Jeremy C. Kallman

A novel <i>DFNA9</i> mutation in the vWFA2 domain of <i>COCH</i> alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site‐specific vestibular and central oculomotor dysfunction

Valerie A. Street, Jeremy C. Kallman, Nahid G. Robertson et al. · American Journal of Medical Genetics Part A · 2005 · 57 citations

A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings

Naomi F. Bramhall, Jeremy C. Kallman, Aimee M. Verrall et al. · BMC Medical Genetics · 2008 · 25 citations · Full text

A DNA Variant within the MYO7A Promoter Regulates YY1 Transcription Factor Binding and Gene Expression Serving as a Potential Dominant DFNA11 Auditory Genetic Modifier

Valerie A. Street, Jin Li, Carol A. Robbins et al. · Journal of Biological Chemistry · 2011 · 16 citations · Full text

Resistance to Noise-Induced Hearing Loss in 129S6 and MOLF Mice: Identification of Independent, Overlapping, and Interacting Chromosomal Regions

Valerie A. Street, Sharon G. Kujawa, Ani Manichaikul et al. · Journal of the Association for Research in Otolaryngology · 2014 · 12 citations · Full text

Biology, Knockout Mouse, Genetics +12

In Search of the DFNA11 Myosin VIIA Low- and Mid-Frequency Auditory Genetic Modifier

Jeremy C. Kallman, James O. Phillips, Naomi F. Bramhall et al. · Otology & Neurotology · 2008 · 11 citations · Full text