Nakaoka H - Search Results

1

Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.

Matsuo H, Yamamoto K, Nakaoka H, Nakayama A, Sakiyama M, Chiba T, Takahashi A, Nakamura T, Nakashima H, Takada Y, Danjoh I, Shimizu S, Abe J, Kawamura Y, Terashige S, Ogata H, Tatsukawa S, Yin G, Okada R, Morita E, Naito M, Tokumasu A, Onoue H, Iwaya K, Ito T, Takada T, Inoue K, Kato Y, Nakamura Y, Sakurai Y, Suzuki H, Kanai Y, Hosoya T, Hamajima N, Inoue I, Kubo M, Ichida K, Ooyama H, Shimizu T, Shinomiya N. Matsuo H, et al. Among authors: nakaoka h. Ann Rheum Dis. 2016 Apr;75(4):652-9. doi: 10.1136/annrheumdis-2014-206191. Epub 2015 Feb 2. Ann Rheum Dis. 2016. PMID: 25646370 Free PMC article.

2

Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.

Nakaoka H, Inoue I. Nakaoka H, et al. J Hum Genet. 2009 Nov;54(11):615-23. doi: 10.1038/jhg.2009.95. Epub 2009 Oct 23. J Hum Genet. 2009. PMID: 19851339 Review.

3

Positional effects of polymorphisms in probe-target sequences on genoplot images of oligonucleotide microarrays.

Cui TL, Nakaoka H, Akiyama K, Kamura H, Hosomichi K, Bae J, Cheong H, Shin H, Yada T, Inoue I. Cui TL, et al. Among authors: nakaoka h. Genet Mol Res. 2010 Mar 23;9(1):524-31. doi: 10.4238/vol9-1gmr737. Genet Mol Res. 2010. PMID: 20391336 Free article.

4

Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution.

Nakaoka H, Takahashi T, Akiyama K, Cui T, Tajima A, Krischek B, Kasuya H, Hata A, Inoue I. Nakaoka H, et al. Stroke. 2010 Aug;41(8):1593-8. doi: 10.1161/STROKEAHA.110.586529. Epub 2010 Jul 1. Stroke. 2010. PMID: 20595659

5

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: nakaoka h. 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

6

TRIM39 and RNF39 are associated with Behçet's disease independently of HLA-B∗51 and -A∗26.

Kurata R, Nakaoka H, Tajima A, Hosomichi K, Shiina T, Meguro A, Mizuki N, Ohono S, Inoue I, Inoko H. Kurata R, et al. Among authors: nakaoka h. Biochem Biophys Res Commun. 2010 Oct 29;401(4):533-7. doi: 10.1016/j.bbrc.2010.09.088. Epub 2010 Sep 27. Biochem Biophys Res Commun. 2010. PMID: 20875797

7

[Genome informatics].

Nakaoka H, Inoue I. Nakaoka H, et al. Nihon Rinsho. 2010 Aug;68 Suppl 8:93-9. Nihon Rinsho. 2010. PMID: 20979269 Review. Japanese. No abstract available.

8

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.

Nakabayashi K, Tajima A, Yamamoto K, Takahashi A, Hata K, Takashima Y, Koyanagi M, Nakaoka H, Akamizu T, Ishikawa N, Kubota S, Maeda S, Tsunoda T, Kubo M, Kamatani N, Nakamura Y, Sasazuki T, Shirasawa S. Nakabayashi K, et al. Among authors: nakaoka h. J Hum Genet. 2011 Nov;56(11):772-8. doi: 10.1038/jhg.2011.99. Epub 2011 Sep 8. J Hum Genet. 2011. PMID: 21900946

9

A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis.

Nakaoka H, Cui T, Tajima A, Oka A, Mitsunaga S, Kashiwase K, Homma Y, Sato S, Suzuki Y, Inoko H, Inoue I. Nakaoka H, et al. PLoS One. 2011;6(9):e25389. doi: 10.1371/journal.pone.0025389. Epub 2011 Sep 28. PLoS One. 2011. PMID: 21980439 Free PMC article.

10

Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders.

Rabbani B, Mahdieh N, Hosomichi K, Nakaoka H, Inoue I. Rabbani B, et al. Among authors: nakaoka h. J Hum Genet. 2012 Oct;57(10):621-32. doi: 10.1038/jhg.2012.91. Epub 2012 Jul 26. J Hum Genet. 2012. PMID: 22832387 Review.

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