Aritoshi Iida

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 11

Top Venues

Nature communications

Human genome variation

Molecular genetics & genomic medicine

Sleep

This page only lists publications with an associated author ORCID identifier.

Publications

Akiko Hida, Aritoshi Iida, Motoki Ukai, Hiroshi Kadotani, Makoto Uchiyama, Takashi Ebisawa, Yuichi Inoue, Shingo Kitamura, Kazuo Mishima
Novel CLOCK and NR1D2 variants in 64 sighted Japanese individuals with non-24-hour sleep-wake rhythm disorder. Sleep (2023)
Yosuke Kawai, Yusuke Watanabe, Yosuke Omae, Reiko Miyahara, Seik-Soon Khor, Eisei Noiri, Koji Kitajima, Hideyuki Shimanuki, Hiroyuki Gatanaga, Kenichiro Hata, Kotaro Hattori, Aritoshi Iida, Hatsue Ishibashi-Ueda, Tadashi Kaname, Tatsuya Kanto, Ryo Matsumura, Kengo Miyo, Michio Noguchi, Kouichi Ozaki, Masaya Sugiyama, Ayako Takahashi, Haruhiko Tokuda, Tsutomu Tomita, Akihiro Umezawa, Hiroshi Watanabe, Sumiko Yoshida, Yu-Ichi Goto, Yutaka Maruoka, Yoichi Matsubara, Shumpei Niida, Masashi Mizokami, Katsushi Tokunaga
Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis. PLoS genetics 19 (12) (2023)
Hong Joo Kim, Payam Mohassel, Sandra Donkervoort, Lin Guo, Kevin O'Donovan, Maura Coughlin, Xaviere Lornage, Nicola Foulds, Simon R Hammans, A Reghan Foley, Charlotte M Fare, Alice F Ford, Masashi Ogasawara, Aki Sato, Aritoshi Iida, Pinki Munot, Gautam Ambegaonkar, Rahul Phadke, Dominic G O'Donovan, Rebecca Buchert, Mona Grimmel, Ana Töpf, Irina T Zaharieva, Lauren Brady, Ying Hu, Thomas E Lloyd, Andrea Klein, Maja Steinlin, Alice Kuster, Sandra Mercier, Pascale Marcorelles, Yann Péréon, Emmanuelle Fleurence, Adnan Manzur, Sarah Ennis, Rosanna Upstill-Goddard, Luca Bello, Cinzia Bertolin, Elena Pegoraro, Leonardo Salviati, Courtney E French, Andriy Shatillo, F Lucy Raymond, Tobias B Haack, Susana Quijano-Roy, Johann Böhm, Isabelle Nelson, Tanya Stojkovic, Teresinha Evangelista, Volker Straub, Norma B Romero, Jocelyn Laporte, Francesco Muntoni, Ichizo Nishino, Mark A Tarnopolsky, James Shorter, Carsten G Bonnemann, J Paul Taylor
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy. Nature communications 13 (1) (2022)
Chihiro Abe-Hatano, Aritoshi Iida, Shunichi Kosugi, Yukihide Momozawa, Chikashi Terao, Keiko Ishikawa, Mariko Okubo, Yasuo Hachiya, Hiroya Nishida, Kazuyuki Nakamura, Rie Miyata, Chie Murakami, Kan Takahashi, Kyoko Hoshino, Haruko Sakamoto, Sayaka Ohta, Masaya Kubota, Eri Takeshita, Akihiko Ishiyama, Eiji Nakagawa, Masayuki Sasaki, Mitsuhiro Kato, Naomichi Matsumoto, Yoichiro Kamatani, Michiaki Kubo, Yoshiyuki Takahashi, Jun Natsume, Ken Inoue, Yu-Ichi Goto
Whole genome sequencing of 45 Japanese patients with intellectual disability. American journal of medical genetics. Part A 185 (5) (2021)
Long Guo, Aritoshi Iida, Gandham SriLakshmi Bhavani, Kalpana Gowrishankar, Zheng Wang, Jing-Yi Xue, Juan Wang, Noriko Miyake, Naomichi Matsumoto, Takanori Hasegawa, Yusuke Iizuka, Masashi Matsuda, Tomoki Nakashima, Masaki Takechi, Sachiko Iseki, Shinsei Yambe, Gen Nishimura, Haruhiko Koseki, Chisa Shukunami, Katta Mohan Girisha, Shiro Ikegawa
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling. Nature communications 12 (1) (2021)
Yukako Nishimori, Aritoshi Iida, Masashi Ogasawara, Mariko Okubo, Yuki Yonenobu, Makoto Kinoshita, Kazuma Sugie, Satoru Noguchi, Ichizo Nishino
TNNI1 Mutated in Autosomal Dominant Proximal Arthrogryposis. Neurology. Genetics 8 (1) (2021)
Yoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, Madoka Mori-Yoshimura, Yasushi Oya, Akihiko Ishiyama, Hirofumi Komaki, Seigo Nakamura, Susumu Fujikawa, Takashi Kanda, Misaki Yamadera, Hiroshi Sakiyama, Shinichiro Hayashi, Ikuya Nonaka, Satoru Noguchi, Ichizo Nishino
ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features. Neurology 95 (11) (2020)
Aritoshi Iida, Kyoko Takano, Eri Takeshita, Chihiro Abe-Hatano, Shinichi Hirabayashi, Yuji Inaba, Shunichi Kosugi, Yoichiro Kamatani, Yukihide Momozawa, Michiaki Kubo, Eiji Nakagawa, Ken Inoue, Yu-Ichi Goto
A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature. Cold Spring Harbor molecular case studies 5 (6) (2019)
Atsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, Mariko Okubo, Yasushi Oya, Gaku Yamanaka, Ikuko Takahashi, Ikuya Nonaka, Satoru Noguchi, Ichizo Nishino
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathy. Molecular genetics & genomic medicine 7 (5) (2019)
Shumpei Uchino, Aritoshi Iida, Atsushi Sato, Keiko Ishikawa, Masakazu Mimaki, Ichizo Nishino, Yu-Ichi Goto
A novel compound heterozygous variant of ECHS1 identified in a Japanese patient with Leigh syndrome. Human genome variation 6 (2019)
Aritoshi Iida, Eri Takeshita, Shunichi Kosugi, Yoichiro Kamatani, Yukihide Momozawa, Michiaki Kubo, Eiji Nakagawa, Kenji Kurosawa, Ken Inoue, Yu-Ichi Goto
A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation. Human genome variation 6 (2018)

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Publication Activity (10 Years)

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Aritoshi Iida