Shin‐ichi Usami - Concepedia

Author

Shin‐ichi Usami

Also Known As

David Steward, E. Aten, Kazuyuki Kainuma, Lassaletta, Luis, S Usami, S. Usami, S.-I. Usami, S.-i. Usami, SHINICHI USAMI, Shin-Ichi Usami

503

Publications

13.2K

Citations

H-Index

183

Concepts

All Affiliations

Shinshu University Hirosaki University Toranomon Hospital Mita Hospital Kyushu University

About

Shin‐ichi Usami is an author at Shinshu University specializing in medicine, audiology, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	81	4.2K
2	Arts	27	39	2.2K
3	Health Sciences	22	27	1.4K
4	Natural Sciences	4	4	133
5	Engineering	2	2	59

Shin‐ichi Usami

228

Publications

11.3K

Citations

H-Index

Page 1

	Year	Citations
Organization of AMPA Receptor Subunits at a Glutamate Synapse: A Quantitative Immunogold Analysis of Hair Cell Synapses in the Rat Organ of Corti Atsushi Matsubara, Jon Henrik Laake, Svend Davanger, Journal of Neuroscience	1996	424
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations Shin‐ichi Usami, Satoko Abe, Mike D. Weston, Human Genetics Pds MutationsNon-syndromic Hearing LossVestibular SystemHealth SciencesMedicine	1999	315
Differential Localization of δ Glutamate Receptors in the Rat Cerebellum: Coexpression with AMPA Receptors in Parallel Fiber–Spine Synapses and Absence from Climbing Fiber–Spine Synapses Alf S. Landsend, Mahmood Amiry‐Moghaddam, Atsushi Matsubara, Journal of Neuroscience	1997	280
Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese Koji Tsukamoto, Hiroaki Suzuki, Daisuke Harada, European Journal of Human Genetics Unique SpectrumMendelian DisorderGenetic DisorderMedicineGenetics	2003	255
Towards a consensus on a hearing preservation classification system Henryk Skarżyńśki, Paul Van de Heyning, Sumit Agrawal, Acta Oto-Laryngologica	2013	215
Prevalence of mitochondrial gene mutations among hearing impaired patients Shin‐ichi Usami Journal of Medical Genetics	2000	197
Towards a Unified Testing Framework for Single-Sided Deafness Studies: A Consensus Paper Paul Van de Heyning, Dayse Távora‐Vieira, Griet Mertens, Audiology and Neurotology	2016	182
A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene Guy Van Camp, Rikkert L. Snoeckx, Nele Hilgert, The American Journal of Human Genetics Stickler Syndrome IsAutoimmune DiseaseMendelian DisorderGenetic DisorderGenetics	2006	181
Genomic Structure and Identification of Novel Mutations in Usherin, the Gene Responsible for Usher Syndrome Type IIa Michael D. Weston, James D. Eudy, Shigetoshi Fujita, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsNovel MutationsMolecular Genetics	2000	180
Expression of the P2X<sub>2</sub>Receptor Subunit of the ATP-Gated Ion Channel in the Cochlea: Implications for Sound Transduction and Auditory Neurotransmission Gary D. Housley, Refik Kanjhan, Nicholas P. Raybould, Journal of Neuroscience	1999	173

Page 1