385
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
Kamatani Y, Matsuda K, Ohishi T, Ohtsubo S, Yamazaki K, Iida A, Hosono N, Kubo M, Yumura W, Nitta K, Katagiri T, Kawaguchi Y, Kamatani N, Nakamura Y. Kamatani Y, et al. Among authors: nakamura y. J Hum Genet. 2008;53(1):64-73. doi: 10.1007/s10038-007-0219-1. Epub 2007 Dec 6. J Hum Genet. 2008. PMID: 18058064
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations.
Unoki H, Takahashi A, Kawaguchi T, Hara K, Horikoshi M, Andersen G, Ng DP, Holmkvist J, Borch-Johnsen K, Jørgensen T, Sandbaek A, Lauritzen T, Hansen T, Nurbaya S, Tsunoda T, Kubo M, Babazono T, Hirose H, Hayashi M, Iwamoto Y, Kashiwagi A, Kaku K, Kawamori R, Tai ES, Pedersen O, Kamatani N, Kadowaki T, Kikkawa R, Nakamura Y, Maeda S. Unoki H, et al. Among authors: nakamura y. Nat Genet. 2008 Sep;40(9):1098-102. doi: 10.1038/ng.208. Nat Genet. 2008. PMID: 18711366
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.
Yasuda K, Miyake K, Horikawa Y, Hara K, Osawa H, Furuta H, Hirota Y, Mori H, Jonsson A, Sato Y, Yamagata K, Hinokio Y, Wang HY, Tanahashi T, Nakamura N, Oka Y, Iwasaki N, Iwamoto Y, Yamada Y, Seino Y, Maegawa H, Kashiwagi A, Takeda J, Maeda E, Shin HD, Cho YM, Park KS, Lee HK, Ng MC, Ma RC, So WY, Chan JC, Lyssenko V, Tuomi T, Nilsson P, Groop L, Kamatani N, Sekine A, Nakamura Y, Yamamoto K, Yoshida T, Tokunaga K, Itakura M, Makino H, Nanjo K, Kadowaki T, Kasuga M. Yasuda K, et al. Among authors: nakamura n, nakamura y. Nat Genet. 2008 Sep;40(9):1092-7. doi: 10.1038/ng.207. Nat Genet. 2008. PMID: 18711367
Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.
Betcheva ET, Mushiroda T, Takahashi A, Kubo M, Karachanak SK, Zaharieva IT, Vazharova RV, Dimova II, Milanova VK, Tolev T, Kirov G, Owen MJ, O'Donovan MC, Kamatani N, Nakamura Y, Toncheva DI. Betcheva ET, et al. Among authors: nakamura y. J Hum Genet. 2009 Feb;54(2):98-107. doi: 10.1038/jhg.2008.14. Epub 2009 Jan 16. J Hum Genet. 2009. PMID: 19158809
A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.
Kamatani Y, Wattanapokayakit S, Ochi H, Kawaguchi T, Takahashi A, Hosono N, Kubo M, Tsunoda T, Kamatani N, Kumada H, Puseenam A, Sura T, Daigo Y, Chayama K, Chantratita W, Nakamura Y, Matsuda K. Kamatani Y, et al. Among authors: nakamura y. Nat Genet. 2009 May;41(5):591-5. doi: 10.1038/ng.348. Epub 2009 Apr 6. Nat Genet. 2009. PMID: 19349983
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