教室案内

論文実績

2018年

  • Takahashi M, Arai Y, Sakuma N, Yabuki K, Sano D, Nishimura G, Oridate N, Usami SI. Cochlear volume as a predictive factor for residual-hearing preservation after conventional cochlear implantation. Acta otolaryngol. 138(4): 345-350. 2018
  • Ikezono T, Matsumura T, Matsuda H, Shikaze S, Saitoh S, Shindo S, Hasegawa S, Oh SH, Hagiwara Y, Ogawa Y, sato H, Tono T, Araki R, maeda Y, Usami SI, Kase Y. The diagnostic performance of a novel ELISA for human CTP (Cochlin-tomoprotein) to detect perilymph leakage. PLoS One. 13(1): e0191498. 2018
  • Moteki H, Isaka Y, Inaba Y, Motobayashi M, Nishio SY, Ohira S, Yano T, Iwasaki S, Shiozawa T, Koike K, Usami SI. A rational approach to identifying newborns with hearing loss caused by congenital cytomegalovirus infection by dried blood spot screening. Acta otolaryngol. 138(8): 708-712. 2018
  • Kobayashi M, Miyagawa M, Nishio SY, Moteki H, Fujikawa T, Ohyama K, Sakaguchi H, Miyanohara I, Sugaya A, Naito Y, Morita SY, Kanda Y, Takahashi M, Ishikawa K, Nagano Y, Tono T, Oshikawa C, Kihara C, Takahashi H, Noguchi Y, Usami SI. WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis. PLoS One. 13(3): e0193359. 2018
  • Nishio SY, Moteki H, Usami SI. Simple and efficient germline copy number variant visualization method for the Ion AmpliSeq™ custom panel. Mol Genet Genomic Med. 678-686. 2018
  • Moteki H, Fujinaga Y, Goto T,Usami SI. Pneumolabyrinth, intracochlear and vestibular fluid loss after cochlear implantation. Auris Nasus Larynx. 45: 1116-1120. 2018
  • Usami SI, Nishio SI. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. GeneReviews(NCBI Bookshelf). 2018
  • Nakatani T, Ueda S, Nishio SI, Usami SI. Introgressive Hybridization of the Erebia ligea Complex(Lepidoptera, Nymphalidae) in the Far Eastern Region. Butterfly Science. 11: 26-37. 2018
  • Abe S, Takeda H, Nishio SY, Usami SI. Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation. Human Genome Variation. 5(23): 1-4. 2018
  • Nakatani T, Ueda S, Nishio SY, Usami SI. Molecular Phylogeny of the Genus Erebia(Lepidoptera,Nymphalidae,Satyrinae) : Species Groups Inferred from Mitochondrial and Nucleus Gene Sequences. Butterfly Science. 12: 27-48. 2018
  • Abe S, Nishio SY,Yokota Y, Moteki H, Kumakawa K, Usami SI. Diagnostic pitfalls for GJB2-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss. Cin Case Rep. 6: 2111-2116. 2018
  • Iwasa YI, Tsukada K, Kobayashi M, Kitano T, Mori K, Yoshimura H, Fukuoka H, Usami SI. Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI. PLoS One. 13(12): e0206891. 2018

