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論文発表 英文publication list

2017

1)       Nishide A, Fujita M, Sato Y, Nagashima K, Takahashi S, Hata A. Income-Related Inequalities in Access to Dental Care Services in Japan. Int J Environ Res Public Health. 12;14, pii: E524, 2017. doi: 10.3390/ijerph14050524.

      

2)       Fujita M, Sato Y, Nagashima K, Takahashi S, Hata A. Impact of geographic accessibility on utilization of the annual health check-ups by income level in Japan: A multilevel analysis. PLoS One. 9;12:e0177091, 2017. doi: 10.1371/journal.pone.0177091.



2016

1)       Fujita M, Sato Y, Nagashima K, Takahashi S, Hata A. Income Related Inequality of Health Care Access in Japan: A Retrospective Cohort Study. PLoS One. 15:e0151690, 2016.

2)       Yamamoto M, Fujita M, Mori C, Hata A. Survey of motivation to participate in a birth cohort. J Hum Genet. 61:787-91, 2016. doi: 10.1038/jhg.2016.60.

   

2015

1)       Fujita M, Sato Y, Nagashima K, Takahashi S, Hata A. Validity assessment of self-reported medication use by comparing to pharmacy insurance claims. BMJ Open. 5: e009490, 2015.

      

2)       Fujita M, Sato Y, Nagashima K, Takahashi S, Hata A. Predictive power of a body shape index for development of diabetes, hypertension, and dyslipidemia in Japanese adults: a retrospective cohort study. PLoS One; 10:e0128972, 2015.

2014

1)       Fujita M, Hata A. Sex and age differences in the effect of obesity on incidence of hypertension in the Japanese population: A large historical cohort study.J Am Soc Hypertens. 8:64-70 ,2014 .


      

2)       Itoh K, Moriguchi R, Yamada Y, Fujita M, Yamato T, Oumi M, Holst JJ, Seino Y. High saturated fatty acid intake induces insulin secretion by elevating gastric inhibitory polypeptide levels in healthy individuals. Nutr Res. 34:653-60 , 2014 .

      

2013

1)       Kuo HC, Hsu YW, Wu CM, Chen SH, Hung KS, Chang WP, Yang KD, Hsieh KS, Chen WC, Onouchi Y, Chang WC.: A replication study for association of ITPKC and CASP3 two-locus analysis in IVIG unresponsiveness and coronary artery lesion in Kawasaki disease. PLoS One; 8: e69685, 2013.



2012

1)       Okamoto N, Hayashi S, Masui A, Kosaki R, Oguri I, Hasegawa T, Imoto I, Makita Y, Hata A, Moriyama K Inazawa J: Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion. J Hum Genet 2012.

 

2)       Inoue H, Mashimo Y, Funamizu M, Yonekura S, Horiguchi S, Shimojo N, Kohno Y, Okamoto Y, Hata A Suzuki Y: Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis. J Hum Genet 2012.

 

3)       Hayashi S, Okamoto N, Chinen Y, Takanashi J, Makita Y, Hata A, Imoto I Inazawa J: Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH). Hum Genet 2012: 131: 99-110.

4)       Hamada H, Suzuki H, Abe J, Suzuki Y, Suenaga T, Takeuchi T, Yoshikawa N, Shibuta S, Miyawaki M, Oishi K, Yamaga H, Aoyagi N, Iwahashi S, Miyashita R, Honda T, Onouchi Y, Terai M, Hata A: Inflammatory cytokine profiles during Cyclosporin treatment for immunoglobulin-resistant Kawasaki disease. Cytokine; 60: 681-5, 2012.

5)       Onouchi Y: Genetics of Kawasaki disease: what we know and don't know. Circ J; 76: 1581-6, 2012.

6)       Tremoulet AH, Pancoast P, Franco A, Bujold M, Shimizu C, Onouchi Y, Tamamoto A, Erdem G, Dodd D, Burns JC: Calcineurin inhibitor treatment of intravenous immunoglobulin-resistant Kawasaki disease. J Pediatr; 161: 506-512, 2012.


7)       Onouchi Y, Ozaki K, Jane C. Burns, Shimizu C, Terai M, Hamada H, Honda T, Suzuki H, Suenaga T, Takeuchi T, Yoshikawa N, Suzuki Y, Yasukawa K, Ebata R, Higashi K, Saji T, Kemmotsu Y, Takatsuki S, Ouchi K, Kishi F, Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Honda A, Kobayashi H, Sato J, Shibuta S, Masakazu Miyawaki M, Ko Oishi K, Hironobu Yamaga H, Aoyagi N, Iwahashi S, Miyashita R, Murata Y, Sasago K, Takahashi A, Kamatani N, Kubo M, Tsunoda T, Hata A, Nakamura Y, Tanaka T, Japan Kawasaki Disease Genome Consortium & US Kawasaki Disease Genetics Consortium: A genome-wide association study identifies three new risk loci for Kawasaki disease. Nat Genet; 44: 517-21, 2012.


