Eliot Shearer, MD, PhD
Assistant Professor of Otolaryngology Head and Neck Surgery
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing
Shearer, A.E., DeLuca, A.P., Hildebrand, M.S., Taylor, K.R., Gurrola, J., Scherer, S., Scheetz, T.E. and Smith, R.J., 2010.
Proceedings of the National Academy of Sciences. 2010.,107(49), pp.21104-21109
Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.
Shearer, A.E., Eppsteiner, R.W., Booth, K.T., Ephraim, S.S., Gurrola II, J., Simpson, A., Black-Ziegelbein, E.A., Joshi, S., Ravi, H., Giuffre, A.C. and Happe, S.,
The American Journal of Human Genetics. 2010, 95(4), pp.445-453.
A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children.
Shearer, A.E., Shen, J., Amr, S., Morton, C.C. and Smith, R.J.
Genetics in Medicine. 2019, 21(11), pp.2614-2630.
Dual-vector gene therapy restores cochlear amplification and auditory sensitivity in a mouse model of DFNB16 hearing loss.
Shubina-Oleinik, O., Nist-Lund, C., French, C., Rockowitz, S., Shearer, A.E. and Holt, J.R.
Science Advances, 2021, 7(51), p.eabi7629