2017年

  • Moteki H, Nishio S, Miyagawa M, Tsukada K, Iwasaki S, Usami S. Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing. Acta Otolaryngol. 137(5): 516-521.2017
  • Korver AM, Smith RJ, Van Camp G, Schleiss MR, Bitner-Glindzicz MA, Lustig LR, Usami SI, Boudewyns AN. Congenital hearing loss. Nat Rev Dis Primers. 3:16094. 2017
  • Nishio SY, Usami SI. The Clinical Next-Generation Sequencing Database: A Tool for the Unified Management of Clinical Information and Genetic Variants to Accelerate Variant Pathogenicity Classification. Hum Mutat. 38(3): 252-259. 2017
  • Van de Heyning P1, T_vora-Vieira D, Mertens G, Van Rompaey V, Rajan GP, M_ller J, Hempel JM, Leander D, Polterauer D, Marx M, Usami SI, Kitoh R, Miyagawa M, Moteki H, Smilsky K, Baumgartner WD, Keintzel TG, Sprinzl GM, Wolf-Magele A, Arndt S, Wesarg T, Zirn S, Baumann U, Weissgerber T, Rader T, Hagen R, Kurz A, Rak K, Stokroos R, George E, Polo R, Medina M, Henkin Y, Hilly O, Ulanovski D, Rajeswaran R, Kameswaran M, Di Gregorio MF, Zernotti ME. Towards a Unified Testing Framework for Single-Sided Deafness Studies: A Consensus Paper. Audiol Neurootol. 21(6): 391-398.2017
  • Morita S, Fujiwara K, Fukuda A, Fukuda S, Nishio SY, Kitoh R, Hato N, Ikezono T, Ishikawa K, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Nishizaki K, Ogawa K, Sano H, Sato H, Sone M, Suzuki M, Takahashi H, Tono T, Yamashita H, Yamasoba T, Usami SI. The clinical features and prognosis of mumps-associated hearing loss: a retrospective, multi-institutional investigation in Japan. Acta Otolaryngol. 137(sup565): S44-S47. 2017
  • Nishio SY, Takumi Y, Usami SI Laser-capture micro dissection combined with next-generation sequencing analysis of cell type-specific deafness gene expression in the mouse cochlea. Hear Res. 348:87-97.2017
  • Noguchi Y, Fukuda S, Fukushima K, Gyo K, Hara A, Nakashima T, Ogawa K, Okamoto M, SatoH, Usami SI, Yamasoba T, Yokoyama T, Kitamura K. A nationwide study on enlargement of the vestibular aqueduct in Japan. Auris Nasus Larynx. 44(1): 33-39.2017
  • Okada M, Hato N, Nishio SY, Kitoh R, Ogawa K, Kanzaki S, Sone M, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami SI. The effect of initial treatment on hearing prognosis in idiopathic sudden sensorineural hearing loss: a nationwide survey in Japan. Acta Otolaryngol. 137(sup565):S30-S33. 2017
  • Usami SI, Kitoh R, Moteki H, Nishio SY, Kitano T, Kobayashi M, Shinagawa J, Yokota Y, Sugiyama K, Watanabe K. Etiology of single-sided deafness and asymmetrical hearing loss. Acta Otolaryngol. 137(sup565): S2-S7. 2017
  • Kitoh R, Nishio SY, Ogawa K, kanzaki S, Hato N, Sone M, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami SI, Nationwide epidemiological survey of idiopathic sudden sensorineural hearing loss in Japan. Acta Otolaryngol. 137(sup565): S8-S16. 2017
  • Wada T, Sano H, Nishio SY Kitoh R, Ikezono T, Iwasaki S, Kaga k, matsubara A, Matsunaga T, Murata T, naito Y, Suzuki M, Takahashi H, Tono T, Yamashita H, Hara A, Usami SI. Differences between acoustic trauma and other types of acute noise-induced hearing loss in terms of treatment and hearing prognosis. Acta Otolaryngol. 137(sup565): S48-S52. 2017
  • Kitoh R, Nishio SY, Usami SI. Prognostic impact of gene polymorphisms in patients with idiopathic sudden sensorineural hearing loss. Acta Otolaryngol. 137(sup565): S24-S29. 2017
