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Identification of five genetic variants as novel determinants of type 2 diabetes mellitus in Japanese by exome-wide association studies.
Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M. Yamada Y, et al. Among authors: mori s. Oncotarget. 2017 Jul 17;8(46):80492-80505. doi: 10.18632/oncotarget.19287. eCollection 2017 Oct 6. Oncotarget. 2017. PMID: 29113320 Free PMC article.
Association of the formiminotransferase N-terminal sub-domain containing gene and thrombospondin, type 1, domain-containing 7A gene with the prevalence of vertebral fracture in 2427 consecutive autopsy cases.
Zhou H, Mori S, Kou I, Fuku N, Naka Mieno M, Honma N, Arai T, Sawabe M, Tanaka M, Ikegawa S, Ito H. Zhou H, et al. Among authors: mori s. J Hum Genet. 2013 Feb;58(2):109-12. doi: 10.1038/jhg.2012.145. Epub 2013 Jan 10. J Hum Genet. 2013. PMID: 23303384
Significant association between hypolipoproteinemia(a) and lifetime risk of cancer: an autopsy study from a community-based Geriatric Hospital.
Mieno MN, Sawabe M, Tanaka N, Nakahara K, Hamamatsu A, Chida K, Sakurai U, Arai T, Harada K, Mori S, Inamatsu T, Ozawa T, Honma N, Aida J, Takubo K, Matsushita S. Mieno MN, et al. Among authors: mori s. Cancer Epidemiol. 2014 Oct;38(5):550-5. doi: 10.1016/j.canep.2014.07.013. Epub 2014 Aug 19. Cancer Epidemiol. 2014. PMID: 25164551
A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population.
Zhou H, Mori S, Tanaka M, Sawabe M, Arai T, Muramatsu M, Mieno MN, Shinkai S, Yamada Y, Miyachi M, Murakami H, Sanada K, Ito H. Zhou H, et al. Among authors: mori s. J Bone Miner Metab. 2015 Nov;33(6):694-700. doi: 10.1007/s00774-014-0636-0. Epub 2015 Jan 31. J Bone Miner Metab. 2015. PMID: 25637295
5,248 results