8)       Kobayashi T, Saji T, Otani T, Takeuchi K, Nakamura T, Arakawa H, Kato T, Hara T, Hamaoka K, Ogawa S, Miura M, Nomura Y, Fuse S, Ichida F, Seki M, Fukazawa R, Ogawa C, Furuno K, Tokunaga H, Takatsuki S, Hara S, Morikawa A; RAISE study group investigators.: Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blinded-endpoints trial. Lancet; 379: 1613-20, 2012.


 

2011

1)       Yasuno K, Bakircioglu M, Low S K, Bilguvar K, Gaal E, Ruigrok Y M, Niemela M, Hata A, Bijlenga P, Kasuya H, Jaaskelainen J E, Krex D, Auburger G, Simon M, Krischek B, Ozturk A K, Mane S, Rinkel G J, Steinmetz H, Hernesniemi J, Schaller K, Zembutsu H, Inoue I, Palotie A, Cambien F, Nakamura Y, Lifton R P Gunel M: Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk. Proc Natl Acad Sci U S A 2011: 108: 19707-12.

 

2)       Yamazaki D, Tabara Y, Kita S, Hanada H, Komazaki S, Naitou D, Mishima A, Nishi M, Yamamura H, Yamamoto S, Kakizawa S, Miyachi H, Miyata T, Kawano Y, Kamide K, Ogihara T, Hata A, Umemura S, Soma M, Takahashi N, Imaizumi Y, Miki T, Iwamoto T Takeshima H: TRIC-A channels in vascular smooth muscle contribute to blood pressure maintenance. Cell Metab 2011: 14: 231-41.

 

3)       Yamamoto M Hata A: A commentary on for what am i participating? The need for communication after receiving consent from biobanking project participants: experience in Japan. J Hum Genet 2011: 56: 405.

 

4)       Suzuki H, Terai M, Hamada H, Honda T, Suenaga T, Takeuchi T, Yoshikawa N, Shibuta S, Miyawaki M, Oishi K, Yamaga H, Aoyagi N, Iwahashi S, Miyashita R, Onouchi Y, Sasago K, Suzuki Y Hata A: Cyclosporin A treatment for Kawasaki disease refractory to initial and additional intravenous immunoglobulin. Pediatr Infect Dis J 2011: 30: 871-6.

 

5)       Oomachi K, Ogata K, Sugawara T, Hagiwara A, Hata A Yamamoto S: Evaluation of contrast visual acuity in patients with retinitis pigmentosa. Clin Ophthalmol 2011: 5: 1459-63.

 

6)       Onouchi Y, Suzuki Y, Suzuki H, Terai M, Yasukawa K, Hamada H, Suenaga T, Honda T, Honda A, Kobayashi H, Takeuchi T, Yoshikawa N, Sato J, Shibuta S, Miyawaki M, Oishi K, Yamaga H, Aoyagi N, Iwahashi S, Miyashita R, Murata Y, Ebata R, Higashi K, Ozaki K, Sasago K, Tanaka T Hata A: ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease. Pharmacogenomics J 2011.

 

7)       Narisawa A, Komatsuzaki S, Kikuchi A, Niihori T, Aoki Y, Fujiwara K, Tanemura M, Hata A, Suzuki Y, Relton C L, Grinham J, Leung K Y, Partridge D, Robinson A, Stone V, Gustavsson P, Stanier P, Copp A J, Greene N D, Tominaga T, Matsubara Y Kure S: Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans. Hum Mol Genet 2011.

 

8)       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: A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. J Hum Genet 2011: 56: 34-40.

 

9)       Hayashi S, Imoto I, Aizu Y, Okamoto N, Mizuno S, Kurosawa K, Honda S, Araki S, Mizutani S, Numabe H, Saitoh S, Kosho T, Fukushima Y, Mitsubuchi H, Endo F, Chinen Y, Kosaki R, Okuyama T, Ohki H, Yoshihashi H, Ono M, Takada F, Ono H, Yagi M, Matsumoto H, Makita Y, Hata A Inazawa J: Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies. J Hum Genet 2011: 56: 110-24.

 

10)     Hattori S, Shimojo N, Mashimo T, Inoue Y, Ono Y, Kohno Y, Okamoto Y, Hata A Suzuki Y: Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population. Jpn J Infect Dis 2011: 64: 242-5.