  • Umesawa M, Kobashi G, Kitoh R, Nishio SY, Ogawa K, Hato N, Sone M, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami SI. Relationships among drinking and smoking habits, history of diseases, body mass index and idiopathic sudden sensorineural hearing loss in Japanese patients. Acta Otolaryngol. 137(sup565): S17-S23. 2017
  • Usami SI. Acute sensorineural hearing loss. Acta Otolaryngol. 137(sup565): S1. 2017
  • Matsuda H, Sakamoto K, Matsumura T, Saito S, Shindo S, Fukushima K, Nishio SY, Kitoh R, Shibasaki O, Ito A, Araki R, Usami SI Suzuki M, Ogawa K, Hasegawa T, Hagiwara Y, Kase Y, Ikezono T. A nationwide multicenter study of the Cochlin tomo-protein detection test: clinical characteristics of perilymphatic fistula cases. Acta Otolaryngol. 137(sup565): S53-S59. 2017
  • Sato H, Kuwashima S, Nishio SY, Kitoh R, Fukuda S, Hara A, Hato N, Ikezono T, Ishikawa K, Iwasaki S, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Ogawa K, Sano H, Sone M, Shojaku H, Takahashi H, Tono T, Yamashita H, Yamasoba T, Usami SI. Epidemiological survey of acute low-tone sensorineural hearing loss. Acta Otolaryngol. 137(sup565): S34-S37. 2017
  • Nishio SY, Usami SI. Outcomes of cochlear implantation for the patients with specific genetic etiologies: a systematic literature review. Acta Otolaryngol. 137(7): 730-742. 2017
  • Yoshida T, Sone M, Kitoh R, Nishio SY, Ogawa K, Kanzaki S, Hato N, Fukuda S, Hara A, Ikezono T, Ishikawa K, Iwasaki S, kaga K, kakehata S, Matsubara A, Matsunaga T, Murata T, Naito Y, Nakagawa T, Nishizaki K, Noguchi Y, Sano H, Sato H, Suzuki M, Shojaku H, Takahashi H, Takeda H, Tono T, Yamashita H, Yamasoba T, Usami SI. Idiopathic sudden sensorineural hearing loss and acute low-tone sensorineural hearing loss: a comparison of the results of a nationwide epidemiological survey in Japan. Acta Otolaryngol. 137(sup565): S38-S59. 2017
  • Kitano T, Miyagawa M, Nishio SY, Moteki H, Oda K, Ohyama K, Miyazaki H, Hidaka H, Nakamura KI, Murata T, Matsuoka R, Ohta Y, Nishiyama N, Kumakawa K, Furutate S, Iwasaki S, Yamada T, Ohta Y, Uehara N, Noguchi Y, Usami SI. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. PLoS ONE. 12(5): e0177636. 2017
  • Iwasaki S, Usami SI, Takahashi H, Kanda Y, Tono T, Doi K, Kumakawa K, Gyo K, Naito Y, Kanzaki S, Yamanaka N, Kaga K. Round Window Application of an Active Middle Ear Implant: A Comparison With Hearing Aid Usage in Japan. Otol Neurotol. 38(6): e145-e151. 2017
  • Arai Y, Takahashi M, Sakuma N, Nishio S, Oridate N, Usami SI. Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar karatoderma Acta Otolaryngol. 2(1): 137-140. 2017
  • Raian G,Tavora-Vieira D,Baumqartner WD,Godey B, M_ller J, O'Driscoll M, Skarzynski H, Skarzynski P, Usami SI,Adunka O,Aqrawal S,Bruce I,De Bodt M,Caversaccio M,Pilsbury H,Gavila　J,Haqen R,haqr A,Kameswaran M,Karltorp E, Kompis M,Kuzovkov V,lassaletta L,Yonqxin L, Lorens A,Manoi M,Martin J,Mertens G,Mlynski R,Parned L,Pulibalathingal S,Radeloff A,Raine CH,Raieswaran R,Schmutzhard J,Sprinzl G,Staecker H,Stephan K,Suqarova S,Zernotti M,Zprpwka P,Van de Heyning P. Hearing preservation cochlear implantation in children: The HEARRING Group consensus and practice guide. Cochlear Implants Int. 26: 1-13. 2017
  • Iki T, Tanaka M, Kitajiri SI, Kita T, Kawasaki Y, Mizukoshi A, Fujibuchi W, nakagawa T, Nakahara T, Ito J, Omori K, Saito MK. Microarray analyses of otospheres derived from the cochlea in the inner ear identify putative transcription factors that regulate the characteristics of otospheres. PLoS ONE 12(6): e0179901. 2017

