Hata A - Search Results

1

Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis.

Ohmori H, Makita Y, Funamizu M, Hirooka K, Hosoi T, Orimo H, Suzuki T, Ikari K, Nakajima T, Inoue I, Hata A. Ohmori H, et al. Among authors: hata a. J Hum Genet. 2002;47(8):400-6. doi: 10.1007/s100380200058. J Hum Genet. 2002. PMID: 12181640

2

Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene.

Ohmori H, Makita Y, Funamizu M, Chiba S, Ohtani K, Suzuki Y, Wakamiya N, Hata A. Ohmori H, et al. Among authors: hata a. J Hum Genet. 2003;48(2):82-5. doi: 10.1007/s100380300011. J Hum Genet. 2003. PMID: 12601552

3

Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis.

Inoue H, Mashimo Y, Funamizu M, Yonekura S, Horiguchi S, Shimojo N, Kohno Y, Okamoto Y, Hata A, Suzuki Y. Inoue H, et al. Among authors: hata a. J Hum Genet. 2012 Mar;57(3):176-83. doi: 10.1038/jhg.2011.148. Epub 2012 Jan 12. J Hum Genet. 2012. PMID: 22237587

4

Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms.

Akagawa H, Narita A, Yamada H, Tajima A, Krischek B, Kasuya H, Hori T, Kubota M, Saeki N, Hata A, Mizutani T, Inoue I. Akagawa H, et al. Among authors: hata a. Hum Genet. 2007 May;121(3-4):377-87. doi: 10.1007/s00439-007-0333-3. Epub 2007 Feb 8. Hum Genet. 2007. PMID: 17287949

5

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: hata a. 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

6

International web-based survey of informed consent procedures in genetic epidemiological studies: towards the establishment of a research coordinator accreditation system.

Yamamoto M, Funamizu M, Muto K, Hata A. Yamamoto M, et al. Among authors: hata a. J Hum Genet. 2009 Dec;54(12):713-20. doi: 10.1038/jhg.2009.103. Epub 2009 Oct 30. J Hum Genet. 2009. PMID: 19881471

7

A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms.

Akagawa H, Tajima A, Sakamoto Y, Krischek B, Yoneyama T, Kasuya H, Onda H, Hori T, Kubota M, Machida T, Saeki N, Hata A, Hashiguchi K, Kimura E, Kim CJ, Yang TK, Lee JY, Kimm K, Inoue I. Akagawa H, et al. Among authors: hata a. Hum Mol Genet. 2006 May 15;15(10):1722-34. doi: 10.1093/hmg/ddl096. Epub 2006 Apr 12. Hum Mol Genet. 2006. PMID: 16611674

8

Association of TNFRSF4 gene polymorphisms with essential hypertension.

Mashimo Y, Suzuki Y, Hatori K, Tabara Y, Miki T, Tokunaga K, Katsuya T, Ogihara T, Yamada M, Takahashi N, Makita Y, Nakayama T, Soma M, Hirawa N, Umemura S, Ohkubo T, Imai Y, Hata A. Mashimo Y, et al. Among authors: hata a. J Hypertens. 2008 May;26(5):902-13. doi: 10.1097/HJH.0b013e3282f6a65e. J Hypertens. 2008. PMID: 18398332

9

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.

Akiyama K, Narita A, Nakaoka H, Cui T, Takahashi T, Yasuno K, Tajima A, Krischek B, Yamamoto K, Kasuya H, Hata A, Inoue I. Akiyama K, et al. Among authors: hata a. J Hum Genet. 2010 Oct;55(10):656-61. doi: 10.1038/jhg.2010.82. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613766

10

SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements.

Uehara DT, Hayashi S, Okamoto N, Mizuno S, Chinen Y, Kosaki R, Kosho T, Kurosawa K, Matsumoto H, Mitsubuchi H, Numabe H, Saitoh S, Makita Y, Hata A, Imoto I, Inazawa J. Uehara DT, et al. Among authors: hata a. J Hum Genet. 2016 Apr;61(4):335-43. doi: 10.1038/jhg.2015.154. Epub 2016 Jan 7. J Hum Genet. 2016. PMID: 26740234

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