 

11)     Harada M, Hirota T, Jodo A I, Hitomi Y, Sakashita M, Tsunoda T, Miyagawa T, Doi S, Kameda M, Fujita K, Miyatake A, Enomoto T, Noguchi E, Masuko H, Sakamoto T, Hizawa N, Suzuki Y, Yoshihara S, Adachi M, Ebisawa M, Saito H, Matsumoto K, Nakajima T, Mathias R A, Rafaels N, Barnes K C, Himes B E, Duan Q L, Tantisira K G, Weiss S T, Nakamura Y, Ziegler S F Tamari M: Thymic stromal lymphopoietin gene promoter polymorphisms are associated with susceptibility to bronchial asthma. Am J Respir Cell Mol Biol 2011: 44: 787-93.

        

12)     Kuo HC, Onouchi Y, Hsu YW, Chen WC, Huang JD, Huang YH, Yang YL, Chao MC, Yu HR, Juan YS, Kuo CM, Yang KD, Huang JS, Chang WC: Polymorphisms of transforming growth factor-β signaling pathway and Kawasaki disease in the Taiwanese population. J Hum Genet; 56: 840-5, 2011.

      

 

2010

1)       Yasuno K, Bilguvar K, Bijlenga P, Low S K, Krischek B, Auburger G, Simon M, Krex D, Arlier Z, Nayak N, Ruigrok Y M, Niemela M, Tajima A, von und zu Fraunberg M, Doczi T, Wirjatijasa F, Hata A, Blasco J, Oszvald A, Kasuya H, Zilani G, Schoch B, Singh P, Stuer C, Risselada R, Beck J, Sola T, Ricciardi F, Aromaa A, Illig T, Schreiber S, van Duijn C M, van den Berg L H, Perret C, Proust C, Roder C, Ozturk A K, Gaal E, Berg D, Geisen C, Friedrich C M, Summers P, Frangi A F, State M W, Wichmann H E, Breteler M M, Wijmenga C, Mane S, Peltonen L, Elio V, Sturkenboom M C, Lawford P, Byrne J, Macho J, Sandalcioglu E I, Meyer B, Raabe A, Steinmetz H, Rufenacht D, Jaaskelainen J E, Hernesniemi J, Rinkel G J, Zembutsu H, Inoue I, Palotie A, Cambien F, Nakamura Y, Lifton R P Gunel M: Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010: 42: 420-5.

 

2)       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: Replication of genetic association studies in asthma and related phenotypes. J Hum Genet 2010: 55: 342-9.

 

3)       Tabara Y, Kohara K, Kita Y, Hirawa N, Katsuya T, Ohkubo T, Hiura Y, Tajima A, Morisaki T, Miyata T, Nakayama T, Takashima N, Nakura J, Kawamoto R, Takahashi N, Hata A, Soma M, Imai Y, Kokubo Y, Okamura T, Tomoike H, Iwai N, Ogihara T, Inoue I, Tokunaga K, Johnson T, Caulfield M, Munroe P, Umemura S, Ueshima H Miki T: Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project. Hypertension 2010: 56: 973-80.

 

4)       Onouchi Y, Ozaki K, Buns J C, 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 J W, Baker A L, Shulman S T, Rowley A H, Yashiro M, Nakamura Y, Wakui K, Fukushima Y, Fujino A, Tsunoda T, Kawasaki T, Hata A Tanaka T: Common variants in CASP3 confer susceptibility to Kawasaki disease. Hum Mol Genet 2010: 19: 2898-906.

 

5)       Nakaoka H, Takahashi T, Akiyama K, Cui T, Tajima A, Krischek B, Kasuya H, Hata A Inoue I: Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution. Stroke 2010: 41: 1593-8.

 

6)       Mamtani M, Matsubara T, Shimizu C, Furukawa S, Akagi T, Onouchi Y, Hata A, Fujino A, He W, Ahuja S K Burns J C: Association of CCR2-CCR5 haplotypes and CCL3L1 copy number with Kawasaki Disease, coronary artery lesions, and IVIG responses in Japanese children. PLoS One 2010: 5: e11458.

 

7)       Fukuda N, Suzuki Y, Sato K, Yajima D, Hayakawa M, Motani H, Kobayashi K, Otsuka K, Nagasawa S Iwase H: Estimation of age from sclerotic glomeruli. Forensic Sci Int 2010: 197: 123 e1-4.

 

8)       Fujita M, Ueno K Hata A: Association of gamma-glutamyltransferase with incidence of type 2 diabetes in Japan. Exp Biol Med (Maywood) 2010: 235: 335-41.

 

9)       Akiyama K, Narita A, Nakaoka H, Cui T, Takahashi T, Yasuno K, Tajima A, Krischek B, Yamamoto K, Kasuya H, Hata A Inoue I: Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms. J Hum Genet 2010: 55: 656-61.

