Towards a consensus on a hearing preservation classification systemHenryk Skarżyńśki, Griet Mertens, Paul Van de Heyning et al.|Acta Oto-Laryngologica|2013Cited by 222
Genomic Structure and Identification of Novel Mutations in Usherin, the Gene Responsible for Usher Syndrome Type IIaMichael D. Weston, William J. Kimberling, Richard J. Smith et al.|The American Journal of Human Genetics|2000Cited by 180
Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing lossSatoko Abe, Yusuke Nakamura, Shin‐ichi Usami|Journal of Human Genetics|2003Cited by 134
Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data reported herein are available in the DDBJ/EMBL/GenBank databases; for details, see the Electronic-Database Information section of this article.Satoko Abe, Yusuke Nakamura, Toyomasa Katagiri et al.|The American Journal of Human Genetics|2003Cited by 127
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patientsKenji Asamura, Shin‐ichi Usami, Satoko Abe et al.|Auris Nasus Larynx|2005Cited by 20