学術論文

Publications (2009)

2017  2016  2015  2014  2013  2012  2011  2010  2009  2008  ~2007

1. Papers from Biobank Japan

Effects of structural variations of APOBEC3A and APOBEC3B genes in chronic hepatitis B virus infection.

Abe H, Ochi H, Maekawa T, Hatakeyama T, Tsuge M, Kitamura S, Kimura T, Miki D, Mitsui F, Hiraga N, Imamura M, Fujimoto Y, Takahashi S, Nakamura Y, Kumada H, Chayama K.
Hepatology Research. 2009 Dec;39(12):1159-68.

 

Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression.

Cha PC, Mushiroda T, Zembutsu H, Harada H, Shinoda N, Kawamoto S, Shimoyama R, Nishidate T, Furuhata T, Sasaki K, Hirata K, Nakamura Y.
Journal of human genetics. 2009 Oct;54(10):572-80.

 

Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation.

Cheung CL, Chan BY, Chan V, Ikegawa S, Kou I, Ngai H, Smith D, Luk KD, Huang QY, Mori S, Sham PC, Kung AW.
Human Molecular Genetics. 18:679-87, 2009.

 

Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk.

Cui R, Kamatani Y, Takahashi A, Usami M, Hosono N, Kawaguchi T, Tsunoda T, Kamatani N, Kubo M, Nakamura Y, Matsuda K.
Gastroenterology. 2009 Nov;137(5):1768-75.

 

CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection.

Hosono N, Kato M, Kiyotani K, Mushiroda T, Takata S, Sato H, Amitani H, Tsuchiya Y,
Yamazaki K, Tsunoda T, Zembutsu H, Nakamura Y, Kubo M.
Clinical Chemistry. 2009 Aug;55(8):1546-54.

 

Estimation of the warfarin dose with clinical and pharmacogenetic data.

International Warfarin Pharmacogenetics Consortium.
The New England journal of medicine. 2009 Feb 19;360(8):753-64.

 

A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.

Kamatani Y, Wattanapokayakit S, Ochi H, Kawaguchi T, Takahashi A, Hosono N, Kubo M, Tsunoda T, Kamatani N, Kumada H, Puseenam A, Sura T, Daigo Y, Chayama K, Chantratita W, Nakamura Y, Matsuda K.
Nature Genetics. 2009 May;41(5):591-5.


 

Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients.

Low SK, Kiyotani K, Mushiroda T, Daigo Y, Nakamura Y, Zembutsu H.
Journal of human genetics. 2009 Oct;54(10):564-71.

 

Lack of association between variations of PDE4D and ischemic stroke in the Japanese population.

Matsushita T, Kubo M, Yonemoto K, Ninomiya T, Ashikawa K, Liang B, Hata J, Doi Y, Kitazono T, Ibayashi S, Iida M, Kiyohara Y, Nakamura Y.
Stroke; a journal of cerebral circulation. 2009 Apr;40(4):1245-51.

 

Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis.

Mori S, Kou I, Sato H, Emi M, Ito H, Hosoi T, Ikegawa S.
Journal of bone and mineral metabolism. 27:213-6, 2009.

 

Association study of TRAF1-C5 polymorphisms with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese.

Nishimoto K, Kochi Y, Ikari K, Yamamoto K, Suzuki A, Shimane K, Nakamura Y, Yano K, Iikuni N, Tsukahara S, Kamatani N, Okamoto H, Kaneko H, Kawaguchi Y, Hara M, Toyama Y, Horiuchi T, Tao K, Yasumoto K, Hamada D, Yasui N, Inoue H, Itakura M, Yamanaka H, Momohara S.
Annals of the rheumatic diseases. 2009 Mar 30.

 

Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1.

Okada Y, Yamada R, Suzuki A, Kochi Y, Shimane K, Myouzen K, Kubo M, Nakamura Y, Yamamoto K.
Arthritis and rheumatism. 2009 Dec;60(12):3582-90.

 

Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individuals.

Omori S, Tanaka Y, Horikoshi M, Takahashi A, Hara K, Hirose H, Kashiwagi A, Kaku K, Kawamori R, Kadowaki T, Nakamura Y, Maeda S.
Diabetologia. 2009 Aug;52(8):1554-60.

 

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.

Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T.
Nature Genetics. 2009 Dec;41(12):1303-7.

 

A single nucleotide polymorphism in the IRF5 promoter region is associated with susceptibility to rheumatoid arthritis in the Japanese population.

Shimane K, Kochi Y, Yamada R, Okada Y, Suzuki A, Miyatake A, Kubo M, Nakamura Y, Yamamoto K.
Annals of the rheumatic diseases 2009 Mar;68(3):377-83.

 

Identification of nectin-4 oncoprotein as a diagnostic and therapeutic target for lung cancer.

Takano A, Ishikawa N, Nishino R, Masuda K, Yasui W, Inai K, Nishimura H, Ito H, Nakayama H, Miyagi Y, Tsuchiya E, Kohno N, Nakamura Y, Daigo Y.
Cancer research. 2009 Aug 15;69(16):6694-703.

 

Serum levels of nicotinamide N-methyltransferase in patients with lung cancer.

Tomida M, Mikami I, Takeuchi S, Nishimura H, Akiyama H.
Journal of cancer research and clinical oncology. 2009 Feb 26.