 

2009

1)   Yamazaki K, Takahashi A, Takazoe M, Kubo M, Onouchi Y, Fujino A, Kamatani N, Nakamura YHata A: Positive association of genetic variants in the upstream region of NKX2-3 with Crohn's disease in Japanese patients. Gut; 58: 228-32, 2009

2)   Yamamoto M, Funamizu M, Muto KHata A: International web-based survey of informed consent procedures in genetic epidemiological studies: towards the establishment of a research coordinator accreditation system. J Hum Genet; 54: 713-20, 2009

3)   Ueno T, Tabara Y, Fukuda N, Tahira K, Matsumoto T, Kosuge K, Haketa A, Matsumoto K, Sato Y, Nakayama T, Katsuya T, Ogihara T, Makita Y, Hata A, Yamada M, Takahashi N, Hirawa N, Umemura S, Miki TSoma M: Association of SLC6A9 gene variants with human essential hypertension. J Atheroscler Thromb; 16: 201-6, 2009

4)   Suzuki Y, Hattori S, Mashimo Y, Funamizu M, Kohno Y, Okamoto Y, Hata AShimojo N: CD14 and IL4R gene polymorphisms modify the effect of day care attendance on serum IgE levels. J Allergy Clin Immunol; 123: 1408-11 e1, 2009

5)   Sugimoto T, Seki N, Shimizu S, Kikkawa N, Tsukada J, Shimada H, Sasaki K, Hanazawa T, Okamoto YHata A: The galanin signaling cascade is a candidate pathway regulating oncogenesis in human squamous cell carcinoma. Genes Chromosomes Cancer; 48: 132-42, 2009

6)   Ruigrok Y M, Rinkel G J, Wijmenga C, Kasuya H, Tajima A, Takahashi T, Hata A, Inoue IKrischek B: Association analysis of genes involved in the maintenance of the integrity of the extracellular matrix with intracranial aneurysms in a Japanese cohort. Cerebrovasc Dis; 28: 131-4, 2009

7)   Kobashi G, Ohta K, Yamada H, Hata A, Minakami H, Sakuragi N, Tamashiro HFujimoto S: 4G/5G variant of plasminogen activator inhibitor-1 gene and severe pregnancy-induced hypertension: subgroup analyses of variants of angiotensinogen and endothelial nitric oxide synthase. J Epidemiol; 19: 275-80, 2009

8)   Imada Y, Fujimoto M, Hirata K, Hirota T, Suzuki Y, Saito H, Matsumoto K, Akazawa A, Katsunuma T, Yoshihara S, Ebisawa M, Shibasaki M, Arinami T, Tamari MNoguchi E: Large scale genotyping study for asthma in the Japanese population. BMC Res Notes; 2: 54, 2009

9)   Hitomi Y, Ebisawa M, Tomikawa M, Imai T, Komata T, Hirota T, Harada M, Sakashita M, Suzuki Y, Shimojo N, Kohno Y, Fujita K, Miyatake A, Doi S, Enomoto T, Taniguchi M, Higashi N, Nakamura YTamari M: Associations of functional NLRP3 polymorphisms with susceptibility to food-induced anaphylaxis and aspirin-induced asthma. J Allergy Clin Immunol; 124: 779-85 e6, 2009

10) Hata A Onouchi Y: Susceptibility genes for Kawasaki disease: toward implementation of personalized medicine. J Hum Genet; 54: 67-73, 2009

11) Fujita M, Ueno K Hata A: Effect of obesity on incidence of type 2 diabetes declines with age among Japanese women. Exp Biol Med (Maywood); 234: 750-7, 2009

12) Fujita M, Ueno K Hata A: Lower frequency of daily teeth brushing is related to high prevalence of cardiovascular risk factors. Exp Biol Med (Maywood); 234: 387-94, 2009

 

2008

1)   Onouchi Y, Gunji T, Burns J C, Shimizu C, Newburger J W, Yashiro M, Nakamura Y, Yanagawa H, Wakui K, Fukushima Y, Kishi F, Hamamoto K, Terai M, Sato Y, Ouchi K, Saji T, Nariai A, Kaburagi Y, Yoshikawa T, Suzuki K, Tanaka T, Nagai T, Cho H, Fujino A, Sekine A, Nakamichi R, Tsunoda T, Kawasaki THata A: ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms. Nat Genet; 40: 35-42, 2008

2)   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 YHata A: Association of TNFRSF4 gene polymorphisms with essential hypertension. J Hypertens; 26: 902-913, 2008

3)   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 ASuzuki Y: Association study of the C3 gene with adult and childhood asthma. J Hum Genet; 53: 728-38, 2008

4)   Inoue H, Kayano S, Aoki Y, Kure S, Yamada A, Hata A, Matsubara YSuzuki Y: Association of the GABRB3 Gene With Nonsyndromic Oral Clefts. Cleft Palate Craniofac J; 45: 261-6, 2008

5)   Cervigni F, Suzuki Y, Ishii THata A: Spatial Accessibility to Pediatric Services. J Community Health, 2008

 

