Suzuki Y - Search Results

1

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.

Shiga Y, Akiyama M, Nishiguchi KM, Sato K, Shimozawa N, Takahashi A, Momozawa Y, Hirata M, Matsuda K, Yamaji T, Iwasaki M, Tsugane S, Oze I, Mikami H, Naito M, Wakai K, Yoshikawa M, Miyake M, Yamashiro K; Japan Glaucoma Society Omics Group (JGS-OG); Kashiwagi K, Iwata T, Mabuchi F, Takamoto M, Ozaki M, Kawase K, Aihara M, Araie M, Yamamoto T, Kiuchi Y, Nakamura M, Ikeda Y, Sonoda KH, Ishibashi T, Nitta K, Iwase A, Shirato S, Oka Y, Satoh M, Sasaki M, Fuse N, Suzuki Y, Cheng CY, Khor CC, Baskaran M, Perera S, Aung T, Vithana EN, Cooke Bailey JN, Kang JH, Pasquale LR, Haines JL; NEIGHBORHOOD Consortium; Wiggs JL, Burdon KP, Gharahkhani P, Hewitt AW, Mackey DA, MacGregor S, Craig JE, Allingham RR, Hauser M, Ashaye A, Budenz DL, Akafo S, Williams SEI, Kamatani Y, Nakazawa T, Kubo M. Shiga Y, et al. Among authors: suzuki y. Hum Mol Genet. 2018 Apr 15;27(8):1486-1496. doi: 10.1093/hmg/ddy053. Hum Mol Genet. 2018. PMID: 29452408 Free PMC article.

2

Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population.

Kanno K, Suzuki Y, Yang X, Yamada A, Aoki Y, Kure S, Matsubara Y. Kanno K, et al. Among authors: suzuki y. J Hum Genet. 2002;47(6):269-74. doi: 10.1007/s100380200038. J Hum Genet. 2002. PMID: 12111375

3

Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma.

Hasegawa K, Tamari M, Shao C, Shimizu M, Takahashi N, Mao XQ, Yamasaki A, Kamada F, Doi S, Fujiwara H, Miyatake A, Fujita K, Tamura G, Matsubara Y, Shirakawa T, Suzuki Y. Hasegawa K, et al. Among authors: suzuki y. Hum Genet. 2004 Sep;115(4):295-301. doi: 10.1007/s00439-004-1157-z. Hum Genet. 2004. PMID: 15278436

4

An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway.

Nakashima K, Hirota T, Obara K, Shimizu M, Jodo A, Kameda M, Doi S, Fujita K, Shirakawa T, Enomoto T, Kishi F, Yoshihara S, Matsumoto K, Saito H, Suzuki Y, Nakamura Y, Tamari M. Nakashima K, et al. Among authors: suzuki y. J Hum Genet. 2006;51(4):284-291. doi: 10.1007/s10038-005-0358-1. Epub 2006 Jan 24. J Hum Genet. 2006. PMID: 16432636

5

Single nucleotide polymorphism-based genome-wide linkage analysis in Japanese atopic dermatitis families.

Enomoto H, Noguchi E, Iijima S, Takahashi T, Hayakawa K, Ito M, Kano T, Aoki T, Suzuki Y, Koga M, Tamari M, Shiohara T, Otsuka F, Arinami T. Enomoto H, et al. Among authors: suzuki y. BMC Dermatol. 2007 Sep 28;7:5. doi: 10.1186/1471-5945-7-5. BMC Dermatol. 2007. PMID: 17900373 Free PMC article.

6

Filaggrin null mutations are associated with atopic dermatitis and elevated levels of IgE in the Japanese population: a family and case-control study.

Enomoto H, Hirata K, Otsuka K, Kawai T, Takahashi T, Hirota T, Suzuki Y, Tamari M, Otsuka F, Fujieda S, Arinami T, Noguchi E. Enomoto H, et al. Among authors: suzuki y. J Hum Genet. 2008;53(7):615. doi: 10.1007/s10038-008-0293-z. Epub 2008 Jun 3. J Hum Genet. 2008. PMID: 18521703 Free article.

7

Association study of the C3 gene with adult and childhood asthma.

Inoue H, Mashimo Y, Funamizu M, Shimojo N, Hasegawa K, Hirota T, Doi S, Kameda M, Miyatake A, Kohno Y, Okamoto Y, Tamari M, Hata A, Suzuki Y. Inoue H, et al. Among authors: suzuki y. J Hum Genet. 2008;53(8):728-738. doi: 10.1007/s10038-008-0304-0. Epub 2008 Jun 20. J Hum Genet. 2008. PMID: 18566738

8

Replication of genetic association studies in asthma and related phenotypes.

Undarmaa S, Mashimo Y, Hattori S, Shimojo N, Fujita K, Miyatake A, Doi S, Kohno Y, Okamoto Y, Hirota T, Tamari M, Hata A, Suzuki Y. Undarmaa S, et al. Among authors: suzuki y. J Hum Genet. 2010 Jun;55(6):342-9. doi: 10.1038/jhg.2010.32. Epub 2010 Apr 16. J Hum Genet. 2010. PMID: 20395963

9

Common variants in CASP3 confer susceptibility to Kawasaki disease.

Onouchi Y, Ozaki K, Buns JC, Shimizu C, Hamada H, Honda T, Terai M, Honda A, Takeuchi T, Shibuta S, Suenaga T, Suzuki H, Higashi K, Yasukawa K, Suzuki Y, Sasago K, Kemmotsu Y, Takatsuki S, Saji T, Yoshikawa T, Nagai T, Hamamoto K, Kishi F, Ouchi K, Sato Y, Newburger JW, Baker AL, Shulman ST, Rowley AH, Yashiro M, Nakamura Y, Wakui K, Fukushima Y, Fujino A, Tsunoda T, Kawasaki T, Hata A, Nakamura Y, Tanaka T. Onouchi Y, et al. Among authors: suzuki h, suzuki y. Hum Mol Genet. 2010 Jul 15;19(14):2898-906. doi: 10.1093/hmg/ddq176. Epub 2010 Apr 27. Hum Mol Genet. 2010. PMID: 20423928 Free PMC article.

10

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.

Kamada F, Aoki Y, Narisawa A, Abe Y, Komatsuzaki S, Kikuchi A, Kanno J, Niihori T, Ono M, Ishii N, Owada Y, Fujimura M, Mashimo Y, Suzuki Y, Hata A, Tsuchiya S, Tominaga T, Matsubara Y, Kure S. Kamada F, et al. Among authors: suzuki y. J Hum Genet. 2011 Jan;56(1):34-40. doi: 10.1038/jhg.2010.132. Epub 2010 Nov 4. J Hum Genet. 2011. PMID: 21048783

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