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J-GLOBAL ID：201801011951118702   Update date: Mar. 19, 2025

Aritoshi Iida

イイダ アリトシ | Aritoshi Iida
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Affiliation and department：
National Center of Neurology and Psychiatry

About National Center of Neurology and Psychiatry


Research field  (3)： Genetics ,  Medical biochemistry ,  Genomics
Research keywords  (2)： 遺伝医学 ,  ゲノム科学
Research theme for competitive and other funds  (5)：
  • 2013 - 2016 Searching for factors associated with progression and prognosis in patients with sporadic amyotrophic lateral sclerosis
  • 2011 - 2013 Elucidation of molecular pathogenesis of amyotrophic lateral sclerosis based on genome analysis
  • 2007 - 2008 Large-scale genome association study of amyotrophic lateral sclerosis in Japanese
  • 1998 - 1999 ポジショナルクローニング法を用いた多脾症/左右内臓逆位原因遺伝子の検索
  • 1996 - 1999 乳癌の遺伝子診断法の確立
Papers (153)：
  • Shunsuke Funaguma, Aritoshi Iida, Yoshihiko Saito, Jantima Tanboon, Francia Victoria De Los Reyes, Kyuto Sonehara, Yu-ichi Goto, Yukinori Okada, Shinichiro Hayashi, Ichizo Nishino. Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosis. Nature Communications. 2025. 16. 1
  • Aki Murayama, Utako Nagaoka, Keizo Sugaya, Rui Shimazaki, Kazuhito Miyamoto, Shiro Matsubara, Masashi Ogasawara, Aritoshi Iida, Ichizo Nishino, Kazushi Takahashi. Sequential development of parkinsonism in two patients with oculopharyngodistal type myopathy in GIPC1-related repeat expansion disorder. Neuromuscular disorders : NMD. 2024. 44. 104465-104465
  • Takeshi Imai, Mitsuhashi S, Isahaya K, Shibata S, Yosuke Kawai, Omae Y, Tokunaga K, NCBN Controls WGS Consortium, Yamano Y. Wilson disease (novel ATP7B variants) with concomitant FLNC-related cardiomyopathy. Human genome variation. 2024. 11. 1. 34
  • Kenta Orimo, Mitsui J, Takashi Matsukawa, Tanaka M, Nomoto J, Hiroyuki Ishiura, Omae Y, Yosuke Kawai, Katsushi Tokunaga, NCBN Controls WGS Consortium, et al. Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genome. Journal of human genetics. 2024. 69. 12. 613-621
  • Pongpakdee S., Apiwattanakul M., Termglinchan T., Witoonpanich R., Dejthevaporn C., Lee T., Wansophonkul S., Yamanaka A., Funaguma S., Iida A., et al. CGG/CCG Repeat Expansions in LOC642361/NUTM2B-AS1 in Thai Patients With Oculopharyngodistal Myopathy. Neurol Genet. 2024. 10. 4. e200170.
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MISC (84)：
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Patents (14)：
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Professional career (1)：
  • 博士(医学)
Association Membership(s) (1)：
THE JAPAN SOCIETY OF HUMAN GENETICS
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

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