2016年

  • Yoshimura H, Miyagawa M, Kumakawa K, Nishio S, Usami S. Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing. J Hum Genet. 61: 419-422. 2016
  • Inaba Y, Motobayashi M, Nishioka M, Kaneko T, Yamauchi S, Kawasaki Y, Shiba N, Nishio S, Moteki H, Miyagawa M, Takumi Y, Usami S, Koike K. Correlation between White Matter Lesions and Intelligence Quptient in patients with Congenital Cytomegalovirus Infection. Pediatr Neurol. 55: 52-57. 2016
  • Kitoh R, Moteki H, Nishio S, Shinden S, Kanzaki S, Iwasaki S, Ogawa K, Usami S. The effects of cochlear implantation in Japanese single-sided deafness patients: five case reports. Acta Otolaryngol. 136: 460-464. 2016
  • Kitoh R, Nishio S, Ogawa K, Okamura M Kitamura K, Gyo K, Sato H, Nakashima T, Fukuda S, Fukushima K, Hara A, Yamasoba T, Usami S. SOD1 gene polymorphisms in sudden sensorineural hearing loss. Acta Otolaryngol. 136: 465-469. 2016
  • Miyagawa M, Nishio S, Usami S. A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology. Otol Neurotol. 37(2): e126-134. 2016
  • Sakuma N, Moteki H, Takahashi M, Nishio S, Arai Y, Yamashita Y, Oridate N, Usami S. An effective screening strategy for deafness in combination with a next-generation sequencing platform: a consecutive analysis. J Hum Genet. 61(3): 230-261. 2016
  • Moteki H, Azaiez H, Booth K.T, Shearer A.E, Sloan C.M, Kolbe D.L, Nishio S, Hattori M, Usami S, Smith R.J.H. Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss population. Clin Genet. 89: 466-472. 2016
  • Karino S, Usami S, Kumakawa K, Takahashi H, Tono T, Naito Y, Doi K, Ito K, Suzuki M, Sakata H, Takumi Y, Iwasaki S, Kakigi A, Yamasoba T. Discrimination of Japanese monosyllables in patients with high-frequency hearing loss. Auris Nasus Larynx. 43:269-280. 2016
  • Moteki H, Azaiez H, Sloan-Heggen CM, Booth K, Nishio S, Wakui K, Yamaguchi T, Kolbe DL, Iwasa Y, Shearer AE, Fukushima Y, Smith RJ, Usami S. Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization. Ann Otol Rhinol Laryngol. 125: 918-923. 2016
  • Mori K, Moteki H, Miyagawa M, Nishio SY, Usami S. Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients. PLoS ONE. 11(9): e0162230. 2016
  • Ueyama T, Ninoyu Y, Nishio S, Miyoshi T, Torii H, Nishimura K, Sugahara K, Sakata H, Thumkeo D, Sakaguchi H, Watanabe N, Usami S, Saito N, Kitajiri S. Constitutive activation of DIA1 (DIAPH1) via C-terminal truncation causes human sensorineural hearing loss. EMBO Molecular Medicine. 8(11): 1310-1324. 2016
  • Moteki H, Nishio S, Miyagawa M, Tsukada K, Iwasaki S, Usami S. Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing. Acta Otolaryngol. 2016
  • Iwasa Y, Nishio S, Usami S. Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients. PLoS One. 11(12): e0166781. 2016
  • Noguchi Y, Fukuda S, Fukushima K, Gyo K, Hara A, Nakashima T, Ogawa K, Okamoto M, Sato H, Usami S, Yamasoba T, Yokoyama T, Kitamura K. A nationwide study on enlargement of the vestibular aqueduct in Japan. Auris Nasus Larynx. 2016
  • Noguchi Y, Takahashi M, Ito T, Fujikawa T, Kawashima Y, Kitamura K. Delayed restoration of maximum speech discrimination scores in patients with idiopathic sudden sensorineural hearing loss. Auris Nasus Larynx. 43: 495-500. 2016

