2019 - 2022 Development of a prediction method for cofactors binding to uncharacterized enzymes using feedback from experimental validations
2018 - 2021 Developing a method for evaluating variants of uncertain significance in humans based on protein structures
2015 - 2018 Development of a method for predicting functional sites in function-unknown splicing isoforms
2015 - 2018 Development of a new method to predict disease-causing mechanisms of missense mutations
2011 - 2013 Analysis of pathophysiology and identification of the causative gene(s) of primary immunodeficiency with B, NK, dendritic cell deficiency
2002 - 2003 タンパク質の配列アライメント法の改良とゲノム機能予測への適用
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Papers (85):
Taichi Shiraishi, Yuta Katayama, Masaaki Nishiyama, Hirotaka Shoji, Tsuyoshi Miyakawa, Taisuke Mizoo, Akinobu Matsumoto, Atsushi Hijikata, Tsuyoshi Shirai, Kouta Mayanagi, et al. The complex etiology of autism spectrum disorder due to missense mutations of CHD8. Molecular Psychiatry. 2024
Dan Tomomasa, Beom Hee Lee, Yuki Hirata, Yuzaburo Inoue, Hidetaka Majima, Yusuke Imanaka, Takaki Asano, Takashi Katakami, Jina Lee, Atsushi Hijikata, et al. Inherited CARD9 deficiency due to a founder effect in east asia. Journal of clinical immunology. 2024. 44. 5. 121-121
Atsushi Hijikata, Mikita Suyama, Shingo Kikugawa, Ryo Matoba, Takuya Naruto, Yumi Enomoto, Kenji Kurosawa, Naoki Harada, Kumiko Yanagi, Tadashi Kaname, et al. Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencing. Nucleic Acids Research. 2024
Shogo Wada, Takeshi Namiki, Aoi Ebata, Takuya Takeichi, Masashi Akiyama, Masafumi Yamada, Atsushi Hijikata, Yutaka Shimomura, Hirokazu Kanegane, Naoko Okiyama. Generalisierte pustulöse Psoriasis, die sich bei einem Patienten mit einer NFKB2-Variante entwickelte. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 2024
Shogo Wada, Takeshi Namiki, Aoi Ebata, Takuya Takeichi, Masashi Akiyama, Masafumi Yamada, Atsushi Hijikata, Yutaka Shimomura, Hirokazu Kanegane, Naoko Okiyama. Generalized pustular psoriasis that developed in a patient with an NFKB2 variant. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 2024