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Results: 1 to 20 of 103

1.

Identification of chromosome 3q28 and ALPK1 as susceptibility loci for chronic kidney disease in Japanese individuals by a genome-wide association study.

Yamada Y, Nishida T, Ichihara S, Kato K, Fujimaki T, Oguri M, Horibe H, Yoshida T, Watanabe S, Satoh K, Aoyagi Y, Fukuda M, Sawabe M.

J Med Genet. 2013 Jun;50(6):410-8. doi: 10.1136/jmedgenet-2013-101518. Epub 2013 Mar 28.

PMID:
23539754
[PubMed - indexed for MEDLINE]
2.

Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study.

Yamada Y, Fuku N, Tanaka M, Aoyagi Y, Sawabe M, Metoki N, Yoshida H, Satoh K, Kato K, Watanabe S, Nozawa Y, Hasegawa A, Kojima T.

Atherosclerosis. 2009 Nov;207(1):144-9. doi: 10.1016/j.atherosclerosis.2009.03.038. Epub 2009 Apr 5.

PMID:
19403135
[PubMed - indexed for MEDLINE]
3.

Association of a genetic variant of BTN2A1 with chronic kidney disease in Japanese individuals.

Yoshida T, Kato K, Horibe H, Oguri M, Fukuda M, Satoh K, Aoyagi Y, Shinkai S, Nozawa Y, Yamada Y.

Nephrology (Carlton). 2011 Sep;16(7):642-8. doi: 10.1111/j.1440-1797.2011.01470.x.

PMID:
21557786
[PubMed - indexed for MEDLINE]
4.

Association of genetic variants with chronic kidney disease in Japanese individuals.

Yoshida T, Kato K, Fujimaki T, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.

Clin J Am Soc Nephrol. 2009 May;4(5):883-90. doi: 10.2215/CJN.04350808. Epub 2009 Apr 30.

PMID:
19406964
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Association of genetic variants with chronic kidney disease in Japanese individuals with type 2 diabetes mellitus.

Yoshida T, Kato K, Yokoi K, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Suzuki T, Nozawa Y, Yamada Y.

Int J Mol Med. 2009 Apr;23(4):529-37.

PMID:
19288030
[PubMed - indexed for MEDLINE]
6.

A single nucleotide polymorphism within DUSP9 is associated with susceptibility to type 2 diabetes in a Japanese population.

Fukuda H, Imamura M, Tanaka Y, Iwata M, Hirose H, Kaku K, Maegawa H, Watada H, Tobe K, Kashiwagi A, Kawamori R, Maeda S.

PLoS One. 2012;7(9):e46263. doi: 10.1371/journal.pone.0046263. Epub 2012 Sep 27.

PMID:
23029454
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genetic risk for myocardial infarction in Japanese individuals with or without chronic kidney disease.

Fujimaki T, Kato K, Yokoi K, Yoshida T, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y.

Int J Mol Med. 2010 May;25(5):743-9.

PMID:
20372818
[PubMed - indexed for MEDLINE]
8.

Association of genetic variants of the α-kinase 1 gene with myocardial infarction in community-dwelling individuals.

Fujimaki T, Horibe H, Oguri M, Kato K, Yamada Y.

Biomed Rep. 2014 Jan;2(1):127-131. Epub 2013 Oct 30.

PMID:
24649083
[PubMed]
Free PMC Article
9.

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

Ferguson JF, Matthews GJ, Townsend RR, Raj DS, Kanetsky PA, Budoff M, Fischer MJ, Rosas SE, Kanthety R, Rahman M, Master SR, Qasim A, Li M, Mehta NN, Shen H, Mitchell BD, O'Connell JR, Shuldiner AR, Ho WK, Young R, Rasheed A, Danesh J, He J, Kusek JW, Ojo AO, Flack J, Go AS, Gadegbeku CA, Wright JT Jr, Saleheen D, Feldman HI, Rader DJ, Foulkes AS, Reilly MP; CRIC Study Principal Investigators.

J Am Coll Cardiol. 2013 Aug 27;62(9):789-98. doi: 10.1016/j.jacc.2013.01.103. Epub 2013 May 30.

PMID:
23727086
[PubMed - indexed for MEDLINE]
Free Article
10.

Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.

Yoshida T, Kato K, Fujimaki T, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Yamada Y.

Genomics. 2009 Mar;93(3):221-6. doi: 10.1016/j.ygeno.2008.11.001. Epub 2008 Dec 6.

PMID:
19056482
[PubMed - indexed for MEDLINE]
Free Article
11.

Association of a polymorphism of BTN2A1 with type 2 diabetes mellitus in Japanese individuals.