 

Targeted serum glycoproteomics for the discovery of lung cancer-associated glycosylation disorders using lectin-coupled ProteinChip arrays.

Ueda K, Fukase Y, Katagiri T, Ishikawa N, Irie S, Sato TA, Ito H, Nakayama H, Miyagi Y, Tsuchiya E, Kohno N, Shiwa M, Nakamura Y, Daigo Y.
Proteomics. 2009 Apr;9(8):2182-92.

 

HLA-DRB1*0901 lowers anti-cyclic citrullinated peptide antibody levels in Japanese patients with rheumatoid arthritis.

Okada Y, Suzuki A, Yamada R, Kochi Y, Shimane K, Myouzen K, Kubo M, Nakamura Y, Yamamoto K.
Annals of the rheumatic diseases. 2009 Oct 22.

 

2. Papers related to personalized medicine

A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.

Nuinoon M, Makarasara W, Mushiroda T, Setianingsih I, Wahidiyat PA, Sripichai O, Kumasaka N, Takahashi A, Svasti S, Munkongdee T, Mahasirimongkol S, Peerapittayamongkol C, Viprakasit V, Kamatani N, Winichagoon P, Kubo M, Nakamura Y, Fucharoen S.
Hum Genet. 2010 Mar;127(3):303-14. doi: 10.1007/s00439-009-0770-2.

 

A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population.

Asano K, Matsushita T, Umeno J, Hosono N, Takahashi A, Kawaguchi T, Matsumoto T, Matsui T, Kakuta Y, Kinouchi Y, Shimosegawa T, Hosokawa M, Arimura Y, Shinomura Y, Kiyohara Y, Tsunoda T, Kamatani N, Iida M, Nakamura Y, Kubo M.
Nat Genet. 2009 Dec;41(12):1325-9.

 

A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.

Ng CC, Yew PY, Puah SM, Krishnan G, Yap LF, Teo SH, Lim PV, Govindaraju S, Ratnavelu K, Sam CK, Takahashi A, Kubo M, Kamatani N, Nakamura Y, Mushiroda T.
J Hum Genet. 2009 Jul;54(7):392-7.

 

Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

Betcheva ET, Mushiroda T, Takahashi A, Kubo M, Karachanak SK, Zaharieva IT, Vazharova RV, Dimova II, Milanova VK, Tolev T, Kirov G, Owen MJ, O'Donovan MC, Kamatani N, Nakamura Y, Toncheva DI.
J Hum Genet. 2009 Feb;54(2):98-107.

 

HLA-B*3505 allele is a strong predictor for nevirapine-induced skin adverse drug reactions in HIV-infected Thai patients.

Chantarangsu S, Mushiroda T, Mahasirimongkol S, Kiertiburanakul S, Sungkanuparph S, Manosuthi W, Tantisiriwat W, Charoenyingwattana A, Sura T, Chantratita W, Nakamura Y.
Pharmacogenet Genomics. 2009 Feb;19(2):139-46.

 

Automated SNPs typing system based on the Invader assay.

Nakahara H, Hosono N, Kitayama T, Sekiguchi K, Kubo M, Takahashi A, Nakamura Y, Yamano Y, Kai K.
Leg Med (Tokyo). 2009 Apr;11 Suppl 1:S111-4.


 

DNA variations in human and medical genetics: 25 years of my experience.

Nakamura Y.
J Hum Genet. 2009 Jan;54(1):1-8. Review.

 

Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population.

Yosifova A, Mushiroda T, Stoianov D, Vazharova R, Dimova I, Karachanak S, Zaharieva I, Milanova V, Madjirova N, Gerdjikov I, Tolev T, Velkova S, Kirov G, Owen MJ, O'Donovan MC, Toncheva D, Nakamura Y.
J Affect Disord. 2009 Sep;117(1-2):87-97.

 

A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E.

Nuinoon M, Makarasara W, Mushiroda T, Setianingsih I, Wahidiyat PA, Sripichai O, Kumasaka N, Takahashi A, Svasti S, Munkongdee T, Mahasirimongkol S, Peerapittayamongkol C, Viprakasit V, Kamatani N, Winichagoon P, Kubo M, Nakamura Y, Fucharoen S.
Hum Genet. 2009 Nov 19.

 

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.

Tomlinson IP, Dunlop M, Campbell H, Zanke B, Gallinger S, Hudson T, Koessler T, Pharoah PD, Niittymakix I, Tuupanenx S, Aaltonen LA, Hemminki K, Lindblom A, Forsti A, Sieber O, Lipton L, van Wezel T, Morreau H, Wijnen JT, Devilee P, Matsuda K, Nakamura Y, Castellvi-Bel S, Ruiz-Ponte C, Castells A, Carracedo A, Ho JW, Sham P, Hofstra RM, Vodicka P, Brenner H, Hampe J, Schafmayer C, Tepel J, Schreiber S, Volzke H, Lerch MM, Schmidt CA, Buch S, Moreno V, Villanueva CM, Peterlongo P, Radice P, Echeverry MM, Velez A, Carvajal-Carmona L, Scott R, Penegar S, Broderick P, Tenesa A, Houlston RS.
Br J Cancer. 2009 Nov 17.

 
ゲノム研究バイオバンク事業 バイオバンク・ジャパン(BBJ)

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