2007

1)   Yatsu K, Mizuki N, Hirawa N, Oka A, Itoh N, Yamane T, Ogawa M, Shiwa T, Tabara Y, Ohno S, Soma M, Hata A, Nakao K, Ueshima H, Ogihara T, Tomoike H, Miki T, Kimura A, Mano S, Kulski J K, Umemura SInoko H: High-resolution mapping for essential hypertension using microsatellite markers. Hypertension; 49: 446-52, 2007

2)   Yamazaki K, Onouchi Y, Takazoe M, Kubo M, Nakamura YHata A: Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients. J Hum Genet; 52: 575-83, 2007

3)   Onouchi Y, Tamari M, Takahashi A, Tsunoda T, Yashiro M, Nakamura Y, Yanagawa H, Wakui K, Fukushima Y, Kawasaki THata A: A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12. J Hum Genet; 52: 179-90, 2007

4)   Matsuzawa D, Hashimoto K, Miyatake R, Shirayama Y, Shimizu E, Maeda K, Suzuki Y, Mashimo Y, Sekine Y, Inada T, Ozaki N, Iwata N, Harano M, Komiyama T, Yamada M, Sora I, Ujike H, Hata A, Sawa AIyo M: Identification of functional polymorphisms in the promoter region of the human PICK1 gene and their association with methamphetamine psychosis. Am J Psychiatry; 164: 1105-14, 2007

5)   Kamada F, Mashimo Y, Inoue H, Shao C, Hirota T, Doi S, Kameda M, Fujiwara H, Fujita K, Enomoto T, Sasaki S, Endo H, Takayanagi R, Nakazawa C, Morikawa T, Morikawa M, Miyabayashi S, Chiba Y, Tamura G, Shirakawa T, Matsubara Y, Hata A, Tamari MSuzuki Y: The GSTP1 gene is a susceptibility gene for childhood asthma and the GSTM1 gene is a modifier of the GSTP1 gene. Int Arch Allergy Immunol; 144: 275-86, 2007

6)   Inoue Y, Shimojo N, Suzuki Y, Campos Alberto E J, Yamaide A, Suzuki S, Arima T, Matsuura T, Tomiita M, Aoyagi M, Hoshioka A, Honda A, Hata AKohno Y: CD14 -550 C/T, Which Is Related to the Serum Level of Soluble CD14, Is Associated with the Development of Respiratory Syncytial Virus Bronchiolitis in the Japanese Population. J Infect Dis; 195: 1618-24, 2007

7)   Harada M, Nakashima K, Hirota T, Shimizu M, Doi S, Fujita K, Shirakawa T, Enomoto T, Yoshikawa M, Moriyama H, Matsumoto K, Saito H, Suzuki Y, Nakamura YTamari M: Functional Polymorphism in the Suppressor of Cytokine Signaling 1 Gene Associated with Adult Asthma. Am J Respir Cell Mol Biol; 36: 491-496, 2007

8)   Gunji T, Onouchi Y, Nagasawa T, Katagiri S, Watanabe H, Kobayashi H, Arakawa S, Noguchi K, Hata A, Izumi YIshikawa I: Functional polymorphisms of the FPR1 gene and aggressive periodontitis in Japanese. Biochem Biophys Res Commun; 364: 7-13, 2007

9)   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 FArinami T: Single nucleotide polymorphism-based genome-wide linkage analysis in Japanese atopic dermatitis families. BMC Dermatol; 7: 5, 2007

10) Campos E, Shimojo N, Inoue Y, Arima T, Suzuki S, Tomiita M, Matsuura T, Hata A, Suzuki Y, Aoyagi MKohno Y: No Association of Polymorphisms in the 5' Region of the CD14 Gene and Food Allergy in a Japanese Population. Allergol Int; 56: 23-7, 2007

11) Akagawa H, Narita A, Yamada H, Tajima A, Krischek B, Kasuya H, Hori T, Kubota M, Saeki N, Hata A, Mizutani TInoue I: Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms. Hum Genet; 121: 377-87, 2007

12) Tanaka M, Koga R, Tsuda H, Imai K, Abe S, Masuda T, Iwamoto M, Nakazono E, Kamohara T, Kinukawa N, Sakata T. Subcutaneous fat accumulation shows a beneficial correlation with serum cholesterol in postmenopausal Japanese women. Experimental Biology and Medicine. 232, 1064-1070, 2007

 

2006

1)   Takikawa K, Haga N, Maruyama T, Nakatomi A, Kondoh T, Makita Y, Hata A, Kawabata HIkegawa S: Spine and rib abnormalities and stature in spondylocostal dysostosis. Spine; 31: E192-7, 2006

2)   Suzuki H, Komiya A, Kamiya N, Imamoto T, Kawamura K, Miura J, Suzuki N, Nakatsu H, Hata AIchikawa T: Development of a nomogram to predict probability of positive initial prostate biopsy among Japanese patients. Urology; 67: 131-6, 2006

