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Appropriate data cleaning methods for genome-wide association study.
Miyagawa T, Nishida N, Ohashi J, Kimura R, Fujimoto A, Kawashima M, Koike A, Sasaki T, Tanii H, Otowa T, Momose Y, Nakahara Y, Gotoh J, Okazaki Y, Tsuji S, Tokunaga K. Miyagawa T, et al. Among authors: tsuji s. J Hum Genet. 2008;53(10):886-893. doi: 10.1007/s10038-008-0322-y. Epub 2008 Aug 12. J Hum Genet. 2008. PMID: 18695938
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.
Miyagawa T, Kawashima M, Nishida N, Ohashi J, Kimura R, Fujimoto A, Shimada M, Morishita S, Shigeta T, Lin L, Hong SC, Faraco J, Shin YK, Jeong JH, Okazaki Y, Tsuji S, Honda M, Honda Y, Mignot E, Tokunaga K. Miyagawa T, et al. Among authors: tsuji s. Nat Genet. 2008 Nov;40(11):1324-8. doi: 10.1038/ng.231. Epub 2008 Sep 28. Nat Genet. 2008. PMID: 18820697
A mutation database for amyotrophic lateral sclerosis.
Yoshida M, Takahashi Y, Koike A, Fukuda Y, Goto J, Tsuji S. Yoshida M, et al. Among authors: tsuji s. Hum Mutat. 2010 Sep;31(9):1003-10. doi: 10.1002/humu.21306. Hum Mutat. 2010. PMID: 20556799
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese.
Iida A, Takahashi A, Kubo M, Saito S, Hosono N, Ohnishi Y, Kiyotani K, Mushiroda T, Nakajima M, Ozaki K, Tanaka T, Tsunoda T, Oshima S, Sano M, Kamei T, Tokuda T, Aoki M, Hasegawa K, Mizoguchi K, Morita M, Takahashi Y, Katsuno M, Atsuta N, Watanabe H, Tanaka F, Kaji R, Nakano I, Kamatani N, Tsuji S, Sobue G, Nakamura Y, Ikegawa S. Iida A, et al. Among authors: tsuji s. Hum Mol Genet. 2011 Sep 15;20(18):3684-92. doi: 10.1093/hmg/ddr268. Epub 2011 Jun 10. Hum Mol Genet. 2011. PMID: 21665992
2,714 results