Miyagawa T - Search Results

1

A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia.

Miyagawa T, Tanaka S, Shimada M, Sakai N, Tanida K, Kotorii N, Kotorii T, Ariyoshi Y, Hashizume Y, Ogi K, Hiejima H, Kanbayashi T, Imanishi A, Ikegami A, Kamei Y, Hida A, Wada Y, Miyamoto M, Takami M, Kondo H, Tamura Y, Taniyama Y, Omata N, Mizuno T, Moriya S, Furuya H, Kato M, Kato K, Ishigooka J, Tsuruta K, Chiba S, Yamada N, Okawa M, Hirata K, Kuroda K, Kume K, Uchimura N, Kitada M, Kodama T, Inoue Y, Nishino S, Mishima K, Tokunaga K, Honda M. Miyagawa T, et al. NPJ Genom Med. 2022 Apr 12;7(1):29. doi: 10.1038/s41525-022-00298-w. NPJ Genom Med. 2022. PMID: 35414074 Free PMC article.

2

Significant association of a single nucleotide polymorphism in the tumor necrosis factor-alpha (TNF-alpha) gene promoter with human narcolepsy.

Hohjoh H, Nakayama T, Ohashi J, Miyagawa T, Tanaka H, Akaza T, Honda Y, Juji T, Tokunaga K. Hohjoh H, et al. Among authors: miyagawa t. Tissue Antigens. 1999 Aug;54(2):138-45. doi: 10.1034/j.1399-0039.1999.540204.x. Tissue Antigens. 1999. PMID: 10488740

3

Identification of a telomeric boundary of the HLA region with potential for predisposition to human narcolepsy.

Miyagawa T, Hohjoh H, Honda Y, Juji T, Tokunaga K. Miyagawa T, et al. Immunogenetics. 2000 Nov;52(1-2):12-8. doi: 10.1007/s002510000245. Immunogenetics. 2000. PMID: 11132147

4

Case-control study with narcoleptic patients and healthy controls who, like the patients, possess both HLA-DRB1*1501 and -DQB1*0602.

Hohjoh H, Terada N, Nakayama T, Kawashima M, Miyagawa T, Honda Y, Tokunaga K. Hohjoh H, et al. Among authors: miyagawa t. Tissue Antigens. 2001 Mar;57(3):230-5. doi: 10.1034/j.1399-0039.2001.057003230.x. Tissue Antigens. 2001. PMID: 11285131

5

Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.

Miyagawa T, Kawashima M, Nishida N, Ohashi J, Kimura R, Fujimoto A, Shimada M, Morishita S, Shigeta T, Lin L, Hong SC, Faraco J, Shin YK, Jeong JH, Okazaki Y, Tsuji S, Honda M, Honda Y, Mignot E, Tokunaga K. Miyagawa T, et al. Nat Genet. 2008 Nov;40(11):1324-8. doi: 10.1038/ng.231. Epub 2008 Sep 28. Nat Genet. 2008. PMID: 18820697

6

Genome-wide association study of panic disorder in the Japanese population.

Otowa T, Yoshida E, Sugaya N, Yasuda S, Nishimura Y, Inoue K, Tochigi M, Umekage T, Miyagawa T, Nishida N, Tokunaga K, Tanii H, Sasaki T, Kaiya H, Okazaki Y. Otowa T, et al. Among authors: miyagawa t. J Hum Genet. 2009 Feb;54(2):122-6. doi: 10.1038/jhg.2008.17. Epub 2009 Jan 23. J Hum Genet. 2009. PMID: 19165232

7

Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia).

Miyagawa T, Honda M, Kawashima M, Shimada M, Tanaka S, Honda Y, Tokunaga K. Miyagawa T, et al. PLoS One. 2009;4(4):e5394. doi: 10.1371/journal.pone.0005394. Epub 2009 Apr 30. PLoS One. 2009. PMID: 19404393 Free PMC article.

8

Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotype.

Miyagawa T, Honda M, Kawashima M, Shimada M, Tanaka S, Honda Y, Tokunaga K. Miyagawa T, et al. J Hum Genet. 2010 Jan;55(1):63-5. doi: 10.1038/jhg.2009.118. Epub 2009 Nov 20. J Hum Genet. 2010. PMID: 19927159

9

Anti-Tribbles homolog 2 autoantibodies in Japanese patients with narcolepsy.

Toyoda H, Tanaka S, Miyagawa T, Honda Y, Tokunaga K, Honda M. Toyoda H, et al. Among authors: miyagawa t. Sleep. 2010 Jul;33(7):875-8. doi: 10.1093/sleep/33.7.875. Sleep. 2010. PMID: 20614847 Free PMC article.

10

An approach based on a genome-wide association study reveals candidate loci for narcolepsy.

Shimada M, Miyagawa T, Kawashima M, Tanaka S, Honda Y, Honda M, Tokunaga K. Shimada M, et al. Among authors: miyagawa t. Hum Genet. 2010 Oct;128(4):433-41. doi: 10.1007/s00439-010-0862-z. Epub 2010 Jul 31. Hum Genet. 2010. PMID: 20677014

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