3)   Omi T, Kumada M, Kamesaki T, Okuda H, Munkhtulga L, Yanagisawa Y, Utsumi N, Gotoh T, Hata A, Soma M, Umemura S, Ogihara T, Takahashi N, Tabara Y, Shimada K, Mano H, Kajii E, Miki TIwamoto S: An intronic variable number of tandem repeat polymorphisms of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene modifies gene expression and is associated with essential hypertension. Eur J Hum Genet; 14: 1295-305, 2006

4)   Nakayama T, Kuroi N, Sano M, Tabara Y, Katsuya T, Ogihara T, Makita Y, Hata A, Yamada M, Takahashi N, Hirawa N, Umemura S, Miki TSoma M: Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension. Hypertension; 48: 512-8, 2006

5)   Nakashima K, Hirota T, Suzuki Y, Akahoshi M, Shimizu M, Jodo A, Doi S, Fujita K, Ebisawa M, Yoshihara S, Enomoto T, Shirakawa T, Kishi F, Nakamura YTamari M: Association of the RIP2 gene with childhood atopic asthma. Allergol Int; 55: 77-83, 2006

6)   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 YTamari M: An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway. J Hum Genet; 51: 284-91, 2006

7)   Nakashima K, Hirota T, Obara K, Shimizu M, Doi S, Fujita K, Shirakawa T, Enomoto T, Yoshihara S, Ebisawa M, Matsumoto K, Saito H, Suzuki Y, Nakamura YTamari M: A functional polymorphism in MMP-9 is associated with childhood atopic asthma. Biochem Biophys Res Commun; 344: 300-7, 2006

8)   Kamada F, Kure S, Kudo T, Suzuki Y, Oshima T, Ichinohe A, Kojima K, Niihori T, Kanno J, Narumi Y, Narisawa A, Kato K, Aoki Y, Ikeda K, Kobayashi TMatsubara Y: A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype-phenotype correlation. J Hum Genet; 51: 455-60, 2006

9)   Hirota T, Hasegawa K, Obara K, Matsuda A, Akahoshi M, Nakashima K, Shirakawa T, Doi S, Fujita K, Suzuki Y, Nakamura YTamari M: Association between ADAM33 polymorphisms and adult asthma in the Japanese population. Clin Exp Allergy; 36: 884-91, 2006

10) 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 C J, Yang T K, Lee J Y, Kimm KInoue I: A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms. Hum Mol Genet; 15: 1722-34, 2006

 

2005

1)   Yokosuka O, Kawai S, Suzuki Y, Fukai K, Imazeki F, Kanda T, Tada M, Mikata R, Hata ASaisho H: Evaluation of clinical usefulness of second-generation HCV core antigen assay: comparison with COBAS AMPLICOR HCV MONITOR assay version 2.0. Liver Int; 25: 1136-41, 2005

2)   Suzuki Y, Yang X, Aoki Y, Kure SMatsubara Y: Mutations in the holocarboxylase synthetase gene HLCS. Hum Mutat; 26: 285-290, 2005

3)   Niihori T, Aoki Y, Ohashi H, Kurosawa K, Kondoh T, Ishikiriyama S, Kawame H, Kamasaki H, Yamanaka T, Takada F, Nishio K, Sakurai M, Tamai H, Nagashima T, Suzuki Y, Kure S, Fujii K, Imaizumi MMatsubara Y: Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. J Hum Genet; 50: 192-202, 2005

4)   Hirota T, Suzuki Y, Hasegawa K, Obara K, Matsuda A, Akahoshi M, Nakashima K, Cheng L, Takahashi N, Shimizu M, Doi S, Fujita K, Enomoto T, Ebisawa M, Yoshihara S, Nakamura Y, Kishi F, Shirakawa TTamari M: Functional haplotypes of IL-12B are associated with childhood atopic asthma. J Allergy Clin Immunol; 116: 789-95, 2005

5)   Hiraide A, Imazeki F, Yokosuka O, Kanda T, Kojima H, Fukai K, Suzuki Y, Hata ASaisho H: Fas polymorphisms influence susceptibility to autoimmune hepatitis. Am J Gastroenterol; 100: 1322-9, 2005

6)   Aoki Y, Niihori T, Kawame H, Kurosawa K, Ohashi H, Tanaka Y, Filocamo M, Kato K, Suzuki Y, Kure SMatsubara Y: Germline mutations in HRAS proto-oncogene cause Costello syndrome. Nat Genet; 37: 1038-40, 2005

 

2004

1)   Yang X, Sakamoto O, Matsubara Y, Kure S, Suzuki Y, Aoki Y, Yamaguchi S, Takahashi Y, Nishikubo T, Kawaguchi C, Yoshioka A, Kimura T, Hayasaka K, Kohno Y, Iinuma KOhura T: Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia. Mol Genet Metab; 81: 335-42, 2004

