Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population-Reference-Cited by-同舟云学术

Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population

Published:2010-05-07 Issue:7 Volume:55 Page:473-476
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Matsushita Tomonaga,Umeno Junji,Hirakawa Yoichiro,Yonemoto Koji,Ashikawa Kyota,Amitani Hanae,Ninomiya Toshiharu,Hata Jun,Doi Yasufumi,Kitazono Takanari,Iida Mitsuo,Nakamura Yusuke,Kiyohara Yutaka,Kubo Michiaki

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201045.pdf

Reference10 articles.

1. Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661–678 (2007).

2. Myocardial Infarction Genetics Consortium. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat. Genet. 41, 334–341 (2009).

3. McPherson, R., Pertsemlidis, A., Kavaslar, N., Stewart, A., Roberts, R., Cox, D. R. et al. A common allele on chromosome 9 associated with coronary heart disease. Science 316, 1488–1491 (2007).

4. Ikram, M. A., Seshadri, S., Bis, J. C., Fornage, M., DeStefano, A. L., Aulchenko, Y. S. et al. Genomewide association studies of stroke. N. Engl. J. Med. 360, 1718–1728 (2009).

5. Kubo, M., Hata, J., Ninomiya, T., Matsuda, K., Yonemoto, K., Nakano, T. et al. A nonsynonymous SNP in PRKCH (protein kinase Cη) increases the risk of cerebral infarction. Nat. Genet. 39, 212–217 (2007).

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