Aiden Eliot Shearer (A Eliot Shearer, Eliot Shearer, A Eliot Shearer)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 21

Top Venues

Human genetics

The Laryngoscope

Laryngoscope investigative otolaryngology

Scientific reports

University of Iowa (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Iowa Aug 01 2009 - May 16 2014

United States

PHD :: Dept of Molecular Physiology and Biophysics

Ohio University Aug 20 2003 - Jun 01 2007

United States

BSC :: Honors Tutorial College

Publications

Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics 143 (3) (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics 143 (3) (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics 143 (3) (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics 143 (3) (2024)
Monica Rodriguez-Valero, Adrian Pastolero, Shelby Redfield, Alma Medrano, Melania Abreu-Gonzalez, Jose Francisco Gallardo-Ollervides, Juan Carlos Cisneros Lesser, Maria Fernanda Hinojosa Valencia, Dennis Poe, Aiden Eliot Shearer
High prevalence of syndromic hearing loss in Mexican children undergoing cochlear implantation. Laryngoscope investigative otolaryngology 9 (3) (2024)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human genetics (2024)
Monica Rodriguez-Valero, Adrian Pastolero, Shelby Redfield, Alma Medrano, Melania Abreu-Gonzalez, Jose Francisco Gallardo-Ollervides, Juan Carlos Cisneros Lesser, Maria Fernanda Hinojosa Valencia, Dennis Poe, Aiden Eliot Shearer
High prevalence of syndromic hearing loss in Mexican children undergoing cochlear implantation. Laryngoscope investigative otolaryngology 9 (3) (2024)
Greg R Licameli, Alicia Wang, Guangwei Zhou, David Faller, Margaret A Kenna, Dennis S Poe, Aiden Eliot Shearer, Linda Oster, Jacob R Brodsky
Vestibular Preservation in Pediatric Cochlear Implantation. The Laryngoscope (2023)
Shelby E Redfield, Pedro De-la-Torre, Mina Zamani, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A Kenna, Go Hun Seo, Sadaf Naz, Hamid Galehdari, Artur A Indzhykulian, Aiden Eliot Shearer, Barbara Vona
PKHD1L1 , A Gene Involved in the Stereociliary Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss. medRxiv : the preprint server for health sciences (2023)
Jalen Benson, Candace Stewart, Margaret A Kenna, Aiden Eliot Shearer
Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients. The Laryngoscope 133 (6) (2022)
Aiden Eliot Shearer, Alicia Wang, Maranda Lawton, Catherine Lachenauer, Jacob R Brodsky, Dennis S Poe, Margaret A Kenna, Greg R Licameli
Pain at the Cochlear Implant Site Requiring Device Removal in Pediatric Patients. The Laryngoscope 132 (10) (2022)
Julia Perry, Shelby E Redfield, Andrea Oza, Stephanie Rouse, Candace K Stewart, Harmon Khela, Tarika Srinivasan, Victoria Albano, Aiden Eliot Shearer, Margaret A Kenna
Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss. The Laryngoscope (2022)
Jalen Benson, Candace Stewart, Margaret A Kenna, Aiden Eliot Shearer
Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients. The Laryngoscope 133 (6) (2022)
Jalen Benson, Candace Stewart, Margaret A Kenna, Aiden Eliot Shearer
Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients. The Laryngoscope 133 (6) (2022)
Wafaa Abbasi, Courtney E French, Shira Rockowitz, Margaret A Kenna, Aiden Eliot Shearer
Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings. Human genetics (2021)
Aiden Eliot Shearer, Marlan R Hansen
Auditory synaptopathy, auditory neuropathy, and cochlear implantation. Laryngoscope investigative otolaryngology 4 (4) (2019)
Aiden Eliot Shearer, Jun Shen, Sami S Amr, Cynthia C Morton, Richard J H Smith, null null
A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Aiden Eliot Shearer, Viral D Tejani, Carolyn J Brown, Paul J Abbas, Marlan R Hansen, Bruce J Gantz, Richard J H Smith
In Vivo Electrocochleography in Hybrid Cochlear Implant Users Implicates TMPRSS3 in Spiral Ganglion Function. Scientific reports 8 (1) (2018)

Aiden Eliot Shearer.css-eqlu8i{font-size:small;padding-left:4px;} (A Eliot Shearer, Eliot Shearer, A Eliot Shearer)

Publication Activity (10 Years)

Top Topics

Top Venues

Aiden Eliot Shearer (A Eliot Shearer, Eliot Shearer, A Eliot Shearer)