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International Journal of Pediatric Otorhinolaryngology|July 22, 2021
Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiersMakoto Hosoya, Masato Fujioka, Kiyomitsu Nara, et al.Mitochondrion|May 22, 2025
Auditory neuropathy spectrum disorder and related auditory features in patients with hearing loss associated with the MT-TS1 m.7471dup variantShujiro Minami, Amina Kida, Satomi Inoue, et al.International Journal of Alzheimer'S Disease|August 31, 2011
High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid: A Possible Extension toward Alzheimer's Disease Biomarker DevelopmentKeiro Shirotani, Satoshi Futakawa, Kiyomitsu Nara, et al.Scientific Reports|April 22, 2023
Correlation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2-related schwannomatosisNaoki Oishi, Masaru Noguchi, Masato Fujioka, et al.Plos Genetics|April 16, 2020
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humansHideki Mutai, Koichiro Wasano, Yukihide Momozawa, et al.Journal of Biochemistry|August 8, 2013
Lectin-dependent inhibition of antigen-antibody reaction: application for measuring α2,6-sialylated glycoforms of transferrinKyoka Hoshi, Yoshinobu Kariya, Kiyomitsu Nara, et al.Scientific Reports|January 20, 2022
Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndromeMasatsugu Masuda, Ayako Kanno, Kiyomitsu Nara, et al.Auris, Nasus, Larynx|June 20, 2020
Differences in hearing levels between siblings with hearing loss caused by GJB2 mutationsMasato Fujioka, Makoto Hosoya, Kiyomitsu Nara, et al.Neurobiology of Aging|April 5, 2011
A unique N-glycan on human transferrin in CSF: a possible biomarker for iNPHSatoshi Futakawa, Kiyomitsu Nara, Masakazu Miyajima, et al.Human Genetics|January 4, 2025
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity searchHideki Mutai, Fuyuki Miya, Kiyomitsu Nara, et al.Pageof 3