Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes

Genomic sequencing.

1984 • 8,343 citations

How the ear's works work

1989 • 852 citations

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

2000 • 463 citations

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling

1999 • 440 citations

RNA surveillance: unforeseen consequences for gene expression, inherited genetic disorders and cancer

1999 • 400 citations

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1998 • 325 citations

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

1999 • 259 citations

Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains

1993 • 218 citations

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

1999 • 186 citations

INHERITED HEARING DEFECTS IN MICE

1995 • 157 citations

Otogelin: A glycoprotein specific to the acellular membranes of the inner ear

1997 • 141 citations

Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals

1999 • 122 citations

mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)

1997 • 104 citations

Inner Ear and Kidney Anomalies Caused by IAP Insertion in an Intron of the Eya1 Gene in a Mouse Model of BOR Syndrome

1999 • 89 citations

Genetic Modification of Hearing in Tubby Mice: Evidence for the Existence of a Major Gene (moth1) Which Protects Tubby Mice from Hearing Loss

1999 • 77 citations

Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss

1999 • 52 citations

Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

1999 • 15 citations

Hear come more genes!

1998 • 14 citations