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Results: 1 to 20 of 99

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.

Ann Rheum Dis. 2015 Feb 2. pii: annrheumdis-2014-206191. doi: 10.1136/annrheumdis-2014-206191. [Epub ahead of print]

2.

Molecular characterization of an intact p53 pathway subtype in high-grade serous ovarian cancer.

Hayano T, Yokota Y, Hosomichi K, Nakaoka H, Yoshihara K, Adachi S, Kashima K, Tsuda H, Moriya T, Tanaka K, Enomoto T, Inoue I.

PLoS One. 2014 Dec 2;9(12):e114491. doi: 10.1371/journal.pone.0114491. eCollection 2014.

3.

Genome-wide linkage and exome analyses identify variants of HMCN1 for splenic epidermoid cyst.

Omer WH, Narita A, Hosomichi K, Mitsunaga S, Hayashi Y, Yamashita A, Krasniqi A, Iwasaki Y, Kimura M, Inoue I.

BMC Med Genet. 2014 Oct 23;15:115. doi: 10.1186/s12881-014-0115-4.

4.

Possible association between dysfunction of vitamin D binding protein (GC Globulin) and migraine attacks.

Nagata E, Fujii N, Hosomichi K, Mitsunaga S, Suzuki Y, Mashimo Y, Tsukamoto H, Satoh T, Osawa M, Inoue I, Hata A, Takizawa S.

PLoS One. 2014 Aug 22;9(8):e105319. doi: 10.1371/journal.pone.0105319. eCollection 2014.

5.

A Bead-based Normalization for Uniform Sequencing depth (BeNUS) protocol for multi-samples sequencing exemplified by HLA-B.

Hosomichi K, Mitsunaga S, Nagasaki H, Inoue I.

BMC Genomics. 2014 Aug 4;15:645. doi: 10.1186/1471-2164-15-645.

6.

Gene expression profiling reveals distinct molecular signatures associated with the rupture of intracranial aneurysm.

Nakaoka H, Tajima A, Yoneyama T, Hosomichi K, Kasuya H, Mizutani T, Inoue I.

Stroke. 2014 Aug;45(8):2239-45. doi: 10.1161/STROKEAHA.114.005851. Epub 2014 Jun 17.

PMID:
24938844
7.

Estrogen promotes Leydig cell engulfment by macrophages in male infertility.

Yu W, Zheng H, Lin W, Tajima A, Zhang Y, Zhang X, Zhang H, Wu J, Han D, Rahman NA, Korach KS, Gao GF, Inoue I, Li X.

J Clin Invest. 2014 Jun;124(6):2709-21. doi: 10.1172/JCI59901. Epub 2014 Apr 24.

8.

A genome-wide association study of third molar agenesis in Japanese and Korean populations.

Haga S, Nakaoka H, Yamaguchi T, Yamamoto K, Kim YI, Samoto H, Ohno T, Katayama K, Ishida H, Park SB, Kimura R, Maki K, Inoue I.

J Hum Genet. 2013 Dec;58(12):799-803. doi: 10.1038/jhg.2013.106. Epub 2013 Oct 31.

PMID:
24172245
9.

Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.

Ichihara S, Yamamoto K, Asano H, Nakatochi M, Sukegawa M, Ichihara G, Izawa H, Hirashiki A, Takatsu F, Umeda H, Iwase M, Inagaki H, Hirayama H, Sone T, Nishigaki K, Minatoguchi S, Cho MC, Jang Y, Kim HS, Park JE, Tada-Oikawa S, Kitajima H, Matsubara T, Sunagawa K, Shimokawa H, Kimura A, Lee JY, Murohara T, Inoue I, Yokota M.

Circ Cardiovasc Genet. 2013 Dec;6(6):569-78. doi: 10.1161/CIRCGENETICS.111.000027. Epub 2013 Oct 11.

10.

HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients.

Jinam TA, Nakaoka H, Hosomichi K, Mitsunaga S, Okada H, Tanaka A, Tanaka K, Inoue I.

Hum Genet. 2013 Dec;132(12):1405-11. doi: 10.1007/s00439-013-1347-7. Epub 2013 Aug 10.

PMID:
23934009
11.

Phase-defined complete sequencing of the HLA genes by next-generation sequencing.

Hosomichi K, Jinam TA, Mitsunaga S, Nakaoka H, Inoue I.

