Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

5,247 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Identification of C21orf59 and ATG2A as novel determinants of renal function-related traits 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 11;8(28):45259-45273. doi: 10.18632/oncotarget.16696. Oncotarget. 2017. PMID: 28410202 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
5,247 results