Shin-Ya Nishio
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Explore the profile of Shin-Ya Nishio including associated specialties, affiliations and a list of published articles.
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130
Citations
1613
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Recent Articles
1.
Maekawa K, Nishio S, Ishikawa K, Takahashi M, Kumakawa K, Okami M, et al.
Genes (Basel)
. 2025 Feb;
16(2).
PMID: 40004452
Background/objectives: Hearing loss is one of the most common sensorineural impairments, and approximately 60% of early-onset cases are due to genetic variations. The otogelin-like protein, encoded by the gene, is...
2.
Kumai T, Nishio S, Moteki H, Katada A, Usami S
Genes (Basel)
. 2025 Feb;
16(2).
PMID: 40004445
Background/objectives: The gene is reported to be the causative gene for non-syndromic recessive sensorineural hearing loss and auditory neuropathy spectrum disorder. About 300 variants have been reported, but there have...
3.
Maekawa K, Nishio S, Miyazaki H, Ohta Y, Oishi N, Kasai M, et al.
Genes (Basel)
. 2025 Jan;
16(1.
PMID: 39858639
belongs to the unconventional myosin superfamily, and the myosin IIIa protein localizes on the tip of the stereocilia of vestibular and cochlear hair cells. Deficiencies in have been reported to...
4.
Arai Y, Nishio S, Goto S, Kobayashi Y, Honkura Y, Ganaha A, et al.
Genes (Basel)
. 2025 Jan;
16(1.
PMID: 39858607
Background/objectives: The gene is responsible for autosomal recessive non-syndromic sensorineural hearing loss and is assigned as DFNB18B. To date, 44 causative variants have been reported to cause non-syndromic hearing loss....
5.
Otsuka S, Morimoto C, Nishio S, Morita S, Kikuchi D, Takahashi M, et al.
Genes (Basel)
. 2025 Jan;
16(1).
PMID: 39858604
Background/objectives: A heterozygous mutation in the gene is responsible for autosomal dominant non-syndromic hearing loss (DFNA6/14/38) and Wolfram-like syndrome, which is characterized by bilateral sensorineural hearing loss with optic atrophy...
6.
Steinacher C, Nishio S, Usami S, Dudas J, Rieder D, Rask-Andersen H, et al.
Int J Mol Sci
. 2024 Dec;
25(23).
PMID: 39684722
We determined the relative expression levels of the receptors , , , and and ligands , , , and with RNAseq analysis on fetal human inner ear samples, located TrkB...
7.
Yoshimura H, Takumi Y, Nishio S, Usami S
J Vis Exp
. 2024 Oct;
(212).
PMID: 39465961
Electric-acoustic stimulation (EAS) is a promising treatment to improve hearing ability in patients with high-frequency hearing loss (HL). In EAS surgeries, shorter electrodes have been preferred to avoid the presence...
8.
Usami S, Nishio S, Gavilan J, Acharya A, Hagr A, Lassaletta L, et al.
Acta Otolaryngol
. 2024 Oct;
144(11-12):602-609.
PMID: 39451138
Background: In cases of congenital sensorineural hearing loss, testing for genetic etiologies and congenital cytomegalovirus (cCMV) infection have become common practice. Aims/objectives: The purpose of this study is to determine...
9.
Usami S, Nishio S, Gavilan J, Van de Heyning P, Mertens G, Karltorp E, et al.
Acta Otolaryngol
. 2024 Oct;
144(10):542-551.
PMID: 39434647
Background: While cochlear implantation (CI) and electric acoustic stimulation (EAS) have a positive outcome in most cases, their effectiveness varies depending on the etiology of the hearing loss. Among the...
10.
Kitoh R, Nishio S, Sato H, Ikezono T, Morita S, Wada T, et al.
Auris Nasus Larynx
. 2024 Jul;
51(4):811-821.
PMID: 38968877
Objective: Acute sensorineural hearing loss represents a spectrum of conditions characterized by sudden onset hearing loss. The "Clinical Practice Guidelines for the Diagnosis and Management of Acute Sensorineural Hearing Loss"...