Onouchi Y - Search Results

1

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population.

Konta A, Ozaki K, Sakata Y, Takahashi A, Morizono T, Suna S, Onouchi Y, Tsunoda T, Kubo M, Komuro I, Eishi Y, Tanaka T. Konta A, et al. Among authors: onouchi y. J Hum Genet. 2016 May;61(5):435-41. doi: 10.1038/jhg.2015.171. Epub 2016 Jan 21. J Hum Genet. 2016. PMID: 26791355

2

Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome.

Onouchi Y, Kurahashi H, Tajiri H, Ida S, Okada S, Nakamura Y. Onouchi Y, et al. J Hum Genet. 1999;44(4):235-9. doi: 10.1007/s100380050150. J Hum Genet. 1999. PMID: 10429362

3

Mapping of a gene responsible for dermatitis in NOA (Naruto Research Institute Otsuka Atrichia) mice, an animal model of allergic dermatitis.

Natori K, Tamari M, Watanabe O, Onouchi Y, Shiomoto Y, Kubo S, Nakamura Y. Natori K, et al. Among authors: onouchi y. J Hum Genet. 1999;44(6):372-6. doi: 10.1007/s100380050181. J Hum Genet. 1999. PMID: 10570907

4

Association studies of 33 single nucleotide polymorphisms (SNPs) in 29 candidate genes for bronchial asthma: positive association a T924C polymorphism in the thromboxane A2 receptor gene.

Unoki M, Furuta S, Onouchi Y, Watanabe O, Doi S, Fujiwara H, Miyatake A, Fujita K, Tamari M, Nakamura Y. Unoki M, et al. Among authors: onouchi y. Hum Genet. 2000 Apr;106(4):440-6. doi: 10.1007/s004390000267. Hum Genet. 2000. PMID: 10830912

5

Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in children.

Takeoka S, Unoki M, Onouchi Y, Doi S, Fujiwara H, Miyatake A, Fujita K, Inoue I, Nakamura Y, Tamari M. Takeoka S, et al. Among authors: onouchi y. J Hum Genet. 2001;46(2):57-63. doi: 10.1007/s100380170109. J Hum Genet. 2001. PMID: 11281413

6

CD40 ligand gene and Kawasaki disease.

Onouchi Y, Onoue S, Tamari M, Wakui K, Fukushima Y, Yashiro M, Nakamura Y, Yanagawa H, Kishi F, Ouchi K, Terai M, Hamamoto K, Kudo F, Aotsuka H, Sato Y, Nariai A, Kaburagi Y, Miura M, Saji T, Kawasaki T, Nakamura Y, Hata A. Onouchi Y, et al. Eur J Hum Genet. 2004 Dec;12(12):1062-8. doi: 10.1038/sj.ejhg.5201266. Eur J Hum Genet. 2004. PMID: 15367912

7

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease.

Yamazaki K, Takazoe M, Tanaka T, Ichimori T, Saito S, Iida A, Onouchi Y, Hata A, Nakamura Y. Yamazaki K, et al. Among authors: onouchi y. J Hum Genet. 2004;49(12):664-668. doi: 10.1007/s10038-004-0204-x. Epub 2004 Oct 19. J Hum Genet. 2004. PMID: 15503241

8

A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12.

Onouchi Y, Tamari M, Takahashi A, Tsunoda T, Yashiro M, Nakamura Y, Yanagawa H, Wakui K, Fukushima Y, Kawasaki T, Nakamura Y, Hata A. Onouchi Y, et al. J Hum Genet. 2007;52(2):179-190. doi: 10.1007/s10038-006-0092-3. Epub 2006 Dec 8. J Hum Genet. 2007. PMID: 17160344

9

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: onouchi y. 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

10

ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms.

Onouchi Y, Gunji T, Burns JC, Shimizu C, Newburger JW, Yashiro M, Nakamura Y, Yanagawa H, Wakui K, Fukushima Y, Kishi F, Hamamoto K, Terai M, Sato Y, Ouchi K, Saji T, Nariai A, Kaburagi Y, Yoshikawa T, Suzuki K, Tanaka T, Nagai T, Cho H, Fujino A, Sekine A, Nakamichi R, Tsunoda T, Kawasaki T, Nakamura Y, Hata A. Onouchi Y, et al. Nat Genet. 2008 Jan;40(1):35-42. doi: 10.1038/ng.2007.59. Epub 2007 Dec 16. Nat Genet. 2008. PMID: 18084290 Free PMC article.

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