2015年

  • Moteki H, Kitoh R, Tsukada K, Iwasaki S, Nishio S, Usami S.
    The advantages of sound localization and speech perception of bilateral electric acoustic stimulation.
    Acta Otolaryngol 135(2):147-153.2015
  • Nishio S, Hayashi Y, Watanabe M, Usami S.
    Clinical application of a custom AmpliSeq library and ion torrent PGM sequencing to comprehensive mutation screening for deafness genes.
    Genet Test Mol Biomarkers. 19: 209-217.2015
  • Moteki H, Yoshimura H, Azaiez H, Booth KT, Shearer AE, Sloan CM, Kolbe DL, Murata T, Smith RJ, Usami S.
    USH2 Caused by GPR98 Mutation Diagnosed by Massively Parallel Sequencing in Advance of the Occurrence of Visual Symptoms.
    Ann Otol Rhinol Laryngol. 124: 123-128. 2015
  • Yoshimura H, Oshikawa C, Nakayama J, Moteki H, Usami S.
    Identification of a novel CLRN1 gene mutation in Usher syndrome type 3: two case reports.
    Ann Otol Rhinol Laryngol. 124: 94-99. 2015
  • Yoshimura H, Hashimoto T, Murata T, Fukushima K, Sugaya A, Nishio S, Usami S.
    Novel ABHD12 mutations in PHARC patients: the differential diagnosis of deaf-blindness.
    Ann Otol Rhinol Laryngol. 124: 77-83. 2015
  • Miyagawa M, Nishio S, Sakurai Y, Hattori M, Tsukada K, Moteki H, Kojima H, Usami S.
    The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.
    Ann Otol Rhinol Laryngol. 124: 193-204. 2015
  • Iwasa Y, Moteki H, Hattori M, Sato R, Nishio S, Takumi Y, Usami S.
    Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patients.
    Ann Otol Rhinol Laryngol. 124: 111-117. 2015
  • Tsukada K, Ichinose A, Miyagawa M, Mori K, Hattori M, Nishio S, Naito Y, Kitajiri S, Usami S.
    Detailed hearing and vestibular profiles in the patients with COCH mutations.
    Ann Otol Rhinol Laryngol. 124: 100-110. 2015
  • Miyagawa M, Nishio S, Hattori M, Takumi Y, Usami S.
    Germinal mosaicism in a family with BO syndrome.
    Ann Otol Rhinol Laryngol. 124: 118-122. 2015
  • Mori K, Moteki H, Kobayashi Y, Azaiez H, Booth KT, Nishio S, Sato H, Smith RJ, Usami S.
    Mutations in LOXHD1 gene cause various types and severities of hearing loss.
    Ann Otol Rhinol Laryngol. 124: 135-141. 2015
  • Mori K, Miyanohara I, Moteki H, Nishio S, Kurono Y, Usami S.
    Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness.
    Ann Otol Rhinol Laryngol. 124: 129-134. 2015
  • Nishio S, Hattori M, Moteki H, Tsukada K, Miyagawa M, Naito T, Yoshimura H, Iwasa Y, Mori K, Shima Y, Sakuma N, Usami S.
    Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.
    Ann Otol Rhinol Laryngol. 124: 6-48. 2015
  • Moteki H, Azaiez H, Booth KT, Hattori M, Sato A, Sato Y, Motobayashi M, Sloan CM, Kolbe DL, Shearer AE, Smith RJ, Usami S.
    Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.
    Ann Otol Rhinol Laryngol. 124: 177-183. 2015
  • Ichinose A, Moteki H, Hattori M, Nishio S, Usami S.
    Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritance.
    Ann Otol Rhinol Laryngol. 124: 142-147. 2015
  • Nishio S, Usami S.
    Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan.
    Ann Otol Rhinol Laryngol. 124: 49-60. 2015
  • Miyagawa M, Nishio S, Ichinose A, Iwasaki S, Murata T, Kitajiri S, Usami S.
    Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencing.
    Ann Otol Rhinol Laryngol. 124: 84-93. 2015
  • Sakuma N, Moteki H, Azaiez H, Booth KT, Takahashi M, Arai Y, Shearer AE, Sloan CM, Nishio S, Kolbe DL, Iwasaki S, Oridate N, Smith RJ, Usami S.
    Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing loss.
    Ann Otol Rhinol Laryngol. 124: 184-192. 2015
  • Moteki H, Shearer AE, Izumi S, Kubota Y, Azaiez H, Booth KT, Sato A, Sloan CM, Kolbe DL, Shearer AE, Smith RJ, Usami S.
    De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.
    Ann Otol Rhinol Laryngol. 124: 169-176. 2015
  • Miyagawa M, Nishio S, Hattori M, Moteki H, Kobayashi Y, Saton H, Watanabe T, Naito Y, Oshikawa C, Usami S.
    Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.
    Ann Otol Rhinol Laryngol. 124: 158-168. 2015
  • Tsukada K, Fukuoka H, Usami S.
    Vestibular functions of hereditary hearing loss patients with GJB2 mutations.
    Ann Otol Rhinol Laryngol. 124: 147-152. 2015
  • Tsukada K, Nishio S, Hattori M, Usami S.
    Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review.
    Ann Otol Rhinol Laryngol. 124: 61-76. 2015
  • Miyagawa M, Nishio S, Kumakawa K, Usami S.
    Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristics.
    Ann Otol Rhinol Laryngol. 124: 148-157. 2015
  • Suzuki N, Okamura K, Yano T, Moteki H, Kitoh R, Takumi Y, Usami S.
    Silicone impression material foreign body in the middle ear: Two case reports and literature review.
    Auris Nasus Larynx. 42: 419-423. 2015
  • Taniguchi M, Matsuo H, Shimizu S, Nakayama A, Suzuki K, Hamajima N, Shinomiya N, Nishio S, Kosugi S, Usami S, Ito J, Kitajiri S.
    Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population.
    J Hum Genet. 60: 613-617. 2015
  • Gavilan J, Adunka O, Aqrawal S, etc.44 Usami S, etc. 4
    Qulity standards for bone conduction implants.
    Acta otolaryngol. 135: 1277-1285. 2015

