Narita A - Search Results

1

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.

Akiyama K, Narita A, Nakaoka H, Cui T, Takahashi T, Yasuno K, Tajima A, Krischek B, Yamamoto K, Kasuya H, Hata A, Inoue I. Akiyama K, et al. Among authors: narita a. J Hum Genet. 2010 Oct;55(10):656-61. doi: 10.1038/jhg.2010.82. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613766

2

Genome-wide linkage analysis of mandibular prognathism in Korean and Japanese patients.

Yamaguchi T, Park SB, Narita A, Maki K, Inoue I. Yamaguchi T, et al. Among authors: narita a. J Dent Res. 2005 Mar;84(3):255-9. doi: 10.1177/154405910508400309. J Dent Res. 2005. PMID: 15723866

3

Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

Krischek B, Narita A, Akagawa H, Kasuya H, Tajima A, Onda H, Yoneyama T, Hori T, Inoue I. Krischek B, et al. Among authors: narita a. J Hum Genet. 2006;51(5):491-494. doi: 10.1007/s10038-006-0379-4. Epub 2006 Mar 17. J Hum Genet. 2006. PMID: 16544051

4

The alanine/threonine polymorphism of the alpha-1-antichymotrypsin (SERPINA3) gene and ruptured intracranial aneurysms in the Japanese population.

Krischek B, Akagawa H, Tajima A, Narita A, Kasuya H, Hori T, Inoue I. Krischek B, et al. Among authors: narita a. Cerebrovasc Dis. 2007;23(1):46-9. doi: 10.1159/000095758. Epub 2006 Sep 12. Cerebrovasc Dis. 2007. PMID: 16968986

5

Using endothelial nitric oxide synthase gene polymorphisms to identify intracranial aneurysms more prone to rupture in Japanese patients.

Krischek B, Kasuya H, Akagawa H, Tajima A, Narita A, Onda H, Hori T, Inoue I. Krischek B, et al. Among authors: narita a. J Neurosurg. 2006 Nov;105(5):717-22. doi: 10.3171/jns.2006.105.5.717. J Neurosurg. 2006. PMID: 17121133

6

Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms.

Akagawa H, Narita A, Yamada H, Tajima A, Krischek B, Kasuya H, Hori T, Kubota M, Saeki N, Hata A, Mizutani T, Inoue I. Akagawa H, et al. Among authors: narita a. Hum Genet. 2007 May;121(3-4):377-87. doi: 10.1007/s00439-007-0333-3. Epub 2007 Feb 8. Hum Genet. 2007. PMID: 17287949

7

Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohort.

Krischek B, Tajima A, Akagawa H, Narita A, Ruigrok Y, Rinkel G, Wijmenga C, Feigl GC, Kim CJ, Hori T, Tatagiba M, Kasuya H, Inoue I. Krischek B, et al. Among authors: narita a. Neuroscience. 2010 Aug 11;169(1):339-43. doi: 10.1016/j.neuroscience.2010.05.002. Epub 2010 May 7. Neuroscience. 2010. PMID: 20452405

8

Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese.

Yamaguchi T, Hosomichi K, Narita A, Shirota T, Tomoyasu Y, Maki K, Inoue I. Yamaguchi T, et al. Among authors: narita a. J Bone Miner Res. 2011 Jul;26(7):1655-61. doi: 10.1002/jbmr.385. J Bone Miner Res. 2011. PMID: 21404329 Free article.

9

Particular human leukocyte antigen alleles are associated with biochemical traits in the Japanese population.

Mitsunaga S, Homma Y, Narita A, Kashiwase K, Okudaira Y, Shiina Y, Inoue I, Inoko H. Mitsunaga S, et al. Among authors: narita a. Hum Immunol. 2011 Jul;72(7):566-70. doi: 10.1016/j.humimm.2011.03.011. Epub 2011 Apr 8. Hum Immunol. 2011. PMID: 21510991

10

Associations between six classical HLA loci and rheumatoid arthritis: a comprehensive analysis.

Mitsunaga S, Suzuki Y, Kuwana M, Sato S, Kaneko Y, Homma Y, Narita A, Kashiwase K, Okudaira Y, Inoue I, Kulski JK, Inoko H. Mitsunaga S, et al. Among authors: narita a. Tissue Antigens. 2012 Jul;80(1):16-25. doi: 10.1111/j.1399-0039.2012.01872.x. Epub 2012 Apr 4. Tissue Antigens. 2012. PMID: 22471586

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