Genome-wide association studies (GWAS) have identified several susceptibility loci for bipolar disorder (BP), most notably ANK3. However, most of the inherited risk for BP remains unexplained. One reason for the limited success may be the genetic heterogeneity of BP. Clinical sub-phenotypes of BP ma
Preliminary genome-wide association study of bipolar disorder in the Japanese population
β Scribed by Eiji Hattori; Tomoko Toyota; Yuichi Ishitsuka; Yoshimi Iwayama; Kazuo Yamada; Hiroshi Ujike; Yukitaka Morita; Masafumi Kodama; Kenji Nakata; Yoshio Minabe; Kazuhiko Nakamura; Yasuhide Iwata; Nori Takei; Norio Mori; Hiroshi Naitoh; Yoshio Yamanouchi; Nakao Iwata; Norio Ozaki; Tadafumi Kato; Toru Nishikawa; Atsushi Kashiwa; Mika Suzuki; Kunihiko Shioe; Manabu Shinohara; Masami Hirano; Shinichiro Nanko; Akihisa Akahane; Mikako Ueno; Naoshi Kaneko; Yuichiro Watanabe; Toshiyuki Someya; Kenji Hashimoto; Masaomi Iyo; Masanari Itokawa; Makoto Arai; Masahiro Nankai; Toshiya Inada; Sumiko Yoshida; Hiroshi Kunugi; Michiko Nakamura; Yoshimi Iijima; Yuji Okazaki; Teruhiko Higuchi; Takeo Yoshikawa
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 128 KB
- Volume
- 150B
- Category
- Article
- ISSN
- 1552-4841
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A variable number tandem repeat (VNTR) polymorphism consisting of multiple copies of a 17-bp repeat in the second intron of the serotonin transporter gene (SERT) has been reported. Different alleles of this VNTR have been found to be associated with bipolar disorder and schizophrenia. These findings