2014年

  • Yano T, Nishio S, Usami S, deafness gene study consortium.
    Frequency of mitochondrial mutation in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening
    J Hum Genet. 59(2): 100-106. 2014
  • Miyagawa M, Nishio S, Usami S.
    Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study
    J Hum Genet. 59(2): 262-268. 2014
  • Yoshimura Y, Iwasaki S, Nishio S, Kumakawa K, Tono T, Kobayasi Y, Sato H, Nagai K, Ishikawa K, Ikezono T, Naito Y, Fukushima K, Oshikawa C, Kimitsuki T, Nakanishi H, Usami S.
    Massively Parallel DNA Sequencing Facilitates Diagnosis of Patients with Usher Syndrome Type 1
    PLoS ONE. 9(3): e90688. 2014
  • Ishikawa K, Naito T, Nishio S, Iwasa Y, Nakamura K, Usami S, Ichimura K.
    A Japanese family showing high-frequency hearing loss with KCNQ4 and TECTA muations.
    Acta Otolaryngol 134(6): 557-563. 2014
  • Yoshimura H, Takumi Y, Nishio S, Suzuki N, Iwasa Y,Usami S.
    Deafness Gene Expression Patterns in the Mouse Cochlea Found by Microarray Analysis
    PLoS ONE. 9(3): e92547. 2014
  • Usami S, Moteki H, Tsukada K, Miyagawa M, Nishio S, Takumi Y, Iwasaki S, Kumakawa K, Naito Y, Takahashi H, Kanda Y, Tono T.
    Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries Acta Otolaryngol. 134(7): 717-727. 2014
  • Abe S, Nagano M, Nishio S, Kumakawa K, Usami S.
    High-frequency involved hearing loss Caused by Novel Mitochondrial DNA Mutation in 16S Ribosomal RNA Gene Otol Neurotol. 35(6): 1087-1090. 2014
  • Tian G, Sawashita J, Kubo J, Nishio S, Hashimoto S, Suzuki N, Yoshimura H, Tsuruoka M, Wang Y, Liu H, Xu Z, Mori M, Kitano M, Hosoe K, Takeda T, Usami S, Higuchi K.
    Ubiquinol-10 supplementation activates mitochondria functions to decelerate senescene in senescene-accelerated mice
    Antioxid Redox Signal 20(16): 2606-2620. 2014
  • Moteki H, Suzuki M, Naito Y, Fujiwara K, Oguchi K, Nishio S, Iwasaki S, Usami S.
    Evaluation of cortical processing of language by use of positron emission tomography in hearing loss children with congenital cytomegalovirus infection
    Int J Pediatr Otorhinolaryngol 78(2): 285-289. 2014
  • Fukumoto M, Amanuma T, Kuwahara Y, Shimura T, Suzuki M, Mori S, Kumamoto H, Saito Y, Ohkubo Y, Duan Z, Sano K, Oguchi T, Kainuma K, Usami S, Kinoshiya K, Lee I, Fukumoto M.
    Guanine nucleotide-binding protein 1 is one of the key molecules contributing to cancer cell radioresistance
    Cancer Sci 105(10): 1351-1359. 2014
  • Takumi Y, Matsumoto N, Byunghyun C, Ono H, Mori K, Tsukada K, Ichinose A,Yoshimura H, Iwasaki S, Komune S, usami S.
    A clinical experience of 'STAMP' plate-guided Bonebridge implantation
    Acta Otolaryngologica 134(10): 1042-1046. 2014
  • Shearer AE, Eppsteiner RW, Booth KT, Ephraim SS, Gurrola J2nd, Simpson A, Black-Ziegelbein EA, Joshi S, Ravi H,Giuffre AC, Happe S, Hildebrand MS, Azaiez H, Bayazit YA, Erdai ME, Lopez-Escamez JA, Gazquez I, Tamayo ML, Gelvez NY, Leal GL, Jalas C, Ekstein J, Yang T, Usami S, Kahrizi K, Bazazzadegan N, Najmabadi H, Scheetz TE, Braun TA, Casavant TL, LeProust EM, Smith RJ.
    Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants
    Am J Hum Genet 95(4): 445-453 2014
  • Takumi Y, Nishio S, Mugridge K, Oguchi T, Hashimoto S, Suzuki N, Iwasaki S, Jolly C, Usami S.
    Gene expression pattern after Insertion of Dexamethasone-Eluting electrode into the Guinea Pig Cochlea
    PLoS ONE 9(10): e110238. 2014
  • Nakagawa T, Kumakawa K, Usami S, Hato N, Tabuchi K, Takahashi M, Fujiwara K, Sasaki A, Komune S, Sakamoto T, Hiraumi H, Yamamoto N, Tanaka S, Tada H, Yamamoto M, Yonezawa A, Ito-Ihara T, Ikeda T, Shimizu A, Tabata Y, Ito J.
    A randomized controlled clinical trial of topical insulin-like growth factor-1 therapy for sudden deafness refractory to systemic corticosteroid treatment
    BMC Medicine 12: 2-8. 2014
  • Matsumoto N, Takumi Y, Cho B, Mori K, Usami S, Yamashita M, hashizume M, Komune S.
    Template-guided implantation of the Bonebridge: clinaical experience
    Eur Arch Otorhinolaryngol 2014

