A. Eliot Shearer

Boston Children's Hospital — United States

Neuroscience · Life Sciences

21h-index2.3kcitations48works3.42yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(31), Hearing Loss and Rehabilitation(12), Ear Surgery and Otitis Media(10), RNA regulation and disease(6), Vestibular and auditory disorders(5)

Publications48 total

DB-OTO Gene Therapy for Inherited Deafness
New England Journal of Medicine·2025· 15 cited
Oral and Oropharyngeal Manifestations of Child Abuse: A State‐of‐the‐Art Review
Otolaryngology·2025
Endocochlear potential contributes to hair cell death in TMPRSS3 hearing loss
Journal of Clinical Investigation·2025· 2 citedOpen Access
A Genomic Analysis of Usher Syndrome: Population‐Scale Prevalence and Therapeutic Targets
American Journal of Medical Genetics Part C Seminars in Medical Genetics·2025· 3 citedOpen Access
Sex Differences in B Cells From the Joints of Children With Oligoarticular Juvenile Idiopathic Arthritis
Arthritis & Rheumatology·2025Open Access
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets
2025· 1 citedOpen Access
Predictors of Posttransplant Lymphoproliferative Disease in Pediatric Patients
The Laryngoscope·2025· 1 citedOpen Access
Novel Phenotypes and Genotype–Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome
Clinical Genetics·2025· 5 citedOpen Access
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes
npj Genomic Medicine·2024· 7 citedOpen Access
Pediatric sporadic Burkitt lymphoma of the head and neck: A case series and analysis of national trends
International Journal of Pediatric Otorhinolaryngology·2024
Long-Read Sequencing Increases Diagnostic Yield for Pediatric Sensorineural Hearing Loss
2024Open Access
High prevalence of syndromic hearing loss in Mexican children undergoing cochlear implantation
Laryngoscope Investigative Otolaryngology·2024· 1 citedOpen Access
The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis
Human Genetics·2024· 6 citedOpen Access
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss
Human Genetics·2024· 6 citedOpen Access
<i>PKHD1L1</i> , A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss
2023· 2 citedOpen Access
Vestibular Preservation in Pediatric Cochlear Implantation
The Laryngoscope·2023· 2 cited
Spiral Ganglion Neuron Regeneration in the Cochlea: Regeneration of Synapses, Axons, and Cells
Springer handbook of auditory research·2023· 1 cited
Genotype-Phenotype Correlations in &lt;i&gt;TMPRSS3&lt;/i&gt; (DFNB10/DFNB8) with Emphasis on Natural History
Audiology and Neurotology·2023· 6 citedOpen Access
Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss
The Laryngoscope·2022· 27 cited
Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients
The Laryngoscope·2022· 10 citedOpen Access
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Frequent Co-authors

Richard J. Smith(21), Michael S. Hildebrand(10), Margaret A. Kenna(9), Shelby Redfield(8), Kevin T. Booth(5), Marlan R. Hansen(5), Greg R. Licameli(5), Christina Sloan-Heggen(4), Carla Nishimura(4), Héla Azaiez(4), Diana L. Kolbe(4), P.L.M. Huygen(4), E. Ann Black-Ziegelbein(3), Thomas L. Casavant(3), Terry A. Braun(3), William J. Kimberling(3), Adam P. DeLuca(3), Bruce J. Gantz(3), Melanie Bahlo(3), Courtney E. French(3)