2)   Yang X, Sakamoto O, Matsubara Y, Kure S, Suzuki Y, Aoki Y, Suzuki Y, Sakura N, Takayanagi M, Iinuma KOhura T: Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent MMAA mutation. Mol Genet Metab; 82: 329-33, 2004

3)   Yamazaki K, Takazoe M, Tanaka T, Ichimori T, Saito S, Iida A, Onouchi Y, Hata ANakamura Y: Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease. J Hum Genet; 49: 664-8, 2004

4)   Tomita Y, Tomida S, Hasegawa Y, Suzuki Y, Shirakawa T, Kobayashi THonda H: Artificial neural network approach for selection of susceptible single nucleotide polymorphisms and construction of prediction model on childhood allergic asthma. BMC Bioinformatics; 5: 120, 2004

5)   Shao C, Suzuki Y, Kamada F, Kanno K, Tamari M, Hasegawa K, Aoki Y, Kure S, Yang X, Endo H, Takayanagi R, Nakazawa C, Morikawa T, Morikawa M, Miyabayashi S, Chiba Y, Karahashi M, Saito S, Tamura G, Shirakawa TMatsubara Y: Linkage and association of childhood asthma with the chromosome 12 genes. J Hum Genet; 49: 115-22, 2004

6)   Onouchi Y, Onoue S, Tamari M, Wakui K, Fukushima Y, Yashiro M, Nakamura Y, Yanagawa H, Kishi F, Ouchi K, Terai M, Hamamoto K, Kudo F, Aotsuka H, Sato Y, Nariai A, Kaburagi Y, Miura M, Saji T, Kawasaki T, Nakamura YHata A: CD40 ligand gene and Kawasaki disease. Eur J Hum Genet; 12: 1062-8, 2004

7)   Ohmori H, Ando Y, Makita Y, Onouchi Y, Nakajima T, Saraiva M J, Terazaki H, Suhr O, Sobue G, Nakamura M, Yamaizumi M, Munar-Ques M, Inoue I, Uchino MHata A: Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. J Med Genet; 41: e51, 2004

8)   Kure S, Sato K, Fujii K, Aoki Y, Suzuki Y, Kato SMatsubara Y: Wild-type phenylalanine hydroxylase activity is enhanced by tetrahydrobiopterin supplementation in vivo: an implication for therapeutic basis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. Mol Genet Metab; 83: 150-6, 2004

9)   Kojima K, Kure S, Kamada F, Hao K, Ichinohe A, Sato K, Aoki Y, Yoichi S, Kubota M, Horikawa R, Utsumi A, Miura M, Ogawa S, Kanazawa M, Kohno Y, Inokuchi M, Hasegawa T, Narisawa KMatsubara Y: Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118R. Mol Genet Metab; 81: 343-6, 2004

10) Kobashi G, Washio M, Okamoto K, Sasaki S, Yokoyama T, Miyake Y, Sakamoto N, Ohta K, Inaba YTanaka H: High body mass index after age 20 and diabetes mellitus are independent risk factors for ossification of the posterior longitudinal ligament of the spine in Japanese subjects: a case-control study in multiple hospitals. Spine; 29: 1006-10, 2004

11) Kobashi G, Hata A, Ohta K, Yamada H, Kato E H, Minakami H, Fujimoto SKondo K: A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene. J Hum Genet; 49: 182-6, 2004

12) Kayano S, Suzuki Y, Kanno K, Aoki Y, Kure S, Yamada AMatsubara Y: Significant association between nonsyndromic oral clefts and arylhydrocarbon receptor nuclear translocator (ARNT). Am J Med Genet; 130A: 40-4, 2004

13) Kanno K, Suzuki Y, Yamada A, Aoki Y, Kure SMatsubara Y: Association between nonsyndromic cleft lip with or without cleft palate and the glutamic acid decarboxylase 67 gene in the Japanese population. Am J Med Genet; 127A: 11-6, 2004

14) Kamada F, Suzuki Y, Shao C, Tamari M, Hasegawa K, Hirota T, Shimizu M, Takahashi N, Mao X Q, Doi S, Fujiwara H, Miyatake A, Fujita K, Chiba Y, Aoki Y, Kure S, Tamura G, Shirakawa TMatsubara Y: Association of the hCLCA1 gene with childhood and adult asthma. Genes Immun; 5: 540-7, 2004

15) Hirota T, Obara K, Matsuda A, Akahoshi M, Nakashima K, Hasegawa K, Takahashi N, Shimizu M, Sekiguchi H, Kokubo M, Doi S, Fujiwara H, Miyatake A, Fujita K, Enomoto T, Kishi F, Suzuki Y, Saito H, Nakamura Y, Shirakawa TTamari M: Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma. J Hum Genet; 49: 370-5, 2004

