Aiden Eliot Shearer M.D., PH.D.
Ear-Nose and Throat Doctor (ENT)
200 Hawkins Dr Dept. Of Otolaryngol Iowa City IA, 52242About
Dr. Aiden Shearer is an ear, nose and throat (ENT) doctor, also known as an otolaryngologist, practicing in Iowa City, IA. Dr. Shearer specializes in diseases and disorders of the ear, nose and throat as well as other parts of the head and neck. Such structures an ENT may work on include the sinuses, larynx (voice box) and mouth in addition to the ear, nose and throat. There are seven areas of expertise that an ENT might specialize in, and these are: allergies; facial reconstructive surgery; head and neck; laryngology; otology/neurotology; pediatric otolaryngology; and rhinology.
Education and Training
Baylor College of Medicine, Houston, Texas
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Bacterial spore inhibition and inactivation in foods by pressure, chemical preservatives, and mild heat.
- Evaluation of a polymerase chain reaction-based system for detection of Salmonella enteritidis, Escherichia coli O157:H7, Listeria spp., and Listeria monocytogenes on fresh fruits and vegetables.
- A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family.
- Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.
- A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.
- Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population.
- Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
- Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with
- DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
- Deafness in the genomics era.
- Solution-based targeted genomic enrichment for precious DNA samples.
- Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
- Genetics: advances in genetic testing for deafness.
- Pre-capture multiplexing improves efficiency and cost-effectiveness of targeted genomic enrichment.
- TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss.
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