2018 - 2021 Molecular, Cellular, and in vivo analysis of SLC12A2, a novel candidate of deafness gene
2018 - 2020 Elucidation of prevalence, clinical features and pathogenic mechanism of PDZD7 mutations which was identified as a novel gene causing nonsyndromic hearing loss
2017 - 2019 Analysis of causative genes for mid-frequency hearing loss using next-generation sequencing
2016 - 2019 Microbiomes of the Normal Middle Ear and Ears With Chronic Otitis Media
2015 - 2018 Molecular functional analysis of ZBTB10, the novel candidate deafness gene associated with cochlear nerve hypoplasia
2012 - 2015 Elucidation of novel genes causing auditory neuropathy
2012 - 2015 Attenuation of Progressive Hearing Loss in DBA/2J Mice by Epigenetic-Modifying Reagents
2012 - 2014 Study of responsible genes for cochlea and cochlear nerve dysplasia
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Papers (80)：
Marie N Shimanuki, Makoto Hosoya, Takanori Nishiyama, Takeshi Wakabayashi, Masafumi Ueno, Hiroyuki Ozawa, Hideki Mutai, Kiyomitsu Nara, Tatsuo Matsunaga, Naoki Oishi. Detailed characterization of auditory neuropathy in Perrault syndrome with TWNK variants. Auris, nasus, larynx. 2024. 51. 6. 933-939
Chika Saegusa, Hideki Mutai, Tsubasa Saeki, Saeko Matsuzaki, Akifumi Mizukoshi, Shin-Ichiro Kitajiri, Tatsuo Matsunaga, Makoto Hosoya, Hideyuki Okano, Masato Fujioka. Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene. Stem cell research. 2024. 79. 103489-103489
Namba K, Mutai H, Matsunaga T, Kaneko H. Structural basis for pathogenic variants of GJB2 and hearing levels of patients with hearing loss. BMC Res Notes. 2024. 17. 131
Kosuke Hashimoto, Toru Miwa, Chie Ono, Kiyomitsu Nara, Hideki Mutai, Toshiyuki Seto, Hirokazu Sakamoto, Tatsuo Matsunaga. Gap Junction Beta-2 p.Val84Met Can Cause Autosomal Dominant Syndromic Hearing Loss With Keratoderma. Cureus. 2024. 16. 2. e54992