BMC Genomics. 2013 May 28;14:355. doi: 10.1186/1471-2164-14-355.

12.

A nonsynonymous variant of IL1A is associated with endometriosis in Japanese population.

Hata Y, Nakaoka H, Yoshihara K, Adachi S, Haino K, Yamaguchi M, Nishikawa N, Kashima K, Yahata T, Tajima A, Watanabe A, Akira S, Hosomichi K, Inoue I, Tanaka K.

J Hum Genet. 2013 Aug;58(8):517-20. doi: 10.1038/jhg.2013.32. Epub 2013 May 2.

PMID:
23635948
13.

Detection of ancestry informative HLA alleles confirms the admixed origins of Japanese population.

Nakaoka H, Mitsunaga S, Hosomichi K, Shyh-Yuh L, Sawamoto T, Fujiwara T, Tsutsui N, Suematsu K, Shinagawa A, Inoko H, Inoue I.

PLoS One. 2013;8(4):e60793. doi: 10.1371/journal.pone.0060793. Epub 2013 Apr 5.

14.

Improved loop-mediated isothermal amplification for HLA-DRB1 genotyping using RecA and a restriction enzyme for enhanced amplification specificity.

Mitsunaga S, Shimizu S, Okudaira Y, Oka A, Tanaka M, Kimura M, Kulski JK, Inoue I, Inoko H.

Immunogenetics. 2013 Jun;65(6):405-15. doi: 10.1007/s00251-013-0690-0. Epub 2013 Mar 9.

PMID:
23474534
15.

Replication study and meta-analysis of human nonobstructive azoospermia in Japanese populations.

Sato Y, Jinam T, Iwamoto T, Yamauchi A, Imoto I, Inoue I, Tajima A.

Biol Reprod. 2013 Apr 11;88(4):87. doi: 10.1095/biolreprod.112.106377. Print 2013 Apr.

16.

Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.

Mitsunaga S, Hosomichi K, Okudaira Y, Nakaoka H, Kunii N, Suzuki Y, Kuwana M, Sato S, Kaneko Y, Homma Y, Kashiwase K, Azuma F, Kulski JK, Inoue I, Inoko H.

J Hum Genet. 2013 Apr;58(4):210-5. doi: 10.1038/jhg.2013.2. Epub 2013 Jan 31.

PMID:
23364395
17.

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

Rabbani B, Mahdieh N, Hosomichi K, Nakaoka H, Inoue I.

J Hum Genet. 2012 Oct;57(10):621-32. doi: 10.1038/jhg.2012.91. Epub 2012 Jul 26. Review.

PMID:
22832387
18.

High-risk ovarian cancer based on 126-gene expression signature is uniquely characterized by downregulation of antigen presentation pathway.

Yoshihara K, Tsunoda T, Shigemizu D, Fujiwara H, Hatae M, Fujiwara H, Masuzaki H, Katabuchi H, Kawakami Y, Okamoto A, Nogawa T, Matsumura N, Udagawa Y, Saito T, Itamochi H, Takano M, Miyagi E, Sudo T, Ushijima K, Iwase H, Seki H, Terao Y, Enomoto T, Mikami M, Akazawa K, Tsuda H, Moriya T, Tajima A, Inoue I, Tanaka K; Japanese Serous Ovarian Cancer Study Group.

Clin Cancer Res. 2012 Mar 1;18(5):1374-85. doi: 10.1158/1078-0432.CCR-11-2725. Epub 2012 Jan 12.

19.

Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk.

Yasuno K, Bakırcıoğlu M, Low SK, Bilgüvar K, Gaál E, Ruigrok YM, Niemelä M, Hata A, Bijlenga P, Kasuya H, Jääskeläinen JE, Krex D, Auburger G, Simon M, Krischek B, Ozturk AK, Mane S, Rinkel GJ, Steinmetz H, Hernesniemi J, Schaller K, Zembutsu H, Inoue I, Palotie A, Cambien F, Nakamura Y, Lifton RP, Günel M.

Proc Natl Acad Sci U S A. 2011 Dec 6;108(49):19707-12. doi: 10.1073/pnas.1117137108. Epub 2011 Nov 21.

20.

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.

PLoS One. 2011;6(9):e25389. doi: 10.1371/journal.pone.0025389. Epub 2011 Sep 28.

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