2013年

  • Iwasaki S, Sano H, Nishio S, Takumi Y, Okamoto M, Usami S, Ogawa K.
    Hearing handicap in adults with unilateral deafness and bilateral hearing loss
    Otol Neurotol. 34(4): 644-649. 2013
  • Yoshida H, Takahashi H, Kanda Y,Usami S.
    Long term speech perception after cochlear implant in pediatric patients with GJB2 mutations
    Auris Nasus Larynx　40(5): 435-439.2013
  • Ganaha A, Kaname T, Yanagi K, Naritomi K, Tono T, Usami S, Suzuki M.
    Pathogenic substitution of IVS15+5G>A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome
    BioMed Central. 14;56: 2-10. 2013
  • Naito T, Nishio S, Iwasa Y, Yano T, Kumakawa K, Abe S, Ishikawa K, Kojima H, Namba A, Oshikawa C, Usami S.
    Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation
    PLoS ONE 8(5): e63231. 2013
  • Iwasaki S, Usami S.
    Hearing loss in children with congenital cytomegalovirus infection
    INTECH　chapter1.1-15. 2013
  • Van de Heyning P. Adunka O. Arauz S. L. Atlas M. Baumgartner W. D. Brill, S. Bruce, I. Buchman C. Caversaccio M. Dillon M. Eikelboom R. Eskilsson G. Gavilan J. Godey B. Green K. Gstoettner W. Hagen R. Han, D. Iwasaki S. Kameswaran M. Karltorp E. Kleine Punte A. Kompis M. Kuthubutheen, J. Kuzovkov, V. Lassaletta L. Li Y. Lorens A. Manikoth M. Martin J. Mlynski R. Mueller J. O'Driscoll M. Parnes L. Pillsbury H. Prentiss S. Pulibalathingal S. Raine C. H. Rajan G. Rajeswaran R. Riechelmann H. Rivas A. Rivas J. A. Senn P. Skarzynski P. H. Sprinzl G. Staecker H. Stephan K. Sugarova S. Usami S. Wolf-Magele A. Yanov Y. Zernotti M. E. Zimmerman, K. Zorowka P. Skarzynski H. Standards of practice in the field of hearing implants
    Cochlear Implants Int. 14(2): 1-5. 2013
  • Ogawa A, Shimizu A, Yoshizaki S, Kanda Y, Kumagami H, Takahashi H, Usami S.
    A case of palmoplantar lichen planus in a patient with congenital sensorineural deafness
    Clin Exp dermatol. 38(1): 30-32. 2013
  • Kainuma K, Yano T, Kitoh R, Naito T, Usami S.
    Prevalence of level V metastasis in head and neck squamous cell carcinoma
    Acta Otolaryngol. 133(2): 218-224. 2013
  • Yoshimura H, Iwasaki S, Kanda Y, Nakanishi H, Murata T, Iwasa Y, Nishio S, Takumi Y, Usami S.
    An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysis.
    Int J Pediatr Otorhinolaryngol. 77(2): 298-302. 2013
  • Miyagawa M, Naito T, Nishio S, Kamatani N, Usami S.
    Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients
    PLoS ONE 8(8): e71381. 2013
  • Miyagwa M,Nishio S, Ikeda T, Fukushima K, Usami S.
    Massively parallel DNA sequencing successfully identifies new causative
    mutations in deafness genes in patients with cochlear implantation and EAS.
    PLoS ONE 8(10): e75793. 2013
  • Iwasa Y, Nishio S, Yoshimura H, Kanda Y, Kumakawa K, Abe S, Naito Y, Nagai K, Usami S.
    OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.
    BMC Med Genet. 14(1): 95. 2013
  • Tsukada K, Moteki H, Fukuoka H, Iwasaki S, Usami S.
    Effects of EAS cochlear implantation surgery on vestibular function
    Acta Otolaryngol. 133(11): 1128-1132. 2013
  • Moteki H, Suzuki M, Naito Y, Fujiwara K, Oguchi K, Nishio S, Iwasaki S, Usami S.
    Evaluation of cortical processing of language by use of positron emission tomography in hearing loss children with congenital cytomegalovirus infection.
    Int J Pediatr Otorhinolaryngol. 78: 285-289. 2013
  • Skarzynski H. van de Heyning P. Agrawal S. Arauz S. L. Atlas M. Baumgartner W. Caversaccio M. de Bodt M. Gavilan J. Godey B. Green K. Gstoettner W. Hage R. Han D. Kameswaran M. Karltorp E. Kompi M. Kuzovkov V. Lassaletta L. Levevre F. Li Y. Manikoth M. Martin J. Mlynski R. Mueller J. O'Driscoll M. Parne L. Prentiss S. Pulibalathingal S. Raine C. H. Rajan G. Rajeswaran R. Rivas J. A. Rivas A. Skarzynski P. H. Sprinzl G. Staecker H. Stephan K. Usami S. Yanov Y. Zernotti M. E. Zimmermann K. Lorens A. Mertens G.
    Towards a consensus on a hearing preservation classification system
    Acta Otolaryngol Suppl. 564: 2-13. 2013

