Kubo M - Search Results

1

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.

Malik R, Chauhan G, Traylor M, Sargurupremraj M, Okada Y, Mishra A, Rutten-Jacobs L, Giese AK, van der Laan SW, Gretarsdottir S, Anderson CD, Chong M, Adams HHH, Ago T, Almgren P, Amouyel P, Ay H, Bartz TM, Benavente OR, Bevan S, Boncoraglio GB, Brown RD Jr, Butterworth AS, Carrera C, Carty CL, Chasman DI, Chen WM, Cole JW, Correa A, Cotlarciuc I, Cruchaga C, Danesh J, de Bakker PIW, DeStefano AL, den Hoed M, Duan Q, Engelter ST, Falcone GJ, Gottesman RF, Grewal RP, Gudnason V, Gustafsson S, Haessler J, Harris TB, Hassan A, Havulinna AS, Heckbert SR, Holliday EG, Howard G, Hsu FC, Hyacinth HI, Ikram MA, Ingelsson E, Irvin MR, Jian X, Jiménez-Conde J, Johnson JA, Jukema JW, Kanai M, Keene KL, Kissela BM, Kleindorfer DO, Kooperberg C, Kubo M, Lange LA, Langefeld CD, Langenberg C, Launer LJ, Lee JM, Lemmens R, Leys D, Lewis CM, Lin WY, Lindgren AG, Lorentzen E, Magnusson PK, Maguire J, Manichaikul A, McArdle PF, Meschia JF, Mitchell BD, Mosley TH, Nalls MA, Ninomiya T, O'Donnell MJ, Psaty BM, Pulit SL, Rannikmäe K, Reiner AP, Rexrode KM, Rice K, Rich SS, Ridker PM, Rost NS, Rothwell PM, Rotter JI, Rundek T, Sacco RL, Sakaue S, Sale MM, Salomaa V, Sapkota BR, Schmidt R, Schmidt… See abstract for full author list ➔ Malik R, et al. Among authors: kubo m. Nat Genet. 2018 Apr;50(4):524-537. doi: 10.1038/s41588-018-0058-3. Epub 2018 Mar 12. Nat Genet. 2018. PMID: 29531354 Free PMC article.

2

Hyperhomocysteinemia and the development of chronic kidney disease in a general population: the Hisayama study.

Ninomiya T, Kiyohara Y, Kubo M, Tanizaki Y, Tanaka K, Okubo K, Nakamura H, Hata J, Oishi Y, Kato I, Hirakata H, Iida M. Ninomiya T, et al. Among authors: kubo m. Am J Kidney Dis. 2004 Sep;44(3):437-45. Am J Kidney Dis. 2004. PMID: 15332216

3

Chronic kidney disease and cardiovascular disease in a general Japanese population: the Hisayama Study.

Ninomiya T, Kiyohara Y, Kubo M, Tanizaki Y, Doi Y, Okubo K, Wakugawa Y, Hata J, Oishi Y, Shikata K, Yonemoto K, Hirakata H, Iida M. Ninomiya T, et al. Among authors: kubo m. Kidney Int. 2005 Jul;68(1):228-36. doi: 10.1111/j.1523-1755.2005.00397.x. Kidney Int. 2005. PMID: 15954912 Free article.

4

C-reactive protein and risk of first-ever ischemic and hemorrhagic stroke in a general Japanese population: the Hisayama Study.

Wakugawa Y, Kiyohara Y, Tanizaki Y, Kubo M, Ninomiya T, Hata J, Doi Y, Okubo K, Oishi Y, Shikata K, Yonemoto K, Maebuchi D, Ibayashi S, Iida M. Wakugawa Y, et al. Among authors: kubo m. Stroke. 2006 Jan;37(1):27-32. doi: 10.1161/01.STR.0000194958.88216.87. Epub 2005 Nov 23. Stroke. 2006. PMID: 16306468

5

A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.

Kubo M, Hata J, Ninomiya T, Matsuda K, Yonemoto K, Nakano T, Matsushita T, Yamazaki K, Ohnishi Y, Saito S, Kitazono T, Ibayashi S, Sueishi K, Iida M, Nakamura Y, Kiyohara Y. Kubo M, et al. Nat Genet. 2007 Feb;39(2):212-7. doi: 10.1038/ng1945. Epub 2007 Jan 7. Nat Genet. 2007. PMID: 17206144

6

Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction.

Hata J, Matsuda K, Ninomiya T, Yonemoto K, Matsushita T, Ohnishi Y, Saito S, Kitazono T, Ibayashi S, Iida M, Kiyohara Y, Nakamura Y, Kubo M. Hata J, et al. Among authors: kubo m. Hum Mol Genet. 2007 Mar 15;16(6):630-9. doi: 10.1093/hmg/ddm005. Epub 2007 Feb 19. Hum Mol Genet. 2007. PMID: 17309882

7

Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients.

Yamazaki K, Onouchi Y, Takazoe M, Kubo M, Nakamura Y, Hata A. Yamazaki K, et al. Among authors: kubo m. J Hum Genet. 2007;52(7):575-583. doi: 10.1007/s10038-007-0156-z. Epub 2007 May 30. J Hum Genet. 2007. PMID: 17534574

8

Impact of Kir6.2 E23K polymorphism on the development of type 2 diabetes in a general Japanese population: The Hisayama Study.

Doi Y, Kubo M, Ninomiya T, Yonemoto K, Iwase M, Arima H, Hata J, Tanizaki Y, Iida M, Kiyohara Y. Doi Y, et al. Among authors: kubo m. Diabetes. 2007 Nov;56(11):2829-33. doi: 10.2337/db06-1709. Diabetes. 2007. PMID: 17965318

9

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: kubo m. 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

10

Polymorphisms in the lymphotoxin alpha gene and the risk of ischemic stroke in the Japanese population. The Fukuoka Stroke Registry and the Hisayama Study.

Hagiwara N, Kitazono T, Kamouchi M, Kuroda J, Ago T, Hata J, Ninomiya T, Ooboshi H, Kumai Y, Yoshimura S, Tamaki K, Fujii K, Nagao T, Okada Y, Toyoda K, Nakane H, Sugimori H, Yamashita Y, Wakugawa Y, Kubo M, Tanizaki Y, Kiyohara Y, Ibayashi S, Iida M. Hagiwara N, et al. Among authors: kubo m. Cerebrovasc Dis. 2008;25(5):417-22. doi: 10.1159/000121342. Epub 2008 Mar 17. Cerebrovasc Dis. 2008. PMID: 18349535

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

2,705 results

Search Page