Hiramatsu M, Oguri M, Kato K, Yoshida T, Fujimaki T, Horibe H, Yokoi K, Watanabe S, Satoh K, Aoyagi Y, Tanaka M, Yoshida H, Shinkai S, Nozawa Y, Murohara T, Yamada Y.

Diabet Med. 2011 Nov;28(11):1381-7. doi: 10.1111/j.1464-5491.2011.03358.x.

PMID:
21672009
[PubMed - indexed for MEDLINE]
12.

Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension.

Yoshida T, Kato K, Yokoi K, Watanabe S, Metoki N, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y.

Hypertens Res. 2009 May;32(5):411-8. doi: 10.1038/hr.2009.22. Epub 2009 Mar 13.

PMID:
19282863
[PubMed - indexed for MEDLINE]
13.

A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.

Yamauchi T, Hara K, Maeda S, Yasuda K, Takahashi A, Horikoshi M, Nakamura M, Fujita H, Grarup N, Cauchi S, Ng DP, Ma RC, Tsunoda T, Kubo M, Watada H, Maegawa H, Okada-Iwabu M, Iwabu M, Shojima N, Shin HD, Andersen G, Witte DR, Jørgensen T, Lauritzen T, Sandbæk A, Hansen T, Ohshige T, Omori S, Saito I, Kaku K, Hirose H, So WY, Beury D, Chan JC, Park KS, Tai ES, Ito C, Tanaka Y, Kashiwagi A, Kawamori R, Kasuga M, Froguel P, Pedersen O, Kamatani N, Nakamura Y, Kadowaki T.

Nat Genet. 2010 Oct;42(10):864-8. doi: 10.1038/ng.660. Epub 2010 Sep 5.

PMID:
20818381
[PubMed - indexed for MEDLINE]
14.

A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese.

Elgazzar S, Zembutsu H, Takahashi A, Kubo M, Aki F, Hirata K, Takatsuka Y, Okazaki M, Ohsumi S, Yamakawa T, Sasa M, Katagiri T, Miki Y, Nakamura Y.

J Hum Genet. 2012 Dec;57(12):766-71. doi: 10.1038/jhg.2012.108. Epub 2012 Sep 6.

PMID:
22951594
[PubMed - indexed for MEDLINE]
15.

Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.

Yang SK, Hong M, Zhao W, Jung Y, Tayebi N, Ye BD, Kim KJ, Park SH, Lee I, Shin HD, Cheong HS, Kim LH, Kim HJ, Jung SA, Kang D, Youn HS, Liu J, Song K.

Inflamm Bowel Dis. 2013 Apr;19(5):954-66. doi: 10.1097/MIB.0b013e3182802ab6.

PMID:
23511034
[PubMed - indexed for MEDLINE]
16.

Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese.

Akamatsu S, Takata R, Haiman CA, Takahashi A, Inoue T, Kubo M, Furihata M, Kamatani N, Inazawa J, Chen GK, Le Marchand L, Kolonel LN, Katoh T, Yamano Y, Yamakado M, Takahashi H, Yamada H, Egawa S, Fujioka T, Henderson BE, Habuchi T, Ogawa O, Nakamura Y, Nakagawa H.

Nat Genet. 2012 Feb 26;44(4):426-9, S1. doi: 10.1038/ng.1104.

PMID:
22366784
[PubMed - indexed for MEDLINE]
17.

Association of genetic variants with myocardial infarction in Japanese individuals with chronic kidney disease.

Fujimaki T, Kato K, Yoshida T, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.

Thromb Haemost. 2009 May;101(5):963-8.

PMID:
19404551
[PubMed - indexed for MEDLINE]
18.

A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.

Osman W, Low SK, Takahashi A, Kubo M, Nakamura Y.

Hum Mol Genet. 2012 Jun 15;21(12):2836-42. doi: 10.1093/hmg/dds103. Epub 2012 Mar 13.

PMID:
22419738
[PubMed - indexed for MEDLINE]
Free Article
19.

Association of TGFbeta1, TNFalpha, CCR2 and CCR5 gene polymorphisms in type-2 diabetes and renal insufficiency among Asian Indians.

Prasad P, Tiwari AK, Kumar KM, Ammini AC, Gupta A, Gupta R, Thelma BK.

BMC Med Genet. 2007 Apr 12;8:20.

PMID:
17428349
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

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.

J Hum Genet. 2011 Nov;56(11):772-8. doi: 10.1038/jhg.2011.99. Epub 2011 Sep 8.

PMID:
21900946
[PubMed - indexed for MEDLINE]

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