2012年

  • Fukuoka H, Takumi Y, Tsukada K, Miyagawa M, Oguchi T, Ueda H, Kadoya M, Usami S.
    Comparison of the diagnostic value of 3T-MRI after intratympanic injection of GBCA,electrocochleography,and glycerol test in patients with Meniere's disease. 
    Acta Otolaryngol. 132:141-145. 2012
  • Iwasaki S. Nishio S., Moteki H., Takumi Y., Fukushima K., Kasai N., Usami S.
    Language development in Japanese children who receive cochlear implant and/or hearing aid
    Int J Pediatr Otorhinolaryngol. 76(3):433-438. 2012
  • Iwasaki S. Suzuki H. Moteki H. Miyagawa M. Takumi Y. Usami S.
    Expeprience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosis
    Acta Oto-Laryngol 132(6); 676-682. 2012
  • Usami S. Nishio S. Nagano M. Abe S. Yamaguchi T.
    Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study
    PLOS ONE. 7(2): e31276. 2012
  • Usami, S. Abe, S. Nishio, S. Sakurai, Y. Kojima, H. Tono, T. Suzuki, N.
    Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis
    Clin Genet. 82(6):514-520. 2012
  • Usami S. Miyagawa M. Nishio S. Moteki H. Takumi Y. Suzuki M. Kitano Y. Iwasaki S.
    Patients with CDH23 mutations and the 1555A>G mitochondrial mutations are good candidates for electric acoustic stimulation(EAS)
    Acta Otolaryngol. 132;377-384. 2012
  • Nakatani T. Usami S. Itoh T.
    Phylogeography of the genus Erebia(Lepidoptera,Nymphalidae) in Bulgaria, inferred by mitochondrial DNA
    Lepidoptera Science. 63; 25-36. 2012
  • Fujiyoshi A. Fukushima K. Taguchi T. Omori K. Kasai N. Nishio S. Sugaya A. Nagayasu R. Konishi T. Sugishita S. Fujita J. Nishizaki K. Shiroma M.
    Syntactic Development in Japanese Hearing-Impaired Children
    Annals of Otology,Rhinology & Laryngology. 121(4); 28-34. 2012
  • Moteki H.Nishio S.Hashimoto S.Takumi Y. Iwasaki S.Takeichi N.Fukuda S.Usami S.
    TECTA mutations in Japanese with mid-Frequency hearing loss affected by zona pellucida domain protein secretion
    J Hum Genet. 57(9); 587-592. 2012
  • Miyagawa M. Nishio S. Usami S.
    Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study
    PLOS ONE. 7(8): e40366. 2012
  • Oguchi T. Suzuki N. Hashimoto S. Chaudhry G.A. Chaudhry F.A. Usami S. Ottersen O.P.
    Inner hair cells of mice express the glutamine transporter SAT1
    Hear Res. 292:59-63. 2012
  • Ogawa A. Shimizu A. Yoshizaki S. Kanda Y. Kumagami H. Takahashi H. Usami S.
    A case of palmoplantar lichen planus in a patient with congenital sensorineural deafness
    Clin Exp dermatol. 38(1): 30-32. 2012
  • Kainuma K. Yano T. Kitoh R. Naito T. Usami S.
    Prevalence of level V metastasis in head and neck squamous cell carcinoma
    Acta Otolaryngol. 133(2): 218-224. 2012
  • Yoshimura H. Iwasaki S. Kanda Y. Nakanishi H. Murata T. Iwasa Y. Nishio S. Takumi Y. Usami S.
    An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysis
    Int J Pediatr Otorhinolaryngol. 77(2): 298-302. 2012
  • Nakatani T. Usami S. Itoh T.
    Historic cycles of fragmentation and expansion in the Alpine butterfly Erebia ligea(Lepidoptera,Nymphalidae) on the Japanese archipelago, inferred from mitochondrial DNA
    Lepidoptera Science. 63(4): 204-216. 2012
  • Usami S. Miyagawa M. Suzuki N. Nishio S.
    GENETICS AND PRESBYCUSIS-MONOGENIC FORM OF AGE RELATED HEARING IMPAIRMENT CAUSED BY CDH23 MUTATIONS
    Journal of hearing Science. 2(4): 1-4. 2012