16) Hasegawa K, Tamari M, Shao C, Shimizu M, Takahashi N, Mao X Q, Yamasaki A, Kamada F, Doi S, Fujiwara H, Miyatake A, Fujita K, Tamura G, Matsubara Y, Shirakawa TSuzuki Y: Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma. Hum Genet; 115: 295-301, 2004

      

17) Tanaka M, Itoh K, Abe S, Imai K, Masuda T, Koga R, Itoh H, Konomi Y, Kinukawa N, Sakata T. Irregular patterns in the daily weight chart at night predict body weight regain. Experimental Biology and Medicine. 229, 940-945, 2004

 

2003

1)   Santer R, Muhle H, Suormala T, Baumgartner E R, Duran M, Yang X, Aoki Y, Suzuki YStephani U: Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects. Mol Genet Metab; 79: 160-6, 2003

2)   Ouchi K, Suzuki Y, Shirakawa TKishi F: Polymorphism of SLC11A1 (formerly NRAMP1) gene confers susceptibility to Kawasaki disease. J Infect Dis; 187: 326-9, 2003

3)   Ohta K, Kobashi G, Hata A, Yamada H, Minakami H, Fujimoto S, Kondo KTamashiro H: Association between a variant of the glutathione S-transferase P1 gene (GSTP1) and hypertension in pregnancy in Japanese: interaction with parity, age, and genetic factors. Semin Thromb Hemost; 29: 653-9, 2003

4)   Ohmori H, Makita Y, Funamizu M, Chiba S, Ohtani K, Suzuki Y, Wakamiya NHata A: Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene. J Hum Genet; 48: 82-5, 2003

5)   Kudo T, Kure S, Ikeda K, Xia A P, Katori Y, Suzuki M, Kojima K, Ichinohe A, Suzuki Y, Aoki Y, Kobayashi TMatsubara Y: Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness. Hum Mol Genet; 12: 995-1004, 2003

6)   Kayano S, Kure S, Suzuki Y, Kanno K, Aoki Y, Kondo S, Schutte B C, Murray J C, Yamada AMatsubara Y: Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion. J Hum Genet; 48: 622-8, 2003

 

2002

1)   Tomida S, Hanai T, Koma N, Honda H, Suzuki YKobayashi T: Artifical Neural Network predictive model for allergic disease using single nucleotide polymorphisms data. J Biosci Bioeng; 93: 470-478, 2002

2)   Ohmori H, Makita Y, Funamizu M, Hirooka K, Hosoi T, Orimo H, Suzuki T, Ikari K, Nakajima T, Inoue IHata A: Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis. J Hum Genet; 47: 400-6, 2002

3)   Ohmi H, Kojima S, Awai Y, Kamata S, Sasaki K, Tanaka Y, Mochizuki Y, Hirooka KHata A: Post-traumatic stress disorder in pre-school aged children after a gas explosion. Eur J Pediatr; 161: 643-8, 2002

4)   Nakamura T, Saionji K, Hiejima Y, Hirayama H, Tago K, Takano H, Tajiri M, Hayashi K, Kawabata M, Funamizu M, Makita YHata A: Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients. Am J Kidney Dis; 39: 1032-9, 2002

5)   Kure S, Kojima K, Ichinohe A, Maeda T, Kalmanchey R, Fekete G, Berg S Z, Filiano J, Aoki Y, Suzuki Y, Izumi TMatsubara Y: Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia. Ann Neurol; 52: 643-6, 2002

6)   Kobashi G, Ohta K, Hata A, Shido K, Yamada H, Fujimoto SKondo K: An association between maternal smoking and preeclampsia in Japanese women. Semin Thromb Hemost; 28: 507-10, 2002

7)   Kobashi G, Hata A, Shido K, Ohta K, Yamada H, Fujimoto SKondo K: The M235T variant of the angiotensinogen gene and the body mass index are useful markers for prevention of hypertension in pregnancy: a tree-based analysis of gene-environment interaction. Semin Thromb Hemost; 28: 501-6, 2002

8)   Kanno K, Suzuki Y, Yang X, Yamada A, Aoki Y, Kure SMatsubara Y: 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. J Hum Genet; 47: 269-74, 2002

9)   Carr A N, Schmidt A G, Suzuki Y, del Monte F, Sato Y, Lanner C, Breeden K, Jing S L, Allen P B, Greengard P, Yatani A, Hoit B D, Grupp I L, Hajjar R J, DePaoli-Roach A AKranias E G: Type 1 phosphatase, a negative regulator of cardiac function. Mol Cell Biol; 22: 4124-35., 2002

10)   l Itoh K, Imai K, Masuda T, Abe S, Tanaka M, Koga R, Itoh H, Matsuyama T, Nakamura M. Relationship between changes in serum leptin levels and blood pressure after weight loss. Hypertension Res. 25, 881-886, 2002

千葉大学大学院 公衆衛生学

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